AU752132B2 - Irrigation solution and method for inhibition of pain, inflammation and spasm - Google Patents

Description

P/00/0011 Regulation 3.2

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT

ORIGINAL

C p® -I OMEROS MEDICAL SYSTEMS, INC Name of Applicant: Actual Inventor: Address for service in Australia: Invention Title: Gregory DEMOPULOS; Pamela Anne PIERCE; Jeffrey A.

HERZ

CARTER SMITH BEADLE 2 Railway Parade Camberwell Victoria 3124 Australia IRRIGATION SOLUTION AND METHOD INHIBITION OF PAIN, INFLAMMATION

SPASMS

FOR

AND

The following statement is a full description of this invention, including the best method of performing it known to us -1A- IRRIGATION SOLUTION AND METHOD FOR INHIBITION OF PAIN, INFLAMMATION AND SPASM I. Field of the Invention SThe present invention relates to surgical irrigation solutions and methods, and 5 particularly for anti-inflammatory, and anti-pain and anti-spasm surgical irrigation solutions.

II. Background of the Invention Arthroscopy is a surgical procedure in which a camera, attached to a remote light source and video monitor, is inserted into an anatomic joint knee,. shoulder, 10 etc.) through a small portal incision in the overlying skin and joint capsule. Through similar portal incisions, surgical instruments may be placed in the joint, their use guided by arthroscopic visualization. As arthroscopists' skills have improved, an increasing number of operative procedures, once performed by "open" surgical technique, now can be accomplished arthroscopically. Such procedures include, for example, partial meniscectiomies and ligament reconstructions in the knee, shoulder acromioplasties and rotator cuff debridements and elbow synovectomies. As a result of widening surgical indications and the development of small diameter arthroscopes, wrist and ankle arthroscopies also have become routine.

Throughout each arthroscopy, physiologic irrigation fluid normal saline or lactated Ringer's) is flushed continuously through the joint, distending the joint capsule and removing operative debris, thereby providing clearer intra-articular visualization. U.S. Patent 4,504,493 to Marshall discloses an isomolar solution of glycerol in water for a non-conductive and optically clear irrigation solution for arthroscopy.

Irrigation is also used in other procedures, such as intravascular diagnostic and therapeutic procedures, urologic procedures and the treatment of bums and any operative wounds. In each case, a physiologic fluid is used to irrigate a wound or body cavity or passage. Conventional physiologic irrigation fluids do not provide analgesic or anti-inflammatory effects.

Alleviating pain and suffering in postoperative patients is an area of special focus in clinical medicine, especially with the growing number of out-patient operations performed each year. The most widely used agents, cyclooxygenase inhibitors ibuprofen) and opioids morphine, fentanyl) have significant side effects, including gastrointestinal irritation/bleeding and respiratory depression. The high incidence of nausea and vomiting related to opioids is especially problematic in the postoperative period. Therapeutic agents aimed at treating postoperative pain 15 while avoiding detrimental side effects are not easily developed because the molecular targets for these agents are distributed widely throughout the body and mediate diverse physiological actions. Despite the significant clinical need to inhibit pain and inflammation, as well as vasospasm and smooth muscle spasm, methods for the delivery of pain, inflammation and spasm inhibitors at effective dosages while minimizing adverse systemic side effects have not been developed. As an example, conventional intravenous, oral or intramuscular) methods of administration of opiate agonists in therapeutic doses frequently is associated with significant adverse side effects, including severe respiratory depression, changes in mood and mental clouding and profound nausea and vomiting.

0•0' 25 Prior studies have demonstrated the ability of endogenous agents, such as serotonin (5-hydroxytryptamine, sometimes referred to herein as bradykinin and histamine, to produce pain and inflammation. Sicuteri, et. al., Serotonin- Bradykinin Potentiation in the Pain Receptors in Man, Life Sci. 4, pp. 309-316 (1965); Rosenthal, Histamine as the Chemical Mediator for Cutaneous Pain, J. Invest. Dermat. 69, pp. 98-105 (1977); Richardson, et. al., Identification of Serotonin M-Receptor Subtypes and their Specific Blockade by a New Class of Drugs, Nature 316, pp. 126-131 (1985); Whalley, et. al., The Effect of Kinin Agonists and Antagonists, Naunyn-Schmiedeb Arch. Pharmacol. 36, pp. 652-57 (1987); Lang, et. al., Chemo-Sensitivity of Fine Afferents from Rat Skin In Vitro, J. Neurophysiol. 63, pp. 887-901 (1990).

For example, 5-HT applied to a human blister base (denuded skin) has been demonstrated to cause pain that can be inhibited by 5-HT 3 receptor antagonists.

Richardson et al., 1985. Similarly, peripherally-applied bradykinin produces pain which can be blocked by bradykinin receptor antagonists. Sicuteri et al., 1965; Whalley et al., 1987; Dray, et. al., Bradykinin and Inflammatory Pain, Trends Neurosci. 16, pp. 99-104 (1993). Peripherally-applied histamine produces vasodilation, itching and pain which can be inhibited by histamine receptor antagonists. Rosenthal, 1977; Douglas, "Histamine and (Serotonin) and their Antagonists", in Goodman, et. al., ed., The Pharmacological Basis of Therapeutics, MacMillan Publishing Company, New York, pp. 605-638 (1985); Rumore, et. al., Analgesic Effects ofAntihistaminics, Life Sci 36, pp. 403-416 (1985). Combinations of these three agonists (5-HT, bradykinin and histamine) applied together have been demonstrated to display a synergistic pain causing effect, producing a long-lasting and intense pain signal. Sicuteri et al., 1965; 15 Richardson et al., 1985; Kessler, et. al., Excitation of Cutaneous Afferent Nerve Endings In Vitro by a Combination of Inflammatory Mediators and Conditioning Effect of Substance P, Exp. Brain Res. 91, pp. 467-476 (1992).

In the body, 5-HT is located in platelets and in central neurons, histamine is found in mast cells, and bradykinin is produced from a larger precursor molecule 20 during tissue trauma, pH changes, temperature changes, etc. Because 5-HT can be released in large amounts from platelets at sites of tissue injury, producing plasma levels 20-fold greater than resting levels (Ashton, et. al., Serotonin as a Mediator of Cyclic Flow Variations in Stenosed Canine Coronary Arteries, Circulation 73, pp. 572-578 (1986)), it is possible that endogenous 5-HT plays a role 25 in producing postoperative pain, hyperalgesia and inflammation. In fact, activated platelets have been shown to excite peripheral nociceptors in vitro. Ringkamp, M., et. al., Activated Human Platelets in Plasma Excite Nociceptors in Rat Skin, In Vitro, Neurosci. Lett. 170, pp. 103-106 (1994)). Similarly, histamine and bradykinin also are released into tissues during trauma. Kimura, et. al., Changes in Bradykinin Level in Coronary Sinus Blood After the Experimental Occlusion of a Coronary Artery, Am Heart J. 85, pp. 635-647 (1973); Douglas, 1985; Dray et. al. (1993).

In addition, prostaglandins also are known to cause pain and inflammation.

Cyclooxygenase inhibitors, ibuprofen, are commonly used to block the production of prostaglandins, thereby reducing prostaglandin-mediated pain and inflammation. Flower, et. al., Analgesic-Antipyretics and Anti-Inflammatory Agents; Drugs Employed in the Treatment of Gout, in Goodman, et. al., ed., The Pharmacological Basis of Therapeutics, MacMillan Publishing Company, New York, pp. 674-715 (1985). Cyclooxygenase inhibitors are associated with some adverse systemic side effects when applied conventionally. For example, indomethacin or keterolac have well recognized gastrointestinal and renal adverse side effects.

As discussed, 5-HT, histamine, bradykinin and prostaglandins cause pain and inflammation. The various receptors through which these agents mediate their effects on peripheral tissues have been known and/or debated for the past two decades.

Most studies have been performed in rats or other animal models. However, there are differences in pharmacology and receptor sequences between human and animal species. There have been no studies conclusively demonstrating the importance of 5-HT, bradykinin or histamine in producing postoperative pain in humans.

Furthermore, antagonists of these mediators currently are not used for postoperative pain treatment. A class of drugs, termed 5-HT and norepinephrine 15 uptake antagonists, which includes amitriptyline, has been used orally with moderate success for chronic pain conditions. However, the mechanisms of chronic versus acute pain states are thought to be considerably different. In fact, two studies in the acute pain setting using amitiiptyline perioperatively have shown no pain-relieving effect of amitriptyline. Levine, et. al., Desipramine Enhances Opiate 20 Postoperative Analgesia, Pain 27, pp. 45-49 (1986); Kerrick, et. al., Low-Dose Amitriptyline as an Adjunct to Opioids for Postoperative Orthopedic Pain: a Placebo-Controlled Trial Period, Pain 52, pp. 325-30 (1993). In both studies the drug was given orally. The second study noted that oral amitriptyline actually produced a lower overall sense of well-being in postoperative patients, which may be due to the drug's affinity for multiple amine receptors in the brain.

Amitriptyline, in addition to blocking the uptake of 5-HT and norepinephrine, is a potent 5-HT receptor antagonist. Therefore, the lack of efficacy in reducing postoperative pain in the previously-mentioned studies would appear to conflict with the proposal of a role for endogenous 5-HT in acute pain. There are a number of reasons for the lack of acute pain relief found with amitriptyline in these two studies.

The first study used amitriptyline preoperatively for one week up until the night prior to surgery whereas the second study only used amitriptyline postoperatively.

Therefore, no amitriptyline was present in the operative site tissues during the actual tissue injury phase, the time at which 5-HT is purported to be released.

Amitriptyline is known to be extensively metabolized by the liver. With oral administration, the concentration of amitriptyline in the operative site tissues may not have been sufficiently high for a long enough time period to inhibit the activity of postoperatively released 5-HT in the second study. Since multiple inflammatory mediators exist, and studies have demonstrated synergism between the inflammatory mediators, blocking only one agent (5-HT) may not sufficiently inhibit the inflammatory response to tissue injury.

There have been a few studies demonstrating the ability of extremely high concentrations 3% solutions 10- 30 mg per milliter) of histamine, (H 1 receptor antagonists to act as local anesthetics for surgical procedures. This anesthetic effect is not believed to be mediated via H1 receptors, but, rather, due to a non-specific interaction with neuronal membrane sodium channels (similar to the action of lidocaine). Given the side effects sedation) associated with these high "anesthetic" concentrations of histamine receptor antagonists, local administration of histamine receptor antagonists currently is not used in the perioperative setting.

III. Summary of the Invention The present invention provides the use of a composition for perioperatively inhibiting pain and inflammation, and/or spasm at a wound during an arthroscopic, urologic, open or other surgical or body cavity procedure by intraprocedurally applying the composition locally to the wound, wherein the composition comprises 20 a solution of a plurality of inhibitory agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the wound, wherein each agent is included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma concentration that would be 6 required to achieve the same level of inhibitory effect at the wound when delivered systemically.

The anti-pain/anti-inflammation agents in the solution include agents selected from the following classes of receptor antagonists, receptor agonists and enzyme inhibitors, each class acting through a differing molecular mechanism of action for pain and inflammation inhibition: serotonin receptor antagonists; (2) serotonin receptor agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein inhibitors; tachykinin receptor antagonists, including neurokininl and neurokinin 2 receptor subtype antagonists; calcitonin gene-related peptide (CGRP) receptor antagonists; interleukin receptor antagonists; inhibitors of enzymes active in the synthetic pathway for arachadonic acid metabolites, including phospholipase inhibitors, including

PLA

2 isoform inhibitors and PLCy isoform inhibitors, cyclooxygenase inhibitors, and lipoxygenase inhibitors; (10) prostanoid receptor antagonists including eicosanoid EP-1 and EP-4 receptor subtype antagonists and thromboxane receptor subtype antagonists; (11) leukotriene receptor antagonists including leukotriene B 4 receptor subtype antagonists and leukotriene D 4 receptor subtype antagonists; (12) opioid receptor agonists, including mu-opiate, delta-opiate, and kappa-opiate receptor subtype agonists; (13) purinoceptor agonists and antagonists including P2X receptor antagonists and P2Y receptor agonists; (14) adenosine triphosphate (ATP)sensitive potassium channel openers; and (15) calcium channel antagonists. Each of the above agents functions both as an anti-inflammatory agent and as an antinociceptive, anti-pain or analgesic, agent. The selection of agents from these classes of compounds is tailored for the particular application.

The invention also provides the use of a composition for inhibiting pain and inflammation at a wound during a medical procedure by applying the composition locally to the wound during the procedure, wherein the composition comprises a solution of the serotoniniA,1B,D,1F receptor agonist sumatriptan included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the wound when delivered systemically.

Several preferred embodiments of the solution of the present invention also include anti-spasm agents for particular applications. For example, anti-spasm agents may be included in solutions used for vascular procedures to limit vasospasm, and for urinary procedures to limit spasm in the urinary tract and bladder wall. For such applications, an anti-spasm agent is utilized in the solution.

For example, an anti-pain/anti-inflammation agent which also serves as an antispasm agent may be included. Suitable anti-inflammatory/anti-pain agents which also act as anti-spasm agents include serotonin receptor antagonists, tachykinin receptor antagonists, ATP-sensitive potassium channel openers and calcium channel antagonists. Other agents which may be utilized in the solution specifically for their anti-spasm properties including endothelin receptor antagonists and the nitric oxide donors (enzyme activators).

The present invention also provides a solution for perioperatively inhibiting pain and inflammation and/or spasm, for use in intraprocedural application to a wound during an arthroscopic, urologic, open or other surgical or body cavity procedure, comprising a solution of a plurality of inhibitory agents at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the wound when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents mixed together in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the wound.

The invention further provides the use of a composition for perioperatively inhibiting pain and inflammation, and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the composition locally to the vascular structure, wherein the composition comprises a solution of a plurality of inhibitory agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through distinct molecular mechanisms of action, wherein each class of agent is selected from the classes of receptor antagonists, receptor agonists, enzyme inhibitors, enzyme activators, ion channel openers, and receptor operated ion channel antagonists, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure, wherein each agent is included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically.

:°oooo The invention also provides a solution for perioperatively inhibiting pain and inflammation and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the solution to the vascular structure, comprising a solution of a plurality of inhibitory agents a concentration or dosage that is sufficient to provide a level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory S agents mixed together in a physiologic liquid carrier, the plurality of agents being 6c selected from a plurality of classes of agents that act through distinct molecular mechanisms of action, wherein each class of agent is selected from the classes of receptor antagonists, receptor agonists, enzyme inhibitors, enzyme activators, ion channel openers, and receptor operated ion channel antagonists, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure.

The invention further provides solution for perioperatively inhibiting pain and inflammation and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the solution to the vascular structure, comprising a solution of a plurality of inhibitory agents a concentration or dosage that is sufficient to provide a predetermined level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma oo concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents mixed together in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure.

The method of the present invention provides for the delivery of a dilute combination of multiple antagonists to the mediators of pain, inflammation and spasm and inhibitory receptor agonists directly to a wound, such as the joint tissue during arthroscopic procedures. Since the active ingredients in the solution are being applied directly to the operative tissues in a continuous fashion, the drugs may be used efficaciously at extremely low doses relative to those doses required for therapeutic effect when the same drugs are delivered orally, intramuscularly or intravascularly. The advantage of low doses of agents is three-fold. The most S important is the absence of systemic side effects which often limit the usefulness of 6d these agents. The low therapeutic dosages utilized in the solution of the present invention minimize es S S S S

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*555 0 S S intravascular absorption of the included agents, thereby also minimizing systemic effects. Additionally, the agents selected for particular applications in the solutions of the present invention are highly specific with regard to the mediators on which they work. This specificity is maintained by the low dosages utilized. Finally, the cost of these active agents per liter is extremely low.

Local administration of the agents via irrigation also guarantees a known concentration at the peripheral target site, regardless of interpatient variability in metabolism, blood flow, etc. Because of the direct mode of delivery, a therapeutic concentration is obtained instantaneously. Thus improved dosage control is provided.

Local administration of the active agents directly to a wound or operative site also substantially reduces degradation of the agents through extracellular processes, i.e., first and second pass metabolism, that would otherwise occur if the agents were given orally, intravenously or intramuscularly. This is particularly true for those active agents that are peptides, which are metabolized rapidly. For example, some agents in 15 the following classes are peptitic: bradykinin receptor antagonists; tachykinin receptor antagonists; opioid receptor agonists; CGRP receptor antagonists; and interleukin receptor antagonists. Local, continuous delivery to the wound or operative site minimizes degradation while also providing for the continuous replacement of that portion of the agent that may be degraded, to ensure that a local therapeutic concentration, sufficient to maintain receptor occupancy, is maintained throughout the duration of the operative procedure.

Local administration 'of the solution throughout a surgical procedure in accordance with the present invention produces a "preemptive analgesic" effect. By occupying the target receptors or inactivating targeted enzymes prior to the initiation of significant operative trauma locally, the agents of the present solution modulate signal transmission to preemptively inhibit the targeted pathologic process. If inflammatory mediators and processes are inhibited before they can exert tissue damage, the benefit is more substantial than if given after the damage has been initiated.

Inhibiting more than one inflammatory mediator by application of the multiple agent solution of the present invention is believed to dramatically reduce the degree of inflammation and pain. The irrigation solutions of the present invention include combinations of drugs, each effective against multiple anatomic receptors or enzymes.

The drug agents are thus simultaneously effective against a combination of pathologic processes, including pain and inflammation, vasospasm and smooth muscle spasm.

The action of these mediators is considered to be synergistic, in that the multiple receptor antagonists and inhibitory agonists of the present invention provide a disproportionately increased efficacy in combination relative to the efficacy of the individual agents. The synergistic action of several of the agents of the present invention are discussed, by way of example, below in the detailed descriptions of those agents.

In addition to arthroscopy, the solution of the present invention may also be applied locally to any human body cavity or passage, operative wound, traumatic wound bums) or in any operative/interventional procedure in which irrigation can be performed. These procedures include, but are not limited to, urological procedures, interventional cardiovascular diagnostic and/or therapeutic procedures, and oral, dental and periodontal procedures. As used herein throughout, the term "wound", unless otherwise specified, is intended to include surgical wounds, operative/interventional sites, traumatic wounds and burns.

Used intra-operatively, the solution should results in a clinically significant decrease in operative sit pain and inflammation relative to currently-used irrigation fluids, thereby decreasing the patient's postoperative analgesic opiate) requirement and, where appropriate, allowing earlier patient mobilization of the operative site. No extra effort on the part of the surgeon and operating room personnel is required to use the present solution relative to conventional irrigation fluids.

8a IV. Brief Description of the Drawings The present invention will now be described in greater detail, by way of example, with reference to the accompanying drawings in which: Figures 1, 2A and 2B provide charts of the percent of vasoconstriction versus time in control arteries, in the proximal segment of subject arteries, and in the distal segment of subject arteries, respectively, for the animal study described in Example VII herein demonstrating the effect on vasoconstriction of infusion with histamine and serotonin antagonists, used in the solutions of the present invention, during balloon angioplasty; and Figures 3 and 4 provide charts of plasma extravasation versus dosage of i: amitriptyline, used in the solution of the present invention, delivered intravenously and intra-articulary, respectively, to knee joints in which extravasation has been induced by introduction of 5-Hydroxytryptamine in the animal study described in Example VIII herein.

*o o V. Detailed Description of the Preferred Embodiment The irrigation solution of the present invention is a dilute solution of multiple pain/inflammation inhibitory agents and anti-spasm agents in a physiologic carrier.

The carrier is a fluid containing physiologic electrolytes, such as normal saline or lactated Ringer's solution. The carrier is preferably a liquid, but for some applications, bums, may be compounded as a paste or salve.

The anti-inflammation/anti-pain agents are selected from the group consisting of: serotonin receptor antagonists; serotonin receptor agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein inhibitors; tachykinin receptor antagonists, including neurokininl and neurokinin 2 receptor subtype antagonists; calcitonin gene-related peptide (CGRP) receptor antagonists; interleukin receptor antagonists; inhibitors of enzymes active in the synthetic pathway for arachadonic acid metabolites, including phospholipase inhibitors, including PLA 2 isoform inhibitors and PLCy isoform inhibitors cyclooxygenase 15 inhibitors, and lipooxygenase inhibitors; (10) prostanoid receptor antagonists including eicosanoid EP-1 and EP-4 receptor subtype antagonists and thromboxane receptor subtype antagonists; (11) leukotriene receptor antagonists including leukotrieneB 4 receptor subtype antagonists and leukotrieneD 4 receptor subtype antagonists; (12) opioid receptor agonists, including mu-opiate, delta-opiate, and kappa-opiate receptor subtype agonists; (13) purinoceptor agonists and antagonists including P2X receptor antagonists and P2Y receptor agonists; (14) adenosine triphosphate (ATP)-sensitive potassium channel openers; and (15) calcium channel antagonists. Suitable anti-inflammatory/anti-pain agents which also act as anti-spasm agents include serotonin receptor antagonists, tachykinin receptor antagonists, 25 ATP-sensitive potassium channel openers and calcium channel antagonists. Other agents which may be utilized in the solution specifically for their anti-spasm properties including endothelin receptor antagonists and the nitric oxide donors (enzyme activators).

In each of the surgical solutions of the present invention, the agents are included in low concentrations and are delivered locally in low doses relative to concentrations and doses required with conventional methods of drug administration to achieve the desired therapeutic effect. It is impossible to obtain an equivalent therapeutic effect by delivering similarly dosed agents via other intravenous, intramuscular or oral) routes of drug administration since drugs given systemically are subject to first- and second-pass metabolism. Each agent is preferably included at a low concentration of 0.1 to 10,000 nanomolar, except for cyclooxygenase inhibitors, which may be required at larger concentrations depending on the particular inhibitor selected. The exact agents selected for use in the solution, and the concentration of the agents, varies in accordance with the particular application, as described below.

A solution in accordance with the present invention can include just a single or multiple pain/inflammation inhibitory agent(s), a single or multiple anti-spasm agent(s), or a combination of both anti-spasm and pain/inflammation inhibitory agents from the enumerated classes, at low concentration. However, due to the aforementioned synergistic effect of multiple agents, and the desire to broadly block pain and inflammation, it is preferred that multiple agents be utilized.

The surgical solutions constitute a novel therapeutic approach to the delivery of multiple pharmacologic agents acting at distinct receptor and enzyme molecular targets. To date, pharmacologic strategies have focused on the development of highly specific drugs that are selective for individual receptor subtypes and enzyme isoforms 15 that mediate responses to individual signaling neurotransmitters and hormones. As an example, endothelin peptides are some of the most potent vasoconstrictors known.

Selective antagonists that are specific for subtypes of endothelin (ET) receptors are being sought by several pharmaceutical companies for use in the treatment of numerous disorders involving elevated endothelin levels in the body. Recognizing the 20 potential role of the receptor subtype ETA in hypertension, these drug companies specifically are targeting the development of selective antagonists to the ETA receptor subtype for the anticipated treatment of coronary vasospasm. This standard pharmacologic strategy, although well accepted, is not optimal since many other vasoconstrictor agents serotonin, prostaglandin, eicosanoid, etc.) simultaneously 25 may be responsible for initiating and -maintaining the vasospastic episode.

Furthermore, despite inactivation of a single receptor subtype or enzyme, activation of other receptor subtypes or enzymes and the resultant signal transmission often can trigger a cascade effect. This explains the significant difficulty in employing a single receptor-specific drug to block a pathophysiologic process in which multiple transmitters play a role. Therefore, targeting only a specific individual receptor subtype, such as ETA, is likely to be ineffective.

In contrast to the standard approach to pharmacologic therapy, the therapeutic approach of the present surgical solutions is based on the rationale that a combination of drugs acting simultaneously on distinct molecular targets is required to inhibit the full spectrum of events that underlie the development of a pathophysiologic state.

Furthermore, instead of targeting a specific receptor subtype alone, the surgical solutions are composed of drugs that target common molecular mechanisms operating in different cellular physiologic processes involved in the development of pain, inflammation, vasospasm, and smooth muscle spasm. In this way, the cascading of additional receptors and enzymes in the nociceptive, inflammatory and spasmodic pathways is minimized by the surgical solutions. In these pathophysiologic pathways, the surgical solutions inhibit the cascade effect both "upstream" and "downstream".

An example of "upstream" inhibition is the cyclooxygenase antagonists in the setting of pain and inflammation. The cyclooxygenase enzymes (COXi and COX 2 catalyze the conversion of arachidonic acid to prostaglandin H which is an intermediate in the biosynthesis of inflammatory and nociceptive mediators including prostaglandins, leukotrienes, and thromboxanes. The cyclooxygenase inhibitors block "upstream" the formation of these inflammatory and nociceptive mediators. This strategy precludes the need to block the interactions of the seven described subtypes of prostanoid receptors with their natural ligands. A similar "upstream" inhibitor 15 included in the surgical solutions is aprotinin, a kallikrein inhibitor. The enzyme kallikrein, a serine protease, cleaves the high molecular weight kininogens in plasma to produce bradykinins, important mediators of pain and inflammation. By inhibition of kallikrein, aprotinin effectively inhibits the synthesis of bradykinins, thereby providing an effective "upstream" inhibition of these inflammatory mediators.

S 20 The surgical solutions also make use of "downstream" inhibitors to control the pathophysiologic pathways. In vascular smooth muscle preparations that have been i precontracted with a variety of neurotransmitters serotonin, histamine, endothelin, and thromboxane) implicated in coronary vasospasm, ATP-sensitive potassium channel openers (KCOs) produce smooth muscle relaxation which is 25 concentration dependent (Quast et al., 1994; Kashiwabara et al., 1994). The KCOs, therefore, provide a significant advantage to the surgical solutions in the settings of vasospasm and smooth muscle spasm by providing "downstream" antispasmodic effects that are independent of the physiologic combination of agonists initiating the spasmodic event. Similarly, NO donors and voltage-gated calcium channel antagonists can limit vasospasm and smooth muscle spasm initiated by multiple mediators known to act earlier in the spasmodic pathway. These same calcium channel antagonists also can provide a "downstream" blockade of inflammation.

Moncada, Flower, R. and Vane, J. in Goodman's and Gilman's Pharmacological Basis of Therapeutics, (7th MacMillan Publ. Inc., pp. 660-5 (1995).

The following is a description of suitable drugs falling in the aforementioned classes of anti-inflammation/anti-pain agents, as well as suitable concentrations for use in solutions, of the present invention. While not wishing to be limited by theory, the justification behind the selection of the various classes of agents which is believed to render the agents operative is also set forth.

A. Serotonin Receptor Antagonists Serotonin is thought to produce pain by stimulating serotonin 2 (5-HT 2 and/or serotonin 3 (5-HT 3 receptors on nociceptive neurons in the periphery. Most researchers agree that 5-HT 3 receptors on peripheral nociceptors mediate the immediate pain sensation produced by 5-HT (Richardson et al., 1985). In addition to inhibiting 5-HT-induced pain, 5-HT 3 receptor antagonists, by inhibiting nociceptor activation, also may inhibit neurogenic inflammation. Barnes et. al., Modulation of Neurogenic Inflammation: Novel Approaches to Inflammatory Disease, Trends in Pharmacological Sciences 11, pp. 185-189 (1990). A study in rat ankle joints, however, claims the 5-HT 2 receptor is responsible for nociceptor activation by Grubb, et. al., A Study of 5-HT-Receptors Associated with Afferent Nerves 15 Located in Normal and Inflamed Rat Ankle Joints, Agents Actions 25, pp. 216-18 (1988). Therefore, activation of 5-HT 2 receptors also may play a role in peripheral pain and neurogenic inflammation.

One goal of the solution of the present invention is to block pain and a multitude of inflammatory processes. Thus 5-HT 2 and 5-HT 3 receptor antagonists 20 are both suitably used, either individually or together, in the solution of the present invention, as shall be described subsequently. Amitriptyline (ElavilTM) is a suitable 2 receptor antagonist for use in the present invention. Amitriptyline has been used clinically for numerous years as an anti-depressant, and is found to have beneficial effects in certain chronic pain patients. Metoclopramide (ReglanTM) is used clinically as an anti-emetic drug, but displays moderate affinity for the 5-HT 3 receptor and can inhibit the actions of 5-HT at this receptor, possibly inhibiting the pain due to release from platelets. Thus it also is suitable for use in the present invention.

Other suitable 5-HT 2 receptor antagonists include imipramine, trazadone, desipramine and ketanserin. Ketanserin has been used clinically for its antihypertensive effects. Hedner, et. al., Effects of a New Serotonin Antagonist, Ketanserin, in Experimental and Clinical Hypertension, Am J of Hypertension, pp. 317s-23s (Jul. 1988). Other suitable 5-HT 3 receptor antagonists include cisapride and ondansetron. Suitable serotoninlB receptor antagonists include yohimbine, N-[-methoxy-3- (4-methyl- -piperanzinyl)phenyl]-2'-methyl-4'- (5-methyl-i, 2, 4- .oxadiazol-3-yl)[1, 1-biphenyl]-4-carboxamide ("GR127935") and methiothepin.

-13- Therapeutic and preferred concentrations for use of these drugs in the solution of the present invention are set forth in Table 1.

Table 1 Therapeutic and Preferred Concentrations of Pain/Inflamnmation Inhibitory Agents Therapeutic Concentrations A-gent QNanomolar) Preferred Concentrations (Nanomolar) S-erotonin, Recept or Antaizonists: amutriptyline imipramine trazodone desipraiine ketanserin Serotonin 3 Receptor Antagonists: metoclopramide 0.1 -1,000 0.1- 1,000 0.1 -1,000 0.1 -1,000 0.1 -1,000 10 -10,000 0.1 -1,000 0.1 -1,000 0.1 -1,000 0.1 -1,000 50-500 50-500 50-500 50-500 50 -500 200 -2,000 cisapride ondansetron Se-rotoniniB (Human 1D,)Antagonists: yohimbine 20 -200 20 -200 50 -500 10- 500 1 -100 GR127935 methiothepin 0.1 500 B. Serotonin Receptor Agonists 5-H1TIB and 5-HT1D receptors are known to inhibit adenylate cyclase activity. Thus including a low dose of these serotoninIA, serotornilB and serotoninID receptor agonists in~ the solution should. inhibit neurons mediating pain and inflammation. The same action is expected from serotoninjE and serotoninIF receptor agonists because these receptors also inhibit adenylate cyclase.

Buspirone is a suitable IA receptor agonist for use in the present invention.

Sumnatriptan is a suitable I A, IB, ID and IF. receptor agonist. A suitable 1l3 and ID receptor agonist is dihydroergotarine. A suitable lE receptor agonist is ergonovine.

Therapeutic and preferred concentrations for these receptor agonists are provided in Table 2.

Table 2 Therapeutic and Preferred Concentrations of Pain/Inflamnmation Inhibitory Agents Therapeutic Concentrations Agent (an o m oar~ *5

S

SerotoninlA Agon ists: buspirone 1 -1,000 1 -1,000 Preferred Concentrations (Nanomolar) 10-200 10 -200 sumatriptan erotonin 1 aBgonists: dihydroergotanine sumnatriptan SerotoninIDAonists: dihydroergotarnine sumatriptan SerotoninlE Aonists: ergonovine SerotoninF Aonists: 0.1 1,000 1 1,3000 0.1 1,000 1 -1,000 10 100 10-200 10 -100 10 -200 10- 2,000 100 -1,000 sumatriptan1-1,0 1-1,000 10 -200 C. Histamine Receptor Antagonists Histamine receptors generally are divided into histamine 1 (HI) and histamine 2 (H2) subtypes. The classic inflammatory response to the peripheral administration of histamine is mediated via the H 1 receptor. Douglas, 1985. Therefore, the solution of the present invention preferably includes a histamine H 1 receptor antagonist.

Promethazine (PhenerganTM) is a commonly used anti-emetic drug which potently blocks H 1 receptors, and is suitable for use in the present invention. Interestingly, this drug also has been shown to possess local anesthetic effects but the concentrations necessary for this effect are several orders higher than that necessary to block H 1 receptors, thus, the effects are believed to occur by different mechanisms. The histamine receptor antagonist concentration in the solution is sufficient to inhibit H 1 receptors involved in nociceptor activation, but not to achieve a "local anesthetic" effect, thereby eliminating the concern regarding systemic side effects.

Histamine receptors also are known to mediate vasomotor tone in the 15 coronary arteries. In vitro studies in the human heart have demonstrated that the histamine 1 receptor subtype mediates contraction of coronary smooth muscle.

S.Ginsburg, et al., Histamine Provocation of Clinical Coronary Artery Spasm: Implications Concerning Pathogenesis of Variant Angina Pectoris, American Heart Vol. 102, pp. 819-822, (1980). Some studies suggest that histamine-induced 20 hypercontractility in the human coronary system is most pronounced in the proximal arteries in the setting of atherosclerosis and the associated denudation of the arterial endothelium. Keitoku, M. et al., Different Histamine Actions in Proximal and Distal Human Coronary Arteries in Vitro, Cardiovascular Research 24, pp. 614-622, (1990). Therefore, histamine receptor antagonists may be included in the cardiovascular irrigation solution.

Other suitable H 1 receptor antagonists include terfenadine, diphenhydramine and amitriptyline. Because amitriptyline is also effective as a serotonin 2 receptor antagonist, it has a dual function as used in the present invention. Suitable therapeutic and preferred concentrations for each of these H 1 receptor antagonists are set forth in Table 3.

Table 3 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent Nanomolar) (Nanomolar) -16- Histamine 1 Receptor Antagonists: promethazine 0.1 1,000 50-200 diphenhydramine 0.1 1,000 50 200 amitriptyline 0.1-1,000 50-500 terfenadine 0.1 1,000 50 500 D. Bradykinin Receptor Antagonists Bradykinin receptors generally are divided into bradykininI (B 1 and bradykinin 2

(B

2 subtypes. Studies have shown that acute peripheral pain and inflammation produced by bradykinin are mediated by the B 2 subtype whereas bradykinin-induced pain in the setting of chronic inflammation is mediated via the B1 subtype. Perkins, et. al., Antinociceptive Activity of the Bradykinin BJ and B2 Receptor Antagonists, des-Arg 9 [Leu 8 ]-BK and HOE 140, in Two Models of Persistent Hyperalgia in the Rat, Pain 53, pp. 191-97 (1993); Dray, et. al., Bradykinin andInflammatory Pain, Trends Neurosci 16, pp. 99-104 (1993), each of 10 which references is hereby expressly incorporated by reference.

At present, bradykinin receptor antagonists are not used clinically. These drugs are peptides (small proteins), and thus they cannot be taken orally, because they S"would be digested. Antagonists to B 2 receptors block bradykinin-induced acute pain and inflammation. Dray et. al., 1993. B 1 receptor antagonists inhibit pain in chronic inflammatory conditions. Perkins et al., 1993; Dray et. al., 1993. Therefore, o* depending on the application, the solution of the present invention preferably includes t either or both bradykinin B 1 and B 2 receptor antagonists. For example, arthroscopy is performed for both acute and chronic conditions, and thus an irrigation solution for arthroscopy could include both B 1 and B 2 receptor antagonists.

Suitable bradykinin receptor antagonists for use in the present invention include the following bradykininI receptor antagonists: the [des-Arg 10 derivative of D-Arg-(Hyp 3 -ThiS-D-Tic 7 -OicS)-BK ("the [des-Arg 10 derivative of HOE 140", available from Hoechst Pharmaceuticals); and [Leu 8 des-Arg 9 -BK. Suitable bradykinin 2 receptor antagonists include: [D-Phe7]-BK; D-Arg-(Hyp 3 -Thi 5 ,8-D-Phe 7 )-BK ("NPC 349"); D-Arg-(Hyp 3 -D-Phe 7 )-BK ("NPC 567"); and D-Arg-(-yp 3 -Thi-D-Tic 7 -Oic 8 )-BK ("HOE 140"). These compounds are more fully described in the previously incorporated Perkins et. al. 1993 and Dray -17et. ad. 1993 references. Suitable therapeutic and preferred concentrations are provided in Table 4.

Table 4 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Concentrations aNano molar) Preferred Concentrations (Nanomolar) .Aptent Bradvkinin, Receptor Antaponists: [Leu 8 des-Arg 9 -BK 1 1,000 1 1,000 50 -500 50 -500 6S es..

V

b*OS

V.

I V

V

V.

V C @0 fl I a**

*G

0 [des-ArgIO] derivative of HOE 140 Bradykinin,) Receptor -Antagonists: [D-Phe 7 -BK 100 -10,000 NPC 349 NPC 567 HOE 140 1 -1,000 1 -1,000 1 -1,000 200 -5,000 50 -500 50 -500 50 -500 V. V V

V

E. Kallikrein Inhibitors The peptide Bradykinin- is an important mediator of pain and inflammation, as noted previously. Bradykinin is produced as a cleavage product by the action of kallikrein on high molecular weight kininogens in plasma. Therefore kallikrein 10 inhibitors are believed to be therapeutic in inhibiting bradykinin production and resultant pain and inflammnation. A suitable kallikrein inhibitor for use in the present invention is aprotinin. Suitable concentrations for use in the solutions of the present invention are set forth below in Table Table Therapeutic and Preferred Concentrations of Pain/nflarnmation Inhibitory Agents Therapeutic Concentrations Agent (Nanomolar) Kallikrein Inhibitor: Preferred Concentrations (Nanomolar) Aprotinen 0.1- 1,000 50-500 most prefer: 200 F. Tachykinin Receptor Antagonists Tachykinins (TKs) are a family of structurally related peptides that include substance P, neurokinin A (NKA) and neurokinin B (NKB). Neurons are the major source of TKs in the periphery. An important general effect of TKs is neuronal stimulation, but other effects include endothelium-dependent vasodilation, plasma protein extravasation, mast cell degranulation and recruitment and stimulation of inflammatory cells. Maggi, Gen. Pharmacol, Vol. 22, pp. 1-24 (1991). Due to the above combination of physiological action mediated by activation of TK receptors, targeting of TK receptors for promotion of analgesia and treatment of neurogenic inflammation.

1. Neurokinin, Receptor Subtype Antagonists Substance P activates the neurokinin receptor subtype referred to as NK-1.

Substance P is an undecapeptide that is present in sensory nerve terminals.

Substance P is known to have multiple actions which produce inflammation and pain 15 in the periphery after C-fiber activation, including vasodilation, plasma extravasation and degranulation of mast cells. Levine, et. al., Peptides and the Primary Afferent Nociceptor, J. Neurosci. 13, p. 2273 (1993). A suitable Substance P antagonist is ([D-Pro'[spiro-gamma-lactam]Leu' o ,Trp"]physalae

("GR

82334"). Other suitable antagonists for use in the present invention which act on the 20 NK-1 receptor are: 1-imino-2-(2-methoxy-phenyl)-ethyl)-7,7-diphenyl-4perhydroisoindolone(3aR,7aR) ("RP 67580"); and 2s,3s-cis-3-(2methoxybenzylamino)-2-benzhydrylquinuclidine ("CP 96,345"). Suitable concentrations for these agents are set forth in Table 6.

Table 6 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Neurokinin 1 Receptor Subtype Antagonists GR 82334 1 1,000 10 500 CP 96,345 1-10,000 100-1,000 -19- RP 67580 0.1-1,000 100-1,000 2. Neurokinin, Receptor Subtype Antagonists Neurokinin A is a peptide which is colocalized in sensory neurons with substance P and which also promotes inflammation and pain. Neurokinin A activates the specific neurokinin receptor referred to as NK2. Edmonds-Alt, et. al., A Potent and Selective Non-Peptide Antagonist of the Neurokinin A (NKj) Receptor, Life Sci. 50:PL101 (1992). In the urinary tract, TKs are powerful spasmogens acting through only the NK-2 receptor in the human bladder, as well as the human urethra and ureter. Maggi, Gen. Pharmacol., Vol. 22, pp. 1-24 (1991). Thus, the desired drugs for inclusion in a surgical solution for use in urological procedures would contain an antagonist to the NK-2 receptor to reduce spasm. Examples of suitable NK2 antagonists include: ((S)-N-methyl-N-[ 4 4 -acetylamino-4phenylpiperidino)-2- 3 4 -dichlorophenyl)butyl]benzamide 48968"); Met- Asp-Trp-Phe-Dap-Leu ("MEN 10,627"); and cyc(Gln-Trp-Phe-Gly-Leu-Met) 659,877"). Suitable concentrations of these agents are provided in Table 7.

Table 7 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Neurokinin, Receptor Subtype Antagonists: MEN 10,627 1-1,000 10-1,000 L 659,877 10-10,000 100-10,000 48968 10-10,000 100-10,000 G. CGRP Receptor Antagonists Calcitonin gene-related peptide (CGRP) is a peptide which is also colocalized in sensory neurons with substance P, and which acts as a vasodilator and potentiates the actions of substance P. Brain, et. al., Inflammatory Oedema Induced by Synergism Between Calcitonin Gene-Related Peptide (CGRP) and Mediators of Increased Vascular Permeability, Br. J. Pharmacol. 99, p. 202 (1985). An example of a suitable CGRP receptor antagonist is alpha-CGRP-(8-37), a truncated version of CGRP. This polypeptide inhibits the activation o f CGRP receptors. Suitable concentrations for this agent are provided in Table 8.

Table 8 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Concentrations Agent (Nanomolar) CGR ReceptorA mtagonist: Preferred Concentrations anmomolar) 10-500 alpha-CGRP-(8-3 7) 1- 1,000 H. Interleukin Receptor Antagonist Interleukins are a family of peptides, classified as cytolcines, produced by leukocytes and other cells in response to inflarnmatory. mediators. Interleukins

(IL)

may be potent hyperalgesic agents peripherally. Ferriera, et. Inierleukin- 10 1 beta as a Potent Hyperalgesic Agent Antagonized by a Tripeptide Analogue, Nature 334, p. 698 (1988). An example of a suitable IEL-lbeta receptor antagonist is Lys-D- Pro-Thr,. which is a truncated version of IL-Ibeta. This tripeptide inhibits the activation of IIL-lbeta receptors. Suitable concentrations for this agent are provided in Table 9.

Table 9 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Aents Therapeutic Concentrations Agent aNanomolar) Interleukin Recept Lys-D-Pro-Thr Preferred Concentrations (Nianomolar) 10-500 or Antagonist: 1-1,000 L. Inhibitors -of Enzymes Active in the Synthetic Pathway for Arachidonic Acid Metabolites 1. Phospholipase Inhibitors The production of arachidonic acid by phospholipase A, (PLA 2 results in a cascade of reactions that produces numerous mediators of inflammation, know as eicosanoids. There are a number of stages throughout this pathway that can be inhibited, thereby decreasing the production of these inflammatory mediators.

Examples of inhibition at these various stages are given below.

Inhibition of the enzyme PLA 2 isoform inhibits the release of arachidonic acid from cell membranes, and therefore inhibits the.production of prostaglandins and leukotrienes resulting in the anti-inflammatory and analgesic properties of these compounds. Glaser, Regulation of Phospholipase A2 Enzymes: Selective Inhibitors and Their Pharmacological Potential, Adv. Pharmacol. 32, p. 31 (1995).

An example of a suitable PLA 2 isoform agonist is manoalide. Suitable concentrations for this agent are included in Table 10. Inhibition ofPLC, isoform also will result in decreased production of prostanoids and leukotrienes, and, therefore, will result in decreased pain and inflammation. An example of a PLC, isoform inhibitor is 1-[6- ((17p-3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl]-lH-pyrrole-2,5-dione Table Therapeutic and Preferred Concentrations of S 15 Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent CNanomolar) (Nanomolar) PLA2 Isoform Inhibitor: manoalide 100-100,000 500-10,000 Cvclooxygenase Inhibitors Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used as anti-inflammatory, anti-pyretic, anti-thrombotic and analgesic agents. Lewis, R.A., Prostaglandins and Leukotrienes, In: Textbook of Rheumatology, 3d ed. (Kelley et. al., eds.), p. 258 (1989). The molecular targets for these drugs are type I and type II cyclooxygenases (COX-1 and COX-2). These enzymes are also known as Prostaglandin H Synthase 1 (constitutive) and 2 (inducible) (PGHS), and catalyze the conversion of arachidonic acid to Prostaglandin H which is an intermediate in the biosynthesis of prostaglandins and thromboxanes. The COX-2 enzyme has been identified in endothelial cells, macrophages, and fibroblasts. This enzyme is induced by IL-1 and endotoxin, and its expression is upregulated at sites of inflammation.

Constitutive activity of COX-1 and induced activity of COX-2 both lead to synthesis of prostaglandins which contribute to pain and inflammation.

NSAIDs currently on the market (diclofenac, naproxen and indomethacin, ibuprofen, etc.) are generally nonselective inhibitors of both isoforms of COX, but -22may show greater selectively for COX-1 over COX-2, although this ratio varies for the different compounds. Uses of COX-1 and 2 inhibitors to block formation of prostaglandins represents a better therapeutic strategy than attempting to block interactions of the natural ligands with the seven described subtypes of prostanoid receptors. Reported antagonists of the eicosanoid receptors (EPI, EP2, EP3) are quite rare and only specific, high affinity antagonists of the Thromboxane A2 receptor have been reported. Wallace, J. and Cirino, G. Trends in Pharm. Sci., Vol. pp. 405-406 (1994).

The use of cyclooxygenase inhibitors is contraindicated in patients with ulcer disease, gastritis or renal impairment. In the United States, the only available injectable form of this class of drugs is ketorolac (ToradolTM), available from Syntex Pharmaceuticals, which is conventionally used intramuscularly or intravenously in postoperative patients but, again, is contraindicated for the above-mentioned categories of patients. The use of ketorolac, or any other cyclooxygenase inhibitor(s), 15 in the solution in substantially lower concentrations than currently used perioperatively may allow the use of this drug in otherwise contraindicated patients.

The addition of a cyclooxygenase inhibitor to the solutions of the present invention adds a distinct mechanism for inhibiting the production of pain and inflammation during arthroscopy or other operative/interventional procedure.

Preferred cyclooxygenase inhibitors for use in the present invention are keterolac and indomethacin. Of these two agents, indomethacin is less preferred because of the relatively high dosages required. Therapeutic and preferred concentrations for use in the solution are provided in Table 11.

Table 11 i 25 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Cvclooxygenase Inhibitors: ketorolac 100- 10,000 800- 5,000 indomethacin 1,000 500,000 10,000 200,000 (most prefer: 10,000-100,000) -23- 3. Lipooxvygenase Inhibitors Inhibition of the enzyme lipooxygenase inhibits the production of leukotrienes, such. as leukotriene which is known to be an important mediator of inflammation and pain. Lewis, Prostaglandins and Leukotrienes, In: Textbook of Rheumatology, 3d ed. (Kelley et. al., eds.), p. 258 (1989). An example of a lipooxygenase antagonist is 2,3, 5-trimethyl-6-( 12-hydroxy-5, 10-dodecadiynyl)- 1,4beazoquinone ("AA 861"), suitable concentrations for which are listed in Table 12.

Table 12 Therapeutic and Preferred Concentrations of Pain/nflammation Inhibitory Agents Therapeutic Concentrations Agent (Lqanornolar) Lipooxygenase Int ibitor: Preferred Concentrations (Nanom-olar) 500-5,000 AA 861 100-10,000 3. Prostanoid Receptor Antagonists Specific prostanoids produced as metabolites of arachidonic acid mediate their inflammatory effects through activation of prostanoid receptors. Examples of classes of specific prostanoid antagonist 's are the eicosanoid EP- 1 and EPA receptor subtype antagonists and the throniboxane receptor subtype antagonists. A suitable prostaglandin E, receptor antagonist is 8 -chlorodibenzb,fJ[1,4]oxazepine-1O(1111carboxylic acid, 2-acetyhydrazide ("SC 19220"). A suitable thromboxane receptor subtype antagonist is [lS-[cla, 203(5Z), 303, 4 a]- 7 3 -[2-(phenylarnino)-carbonyl] 20 hydrazino] methyl]-7-oxobicyclo..[2,2,1]-hept-2-yl]-5-heptanoic acid ("SQ 29548").

Suitable concentrations for these agents are set forth in Table 13.

Table 13 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory ents Therapeutic Preferred Concentrations Concentrations ent (an~omolar (anornolar) Eicosanoid EP-l Antaonist: SC 19220 SC 9220100- 10,000 500-5,000 -24- K. Leukotriene Receptor Antagonists The leukotrienes

(LTB

4

LTC

4 and LTD 4 are products of the pathway of arachidonic acid metabolism that are generated enzymatically and have important biological properties. Leukotrienes are implicated in a number of pathological conditions including inflammation. Specific antagonists are currently being sought by many pharmaceutical companies for potential therapeutic intervention in these pathologies. Halushka, et al., Annu. Rev. Pharmacol. Toxicol. 29: 213- 239 (1989); Ford-Hutchinson, A. Crit. Rev. Immunol. 10: 1-12 (1990). The LTB 4 receptor is found in certain immune cells including eosinophils and neutrophils.

LTB

4 binding to these receptors results in chemotaxis and lysosomal enzyme release thereby contributing to the process of inflammation. The signal transduction process associated with activation of the LTB 4 receptor involved G-protein-mediated stimulation of phosphotidy (P metabolism and elevation of intracellular calcium.

An example of a suitable leukotriene B4 receptor antagonist is SC 15 2 -(cyclopropylmethyl)3 -methoxy-4-[(methylamino)-carbonyl]phenoxy)propoxy)- 3, 4 -dihydro-8-propyl-2H- -benzopyran-2-propanoic acid ("SC 53228").

Concentrations for this agent that are suitable for the practice of the present invention are provided in Table 14. Other suitable leukotriene B. receptor antagonists include [3--2(7-chloro-2-quinolinyl)ethenyl]phenyl] 3 -(dimethylamino-3-oxopropyl)thio] methyl]thio propanoic acid ("MK 0571") and the drugs LY 66,071 and ICI 20,3219.

MK 0571 also acts as a LTD 4 receptor subtype antagonist.

Table 14 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations A.*.ent (Nanomolar) (Nanomolar) Leukotriene B 1 Antagonist: SC 53228 100-10,000 500-5,000 L. Opioid Receptor Agonists Opiate receptors are anti-nociceptive and, therefore, agonists to these receptors are desirable. Opiate receptors include the mu, delta and kappa opiate receptor subtypes. The mu receptors are located on sensory neuron terminals in the periphery and activation of these receptors inhibits sensory neuron activity. Basbaum, et. al., Opiate analgesia: How Central is a Peripheral Target?, N. Engl. J.

Med., 325:1168 (1991). Delta and kappa receptors are located on sympathetic efferent terminals and inhibit the release of prostaglandins, thereby inhibiting pain and inflammation. Taiwo, et. al., Kappa- andDelta-Opoids Block Sympathetically Dependent Hyperalgesia, J. NeuroscL, Vol. 11, page 928 (1991). Examples of suitable mu-opiate receptor agonists are fentanyl and Try-D-Ala-Gly-[N-MePhe]- NH(CH 2)2 ("DAMGO"). An example of a suitable delta-opiate receptor agonist is [D-Pen 2 ,D-Pen']enkephalin ("DPDPE"). An example of a suitable kappa-opiate receptor agonist is (trans)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidnyl)cyclohexyl]benzene acetamide ("U50,488"). Suitable concentrations for each of these agents are set forth in Table Table Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred o*e Concentrations Concentrations Aent (Nanomolar) (Nanomolar) Mu-Opiate Agonist: DAMGO 0.1-100 0.5-20 fentanyl 0.1-100 0.5-20 Delta-Opiate Agonist: DPDPE 0.1-500 1.0-100 Kappa-Opiate Agonist: U50,488 0.1-500 1.0-100 M. Purinoceptor Antagonists and Agonists Extracellular ATP acts as a signaling molecule through interactions with P 2 purinoceptors. One major class of purinoceptors are the P2x purinoceptors which are ligand-gated ion channels possessing intrinsic ion channels permeable to Na and Ca'. P 2 receptors described in sensory neurons are important for primary afferent neurotransmission and nociception. ATP is known to depolarize sensory neurons and plays a role in nociceptor activation since ATP released from damaged cells stimulates P2X receptors leading to depolarization of nociceptive nerve-fibre terminals. The

P

2 X receptor has a highly restricted distribution (Chen, et. al., Nature, Vol.

377, pp. 428-431 (1995)) since it is selectively expressed in sensory C-fibre nerves that run into the spinal cord and many of these C-fibres are known to carry the receptors for painful stimuli. Thus, the highly restricted localization of expression for the P2X2 receptor subunits make these subtypes excellent targets for analgesic action.

Suitable antagonists of P 2 x/ATP purinoceptors for use in the present invention include, by way of example, suramin and pyridoxylphosphate-6-azophenyl- 2,4-disulfonic acid ("PPADS"). Suitable concentrations for these agents are provided in Table 16.

Agonists of the P2y receptor, a G-protein coupled receptor, are known to effect smooth muscle relaxation through elevation of IP3 levels with a subsequent increase in intracellular calcium. An example of a P2y receptor agonist is 2-me-S-

ATP.

Table 16 15 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Purinoceptor Antagonists: suramin 100-100,000 10,000-100,000 PPADS 100-100,000 10,000-100,000 N. Adenosine Triphosphate (ATP)-Sensitive Potassium Channel Openers ATP-sensitive potassium channels have been discovered in numerous tissues, including brain, and binding studies using radiolabeled ligands have confirmed their 20 existence. Opening of these channels causes potassium efflux and hyperpolarizes ***the cell piembrane. This hyperpolarization induces a reduction in intracellular free calcium through inhibition of voltage-dependent calcium (Ca 2 channels and receptor operated Ca 2 channels. These combined actions drives the cell into a relaxed state, i.e. one which is more resistant to activation. K' channel openers (KCOs) have been shown to prevent stimulus coupled secretion and are considered to act on prejunctional neuronal receptors and thus will inhibit effects due to nerve stimulation and release of inflammatory mediators. Quast, et. al., Cellular Pharmacology of -27- Potassium Channel Openers in Vascular Smooth Muscle Cardiovasc. Res., Vol. 28, pp. 805-810 (1994).

ATP-sensitive potassium channels have been discovered in vascular and nonvascular smooth muscle and binding studies with radiolabeled ligands have confirmed their existence. Opening of these channels hyperpolarizes the cell membrane and in so doing, drives the smooth muscle cell into a relaxed state or one which is more resistant to activation, hence achieving vasorelaxation. K* channel openers (KCO) have been characterized as having potent antihypertensive activity in vivo and vasorelaxant activity in vitro. There is no known precedent in the medical literature demonstrating therapeutic utilization of these agents as anti-inflammatory, anti-nociceptive and bladder anti-spasm agents.

Synergistic interactions between endothelin (ETA) antagonists and openers of ATP-sensitive potassium channels (KCOs) are expected in achieving vasorelaxation or smooth muscle relaxation. A rationale for dual use is based upon the fact that these drugs have different molecular mechanisms of action in promoting relaxation of .smooth muscle and prevention ofvasospasm. An initial intracellular calcium elevation in smooth muscle cells induced by ETA receptor subsequently triggers activation of voltage-dependent channels and the entry of extracellular calcium which is required for contraction. Antagonists of the ETA receptor will specifically block this receptor 20 mediated effect but not block increases in calcium triggered by activation of other G-protein coupled receptors on the muscle cell.

Potassium-channel opener drugs, such as pinacidil, will open these channels o* 9* causing K efflux and hyperpolarization of the cell membrane. This hyperpolarization will act to reduce contraction mediated by other receptors by the following mechanisms: induces a reduction in intracellular free calcium through inhibition of voltage-dependent Ca channels by reducing the opening probability of both L-type es* and T-type calcium channels, restrains agonist induced (receptor operated channels) Ca release from intracellular sources through inhibition of IP3 formation, and lowers the efficiency of calcium as an activator of contractile proteins.

Consequently, combined actions of these two classes of drugs will clamp the target cells into a relaxed state or one which is more resistant to activation.

Suitable ATP-Sensitive K* Channel Openers for the practice of the present invention include: (-)pinacidil; cromakalin; nicorandil; minoxidil; N-cyano-N'-[1,1dimethyl-[2,2,3,3-'H]propyl]-N"-(3-pyridinyl)guanidine 1075"); and N-cyano-N'- 2 -nitroxyethyl)-3-pyridinecarboximidamide monomethansulphonate ("KRN 2391").

Concentrations for these agents are set forth in Table 17.

-28- Table 17 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) ATP-Sensitive K* Channel Opener: cromakalin 10-10,000 100-10,000 nicorandil 10-10,000 100-10,000 minoxidil 10-10,000 100-10,000 P 1075 0.1-1,000 10-1,000 KRN 2391 1-10,000 100-1,000 o (-)pinacidil 1-10,000 100-1,000 O. Calcium Channel Antagonists Calcium channel antagonists are a distinct group of drugs that interfere with the transmembrane flux of calcium ions required for activation of cellular responses mediating neuroinflammation. Calcium entry into platelets and white blood cells is a key event mediating activation of responses in these cells. Furthermore, the role of :bradykinin receptors and neurokinin receptors (NK1 and NK2) in mediating 10 neuroinflammation, signal transduction pathway includes increases in intracellular calcium, thus leading to activation of calcium channels on the plasma membrane. In many tissues, calcium channel antagonists, such as nifedipine, can reduce the release of arachidonic acid, prostaglandins, and leukotrienes that are evoked by various stimuli. Moncada, Flower, R. and Vane, J. in Goodman's and Gilman's Pharmacological Basis of Therapeutics, (7th MacMillan Publ. Inc., pp. 660-5 (1995).

Calcium channel antagonists also interfere with the transmembrane flux of calcium ions required by vascular smooth muscle for contractions. This effect provides the rationale for the use of calcium antagonists in the proposed use in perioperative procedures in which the goal is to alleviate vasospasm and relaxation of smooth muscle. The dihydropyridines, including nisoldipine act as specific inhibitors (antagonists) of the voltage-dependent gating of the L-type subtype of calcium channels. Systemic administration of the calcium channel antagonist nifedipine during cardiac surgery has been previously utilized to prevent or minimize coronary artery vasospasm. Seitelberger, et. al., Circulation, Vol. 83, pp. 460-468 (1991). Again, there is no known precedent in the medical literature demonstrating therapeutic utilization of these agents as anti-inflammatory, anti-nociceptive and bladder antispasm agents.

Calcium channel antagonists, which are among the antipain/inflammation/spasm agents useful in the present invention, exhibit synergistic effect when combined with other agents of the present invention. Calcium (Ca 2 channel antagonists and nitric oxide (NO) donors interact in achieving vasorelaxation or smooth muscle relaxation, in inhibiting spasm activity. A rationale for dual use is based, upon the fact that these drugs have different molecular mechanisms of action, may not be completely effective in achieving relaxation used alone, and may have 15 different time periods of effectiveness. In fact, there are numerous studies showing that calcium channel antagonists alone cannot achieve complete relaxation of vascular muscle that has been precontracted with a receptor agonist.

The effect ofnisoldipine, used alone and in combination with nitroglycerin, on spasm of the internal mammary artery (IMA) showed that the combination of the two 20 drugs produced a large positive synergistic effect in the prevention of contraction (Liu et al., 1994). These studies provide a scientific basis for combination of a calcium channel antagonist and nitric oxide (NO) donor for the most efficacious i prevention of vasospasm and for relaxation of smooth muscle. Examples of systemic administration of nitroglycerin and nifedipine during cardiac surgery to prevent and 25 treat myocardial ischemia or coronary artery vasospasm have been reported (Cohen et al., 1983; Seitelberger et al., 1991).

Calcium channel antagonists also exhibit synergistic effect with endothelin receptor subtype A (ETA) antagonists. Yanagisawa and coworkers observed that dihydropyridine antagonists, calcium channel antagonists, blocked effects ofET-l an endogenous agonist at the ETA receptor in coronary arterial smooth muscle and hence speculated that ET-1 is an endogenous agonist of voltage-sensitive calcium channels.

It has been found that the sustained phase of intracellular calcium elevation in smooth muscle cells induced by ETA receptor activation requires extracellular calcium and is at least partially blocked by nicardipine. Thus, the inclusion of a calcium channel antagonist would be expected to synergistically enhance the actions of an ETA antagonist when combined in a surgical solution.

Calcium channel antagonists and ATP-sensitive potassium channel openers likewise exhibit synergistic action. Potassium channels that are ATP-sensitive

(KATP)

couple the membrane potential of a cell to the cell's metabolic state via sensitivity to adenosine nucleotides. KATP channels are inhibited by intracellular ATP but are stimulated by intracellular nucleotide diphosphates. The activity of these channels is controlled by the electrochemical driving force to potassium and intracellular signals ATP or a G-protein), but are not gated by the membrane potential per se. KAT

P

channels hyperpolarize the membrane and thus allow them to control the resting potential of the cell. ATP-sensitive potassium currents have been discovered in skeletal muscle, brain, and vascular and nonvascular smooth muscle and binding studies with radiolabeled ligands have confirmed the existence of these channels which are the receptor targets for the potassium-channel opener drugs such as pinacidil.

Opening of these channels causes potassium efflux and hyperpolarizes the cell membrane. This hyperpolarization induces a reduction in intracellular free calcium 15 through inhibition of voltage-dependent Ca channels by reducing the opening probability of both L-type and T-type calcium channels, restrains agonist induced (receptor operated channels) Ca" release from intracellular sources through inhibition ofinositol triphosphate (IP3) formation, and lowers the efficiency of calcium as an activator of contractile proteins. These combined actions of these two classes of drugs will clamp the target cells into a relaxed state or one which is more resistant to activation.

Finally, calcium channel antagonists and tachykinin and bradykinin antagonists exhibit synergistic effects in mediating neuroinflammation. The role of neurokinin receptors in mediating neuroinflammation has been established. The neurokinin, 25 (NK1) and neurokinin 2 (NK2) receptor (members of the G-protein coupled superfamily) signal transduction pathway includes increases in intracellular calcium, *thus leading to activation of calcium channels on the plasma membrane. Similarly, activation of bradykinin, (BK2) receptors is coupled to increases in intracellular calcium. Thus, calcium channel antagonists interfere with a common mechanism involving elevation of intracellular calcium, part of which enters through L-type channels. This is the basis for synergistic interaction between calcium channel antagonists and antagonists to these receptors.

Suitable calcium channel antagonists for the practice of the present invention include nisoldipine, nifedipine, nimodipine, lacidipine and isradipine. Suitable concentrations for these agents are set forth in Table 18.

-31- Table 18 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Calcium Channel Antagonists: nisoldipine 1-10,000 100-1,000 nifedipine 1-10,000 100-5,000 nimodipine 1-10,000 100-5,000 lacidipine 1-10,000 100-5,000 isradipine 1-10,000 100-5,000 P. Anti-Spasm Agents 1. Multifunction Agents Several of the anti-pain/anti-inflammatory agents described above also serve to inhibit vasoconstriction or smooth muscle spasm. As such, these agents also perform the function of an anti-spasm agent, and thus are beneficially used in vascular and urinary applications. Anti-inflammatory/anti-pain agents that also serve as anti-spasm 10 agents include: serotonin receptor antagonists, particularly, serotonin 2 antagonists; tachykinin receptor antagonists, ATP-sensitive potassium channel openers and calcium channel antagonists.

2. Nitric Oxide Donors Nitric oxide donors may be included in the solutions of the present invention particularly for their anti-spasm activity. Nitric oxide (NO) plays a critical role as a molecular mediator of many physiological processes, including vasodilation and regulation of normal vascular tone. Within endothelial cells, an enzyme known as NO synthase (NOS) catalyzes the conversion of L-arginine to NO which acts as a diffusible second messenger and mediates responses in adjacent smooth muscle cells.

NO is continuously formed and released by the vascular endothelium under basal conditions which inhibits contractions and controls basal coronary tone and is produced in the endothclium in response to various antagonists (such as acetylcholine) -32and other endothelium dependent vasodilators. Thus, regulation of NO synthase activity and the resultant levels of NO are key molecular targets controlling vascular tone. Muramatsu, et. al., Coron. Artery Dis., Vol. 5, pp. 815-820 (1994).

Synergistic interactions between NO donors and openers of ATP-sensitive potassium channels (KCOs) are expected to achieve vasorelaxation or smooth muscle relaxation. A rationale for dual use is based upon the fact that these drugs have different molecular mechanisms of action in promoting relaxation of smooth muscle and prevention of vasospasm. There is evidence from cultured coronary arterial smooth muscle cells that the vasoconstrictors: vasopressin, angotensin II and endothelin, all inhibit KA, currents through inhibition of protein kinase A. In addition, it has been reported that KA, current in bladder smooth muscle is inhibited by muscarinic agonists. The actions of NO in mediating smooth relaxation occur via independent molecular pathways (described above) involving protein kinase G. This suggests that the combination of the two drugs will be more efficacious in relaxing 15 smooth muscle than employing a single drug alone.

Suitable nitric oxide donors for the practice of the present invention include nitroglycerine, sodium nitroprusside, the drug FK409, 3 -morpholinosydnonimine or linsidomine chlorohydrate, and S-nitroso-N-acetylpenicillamine

("SNAP").

Concentrations for these agents are set forth in Table 19.

20 Table 19 Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred Concentrations Concentrations

S"

geint (Nanomolar) (Nanomolar) Nitric Oxide Donors: Nitroglycerin 10-10,000 100-1,000 sodium nitroprusside 10-10,000 100-1,000 SIN-1 10-10,000 100-1,000 SNAP 10-10,000 100-1,000 FK409 1-1,000 10-100 3. Endothelin Receptor Antagonists Endothelin is a 21 amino acid peptide that is one of the most potent vasoconstrictors known. Three different human endothelin peptides, designated ETI, ET2 and ET3 have been described which mediate their physiological effects through at least two receptor subtypes referred to as ETA and ETB receptors. The heart and the vascular smooth muscles contain predominantly ETA receptors and this subtype is responsible for contraction in these tissues. Furthermore, ETA receptors have often been found to mediate contractile responses in isolated smooth muscle preparations.

Antagonists of ETA receptors have been found to be potent antagonists of human coronary artery contractions. Thus, antagonists to the ETA receptor should be therapeutically beneficial in the perioperative inhibition of coronary vasospasm and may additionally be useful in inhibition of smooth muscle contraction in urological applications. Miller, et. al., Trends in Pharmacol. Sci., Vol. 14, pp. 54-60 (1993).

15 Suitable endothelin receptor antagonists include: cyclo(D-Asp-Pro-D-Val- Leu-D-Trp) ("BQ 123"); (N,N-hexamethylene)-carbamoyl-Leu-D-Trp-(CHO)-D- Trp-OH ("BQ 610"); 1-hexahydro-1H-azepinyl]-carbonyl]amino- 4-methyl-pentanoyl) amino-3-(3 [1-methyl- 1H-indodyl])propionylamino-3 (2-pyridyl) propionic acid ("FR 139317"); cyclo(D-Asp-Pro-D-Ile-Leu-D-Trp) ("JKC 301"); 20 cyclo(D-Ser-Pro-D-Val-Leu-D-Trp) ("JK 302"); and 5-(dimethylamino)-N-(3,4- ("BMS 182874"). Concentrations for a representative two of these agents is set forth in Table Table Therapeutic and Preferred Concentrations of Pain/Inflammation Inhibitory Agents Therapeutic Preferred S Concentrations Concentrations Agent (Nanomolar) (Nanomolar) Endothelin Receptor Antagonists: BQ 123 0.01-1,000 10-1,000 FR 139317 1-100,000 100-10,000 VL Method of Application The solution of the present invention has applications for a variety of operative/interventional procedures, including surgical and diagnostic and therapeutic techniques. Applications include use as a perioperatively applied irrigation solution during arthroscopic surgery of anatomic joints, urological procedures and intravascular diagnostic and therapeutic procedures. As used herein throughout, the term "perioperative" is intended to mean application of the solution during the course of an operative or interventional medical procedure, and for many procedures will preferably also entail application of the solution prior to the initiation of the procedure. Such procedures conventionally utilize physiologic irrigation fluids, such as normal saline or lactated Ringer's, applied to the surgical site by techniques well know to those of ordinary skill in the art. The method of the present invention involves substituting the anti-pain/anti-inflammatory/anti-spasm irrigation solution of the present invention for conventionally applied irrigation fluids. The irrigation solution is applied to the wound or surgical site prior to the initiation of the procedure, preferably before tissue trauma, and continuously throughout the duration of the procedure, to preemptively block pain and inflammation and/or spasm. As used .15 herein throughout, the term "irrigation" is intended to mean the flushing of a wound or anatomic structure with a stream of liquid. As used herein throughout, the term "continuously" is intended to also include situations in which there is repeated and e: frequent irrigation of wounds at a frequency sufficient to maintain a predetermined therapeutic local concentration of the applied agents, and applications in which there may be intermittent cessation of irrigation fluid flow necessitated by operating technique.

S Arthroscopic techniques for which the present solution may be employed include, by way of non-limiting example, partial meniscectomies and ligament reconstructions in the knee, shoulder acromioplasties, rotator cuff debridements, 25 elbow synovectomies, and wrist and ankle arthroscopies. The irrigation solution is continuously supplied intraoperatively to the joint at a flow rate sufficient to distend the joint capsule, to remove operative debris, and to enable unobstructed intraarticular visualization.

A suitable irrigation solution for control of pain and edema during such arthroscopic techniques is provided in Example I herein below. For arthroscopy, it is preferred that the solution include a combination, and preferably all, or any of the following: a serotonin 2 receptor antagonist, a serotonin 3 receptor antagonist, a histamine 1 receptor antagonist, a serotonin receptor agonist acting on the 1A, 1B, ID, 1F and/or lE receptors, a bradykinin 1 receptor antagonist, a bradykinin 2 receptor antagonist, and a cyclooxygenase inhibitor, and preferably all of the above agents.

This solution utilizes extremely low doses of these pain and inflammation inhibitors, due to the local application of the agents directly to the operative site during the procedure. For example, less than 0.05 mg of amitriptyline (a suitable serotonin 2 and histamine 1 "dual" receptor antagonist) is needed per liter of irrigation fluid to provide substantial local tissue concentrations that would inhibit 5-HT 2 and HI receptors. This dosage is extremely low relative to the 10-25 mg of oral amitriptyline that is the usual starting dose for this drug.

In each of the surgical solutions of the present invention, the agents are included in low concentrations and are delivered locally in low doses relative to concentrations and doses required with conventional methods of drug administration to achieve the desired therapeutic effect. It is impossible to obtain an equivalent therapeutic effect by delivering similarly dosed agents via other intravenous, intramuscular or oral) routes of drug administration since drugs given systemically are subject to first- and second-pass metabolism.

15 For example, using a rat model of arthroscopy, the inventors examined the ability of amitriptyline, a 5-HT 2 antagonist, to inhibit 5-HT-induced plasma extravasation in the rat knee in accordance with the present invention. This study, described more fully below in Example VIII, compared the therapeutic dosing of amitriptyline delivered locally intra-articularly) at the knee and intravascularly.

20 The results demonstrated that intra-articular administration of amitriptyline required total dosing levels approximately 200-fold less than were required via the intravenous route to obtain the same therapeutic effect. Given that only a small fraction of the drug delivered intra-articularly is absorbed by the local synovial tissue, the difference in plasma drug levels between the two routes of administration is much greater than 25 the difference in total amitriptyline dosing levels.

Practice of the present invention should be distinguished from conventional intra-articular injections of opiates and/or local anesthetics at the end of arthroscopic or "open" joint knee, shoulder, etc.) procedures. The solution of the present invention is used for continuous infusion throughout the surgical procedure to provide preemptive inhibition of pain and inflammation. In contrast, the high concentrations necessary to achieve therapeutic efficacy with a constant infusion of local anesthetics, such as lidocaine solutions), would result in profound systemic toxicity.

Upon completion of the procedure of the present invention, it may be desirable to inject or otherwise apply a higher concentration of the same pain and inflammation inhibitors as used in the irrigation solution at the operative site, as an alternative or supplement to opiates.

The solution of the present invention also has application in intravascular diagnostic and therapeutic procedures to potentially decrease vessel wall spasm, platelet aggregation and nociceptor activation produced by vessel manipulation. A suitable solution for such techniques is disclosed in Example II herein below. The intravascular solution preferably includes any combination, and preferably all, of the following: a 5-HT 2 receptor antagonist (Saxena, P. et. al., Cardiovascular Effects of Serotonin Inhibitory Agonists and Antagonists, J Cardiovasc Pharmacol (Suppl. pp. S17-S34 (1990); Douglas, 1985); a 5-HT 3 receptor antagonist to block activation of these receptors on sympathetic neurons and C-fiber nociceptive neurons in the vessel walls, which has been shown to produce brady- and tachycardia (Saxena et. al. 1990); a bradykinin 1 receptor antagonist; and a cyclooxygenase inhibitor to prevent production of prostaglandins at tissue injury sites, which decreases pain and inflammation. In addition, the intravascular solution also preferably will contain a serotoninlB (also known as serotoninDip) antagonist because serotonin has been shown to produce significant vascular spasm via activation of the serotoniniB receptors in humans. Kaumann, AJ., et al., Variable Participation .of 5-HTl-Like Receptors and 5-HT2 Receptors in Serotonin-Induced Contraction of Human Isolated Coronary Arteries, Circulation 90, pp. 1141-53 (1994). This excitatory action of serotoninlB receptors in vessel walls, resulting in vasoconstriction, is in contrast to the previously-discussed inhibitory action of serotoninlB receptors in neurons. For the purpose of the intravascular solution, the term "pain/inflammation inhibitory agents" is intended to also include vessel wall spasm and platelet aggregation inhibitory agents.

The solution of the present invention also has utility for reducing pain and 25 inflammation associated with urological procedures, such as trans-urethral prostate resection and similar urological procedures utilizing a laser. Studies have demonstrated that serotonin, histamine and bradykinin produce inflammation in lower urinary tract tissues. Schwartz, et. al., Vascular Leakage in the Kidney and Lower Urinary Tract: Effects of Histamine, Serotonin and Bradykinin, Proc Soc Exp Biol Med 140, pp. 535-539 (1972). A suitable irrigation solution for urological procedures is disclosed in Example m herein below. The solution preferably includes a combination, and preferably all, of the following: a histamine 1 receptor antagonist to inhibit histamine-induced pain and inflammation; a 5-HT 3 receptor antagonist to block activation of these receptors on peripheral C-fiber nociceptive neurons; a bradykinin 1 antagonist; a bradykinin 2 antagonist; and a cyclooxygenase inhibitor to decrease pain/inflammation produced by prostaglandins at the tissue injury sites.

Preferably an anti-spasm agent is also included to prevent spasm in the urethral canal and bladder wall spasm.

The solution of the present invention may also be employed perioperatively for the inhibition of pain and inflammation in surgical.wounds, as well as to reduce pain and inflammation associated with bums. Burs result in the release of a significant quantity of biogenic amines, which not only produce pain and inflammation, but also result in profound plasma extravasation (fluid loss), often a life-threatening component of severe burs. Holliman, et. al., The Effect of Ketanserin, a Specific Serotonin Antagonist, on Bur Shock Hemodynamic Parameters in a Porcine Burn Model, J Trauma 23, pp. 867-871 (1983). The solution disclosed in Example I for arthroscopy may also be suitably applied to a wound or burn for pain and inflammation control. The agents of the solution of Example I may alternately be carried at the same concentrations in a paste or salve base, for application to the burn or wound.

VII. Examples The following are several formulations in accordance with the present invention suitable for certain operative procedures followed by a summary of two clinical studies utilizing the agents of the present invention.

A. Example 1 Irrigation Solution for Arthroscopy The following composition is suitable for use in anatomic joint irrigation during arthroscopic procedures. Each drug is solubilized in a carrier fluid containing physiologic electrolytes, such as normal saline or lactated Ringer's solution, as are the remaining solutions described in subsequent examples.

Concentration Class of Agent Drug (Nanomolar): Most Therapeutic Preferred Preferred serotonin 2 antagonist amitriptyline 0.1-1,000 50-500 100 serotonin 3 antagonist metoclopramide 10-10,000 200-2,000 1,000 histamineI antagonist amitriptyline 0.1-1,000 50-500 200 serotoninlA, IB, 1D, 1F sumatriptan 1-1,000 10-200 inhibitory agonist bradykininI antagonist [des-Arg l o 1-1,000 50-500 200 v derivative of HOE 140 HOE 140 bradykinin 2 antagonist 1- 1,000 50-500 B. Example HI Irrigation Solution for Intravascular Therapeutic Procedures The following drugs and concentration ranges in solution in a physiologic carrier fluid are suitable for use in irrigating operative sites during intravascular procedures.

Class of Agent 4 0.4 oe.

.oa .o 6 serotonin 2 antagonist serotonin 3 antagonist serotoninlB antagonist bradykiin, antagonist cyclooxygenase inhibitor trazodone metoclopraniide yohirnbine [des-ArgIO] derivative of HOE 140 ketorolac Concentration (Nanomolar): Therapeutic 0.1-1,000 10-10,000 0.1-1,000 1-1,000 100-10,00.0 Preferred 50-500 200-2,000 50-500 50-500 Most Preferred 200 1,000 200 200 800-5,000 3,000 C. Examnplel l Irrigation Solution for Urolopic Procedures The folowing drugs and concentration ranges in solution in a physiologic carrier fluid are suitable for use in irrigating operative sites during urological 10 procedures.

Class of Agzent Histamine, antagonist serotonin 3 antagonist bradykiin, antagonist bradykiin 2 antagonist cyclooxygenase inhibitor terfenadine metoclopramnide [des-Arg' 0 derivative of HOE 140 HOE 140 ketorolac Concentration (Nanomnolar): Therapeutic 0.1-1,000 10-10,000 1-1,000 1-1,000 100-10,000 Preferred 50-500 200-2,000 50-500 50-500 800-5,000 Most Preferred 200 1,000 200 200 3,000 D. Example IV Irrigation Solution for Arthroscopy. Burns. General Sur-ica] Wounds and Oral/Dental Ap~plications The following composition is preferred for use in anatQmnic irrigation during arthroscopic and oral/dental procedures and the management of burns and general surgical wounds. YWle the solution set forth in Example I is suitable for use with the present -invention, the following solution is even more preferred because of expected higher efficacy.

S. S S S.

S

S

S S *5 5.555.

*S

S

*SSS

Class of Agent serotonin 2 antagonist serotonin 3 antagonist histamine, antagonist serotonin IA, lB, ID, 1F agonist cyclooxygenase inhibitor neurokininjantagonist neurokinin 2 antagonist purine 2 Xantagonist ATP-sensitive K+ channel agonist Ca 2 channel antagonist kallikrein inhibitor amitriptyline metoclopranide amnitriptyline sumatriptan ketorolac GR 82334 ()SR 48968

PPADS

()pinacidil nifedipine Concentration (Nanomolar): Therapeutic 0.1 -1,000 10 -10,000 0.1 -1,000 1 -1,000 100 -10,000 1 -1,000 1 -1,000 100 100,000 1 -10,000 1 -10,000 Preferred 50-500 200 -2,000 50-500 10 -200 800 -5,000 10- 500 10 -500 10,000- 100,000 100 -1,000 100-5,000 Most Preferred 200 1,000 200 100 3,000 200 200 50,000 500 1,000 aprotinin 0.1 -1,000 5-0 0 50-500 200 E. Example V Irrination Solution for Intravascular Therapeutic Procedures The folowing drugs and concentration ranges in solution in a physiologic carrier fluid are preferred for use in irrigating operative sites during intravascular procedures. Again, this solution is Example II above for higher efficacy.

preferred relative -to the solution set forth in Concentration (Nanomolar): Therapeutic Class of Agent Drug Preferred most Preferred 200 serotonin 2 antagonist trazodone 0.1 -1,000 50-500 cyclooxygenase inhibitor ketorolac 100- 10,000 0.01 -1,000 1 -10,000 endothelin antagonist BQ 123

C.

Ge C

*CCS

C.

C

C.

C. C C C

C

C C

.CC.CC

C. C C

C

CS..

SC..

ATP-sensitive K+ channel agonist Ca 2 channel antagonist nitric oxide donor pinacidil 800 -5,000 10 -1,000 100 -1,000 100 -1,000 100 -1,000 3,000 500 500 500 nisoldipine 1 10,000 SIN-i 10 -10,000 500 F. Example VI Irrigation Solution for Urologic Procedures The following drugs and concentration ranges in solution in a physiologic 10 carrier fluid are preferred for use in irrigating operative sites during urologic procedures. The solution is believes to have even higher efficacy than the solution set forth in prior Example ]f.

Class of Agent serotonin 2 antagonist histamidne 1 antagonist cyclooxygenase inhibitor LY 53857 terfenadine ketorolac SR 48968 Concentration (Nanomolar): Therapeutic 0.1 -500 0.1 -1,000 100 10,000 1 -100 50 -500 200 Most Preferred Preferred 800 -5,000 3,000 .neurokinin 2 antagonist 1-100 1 0 1-1,000 10-500 -41purine-xantagonist PPADS 100 100,000 10,000 50,000 100,000 ATP-sensitive K pinacidil 1 10,000 100 1,000 500 channel agonist Ca 2 channel nifedipine 1 10,000 100- 5,000 1,000 antagonist kallikrein inhibitor aprotinin 0.1 1,000 50 500 200 nitric oxide donor SIN-1 10 10,000 100 1,000 500 G. Example VII Balloon Dilatation of Normal Iliac Arteries in the New Zealand White Rabbit and the Influence ofHistamine/Serotonin Receptor Blockade on the Response The purpose of this study was twofold. First, a new in vivo model for the 5 study of arterial tone was employed. The time course of arterial dimension changes before and after balloon angioplasty is described below. Second, the role of histamine and serotonin together in the control of arterial tone in this setting was then studied by the selective infusion of histamine and serotonin receptor blocking agents into arteries before and after the angioplasty injury.

1. Design Considerations This study was intended to describe the time course of change in arterial S" lumen dimensions in one group of arteries and to evaluate the effect of histamine/serotonin receptor blockade on these changes in a second group of similar arteries. To facilitate the comparison of the two different groups, both groups were S 15 treated in an identical manner with the exception of the contents of an infusion performed during the experiment. In control animals (arteries), the infusion was normal saline (the vehicle for test solution). The histamine/serotonin receptor blockade treated arteries received saline containing the blocking agents at the same rate and at the same part of the protocol as control animals. Specifically, the test solution included: the serotonin 3 antagonist metoclopramide at a concentration of 16.0 IM; the serotonin 2 antagonist trazodone at a concentration of 1.6pM; and the histamine antagonist promethazine at concentrations of 1.0pM, all in normal saline. This study was performed in a prospective, randomized and blinded manner.

Assignment to the specific groups was random and investigators were blinded to -42infusion solution contents (saline alone or saline containing the histamine/serotonin receptor antagonists) until the completion of the angiographic analysis.

2. Animal Protocol This protocol was approved by the Seattle Veteran Affairs Medical Center Committee on Animal Use and the facility is fully accredited by the American Association for Accreditation of Laboratory Animal Care. The iliac arteries of 3-4 kg male New Zealand white rabbits fed a regular rabbit chow were studied. The animals were sedated using intravenous xylazine (5 mg/kg) and Ketamine (35 mg/kg) dosed to effect and a cutdown was performed in the ventral midline of the neck to isolate a carotid artery. The artery was ligated distally, an arteriotomy performed and a French sheath was introduced into the descending aorta. Baseline blood pressure and heart rate were recorded and then an angiogram of the distal aorta and bilateral iliac arteries was recorded on 35 mm cine film (frame rate 15 per second) using hand injection of iopamidol 76% (Squibb Diagnostics, Princeton, NJ) into the descending 15 aorta. For each angiogram, a calibration object was placed in the radiographic field of view to allow for correction for magnification when diameter measurements were made. A 2.5 French infusion catheter (Advanced Cardiovascular Systems, Santa Clara, CA) was placed through the carotid sheath and positioned 1-2 cm above the aortic bifurcation. Infusion of the test solution either saline alone or saline 20 containing the histamine/serotonin receptor antagonists was started at a rate of 5 cc per minute and continued for 15 minutes. At 5 minutes into the infusion, a second angiogram was performed using the previously described technique then a 2.5 mm balloon angioplasty catheter (the Lightning, Cordis Corp., Miami, FL) was rapidly advanced under fluoroscopic guidance into the left and then the right iliac arteries. In each iliac the balloon catheter was carefully positioned between the proximal and distal deep femoral branches using bony landmarks and .the balloon was inflated for 30 seconds to 12 ATM of pressure. The balloon catheter was inflated using a dilute solution of the radiographic contrast agent so that the inflated balloon diameter could be recorded on cine film. The angioplasty catheter was rapidly removed and another angiogram was recorded on cine film at a mean of 8 minutes after the infusion was begun. The infusion was continued until the 15 minute time point and another angiogram (the fourth) was performed. Then the infusion was stopped (a total of cc of solution had been infused) and the infusion catheter was removed. At the minute time point (15 minutes after the infusion was stopped), a final angiogram was recorded as before. Blood pressure and heart rate were recorded at the 15 and -43minute time points immediately before the angiograms. After the final angiogram, the animal was euthanized with an overdose of the anesthetic agents administered intravenously and the iliac arteries were retrieved and immersion fixed in formation for histologic analysis.

3. Angiographic Analysis The angiograms were recorded on 35 mm cine film at a frame rate of 15 per second. For analysis, the angiograms were projected from a Vanguard projector at a distance of 5.5 feet. Iliac artery diameters at prespecified locations relative to the balloon angioplasty site were recorded based on hand held caliper measurement after correction for magnification by measurement of the calibration object. Measurements were made at baseline (before test solution infusion was begun), 5 minutes into the infusion, immediately post balloon angioplasty (a mean of 8 minutes after the test solution was begun), at 15 minutes (just before the infusion was stopped) and at 30 minutes (15 minutes after the infusion was stopped). Diameter measurements 15 were made at three sites in each iliac artery: proximal to the site of balloon dilatation, at the site of balloon dilatation and just distal to the site of balloon dilatation.

The diameter measurements were then converted to area measurements by the formula: Area (Pi)(Diameter)/4.

20 For calculation of vasoconstriction, baseline values were used to represent the maximum area of the artery and percent vasoconstriction was calculated as: Vasoconstriction {Baseline area Later time point area)/Baseline area) xl00.

4. Statistical Methods All values are expressed as mean 1 standard error of the mean. The time course of vasomotor response in control arteries was assessed using one way analysis of variance with correction for repeated measures. Post hoc comparison of data between specific time points was performed using the Scheffe test. Once the time points at which significant vasoconstriction occurred had been determined in control arteries, the control and histamine/serotonin receptor antagonist treated arteries were compared at those time points where significant vasoconstriction occurred in control arteries using multiple analysis of variance with treatment group identified as an independent variable. To compensate for the absence of a single a priori stated -44hypothesis, a p value <0.01 was considered significant. Statistics were performed using Statistica for Windows, version 4.5, (Statsoft, Tulsa, OK).

Results The time course of arterial dimension changes before and after balloon angioplasty in normal arteries receiving saline infusion was evaluated in 16 arteries from 8 animals (Table 21). Three segments of each artery were studied: the proximal segment immediately upstream from the balloon dilated segment, the balloon dilated segment and the distal segment immediately downstream from the balloon dilated segment. The proximal and distal segments demonstrated similar patterns of change in arterial dimensions: in each, there was significant change in arterial diameter when all time points were compared (proximal segment, p=0.0002 and distal segment, p<0.001, ANOVA). Post hoc testing indicated that the diameters at the immediate post angioplasty time point were significantly less than the diameters at baseline or at the 30 minute time point in each of these segments. On the other hand, the arterial 15 diameters in each segment at the 5 minute, 15 minute and 30 minute time points were similar to the baseline diameters. The balloon dilated segment showed lesser changes in arterial dimension than the proximal and distal segments. The baseline diameter of this segment was 1.82±0.05 mm; the nominal inflated diameter of the balloon used for angioplasty was 2.5 mm and the actual measured inflated diameter of the balloon was 20 2.20±0.03 mm (p<0.0001 vs. baseline diameter of the balloon treated segment).

Thus, the inflated balloon caused circumferential stretch of the balloon dilated segment, but there was only slight increase in lumen diameter from baseline to the 30 minute time point (1.82-0.05 mm to 1.94±0.07 mm, p=NS by post hoc testing).

Table 21 25 Angioraphically determined lumen diameters at the specified times before and after balloon dilatation of normal iliac arteries.

Segment Baseline 5 Minute Immediate 15 Minute 30 Minute Post PTA Proximal' 2.18±0.7 2.03±0.7 1.81±0.08* 2.00±.08 2.23±.08 Balloon 2 1.82±.05 1.77±.03 1.79±.05 1.70±.04 1.94±.07 Distal 3 1.76±.04 1.68±.04** 1.43±.04* 1.54±.03 1.69±.06 All measurements in mm. Means±SEM.PTA percutaneous transluminal angioplasty.

Sp=0.0002 (ANOVA within group comparison),' p=0.03 (ANOVA within group comparison), 3 p<0.0001 (ANOVA within group comparison). N=16 at all time points.

p<0.01 versus baseline and 30 minute diameter measurements (Scheffe test for post hoc comparisons).

p<0.01 versus immediate post PTA measurements (Scheffe test for post hoc comparisons). All other post hoc comparisons were not significant using the p<0.01 threshold.

Arterial lumen diameters were used to calculate lumen area then the area measurements were used to calculate percent vasoconstriction by comparison of the minute, immediate post angioplasty, 15 and 30 minute data to the baseline measurements. The proximal and distal segment data expressed as percent vasoconstriction are shown in FIGURE 1; the changes in the amount of vasoconstriction over time are significant (in the proximal segment, p=0.

00 0 8 in the ""distal segment, p=0.0001, ANOVA). Post hoc testing identifies the vasoconstriction at the immediate post angioplasty time point as significantly different from that present at the 30 minute time point (P<0.001 in both segments). In the distal segment, the immediate post angioplasty vasoconstriction was also significantly less than that at 5 minutes no other differences in intra-time point comparisons were significant by post hoc testing.

The luminal changes in control arteries can be summarized as follows: 20 1) Vasoconstriction with loss of approximately 30% of baseline luminal area occurs in the segments of artery proximal and distal to the balloon dilated segment immediately after balloon dilatation. There are trends to smaller amounts of vasoconstriction in the proximal and distal segments before dilatation and at the 15 minute time point (approximately 7 minutes after dilatation) also but, by the 30 minute time point 25 (approximately 22 minutes after dilatation), a trend towards vasodilatation has *replaced the previous vasoconstriction; 2) In the balloon dilated segment, only minor changes in lumen dimensions are present, and, despite the use of a balloon with a significantly larger inflated diameter than was present in this segment at baseline, there was no significant increase in lumen diameter of the dilated segment. These findings lead to a conclusion that any effects of the putative histamine/serotonin treatment would only be detectable in the proximal and distal segments at the time points where vasoconstriction was present.

The histamine/serotonin receptor blockade solution was infused into 16 arteries (8 animals); angiographic data was available at all time points in 12 arteries. Heart rate and systolic blood pressure measurements were available in a subset of animals (Table 22). There were no differences in heart rate or systolic blood pressure when the two animal groups were compared within specific time -46points. Histamine/serotonin treated animals showed trends toward a decrease in the systolic blood pressure from baseline to 30 minutes (-14±5 mm Hg, p=0.04) and a lower heart rate (-26±10, p=0.05). Within the control animals, there was no change in heart rate or systolic blood pressure over the duration of the experiment.

Table 22 Systolic blood pressure and heart rate measurements in control and histamine/serotonin treated animals.

Group Baseline 5 Minute 15 Minute 30 Minute

(N)

Systolic Blood Pressure Control 83±4 84±4 82±6 80±4 (8) Histamine/Serotonin 93±5 87±9 82±9 80±8 Heart Rate Control 221±18 234±18 217±23 227±22 Histamine/Serotonin 232±8 232±8 209±14 206±12 Systolic blood pressure in mm Hg and heart rate in beats per minute. Mean±SEM.

p=0.04 for decrease in systolic blood pressure from baseline to 30 minutes and **p=0.05 for decrease in heart rate from baseline to 30 minutes within the histamine/serotonin treated animals.

The proximal and distal segments of histamine/serotonin treated arteries were compared to control arteries using the percent vasoconstriction measurement.

FIGURE 2A shows the effects of the histamine/serotonin infusion on proximal 15 segment vasoconstriction relative to the vasoconstriction present in the control arteries. When the findings in the two treatment groups were compared at the baseline immediate post angioplasty and 15 minute time point, histamine/serotonin infusion resulted in significantly less vasoconstriction compared to the control saline infusion (p=0.003. 2-way ANOVA). Comparison of the two treatment groups in the distal segment is illustrated in FIGURE 2B. Despite observed differences in mean diameter measurements in the distal segment, solution treated vessels exhibited less vasoconstriction than saline treated control vessels at baseline, immediate postangioplasty and 15 minute time points, this pattern did not achieve statistical significance (p=0.32, 2-way ANOVA). Lack of statistical significance may be attributed to smaller than expected vasoconstriction valves in the control vessels.

-47- H. Example VIII Amitriptyline Inhibition of Knee Joint Plasma Extravasation Comparison ofIntra-Articular Versus Intravenous Routes of Administration The following study was undertaken in order to compare two routes of administration of the 5-HT 2 receptor antagonist, amitriptyline: 1) continuous intraarticular infusion; versus 2) intravenous injection, in a rat knee synovial model of inflammation. The ability of amitriptyline to inhibit 5-HT-induced joint plasma extravasation by comparing both the efficacy and total drug dose of amitriptyline delivered via each route was determined.

1. Animals Approval from the Institutional Animal Care Committee at the University of California, San Francisco was obtained for these studies. Male Sprague-Dawley rats (Bantin and Kingman, Fremont, CA) weighing 300 450 g were used in these studies.

15 Rats were housed under controlled lighting conditions (lights on 6 A.M. to 6 with food and water available ad libitum.

2. Plasma Extravasation Rats were anesthetized with sodium pentobarbital (65 mg/kg) and then given a ta i l vein injection of Evans Blue dye (50 mg/kg in a volume of 2.5 ml/kg), which is S. 20 used as a marker for plasma protein extravasation. The knee joint capsule was exposed by excising the overlying skin, and a 30-gauge needle was inserted into the joint and used for the infusion of fluid. The infusion rate (250 pl/min was controlled by a Sage Instruments Syringe pump (Model 341B, Orion Research Inc., Boston, MA). A 25-gauge needle was also inserted into the joint space and perfusate fluid was extracted at 250 gl/min, controlled by a Sage Instruments Syringe pump (Model 351).

The rats were randomly assigned to three groups: 1) those receiving only intra-articular (IA) 5-HT (1 pM), 2) those receiving amitriptyline intravenously (TV) (doses ranging from 0.01 to 1.0 mg/kg) followed by IA 5-HT (1 mM), and 3) those receiving amitriptyline intra-articularly (IA) (concentrations ranging from 1 to.

100 nM) followed by IA 5-HT (1 M) plus IA amitriptyline. In all groups, baseline plasma extravasation levels were obtained at the beginning of each experiment by perfusing 0.9% saline intra-articularly and collecting three perfusate samples over a min. period (one every 5 min). The first group was then administered 5-HT IA for a total of 25 min. Perfusate samples were collected every 5 min for a total of 25 min.

-48- Samples were then analyzed for Evans Blue dye concentration by spectrophotometric measurement of absorbance at 620 nm, which is linearly related to its concentration (Carr and Wilhelm, 1964). The IV amitriptyline group was administered the drug during the tail vein injection of the Evans Blue dye. The knee joints were then perfused for 15 min with saline (baseline), followed by 25 min perfusion with (1 IM). Perfusate samples were collected every 5 min for a total of 25 min. Samples were then analyzed using spectrophotometry. In the IA amitriptyline group, amitriptyline was perfused intra-articularly for 10 min after the 15 min saline perfusion, then amitriptyline was perfused in combination with 5-HT for an additional 25 min. Perfusate samples were collected every 5 min and analyzed as above.

Some rat knees were excluded from the study due to physical damage of knee joint or inflow and outflow mismatch (detectable by presence of blood in perfusate and high baseline plasma extravasation levels or knee joint swelling due to improper needle placement).

a. 5-HT-Induced Plasma Extravasation Baseline plasma extravasation was measured in all knee joints tested (total n=22). Baseline plasma extravasation levels were low, averaging 0.022 0.003 absorbance units at 620 nm (average standard error of the mean). This baseline extravasation level is shown in Figures 1 and 2 as a dashed line.

20 5-HT (1 pM) perfused into the rat knee joint produces a time-dependent increase in plasma extravasation above baseline levels. During the 25 min perfusion Sof 5-

H

T intra-articularly, maximum levels of plasma extravasation were achieved by min and continued until the perfusion was terminated at 25 min (data not shown).

Therefore, 5-HT-induced plasma extravasation levels reported are the average of the 15, 20 and 25 min time points during each experiment. 5-HT-induced plasma extravasation averaged 0.192 0.011, approximately an 8-fold stimulation above baseline. This data is graphed in FIGURES 3 and 4, corresponding to the dose of IV amitriptyline and the concentration ofIA amitriptyline, respectively.

b. Effect of Intravenous Amitriptyline on 5-HT-Induced Plasma Extravasation Amitriptyline administered via tail vein injection produced a dose-dependent decrease in 5-HT-induced plasma extravasation as shown in FIGURE 3. The IC 5 o for IV amitriptyline inhibition of 5-HT-induced plasma extravasation is approximately 0.025 mg/kg. 5-HT-induced plasma extravasation is completely inhibited by an IV amitriptyline dose of mg/kg, the plasma extravasation averaging 0.034 0.010.

-49c. Effect of Intra-articular amitriPtvline on 5-HT-Induced Plasma Extravasation Amitriptyline administered alone in increasing concentrations intra-articularly did not affect plasma extravasation levels relative to baseline, with the plasma extravasation averaging 0.018 0.002 (data not shown). Amitriptyline co-perfused in increasing concentrations with 5-HT produced a concentration-dependent decrease in plasma extravasation as shown in FIGURE 4. 5-HT-induced plasma extravasation in the presence of 3 nM IA amitriptyline was not significantly different from that produced by 5-HT alone, however, 30 nM amitriptyline co-perfused with produced a greater than 50% inhibition, while 100 nM amitriptyline produced complete inhibition of 5-HT-induced plasma extravasation. The ICso for IA amitriptyline inhibition of 5-HT-induced plasma extravasation is approximately nM.

The major finding of the present study is that 5-HT (1 pM) perfused intraarticularly in the rat knee joint produces a stimulation of plasma extravasation that is approximately 8-fold above baseline levels and that either intravenous or intraarticular administration of the 5-HT 2 receptor antagonist, amitriptyline, can inhibit plasma extravation. The total dosage of administered amitriptyline, however, differs dramatically between the two methods of drug delivery. The ICso for IV amitriptyline inhibition of 5-HT-induced plasma extravasation is 0.025 mg/kg, or 20 7.5 x 10-' mg in a 300 g adult rat. The ICso for IA amitriptyline inhibition of induced plasma extravasation is approximately 20 nM. Since 1 ml of this solution was delivered every five minutes for a total of 35 min during the experiment, the total dosage perfused into the knee was 7 ml, for a total dosage of 4.4 x 10 5 mg perfused into the knee. This IA amitriptyline dose is approximately 200-fold less than the IV 25 amitriptyline dose. Furthermore, it is likely that only a small fraction of the IA perfused drug is systemically absorbed, resulting in an even greater difference in the total delivered dose of drug.

Since 5-HT may play an important role in surgical pain and inflammation, as discussed earlier, 5-HT antagonists such as amitriptyline may be beneficial if used during the perioperative period. A recent study attempted to determine the effects of oral amitriptyline on post-operative orthopedic pain (Kerrick et al., 1993). An oral dose as low as 50 mg produced undesirable CNS side-effects, such as a "decreased feeling of well-being". Their study, in addition, also showed that oral amitriptyline produced higher pain scale scores than placebo (P0.05) in the post-operative patients.

Whether this was due to the overall unpleasantness produced by oral amitriptyline is not known. In contrast, an intra-articular route of administration allows extremely

Claims (45)

1. The use of a composition for perioperatively inhibiting pain and inflammation, and/or spasm at a wound during an arthroscopic, urologic, open or other surgical or body cavity procedure by intraprocedurally applying the composition locally to the wound, wherein the composition comprises a solution of a plurality of inhibitory agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the wound, wherein each agent is included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the wound when delivered systemically.

2. The use of the composition of Claim 1 by continuously irrigating the wound with the solution during the medical procedure.

3. The use of the composition of Claim 1, wherein each agent in the 20 composition has a concentration of no greater than 100,000 nanomolar. "0'0 4. The use of the composition of Claim 3, wherein each agent in the composition has a concentration of no greater than 10,000 nanomolar. The use of the composition of Claim 1, wherein the classes of agents comprise pain/inflammation inhibitory agent classes selected from the group consisting of: serotonin receptor antagonists; serotonin receptor agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein inhibitors; neurokinin 2 receptor antagonists comprising: neurokininl receptor subtype Jl/N antagonists and neurokinin 2 receptor subtype antagonists; calcitonin gene-related 004095408 52 peptide receptor antagonists; interleukin receptor antagonists; phospholipase inhibitors comprising PLA 2 isoform and PLCy isoform inhibitors; cyclooxygenase inhibitors; lipooxygenase inhibitors; prostanoid receptor antagonists comprising eicosanoid EP-1 and EP-4 receptor subtype antagonists and thromboxane receptor subtype antagonists; leukotriene receptor antagonists comprising leukotriene B 4 and D 4 receptor subtype antagonists; opioid receptor agonists comprising mu-opiate receptor subtype agonists, delta-opiate receptor subtype agonists, and kappa-opiate receptor subtype agonists; purinoceptor agonists and antagonists comprising P2Y receptor agonists and P 2 x receptor antagonists; and ATP-sensitive potassium 10 channel openers. i' 6. The use of the composition of Claim5, wherein the selected pain/inflammation inhibitory agents have concentrations of: 0.1 to 10,000 nanomolar for serotonin receptor antagonists; 0.1 to 2,000 nanomolar for serotonin receptor agonists; 0.1 to 1,000 nanomolar for histamine receptor antagonists; 1 to 10,000 nanomolar for bradykinin receptor antagonists; 0.1 to 1,000 nanomolar for kallikrein inhibitors; 0.1 to 10,000 nanomolar for neurokinin, receptor subtype antagonists; 1.0 to 10,000 nanomolar for neurokinin 2 receptor subtype antagonists; 1 to 1,000 nanomolar for calcitonin gene-related peptide antagonists; 1 to 1,000 nanomolar for interleukin antagonists; 100 to 100,000 nanomolar for PLA 2 isoform *0000 20 inhibitors; 100 to 200,000 nanomolar for cyclooxygenase inhibitors; 100 to 10,000 nanomolar for lipooxygenase inhibitors; 100 to 10,000 nanomolar for eicosanoid EP-1 receptor subtype antagonists; 100 to 10,000 nanomolar for leukotriene B 4 receptor subtype antagonists; 0.1 to 100 nanomolar for mu-opiate receptor subtype agonists; 0.1 to 500 nanomolar for delta-opiate receptor subtype agonists; 0.1 to 500 nanomolar for kappa-opiate receptor subtype agonists; 100 to 100,000 nanomolar for purinoceptor antagonists; and 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel'openers. 004095408 53

7. The use of the composition of Claim 1, wherein at least one of the selected classes of agents in the composition comprises a class of anti-spasm agents for the inhibition of smooth muscle spasm.

8. The use of the composition of Claim 7, wherein the anti-spasm agent or agents is selected from the group consisting of serotonin 2 receptor subtype antagonists, tachykinin receptor antagonists, nitric oxide donors, ATP-sensitive potassium channel openers and endothelin receptor antagonists.

9. The use of the composition of Claim 8, wherein the selected anti- spasm agent or agents have concentrations of: 0.1 to 10,000 nanomolar for serotonin2 receptor antagonists; 0.1 to 10,000 nanomolar for tachykinin receptor antagonists; 1.0 to 10,000 nanomolar for nitric oxide donors; 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers; and 0.01 to 100,000 nanomolar for endothelin receptor antagonists.

10. The use of the composition of Claim 1, wherein the classes of agents in the composition comprise: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; ion channel openers; and ion channel antagonists.

11. The use of the composition of Claim 10, wherein the classes of agents in the composition comprise only: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; ion channel openers; and receptor operated ion 20 channel antagonists. S12. The use of the composition of Claim 11, wherein the classes of agents in the composition comprise only: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; and ion channel openers.

13. The use of the composition of Claim 1, wherein the application step comprises irrigating an open surgical wound, a body cavity wound or an anatomic joint during arthroscopic surgery.

14. The use of the composition of Claim 13, wherein the solution comprises selected pain/inflammation inhibitory agents which comprise: a 004095408 54 serotonin 2 receptor antagonist having a concentration of 50 to 500 nanomolar; a serotonin 3 receptor antagonist having a concentration of 200 to 2,000 nanomolar; a histamine, receptor antagonist having a concentration of 50 to 500 nanomolar; a serotonin receptor agonist having a concentration of 100 to 200 nanomolar; a cyclooxygenase inhibitor having a concentration of 800 to 5,000 nanomolar; a neurokinin, receptor subtype antagonist having a concentration of 10 to 500 nanomolar; a neurokinin 2 receptor subtype antagonist having a concentration of to 500 nanomolar; a purinoceptor antagonist having a concentration of 10,000 to 100,000 nanomolar; an ATP-sensitive potassium channel opener having a 10 concentration of 100 to 1,000 nanomolar; and a kallikrein inhibitor having a concentration of 50 to 500 nanomolar.

15. The use of the composition of Claim 1, wherein the application step comprises irrigating at least a portion of the urinary tract during a urological procedure.

16. The use of the composition of Claim 15, wherein the irrigation solution utilized comprises at least one selected anti-spasm agent and at least one selected pain/inflammation inhibitory agent, the selected agents comprising: a .serotonin2 receptor subtype antagonist having a concentration of 1 to 100 nanomolar; a histamine receptor subtype antagonist having a concentration of 50 to 20 500 nanomolar; a cyclooxygenase inhibitor having a concentration of 800 to 5,000 nanomolar; a neurokinin2 receptor subtype antagonist having a concentration of to 500 nanomolar; a purinoceptor antagonist having a concentration of 10,000 to 100,000 nanomolar; an ATP-sensitive potassium channel opener having a concentration of 100 to 1,000 nanomolar; a kallikrein inhibitor having a concentration of 50 to 500 nanomolar; and a nitric oxide donor having a concentration of 100 to 1,000 nanomolar. 004095408

17. The use of the composition of Claim 1, wherein the solution comprises a serotonin receptor antagonist.

18. The use of the composition of Claim 1, wherein the solution comprises an ATP-sensitive potassium channel agonist.

19. The use of the composition of Claim 1, wherein the solution comprises a calcium channel antagonist at a concentration of no more than 100,000. A solution for perioperatively inhibiting pain and inflammation and/or spasm, for use in intraprocedural application to a wound during an arthroscopic, urologic, open or other surgical or body cavity procedure, comprising a solution of a 10 plurality of inhibitory agents at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma o. concentration that would be required to achieve the same level of inhibitory effect at the wound when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents mixed together in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the wound. 20 21. The solution of Claim 20, wherein the classes of agents comprise pain/inflammation inhibitory agent classes selected from the group consisting of: serotonin receptor antagonists; serotonin receptor agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein inhibitors; neurokinin receptor antagonists comprising neurokinin receptor subtype antagonists and neurokinin 2 receptor subtype antagonists; calcitonin gene-related peptide antagonists; interleukin antagonists; phospholipase inhibitors comprising PLA 2 isoform and PLCy isoform inhibitors; cyclooxygenase inhibitors; lipooxygenase S v inhibitors; prostanoid receptor antagonists comprising eicosanoid EP-1 and EP-4 004095408 56 receptor subtype antagonists and thromboxane receptor subtype antagonists; leukotriene receptor antagonists comprising leukotriene B 4 and D 4 receptor subtype antagonists; opioid receptor agonists comprising mu-opiate receptor subtype agonists, delta-opiate receptor subtype agonists, and kappa-opiate receptor subtype agonists; purinoceptor agonists and antagonists comprising P2Y receptor agonists and P2x receptor antagonists; and ATP-sensitive potassium channel openers.

22. The solution of Claim 21, wherein the pain/inflammation inhibitory agents in the solution have concentrations of: 0.1 to 10,000 nanomolar for serotonin receptor antagonists; 0.1 to 2,000 nanomolar for serotonin receptor agonists; 0.1 to 10 1,000 nanomolar for histamine receptor antagonists; 1 to 10,000 nanomolar for bradykinin receptor antagonists; 0.1 to 1,000 nanomolar for kallikrein inhibitors; 0.1 to 10,000 nanomolar for neurokinin, receptor subtype antagonists; 1.0 to 10,000 nanomolar for neurokinin 2 receptor subtype antagonists; 1 to 1,000 nanomolar for calcitonin gene-related peptide receptor antagonists; 1 to 1,000 nanomolar for interleukin receptor antagonists; 100 to 100,000 nanomolar for phospholipase inhibitors; 100 to 200,000 nanomolar for cyclooxygenase inhibitors; 100 to 10,000 nanomolar for lipooxygenase inhibitors; 100 to 10,000 nanomolar for eicosanoid EP-1 receptor antagonists; 100 to 10,000 nanomolar for leukotriene B 4 receptor antagonists; 0.1 to 100 nanomolar for mu-opiate receptor subtype agonists; 0.1 to 20 500 nanomolar for delta-opiate receptor subtype agonists; 0.1 to 500 nanomolar for kappa-opiate receptor subtype agonists; 100 to 100,000 nanomolar for purinoceptor antagonists; and 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers.

23. The solution of Claim 20, wherein at least one of the selected classes of agents in the irrigation solution comprises a class of anti-spasm agents for inhibiting smooth muscle spasm. 004095408 57 23. The solution of Claim 20, wherein at least one of the selected classes of agents in the irrigation solution comprises a class of anti-spasm agents for inhibiting smooth muscle spasm.

24. The solution of Claim 23, wherein the anti-spasm agents are selected from the group consisting of: serotonin 2 receptor subtype antagonists; tachykinin receptor antagonists; nitric oxide donors; ATP-sensitive potassium channel openers; calcium channel antagonists; and endothelin receptor antagonists. The solution of Claim 24, wherein the anti-spasm agents have concentrations of: 0.1 to 10,000 nanomolar for serotonin2 receptor subtype antagonists; 0.1 to 10,000 nanomolar for tachykinin receptor antagonists; 1.0 to 10,000 nanomolar for nitric oxide donors; 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers; and 0.01 to 100,000 nanomolar for endothelin receptor antagonists.

26. The solution of Claim 20, wherein each agent has a concentration of no more than 100,000 nanomolar.

27. The solution of Claim 26, wherein each agent has a concentration of no more than 10,000 nanomolar.

28. The solution of Claim 20, wherein the classes of agents in the solution comprise: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme 20 activators; ion channel openers; and ion channel antagonists. ee 29. The solution of Claim 28, wherein the classes of agents in the solution comprise only: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; ion channel openers; and receptor operated ion channel antagonists. The solution of Claim 29, wherein the classes of agents in the solution comprise only: receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; and ion channel openers. 004095408 58

31. The solution of Claim 20, wherein the solution comprises a calcium channel antagonist at a concentration of no more than 100,000.

32. The use of a composition for perioperatively inhibiting pain and inflammation, and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the composition locally to the vascular structure, wherein the composition comprises a solution of a plurality of inhibitory agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through distinct molecular mechanisms of action, wherein each class of agent is selected from the classes of receptor antagonists, receptor agonists, enzyme inhibitors, enzyme activators, ion channel openers, and receptor operated ion channel antagonists, the agents collectively o o being effective for the inhibition of pain and inflammation and/or spasm, at the a vascular structure, wherein each agent is included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically.

33. The use of the composition of Claim 22 by continuously irrigating the 20 vascular structure with the solution during the medical procedure.

34. The use of the composition of Claim 32 wherein each agent in the composition has a concentration of no greater than 100,000 nanomolar. The use of the composition of Claim 34, wherein each agent in the composition has a concentration of no greater than 10,000 nanomolar.

36. The use of the composition of Claim 32, wherein the classes of agents in the composition comprise pain/inflammation inhibitory agent classes selected from the group consisting of: serotonin receptor antagonists; serotonin receptor ,agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein 004095408 59 eicosanoid EP-1 and EP-4 receptor subtype antagonists and thromboxane receptor subtype antagonists; leukotriene receptor antagonists comprising leukotriene B 4 and D 4 receptor subtype antagonists; opioid receptor agonists comprising mu-opiate receptor subtype agonists, delta-opiate receptor subtype agonists, and kappa-opiate receptor subtype agonists; purinoceptor agonists and antagonists comprising P2Y receptor agonists and P 2 x receptor antagonists; and ATP-sensitive potassium channel openers.

37. The use of the composition of Claim 35, wherein the selected pain/inflammation inhibitory agents have concentrations of: 0.1 to 10,000 10 nanomolar for serotonin receptor antagonists; 0.1 to 2,000 nanomolar for serotonin receptor agonists; 0.1 to 1,000 nanomolar for histamine receptor antagonists; 1 to 10,000 nanomolar for bradykinin receptor antagonists; 0.1 to 1,000 nanomolar for .kallikrein inhibitors; 0.1 to 10,000 nanomolar for neurokininl receptor subtype antagonists; 1.0 to 10,000 nanomolar for neurokinin 2 receptor subtype antagonists; 1 to 1,000 nanomolar for calcitonin gene-related peptide antagonists; 1 to 1,000 nanomolar for interleukin antagonists; 100 to 100,000 nanomolar for PLA 2 isoform *2 inhibitors; 100 to 200,000 nanomolar for cyclooxygenase inhibitors; 100 to 10,000 nanomolar for lipooxygenase inhibitors; 100 to 10,000 nanomolar for eicosanoid EP-1 receptor subtype antagonists; 100 to 10,000 nanomolar for leukotriene B 4 20 receptor subtype antagonists; 0.1 to 100 nanomolar for mu-opiate receptor subtype agonists; 0.1 to 500 nanomolar for delta-opiate receptor subtype agonists; 0.1 to 500 nanomolar for kappa-opiate receptor subtype agonists; 100 to 100,000 nanomolar for purinoceptor antagonists; and 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers.

38. The use of the compound of Claim 32, wherein at least one of the selected classes of agents in the composition comprises a class of spasm inhibitory agents targeting an enzyme, a receptor, an ATP-sensitive potassium channel or a 004095408 receptor operated ion channel, for the inhibition of vascular or smooth muscle spasm.

39. The use of the composition of Claim 38, wherein the spasm inhibitory agent or agents is selected from the group consisting of serotonin 2 receptor subtype antagonists, tachykinin receptor antagonists, nitric oxide donors, ATP-sensitive potassium channel openers and endothelin receptor antagonists. The use of the composition of Claim 39, wherein the selected spasm inhibitory agent or agents have concentrations of: 0.1 to 10,000 nanomolar for serotonin2 receptor antagonists; 0.1 to 10,000 nanomolar for tachykinin receptor antagonists; 1.0 to 10,000 nanomolar for nitric oxide donors; 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers; and 0.01 to 100,000 nanomolar for endothelin receptor antagonists.

41. The use of the composition of Claim 32 wherein the solution utilized comprises at least one selected spasm inhibitory agent and at least one selected pain/inflammation inhibitory agent, the selected agents comprising: a serotonin 2 receptor antagonist having a concentration of 50 to 500 nanomolar; a cyclooxygenase inhibitor having a concentration of 800 to 5,000 nanomolar; an endothelin receptor antagonist having a concentration of 10 to 1,000 nanomolar; an ATP-sensitive potassium channel opener having a concentration of 100 to 1,000 20 nanomolar; and a nitric oxide donor having a concentration of 100 to 1,000 nanomolar.

42. The use of the composition of Claim 32 wherein the solution comprises a serotonin receptor antagonist.

43. The use of the composition of Claim 32 wherein the solution comprises an ATP-sensitive potassium channel agonist.

44. The use of the composition of Claim 32, wherein the classes of agents in the solution comprise a pain/inflammation inhibitory agent class. 004095408 61 A solution for perioperatively inhibiting pain and inflammation and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the solution to the vascular structure, comprising a solution of a plurality of inhibitory agents a concentration or dosage that is sufficient to provide a level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents mixed together in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through distinct molecular mechanisms of action, wherein each class of agent is selected from the classes of receptor antagonists, receptor o agonists, enzyme inhibitors, enzyme activators, ion channel openers, and receptor operated ion channel antagonists, the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure.

46. The solution of Claim 45, wherein the classes of agents comprise pain/inflammation inhibitory agent classes selected from the group consisting of: serotonin receptor antagonists; serotonin receptor agonists; histamine receptor antagonists; bradykinin receptor antagonists; kallikrein inhibitors; neurokinin 20 receptor antagonists comprising neurokinin, receptor subtype antagonists and neurokinin 2 receptor subtype antagonists; calcitonin gene-related peptide antagonists; interleukin antagonists; phospholipase inhibitors comprising PLA 2 isoform and PLCy isoform inhibitors; cyclooxygenase inhibitors; lipooxygenase inhibitors; prostanoid receptor antagonists comprising eicosanoid EP-1 and EP-4 receptor subtype antagonists and thromboxane receptor subtype antagonists; leukotriene receptor antagonists comprising leukotriene B 4 and D 4 receptor subtype antagonists; opioid receptor agonists comprising mu-opiate receptor subtype Sagonists, delta-opiate receptor subtype agonists, and kappa-opiate receptor subtype 004095408 62 agonists; purinoceptor agonists and antagonists comprising P2Y receptor agonists and P2x receptor antagonists; and ATP-sensitive potassium channel openers.

47. The solution of Claim 46, wherein the pain/inflammation inhibitory agents in the solution have concentrations of: 0.1 to 10,000 nanomolar for serotonin receptor antagonists; 0.1 to 2,000 nanomolar for serotonin receptor agonists; 0.1 to 1,000 nanomolar for histamine receptor antagonists; 1 to 10,000 nanomolar for bradykinin receptor antagonists; 0.1 to 1,000 nanomolar for kallikrein inhibitors; 0.1 to 10,000 nanomolar for neurokinin receptor subtype antagonists; 1.0 to 10,000 nanomolar for neurokinin 2 receptor subtype antagonists; 1 to 1,000 nanomolar for calcitonin gene-related peptide receptor antagonists; 1 to 1,000 nanomolar for interleukin receptor antagonists; 100 to 100,000 nanomolar for phospholipase inhibitors; 100 to 200,000 nanomolar for cyclooxygenase inhibitors; 100 to 10,000 0 nanomolar for lipooxygenase inhibitors; 100 to 10,000 nanomolar for eicosanoid o EP-1 receptor antagonists; 100 to 10,000 nanomolar for leukotriene B 4 receptor antagonists; 0.1 to 100 nanomolar for mu-opiate receptor subtype agonists; 0.1 to 500 nanomolar for delta-opiate receptor subtype agonists; 0.1 to 500 nanomolar for 00 kappa-opiate receptor subtype agonists; 100 to 100,000 nanomolar for purinoceptor antagonists; and 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers. 20 48. The solution of Claim 45, wherein at least one of the selected classes of agents in the solution comprises a class of anti-spasm agents for inhibiting vascular spasm or smooth muscle spasm.

49. The solution of Claim 48, wherein the anti-spasm agents are selected from the group consisting of: serotonin 2 receptor subtype antagonists; tachykinin receptor antagonists; nitric oxide donors; ATP-sensitive potassium channel openers; and endothelin receptor antagonists. 004095408 63 The solution of Claim 49, wherein the anti-spasm agents have concentrations of: 0.1 to 10,000 nanomolar for serotonin 2 receptor subtype antagonists; 0.1 to 10,000 nanomolar for tachykinin receptor antagonists; 1.0 to 10,000 nanomolar for nitric oxide donors; 0.1 to 10,000 nanomolar for ATP-sensitive potassium channel openers; and 0.01 to 100,000 nanomolar for endothelin receptor antagonists.

51. The solution of Claim 45, wherein each agent in the solution has a concentration of no more than 100,000 nanomolar.

52. The solution of Claim 51, wherein each agent in the solution has a concentration of no more than 10,000 nanomolar. 0

53. The solution of Claim 45, wherein the classes of agents in the solution comprise a pain/inflammation inhibitory agent class.

54. The use of a composition for inhibiting pain and inflammation at a wound during a medical procedure by applying the composition locally to the wound during the procedure, wherein the composition comprises a solution of the serotoninlA,IB,1D,1F receptor agonist sumatriptan included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the wound when delivered locally to the wound and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of 20 inhibitory effect at the wound when delivered systemically.

55. The use of a composition for perioperatively inhibiting pain and inflammation, and/or spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the composition locally to the vascular structure, wherein the composition comprises a solution of a plurality of inhibitory agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through distinct molecular mechanisms of action which mediate pain and inflammation or spasm, the agents collectively being 004095408 64 effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure, wherein each agent is included at a concentration or dosage that is sufficient to provide a level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically.

56. The use of the composition of Claim55, wherein the solution comprises a calcium channel antagonist at a concentration of no more than 100,000.

57. The use of the composition of Claim 55, wherein the classes of agents are selected from receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; ion channel openers; receptor operated ion channel antagonists and T-type voltage-dependent calcium channel antagonists. V0 58. A solution for perioperatively inhibiting pain and inflammation and/or 1 o S:spasm at a vascular structure during an intravascular procedure by intraprocedurally applying the solution to the vascular structure, comprising a solution of a plurality of inhibitory agents a concentration or dosage that is sufficient to provide a .00. predetermined level of inhibitory effect at the vascular structure when delivered locally to the vascular structure and that results in a plasma concentration that is less 0.°00 than a plasma concentration that would be required to achieve the same level of inhibitory effect at the vascular structure when delivered systemically, the agents selected from pain/inflammation inhibitory agents and spasm inhibitory agents mixed together in a physiologic liquid carrier, the plurality of agents being selected from a plurality of classes of agents that act through differing molecular mechanisms at distinct molecular targets which mediate pain and inflammation or spasm the agents collectively being effective for the inhibition of pain and inflammation and/or spasm, at the vascular structure.

59. The solution of Claim 58, wherein the solution comprises a calcium ,channel antagonist at a concentration of no more than 100,000. 004095408 The solution of Claim 58, wherein the classes of agents are selected from receptor agonists; receptor antagonists; enzyme inhibitors; enzyme activators; ion channel openers; receptor operated ion channel antagonists and T-type voltage-dependent calcium channel antagonists.

61. Use of a composition as defined in Claim 1 substantially as hereinbefore described with reference to any one of the Examples. DATED: 9 July 2002 FREEHILLS CARTER SMITH BEADLE Patent Attorneys for the Applicant: OMEROS MEDICAL SYSTEMS, INC o* S