WO2002041844A2 - Composition chimiotherapeutique renfermant une pate de phosphate de calcium nanocristallin - Google Patents

Composition chimiotherapeutique renfermant une pate de phosphate de calcium nanocristallin Download PDF

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WO2002041844A2
WO2002041844A2 PCT/US2001/051419 US0151419W WO0241844A2 WO 2002041844 A2 WO2002041844 A2 WO 2002041844A2 US 0151419 W US0151419 W US 0151419W WO 0241844 A2 WO0241844 A2 WO 0241844A2
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calcium phosphate
composition
phosphate
calcium
nanocrystalline
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PCT/US2001/051419
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WO2002041844A3 (fr
WO2002041844A9 (fr
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Dosuk D. Lee
Maria Aiolova
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Etex Corporation
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Publication of WO2002041844A3 publication Critical patent/WO2002041844A3/fr
Publication of WO2002041844A9 publication Critical patent/WO2002041844A9/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A61K9/0024—Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue

Definitions

  • the present invention relates to pharmaceutical compositions and methods for the treatment of cancer.
  • MacroMed reports the use of a biodegradable polymer having reverse thermal gelation properties for intra-tumoral injections. Under the tradename OncoGelTM, the poly(lactide-co-glycolide)-based polymer is deliverable through a small-gauge (25) needle and localized delivery is reported. See, U.S. Patent No. 5,702,717 for further information on the polymeric material. Hydroxyapatite is a major mineral in bone and teeth. It demonstrates excellent biocompatibility with bony tissue and has been used in the orthopedic industry as bone-filling material.
  • Anticancer agents such as adriamycin, cis-platin and methotrexate have been incorporated into porous hydroxyapatite beads and blocks, and sustained release of the agents have been demonstrated.
  • Administration of the drug-loaded blocks to a tumor site in a cancer rat model resulted in increased life span and reduction in body weight loss.
  • hydroxyapatite ceramics typically are dense, highly crystalline materials, and as such, are poorly resorbable.
  • Porosity must be engineered into the material to permit drug uptake during drug loading and drug release at the tumor site.
  • Engineering of the hydroxyapatite block for a particular drug release profile is difficult and not easily reproducible.
  • An additional limitation of use of a hydroxyapatite solid block or bead is that it requires surgical implantation.
  • Calcium phosphate cements are compositions having one or more dry components and a liquid which combine to form a material that is capable of setting into a solid calcium phosphate product.
  • Materials that set into solid calcium phosphate mineral products are of particular interest as such products can closely resemble the mineral phase of natural bone, are potentially remodelable, and are biocompatible.
  • Patents of interest describing calcium phosphate cements include: 4,684,673 to Adachi et al.; 5,037,639 to tung et al., 5,683,461, 5,676,976 and 5,650,176 to Lee et al; 4,108,690, 5,968,253 to Posner et al.
  • Constantz et al. "Skeletal Repair by in Situ Formation of the Mineral Phase of Bone," Science (Mar. 24, 1995) 267: 1796-1798, describes a calcium phosphate cement comprising ⁇ -tricalcium phosphate, monocalcium phosphate monohydrate (MCPM), and CaC0 3 . Also of interest is Otsuka et al. "A Novel Skeletal Drug Delivery System Using Self-Setting Calcium Phosphate Cement. 9: Effects of the Mixing Solution Volume on Anticancer Drug Release from Homogeneous Drug-loaded Cement" J. Pharm. Sci.
  • an anticancer agent delivery system that combines desirable delivery characteristics (e.g. resorbability, controlled release, biocompatibility) in conjunction with the ability to be injectable, and thus able to administer the therapeutic mixture by syringe or cannula.
  • the present invention provides a nanocrystalline or poorly crystalline calcium phosphate composition for use in the local treatment of cancer.
  • the composition demonstrates excellent biocompatibility, controlled drug release and ease of administration.
  • the composition readily incorporates the drug with simple mixing and can be administered without invasive surgery by injection or by cannula.
  • the setting and crystallization properties of the composition are not significantly affected by the addition of a therapeutic agent.
  • the nanocrystalline or poorly crystalline features of the calcium phosphate carrier provide ideal drug delivery and bioresorption profiles.
  • a method for treating cancer in a mammal in which an anticancer composition is administered to a tumor site of the mammal.
  • the composition includes a mixture of an anticancer agent and a calcium phosphate paste, and the paste includes one or more nanocrystalline or poorly crystalline calcium phosphates and a physiologically acceptable fluid.
  • the paste has an injectable or formable consistency at the time of administration and is hardenable at the tumor site.
  • each calcium phosphate has a Ca/P ratio of less than or equal to 1.7.
  • the anticancer agent is selected from the group consisting of methotrexate, cis-platin, prednisone, hydroxyprogesterone, medrioxyprogesterone acetate, megestrol acetate, diethylstilbestrol, testosterone propionate, fluoxymesterone, vinblastine, vincristine, vindesine, daunorubicin, doxorubicin, hydroxyurea, procarbazine, aminoglutethimide, mechlorem-ui-iine, cyclophosphamide, mephalan, uracil mustard, chlorambucil, busulfan, carmustine, lomusline, dacarbazine (DTIC, dimethyltriazenomideazolecarboxamide), fluorouracil, 5-fluorouracil, cytarabine, cytosine arabinoxide, mercaptopurine, 6- mercaptomurine, tamoxifan, paclitaxel
  • the anticancer composition is administered to the tumor site by cannula or by injection, or the anticancer composition is administrable by cannula or injection more than five minutes after its preparation, or the anticancer composition is administrable by cannula or injection more than twenty minutes after its preparation.
  • the paste hardens into an apatitic calcium phosphate.
  • the nanocrystalline or poorly crystalline calcium phosphate paste comprises a calcium phosphate selected from the group consisting of poorly crystalline apatitic (PCA) calcium phosphates (PC A), dicalcium phosphates, such as dicalcium phosphate dihydrate (DCPD) and dicalcium phosphate anhydrous (DCPA), tricalcium phosphates (TCP), monetite, monocalcium phosphate monohydrate (MCPM), hetpacalcium phosphate, calcium pyrophosphate, calcium metaphosphate, octacalcium phosphates (OCP), hydroxyapatites (HA), or at least one of the nanocrystalline or poorly crystalline calcium phosphates is a poorly crystalline apatitic calcium phosphate.
  • PCA poorly crystalline apatitic calcium phosphates
  • DCPD dicalcium phosphate dihydrate
  • DCPA dicalcium phosphate anhydrous
  • TCP tricalc
  • each of the one or more nanocrystalline or poorly crystalline calcium phosphates has a calcium to phosphate ratio in the range of 1.0 to 1.67, or in the range of 1.3 to 1.67.
  • the nanocrystalline or poorly crystalline calcium phosphate paste has an overall calcium to phosphate ratio in the range of 1.0 to 1.7, or in the range of 1.40 to 1.65.
  • the nanocrystalline or poorly crystalline calcium phosphate paste comprises a physiologically acceptable fluid in an amount sufficient to produce a paste having injectable or formable consistency.
  • a therapeutically effect amount of anticancer agent is released from the composition for a time greater than one week, or for a time greater than two week, or for a time greater than one month, or for a time greater than three months.
  • delivery of the anticancer therapy to the tumor site is sufficient to prevent increase of tumor mass without significant weight loss of the mammal, or delivery of the anticancer therapy to the tumor site is sufficient to result in a decrease in tumor mass without significant weight loss in the mammal.
  • an anticancer composition includes a mixture of a physiologically effective amount of an anticancer agent and a calcium phosphate paste including one or more nanocrystalline or poorly crystalline calcium phosphate and a physiologically acceptable fluid.
  • the paste has an injectable or formable consistency at the time of administration and hardenable at the tumor site.
  • each calcium phosphate having a Ca/P ratio of less than or equal to 1.7.
  • the anticancer agent is selected from the group consisting of mefhotrexate, cis-platin, prednisone, hydroxyprogesterone, medrioxyprogesterone acetate, megestrol acetate, diethylstilbestrol, testosterone propionate, fluoxymesterone, vinblastine, vincristine, vindesine, daunorubicin, doxorubicin, hydroxyurea, procarbazine, aminoglutethimide, mechlorethamine, cyclophosphamide, mephalan, uracil mustard, chlorambucil, busulfan, carmustine, lomusline, dacarbazine (DTIC, dimethyltriazenon-rideazolecarboxamide), fluorouracil, 5-fluorouracil, cytarabine, cytosine arabinoxide, mercaptopurine, 6- mercaptomurine, tamoxifan, paclitaxel,
  • the nanocrystalline or poorly crystalline calcium phosphate cement comprises a calcium phosphate selected from the group consisting of amorphous calcium phosphate, poorly crystalline apatitic (PCA) calcium phosphates (PCA), dicalcium phosphates, such as dicalcium phosphate dihydrate (DCPD) and dicalcium phosphate anhydrous (DCPA), tricalcium phosphates (TCP), monetite, monocalcium phosphate monohydrate (MCPM), hetpacalcium phosphate, calcium pyrophosphate, calcium metaphosphate, octacalcium phosphates (OCP), hydroxy apatites (HA), or at least one of the nanocrystalline or poorly crystalline calcium phosphates is selected from the group consisting of amorphous calcium phosphate and poorly crystalline apatitic calcium phosphate.
  • PCA poorly crystalline apatitic calcium phosphates
  • DCPD dicalcium phosphate dihydrate
  • DCPA dicalcium phosphate anhydrous
  • each of the one or more nanocrystalline or poorly crystalline calcium phosphates has a calcium to phosphate ratio in the range of 1.3 to 1.67, or the nanocrystalline or poorly crystalline calcium phosphate paste has an overall calcium to phosphate ratio in the range of 1.0 to 1.7, in the range of 1.0 to 1.67 or in the range of 1.40 to 1.65.
  • the anticancer composition is of a consistency administrable to the tumor site by cannula or by injection.
  • the nanocrystalline or poorly crystalline calcium phosphate paste comprises a physiologically acceptable fluid in an amount sufficient to produce a paste having injectable or formable consistency for at least five minutes, or for at least twenty minutes.
  • the nanocrystalline or poorly crystalline calcium phosphate paste is hardenable into an apatitic calcium phosphate.
  • a therapeutically effect amount of anticancer agent is released from the composition for a time greater than one week, or for a time greater than two week, or for a time greater than one month, or for a time greater than three months.
  • delivery of the anticancer therapy to the tumor site is sufficient to at least prevent increase of tumor mass without significant weight loss of the mammal, or delivery of the anticancer therapy to the tumor site is sufficient to prevent a decrease in tumor mass without significant weight loss in the mammal.
  • the particle size of the calcium phosphate is selected to provide a desired release kinetic of the anticancer drug.
  • kits for use in preparing a flowable anticancer composition that remain injectable for at least about 20 minutes includes dry ingredients having a nanocrystalline or poorly crystalline calcium phosphate and a second calcium phosphate in a proportion of about 1:10 to 10:1 by weight; a physiologically acceptable aqueous lubricant in an amount sufficient to produce a flowable product upon combination with the dry ingredients; and an anticancer agent in an amount ranging from about 0.01 to 10 wt. % of the dry ingredients.
  • the kit further includes a means of mixing the dry ingredients and the lubricant, or an injecting means.
  • nanocrystalline calcium phosphate NCP
  • NCP nanocrystalline calcium phosphate
  • a means of mixing the dry ingredients and the lubricant or an injecting means.
  • nanocrystalline calcium phosphate NCP
  • a means of mixing the dry ingredients and the lubricant or an injecting means.
  • nanocrystalline calcium phosphate NCP
  • a means of mixing the dry ingredients and the lubricant or an injecting means.
  • nanocrystalline calcium phosphate is meant a calcium phosphate solid which exhibits crystalline domains on the order of nanometers or Angstroms.
  • NCP materials may include localized structure based upon well-known calcium phosphates, such as hydroxyapatite, tricalcium apatite, octacalcium phosphate, etc.; however, long-range order is substantially absent.
  • Exemplary NCP materials based upon hydroxyapatite are found in United States Patent No
  • PCA calcium phosphate a synthetic calcium phosphate of apatitic structure demonstrating only short-range crystallinity.
  • the PCA calcium phosphate is not necessarily restricted to a single calcium phosphate phase, provided is demonstrates the characteristic X-ray diffraction pattern of an apatitic mineral, namely two broad peaks in the region of 20-35° with a peak centered at 26° and a second peak centered at 32°.
  • Exemplary PCA calcium phosphate materials are found in U.S.S.N. 08/729,342, hereby incorporated by reference.
  • Figure 1 is a plot of the % tumor mass change over time in C3H mice for 25 mg kg cisplatin dose in calcium phosphate delivery vehicle (A), calcium phosphate delivery vehicle alone (?$), no treatment (+), and systemic IV administration of cisplatin (-);
  • Figure 2 is a plot of total body weight over time for C3H mice treated with cisplatin in calcium phosphate delivery vehicle of the invention ( ⁇ ), and for rats treated with a positive control (intravenous administration) ( ⁇ );
  • Figure 3 is a plot of the % tumor mass change over time for C3H mice for 25 mg/kg cisplatin dose in calcium phosphate delivery vehicle (A), calcium phosphate delivery vehicle alone ( ⁇ :), no treatment (+), and systemic IV administration of cisplatin (-); and
  • Figure 4 is a plot of total body weight over time for C3H mice treated with cisplatin in calcium phosphate delivery vehicle of the invention ( ⁇ ), and for rats treated with a positive control (intravenous administration) ( ⁇ ).
  • the nanocrystalline calcium phosphate composition of the invention demonstrates excellent biocompatibility, controlled drug release and ease of administration.
  • the composition readily incorporates the drug with simple mixing and can be administered without invasive surgery by injection or by cannula.
  • the flowable material may be injected into a cancellous bone void and the material sets into a solid calcium phosphate product that is capable of withstanding physiological loads, making such products extremely attractive for use in the treatment of bone tumors.
  • the composition may similarly be injected into soft-tissue tumors.
  • the flowable nature of the calcium phosphate composition of the invention allows the mixture to flow around and into the tumor, where it hardens into a calcium phosphate cement.
  • the tumor may be encapsulated thereby in the hardened calcium phosphate cement which confines the cancer cells of the tumor and helps to prevent metastasis.
  • the calcium phosphate paste may include any nanocrystalline or poorly crystalline calcium phosphate material in which the chemical composition and material properties have been selected to provide the desired flow properties and bioresorption.
  • the desired flow properties include the ability to deliver the calcium phosphate composition by syringe or cannula.
  • the paste is considered "injectable" if it is capable of passing through a 16 gauge needle. In preferred embodiments, injectability is maintained after storage, for example, for one minute, five minutes, ten minutes and most preferably 30 minutes. Injectability is evaluated by determining the ability to inject 1 cc of paste material through a 16 gauge needle or smaller, with only finger or hand pressure being applied by the user. The material is capable of injection through small gauge needles, e.g., 18-gauge to 25-gauge needles.
  • the paste is made up of a dry powder component, a liquid component and an anticancer agent.
  • the dry component includes one or more nanocrystalline calcium phosphates.
  • Each calcium phosphate has a calcium to phosphate (Ca/P) ratio of less than or equal to 1.7, and preferably a Ca/P ratio in the range of 1.0-1.65.
  • Calcium phosphates of interest include, but are not limited to, calcium phosphates such as poorly crystalline apatitic (PCA) calcium phosphates (PCA), dicalcium phosphates, such as dicalcium phosphate dihydrate (DCPD) and dicalcium phosphate anhydrous (DCPA), tricalcium phosphates (e.g., ⁇ - and ⁇ -TCPs), monetite, monocalcium phosphate monohydrate (MCPM), hetpacalcium phosphates, calcium pyrophosphates, calcium metaphosphates, octacalcium phosphates (OCP), hydroxyapatites (HA), which are nanocrystalline or poorly crystalline in nature.
  • PCA poorly crystalline apatitic calcium phosphates
  • DCPD dicalcium phosphate dihydrate
  • DCPA dicalcium phosphate anhydrous
  • tricalcium phosphates e.g., ⁇ - and ⁇ -TCPs
  • monetite
  • calcium phosphates are described by Driessen (1995), which is hereby incorporated by reference. Carbonated or otherwise substituted versions of these calcium phosphates are also contemplated in the invention. Calcium deficient or poorly crystalline apatitic calcium phosphates having a Ca/P ratio of about 1.0-1.65, preferably 1.0-1.6, or 1.0-1.5 or 1.0-1.4, or 1.50-1.65, and more particularly 1.55-1.65, are preferred. Another preferred calcium phosphate is nanocrystalline calcium phosphate (NCP), in particular a hydroxyapatitic NCP.
  • NCP nanocrystalline calcium phosphate
  • the preferred nanocrystalline calcium phosphates, NCP, or PCA calcium phosphate may be used alone, or in combination with each other, or individually with a second calcium phosphate to form the dry component of the composition.
  • Suitable second calcium phosphates are those which are capable of reacting with the primary calcium phosphate to form a hardened cement.
  • Exemplary calcium phosphates include dicalcium phosphates, such as dicalcium phosphate dihydrate (DCPD) and dicalcium phosphate anhydrous (DCPA), tricalcium phosphates (TCP), monetite, monocalcium phosphate monohydrate (MCPM), hetpacalcium phosphate, calcium pyrophosphate, calcium metaphosphate, octacalcium phosphates (OCP), hydroxyapatites (HA).
  • a preferred dry powder combination is a nanocrystalline calcium phosphate and dicalcium phosphate, e.g., DCPD.
  • Another preferred embodiment is a poorly crystalline apatitic calcium phosphate and a dicalcium phosphate.
  • a detailed description of the preparation and characteristics of suitable calcium phosphates can be found in U.S. Patent No. 5,783,217, which is hereby incorporated by reference.
  • a particularly preferred dry component is a combination of calcium phosphate powders which react to form an apatitic calcium phosphate.
  • Hydroxy apatite is the mineral component of naturally-occurring bone having a Ca/P ratio of 1.67, although the actual Ca/P ratio of bone varies between 1.5 and 1.7.
  • the composition and relative amounts of the dry powder components preferably are selected to provide an overall Ca/P ratio in the range of 1.0-1.7, or 1.3-1.65, or 1.4-1.6, or preferably close to that of naturally-occurring bone, that is in the range of 1.45 to 1.7. It has been observed that calcium-deficient compositions exhibit more rapid, resorption characteristics. In some embodiments where rapid resorption is desired, it may be desired to use select dry powder components to provide an overall Ca/P ratio of less than 1.67, and preferably in the range of 1.4 to 1.65.
  • the composition of the invention also includes one or more anticancer agents.
  • the anticancer agent may be introduced with the powder component, or with the liquid component of the composition, or it may be separately added to the composition.
  • Suitable anticancer agents may be one or more of known chemotherapy drugs such as methotrexate, cis-platin, prednisone, hydroxyprogesterone, medrioxyprogesterone acetate, megestrol acetate, diethylstilbestrol, testosterone propionate, fluoxymesterone, vinblastine, vincristine, vindesine, daunorubicin, doxorubicin, hydroxyurea, procarbazine, aminoglutethimide, mechlorethamine, cyclophosphamide, mephalan, uracil mustard, chlorambucil, busulfan, carmustine, lomusline, dacarbazine (DTIC, 5 dimethyltxiazenomideazolecarboxarnide), fluorouracil,
  • the amount of anticancer agent that is present in the cement will be sufficient to provide a composition that at least prevents tumor growth in the region where the composition has been introduced as compared to a control. In preferred embodiments, the amount and effectiveness of the anticancer agent is sufficient to reduce the tumor size or even to
  • two or more anticancer agents are included in the composition.
  • Certain combination therapies have been identified as particularly effective and are found in Table 2.
  • the amount of anticancer agent that is present in the cement will generally range from about 0.01 to 10, usually from about 0.01 to 5.0 and more usually from about 0.01 to 3.0% by weight of the dry ingredients of the cement. Table 2.
  • kits comprising the subject chemotherapeutic delivery vehicle, where the dry and liquid components may be present in separate containers in the kit, or some of the components may be combined into one container, such as a kit wherein the dry nanocrystalline or poorly crystalline calcium phosphate components are present in a first container and the liquid components are present in a second container. Instructions for use may also be included.
  • the kit preferably includes dry ingredients comprising amorphous calcium phosphate, nanocrystalline or PCA calcium phosphate and a second calcium phosphate in a proportion of about 1 : 10 to 10:1 by weight, and preferably about 50:50 by weight; a physiologically acceptable aqueous lubricant (liquid component) in an amount sufficient to produce a flowable product upon combination with said dry ingredients; and an anticancer agent in an amount sufficient to produce the desired pharmaceutical effect and typically ranging from about 0.01 to 10 wt. % of said dry ingredients. Due to the need to carefully titrate the amount of anti-cancer agent based upon patient body mass and tumor size, the agent may be added separately. The agent may be added to the liquid component prior to mixing with the dry component, or it may be added to the injectable paste, once formed.
  • the dry components and the liquid components will be combined using any suitable means to produce a homogeneous, flowable paste-like material having the characteristics described above.
  • One suitable means of combining the dry and liquid components is a mortar and pestle, with which the liquid and solid components are mixed to produce the flowable paste.
  • the calcium phosphate composition is formed into an injectable gel or solid nanoparticle paste by the addition of a liquid component or lubricant.
  • the liquid component is a physiologically acceptable liquid, such as but not limited to, water, saline, sodium phosphates, buffer solutions, serum, or tissue culture media.
  • the liquid component may include one or more solutes, selected to buffer the liquid, stabilize the anti-cancer agent, or otherwise modify the properties of the calcium phosphate composition, e.g., modify reaction and hardening times or modify the composition or crystallinity of the product calcium phosphate.
  • sodium phosphate is typically used to accelerate the hardening of the calcium phosphate paste.
  • the preferred calcium phosphate paste may be designed to absorb, bind, entrap or otherwise contain the anticancer agent.
  • the calcium phosphate cements, paste-like compositions and products are combined with an anticancer agent for its local delivery to a physiological site of interest.
  • the calcium phosphate paste containing the anticancer agent remains formable and injectable at room temperature, facilitating the administration of the composition to a tumor site by injection or by cannula.
  • the calcium phosphate cement may be selected to set rapidly or slowly at room temperatures. In many instances it will be advantageous to have the calcium phosphate paste set slowly at room temperature, for example, to allow the medical professional adequate time to administer the therapeutic composition to the tumor site. For example, the calcium phosphate paste may remain flowable and injectable at room temperatures for a significant time, e.g., more than 5 minutes, more than 10 minutes, more than 20 minutes, and up to an hour. The calcium phosphate paste should nonetheless set rapidly under physiological conditions, e.g., less than 20 minutes, less than 10 minutes and preferably within 5 minutes.
  • preferred calcium phosphate compositions exhibit a "dual setting" characteristic in that they are slow to set at about room temperature, e.g., 20-25 °C, yet set rapidly at physiological temperatures e.g., 35-40 °C.
  • a composition including PCA calcium phosphate as one of the components may be used.
  • accelerators may be added to the composition.
  • exemplary accelerators include water-soluble sodium salts, such as sodium phosphate, sodium succinate, sodium lactate, sodium chloride, sodium acetate and the like.
  • Setting times may be determined using well-established standards, such as the Gillmore needle test (ASTM C 266-89 Standard Test Method of Time of Setting of Hydraulic-Cement Paste by Gillmore Needles) and the needle penetration test C 403/C 403M-95 Standard Test Method for Time of Setting of Concrete Mixtures by Penetration Resistance. The effect of the anticancer agent on the setting times may be determined using these tests as well.
  • the calcium phosphate composition may be formulated to be resorbable over a preselected period of time.
  • Calcium phosphate cements may be prepared which resorb within at least about 1 week, within about one month, within about one month and preferably within a year, so that the calcium phosphate cement may release the anticancer agent into their local environment for as long as is needed, depending on the specific cement from which the composition is prepared.
  • the subject compositions find use as anticancer agent delivery vehicles, i.e.
  • anticancer agent depots in which the local delivery of an anticancer agent for an extended period of time is desired.
  • the subject compositions find particular use as local anticancer agent delivery vehicles for bone tissue, particularly cancellous bone tissue. In most cases, the anticancer compositions are resorbable.
  • Resorbable calcium phosphate cements biodegrade over time, ultimately leaving little or no residual material in the body. Resorbability generally eliminates the need for surgical removal of the delivery vehicle, after completion of chemotherapy. Resorbable calcium phosphate cements also allow the controlled delivery of active agents to a the tumor site at a specific rate.
  • the anticancer agent typically is delivered to a tumor site at a rate comparable to the resorption rate.
  • Custom designed resorbability characteristics of the anticancer composition provides for selected delivery rates.
  • weakly resorbing calcium phosphate cements will be used to provide a slow release delivery of the anticancer agent to the tumor site.
  • the calcium phosphate cement will be strongly resorbable and provide a means to deliver a fast, quick dose of the anticancer agent to the tumor site.
  • a combination of weakly and strongly resorbable calcium phosphates will be used to produce a variable or pulsatile kinetic release. The resorption rate, and therefore the delivery rate, can be adjusted to hours, days, weeks, months, and even years by varying the preparations of the variously resorbing components.
  • a strongly resorbing calcium phosphate is characterized as follows: when at least 0.1 gram (preferably 0.1-0.5 g) is implanted in an osseous, subcutaneous or intramuscular site, at least 80% of the material is resorbed within one year. In more preferred embodiments, 0.5 gram of the calcium phosphate will be resorbed within nine months, six months, three months, and ideally one month or less, depending of the desired delivery profile desired at the tumor site. Weakly resorbable means that less than 80% of 0.1 gram of starting calcium phosphate is resorbed after one year. Resorption, as used herein, encompasses solubility based dissolution processes, as well as active cellular or enzyme based processes.
  • the inventive calcium phosphate cements can be tailored to have linear resorption rates, and can be tailored to avoid initial high concentration spikes where undesirable.
  • Resorbability of the calcium phosphate vehicles also may be varied through the adjustment of one or more physical parameters including vehicle size, vehicle particle size, porosity, density, and/or crystallinity.
  • vehicle size For example, monolithic devices, on the order of one gram will resorb more slowly than one gram of the same material when in particulate form. Two or more of these parameters will generally be adjusted in concert to fine-tune the final resorption rate.
  • particle sizes may be controlled by careful control of the precipitation rate. Rapid precipitation, followed by rapid harvesting of the precipitate, is useful in the production of small particle sizes (e.g. particle size ranging from 5 nm to 150 nm) of low crystallinity.
  • Cements can be induced to form particulates during hardening through the use of an emulsifying agent and injection of the cement as an emulsion.
  • Emulsifying agents will be solubilized from the hardened material leaving a macropore matrix.
  • Suitable emulsifying agents include lethicin, dimethicone, and the like.
  • Density of the hardened calcium phosphate composition also has a significant effect on resorption rates. Different calcium phosphate compositions result in different density and grain sizes. Higher density or larger grain size, of course, reduce resorption rates. Leachable or biodegradable materials may be incorporated into the paste that may be subsequently removed in vivo, e.g., by dissolution or cellular action, so that a porous vehicle results. Suitable additives should of course be biocompatible and physiologically acceptable at the doses required to are discussed in Driessens et al. in Enclyclopedic Handbook of Biomaterials and Bioengineering. Chapter 31, “Calcium Phosphate Bone Cements”, Wise (Ed.), Marcel Dekker (1995).
  • Selection of the particular calcium phosphates may be made to provide a desired resorption rate in the device.
  • Control of the calcium phosphate cement degree of crystallinity and crystal size may be used to affect the overall vehicle resorption rate.
  • poorly crystalline forms are believed to resorb more slowly than less crystalline forms, e.g., amorphous calcium phosphates. This may be an advantage in some applications where sustained release over long time periods is desired.
  • calcium phosphate cements prepared with nanocrystalline calcium phosphate, and in particular with nanocrystalline calcium phosphate and dicalcium phosphate dihydrate resorb slowly, e.g., over the course of more than one month.
  • Increased resorption rates may be achieved through the production of apatitic calcium phosphates containing lattice defects, such as ionic vacancies or substitutions.
  • Preferred embodiments include carbonated or otherwise calcium deficient apatites, i.e., Ca/P ⁇ 1.67, all of which tend to have increased in vivo resorption rates.
  • Each type of calcium phosphate cement may be preferred in specific therapeutic settings.
  • the inventive delivery vehicle can be of any porosity that provides the desirable characteristics for anticancer drug delivery. Porosity facilitates both the diffusion of substances to and rom the inventive material and, in certain applications, the penetration of cells and cell processes into the material matrix. Accordingly, calcium phosphate cements of lower porosity tend to resorb more slowly in vivo than those of higher porosity; therefore, the greater the porosity, the greater the rate of resorption. In one embodiment of the invention, porosity is increased through the use of a dry mixture of controlled particle size reactants. For example, a reactant with a larger particle size (e.g. 300-500 ⁇ m) will produce a more porous material. Soluble porogens may also be used to control the porosity of the calcium phosphate material.
  • certain molecular factors may be incorporated into the vehicle that can be used to affect its resorption rate by influencing the cellular or enzymatic processes that ordinarily mediate vehicle resorption in the body.
  • These incorporated factors are often biologically active molecules or collections thereof, which affect bone metabolic processes, such as the activity of osteoclasts and/or osteoblasts.
  • the incorporated factors attract or otherwise affect the activity of one or more of macrophages, monocytes, or foreign body giant cells.
  • useful factors include: growth factors, enzyme inhibitors, extracellular matrix components, cytokines and the like.
  • Incorporation of factors, which attract or inhibit osteogenic cells and/or macrophages, can have a significant effect on calcium phosphate cement resorption rate.
  • incorporation of bone morphogenetic protein into the inventive calcium phosphate cements will lead to more rapid resorption of the vehicle, particularly in soft tissue implant sites.
  • factors that attract osteoclasts e.g. interleukin-1, lymphotoxin, calcitonin,
  • Osteoclast or macrophage activity inhibitors e.g. neutral phosphate, glucocorticoids, plicamycin, gallium nitrate
  • Extracellular matrix components such as laminen, RDG peptides, collagen, fibronectin may also be included with the calcium phosphate cements.
  • Further guidance regarding specific factors useful in the regulation of calcium phosphate resorption rates can be found in PCT/US97/18528, incorporated by reference herein. Generally, these factors will be incorporated into the inventive calcium phosphate cements as a concentration of less than 20% wt/wt preferably less than 10% and in most embodiments, less than 5%. In many instances, calcium phosphate cement resorbability is preferred; however, it is not always required or desired. In some embodiments, a calcium phosphate cement that is either weakly resorbable or substantially non-resorbable may be used.
  • a non-resorbable calcium phosphate cement may be used when prolonged chemotherapy is required over a matter of several years.
  • a non-resorbable calcium phosphate cement may also be desirable in cases when the calcium phosphate cement is used additionally as a support matrix for tissue repair or growth, as a treatment for a disease.
  • Non-resorbable calcium phosphate calcium phosphate cements can remain in the body without detrimental effects to the host due to their excellent biocompatibility.
  • non-resorbable calcium phosphate cements may be surgically removed following the desired delivery period.
  • Suitable non-resorbable or weakly resorbable calcium phosphate calcium phosphate cements include those prepared from sintered hydroxyapatite.
  • resorption rates may be established empirically by using intramuscular or subcutaneous implantation of the calcium phosphate cement in one or more small animal models to assess the exact effect of formulation adjustments on calcium phosphate cement resorption rates.
  • candidate formulations may be tested simultaneously and resorption rates can be compared at various time points using standard histological, radiographic or other methods know to the art.
  • the calcium phosphate paste may also be formulated in a manner which enhances its receptiveness to the cancer cells.
  • the pH of the delivery vehicle may be tailored to be particularly receptive to cancer cells. Cancer cells typically produce an environment that is of lower pH (more acidic) than that associated with healthy host cells.
  • the composition of the calcium phosphate paste may be selected to provide a resultant hardened calcium phosphate having a pH which enhances the effectiveness of the anticancer therapy.
  • Practitioners of calcium phosphate chemistry will know to use those calcium phosphates having the least solubility (for longer release times) at the expected pH at physiological temperatures.
  • the composition is selected for pH stability at neutrality or under slightly acidic conditions.
  • Guidance for preparations of calcium phosphate cements of differing pHs can be found in the solubility isotherm data such as that provided by Brown in "Phase relationships in the ternary system CaO-P 2 0 5 -H 2 0 at 25 C," Amer. Ceram. Soc. 75: 17 (1992) and by J.C.
  • the invention also provides a method for the treatment of cancer.
  • the method includes administering an anticancer composition to a tumor site of a patient.
  • the anticancer composition includes a mixture of an anticancer agent in a calcium phosphate paste delivery vehicle.
  • the paste is made up of two or more calcium phosphates and a physiologically acceptable fluid, each calcium phosphate having a Ca/P ratio of less than or equal to 1.7.
  • the paste is injectable or formable at the time of administration which allows the paste to be introduced directly at and into the tumor. The paste then hardens rapidly at the tumor site.
  • the method of the invention has been investigated for the treatment of breast and prostate cancer, although the methods and compositions described herein may be readily adapted for the treatment of many kinds of cancer.
  • Example 1 This example illustrates the typical formation of a nanocrystalline calcium phosphate (NCP) gel for use in a drug delivery preparation for delivery of a chemotherapeutic.
  • NCP nanocrystalline calcium phosphate
  • a solution of 218 g of disodium Na 2 HP0 4 -12 H 2 0 in 1.2 liters of distilled water and a solution of 70 g of Ca(N0 3 ) 2 -4H 2 0 in 0.5 liters of distilled water were prepared.
  • the calcium solution was quickly poured into the phosphate solution at room temperature with stirring. Precipitation was immediate and substantially complete.
  • the precipitate was adjusted to pH 6.4 by the addition of sodium hydroxide solution in order to avoid the formation of acidic calcium phosphates.
  • the precipitate was aged at room temperature for 5 minutes prior to filtration.
  • the precipitate was then filtered through a Buchner filter (with a total surface about 0.1 m 2 ), and was washed by about 3 liters of distilled water.
  • a gel cake of nanocrystalline calcium phosphate obtained on the filter paper.
  • Example 2 This example illustrates the typical formation of a nanocrystalline calcium phosphate (NCP) powder for use in a drug delivery preparation for delivery of a chemotherapeutic.
  • the calcium phosphate apatite material was prepared according to example 3 but with the following modifications.
  • the washed precipitate was collected using a spatula and immersed into liquid nitrogen in a 2.5 L container. Following freezing, the container was transferred into a vacuum chamber for 24 hours (10 "1 - 10 "2 torr), until a fine and dry powder was obtained.
  • Example 3 This example illustrates the preparation of an apatitic calcium phosphate drug delivery agent for delivery of a chemotherapeutic using NCP powder.
  • NCP was made by combining two solutions at room temperature.
  • Solution A contained 87.6 g calcium nitrate tetrahydrate in 624 mL of distilled water (pH 5.45).
  • Solution B contained 203.7 g dibasic sodium phosphate heptahydrate and 100.0 g sodium bicarbonate in 2000 mL of distilled water. After mixing together for two minutes at room temperature (pH 6.60), 42 mL of 10% wt/wt NaOH solution was added to the reaction mixture over 11 minutes to bring the pH to 7.29. The mixture was filtered by vacuum filtration (650 mL per funnel) and washed four times with 1000 mL of distilled water. After the last wash, the material was covered in liquid nitrogen and lyophilized for 24 hours. After lyophilization, the powder was pushed through a 500 ⁇ m sieve.
  • DCPD Dicalcium phosphate dihydrate
  • the nanocrystalline calcium phosphate material was physically dry-mixed with DCPD at 50:50 weight percent using a mortar and pestle for 3-5 minutes. Water (1 ml/g of mixed material) was then added to the powder mixture to yield a hydrated precursor of paste-like consistency. The amount of H 2 0 added varied, depending on whether a thick or thin paste was desired.
  • the paste material was then placed in a moist tissue environment where upon reaching body temperature (37°C), it hardened into a solid mass. The hardening process could be delayed for several hours by placing it into a refrigerating temperature of 4°C.
  • Example 4 The goal of this study was to use a calcium phosphate material as a delivery vehicle for cisplatin at a mammary tumor site and to evaluate the effectiveness of cisplatin-calcium phosphate delivery system in treating MTGB Mouse cancer tumors in C3H mice.
  • a protocol was established to administer a two component calcium phosphate delivery vehicle using the material of Example 6 to a tumor interior.
  • the material was tested at two different cisplatin dosage levels and compared against a systemically delivered control.
  • Table 4 includes the protocol used for the mice study (total of 80 athymic nude mice).
  • mice were C3H mice (approx. 20 g). They were housed in solid bottom mouse cages maintained within a semi-rigid isolator. They were fed an 18% protein, 5% fat rodent laboratory chow fed ad-lib, gamma-irradiated prior to use. Water was sterile filtered and provided in water bottles. Ambient temperature is 72 degrees F +/- 5 degrees with a relative humidity of 50% +/- 20%.
  • mice were innoculated subcutaneously in the flank area with 1 x 10 6 tumor cell in 0.1 mL of RPMI culture medium. After tumors had grown to 8-10 mm, 0.1 cc of treatment or control materials (except for positive systemic controls which were administered by TV) were injected directly into the tumor with an 18-gauge needle.
  • the positive control cisplatin solution was prepared by dissolving a specified amount of cisplatin in sterile saline for injection through a 25 gauge needle directly into the tumor.
  • the appropriate calcium phosphate delivery vehicle was supplied as a sterile powder in a preweighed package.
  • each powder was hydrated with the appropriate amount of saline and loaded into a 0.1 cc syringe for injection through a 16 gauge needle.
  • Each material was mixed on site and immediately injected at the tumor site using a 1 cc syringe with a Luer-Lok® tip and a 16-gauge needle.
  • each animal was weighed and its tumor size was recorded, using hand-held calipers for the measurements. Mice were sacrificed when tumor mass was greater than 10% of body weight. Animals were monitored over a 20-day period for changes in body weight and tumor mass. Tumor shrinkage accompanied by the absence of toxic side effects (as determined by loss of body weight) was considered an indication of successful treatment.
  • Figure 1 is a plot of the % tumor mass change over time for 25 mg/kg cisplatin dose in calcium phosphate delivery vehicle (A), calcium phosphate delivery vehicle alone ($1$), no treatment (+), and systemic IV administration of 25 mg/kg cisplatin (-).
  • negative control animals curves ( ⁇ ) and (+)
  • the plot clearly demonstrates that the cisplatin locally delivered to the tumor in a calcium phosphate delivery vehicle based on NCP/DCPD matched the ability of intravenous delivery of cisplatin (positive control); however, positive control animals died on Day 5 due to excessive weight loss. See, Figure 2.
  • Example 5 The goal of this study was to use a calcium phosphate material as a delivery vehicle for cisplatin at a prostate cancer tumor site and to evaluate the effectiveness of cisplatin-calcium phosphate delivery system in treating DU-145 human cancer tumors in nude mice.
  • a protocol was established to administer a two component calcium phosphate delivery vehicle using the material of Example 6 to a tumor interior.
  • the material was tested at two different cisplatin dosage levels and compared against a systemically delivered control.
  • Table 5 includes the protocol used for the mice study (total of 36 -NI /NU-nuBR nude mice).
  • mice were female 5-6 week old Crl:NU/NU-nuBR, which are nude outbred mice, mice (approx. 17-21 g). They were housed in solid bottom mouse cages maintained within a semi-rigid isolator. They were fed a 18% protein, 5% fat rodent laboratory chow fed ad-lib, gamma- irradiated prior to use. Water was sterile filtered and provided in water bottles. Ambient temperature is 72 degrees F +/- 5 degrees with a relative humidity of 50% +/- 20%.
  • mice were innoculated subcutaneously in the flank area with 2 x 10 6 tumor cell in 0.1 mL of RPMI culture medium with 30% Matrigel. After tumors had grown to 100 ⁇ 35 mg, 0.1 cc of treatment or control materials (except for positive systemic controls which were administered by IV) were injected directly into the tumor with an 18-gauge needle.
  • the positive control cisplatin solution was prepared by dissolving a specified amount of cisplatin in sterile saline for injection through a 25 gauge needle directly into the tumor.
  • the appropriate calcium phosphate delivery vehicle was supplied as a sterile powder in a preweighed package.
  • each powder was hydrated with the appropriate amount of saline and loaded into a 0.1 cc syringe for injection through a 16 gauge needle.
  • Each material was mixed on site and immediately injected at the tumor site using a 1 cc syringe with a Luer- Lok® tip and a 16-gauge needle.
  • each animal was weighed and its tumor size was recorded, using hand-held calipers for the measurements. Mice were sacrificed when two consecutive tumor mass measurements greater than 1000 mg were recorded. Animals were monitored over a 20-plus day period for changes in body weight and tumor mass. Tumor shrinkage accompanied by the absence of toxic side effects (as determined by loss of body weight) was considered an indication of successful treatment.
  • Figure 3 is a plot of the % tumor mass change over time for (a) 25 mg/kg cisplatin dose in calcium phosphate delivery vehicle, (b) calcium phosphate delivery vehicle alone, (c) no treatment and (d) systemic IV administration of 25 mg/kg cisplatin.
  • negative control animals curve (b)
  • curve (b) which received no chemotherapy, demonstrated rapid and excessive tumor growth.
  • the animals were sacrificed on Day 14 due to excessive tumor load.
  • the plot clearly demonstrates that the cisplatin locally delivered to the tumor in a calcium phosphate delivery vehicle based on NCP/DCPD matched the ability of intravenous delivery of cisplatin (positive control) to contain tumor growth; however, positive control animals died on Day 4 due to excessive weight loss. See, Figure 4. Positive control animals, however, remained active and apparently healthy over the 21 day observation period.

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Abstract

La présente invention concerne une méthode et une composition utiles pour traiter le cancer chez un mammifère. La méthode consiste à administrer au mammifère à l'endroit de la tumeur, une composition anticancéreuse et une pâte de phosphate de calcium nanocristallin ou faiblement cristallin, ladite pâte étant formée d'au moins un phosphate de calcium et d'un fluide physiologiquement acceptable, la pâte présentant une consistance qui permet de l'injecter ou de la façonner au moment de l'administration, cette pâte durcissant à l'endroit de la tumeur.
PCT/US2001/051419 2000-10-20 2001-10-19 Composition chimiotherapeutique renfermant une pate de phosphate de calcium nanocristallin WO2002041844A2 (fr)

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Cited By (8)

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WO2005074991A1 (fr) * 2004-02-09 2005-08-18 Kabushiki Kaisha Sangi Agent antitumoral
EP2076241A2 (fr) * 2006-07-12 2009-07-08 McGILL UNIVERSITY Particules fibreuses de pyrophosphage de calcium, procédés de fabrication et méthodes d'utilisation
US8124118B2 (en) 2003-10-22 2012-02-28 Lidds Ab Composition comprising biodegradable hydrating ceramics for controlled drug delivery
US8293274B2 (en) 2005-04-06 2012-10-23 Kabushiki Kaisha Sangi Intestinal absorptive anti-tumor agent
US8790679B2 (en) 2002-12-20 2014-07-29 Xeris Pharmaceuticals, Inc. Intracutaneous paste composition
AU2014200476B2 (en) * 2002-12-20 2015-05-28 Xeris Pharmaceuticals, Inc. Intracutaneous injection
CN109432493A (zh) * 2018-09-26 2019-03-08 四川大学 纳米羟基磷灰石涂层多孔钛支架及其制备方法和应用
SE2130219A1 (en) * 2021-08-08 2023-02-09 Aduro Mat Ab Controlled drug release material

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US5085861A (en) * 1987-03-12 1992-02-04 The Beth Israel Hospital Association Bioerodable implant composition comprising crosslinked biodegradable polyesters
US5462751A (en) * 1990-06-22 1995-10-31 The Regeants Of The University Of California Biological and pharmaceutical agents having a nanomeric biodegradable core
US5782971A (en) * 1991-06-28 1998-07-21 Norian Corporation Calcium phosphate cements comprising amorophous calcium phosphate

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US4016252A (en) * 1972-04-06 1977-04-05 Institut Pasteur Calcium phosphate gel for adsorbing vaccines
US5085861A (en) * 1987-03-12 1992-02-04 The Beth Israel Hospital Association Bioerodable implant composition comprising crosslinked biodegradable polyesters
US5462751A (en) * 1990-06-22 1995-10-31 The Regeants Of The University Of California Biological and pharmaceutical agents having a nanomeric biodegradable core
US5782971A (en) * 1991-06-28 1998-07-21 Norian Corporation Calcium phosphate cements comprising amorophous calcium phosphate
US5782971B1 (en) * 1991-06-28 1999-09-21 Norian Corp Calcium phosphate cements comprising amorophous calcium phosphate

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8790679B2 (en) 2002-12-20 2014-07-29 Xeris Pharmaceuticals, Inc. Intracutaneous paste composition
EP3597262A1 (fr) * 2002-12-20 2020-01-22 Xeris Pharmaceuticals, Inc. Formulation pour injection intracutanée
US9314424B2 (en) 2002-12-20 2016-04-19 Xeris Pharmaceuticals, Inc. Pastes for injection of a therapeutic agent
AU2014200476C1 (en) * 2002-12-20 2015-12-03 Xeris Pharmaceuticals, Inc. Intracutaneous injection
AU2014200476B2 (en) * 2002-12-20 2015-05-28 Xeris Pharmaceuticals, Inc. Intracutaneous injection
US8124118B2 (en) 2003-10-22 2012-02-28 Lidds Ab Composition comprising biodegradable hydrating ceramics for controlled drug delivery
EP1680089B1 (fr) * 2003-10-22 2013-09-11 Lidds AB Composition comprenant des ceramiques d'hydratation biodegradables pour une administration de medicaments controlee
US9034359B2 (en) 2003-10-22 2015-05-19 Lidds Ab Composition comprising biodegradable hydrating ceramics for controlled drug delivery
JP4982084B2 (ja) * 2004-02-09 2012-07-25 株式会社サンギ 抗腫瘍剤
JPWO2005074991A1 (ja) * 2004-02-09 2007-10-11 株式会社サンギ 抗腫瘍剤
WO2005074991A1 (fr) * 2004-02-09 2005-08-18 Kabushiki Kaisha Sangi Agent antitumoral
US8293274B2 (en) 2005-04-06 2012-10-23 Kabushiki Kaisha Sangi Intestinal absorptive anti-tumor agent
US8084060B2 (en) 2006-07-12 2011-12-27 Nanunanu Ltd. Fibrous calcium pyrophosphate particles and methods of making and using same
WO2008006204A3 (fr) * 2006-07-12 2011-02-03 Mcgill University Particules fibreuses de pyrophosphage de calcium, procédés de fabrication et méthodes d'utilisation
EP2076241A2 (fr) * 2006-07-12 2009-07-08 McGILL UNIVERSITY Particules fibreuses de pyrophosphage de calcium, procédés de fabrication et méthodes d'utilisation
EP2076241A4 (fr) * 2006-07-12 2012-10-03 Nanunanu Ltd Particules fibreuses de pyrophosphage de calcium, procédés de fabrication et méthodes d'utilisation
CN109432493A (zh) * 2018-09-26 2019-03-08 四川大学 纳米羟基磷灰石涂层多孔钛支架及其制备方法和应用
CN109432493B (zh) * 2018-09-26 2021-04-06 四川大学 纳米羟基磷灰石涂层多孔钛支架及其制备方法和应用
SE2130219A1 (en) * 2021-08-08 2023-02-09 Aduro Mat Ab Controlled drug release material
SE545583C2 (en) * 2021-08-08 2023-10-31 Aduro Mat Ab Controlled drug release material

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