WO2002051403A1 - Compositions of stable t3 and methods of use thereof - Google Patents

Compositions of stable t3 and methods of use thereof Download PDF

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Publication number
WO2002051403A1
WO2002051403A1 PCT/US2001/044855 US0144855W WO02051403A1 WO 2002051403 A1 WO2002051403 A1 WO 2002051403A1 US 0144855 W US0144855 W US 0144855W WO 02051403 A1 WO02051403 A1 WO 02051403A1
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composition
composition according
administered
cardiac
serum albumin
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PCT/US2001/044855
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French (fr)
Inventor
Irwin Klein
Kaie Ojamaa
Leo Rubin
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Resuscitek, Inc.
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Priority to CA2432523A priority Critical patent/CA2432523C/en
Priority to JP2002552548A priority patent/JP2004525874A/en
Priority to DE60130145T priority patent/DE60130145T2/en
Priority to EP01272465A priority patent/EP1351673B1/en
Priority to ES01272465T priority patent/ES2291274T3/en
Priority to AT01272465T priority patent/ATE370729T1/en
Publication of WO2002051403A1 publication Critical patent/WO2002051403A1/en

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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
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • 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
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/02—Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention relates generally to a stable aqueous formulation of T 3 for treating patients to restore effective cardiac function.
  • Serum albumin is a serum protein fraction involved in maintaining blood osmotic pressure and is used as a plasma substitute in shock treatment. Serum Albumin also contributes to many body transport and regulatory processes. Like many other substances, such as N-oxy trimethyl amines, amino acids, alkylated amino acids, and sugars, serum albumin is used as a protein protectant to stabilize proteins against denaturation and to preserve enzymatic activity as well as in formulation of biomedicals.
  • U.S. Patent No. 5,876,992 discloses the use of serum albumin, together with disaccharides or their derivatives to stabilize proteins. Serum albumin has been used to preserve the integrity of urinary proteins.
  • Thyroid hormones include the L-forms of thyroxine (4-(4-Hydroxy-3,5- diiodophenyl)-3,5-diidotyrosine; hereinafter T 4 ) and 3, 5, 3'-triiodothyronine (T ). They can be obtained from natural sources, such as bovine thyroid glands or synthesized. U.S. Patent No. 2,803,654.
  • Thyroid hormones administered to patients with cardiovascular compromise restore or improve cardiac rhythm and function. Thyroid hormones increase heart rate and heart beat force thus increasing cardiac output and are found to be significantly decreased during cardiac arrest. Wortsman et al. (1987) Arch. Intern. Med. 147:245-248. An infusion of thyroid hormone effects cardiac resuscitation in patients undergoing cardiac arrest, cardiac standstill, electro-mechanical dissociation and a variety of other cardiac conditions. The effect of thyroid hormone is almost immediate and occurs even where standard treatments have failed. Thyroid hormones are also therapeutically effective in other cardiac indications such as cardiomyopathies and bradyarrhythmias. Of the thyroid hormones, T is normally synthesized in smaller quantities than T 4 and presents in blood and the thyroid gland.
  • T 3 is more potent and the onset of its effect is more rapid than T 4 and is synthesized in the thyroid gland and by metabolism of T 4 in peripheral tissues by the enzyme 5' deiodinase.
  • T 4 has been the preferred thyroid hormone in clinical use today, largely due to its availability and relatively long half-life of 6-7 days because T 4 binds avidly to thyroxine-binding globulin in human serum and is thus protected from metabolism and excretion.
  • T 3 has higher potency and more rapid effect than T 4 in resuscitate patients undergoing cardiac arrest.
  • T 3 is unstable in aqueous solution with an extremely short half-life. This short half-life has limited the application of T 3 in treating patients, especially in emergency situations where the injection of an aqueous thyroid hormone solution is required.
  • the invention encompasses a stable aqueous pharmaceutical composition containing T 3 , serum albumin and water. Dried samples for reconstitution are also encompassed by the invention as are various pharmaceutical preparations.
  • the invention further relates to a method for emergency treatment of a patient with cardiac arrest, and with cardiac electrical standstill, to restore effective cardiac function, by administering to the patient a therapeutically effective amount of a pharmaceutical composition of T , serum albumin and water.
  • Figure 1 describes mortality rate as a function of the level of thyroid hormone during acute myocardial infarction.
  • Figure 2 shows hemodynamic data after defibrillation (5 min-VF).
  • FIG. 3 describes detailed procedures for testing the effectiveness of T 3a (Protocol 1).
  • Figure 4(A-H) shows the effects of T 3a injections on blood T 3 levels.
  • FIG. 5 shows left ventricle (LV) pressure after T 3a injection.
  • Figure 6 provides results of several animal model studies of T 3a .
  • * indicates where ECG data points do not totally correlate with the pressures below; it is only shown to distinguish between ventricular fibrillation (VF) and sinus rhythm here.
  • Figure 7(A-I) shows the serum total T 3 levels (ng/dl) as a function of time after T a injection during cardiac resuscitation in dogs.
  • Figure 8 is a graph depicting pH-dependent T 3 and T 3a stability measured over 13 months.
  • Figure 9 is a graph depicting serum T levels after T 3 injection during cardiac resuscitation in dogs.
  • Figure 10 is a graph depicting serum T 3 levels after a single 5 ⁇ g/kg dose of
  • FIG. 11 is a graph depicting serum T 3 after 100 ⁇ g/kg bolus dose of T
  • Figure 12 is a graph depicting the half-life of serum T 3 after a single injection.
  • Figure 13 is a graph depicting 125 I-T 3 uptake into rat neonatal myocyte nuclear fraction.
  • the invention provides a stable liquid composition containing T 3 or an analog thereof, serum albumin and water, where the T 3 has a half-life of at least five days at a temperature range of -30°C and 70°C, preferably -10°C and 50°C and more preferably 0°C and 30°C.
  • the compositions described herein are suitable for use in any condition for which T 3 is indicated.
  • the invention also provides a method for treatment, of a patient with cardiac arrest and cardiac electrical standstill to restore effective cardiac function, comprising administering to the patient a therapeutically effective amount of the composition.
  • the T 3 in the composition has a half-life of or at least two weeks, preferably at least one month, more preferably at least three months, even more preferably at least six months and most preferably at least one year.
  • the composition has a T 3 and serum albumin ration of between 0.001 and 0.1, preferably between 0.002 and 0.05.
  • the serum albumin is a human serum albumin or a bovine serum albumin.
  • T 3 in the composition has a concentration of between 0.01 mg/ml and 1.0 mg/ml, preferably between 0.02 mg/ml and 0.8 mg/ml and more preferably between 0.1 mg/ml and 0.5 mg/ml.
  • compositions can further comprise other pharmaceutically effective or acceptable compositions such as epinephrine, adrenaline and any excipients.
  • Pharmaceutically acceptable excipients are isotonic and include, without limitation, saline and phosphate buffered saline.
  • compositions of the present invention allow the use and manufacture of a variety of compositions not previously available. Methods of making such compositions are known in the art, but have been previously unavailable for use with T 3 .
  • compositions for different delivery means are provided herein. These compositions include, without limitation, those suitable for use in intravenous, direct cardiac, parenteral, mucosal, intranasal, by-inhalation and buccal administration.
  • compositions are particularly suitable for use in by-inhalation delivery.
  • Aqueous solutions are far more effective at drug delivery than dry formulations but are not often used due to the instability and tendency of many drugs to aggregate in solution.
  • Methods of making compositions for by-inhalation etc are known in the art.
  • U.S. Patent No. 5,011,678 describes suitable compositions containing a pharmaceutically active substance, a biocompatible amphiphilic steroid and a biocompatible carbon propellant.
  • U.S. Patent No. 5,006,343 describes suitable compositions containing liposomes, pharmaceutically active substances and an amount of alveolar surfactant protein to enhance transport of the liposomes across a pulmonary surface.
  • the composition is administered by direct injection to a heart cavity of the patient, or direct parenteral injection into a central venous line of the patient, or is administered by parenteral injection or parenteral intravenous injection, or directly to the pulmonary system of the patient, or directly to the pulmonary system by direct endotracheal injection, or directly to the pulmonary system by infusion through a respiratory airway of the patient, or in at least one rapid bolus injection.
  • the composition can also be administered via drip from an intravenous line.
  • the term "therapeutically effective amount” means a dosage of T 3 preferably between 0.1 and 20 ⁇ g/kg of body weight, preferably between 0.2 and 10 ⁇ g/kg and more preferably between 0.3 and 5 ⁇ g kg although dosages of up to at least 100 ⁇ g/kg are effective. Surprisingly, dosages of 5 ⁇ g/kg and 100 ⁇ g/kg appear to result in similar physiologic distribution. Therefore, the composition allows for use of a low concentration of T 3 to achieve a therapeutically effective endpoint.
  • a therapeutically effective amount is also used to describe the amount required to treat any condition that responds to T 3 . Preferably the amount is sufficient restore effective cardiac function in a patient in need thereof.
  • T a represents a composition of T 3 and serum albumin.
  • T 3a has a pH range of 2.5 to 11.5, preferably 4.0 to 10, more preferably 6.0 to 8.0 and most preferably 6.5 to, 7.5.
  • the invention also includes packaged combinations for parenteral administration of liquid T 3 formulation to patients with cardiovascular compromise.
  • packaged combinations include a device suitable for injecting T 3 formulation alone or in combination either dissolved in a physiologically acceptable diluent in combination with a physiologically acceptable diluent for dilution just prior to use.
  • the diluent can be formulated to additionally contain various therapeutically effective substances which enhance the heart functions including but not limited to calcium and magnesium in therapeutically acceptable amounts. It is apparent from the following examples that T a effects cardiac resuscitation when other standard treatments have failed. T 3a did not cause any symptoms of hyperthyroidism in the treated dogs. T is the preferred thyroid hormone for use in humans despite the fact that T has heretofore not been used clinically, as T 3 has high specific activity and does not persist after administration so as to decrease or eliminate the need for subsequent 3-blocker therapy.
  • the following examples are provided to illustrate but not limit the invention.
  • the examples show the stability of T 3a compared to T 3 alone, particularly in a pH neutral environment and the cardiac benefit of T 3 in the immediate period following drug administration during cardiopulmonary resuscitation.
  • Example 1 Thyroid hormones during acute myocardial infarction as an indicator for mortality
  • thyroid hormone system may be temporarily downgraded. This "sick euthyroid syndrome" has been regarded as an adaptive response to conserve energy. However, thyroid hormone also reduces systemic vascular resistance, improves systolic and diastolic function and has beneficial effects on platelet function and lipids. Recent experimental data indicate thyroid hormone treatment is of value for some patients with cardiac disease.
  • Thyroid hormone values during acute myocardial infarction are of importance for the prognosis.
  • a comparison of thyroid hormone levels on arrival to the CCU in 331 consecutive pts (age 68 ⁇ 12 yrs) with acute myocardial infarction to a healthy control shows a significant down-regulation of the thyroid hormone system.
  • a serum concentration of reverse T 3 (rT 3 ) over the median value 0.41 nmol/L was identified as an independent risk factor after myocardial infarction.
  • the odds ratio for death within the first month was 10,8 (95% conf. interval 2,3-51,7 p 0,003) and within one year 3,0 (1,2-7,3 p 0,02).
  • Figure 1 shows the percent of survival versus time.
  • a 8.5Fr. catheter sheath was introduced into the right femoral vein and a 7Fr.
  • MP A2 Multipurpose high flow catheter (catalog no. 527-742, Cordis, USA) with open end and side holes was placed into the right ventricle for T 3a injections.
  • Another 7Fr. catheter sheath was introduced into the left femoral artery and a 6Fr.
  • pigtail catheter (catalog no. 527-654S, 110 cm, 155° angled) was placed into the descending aorta for the collection of aortic blood samples after T 3a injections into the right ventricle.
  • ECG Hewlett-Packard, Model No. 78346A, Serial No.
  • a temperature-monitoring device (T. SIN, Japan, designed for YSI series 400 thermistors), connected to the data acquisition system, was introduced into the external ears of all the animals to continuously measure body temperature. Fibrillation
  • the two distal ends of the 7Fr. Bipolar Multipurpose A-2 Electrode Catheter were connected to a Transformer.
  • the electrical system can deliver 15 V, 20mA AC current through the pacing catheter system.
  • the anesthesia was stopped.
  • a venous blood sample from the right ventricle was obtained. Lid reflexes returned in several minutes.
  • the lid reflexes were checked by the finger method system and when frequent blinking of the lids was obtained, procedures for the ventricular fibrillation were carried out.
  • 15 V, 20ma AC were directly passed through the left ventricular myocardium via the pacing catheter to fibrillate the heart.
  • the time period for the electrical induction of ventricular fibrillation was an average of 4-5 seconds. Occasionally, longer periods of between 5 and 15 seconds of electrical induction were needed to induce ventricular fibrillation.
  • CPR was initiated using a Michigan Instruments THUMPER ® (Michigan Instruments, Grand Rapids, Ml, Model no. 1004, Serial no. 2252) set to generate an arterial peak pressure during compression of at least 60 mm Hg, simulating a palpable pulse generated by manual chest compression was carried out according to the American Heart Association instructions.
  • the force of compression necessary to achieve this baseline condition was recorded and not altered during subsequent provision of chest compressions. Ventilation was pressure limited (30 cm H 2 O), providing 100% oxygen.
  • the compression rate was set at 60 compressions/min with a compression/relaxation ratio of 1 : 1 and a compression/ventilation ratio of 5 : 1.
  • T 3a was given 30 seconds before defibrillation.
  • T 3a injection was given 60 to 90 seconds after defibrillation.
  • Phase lb restoration of spontaneous circulation was achieved in 7 out of 8 animals with the changes to the protocol.
  • One animal (T 3 #15) had an aortic dissection during the procedure, and was thus excluded from the study.
  • Two animals had recovery of spontaneous circulation without T 3a .
  • Further experimental chronic laboratory and human clinical studies are needed to determine efficacy of using this drug and new CPR techniques. Advanced Cardiac Life Support using T 3
  • defibrillatory shocks were administered according to the Advanced Cardiac Life Support algorithm, starting with an initial energy level of 200 joules, then increased to 300 joules, and if still not successful, to 360 joules.
  • Lidocaine, atropine, and epinephrine were not used for cardiac resuscitation.
  • a Physio-Control Life Pack 9A system (Physio-Control Inc., Medtronic, US) was used to defibrillate the animals.
  • Patient ECG cable (3-lead, AHA, Physio-Control PN 9-10418-02) was connected to all the animals for simultaneous synchronous or asynchronous defibrillation.
  • QUICK-COMBO defibrillation cables (Physio-Control PN 806717) were used with EDGE SYSTEMTM therapy electrodes were attached to all animals.
  • One electrode (+, black cable connector) was placed left lateral to the animal's sternum with the center of the electrode in the left mid-axillary line towards the apex of the myocardium.
  • Another electrode (-, red cable connector) was placed at the apical aspect of the right lateral portion of the animal's chest in the right mid-axillary line.
  • Example 3 Triiodothyronine-human serum albumin preparation CLW) 100 ⁇ g T 3 /ml (1.5 x 10 "4 M) was combined with a physiological concentration of 5% human serum albumin (HSA, 50 mg/ml, 762 ⁇ M) at pH 7.2. The binding affinity between T 3 and albumin is low, the hormone-albumin complex dissociates rapidly.
  • HSA human serum albumin
  • the examples provided herein show that the high capacity-low affinity binding complex is ideal in its ability to bind more than 1000 times normal serum T concentrations, maintain the T 3 in solution at neutral pH and make T rapidly available to tissues after intravenous administration.
  • albumin (66 kD) binds approximately 15-20% of the total serum T 3 .
  • the remaining T 3 is bound by other blood proteins including thyroxine-binding globulin (TBG) and transthyretin, so that 99% of the hormone in serum is protein- bound.
  • T 3a preparations contain approximately 90% albumin-bound T 3 , which, when administered, dissociates rapidly.
  • Preparation of the T a composition combination of 5% human serum albumin with a T /sodium hydroxide solution (10 mg T 3 /ml 0.05 N NaOH) produces a T 3a preparation which is a neutral pH 7.2 and is
  • T 3a The T preparation used in these studies was in the T 3a formulation prepared as follows. (1) T 3 was dissolved in a physiological concentration of human serum albumin (HSA) (50 mg/ml), at a concentration of 0.10 mg /ml and pH 7.4. The samples were stored at room temperature, (2) T 3a was injected as a bolus dose of 4 ⁇ g/kg body weight approximately one minute after defibrillation was initiated and
  • HSA human serum albumin
  • HVS-02 Fibrillator and Defibrillator were used in the tests.
  • the operating instructions for the HVS-02 Fibrillator and Defibrillator can be found in the Manual for HVS-02 Fibrillator and Defibrillator.
  • Tables 1 and 2 showed the hemodynamic parameters during 2-phase intervention with T 3a in fibrillation and defibrillation procedures.
  • phase lb restoration of spontaneous circulation was achieved in 7 out of the 8 animalstested.
  • Table 1 one animal (T 3 #15) had an aortic dissection and was thus precluded from the procedure and two animals had recovery of spontaneous circulation without T a .
  • the circulation was unstable and required epinephrine and external compression to maintain the circulation.
  • the period of non-support before applying CPR was extended to 6 minutes and this animal (T #18) had full recovery of the circulation with T a .
  • T 3a was clearly effective in restoration of spontaneous cardiopulmonary circulation in the preliminary study.
  • T 3a The triiodo-L-thyronine preparation used in these studies was in the T 3a formulation prepared as follows. T was dissolved in a physiological concentration of human serum albumin (HSA) (50 mg/ml), at a concentration of 0.10 mg / ml at pH 7.4. The samples were stored at room temperature for specific lengths of time as indicated in Figure 8.
  • HSA human serum albumin
  • T was dissolved in 0.05N NaOH/saline and the pH adjusted to pH 7 or pH 10 to provide two other preparations of T 3 at a concentration of 0.10 mg/ml. These two preparations were stored under similar conditions as T a and are shown in Figure 8 as T 3 -pH 10 and T 3 -pH 7. The total T concentration in all the stock T 3 preparations were determined when initially made and at the times indicated using the radioimmunoassay described herein.
  • the results presented in Figure 8 show the following.
  • the T 3 concentration in the T a formulation remained unchanged from the original preparation for over 13 months of analysis.
  • the concentration of T 3 in saline solution at pH 10 was decreased to 71 ⁇ 7% of the original preparation after 13 months of storage at room temperature.
  • the concentration of T 3 in saline solution at pH 7 was decreased to 14 ⁇ 5% of the original preparation when measured following 2 months of storage at room temperature.
  • the T 3a stored at 37°C for 13 months retained 87 + 5% of the initial T 3 concentration.
  • Figure 9 shows serum T 3 levels in the dog model of cardiac resuscitation in which dogs were given 4 ⁇ g T 3 /kg body weight immediately after fibrillation and cardiac arrest. The desired effect was seen, that is the T 3 dosing in resuscitation as a requirement for an immediate effect of T (within 30 min.) on the heart followed by rapid degradation of T 3 from serum.
  • Figure 12 shows the log plot of T 3 in serum over a time period calculated T 3 half-life of seven (7) hours.
  • T 3 uptake into the heart was followed by treating the cells with radio-labeled T 3 ( I-T 3 ).

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Abstract

This invention provides a stable composition containing T3 serum albumin and water, wherein the T3 has a half-life of at least five days, particularly at neutral pH. This ivention further provides a method for emergency treatment of a patient with cardiac arrest and with cardiac electrical standstill to restore effective cardiac function, comprising administering to the patient a therapeutically effective amount of stable composition.

Description

COMPOSITIONS OF STABLE T3 AND METHODS OF USE THEREOF FIELD OF THE INVENTION
The present invention relates generally to a stable aqueous formulation of T3 for treating patients to restore effective cardiac function. BACKGROUND OF THE INVENTION
Serum albumin is a serum protein fraction involved in maintaining blood osmotic pressure and is used as a plasma substitute in shock treatment. Serum Albumin also contributes to many body transport and regulatory processes. Like many other substances, such as N-oxy trimethyl amines, amino acids, alkylated amino acids, and sugars, serum albumin is used as a protein protectant to stabilize proteins against denaturation and to preserve enzymatic activity as well as in formulation of biomedicals. U.S. Patent No. 5,876,992 discloses the use of serum albumin, together with disaccharides or their derivatives to stabilize proteins. Serum albumin has been used to preserve the integrity of urinary proteins. U.S. Patent No. 5,679,318. In addition, serum albumin solubilizes paclitaxel in aqueous solution. WO 00/06152.
Thyroid hormones include the L-forms of thyroxine (4-(4-Hydroxy-3,5- diiodophenyl)-3,5-diidotyrosine; hereinafter T4) and 3, 5, 3'-triiodothyronine (T ). They can be obtained from natural sources, such as bovine thyroid glands or synthesized. U.S. Patent No. 2,803,654.
Thyroid hormones administered to patients with cardiovascular compromise restore or improve cardiac rhythm and function. Thyroid hormones increase heart rate and heart beat force thus increasing cardiac output and are found to be significantly decreased during cardiac arrest. Wortsman et al. (1987) Arch. Intern. Med. 147:245-248. An infusion of thyroid hormone effects cardiac resuscitation in patients undergoing cardiac arrest, cardiac standstill, electro-mechanical dissociation and a variety of other cardiac conditions. The effect of thyroid hormone is almost immediate and occurs even where standard treatments have failed. Thyroid hormones are also therapeutically effective in other cardiac indications such as cardiomyopathies and bradyarrhythmias. Of the thyroid hormones, T is normally synthesized in smaller quantities than T4 and presents in blood and the thyroid gland. However, on a molecular basis, T3 is more potent and the onset of its effect is more rapid than T4 and is synthesized in the thyroid gland and by metabolism of T4 in peripheral tissues by the enzyme 5' deiodinase. T4 has been the preferred thyroid hormone in clinical use today, largely due to its availability and relatively long half-life of 6-7 days because T4 binds avidly to thyroxine-binding globulin in human serum and is thus protected from metabolism and excretion. T3 has higher potency and more rapid effect than T4 in resuscitate patients undergoing cardiac arrest. However, T3 is unstable in aqueous solution with an extremely short half-life. This short half-life has limited the application of T3 in treating patients, especially in emergency situations where the injection of an aqueous thyroid hormone solution is required.
Although a stable T3 formulation is desirable and needed in treating patients with heart disease, there has been no report or actual use of a stable aqueous T3 formulation. The present invention addresses this longstanding need and desire in the art.
Various documents are cited in this application. Each of these documents is hereby incorporated herein by reference. SUMMARY OF THE INVENTION The invention encompasses a stable aqueous pharmaceutical composition containing T3, serum albumin and water. Dried samples for reconstitution are also encompassed by the invention as are various pharmaceutical preparations.
The invention further relates to a method for emergency treatment of a patient with cardiac arrest, and with cardiac electrical standstill, to restore effective cardiac function, by administering to the patient a therapeutically effective amount of a pharmaceutical composition of T , serum albumin and water. BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 describes mortality rate as a function of the level of thyroid hormone during acute myocardial infarction. Figure 2 shows hemodynamic data after defibrillation (5 min-VF).
Figure 3 describes detailed procedures for testing the effectiveness of T3a (Protocol 1). Figure 4(A-H) shows the effects of T3a injections on blood T3 levels.
Figure 5 shows left ventricle (LV) pressure after T3a injection.
Figure 6 provides results of several animal model studies of T3a. In Figures 6G and H, * indicates where ECG data points do not totally correlate with the pressures below; it is only shown to distinguish between ventricular fibrillation (VF) and sinus rhythm here.
Figure 7(A-I) shows the serum total T3 levels (ng/dl) as a function of time after T a injection during cardiac resuscitation in dogs.
Figure 8 is a graph depicting pH-dependent T3 and T3a stability measured over 13 months.
Figure 9 is a graph depicting serum T levels after T3 injection during cardiac resuscitation in dogs.
Figure 10 is a graph depicting serum T3 levels after a single 5 μg/kg dose of
T3. Figure 11 is a graph depicting serum T3 after 100 μg/kg bolus dose of T
Figure 12 is a graph depicting the half-life of serum T3 after a single injection.
Figure 13 is a graph depicting 125I-T3 uptake into rat neonatal myocyte nuclear fraction. DETAILED DESCRIPTION OF THE INVENTION
The invention provides a stable liquid composition containing T3 or an analog thereof, serum albumin and water, where the T3 has a half-life of at least five days at a temperature range of -30°C and 70°C, preferably -10°C and 50°C and more preferably 0°C and 30°C. The compositions described herein are suitable for use in any condition for which T3 is indicated. The invention also provides a method for treatment, of a patient with cardiac arrest and cardiac electrical standstill to restore effective cardiac function, comprising administering to the patient a therapeutically effective amount of the composition.
In one embodiment of the invention, the T3 in the composition has a half-life of or at least two weeks, preferably at least one month, more preferably at least three months, even more preferably at least six months and most preferably at least one year. In another embodiment of the invention, the composition has a T3 and serum albumin ration of between 0.001 and 0.1, preferably between 0.002 and 0.05. In another embodiment of the invention, the serum albumin is a human serum albumin or a bovine serum albumin. In yet another embodiment of the invention, T3 in the composition has a concentration of between 0.01 mg/ml and 1.0 mg/ml, preferably between 0.02 mg/ml and 0.8 mg/ml and more preferably between 0.1 mg/ml and 0.5 mg/ml.
The compositions can further comprise other pharmaceutically effective or acceptable compositions such as epinephrine, adrenaline and any excipients. Pharmaceutically acceptable excipients are isotonic and include, without limitation, saline and phosphate buffered saline.
The increased stability and solubility under physiologic conditions of T3 in the composition of the present invention allows the use and manufacture of a variety of compositions not previously available. Methods of making such compositions are known in the art, but have been previously unavailable for use with T3. Various compositions for different delivery means are provided herein. These compositions include, without limitation, those suitable for use in intravenous, direct cardiac, parenteral, mucosal, intranasal, by-inhalation and buccal administration.
The compositions are particularly suitable for use in by-inhalation delivery. Aqueous solutions are far more effective at drug delivery than dry formulations but are not often used due to the instability and tendency of many drugs to aggregate in solution. Methods of making compositions for by-inhalation etc are known in the art. U.S. Patent No. 5,011,678 describes suitable compositions containing a pharmaceutically active substance, a biocompatible amphiphilic steroid and a biocompatible carbon propellant. U.S. Patent No. 5,006,343 describes suitable compositions containing liposomes, pharmaceutically active substances and an amount of alveolar surfactant protein to enhance transport of the liposomes across a pulmonary surface.
In a further embodiment of the invention, the composition is administered by direct injection to a heart cavity of the patient, or direct parenteral injection into a central venous line of the patient, or is administered by parenteral injection or parenteral intravenous injection, or directly to the pulmonary system of the patient, or directly to the pulmonary system by direct endotracheal injection, or directly to the pulmonary system by infusion through a respiratory airway of the patient, or in at least one rapid bolus injection. The composition can also be administered via drip from an intravenous line. As used herein, the term "therapeutically effective amount" means a dosage of T3 preferably between 0.1 and 20 μg/kg of body weight, preferably between 0.2 and 10 μg/kg and more preferably between 0.3 and 5 μg kg although dosages of up to at least 100 μg/kg are effective. Surprisingly, dosages of 5 μg/kg and 100 μg/kg appear to result in similar physiologic distribution. Therefore, the composition allows for use of a low concentration of T3 to achieve a therapeutically effective endpoint. A therapeutically effective amount is also used to describe the amount required to treat any condition that responds to T3. Preferably the amount is sufficient restore effective cardiac function in a patient in need thereof.
Throughout the present application, T a represents a composition of T3 and serum albumin. T3a has a pH range of 2.5 to 11.5, preferably 4.0 to 10, more preferably 6.0 to 8.0 and most preferably 6.5 to, 7.5.
The invention also includes packaged combinations for parenteral administration of liquid T3 formulation to patients with cardiovascular compromise. Such packaged combinations include a device suitable for injecting T3 formulation alone or in combination either dissolved in a physiologically acceptable diluent in combination with a physiologically acceptable diluent for dilution just prior to use. The diluent can be formulated to additionally contain various therapeutically effective substances which enhance the heart functions including but not limited to calcium and magnesium in therapeutically acceptable amounts. It is apparent from the following examples that T a effects cardiac resuscitation when other standard treatments have failed. T3a did not cause any symptoms of hyperthyroidism in the treated dogs. T is the preferred thyroid hormone for use in humans despite the fact that T has heretofore not been used clinically, as T3 has high specific activity and does not persist after administration so as to decrease or eliminate the need for subsequent 3-blocker therapy.
The following examples are provided to illustrate but not limit the invention. The examples show the stability of T3a compared to T3 alone, particularly in a pH neutral environment and the cardiac benefit of T3 in the immediate period following drug administration during cardiopulmonary resuscitation.
Example 1 Thyroid hormones during acute myocardial infarction as an indicator for mortality
In severe illness, including cardiac disease, the thyroid hormone system may be temporarily downgraded. This "sick euthyroid syndrome" has been regarded as an adaptive response to conserve energy. However, thyroid hormone also reduces systemic vascular resistance, improves systolic and diastolic function and has beneficial effects on platelet function and lipids. Recent experimental data indicate thyroid hormone treatment is of value for some patients with cardiac disease.
Thyroid hormone values during acute myocardial infarction are of importance for the prognosis. A comparison of thyroid hormone levels on arrival to the CCU in 331 consecutive pts (age 68±12 yrs) with acute myocardial infarction to a healthy control shows a significant down-regulation of the thyroid hormone system. In a multivariate analysis considering age, sex, thyroid hormones, CKB, previous myocardial infarction, angina, heart failure and diabetes, a serum concentration of reverse T3 (rT3) over the median value 0.41 nmol/L was identified as an independent risk factor after myocardial infarction. The odds ratio for death within the first month was 10,8 (95% conf. interval 2,3-51,7 p 0,003) and within one year 3,0 (1,2-7,3 p 0,02).
Figure 1 shows the percent of survival versus time. Thus the increased serum concentrations of rT3 in patients with acute myocardial infarction is a new, not previously identified independent risk factor for death within the first year of the event.
Example 2 Experimental Details
Anesthesia
All animals were fasted overnight and anesthesia was induced by intravenous sodium thiopental (Pentothal sodium 15-25 mg/kg). After intubation and ventilation by a ventilator (North American Drager, Anesthesia and Ventilator, Model AVE-K,
Serial No. 5033), anesthesia was maintained by 2% isoflurane (Isoflurane Vaporizer,
R- Vapor, R-24045), and oxygen. ECG (Hewlett Packard Model No. 78346A). Oxygen saturation was monitored continuously. Preoperatively, all animals received Acepromazine maleate, 0.25-0.5 mg, I.M, lactated Ringer's solution was given intravenously (250 ml - 350 ml/hr) during the procedure. Methods A 8.5Fr. catheter sheath was introduced into the right femoral artery and the side arm was connected to a fluid transducer for the continuous measurement of systemic arterial blood pressure. A 7Fr. Bipolar Multipurpose A-2 Electrode Catheter, 1 Lumelec™ (Lot no. 30395908, Catalog no. 528-724, Cordis, USA) tipped with pressure transducer with 2 side holes, 2 electrodes with an open end, 125 cm long, and 0.038 inch diameter, was advanced through the catheter sheath, and placed into the left ventricle. Continuous measurement of the systemic left ventricular pressure was obtained. Analog signals from the pressure transducers were obtained using an amplifier (PM-1000, CWE Inc., Ardmore, PA).
A 8.5Fr. catheter sheath was introduced into the right femoral vein and a 7Fr. MP A2, Multipurpose high flow catheter (catalog no. 527-742, Cordis, USA) with open end and side holes was placed into the right ventricle for T3a injections. Another 7Fr. catheter sheath was introduced into the left femoral artery and a 6Fr. pigtail catheter (catalog no. 527-654S, 110 cm, 155° angled) was placed into the descending aorta for the collection of aortic blood samples after T3a injections into the right ventricle. ECG (Hewlett-Packard, Model No. 78346A, Serial No.
2320A00522) was continuously monitored. A temperature-monitoring device (T. SIN, Japan, designed for YSI series 400 thermistors), connected to the data acquisition system, was introduced into the external ears of all the animals to continuously measure body temperature. Fibrillation
The two distal ends of the 7Fr. Bipolar Multipurpose A-2 Electrode Catheter were connected to a Transformer. The electrical system can deliver 15 V, 20mA AC current through the pacing catheter system. The anesthesia was stopped. A venous blood sample from the right ventricle was obtained. Lid reflexes returned in several minutes.
The lid reflexes were checked by the finger method system and when frequent blinking of the lids was obtained, procedures for the ventricular fibrillation were carried out. 15 V, 20ma AC were directly passed through the left ventricular myocardium via the pacing catheter to fibrillate the heart. The time period for the electrical induction of ventricular fibrillation was an average of 4-5 seconds. Occasionally, longer periods of between 5 and 15 seconds of electrical induction were needed to induce ventricular fibrillation. Cardiac Resuscitation using Thumper
After 4.5 minutes of untreated ventricular fibrillation and without any respiratory support, CPR was initiated using a Michigan Instruments THUMPER® (Michigan Instruments, Grand Rapids, Ml, Model no. 1004, Serial no. 2252) set to generate an arterial peak pressure during compression of at least 60 mm Hg, simulating a palpable pulse generated by manual chest compression was carried out according to the American Heart Association instructions.
The force of compression necessary to achieve this baseline condition was recorded and not altered during subsequent provision of chest compressions. Ventilation was pressure limited (30 cm H2O), providing 100% oxygen. The compression rate was set at 60 compressions/min with a compression/relaxation ratio of 1 : 1 and a compression/ventilation ratio of 5 : 1.
Data acquisition (10 minutes longer a file) was started at 4 minutes after ventricular fibrillation to cover the entire procedure after defibrillation and recovery. Two infusions of sodium bicarbonate (0.5 mEqv/kg) were given during THUMPER CPR within 2-minutes range to correct the base deficit.
Phase la was dedicated towards developing the basic methodology in the initial experiments, manual chest compression (CPR) and an internal defibrillator were employed. Induction of ventricular fibrillation and defibrillation were problematic with the internal electrodes because of the size mismatch: electrodes designed for humans being used in a smaller sized animal. In later experiments, the internal system was replaced with an LV pacing catheter connected to AC current via a step-down transformer (to induce ventricular fibrillation), and a new external, "hands-off defibrillator. The manual chest compression was replaced with a THUMPER CPR system.
In the experiments, T3a was given 30 seconds before defibrillation. Preferably, T3a injection was given 60 to 90 seconds after defibrillation. In Phase lb, restoration of spontaneous circulation was achieved in 7 out of 8 animals with the changes to the protocol. One animal (T3 #15) had an aortic dissection during the procedure, and was thus excluded from the study. Two animals had recovery of spontaneous circulation without T3a. Further experimental chronic laboratory and human clinical studies are needed to determine efficacy of using this drug and new CPR techniques. Advanced Cardiac Life Support using T3
At 6 minutes after inducing V-fib, defibrillatory shocks were administered according to the Advanced Cardiac Life Support algorithm, starting with an initial energy level of 200 joules, then increased to 300 joules, and if still not successful, to 360 joules. Lidocaine, atropine, and epinephrine were not used for cardiac resuscitation.
A Physio-Control Life Pack 9A system (Physio-Control Inc., Medtronic, US) was used to defibrillate the animals. Patient ECG cable (3-lead, AHA, Physio-Control PN 9-10418-02) was connected to all the animals for simultaneous synchronous or asynchronous defibrillation. QUICK-COMBO defibrillation cables (Physio-Control PN 806717) were used with EDGE SYSTEM™ therapy electrodes were attached to all animals. One electrode (+, black cable connector) was placed left lateral to the animal's sternum with the center of the electrode in the left mid-axillary line towards the apex of the myocardium. Another electrode (-, red cable connector) was placed at the apical aspect of the right lateral portion of the animal's chest in the right mid-axillary line.
200 joules of counter shock were administered to defibrillate the animals. In one animal, a further counter shock was needed. The THUMPER CPR was continued until spontaneous circulation was recovered. At 60 to 90 seconds after defibrillation, a bolus dose of T3a was injected into the right ventricle. The aortic pressure trace was momentarily set to zero to denote the time of the T3a injection. Thirty seconds later, a left ventricular blood sample was collected to determine the T3a blood level. Shortly after T3a injections (30 to 90 seconds), restoration of the spontaneous circulation was achieved in most instances.
Restoration of the spontaneous circulation was defined as a pulsatile rhythm with a systolic arterial pressure of at least 60 mmHg. No further interventions or drugs were given. Lactated Ringer's Fluid infusion was maintained at about 10 mL/kg/hr. The animal was reconnected to the ventilator and after several minutes isoflurane anesthesia was restarted at a rate of 0.5%. Anesthesia was carefully maintained to avoid the cardiac decompensation. The animal was observed for another 30 minutes for any further changes in the arterial and left ventricular pressures. Another venous blood sample was taken after 15 minutes of ventricular fibrillation. Representative results are shown in Figures 2-6.
Example 3 Triiodothyronine-human serum albumin preparation CLW) 100 μg T3/ml (1.5 x 10"4 M) was combined with a physiological concentration of 5% human serum albumin (HSA, 50 mg/ml, 762 μM) at pH 7.2. The binding affinity between T3 and albumin is low, the hormone-albumin complex dissociates rapidly. The examples provided herein show that the high capacity-low affinity binding complex is ideal in its ability to bind more than 1000 times normal serum T concentrations, maintain the T3 in solution at neutral pH and make T rapidly available to tissues after intravenous administration.
In the body, albumin (66 kD) binds approximately 15-20% of the total serum T3. The remaining T3 is bound by other blood proteins including thyroxine-binding globulin (TBG) and transthyretin, so that 99% of the hormone in serum is protein- bound.
Binding characteristics of T3 to albumin in phosphate-buffered saline at 37°C provide association constants of 1.0 x 105 M"1 at site 1 and 6.9 x 103 M"1 at sites 2-6. Gray (1979), Hormones in Blood, eds.; 3rd ed. Vol. 1. London: Academic, p. 576. As shown herein, T3a preparations contain approximately 90% albumin-bound T3, which, when administered, dissociates rapidly. Preparation of the T a composition: combination of 5% human serum albumin with a T /sodium hydroxide solution (10 mg T3/ml 0.05 N NaOH) produces a T3a preparation which is a neutral pH 7.2 and is
100%) soluble in solution.
Example 4 Studies of Cardiac Resuscitation with T^and Bioavailability of Tja Composition
The T preparation used in these studies was in the T3a formulation prepared as follows. (1) T3 was dissolved in a physiological concentration of human serum albumin (HSA) (50 mg/ml), at a concentration of 0.10 mg /ml and pH 7.4. The samples were stored at room temperature, (2) T3a was injected as a bolus dose of 4 μg/kg body weight approximately one minute after defibrillation was initiated and
(3) a baseline serum T3 value was obtained for each animal before ventricular fibrillation was induced. Subsequent blood samples were obtained from the arterial circulation at 0.5 to 1.5 minutes after the bolus injection, and also at 15 to 20 minutes and 30 minutes, respectively. The changes in serum T3 concentration are shown in Figure 7, the serum total T3 levels (ng/dl) as a function of time after injection. The baseline serum T3 level of 87 ± 6 ng/dl is within the physiological range for canines, and this was increased 100-fold one minute after bolus T3 injection, and remained high over the 30 minute period of cardiac resuscitation.
Example 5 Immunoassay for Tja and the determination of hemodynamic parameters during 2-phase intervention with T » drug in fibrillation and defibrillation procedures
Before sending the blood sample for immunoassay, in each experiment all the blood samples were collected in red-topped serum separator tubes. The tubes were centrifuged at 2500 rpm on a tabletop centrifuge for 10 minutes at 4°C to separate the cells from the serum. The blood samples were then stored and frozen at -4°C.
The results section was divided into Phases la (n=9) and lb (n=8). The hemodynamic data were not consistently available in Phase la as there was no spontaneous or induced recovery except for 3 animals. Use of T a was limited to only 3 dogs in this phase although epinephrine was used in 5 of them. This phase was dedicated towards the development of the Phase lb parameters.
In Phase lb, 2 animals showed spontaneous recovery, hi one animal, the hemodynamic pressures were not stable and needed injection of epinephrine (0.1 mg/kg) to increase the reduced hemodynamic pressures. The other animal had spontaneous recovery after 4.5 minutes of ventricular fibrillation. The pressures were comparatively stable in this animal although lower than pre-VF hemodynamic data. In the same animal, we induced a 6-minute ventricular fibrillation and gave CPR for two minutes. The animal was defibrillated and given a T3a injection after 60 seconds. The animal was maintained on Thumper CPR for additional 1-2 minutes and was resuscitated completely. The animal was observed for another 30 minutes and the pressures were completely stable. The hemodynamic pressures were higher then the pro-VF hemodynamic data. HVS-02 Fibrillator and Defibrillator were used in the tests. The operating instructions for the HVS-02 Fibrillator and Defibrillator can be found in the Manual for HVS-02 Fibrillator and Defibrillator. Tables 1 and 2 showed the hemodynamic parameters during 2-phase intervention with T3a in fibrillation and defibrillation procedures.
Table 1
Phase lb (Precise T 3a orkin g section) = 8 animals (test)
Test Time frame S. AoP D. AoP S. LVP Defib. Recover τ3a Epi
No. mmHg mmHg mmHg Type use use
18 Pre-VF 113.8 95.5 118.7 VF+CPR (4.5m) 44.5 39.6 70.1
After D-Fib+T3a 86.4 62.6 107.5 External Yes No No
Post T3a (15m) 88.1 72.2 95.6 Yes No
18 Pre-VF 92.5 80.5 100.1 VF+CPR (6.5m) 44.5 32.1 72.1
After DFib+T3a 103.3 80.7 109.6 External Yes Yes
Post T3a (15m) 102.1 80.5 107.2 Yes No
17 Pre-VF 86.6 76.9 107.4 VF+CPR 59.3 37.5 73.6
After D-Fib+T3a 63.7 37.5 84.0 External Yes Yes
Post T3a (15m) 89.3 76.1 110.2 Yes No
16 Pre-VF 83.1 65.5 89.2 VF+CPR 81.1 42.3 84.1
After D-Fib+T3a 89.6 63.1 102.3 External Yes Yes
Post T3a (15m) 134.1 111.1 138.8 Yes No
15 Pre-VF 98.7 68.0 Aortic VF-Defib No** Dissectio n*
14 Pre-VF 134.1 108.5 137.1 VF+CPR 60.1 35.5 70.2
After D-Fib+T3a 60.2 41.3 80.3 External Yes Yes
Post T3a (15m) 93.7 76.7 99.3 Yes No
13 Pre-VF 80.7 68.0 89.9 VF+CPR 80.6 64.5 87.2
After D-Fib+ 56.7 45 80.0 External Yes No
Post - (15m) 82.7 64.0 103.0 Yes Yes
12 Pre-VF ■ 108.3 71.2 110.5 VF+CPR 58.4 40.5 77.5
After D-Fib+ T3a 62.3 34.9 80.2 External Yes Yes
Post T3a (15m) 81.4 45.5 115.6 Yes No
11 Pre-VF 106.7 78.4 118.5 VF+CPR 52.3 32.1 80.1
After D-Fib+ T3a 58.8 34.4 88.9 External Yes Yes
Post T3a (15m) 117.5 108.1 85.5 Yes No
10 Pre-VF 134.1 108.5 137.1 VF+CPR 81.1 42.3 84.1
After D-Fib+ T3a 89.6 63.1 102.3 External Yes Yes No
Post T3a (15m) 134.1 111.1 138.8 Yes No
* Aortic dissection occurred during blind manipulation of the LV pacing catheter. In Phase lb, restoration of spontaneous circulation was achieved in 7 out of the 8 animalstested. In Table 1, one animal (T3 #15) had an aortic dissection and was thus precluded from the procedure and two animals had recovery of spontaneous circulation without T a. Moreover, in one of these eight animals, the circulation was unstable and required epinephrine and external compression to maintain the circulation. Furthermore, in one animal, the period of non-support before applying CPR was extended to 6 minutes and this animal (T #18) had full recovery of the circulation with T a. In this phase, i.e. Phase lb, T3a was clearly effective in restoration of spontaneous cardiopulmonary circulation in the preliminary study.
Table 2
Phase la (Methodology section) = 9 animals (test)
Test Time frame S. AoP D. AoP S. LVP Defib. Recover Ta, Epi
No. mmHg mmHg mmHg Type Use use
Pre-VF 90 62.5 95.5 VF+CPR* 55 32.0 60.0
After D-Fib+T3a External No Yes No
Post T3a (15m) No No
Pre-VF 96.0 70.1 98.5 VF+CPR 45 25.5 50
After D-Fib+T3a 60 35.6 68.7 External Yes Yes
Post T3a (15m) 80.1 60.3 85.5 Yes No
Pre-VF 122.3 97.7 133.3 VF+CPR
After D-Fib+T3a External No Yes Post T3a (15m) ** No No
Pre-VF 90 60 98 VF+CPR*** 60 32 68
After D-Fib+T3a 77 50 85 External Yes Yes Yes
Post T3a (15m) 93.7 77 99 *** Yes Yes
Pre-VF 98 68 See VF+CPR note
After D-Fib+ Internal No No Yes
Post - (15m) No Yes
Pre-VF 80 65 89 VF+CPR t
After D-Fib+ Internal No No Yes
Post - (15m) No Yes
Pre-VF 86 60 90 VF+CPR
After D-Fib+ Internal Yes No Yes
Post T3 (15m) External No
Pre-VF 89 65 96
VF+CPR 60 48 66 ******
After D-Fib+ 65 50 84.0 Internal5 Yes No No
Post - (15m) 89.3 76.1 110.2 Yes Yes
Pre-VF 80 65 90 VF+CPR Ψ After D-Fib+ Internalψ No No Post - (15m)
* Thumper did not work out in this large dog and CPR was given by manual chest compression • ** Defibrillation was not possible and it appeared that defibrillator was not working properly
• *** Fibrillation and defibrillation procedures were tested 3 times in this animal to test for the first time, the external defibrillator. After a 2 minute wait, the animal was given 1 mg of epinephrine plus sodium bicarbonate and CPR, to defibrillate the animal. The same experiments were done with a 3-minute interval, and this time, T3a was also used after epinephrine and the dog was defϊbrillated with normal pressure development. We further performed the same experiments with 4-minute interval using T a. The results were immediate and the animal developed pressure very rapidly. The dog was fully recovered.
• ****ϊ" The electrodes for the internal defibrillation procedure were partially moved, especially the one with the superior vena cava. Defibrillation was not immediately achieved. Epinephrine and lidocaine injections were given. Finally the animal was defibrillated (50 joules) although there was not any generated pressure development.
• % Animal was fibrillated and defibrillation was not achieved by 920 volts, 14 ms, resistance 70 ohms, and 49.2 joules of shock. No blood pressure recovery was observed. The animal was defibrillated 3-4 times with an injection of 1 mL of epinephrine to achieve defibrillation. However, there was no spontaneous recovery. Cardiac massage was given compressing the heart directly by opening the chest. The study on this animal ended here.
• ***** Fibrillation was for 3 minutes. After defibrillation; but there was no pulse. The animal went into VF again and was defibrillated. There was low pressure and the external defibrillator was applied. Full function was not recovered. Pentobarbital anesthesia was used for this study.
• ******ξ The animal was defϊbrillated several times, one at 2 minutes. The animal fully recovered without any drug. At 3 minutes, epinephrine was required although it needed 3 shocks. The animal was fibrillated, but after another 3 minutes, could not be recovered. • ψ The internal electrodes moved several times during fibrillation procedure due to position change of the dog. The defibrillation procedure was unsuccessful. Phase la was dedicated towards developing the basic methodology.
Restoration of circulation was achieved in 3 animals out of 7 using manual chest compression (CPR). In 3 animals, the hemodynamic data after defibrillation were less than the pre-fibrillatory data. It was found that induction of ventricular fibrillation (VF) was problematic with the internal electrodes and defibrillation was problematic because of the size mismatch, i.e. electrodes designed for humans being used in a smaller sized animal. In the experiments, internal defibrillator was used for the preliminary experiments and T3a was given just before defibrillation (30 seconds). Moreover, THUMPER CPR was used in the last 2 dogs instead of manual CPR. Thumper CPR worked well and it was used for the subsequent T3a experiments of Phase lb. Manual chest compression was maintained for another 5 minutes after defibrillation and T3a or epinephrine injections. Bolus epinephrine injection (100 μg/kg) was used in 5 random dogs.
Example 6 Studies to determine the stability of Tja compared with T3 alone
The triiodo-L-thyronine preparation used in these studies was in the T3a formulation prepared as follows. T was dissolved in a physiological concentration of human serum albumin (HSA) (50 mg/ml), at a concentration of 0.10 mg / ml at pH 7.4. The samples were stored at room temperature for specific lengths of time as indicated in Figure 8.
T was dissolved in 0.05N NaOH/saline and the pH adjusted to pH 7 or pH 10 to provide two other preparations of T3 at a concentration of 0.10 mg/ml. These two preparations were stored under similar conditions as T a and are shown in Figure 8 as T3-pH 10 and T3-pH 7. The total T concentration in all the stock T3 preparations were determined when initially made and at the times indicated using the radioimmunoassay described herein.
The results presented in Figure 8 show the following. The T3 concentration in the T a formulation remained unchanged from the original preparation for over 13 months of analysis. The concentration of T3 in saline solution at pH 10 was decreased to 71 ± 7% of the original preparation after 13 months of storage at room temperature. The concentration of T3 in saline solution at pH 7 was decreased to 14 ± 5% of the original preparation when measured following 2 months of storage at room temperature. The T3a stored at 37°C for 13 months retained 87 + 5% of the initial T3 concentration.
Example 7 Studies to Determine the Pharmacokinetics of T^ in vivo The half-life and stability of Tj in serum after a single bolus dose
Figure 9 shows serum T3 levels in the dog model of cardiac resuscitation in which dogs were given 4 μg T3/kg body weight immediately after fibrillation and cardiac arrest. The desired effect was seen, that is the T3 dosing in resuscitation as a requirement for an immediate effect of T (within 30 min.) on the heart followed by rapid degradation of T3 from serum.
The results showed that the serum T3 levels increased to greater than 9000 ng/dl within 2 minutes of drug administration. These serum T3 levels were maintained at this high level for 30 minutes. Pharmacokinetic studies in a rodent model To further study the degradation or decrease of serum T3 following a bolus dose of drug, the following studies were performed. Rats were injected intramuscularly with two doses of T3: 5 μg/Kg and 100 μg/Kg body wt. Blood samples were collected over a 72 hour period and total T3 was measured in serum by radioimmunoassay as described herein. The results are shown in Figures 10 and 11. Figures 10 and 11 show the following. The rapid increase in serum T3 levels was proportional to the bolus dose administered. Peak values were obtained within 30 minutes of drug administration. Within 2 hours of drug injection, the serum T3 levels decreased significantly to 90% and 64% of the peak values for the low and high doses, respectively. By 24 hours after injection of the drag, the serum T3 levels had decreased to 10% of peak values, and were within normal physiological range. The half-life of T3 in serum after injection of either 5 μg/kg or 100 μg T3/kg body weight was identical.
Figure 12 shows the log plot of T3 in serum over a time period calculated T3 half-life of seven (7) hours. Example 8
Studies to determine uptake of T3 into the cardiac mvocvte:
In order to understand the potential biological benefit of T3 on the heart following cardiopulmonary resuscitation, it is important to document the uptake of the drug into the cardiac myocyte within the time frame used for the resuscitation procedure.
Studies were designed to measure the rate of uptake of T3 into the heart using purified cultured cardiac myocytes. The time course of T3 uptake into the cardiac myocyte was followed by treating the cells with radio-labeled T3 ( I-T3).
The results showed that T3 is detected in the nucleus of the cell within 5 minutes of exposure to T3 at a dose of 10" M (serum levels of T3 equivalent to 650 ng/dl), and that the T uptake reached saturation by approximately 2 hours. These results are illustrated in Figure 13.
Having thus described in detail preferred embodiments of the present invention, it is to be understood that the invention defined by the appended claims is not to be limited by particular details set forth in the above description as many apparent variations thereof are possible without departing from the spirit or scope thereof.

Claims

1. A composition comprising T3, serum albumin and water wherein the stability of T3 is increased.
2. The composition according to claim 1, wherein the T3 has a half-life of at least five days at a temperature range of about -30°C to 70°C.
3. The composition according to claim 1, wherein further comprising a pharmaceutically acceptable excipient.
4. The composition according to claim 3, suitable for use in intravenous administration.
5. The composition according to claim 3, suitable for use in direct cardiac administration.
6. The composition according to claim 3, suitable for use in parenteral administration.
7. The composition according to claim 3, suitable for use in mucosal administration.
8. The composition according to claim 7, wherein the mucosal administration is selected from the group consisting of intranasal, by-inhalation and buccal.
9. The composition according to claim 8, wherein the T3 has a half-life of at least two weeks.
10. The composition according to claim 1, wherein the T3 has a half-life of at least one month.
11. The composition according to claim 1, wherein the T3 has a half-life of at least three months.
12. The composition according to claim 1, wherein the T3 has a half-life of at least six months.
13. The composition according to claim 1, wherein the T3 has a half-life of at least twelve months.
14. The composition according to claim 1, wherein the ratio of T3 and the serum albumin is between about 0.001 and 0.1.
15. The composition according to claim 1, wherein the ratio of T3 and the serum albumin is between 0.002 and 0.05.
16. The composition according to claim 3, wherein the serum albumin is human serum albumin.
17. The composition according to claim 3, wherein the serum albumin is bovine serum albumin.
18. The composition according to claim 1 , wherein the T3 has a concentration of between 0.02 mg/ml and 0.8 mg/ml.
19. The composition according to claim 1, wherein the T has a concentration of between 0.01 mg/ml and 1.0 mg/ml.
20. The composition according to claim 1, wherein the T3 has a concentration of between 0.1 mg/ml and 0.5 mg/ml.
21. The composition according to claim 1, wherein the T3 has a concentration of about 0.1 mg/ml.
22. The composition according to claim 1 , wherein the pH range is about 2.5 to 11.5.
23. The composition according to claim 1 , wherein the pH range is about 4.0 to 10.
24. The composition according to claim 1, wherein the pH range is about 6.0 to 8.0.
25. The composition according to claim 1 , wherein the pH range is about 6.5 to 7.5.
26. A method of treating of a patient with cardiac arrest, or with cardiac electrical standstill, to restore effective cardiac function, comprising administering to the patient a therapeutically effective amount of the composition according to claim 1.
27. The method according to claim 26, wherein the cardiac arrest is caused by electromechanical dissociation.
28. The method according to claim 26, wherein the cardiac electrical standstill is caused by a disease.
29. The method according to claim 26, wherein the composition is administered by direct injection to a heart cavity of the patient, or direct parenteral injection into a central venous line of the patient.
30. The method according to claim 26, wherein the composition is administered by parenteral injection or parenteral intravenous injection.
31. The method according to claim 26, wherein the composition is administered directly to the pulmonary system of the patient.
32. The method according to claim 26, wherein the composition is administered directly to the pulmonary system by direct endotracheal injection.
33. The method according to claim 26, wherein the composition is administered directly to the pulmonary system by infusion through a respiratory airway of the patient.
34. The method according to claim 26, wherein the composition is administered in at least one rapid bolus injection.
35. The method according to claim 26, wherein the composition is administered at between 0.1 and 20 μg T3 per kg of body weight.
36. The method according to claim 26, wherein the composition is administered at between 0.2 and 10 μg T3 per kg of body weight.
37. The method according to claim 26, wherein the composition is administered at between 0.3 and 5 μg T3 per kg of body weight.
38. The method according to claim 26, wherein the composition is administered at 100 μg T3 per kg of body weight.
39. The method according to claim 26, wherein the composition is administered via intravenous drip.
40. The method according to claim 26, wherein the composition is administered via mucosal delivery.
PCT/US2001/044855 2000-12-21 2001-11-30 Compositions of stable t3 and methods of use thereof WO2002051403A1 (en)

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CA2432523A CA2432523C (en) 2000-12-21 2001-11-30 Compositions of stable t3 and methods of use thereof
JP2002552548A JP2004525874A (en) 2000-12-21 2001-11-30 Composition of stable T3 and method of use thereof
DE60130145T DE60130145T2 (en) 2000-12-21 2001-11-30 STABLE T3 COMPOSITIONS AND ITS APPLICATION
EP01272465A EP1351673B1 (en) 2000-12-21 2001-11-30 Compositions of stable t3 and use thereof
ES01272465T ES2291274T3 (en) 2000-12-21 2001-11-30 COMPOSITIONS OF STABLE T3 AND METHODS OF USE OF THE SAME.
AT01272465T ATE370729T1 (en) 2000-12-21 2001-11-30 STABLE T3 COMPOSITIONS AND THEIR APPLICATION

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020144073A1 (en) 2019-01-09 2020-07-16 Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. L-triiodothyronine (t3) for use in limiting microvascular obstruction

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326618A1 (en) * 1987-03-04 1989-08-09 Nippon Hypox Laboratories Incorporated Medicinal composition containing albumin as carrier and process for its preparation
EP0337467A2 (en) * 1988-04-15 1989-10-18 Roche Diagnostics GmbH Method for the determination of thyroxine and a standard solution therefore
GB2240474A (en) * 1990-02-05 1991-08-07 British Tech Group Thyroid hormone cardiac treatment
EP0583717A1 (en) * 1992-08-14 1994-02-23 Roche Diagnostics GmbH Process and standard solution for the determination of thyroxine (T4) or triiodothyronine (T3)
US5795789A (en) * 1997-06-04 1998-08-18 Dade Behring Inc. Standard solution for the determination of thyroid function

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3895782B2 (en) * 1992-10-26 2007-03-22 生化学工業株式会社 Chondroitinase composition and injectable preparation containing the same
JP2622653B2 (en) * 1992-12-18 1997-06-18 三洋化成工業株式会社 Thyroid hormone aqueous solution
JPH06213598A (en) * 1993-01-19 1994-08-02 Mitsubishi Electric Corp Guided missile
JP3428225B2 (en) * 1995-04-28 2003-07-22 三菱ウェルファーマ株式会社 Porphyrin metal complex-albumin inclusion compound and oxygen carrier
EA200001252A1 (en) * 1998-05-29 2001-06-25 Байоджен, Инк. COMPOSITION OF THE RECOMBINANT INTERFERON-β-1A (IFN-β-1A) PERSON

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326618A1 (en) * 1987-03-04 1989-08-09 Nippon Hypox Laboratories Incorporated Medicinal composition containing albumin as carrier and process for its preparation
EP0337467A2 (en) * 1988-04-15 1989-10-18 Roche Diagnostics GmbH Method for the determination of thyroxine and a standard solution therefore
GB2240474A (en) * 1990-02-05 1991-08-07 British Tech Group Thyroid hormone cardiac treatment
EP0583717A1 (en) * 1992-08-14 1994-02-23 Roche Diagnostics GmbH Process and standard solution for the determination of thyroxine (T4) or triiodothyronine (T3)
US5795789A (en) * 1997-06-04 1998-08-18 Dade Behring Inc. Standard solution for the determination of thyroid function

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020144073A1 (en) 2019-01-09 2020-07-16 Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. L-triiodothyronine (t3) for use in limiting microvascular obstruction

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CA2432523C (en) 2014-06-03
DE60130145T2 (en) 2008-05-15
ES2291274T3 (en) 2008-03-01
JP2009120625A (en) 2009-06-04
ATE370729T1 (en) 2007-09-15
EP1351673B1 (en) 2007-08-22
CA2432523A1 (en) 2002-07-04
EP1351673A1 (en) 2003-10-15
JP2005060409A (en) 2005-03-10
JP2004525874A (en) 2004-08-26

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