AU2093497A

AU2093497A – Pharmaceutical compositions containing buffered ortho ester polymers
– Google Patents

AU2093497A – Pharmaceutical compositions containing buffered ortho ester polymers
– Google Patents
Pharmaceutical compositions containing buffered ortho ester polymers

Info

Publication number
AU2093497A

AU2093497A
AU20934/97A
AU2093497A
AU2093497A
AU 2093497 A
AU2093497 A
AU 2093497A
AU 20934/97 A
AU20934/97 A
AU 20934/97A
AU 2093497 A
AU2093497 A
AU 2093497A
AU 2093497 A
AU2093497 A
AU 2093497A
Authority
AU
Australia
Prior art keywords
ortho ester
acid
ester polymer
pharmaceutically acceptable
formula
Prior art date
1996-03-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Application number
AU20934/97A
Other versions

AU722303B2
(en

AU722303C
(en

Inventor
Robert Gurny
Cyrus Tabatabay
Monia Zignani
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Individual

Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1996-03-05
Filing date
1997-02-26
Publication date
1997-09-22

1997-02-26
Application filed by Individual
filed
Critical
Individual

1997-09-22
Publication of AU2093497A
publication
Critical
patent/AU2093497A/en

2000-07-27
Publication of AU722303B2
publication
Critical
patent/AU722303B2/en

2001-12-06
Application granted
granted
Critical

2001-12-06
Publication of AU722303C
publication
Critical
patent/AU722303C/en

2017-02-26
Anticipated expiration
legal-status
Critical

Status
Ceased
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

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

A61K9/20—Pills, tablets, discs, rods

A61K9/2004—Excipients; Inactive ingredients

A61K9/2022—Organic macromolecular compounds

A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers

A61K9/204—Polyesters, e.g. poly(lactide-co-glycolide)

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

A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite

A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides

A61K47/12—Carboxylic acids; Salts or anhydrides thereof

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

A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers

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

A61K9/20—Pills, tablets, discs, rods

A61K9/2004—Excipients; Inactive ingredients

A61K9/2013—Organic compounds, e.g. phospholipids, fats

Abstract

A pharmaceutical composition for the controlled release of therapeutic agents from carboxylic acid ortho ester polymers contains a pharmaceutically acceptable salt of an acid, which together with the acid R1-COOH liberated from the decomposition of the ortho ester polymer forms a buffer system in a physiologically acceptable pH range.

Description

Pharmaceutical Compositions Containing Buffered Ortho Ester Polymers
The present invention relates to a pharmaceutical composition for the controlled release of therapeutic agents from carboxylic acid ortho ester polymers and to a process for the preparation of said pharmaceutical compositions.
Background of the invention
Carboxylic acid ortho ester polymers consisting essentially of monomer repeating units of the partial formula

wherein Ri represents hydrogen or Cι- -alkyl and A represents a hydrocarbon chain of the formula
R-C-(CH2)-C— (CH2)n- (I A),
wherein Ra, Rb und Rc independently of one another represent hydrogen or Cι-4-alkyl, and m and n independently of one another represent zero or integers from one to three; methods for preparing such ortho esters and their utility as carriers in so-called controlled release pharmaceutical compositions have been disclosed in Published International Patent Application (WO) 91/03510, International Publication Date: Aug. 23, 1990.
The slow hydrolysis of these carboxylic acid ortho ester polymers and the controlled release of therapeutic agents from the polymer matrix has been disclosed in Published International Patent Application (WO) 93/00383, International Publication Date: June 18, 1992. Under physiologically acceptable conditions of pH 7.4, the hydrolysis of the ortho ester polymer (I) has been observed. This hydrolysis could formally be regarded as the reversal of the polymerisation step, whereupon a triol of the formula
OH
I (in
OH-A OH ‘

is generated and the acid R,-COOH is being liberated. When an carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula

is hydrolyzed, the acid CH3COOH is liberated. Upon progressive hydrolysis of the ortho ester polymers, an increasing amount of carboxylic acids RiCOOH is being liberated. This causes a decrease of the pH-level in-vitro from values of about 6.5 to 4.5 to even lower values in 1 -5 days depending on the moleclur weight of the polymer.
This decreasing pH-level renders pharmaceutical compositions or administration systems containing the above-mentioned carboxylic acid ester ortho ester polymers less feasible for various types of administration, especially intramuscular, subcutaneous and intraocular administration, since it has firmly been established that the injection of a formulation with an acidic pH could trigger inflammation, cf. Sekizawa etal., J. Toxicol. Sci. 19, 25-35 (1994).
The addition of a base to achieve neutralization is deemed unsuitable, since basic substances produce a local pH level above 8 at the site of addition. This is not acceptable for implants and for various modes of administration, especially intravenous and intraocular administration.
Objects of the invention
Accordingly, the problem to which the present invention relates may be defined as follows: It is desirable to provide a pharmaceutical dosage form for the controlled release of active agents from carboxylic acid ortho ester polymers. To solve this problem, it is necessary to maintain the pH-level in a physiologically acceptable constant range between 5.0 and 7.5.
This problem has been solved by adding a pharmaceutically acceptable salt of an acid, which together with the acid being liberated from the decomposition of the carboxylic acid ortho ester polymer (I) forms a buffer system in a physiologically acceptable pH-range.

General Description of the Invention
The present invention, therefore, relates to a pharmaceutical composition for the controlled release of therapeutic agents from a polymer comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula

wherein R, represents hydrogen or C^-alkyl, and A represents a hydrocarbon chain of the formula
R-C— (CH2)-C— (CH2)n— (I A),
wherein Ra, Rb und Rc independently of one another represent hydrogen or C -alkyl, and m and n independently of one another represent zero or integers from one to three; c) a pharmaceutically acceptable salt of an acid, which together with the acid Ri-COOH being liberated from the decomposition of the carboxylic acid ortho ester polymer (I) forms a buffer system in a physiologically acceptable pH-range; and the following optional components: d) further pharmaceutically acceptable additives; and’or e) a pharmaceutically acceptable carrier liquid.
The pharmaceutical composition is suitable for implants and also for various types of administration, especially parenteral administration by injection, e.g. intramuscular, subcutaneous, subconjunctival, intraocular or periodental administration. The controlled release of the active agent administered follows an approximate «zero order» pattern (constant amounts of active agent are released within defined time periods). The decomposition products of the polyortho esters defined above are physiologically acceptable and no removal of undesirable decomposition products from the site of administration is deemed necessary.

The general terms used throughout the specification of this invention are preferably defined as follows:
The term pharmaceutical composition defines a mixture containing the therapeutic agent or combination of therapeutic agents to be administered in the selected dosage form to a host in a therapeutic method of treating the disease or condition indicated. Intramuscular and intraocular administration of the pharmaceutical composition are particularly preferred.
Component a)
The term therapeutic agent as used herein is intended to define a compound or composition of matter which, when administered to a human being or an animal, induces a desired pharmacological and/or physiological effect by local and/or systemic action. In general, this term includes therapeutic or prophylactic agents in all major therapeutic/ prophylactic areas of medicine. Suitable therapeutic agents include the following pharmaceutical agents: antiinflammatory agents, for example dexamethasone, sodium dexamethasone sulfate, hydrocortisone or prednisolone, coronary dilators, for example ntfedipine, isosorbitol dinitrate, nitroglycerine, diltiazem, trapidil, dipyridamole or dilazep, prostaglandins, for example prostaglandin E1( E2 or FZA, peripheral vasodilators, for example ifenprodil, cine- pazet maleate, cyclandelate, cinnarizine or pentoxyphylline, antibiotics, for example ampicillin, amoxycillin, cephalexin, cephradine, cefroxadin, cefaclor, erythromycin, bacampi- cillin, minocycline or chloramphenicol, antispasmodics, for example propantheline, atropine or scopolamine, antitussives and antiasthmatics, for example theophylline, aminophylline, methylephedrine, procatechol, trimethoquinol, codeine, clofedanolol or dextromethorphan, diuretics, for example furosemide or acetazolamide, muscle relaxants, for example chlor- phenesin carbamate, tolperison, eperison or baclofen, mild tranquilisers, for example oxazolam, diazepam, clotiazepam, medazepam, temazepam or fludiazepam, potent tranquilisers, for example sulpiride, clocapramine or zotepin, beta-blockers, for example pindolol, propranolol, carteolol, oxprenolol, metoprolol or labetalol, antiarrhythmics, for example procainamide, disopyramide, ajimalin or quinidine, antigout agents, such as allopurinol, anticoagulants, such as ticlopidine, antiepileptics, for example phenytoin or valproat, antihistamines, for example chlorpheniramine, clemastine, mequitazine, ali emazine, cyproheptadine, agents for treating nausea and dizziness, for example diphenidol, methochlopromide, domperidone or betahistine, antihypertensives, for example reserpine, rescinnamine, methyldopa, prazosin, clonidine or budralazin, sympathomimetics,

for example dihydroergotamine, isoproterenol or etilefrin, expectorants, for example brom- hexine, carbocisteine, L-ethylcysteine or L-methylcysteine, oral antidiabetics, for example glibenclamide or tolbutamide, cardiovascular agents, for example ubidecarenon or adenosine.
Therapeutic agents can be converted into pharmaceutically acceptable salts, for example into a hydrobromide, hydrochloride, mesylate, acetate, succinate, lactate, tartrate, fumarate, sulfate or maleate salt.
Preferred therapeutic agents are immunosuppressants, such as cyclosporin, cytostatics, such as edatrexate (10-EDAM), doxorubicin, cytarabine, trifosamide, cyclophosphamide, fluorouracil or methotrexate and zinc phthalocyanine as well as water-soluble sulfo deriva¬ tives of phthalocyanine, for example tetrasulfophthalocyanine, which can be used in photo- dynamic chemotherapy.
The therapeutic agents mentioned above are present in the pharmaceutical composition either as individual agents or in fixed combinations with other therapeutic agents. The dose administered is the dose prescribed for each agent, the mode of administration intended and the disease and condition indicated for therapy.
In preferred embodiments of the invention, therapeutic agents are administered by subconjunctival and intraocular injection, such as 5-fluorouracil (5-FU) and mitomycin, after glaucoma filtering surgery; 5-FU or dexamethasone for the treatment of proliferative vitroretinopathy; by subcutaneous and intramuscular injection, such as naitrexone as narcotic antagonisms; insulin for .treatment of diabetes mellitus, norethisterone and levonorgestrel as contraceptive agents; demineralized bone matrix and bone graft agents for bone formation; 5-FU and naitrexone for the treatment of tumors, pyrimethamine or halofantrine for prophylaxis of malaria, homosulphanilamid for the treatment of burned skin, or tetracycline for periodontal injection.
Component bϊ
A suitable bioerodible carboxylic acid ortho ester polymer present in the pharmaceutical composition consists essentially of monomer repeating units of the partial formula

wherein Ri represents hydrogen or Cι-4-alkyl and A represents a hydrocarbon chain of the formula
FL R.
R.-C—(CH2)-C— (CH2)n- (I A),
wherein Ra, Rb und Rc independently of one another represent hydrogen or C^-alkyl, and m and n independently of one another represent zero or integers from one to three;
A particularly preferred carboxylic acid ortho ester polymer present in the pharmaceutical composition consists essentially of monomer repeating units of the partial formula

The term bioerodible as used herein to describe the properties of the defined ortho ester polymers is synonymous with the term biodegradable. These terms denote the property of a body of solid or semisolid polymers to undergo degradation, erosion and solubilization as a result of hydrolysis of labile linkages at the physiological conditions of use.
Monomer repeating units of the partial formula I are structurally recurring units or monomer units of the carboxylic acid ortho ester polymers provided by the present invention. The monomer repeating units may be the same or different; when different, they may be ar¬ ranged in block sequential order or random fashion. When all monomer repeating units are the same or identical, the polymer is called a homopolymer. When there are 2 or more different monomer repeating units in a polymer, the polymer is called a copolymer. The present invention comprises pharmaceutical compositions containing copolymers and homopolymers. Homopolymers are particularly preferred.
In the monomer repeating units of the partial formula (I) Ri represents hydrogen or Ci-t-alkyl, e.g. methyl, ethyl, n- or isopropyl or n-butyl. Methyl is particularly preferred. In ortho ester polymers wherein R, represents methyl, acetic acid is liberated upon hydrolysis of the polymer.

In a hydrocarbon chain of the formula
R.-?-(CH2)-C— (CH2)- (I A),
Ra, R and Rc preferably represent hydrogen. One or two of Ra, Rb and Rc may represent hydrogen and the other(s) d^-alky!, particularly methyl. In the alternative, Ra, Rb and Rc may all represent identical or different d-t-alkyl groups. The parameters m and n indepen¬ dently of one another represent zero or integers from one to three; m preferably is zero and n preferably is three.
The preparation of the carboxylic acid ortho ester polymers is known and comprises the following steps: A triol of the formula
OH
OH-A — OH (,,)’ wherein A represents the alkylene chain of the formula IA defined above, is reacted under the conditions of a condensation reaction with a carboxylic acid ortho ester of the formula

wherein Oalk represents the Cι- -alkoxy group and Ri is as defined above, to give an ortho ester polymer consisting essentially of monomer repeating units of the partial formula

wherein A represents the alkylene chain of the formula IA.
The synthesis reaction of the ortho ester monomer (III) and the triol (II) is carried out neat or in an aprotic solvent such as tetrahydrofuran (THF), cyclohexane, ethylene glycol dimethyl ether (glyme) or the like. Typical concentrations of the reactants may range from essentially 100% (neat) down through about 10% by weight or lower, when solvent is used. The presence of anhydrous conditions is maintained. The reaction can be carried out under reflux conditions and thus, depending upon the solvent, at temperatures in the range of 50- 150°C, preferably 50-90°C. The approximate molar ratio of the reactants is about 1 :1. It is

typically preferred to carry out the reaction in the presence of an acid catalyst. Examples of suitable acid catalysts include p-toluenesulfonic acid and methanesulfonic acid. The amount of acid catalyst can range from 0% (based on its optional presence) to about 1 % molar (based on the amount of triol present).
A preferred synthesis comprises reacting under the conditions of a condensation reaction mentioned above the triol of the formula CH2-CH-(CH2)a— CH,
OH OH OH with the acetic acid ester of the formula

wherein Oalk represents the Cι-.-alkoxy group, to give an acetic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula

Component c
A pharmaceutically acceptable salt of an acid, which together with the acid Ri-COOH being liberated from the decomposition of the ortho ester polymer (I) forms a buffer system in a physiologically acceptable pH-range, is defined by the definition of Ri in the ortho ester polymer (I). The pH-level in a physiologically acceptable range is between 6.5 and 7.5. The pH of 7.5 must not be exceeded when intraocular or intramuscular administration is intended.
When R! is hydrogen, formic acid will be liberated upon hydrolysis of the ortho ester poly¬ mer (I). A suitable pharmaceutically acceptable salt of formic acid is, e.g. sodium or potassium formiate. When Ri is methyl, acetic acid will be liberated upon hydrolysis. A pharmaceutically acceptable salt of acetic acid is, e.g. sodium or potassium acetate.
When RT is ethyl, n-propyl or n-butyl, the corresponding C3-, C -, or C5 -carboxylic acids will be liberated upon hydrolysis. Preferred pharmaceutically acceptable acids of these acids

are the sodium salts. The addition of pharmaceutically acceptable salts of other acids is also possible. Their structure is unrelated with the group Ri in the ortho ester polymer (I), but these salts also form together with the acid R COOH being liberated from the decomposition of the ortho ester polymer (I) a buffer system in the physiologically acceptable pH-range defined above. Such salts are, for example, sodium citrate, salts from amino acids, sodium ascorbate, glycolate, lactate, tartrate, maleate, fumarate, maleinate, succinate, benzoate and others.
Pharmaceutically acceptable salts of the acids defined above have the particular advantage of buffering the pharmaceutical composition on acceptable pH-levels. In the beginning and in all subsequent stages of the hydrolytic decomposition of the ortho ester polymer (I) biocompatibility is maintained. Initial raises of the pH-level when decomposition begins, to basic pH-levels and subsequent lowering to acidic pH-levels is avoided.
The amount of the salt added is determined by the amount of the ortho ester polymer pre¬ sent in the pharmaceutical composition. The addition of molar equivalent amounts of salt is preferred. For each molar amount of acid liberated, the addition of a molar amount of the above-defined salt is suggested. The salt may also be added in less than equivalent and excess amounts, e.g. up to 2 molar equivalents.
Component d)
Suitable pharmaceutically acceptable additives are determined by the dosage form for the intended mode of administration, e.g. parenteral administration. A preferred mode of administration is especially intramuscular and subcutaneous, but also topical, e.g. ocular.
Additives for topical formulations are listed in standard textbooks, e.g. Remington’s Pharmaceutical Sciences or Hagers Handbuch der Pharmazeutischen Praxis. Topical formulations are in particular creams, ointments, gels, pastes or topically administered aerosols and also suspensions of nanoparticles or ophthalmic compositions. Suitable additives for topical and especially ophthalmic compositions are in particular inert carriers, solubilizers, tonicity-increasing agents, buffer substances, preservatives, thickeners, and other adjuncts. Such additives are e.g. vegetable oil, mineral oil containing hydroxyethyl cellulose, ethyl oleate, carboxymethyl cellulose, polyvinyl pyrrolidone, and other non-toxic

water-soluble polymers intended for ophthalmic use, e.g. cellulose ethers such as methyl cellulose, alkali metal salts of carboxymethyl cellulose or hydroxym ethyl, hydroxyethyl, or hydroxypropyl cellulose, acrylates or methacrylates such as salts of polyacrylic acid or ethyl acrylate, polyacrylamides, natural products such as gelatin, alginates, pectins, tragacanth, karaya gum, xanthan gum, carrageenan, agar or acacia, starch derivatives such as starch acetate and hydroxypropyl starch, and also other synthetic additives such as polyvinyl alcohol, polyvinylpyrrolidone, polyvinyl methyl ether, polyethylene oxide, preferably crosslinked polyacrylic acid, such as neutral Carbopolβ» or mixtures of these polymers.
Tonicity-enhancing agents are, for example, ionic compounds, such as alkali metal or alkaline earth metal halides, e.g. CaCI2, KBr, KCI, LiCI, Nal, NaBr, or NaCl, or boric acid. Non-ionic tonicity-enhancing agents are, for example, urea, glycerol, sorbitol , mannitol, propyiene glycol, or dextrose. Sufficient tonicity-enhancing agent is added that the oph¬ thalmic composition has an osmolality in a preferred range of about 50 to 400 mOsmol.
Examples of preservatives are quaternary ammonium salts such as cetrimide, benzalk- onium chloride, alkylmercury salts of thiosalicylic acid such as thiomersal, phenylmercury nitrate, acetate, or borate, parabens such as methylparaben or propylparaben, alcohol, e.g. chlorobutanol, benzyl alcohol, or phenylethanol, guanidine derivatives, e.g. chlorhexidine, or polyhexamethylenebiguanide, or sorbic acid. If desired, the amount of preservative which is necessary to ensure sterility is added to the ophthalmic composition.
Component e)
A suitable pharmaceutically acceptable carrier liquid is defined by the intended mode of administration. If intramuscular administration is intended, oily carrier liquids, such as propyiene glycol, polyethylene glycol, sesame oil or olive oil, but also lecithin, may be added. Carrier liquids are particularly preferred when intramuscular, or intraocular administration is intended. The carrier liquid ethanol, if desired, is added in the degree of purity (96 %) prescribed for injection formulations in accordance with the regulations of national pharmacopoeias, such as The U.S. Pharmacopoeia (USP) or Deutsches Arzneibuch (DAB). The proportion of ethanol can vary within wide limits from approximately 1 % to approximately 50 %, preferably from approximately 1 % to approximately 10 %. The

carrier liquid water has the degree of purity prescribed for intravenous administration and is germ- and pyrogen-free in accordance with the regulations of the national pharmacopoeias.
Preferred embodiments of the invention
The present invention particularly relates to a pharmaceutical composition comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula

c) a pharmaceutically acceptable salt of an acid, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I’) forms a buffer system in a physiologically acceptable pH-range; and, optionally, d) further pharmaceutically acceptable additives.
An especially preferred embodiment of the invention relates to a pharmaceutical composition comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic ortho ester polymer consisting essentially of monomer repeating units of the partial formula (I’); c) the alkali metal salt X*CH3COO’, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I’) forms a buffer system in the physiologically acceptable pH-range of 5.5 – 7.5; and, optionally, d) further pharmaceutically acceptable additives.
A highly preferred embodiment of the invention relates to a pharmaceutical composition comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a non-rigid, bioerodible ortho ester polymer consisting essentially of monomer repeating units of the partial formula (I’); c) the sodium salt Na*CH3COO», which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (!’), forms a buffer system;

d) further pharmaceutically acceptable additives suitable for intraocular administration.
The present invention also relates to a process for the preparation of the above-mentioned pharmaceutical composition which process comprises preparing a non-rigid, bioerodible ortho ester polymer consisting essentially of monomer repeating units of the partial formula (I) mentioned above; and adding and mixing, in any order of the subsequent process steps, component a), the therapeutic agent or a combination of therapeutic agents to be admini¬ stered; component c), a pharmaceutically acceptable salt of an acid, which together with the acid RrCOOH being liberated from the decomposition of the ortho ester polymer (I), forms a buffer system in a physiologically acceptable pH-range; and, optionally, component d), further pharmaceutically acceptable additives; and/or component e), a pharmaceutically acceptable carrier liquid.
Mixing can be effected by vigorous shaking when using a dispersing machine, for example a Vortex mixer, or using dispersing machines produced by IKA (Staufen, Germany), a static mixer and conventional stirring machines having a propeller or paddle blade or using a magnetic stirrer or phase mixer. In order to obtain an especially homogeneous mixture, stirring is carried out at high speed. Approximately from 0.1 to 50 % by weight of the constituents (without the water component), based on the total weight of the mixture, preferably approximately from 2 to 20 % by weight, can be dispersed in the carrier liquid.
The following Example illustrates the invention:
Example 1 a) synthesis of the ortho ester polymer
34.68 g (300 mMol) of trimethyl ortho acetate (99 % – Aldrich Chemie, Steinheim Germany) are mixed under anhydrous conditions with 40.25 g (300 mMol) of 1 ,2,6-hexanetriol (98 % – Aldrich). The mixture is introduced into a round bottom flask, placed on a magnetic stirrer with 400 ml of cyclohexane added. The reaction is catalyzed by the addition of 25 mg p- TSA: p-toluenesulfonic acid (Fluka). The reaction flask is equipped with a distillation column and heated to 120°C under argon atmosphere and vigorous stirring. In a first step, the reac¬ tion by-product methanol is removed at 54°C during the first 4 h of the distillation. In a se¬ cond step, the temperature at the column head climbs above 54°C. The distillation flow is decreased and the solution is heated for an additional 6 h until the boiling point of 81 °C is

reached. The solution then is cooled to room temperature, and 10 drops of triethylamine (Fluka) are added to neutralize the acid catalyst. Excess solvent is pured off and the poly¬ mer is dried overnight under vacuum at 40°C. The polymer is then purified by dissolution in 100 ml of tetrahydrofurane (THF) and and precipitation in 500 ml anhydrous methanol con¬ taining 10 drops of triethylamine. After separating off the solvent, the polymer is dried under high vacuum for 48 h. An 0.2 μ air filter is added during the solvent evaporation in order to avoid air contamination when the vacuum is broken. No bacterial growth has been observed after 48 h of incubation of test samples at 37CC.
b) preparation of the drug loaded polymer
A 5-fluorouracil (5-FU) loaded polymer is prepared by mixing under laminar flow 25 mg of gamma-sterilized (2.0 Mrad) 5-FU and 12.5 mg of sodium acetate and dispersing the mixture with 2.5 g of aseptically prepared poly ortho ester polymer. This mixture is suitable as implant or for intraocular administration.
c) pH determination
The pH was measured during hydrolysis of the ortho ester polymer in order to assess the decrease of pH induced by the release of acetic acid.
1g (w/w) ortho ester polymer (POE) and 10ml 0.9% sodium chloride solution were placed in an incubator (Haling, Aigle, Switzerland) at 37°C under light shaking (100U/min). The pH measurements were taken every days during the first week and then every week until degradation was complete, with a pH-meter Mettler DL25 (Nanikon-Uster, Switzerland) and a combined pH-glass microelectrode.
Some results are shown in the accompanying drawing in which
Figure 1 is a graph showing pH profiles of the POE containing 5-FU, with or without addi¬ tion of sodium acetate, and
Figure 2 is a graph showing 5-FU release profiles with and without addition of acetate.
As shown in Figure 1 stabilization of the pH level between 5 and 6 is observed upon addition of sodium acetate. Without addition of acetate the pH level falls below 4 after

one week, and thereafter further to 2.5.
Figure 2 shows that the release of 5-FU is only slightly affected by the adjunction of 0.5% sodium acetate.

Claims (10)

Claims

1. A pharmaceutical composition for the controlled release of therapeutic agents from a polymer matrix comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula
wherein Ri represents hydrogen or CM-alkyl and A represents a hydrocarbon chain of the formula
wherein Ra, R und Rc independently of one another represent hydrogen or d^-alkyl, and m and n independently of one another represent zero or integers from one to three; c) a pharmaceutically acceptable salt of an acid, which together with the acid RrCOOH being liberated from the decomposition of the ortho ester polymer (I) forms a buffer system in a physiologically acceptable pH-range; and the following optional components: d) further pharmaceutically acceptable additives; and or e) a pharmaceutically acceptable carrier liquid.

2. A pharmaceutical composition according to claim 1 comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula
c) a pharmaceutically acceptable salt of an acid, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I’) forms a buffer system in a physiologically acceptable pH-range; and, optionally, d) further pharmaceutically acceptable additives.

3. A pharmaceutical composition according to claim 2 comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a bioerodible carboxylic ortho ester polymer consisting essentially of monomer repeating units of the partial formula (I’); c) the alkali metal salt X+CH3COO’, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I’) forms a buffer system in the physiologically acceptable pH-range of 5.5 – 7.5; and, optionally, d) further pharmaceutically acceptable additives.

4. A pharmaceutical composition according to claim 3 comprising: a) the therapeutic agent or a combination of therapeutic agents to be administered; b) a non-rigid, bioerodible ortho ester polymer consisting essentially of monomer repeating units of the partial formula (I’); c) the sodium salt Na*CH3COO’, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (!’), forms a buffer system; d) further pharmaceutically acceptable additives suitable for intraocular administration.

5. A process for the preparation of the pharmaceutical composition according to claim 1 , which comprises reacting under the conditions of a condensation reaction a triol of the formula
OH
OH— A — OH M* wherein A represents the alkylene chain of the formula IA defined in claim 1 , with a carboxylic acid ortho ester of the formula
Oalk
Rr Oalk
< (HI). Oalk wherein Oalk represents the d^-alkoxy group, to give a carboxylic acid ortho ester polymer consisting essentially of monomer repeating units of the partial formula wherein A represents the alkylene chain of the formula IA defined in claim 1 ; and adding, in any order of the subsequent process steps, component a), the therapeutic agent or a combination of therapeutic agents to be administered; component c), a pharmaceutically acceptable salt of an acid, which together with the acid RrCOOH being liberated from the decomposition of the ortho ester polymer (I), forms a buffer system in a physiologically acceptable pH-range; and, optionally, component d), further pharmaceutically acceptable additives; and/or component e), a pharmaceutically acceptable carrier liquid. 6. A process for the preparation of the pharmaceutical composition according to claim 5, which comprises reacting under the conditions of a condensation reaction the triol of the formula CH— CH— (CH2)3— CH2 j.j OH OH OH with the acetic acid ester of the formula wherein Oalk represents the Cι-«-alkoxy group, to give an ortho ester polymer consisting essentially of monomer repeating units of the partial formula and adding, in any order of the subsequent process steps, component a), the therapeutic agent or a combination of therapeutic agents to be administered; component c), a pharma¬ ceutically acceptable salt of an acid, which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I'), forms a buffer system in a physio¬ logically acceptable pH-range; and, optionally, compnent d), further pharmaceutically acceptable additives; and/or component e), a pharmaceutically acceptable carrier liquid. 7. A process according to claim 6, which comprises adding component c), the alkali metal salt X^HaCOO', which together with the acid CH3COOH being liberated from the decomposition of the ortho ester polymer (I') forms a buffer system in the physiologically acceptable pH-range of 5.5 - 7.5. 8. A process according to claim 7, which comprises adding component c), the sodium salt Na*CH3COO', which together with the acid CH3COOH being liberated from the decom¬ position of the ortho ester polymer (F) forms a buffer system. 9. A pharmaceutical administration system obtainable by the process according to claim 5. 10. A pharmaceutical composition according to claim 1 for use in a therapeutic method of treating the human or animal body. AU20934/97A 1996-03-05 1997-02-26 Pharmaceutical compositions containing buffered ortho ester polymers Ceased AU722303C (en) Applications Claiming Priority (3) Application Number Priority Date Filing Date Title EP96103391 1996-03-05 EP96103391 1996-03-05 PCT/EP1997/000906 WO1997032606A1 (en) 1996-03-05 1997-02-26 Pharmaceutical compositions containing buffered ortho ester polymers Publications (3) Publication Number Publication Date AU2093497A true AU2093497A (en) 1997-09-22 AU722303B2 AU722303B2 (en) 2000-07-27 AU722303C AU722303C (en) 2001-12-06 Family ID=8222532 Family Applications (1) Application Number Title Priority Date Filing Date AU20934/97A Ceased AU722303C (en) 1996-03-05 1997-02-26 Pharmaceutical compositions containing buffered ortho ester polymers Country Status (11) Country Link US (1) US6440460B1 (en) EP (1) EP0885014B1 (en) JP (1) JP4225570B2 (en) KR (1) KR100441821B1 (en) AT (1) ATE226450T1 (en) AU (1) AU722303C (en) DE (1) DE69716586T2 (en) DK (1) DK0885014T3 (en) ES (1) ES2185911T3 (en) PT (1) PT885014E (en) WO (1) WO1997032606A1 (en) Families Citing this family (20) * Cited by examiner, † Cited by third party Publication number Priority date Publication date Assignee Title US20030040790A1 (en) 1998-04-15 2003-02-27 Furst Joseph G. Stent coating US20020099438A1 (en) * 1998-04-15 2002-07-25 Furst Joseph G. Irradiated stent coating US7967855B2 (en) 1998-07-27 2011-06-28 Icon Interventional Systems, Inc. Coated medical device US8070796B2 (en) 1998-07-27 2011-12-06 Icon Interventional Systems, Inc. Thrombosis inhibiting graft US7168489B2 (en) * 2001-06-11 2007-01-30 Halliburton Energy Services, Inc. Orthoester compositions and methods for reducing the viscosified treatment fluids US8016881B2 (en) 2002-07-31 2011-09-13 Icon Interventional Systems, Inc. Sutures and surgical staples for anastamoses, wound closures, and surgical closures EP1537163B1 (en) 2002-09-09 2008-10-29 Nektar Therapeutics Al, Corporation Method for preparing water-soluble polymer derivatives bearing a terminal carboxylic acid US7691381B2 (en) * 2004-04-15 2010-04-06 Allergan, Inc. Stabilized biodegradable neurotoxin implants US20060200048A1 (en) * 2005-03-03 2006-09-07 Icon Medical Corp. Removable sheath for device protection US9107899B2 (en) 2005-03-03 2015-08-18 Icon Medical Corporation Metal alloys for medical devices WO2006110197A2 (en) 2005-03-03 2006-10-19 Icon Medical Corp. Polymer biodegradable medical device US7540995B2 (en) 2005-03-03 2009-06-02 Icon Medical Corp. Process for forming an improved metal alloy stent US20080114076A1 (en) * 2006-11-09 2008-05-15 Alcon Manufacturing Ltd. Punctal plug comprising a water-insoluble polymeric matrix ZA200902587B (en) * 2006-11-09 2010-06-30 Alcon Res Ltd Water insoluble polymer matrix for drug delivery US20110293549A1 (en) 2009-02-03 2011-12-01 Athena Cosmetics, Inc. Composition, method and kit for enhancing hair US8398916B2 (en) 2010-03-04 2013-03-19 Icon Medical Corp. Method for forming a tubular medical device BR112016030273A2 (en) 2014-06-24 2017-08-22 Icon Medical Corp MEDICAL DEVICE AND METHOD FOR FORMING SAID DEVICE WO2017151548A1 (en) 2016-03-04 2017-09-08 Mirus Llc Stent device for spinal fusion EP3474820A1 (en) 2017-08-24 2019-05-01 Novo Nordisk A/S Glp-1 compositions and uses thereof WO2021144477A1 (en) 2020-02-18 2021-07-22 Novo Nordisk A/S Glp-1 compositions and uses thereof Family Cites Families (11) * Cited by examiner, † Cited by third party Publication number Priority date Publication date Assignee Title US4093709A (en) 1975-01-28 1978-06-06 Alza Corporation Drug delivery devices manufactured from poly(orthoesters) and poly(orthocarbonates) US4010196A (en) * 1975-06-25 1977-03-01 American Home Products Corporation Linear polyester salts US4268643A (en) * 1979-10-25 1981-05-19 Societa Italiana Resine S.I.R. S.P.A. Process for improving the stability of acetal polymers EP0052916B1 (en) * 1980-11-10 1985-01-02 Alza Corporation Erodible polymer containing erosion rate modifier US4346709A (en) * 1980-11-10 1982-08-31 Alza Corporation Drug delivery devices comprising erodible polymer and erosion rate modifier DE3642662A1 (en) * 1986-10-02 1988-04-14 Hoechst Ag PARENTERAL DEPOT PREPARATIONS OF REGULATORY PEPTIDES CONTAINING CALCIUM ACETATE-GLYCERIN ADDUCT, METHOD FOR THE PRODUCTION THEREOF AND THE USE OF THE ADDUCT US5030457A (en) 1989-08-28 1991-07-09 Pharmaceutical Delivery Systems, Inc. Bioerodible polymers useful for the controlled release of therapeutic agents EP0489843A4 (en) 1989-08-28 1992-08-12 Pharmaceutical Delivery Systems, Inc. Bioerodible polymers useful for the controlled release of therapeutic agents AU2261592A (en) 1991-06-20 1993-01-25 Pharmaceutical Delivery Systems, Inc. Pulsed release of high molecular weight therapeutic agents from bioerodible polymer compositions US5700485A (en) * 1992-09-10 1997-12-23 Children's Medical Center Corporation Prolonged nerve blockade by the combination of local anesthetic and glucocorticoid US5869079A (en) * 1995-06-02 1999-02-09 Oculex Pharmaceuticals, Inc. Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents 1997 1997-02-26 PT PT97906128T patent/PT885014E/en unknown 1997-02-26 JP JP53141397A patent/JP4225570B2/en not_active Expired - Fee Related 1997-02-26 WO PCT/EP1997/000906 patent/WO1997032606A1/en active IP Right Grant 1997-02-26 AT AT97906128T patent/ATE226450T1/en not_active IP Right Cessation 1997-02-26 US US09/117,359 patent/US6440460B1/en not_active Expired - Fee Related 1997-02-26 AU AU20934/97A patent/AU722303C/en not_active Ceased 1997-02-26 ES ES97906128T patent/ES2185911T3/en not_active Expired - Lifetime 1997-02-26 DK DK97906128T patent/DK0885014T3/en active 1997-02-26 EP EP97906128A patent/EP0885014B1/en not_active Expired - Lifetime 1997-02-26 DE DE69716586T patent/DE69716586T2/en not_active Expired - Fee Related 1997-02-26 KR KR10-1998-0706905A patent/KR100441821B1/en not_active IP Right Cessation Also Published As Publication number Publication date AU722303B2 (en) 2000-07-27 EP0885014B1 (en) 2002-10-23 AU722303C (en) 2001-12-06 ATE226450T1 (en) 2002-11-15 KR100441821B1 (en) 2004-10-15 ES2185911T3 (en) 2003-05-01 EP0885014A1 (en) 1998-12-23 WO1997032606A1 (en) 1997-09-12 JP2000506148A (en) 2000-05-23 DE69716586T2 (en) 2003-07-17 PT885014E (en) 2003-02-28 DK0885014T3 (en) 2003-02-24 DE69716586D1 (en) 2002-11-28 KR19990087477A (en) 1999-12-27 JP4225570B2 (en) 2009-02-18 US6440460B1 (en) 2002-08-27 Similar Documents Publication Publication Date Title AU722303C (en) 2001-12-06 Pharmaceutical compositions containing buffered ortho ester polymers US5336505A (en) 1994-08-09 Bioerodible polymers useful for the controlled release of therapeutic agents JP4491560B2 (en) 2010-06-30 Topical composition for delivery of prostaglandin E1 US7560120B2 (en) 2009-07-14 Vehicles for delivery of biologically active substances US5461140A (en) 1995-10-24 Bioerodible polymers for solid controlled release pharmaceutical compositions KR970007898B1 (en) 1997-05-17 Skin penetration enhancement using free base and acid addition salt combinations of active agents CA2316485C (en) 2008-01-22 Sustained-release pharmaceutical composition US7914803B2 (en) 2011-03-29 Ophthalmic compositions containing a synergistic combination of three polymers KR20030060769A (en) 2003-07-16 Topical compositions containing prostaglandin E1 JP2555555B2 (en) 1996-11-20 Antifungal topical formulation JP2000516614A (en) 2000-12-12 Compositions for pharmaceutical applications IL276569B2 (en) 2023-06-01 Hypertonic pharmaceutical compositions containing an anti-platinum chemoprotectant agent JPH10501814A (en) 1998-02-17 In situ gel-forming delivery vehicles for biological agents and methods of use AU608268B2 (en) 1991-03-28 Nasal solutions JPS605567B2 (en) 1985-02-12 Oxytetracycline preparation CA2243988C (en) 2006-05-02 Pharmaceutical compositions containing buffered ortho ester polymers JPH0764754B2 (en) 1995-07-12 Transdermal absorption enhancer and external preparation for skin containing the same CA1263602A (en) 1989-12-05 Transdermal delivery of azatadine JPH0660097B2 (en) 1994-08-10 Pharmaceutical formulation JPS632926A (en) 1988-01-07 Stable injectable antiemetic composition KR900002745B1 (en) 1990-04-28 Process for preparing stable injectable antiemetic composition US6342241B1 (en) 2002-01-29 Medical composition of hydroxy acid-based oligomer JP2847391B2 (en) 1999-01-20 Stable lyophilized powder injection IE49934B1 (en) 1986-01-08 Long acting sulfonamide injectable compositions JPH0717521B2 (en) 1995-03-01 Composition for outer skin administration Legal Events Date Code Title Description 2000-08-31 DA2 Applications for amendment section 104 Free format text: FT="THE" NATURE OF THE PROPOSED AMENDMENT IS AS SHOWN IN THE STATEMENT(S) FILED 20000731 2001-04-26 DA3 Amendments made section 104 Free format text: THE NATURE OF THE AMENDMENT IS AS WAS NOTIFIED IN THE OFFICIAL JOURNAL DATED 20000831 2001-06-14 DA2 Applications for amendment section 104 Free format text: THE NATURE OF THE PROPOSED AMENDMENT IS AS SHOWN IN THE STATEMENT(S) FILED 20010305 2001-12-06 DA3 Amendments made section 104 Free format text: THE NATURE OF THE AMENDMENT IS AS WAS NOTIFIED IN THE OFFICIAL JOURNAL DATED 20010614
Download PDF in English