Prevention of molecular weight reduction of the polymer, impurity formation and gelling in polymer compositions
Polymer and drug containing compositions and method of preparing such compositions are disclosed. The dispersed phase formulation has a polymer, a pharmaceutically or biologically active agent and a small fraction of low pKa acid additive. Stable, filter sterilizable, non-gelling solutions containing GnRH analogues at least at levels typically used in sustained release formulations and a method of increasing solubility of a high level of a GnRH analogue or a freeze-dried antgonist of GnRH in a polymer containing solution are also disclosed. The amount of the acid additive in the polymer solution is such that it is sufficient to increase the solubility of the high level of the GnRH analogue in the polymer solution without affecting the release characteristics of the microspheres prepared therefrom.
1. A method of preparing a polymer solution for use in an injectable sustained release formulation comprising:
dissolving or dispersing a nucleophilic compound that is a polypeptide or a pharmaceutically acceptable salt thereof, capable of catalyzing ester bond cleavage and causing molecular weight reduction of the polymer, and an amount of an acid additive consisting of one or more low pKa acids in a solvent to form a first organic solution or suspension;
dissolving an amount of a biocompatible and biodegradable polymer in a solvent to form a second organic solution; wherein the polymer is poly(d,1-lactic acid), poly(1-lactic acid), poly(glycolic acid) or copolymers thereof; and
mixing the first organic solution or suspension and the second solution to form the polymer solution for use in the injectable sustained release formulation, wherein the amount of an acid additive in the polymer solution is only a fraction relative to the amount of the polymer and is sufficient to reduce molecular weight reduction of the polymer caused by the nucleophilic compound.
2. The method of claim 1 , wherein the acid additive is one low pKa acid.
3. The method of claim 2 , wherein the acid additive is lactic acid, glycolic acid, glacial acetic acid, glyceric acid, benzoic acid, propanoic acid or carboxy terminated oligomers of lactic acid, carboxy terminated oligomers of glycolic acid or a combination of these acids.
4. The method of claim 1 , wherein the solvent in the first and second organic solution is a biocompatible solvent selected from the group consisting of methanol, ethanol, dimethyl sulfoxide (DMSO), dimethylformamide, dichloromethane (DCM), N-methylpyrrolidone, dimethyl acetamide (DMAc) or combinations thereof.
5. The method of claim 1 , wherein the amount of acid additive is about 2% to about 50% by weight of the polymer.
6. A method for preparing a polymer solution for use in an injectable sustained release formulation comprising:
mixing a nucleophilic substance capable of catalyzing ester bond cleavage and causing molecular weight reduction of the polymer, an amount of an acid additive consisting of one or more low pKa acids, a biocompatible and biodegradable polymer, and a solvent for the polymer; wherein the polymer is poly(d,1-lactic acid), poly(1-lactic acid), poly(glycolic acid) or copolymers thereof, and
wherein the amount of acid additive is such that the polymer in the injectable sustained release formulation is less susceptible to molecular weight reduction as compared to the polymer in the polymer solution without the acid additive.
7. The method of claim 6 , wherein the nucleophilic substance is a peptide, ketotifen, thioridazine, olanzapine, risperidone, oxybutynin, naltrexone, octreotide, leuprolide, orntide or Woc4D or pharmaceutically acceptable salts thereof.
8. The method of claim 6 , wherein the acid additive is one low pKa acid.
9. The method of claim 8 , wherein the acid additive is lactic acid, glycolic acid, acetic acid, glyceric acid, benzoic acid, propanoic acid or carboxy terminated oligomers of lactic acid, carboxy terminated oligomers of glycolic acid or a combination of these acids.
10. The method of claim 6 , wherein the amount of acid additive is about 0.1% to about 50% by weight of the polymer.
11. The method of claim 6 , wherein the polymer is a copolymer of poly-D,L-lactide and poly-D,L-lactide-co-glycolide having a molar ratio of lactide to glycolide in the range from 100:0 to 50:50.