Analysis of amino acid copolymer compositions

Patent metadata

Field	Value
Publication number	US-10160992-B2
Application number	US-201815861036-A
Country	US
Kind code	B2
Filing date	Jan 3, 2018
Priority date	Apr 16, 2008
Publication date	Dec 25, 2018
Grant date	Dec 25, 2018

Abstract

Methods for analyzing, selecting, characterizing or classifying compositions of a co-polymer, e.g., glatiramer acetate are described. The methods entail analysis of pyro-glutamate in the composition, and, in some methods, comparing the amount of pyro-glutamate present in a composition to a reference standard.

First claim

What is claimed is:

1. A method for manufacturing a pharmaceutical composition comprising glatiramer acetate, the method comprising:
preparing an amino acid copolymer of L-glutamic acid, L-alanine, L-lysine, and L-tyrosine, wherein the preparing step comprises co-polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)-protected L-lysine, and L-tyrosine to generate a first material; treating the first material to deprotect the benzyl-protected L-glutamic acid therein and to partially depolymerize the first material, thereby generating a second material; treating the second material to deprotect the TFA-protected L-lysine to produce a third material; and purifying the third material, to thereby produce the copolymer of L-glutamic acid, L-alanine, L-lysine, and L-tyrosine;
measuring the pyro-glutamate content of the second material in a sample of the second material or measuring the pyro-glutamate content of the third material in a sample of the third material copolymer in a sample of the copolymer;
processing the copolymer to produce a pharmaceutical composition comprising glatiramer acetate only if the measured pyro-glutamate content in the sample of the second material or the sample of the third material is within 2000-7000 parts per million (ppm) on a dry weight/dry weight basis,
thereby producing a pharmaceutical composition comprising glatiramer acetate.

2. The method of claim 1 wherein: the step of deprotecting the TFA-protected L-lysine comprises treating the second material with aqueous piperidine.

3. The method of claim 1 , wherein co-polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)-protected L-lysine, and L-tyrosine to generate a first material comprises contacting the N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)-protected L-lysine, and L-tyrosine with diethylamine.

4. The method of claim 2 , wherein co-polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)-protected L-lysine, and L-tyrosine to generate a first material comprises contacting the N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)-protected L-lysine, and L-tyrosine with diethylamine.

5. The method of claim 1 , wherein treating the first material to deprotect the benzyl-protected L-glutamic acid therein and to partially depolymerize the first material comprises treating the first material with anhydrous 33% HBr in acetic acid.

6. The method of claim 2 , wherein treating the first material to deprotect the benzyl-protected L-glutamic acid therein and to partially depolymerize the first material comprises treating the first material with anhydrous 33% HBr in acetic acid.

7. The method of claim 3 , wherein treating the first material to deprotect the benzyl-protected L-glutamic acid therein and to partially depolymerize the first material comprises treating the first material with anhydrous 33% HBr in acetic acid.

8. The method of claim 1 , wherein the step of measuring the pyro-glutamate content of the second material in a sample of the second material or measuring the pyro-glutamate content of the third material in a sample of the third material copolymer in a sample of the copolymer comprises obtaining a sample of a manufacturing batch.

9. The method of claim 1 , wherein the step of measuring pyro-glutamate content of the second material in a sample of the second material or measuring the pyro-glutamate content of the third material in a sample of the third material comprises contacting the second material in a sample of the second material or contacting the third material in a sample of the third material copolymer in a sample of the copolymer with pyroglutamate aminopeptidase.

10. The method of claim 1 , wherein the step of measuring pyro-glutamate content comprises determining the ppm of pyro-glutamate on a dry weight/dry weight basis.

11. The method of claim 1 , further comprising packaging, labeling, or releasing into commerce the pharmaceutical composition comprising glatiramer acetate.

12. The method of claim 1 , further comprising offering for sale or selling the pharmaceutical composition comprising glatiramer acetate.

13. The method of claim 1 , further comprising shipping or moving to a Previously Presented location the pharmaceutical composition comprising glatiramer acetate.

14. The method of claim 1 , wherein the glatiramer acetate has an Mp of 5000-9000 Da.

15. The method of claim 1 further comprising measuring the peak average molecular weight (Mp) of the glatiramer acetate.

16. The method of claim 15 wherein the measured peak average molecular weight of the glatiramer acetate is 5000-9000 Da.

Assignees

• Momenta Pharmaceuticals Inc

Inventors

• Zhu Xiangping
• Shriver Zachary
• Jiang Yanjie
• Bauer Corinne
• Anderson James Eric
• Ahern Peter James

Classifications

• G01N33/6812

  Assays for specific amino acids · CPC title

• A61K31/785

  Polymers containing nitrogen · CPC title

• C12Q1/37 Primary

  involving peptidase or proteinase · CPC title

• C08G69/10

  Alpha-amino-carboxylic acids {(polysuccinimides C08G73/1092)} · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title