IP Library Granted Patent US 8,021,652
Granted Patent B2
US 8,021,652 · App. 10/554,637 · Granted Sep 20, 2011

Biodegradable branched polylactide derivatives capable of forming polymeric micelles, and their preparation method and use

Assignee: Samyang Corporation
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Quick Facts
Patent No.
US 8,021,652
App. No.
10/554,637
Granted
Sep 20, 2011
Kind
B2
Abstract

The present invention relates to a biodegradable branched polylactic acid derivative of formula 1, and preparation method and use thereof: <formula 1> 1-(R—X) n wherein each of X, R, I and n is defined as in the detailed description.

Claims (25)

1. A micellar composition comprising a branched polylactic acid derivative of formula (I) for forming micelles in an aqueous solution with a pH of 4 or more:

I—(R—X) n   (1)

Wherein,

R is —[R 1 ] k —[R 2 ] m —,

wherein R 1 is —C(═O)—CHZ—O—,

R 2 is selected from the group consisting of —C(═O)—CHY—O—, —C(═O)—CH 2 CH 2 CH 2 CH 2 CH 2 —O— and —C(═O)—CH 2 —O—CH 2 CH 2 —O—, wherein each of Z and Y is selected from the group consisting of hydrogen, methyl, and phenyl,

k is an integer of 1-30,

m is an integer of 0-30;

X is —C(═O)—(CH 2 ) a —C(═O)—O-M, wherein a is an integer of 0-10, M is selected from the group consisting of hydrogen, sodium, potassium, and lithium;

I is a diol or a polyol having 3-12 hydroxy groups;

n is the same as the number of hydroxy groups that I has, and wherein I is selected from the group consisting of ethylene glycol, propanediol, butanediol, pentanediol, hexanediol, glycerol, erythritol, threitol, pentaerythritol, xylitol, adonitol, sorbitol, mannitol, disaccharide and trisaccharide, and wherein the branched polylactic acid derivative has a number average molecular weight of 1,000-18,000 Dalton.

2. The micellar composition according to claim 1 , wherein R is mono polymer or copolymer which is one or more selected from the group consisting of lactide, glycolide, caprolactone, 1,4-dioxane-2-one, and mandelic acid.

3. The micellar composition according to claim 1 , wherein M is sodium, potassium or lithium.

4. The micellar composition according to claim 1 , wherein the disaccharide is selected from the group consisting of palatinose, maltose monohydrate and maltitol, and the trisaccharide is D-raffinose pentahydrate.

5. A method of preparing the polylactic acid derivative described in any one of claims 1 and 2 to 4 , comprising the steps of

1) polymerizing a monomer of lactides in the presence of an initiator and a catalyst to obtain a branched polylactic acid;

2) dissolving the branched polylactic acid obtained in step 1) in a water-miscibile organic solvent, purifying the branched polylactic acid by adding an aqueous solution with a pH of 7 or more, and drying in vacuum, to obtain a powder form of the branched polylactic acid; and

3) reacting the branched polylactic acid derivative obtained in step 2) with succinic anhydride or a dichloride compound to obtain the branched polylactic acid derivative containing terminal carboxy group, wherein the initiator of step 1) is selected from the group consisting of ethylene glycol, propanediol, butanediol, pentanediol, hexandiol, glycerol, erythritol, threitol, pentaerythritol, xylitol, adonitol, sorbitol, mannitol, disaccharide and trisaccharide, and wherein the branched polylactic acid derivative has a number average molecular weight of 1,000-18,000 Dalton.

6. The method according to claim 5 , further comprising the step of adding an alkali metal salt to the branched polylactic acid derivative obtained in step 3) to obtain the branched polylactic acid derivative containing carboxy alkali metal salt terminal group.

7. The method according to claim 5 , wherein the disaccharide is selected from the group consisting of palatinose, maltose monohydrate and maltitol, and the trisaccharide is D-raffinose pentahydrate.

8. The method according to claim 5 , wherein in step 3, the branched polylactic acid derivative is reacted with a compound which is selected from the group consisting of succinic anhydride, oxalyl chloride, malonyl chloride, succinyl chloride, glutaryl chloride, adipoyl chloride, sebacoyl chloride, and dochecadioyl dichloride.

9. The method according to claim 6 , wherein the alkali metal salt is selected from the group consisting of sodium hydrogen carbonate, sodium carbonate, potassium hydrogen carbonate, potassium carbonate, and lithium carbonate.

10. The micellar composition according to any one of claims 1 and 2 - 4 , wherein said composition is for a poorly, water-soluble drug delivery agent.

11. A pharmaceutical composition containing the polylactic acid derivative described in any one of claims 1 and 2 to 4 and a poorly, water-soluble drug.

12. The micellar composition according to claim 1 , wherein said branched polylactic acid derivative entrap drugs in the micelles by forming stable micelles in aqueous solution and solubilizing poorly water-soluble drugs within the micelles.

Assignments (4)
CHANGE OF ADDRESS Recorded Nov 3, 2021
From: SAMYANG BIOPHARMACEUTICALS CORPORATION
To: SAMYANG BIOPHARMACEUTICALS CORPORATION
Reel/Frame 058013/0696 →
MERGER Recorded Nov 3, 2021
From: SAMYANG BIOPHARMACEUTICALS CORPORATION
To: SAMYANG HOLDINGS CORPORATION
Reel/Frame 058013/0766 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2012
From: SAMYANG CORPORATION
To: SAMYANG BIOPHARMACEUTICALS CORPORATION
Reel/Frame 027811/0667 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2005
From: SEO, MIN-HYO; KIM, BONG-OH; CHOI, IN-JA; SHIM, MYUNG-SEOB
To: SAMYANG CORPORATION
Reel/Frame 018125/0997 →
Priority Claims (1)
KR 10-2003-0087459 · Dec 4, 2003 · national
Continuity (1)
Related Publication 20070003625A1 · Jan 4, 2007