Novel drug release profiles from micellar solutions of PLA-PEO-PLA triblock copolymers

被引:102
作者
Agrawal, SK
Sanabria-DeLong, N
Coburn, JM
Tew, GN
Bhatia, SR
机构
[1] Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
[2] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
关键词
polylactic acid; polyethylene oxide; triblock; controlled release; micelles;
D O I
10.1016/j.jconrel.2005.12.024
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have achieved nearly zero order sustained release behavior for periods up to 10-20 days for two hydrophobic drugs, sulindac and tetracame, from 5 wt.% micellar solutions of poly(lactide)-poly(ethylene oxide)-poly(lactide) (PLA-PEO-PLA) triblock copolymer. The effect of PLA block length and crystallinity on the drug release profiles was studied. A series of polymers with constant PEO molecular weight of 8900Da and PLA molecular weight varying in the range of 4100-650ODa were examined. Drug release was found to be much faster for polymers with crystalline PLA blocks as compared to those with amorphous PLA blocks. The drug release rate also depends significantly on the length of the PLA block. Sustained release of sulindac was observed up to 20 days, and for tetracaine up to 10 days. By comparison, release of these drugs without polymeric carriers occurs over 4-6h. This result, along with a proposed mechanism for drug release, suggests that polymer-drug interactions significantly impact release profiles, causing slow and sustained release of the drug. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 71
页数:8
相关论文
共 35 条
[1]   Rheological studies of PLLA-PEO-PLLA triblock copolymer hydrogels [J].
Aamer, KA ;
Sardinha, H ;
Bhatia, SR ;
Tew, GN .
BIOMATERIALS, 2004, 25 (06) :1087-1093
[2]  
AGARWAL SK, 2005, MAT RES SOC S P, V844
[3]   Lipophilicity behavior of model and medicinal compounds containing a sulfide, sulfoxide, or sulfone moiety [J].
Caron, G ;
Gaillard, P ;
Carrupt, PA ;
Testa, B .
HELVETICA CHIMICA ACTA, 1997, 80 (02) :449-462
[4]   Synthesis and characterization of [L]-lactide - Ethylene oxide multiblock copolymers [J].
Chen, XH ;
McCarthy, SP ;
Gross, RA .
MACROMOLECULES, 1997, 30 (15) :4295-4301
[5]   Drug-releasing behavior of MPEG/PLA block copolymer micelles and solid particles controlled by component block length [J].
Choi, SK ;
Kim, D .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 83 (02) :435-445
[6]   Release from polymeric prodrugs: Linkages and their degradation [J].
D'Souza, AJM ;
Topp, EM .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (08) :1962-1979
[7]   Solubilization and interaction of sulindac with polyvinylpyrrolidone K30 in the solid state and in aqueous solution [J].
de Ilarduya, MCT ;
Martín, C ;
Goñi, MM ;
Martínez-Ohárriz, MC .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1998, 24 (03) :295-300
[8]   BIODEGRADABLE LONG-CIRCULATING POLYMERIC NANOSPHERES [J].
GREF, R ;
MINAMITAKE, Y ;
PERACCHIA, MT ;
TRUBETSKOY, V ;
TORCHILIN, V ;
LANGER, R .
SCIENCE, 1994, 263 (5153) :1600-1603
[9]   Partition coefficients (n-octanol/water) of N-butyl-p-aminobenzoate and other local anesthetics measured by reversed-phase high-performance liquid chromatography [J].
Grouls, RJE ;
Ackerman, EW ;
Korsten, HHM ;
Hellebrekers, LJ ;
Breimer, DD .
JOURNAL OF CHROMATOGRAPHY B, 1997, 694 (02) :421-425
[10]   TREATMENT OF ADENOSINE-DEAMINASE DEFICIENCY WITH POLYETHYLENE-GLYCOL MODIFIED ADENOSINE-DEAMINASE [J].
HERSHFIELD, MS ;
BUCKLEY, RH ;
GREENBERG, ML ;
MELTON, AL ;
SCHIFF, R ;
HATEM, C ;
KURTZBERG, J ;
MARKERT, ML ;
KOBAYASHI, RH ;
KOBAYASHI, AL ;
ABUCHOWSKI, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (10) :589-596