The preparation of polymerizable, optically active non-steroidal anti-inflammatory drugs derivatives by irreversible enzymatic methods

被引:23
作者
Cai, Xiao-Qing [1 ]
Wang, Na [1 ]
Lin, Xian-Fu [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
NSAIDs; irreversible resolution; enantioselectivity; lipases; prodrug; vinyl esters;
D O I
10.1016/j.molcatb.2006.02.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A lipase-catalyzed irreversible resolution of 2-arylpropionic acids was developed using the corresponding racemic vinyl esters as activated substrates. The obtained products, (S)-ketoprofen vinyl ester, (S)-naproxen vinyl ester and (S)-ibuprofen vinyl ester would be useful as significant monomers for polymeric drug. The effect of enzyme sources, solvent, water amount and temperature on the hydrolysis resolution was investigated. Optically active, polymerizable ketoprofen prodrug can be obtained with excellent enantioselectivity (ee similar to 90%) after optimization of the reaction conditions. Lipased-catalyzed transesterification of (R,S)-ketoprofen vinyl esters with various alcohols was also studied. The use of vinyl ester effectively enhanced the enantio selectivity compared with other common ester, such as ethyl and butyl esters. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 57
页数:7
相关论文
共 27 条
[1]   NAPROXEN 1-ALKYLAZACYCLOALKAN-2-ONE ESTERS AS DERMAL PRODRUGS - IN-VITRO EVALUATION [J].
BONINA, FP ;
MONTENEGRO, L ;
GUERRERA, F .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 100 (1-3) :99-105
[2]   THE METABOLIC CHIRAL INVERSION AND DISPOSITIONAL ENANTIOSELECTIVITY OF THE 2-ARYLPROPIONIC ACIDS AND THEIR BIOLOGICAL CONSEQUENCES [J].
CALDWELL, J ;
HUTT, AJ ;
FOURNELGIGLEUX, S .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (01) :105-114
[3]   Polymeric prodrug for release of an antitumoral agent by specific enzymes [J].
Cavallaro, G ;
Pitarresi, C ;
Licciardi, M ;
Giammona, G .
BIOCONJUGATE CHEMISTRY, 2001, 12 (02) :143-151
[4]   A 2-PROPANOL TREATMENT INCREASES THE ENANTIOSELECTIVITY OF CANDIDA-RUGOSA LIPASE TOWARD ESTERS OF CHIRAL CARBOXYLIC-ACIDS [J].
COLTON, IJ ;
AHMED, SN ;
KAZLAUSKAS, RJ .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (01) :212-217
[5]  
CRESCENZO GD, 2000, J MOL CATAL B-ENZYM, V9, P45
[6]  
DUCET A, 1998, ENZYME MICROB TECHNO, V22, P212
[7]  
HERNAIZ MJ, 1994, TETRAHEDRON, V50, P10749
[8]   Enzymatic production of enantiopure ketoprofen in a solvent-free two-phase system [J].
Jin, JN ;
Lee, SH ;
Lee, SB .
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2003, 26 (3-6) :209-216
[9]   Improved enantioselectivity of Candida rugosa lipase towards ketoprofen ethyl ester by a simple two-step treatment [J].
Kim, MG ;
Lee, EG ;
Chung, BH .
PROCESS BIOCHEMISTRY, 2000, 35 (09) :977-982
[10]   RULES FOR OPTIMIZATION OF BIOCATALYSIS IN ORGANIC-SOLVENTS [J].
LAANE, C ;
BOEREN, S ;
VOS, K ;
VEEGER, C .
BIOTECHNOLOGY AND BIOENGINEERING, 1987, 30 (01) :81-87