The manufacturing techniques of various drug loaded biodegradable poly(lactide-co-glycolide) (PLGA) devices

被引:1776
作者
Jain, RA [1 ]
机构
[1] NanoSystems, King Of Prussia, PA 19406 USA
关键词
biodegradable; poly(lactide-co-glycolide) (PLGA); bioresorbable;
D O I
10.1016/S0142-9612(00)00115-0
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A considerable research has been conducted on drug delivery by biodepradable polymeric devices, following the entry of bioresorbable surgical sutures in the market about two decades ago. Amongst the different classes of biodegradable polymers, the thermoplastic aliphatic poly(esters) like poly(lactide) (PLA), poly(glycolide) (PGA), and especially the copolymer of lactide and glycolide, poly(lactide-co-glycolide) (PLGA) have generated immense interest due to their favorable properties such as good biocompatibility, biodegradability, and mechanical strength. Also, they are easy to formulate into different devices for carrying a variety of drug classes such as vaccines, peptides, proteins, and micromolecules. Also, they have been approved by the Food and Drug Administration (FDA) for drug delivery. This review discusses the various traditional and novel techniques (such as in situ microencapsulation) of preparing various drug loaded PLGA devices, with emphasis on preparing microparticles. Also, certain issues about other related biodegradable polyesters are discussed. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2475 / 2490
页数:16
相关论文
共 191 条
[1]   Antisense oligonucleotide delivery to cultured macrophages is improved by incorporation into sustained-release biodegradable polymer microspheres [J].
Akhtar, S ;
Lewis, KJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 151 (01) :57-67
[2]   BIODEGRADABLE MICROSPHERES AS CONTROLLED-RELEASE TETANUS TOXOID DELIVERY SYSTEMS [J].
ALONSO, MJ ;
GUPTA, RK ;
MIN, C ;
SIBER, GR ;
LANGER, R .
VACCINE, 1994, 12 (04) :299-306
[3]   DETERMINANTS OF RELEASE RATE OF TETANUS VACCINE FROM POLYESTER MICROSPHERES [J].
ALONSO, MJ ;
COHEN, S ;
PARK, TG ;
GUPTA, RK ;
SIBER, GR ;
LANGER, R .
PHARMACEUTICAL RESEARCH, 1993, 10 (07) :945-953
[4]  
ALPAR HO, 1995, P INT S CONTROL REL, V22, P564
[5]   PREPARATION OF BIODEGRADABLE MICROSPHERES AND MICROCAPSULES .2. POLYACTIDES AND RELATED POLYESTERS [J].
ARSHADY, R .
JOURNAL OF CONTROLLED RELEASE, 1991, 17 (01) :1-21
[6]  
BENOIT MA, 1996, P INT C ADV CONTR DE, P69
[7]   Study of the influence of several stabilizing agents on the entrapment and in vitro release of pBC 264 from poly(lactide-co-glycolide) microspheres prepared by a W/O/W solvent evaporation method [J].
BlancoPrieto, MJ ;
Leo, E ;
Delie, F ;
Gulik, A ;
Couvreur, P ;
Fattal, E .
PHARMACEUTICAL RESEARCH, 1996, 13 (07) :1127-1129
[8]  
BLANCOPRIETO MJ, 1996, P INT S CONTROLLED R, V23, P853
[10]   RESORPTION RATE, ROUTE OF ELIMINATION, AND ULTRASTRUCTURE OF IMPLANT SITE OF POLYLACTIC ACID IN ABDOMINAL-WALL OF RAT [J].
BRADY, JM ;
CUTRIGHT, DE ;
MILLER, RA ;
BATTISTONE, GC ;
HUNSUCK, EE .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1973, 7 (02) :155-166