Bovine serum albumin loaded poly(lactide-co-glycolide) microspheres: the influence of polymer purity on particle characteristics

被引:29
作者
Bittner, B
Ronneberger, B
Zange, R
Volland, C
Anderson, JM
Kissel, T
机构
[1] Univ Marburg, Dept Pharmaceut & Biopharm, D-35032 Marburg, Germany
[2] Case Western Reserve Univ, Dept Macromol Sci, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
关键词
microsphere; poly(lactide-co-glycolide); bovine serum albumin; DL-lactide and glycolide monomers and oligomers; ultrafiltration; in vitro and in vivo biocompatibility; in vivo degradation;
D O I
10.3109/02652049809006876
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
To study the influence of polymer purity on microsphere characteristics, bovine serum albumin (BSA) loaded biodegradable microspheres were prepared by spray drying using two samples of poly(lactide-co-glycolide), PLG, (50:50, mwt = 35 and 69 kDa). Polymer properties were varied by DL-lactide and glycolide addition or by ultrafiltration. While the effective drug loading was not affected by polymer purity, Tg was decreased with increasing monomer and oligomer content. The removal of these low molecular weight substances by ultrafiltration led to a narrower molecular weight distribution compared to the untreated PLG. Concerning the polymer with the higher molecular weight, microsphere morphology was also strongly affected by polymer composition. In contrast to the non-modified PLG, monomer addition yielded particles with a much smoother surface structure. Moreover, in vitro cytotoxicity of the microspheres prepared from the polymer pretreated by ultrafiltration was significantly reduced, whereas monomer addition caused a dramatic decrease of cells surviving contact with the microsphere extract. The in vivo degradation rate of the ultrafiltered microspheres was decreased and as a result, protein release at later times was slowed down. Furthermore, depending on the effective drug loading level, monomer addition resulted in a decrease in the initial protein burst. It can be concluded that the effect of low molecular weight impurities in a polymer on microsphere characteristics and on cytotoxicity cannot be ignored. Their elimination is possible by ultrafiltration.
引用
收藏
页码:495 / 514
页数:20
相关论文
共 42 条
[1]  
ANDERSON JM, 1994, EUR J PHARM BIOPHARM, V40, P1
[2]   Influence of the preparation method on residual solvents in biodegradable microspheres [J].
Bitz, C ;
Doelker, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 131 (02) :171-181
[3]   THE EFFECT OF THE ADDITION OF LOW-MOLECULAR WEIGHT POLY(DL-LACTIDE) ON DRUG RELEASE FROM BIODEGRADABLE POLY(DL-LACTIDE) DRUG DELIVERY SYSTEMS [J].
BODMEIER, R ;
OH, KH ;
CHEN, H .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 51 (01) :1-8
[4]   PREPARATION OF BIODEGRADABLE POLY (+/-) LACTIDE MICROPARTICLES USING A SPRAY-DRYING TECHNIQUE [J].
BODMEIER, R ;
CHEN, HG .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1988, 40 (11) :754-757
[5]   FACTORS INFLUENCING THE RELEASE OF PEPTIDES AND PROTEINS FROM BIODEGRADABLE PARENTERAL DEPOT SYSTEMS [J].
BODMER, D ;
KISSEL, T ;
TRAECHSLIN, E .
JOURNAL OF CONTROLLED RELEASE, 1992, 21 (1-3) :129-137
[6]   SUSTAINED-RELEASE OF NERVE GROWTH-FACTOR FROM BIODEGRADABLE POLYMER MICROSPHERES [J].
CAMARATA, PJ ;
SURYANARAYANAN, R ;
TURNER, DA ;
PARKER, RG ;
EBNER, TJ .
NEUROSURGERY, 1992, 30 (03) :313-319
[7]   CONTROLLED DELIVERY SYSTEMS FOR PROTEINS BASED ON POLY(LACTIC GLYCOLIC ACID) MICROSPHERES [J].
COHEN, S ;
YOSHIOKA, T ;
LUCARELLI, M ;
HWANG, LH ;
LANGER, R .
PHARMACEUTICAL RESEARCH, 1991, 8 (06) :713-720
[8]   SPRAY-DRIED POLYLACTIDE MICROSPHERE PREPARATION - INFLUENCE OF THE TECHNOLOGICAL PARAMETERS [J].
CONTE, U ;
CONTI, B ;
GIUNCHEDI, P ;
MAGGI, L .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (03) :235-258
[9]   QUALITY IMPROVEMENT OF SPRAY-DRIED, PROTEIN-LOADED D,L-PLA MICROSPHERES BY APPROPRIATE POLYMER-SOLVENT SELECTION [J].
GANDER, B ;
WEHRLI, E ;
ALDER, R ;
MERKLE, HP .
JOURNAL OF MICROENCAPSULATION, 1995, 12 (01) :83-97
[10]   BIODEGRADABLE POLYMERS FOR USE IN SURGERY - POLYGLYCOLIC-POLY(ACTIC ACID) HOMOPOLYMERS AND COPOLYMERS .1. [J].
GILDING, DK ;
REED, AM .
POLYMER, 1979, 20 (12) :1459-1464