Preparation and Characterization of BSA-Loaded Microspheres Based on Polyanhydrides

被引:12
作者
Yu, Yang [1 ]
Lu, Tingli [1 ]
Zhao, Wen [1 ]
Sun, Weiguang [1 ]
Chen, Tao [1 ,2 ]
机构
[1] Northwestern Polytech Univ, Fac Life Sci, Key Lab Space Biosci & Biotechnol, Xian 710072, Peoples R China
[2] Liposome Res Ctr Shaanxi Prov, Xian 710075, Peoples R China
关键词
polyanhydrides; protein; microspheres; degradation; release; POLY-DL-LACTIDE-POLY(ETHYLENE GLYCOL) MICROSPHERES; CONTROLLED DELIVERY SYSTEMS; FABRICATION METHOD; PROTEIN RELEASE; SERUM-ALBUMIN; STABILIZATION; DEGRADATION; NANOPARTICLES; ENCAPSULATION; COPOLYMERS;
D O I
10.1002/app.33546
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of biodegradable PEG-containing polyanhydrides composed of sebacic acid, 1, 6-bis(p-carboxyphenoxy) hexane, and poly (ethylene glycol) (PEG) were used as matrix material for BSA-loaded microspheres. The effects of polymer composition on the microsphere size, entrapment efficiency, in vitro degradation, and in vitro protein release were studied. Microspheres in the size range of 0.8-10 mu m were fabricated via a modified double emulsion method and were characterized using scanning electron microscopy. As the content or the molecular weight of PEG was increased in the copolymer, a proportional increase was found in the particle size and the efficiency of BSA could be controlled by varying the polymer composition, increasing as the PEG proportion increased. In vitro release studies of BSA from polyanhydride microspheres revealed that the increased amounts of PEG within microspheres could accelerate the release rate of protein. These studies indicate that the PEG-containing polyanhydrides hold potential for protein delivery applications. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 121: 352-358, 2011
引用
收藏
页码:352 / 358
页数:7
相关论文
共 33 条
[1]   PLGA-mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in Vivo drug residence in blood properties [J].
Avgoustakis, K ;
Beletsi, A ;
Panagi, Z ;
Klepetsanis, P ;
Karydas, AG ;
Ithakissios, DS .
JOURNAL OF CONTROLLED RELEASE, 2002, 79 (1-3) :123-135
[2]   Microspheres for protein delivery prepared from amphiphilic multiblock copolymers 2. Modulation of release rate [J].
Bezemer, JM ;
Radersma, R ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 2000, 67 (2-3) :249-260
[3]   Protein encapsulation in biodegradable amphiphilic microspheres [J].
Bouillot, P ;
Ubrich, N ;
Sommer, F ;
Duc, TM ;
Loeffler, JP ;
Dellacherie, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 181 (02) :159-172
[4]   Effects of solvent selection and fabrication method on the characteristics of biodegradable poly(lactide-co-glycolide) microspheres containing ovalbumin [J].
Cho, SW ;
Song, SH ;
Choi, YW .
ARCHIVES OF PHARMACAL RESEARCH, 2000, 23 (04) :385-390
[5]  
CLELAND JL, 1993, CRIT REV THER DRUG, V10, P307
[6]   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
[7]  
Conix A., 1966, Macromolecule Synthesis, V2, P95
[8]   Optimization of preparative conditions for poly-DL-lactide-polyethylene glycol microspheres with entrapped Vibrio Cholera antigens [J].
Deng, XM ;
Li, XH ;
Yuan, ML ;
Xiong, CD ;
Huang, ZT ;
Jia, WX ;
Zhang, YH .
JOURNAL OF CONTROLLED RELEASE, 1999, 58 (02) :123-131
[9]   In vitro degradation and release profiles for poly-dl-lactide-poly(ethylene glycol) microspheres containing human serum albumin [J].
Deng, XM ;
Zhou, SB ;
Li, XH ;
Zhao, J ;
Yuan, ML .
JOURNAL OF CONTROLLED RELEASE, 2001, 71 (02) :165-173
[10]   Encapsulation, stabilization, and release of BSA-FITC from polyanhydride microspheres [J].
Determan, AS ;
Trewyn, BG ;
Lin, VSY ;
Nilsen-Hamilton, M ;
Narasimhan, B .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :97-109