Polyphosphoester microspheres for sustained release of biologically active nerve growth factor

被引:108
作者
Xu, XY
Yu, H
Gao, SJ
Mao, HQ
Leong, KW
Wang, S
机构
[1] Natl Univ Singapore, Inst Mat Res & Engn, Mol & Biomat Lab, Singapore 117602, Singapore
[2] Johns Hopkins Singapore, Singapore 117597, Singapore
[3] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
关键词
nerve growth factor; polymeric microsphere; polyphosphoester; nerve regeneration;
D O I
10.1016/S0142-9612(02)00116-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Controlled delivery of neurotrophic proteins to a target tissue by biodegradable polymer microspheres has been explored widely for its potential applications in the treatment of various disorders in the nervous system. We investigated in this study the potential of polyphosphoester microspheres as carriers for the sustained release of nerve growth factor (NGF), a water-soluble neurotrophic protein. Two polyphosphoesters (PPEs), P(BHET-EOP/TC) and P(DAPG-EOP), as well as poly(lactide/glycolic acid) (PLGA), were used to fabricate microspheres by a W/O/W emulsion and solvent evaporation/extraction method. With bovine serum albumin as a model protein to optimize processing parameters, P(DAPG-EOP) microspheres exhibited a lower burst effect but similar protein entrapment levels and efficiencies when compared with those made of PLGA. Bioactive NGF Could be released for at least 10 weeks from the P(DAPG-EOP) microspheres, as confirmed by a neurite outgrowth assay of the PC12 cells. These NGF containing microspheres were incorporated into the nerve guide conduits that were implanted to bridge a 10 turn gap in a rat sciatic nerve model. Two weeks after implantation, immunostaining with an antibody against the neurofilament protein confirmed the presence of axons at the distal end of regenerated cables within the NGF microsphere-loaded conduits. These results demonstrated the feasibility of using biodegradable PPEs for microencapsulation of NGF and provided a basis for future therapeutic application of the microspheres. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3765 / 3772
页数:8
相关论文
共 25 条
[1]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[2]  
[Anonymous], ENCY CONTROLLED DRUG
[3]   POLYLACTIC ACID MICROSPHERES CONTAINING QUINIDINE BASE AND QUINIDINE SULFATE PREPARED BY THE SOLVENT EVAPORATION TECHNIQUE .1. METHODS AND MORPHOLOGY [J].
BODMEIER, R ;
MCGINITY, JW .
JOURNAL OF MICROENCAPSULATION, 1987, 4 (04) :279-288
[4]   Bovine serum albumin release from poly(alpha-hydroxy acid) microspheres: Effects of polymer molecular weight and surface properties [J].
Boury, F ;
Marchais, H ;
Proust, JE ;
Benoit, JP .
JOURNAL OF CONTROLLED RELEASE, 1997, 45 (01) :75-86
[5]   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
[6]   LOCAL CONTROL OF NEURITE DEVELOPMENT BY NERVE GROWTH-FACTOR [J].
CAMPENOT, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (10) :4516-4519
[7]   Delivering neuroactive molecules from biodegradable microspheres for application in central nervous system disorders [J].
Cao, XD ;
Shoichet, MS .
BIOMATERIALS, 1999, 20 (04) :329-339
[8]  
Cleland J L, 1997, Pharm Biotechnol, V10, P1
[9]   SYNTHESIS AND CHARACTERIZATION OF PUTRESCINE-BASED POLY(PHOSPHOESTER-URETHANES) [J].
DAHIYAT, BI ;
HOSTIN, E ;
POSADAS, EM ;
LEONG, KW .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1993, 4 (05) :529-543
[10]   NERVE GROWTH-FACTOR FACILITATES REGENERATION ACROSS NERVE GAPS - MORPHOLOGICAL AND BEHAVIORAL-STUDIES IN RAT SCIATIC-NERVE [J].
DERBY, A ;
ENGLEMAN, VW ;
FRIERDICH, GE ;
NEISES, G ;
RAPP, SR ;
ROUFA, DG .
EXPERIMENTAL NEUROLOGY, 1993, 119 (02) :176-191