Microparticles of novel branched copolymers of lactic acid and amino acids: Preparation and characterization

被引:32
作者
Caponetti, G
Hrkach, JS
Kriwet, B
Poh, M
Lotan, N
Colombo, P
Langer, R
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Univ Parma, Dipartimento Farmaceut, I-43100 Parma, Italy
[3] Technion Israel Inst Technol, Dept Biomed Engn, IL-32000 Haifa, Israel
关键词
D O I
10.1021/js970457f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The preparation and characterization of microparticles produced from a new class of functionalized, biodegradable, comblike graft copolymers is presented. The copolymers are polyester-polyamino acid hybrids, composed of a poly(L-lactic acid-co-L-lysine) (PLAL) backbone, and poly(L-lysine), poly(D,L-alanine) or poly(L-aspartic acid) side chains extending from the lysine residues of PLAL. The microparticles have been characterized with regard to their surface properties, morphology, and size. Thus, electron spectroscopy for chemical analysis data and results of Zeta potential measurements suggest that the polyamino acid side chains tend to concentrate at the surface of the particles. Also, analyses by environmental scanning electron microscopy and confocal scanning laser microscopy indicate that particles carrying poly(lysine) chains have an unusual porous structure, most probably due to the combined effects of the amphiphilic, polyelectrolyte, and chemical nature of the composing copolymer, as well as of the particular preparation technique employed. The capabilities of the microparticles to serve as carriers in controlled drug release and delivery devices were demonstrated by encapsulation and release of rhodamine B, a low molecular weight drug model.
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收藏
页码:136 / 141
页数:6
相关论文
共 26 条
[1]   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
[2]   SYNTHESIS AND RGD PEPTIDE MODIFICATION OF A NEW BIODEGRADABLE COPOLYMER - POLY(LACTIC ACID-CO-LYSINE) [J].
BARRERA, DA ;
ZYLSTRA, E ;
LANSBURY, PT ;
LANGER, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (23) :11010-11011
[3]   RECENT ADVANCES ON THE USE OF BIODEGRADABLE MICROPARTICLES AND NANOPARTICLES IN CONTROLLED DRUG-DELIVERY [J].
BRANNONPEPPAS, L .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 116 (01) :1-9
[4]  
CAPONETTI G, UNPUB
[5]  
Chasin M., 1990, Biodegradable polymers as drug delivery systems, V45
[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]   NANOPARTICLES AND MICROPARTICLES FOR THE DELIVERY OF POLYPEPTIDES AND PROTEINS [J].
COUVREUR, P ;
PUISIEUX, F .
ADVANCED DRUG DELIVERY REVIEWS, 1993, 10 (2-3) :141-162
[8]  
COUVREUR P, 1995, EUR J PHARM BIOPHARM, V41, P2
[9]   MICROSPHERES FOR TARGETING DRUGS TO SPECIFIC BODY SITES [J].
DAVIS, SS ;
ILLUM, L ;
MOGHIMI, SM ;
DAVIES, MC ;
PORTER, CJH ;
MUIR, IS ;
BRINDLEY, A ;
CHRISTY, NM ;
NORMAN, ME ;
WILLIAMS, P ;
DUNN, SE .
JOURNAL OF CONTROLLED RELEASE, 1993, 24 (1-3) :157-163
[10]   Large porous particles for pulmonary drug delivery [J].
Edwards, DA ;
Hanes, J ;
Caponetti, G ;
Hrkach, J ;
BenJebria, A ;
Eskew, ML ;
Mintzes, J ;
Deaver, D ;
Lotan, N ;
Langer, R .
SCIENCE, 1997, 276 (5320) :1868-1871