Preparation and characterization of melittin-loaded poly (DL-lactic acid) or poly (DL-lactic-co-glycolic acid) microspheres made by the double emulsion method

被引:147
作者
Cui, F [1 ]
Cun, DM [1 ]
Tao, AJ [1 ]
Yang, MS [1 ]
Shi, K [1 ]
Zhao, M [1 ]
Guan, Y [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Shenyang 110016, Peoples R China
关键词
biodegradable microspheres; melittin; W-1/O/W-2 emulsion-solvent evaporation technique;
D O I
10.1016/j.jconrel.2005.07.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The water soluble peptide, melittin, isolated from bee venom and composed of twenty-six amino acids, was encapsulated in poly (DL-lactic acid, PLA) and poly (DL-lactic-co-glycolic acid, PLGA) microspheres prepared by a multiple emulsion [(W-1/O)W-2] solvent evaporation method. The aim of this work was to develop a controlled release injection that would deliver the melittin over a period of about one month. The influence of various preparation parameters, such as the type of polymer, its concentration, stabilizer PVA concentration, volume of internal water phase and level of drug loading on the characteristics of the microspheres and drug release was investigated. It was found that the microspheres of about 5 mu m in size can be produced in high encapsulation (up to 90%), and the melittin content in the microspheres was up to 10% (w/w). The drug release profiles in vitro exhibited a significant burst release, followed by a lag phase of little or no release and then a phase of constant melittin release. The type of polymer used was a critical factor in controlling the release of melittin from the microspheres. In this study, the rate of peptide release from the microspheres correlated well with the rate of polymer degradation. Moreover, melittin was released completely during the study period of 30 days, which agreed well with the polymer degradation rate. (c) 2005 Published by Elsevier B.V.
引用
收藏
页码:310 / 319
页数:10
相关论文
共 21 条
[1]  
ANGELIKA N, 2001, J AM CHEM SOC, V123, P7407
[2]   CONFORMATION AND AGGREGATION OF MELITTIN - DEPENDENCE ON PH AND CONCENTRATION [J].
BELLO, J ;
BELLO, HR ;
GRANADOS, E .
BIOCHEMISTRY, 1982, 21 (03) :461-465
[3]   Recombinant human growth hormone poly(lactic-co-glycolic acid) microsphere formulation development [J].
Cleland, JL ;
Johnson, OL ;
Putney, S ;
Jones, AJS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :71-84
[4]   PREPARATION OF POROUS AND NONPOROUS BIODEGRADABLE POLYMERIC HOLLOW MICROSPHERES [J].
CROTTS, G ;
PARK, TG .
JOURNAL OF CONTROLLED RELEASE, 1995, 35 (2-3) :91-105
[5]   Controlled release of anti-cocaine catalytic antibody from biodegradable polymer microspheres [J].
Homayoun, P ;
Mandal, T ;
Landry, D ;
Komiskey, H .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (07) :933-938
[6]   THE PREPARATION AND CHARACTERIZATION OF POLY(LACTIDE-CO-GLYCOLIDE) MICROPARTICLES .2. THE ENTRAPMENT OF A MODEL PROTEIN USING A (WATER-IN-OIL)-IN-WATER EMULSION SOLVENT EVAPORATION TECHNIQUE [J].
JEFFERY, H ;
DAVIS, SS ;
OHAGAN, DT .
PHARMACEUTICAL RESEARCH, 1993, 10 (03) :362-368
[7]  
JUTEL M, 1995, J IMMUNOL, V154, P4187
[8]   Stability and release characteristics of poly(D,L-lactide-co-glycolide) encapsulated CaPi-DNA coprecipitation [J].
Li, YP ;
Ogris, M ;
Pelisek, J ;
Röedl, W .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 269 (01) :61-70
[9]  
OGAWA Y, 1988, CHEM PHARM BULL, V36, P1095
[10]   THE PREPARATION AND CHARACTERIZATION OF POLY(LACTIDE-CO-GLYCOLIDE) MICROPARTICLES .3. MICROPARTICLE/POLYMER DEGRADATION RATES AND THE IN-VITRO RELEASE OF A MODEL PROTEIN [J].
OHAGAN, DT ;
JEFFERY, H ;
DAVIS, SS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 103 (01) :37-45