Optimization of preparative conditions for poly-DL-lactide-polyethylene glycol microspheres with entrapped Vibrio Cholera antigens

被引:88
作者
Deng, XM [1 ]
Li, XH
Yuan, ML
Xiong, CD
Huang, ZT
Jia, WX
Zhang, YH
机构
[1] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing 100080, Peoples R China
[3] W China Univ Med Sci, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
poly-dl-lactide-polyethylene glycol; Vibrio Cholera antigen; microsphere; loading efficiency; release profile;
D O I
10.1016/S0168-3659(98)00147-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly-dl-lactide-polyethylene glycol (PELA) with different contents of polyethylene glycol(PEG) were synthesized and the PEG content was estimated according to the integral height of hydrogen shown in H-1-NMR. PELA microspheres containing V. cholera antigen, outer membrane protein (OMP) were prepared by a water-in-oil-in-water (W/O/W) based on solvent evaporation procedure. Antigen microspheres with smooth surface, suitable size for oral administration (0.5-5 mu m), high loading efficiency (about 60%) and low level of residual solvent (lower than 20ppm) were obtained. Microspheres prepared from PELA with PEG content of about 10% achieved the highest loading efficiency among PELA copolymers and poly-dl-lactide (PLA) homopolymer, which suggested that microspheres size, morphology and the precipitation rate of polymer showed considerable relations with OMP loading efficiency. The regulation of the solvent components of the oil phase contributes to a stable emulsion W/O, and it is concluded that the stable emulsion W/O plays a significant role in improving the protein loading efficiency of obtained microspheres. The addition of stabilizer, such as gelatin and polyvinyl alcohol, into the internal water phase before emulsification produced no significant difference in OMP entrapment and microspheres size. A higher OMP loading efficiency was achieved by adding NaCl or adjusting the pH at the iso-electric point of OMP in the external water phase. It was indicated in vitro that PELA microspheres with smaller size showed larger extent of initial release and higher release rate, whereas microspheres with the diameter of 2.17 mu m showed no apparent burst effect. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 131
页数:9
相关论文
共 21 条
  • [1] DETERMINANTS OF RELEASE RATE OF TETANUS VACCINE FROM POLYESTER MICROSPHERES
    ALONSO, MJ
    COHEN, S
    PARK, TG
    GUPTA, RK
    SIBER, GR
    LANGER, R
    [J]. PHARMACEUTICAL RESEARCH, 1993, 10 (07) : 945 - 953
  • [2] Influence of the preparation method on residual solvents in biodegradable microspheres
    Bitz, C
    Doelker, E
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 131 (02) : 171 - 181
  • [3] CHALLACOMBE SJ, 1992, IMMUNOLOGY, V76, P164
  • [4] CONTROLLED DELIVERY SYSTEMS FOR PROTEINS BASED ON POLY(LACTIC GLYCOLIC ACID) MICROSPHERES
    COHEN, S
    YOSHIOKA, T
    LUCARELLI, M
    HWANG, LH
    LANGER, R
    [J]. PHARMACEUTICAL RESEARCH, 1991, 8 (06) : 713 - 720
  • [5] SYNTHESIS AND CHARACTERIZATION OF BLOCK COPOLYMERS FROM D,L-LACTIDE AND POLY(ETHYLENE GLYCOL) WITH STANNOUS CHLORIDE
    DENG, XM
    XIONG, CD
    CHENG, LM
    XU, RP
    [J]. JOURNAL OF POLYMER SCIENCE PART C-POLYMER LETTERS, 1990, 28 (13) : 411 - 416
  • [6] CONTROLLED VACCINE RELEASE IN THE GUT-ASSOCIATED LYMPHOID-TISSUES .1. ORALLY-ADMINISTERED BIODEGRADABLE MICROSPHERES TARGET THE PEYERS PATCHES
    ELDRIDGE, JH
    HAMMOND, CJ
    MEULBROEK, JA
    STAAS, JK
    GILLEY, RM
    TICE, TR
    [J]. JOURNAL OF CONTROLLED RELEASE, 1990, 11 (1-3) : 205 - 214
  • [7] BIODEGRADABLE MICROSPHERES AS A VACCINE DELIVERY SYSTEM
    ELDRIDGE, JH
    STAAS, JK
    MEULBROEK, JA
    MCGHEE, JR
    TICE, TR
    GILLEY, RM
    [J]. MOLECULAR IMMUNOLOGY, 1991, 28 (03) : 287 - 294
  • [8] PARAMETERS AFFECTING THE IMMUNOGENICITY OF MICROENCAPSULATED TETANUS TOXOID
    ESPARZA, I
    KISSEL, T
    [J]. VACCINE, 1992, 10 (10) : 714 - 720
  • [9] THE FORMULATION AND STABILITY OF MULTIPLE EMULSIONS
    FLORENCE, AT
    WHITEHILL, D
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1982, 11 (04) : 277 - 308
  • [10] 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
    JEFFERY, H
    DAVIS, SS
    OHAGAN, DT
    [J]. PHARMACEUTICAL RESEARCH, 1993, 10 (03) : 362 - 368