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    谭红香, 叶建东, 柯渔. 以PHBV-PLGA为载体的硫酸庆大霉素缓释微球[J]. 功能高分子学报, 2009, 22(1): 12-16.
    引用本文: 谭红香, 叶建东, 柯渔. 以PHBV-PLGA为载体的硫酸庆大霉素缓释微球[J]. 功能高分子学报, 2009, 22(1): 12-16.
    Poly(Hydroxybutyrate-Hydroxyvalerate)-Poly(Lactide-co-Glycolide) SustainedRelease Microspheres Entrapping Gentamicin Sulfate[J]. Journal of Functional Polymers, 2009, 22(1): 12-16.
    Citation: Poly(Hydroxybutyrate-Hydroxyvalerate)-Poly(Lactide-co-Glycolide) SustainedRelease Microspheres Entrapping Gentamicin Sulfate[J]. Journal of Functional Polymers, 2009, 22(1): 12-16.

    以PHBV-PLGA为载体的硫酸庆大霉素缓释微球

    Poly(Hydroxybutyrate-Hydroxyvalerate)-Poly(Lactide-co-Glycolide) SustainedRelease Microspheres Entrapping Gentamicin Sulfate

    • 摘要: 以生物可降解聚羟基丁酸酯和羟基戊酸酯的共聚物(PHBV)、乙交酯和丙交酯的无规共聚物(PLGA)两种高分子作为壁材,采用复乳溶剂挥发法,制备了包裹硫酸庆大霉素(GS)的载药微球。在扫描电镜下观察到所得微球表面呈多孔状,为球形或椭圆形,粒径在20~80 μm。分析结果表明,包封率在60%以上,在体外16~20 d内药物全部释放,90 d微球体外降解50%左右。

       

      Abstract: Biodegradable poly(hydroxybutyrate-hydroxyvalerate)-poly(lactide-co-glycolide) (PHBV-PLGA) microspheres with gentamicin-loading were prepared and characterized by solid-oil-oil-water method. The diameter of the microspheres with spherical or ellipsoidal shape ranges in 20-80 μm and the encapsulation efficiency of gentamicin sulfate is more than 60%. The cumulative rate of drug-release reaches 100% in 16-20 d. In addition, the degradation properties are investigated. The cumulative drug release is about 50% in 90 d in phosphate buffer solution.

       

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