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Characterization of anti-cancer drug materials loaded poly (3-hydroxybutyrate-co-3-hydroxyhexanoate) microspheres for drug delivery system in biochemical material system

机译:抗癌药物的表征负载聚(3-羟基丁酸酯-CO-3-羟基己酸酯)微球,用于生化材料体系中的药物递送系统

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Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) is one of the components of polyhydroxyalkanoates (PHAs) and some of its mechanical properties have been shown to improve over poly (3-hydroxybutyrate) (PHB) and poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV). The investigation of PHBHHx microspheres as a drug delivery system was prepared by emulsion-solvent evaporation method for the sustained release of anti-cancer drug 5-fluorouracil (5-FU) and cyclosporin A (CsA). The mean diameter of the PHBHHx microspheres ranged from 5.24 to 22.10μm dependent on the different processing parameters. The PHBHHx concentration, emulsifier concentration, anti-cancer drug dosage, and agitation speed, were optimized according to the encapsulation efficiency of 4% PHBHHx, 0.5% SDS, 10 mg anti-cancer drug, and 500 rpm. Under optimized conditions, the encapsulation efficiency of 5-FU and CsA microspheres were 7.19% and 96.44%, respectively. The morphologies of scanning electron microscope (SEM) suggested that PHBHHx microspheres were relatively smooth that provided better dispersion compared to PHB microspheres. The in vitro release profiles indicated 32.42% of 5-FU and 30.61% of CsA were released from PHBHHx microspheres during the initial burst phase, and the drug release from PHBHHx microsphere could be detected even after one month. The characteristics of PHBHHx microspheres demonstrated the feasibility of PHBHHx microsphere as a novel matrix for drug release system. With positive maintenance of the therapeutic concentrations of the drug, side effects can be reduced and patient compliance can be improved.
机译:聚(3-羟基丁酸酯-CO-3-羟基己酸酯)(PHBHHHX)是多羟基烷烷(PHA)的组分之一,并且已经显示出一些机械性能改善聚(3-羟基丁酸盐)(PHB)和聚(3 - 羟基丁酸酯-CO-3-羟基戊戊酸盐)(PHBV)。通过乳液 - 溶剂蒸发方法制备对药物递送系统的PHBHHX微球的研究,用于持续释放抗癌药物5-氟尿嘧啶(5-FU)和环孢菌素A(CSA)。 PHBHHX微球的平均直径范围为5.24至22.10μm,依赖于不同的加工参数。根据4%PHBHHHX,0.5%SDS,10mg抗癌药和500rpm的包封效率优化PHBHHX浓度,乳化剂浓度,抗癌药物剂量和搅拌速度。在优化条件下,5-FU和CSA微球的包封效率分别为7.19%和96.44%。扫描电子显微镜(SEM)的形态表明PHBHHX微球相对平滑,与PHB微球相比,提供更好的分散体。在初始爆破阶段,体外释放曲线的32.42%的5-FU和30.61%的CSA释放来自PHBHHX微球,即使在一个月后,也可以检测来自PHBHHX微球的药物释放。 PHBHHX微球的特征表明PHBHHX微球作为药物释放系统的新基质的可行性。通过阳性维持药物的治疗浓度,可以减少副作用,并且可以提高患者的顺应性。

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