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Microspheres prepared with biodegradable PHBV and PLA polymers as prolonged-release system for ibuprofen: in vitro drug release and in vivo evaluation

机译:用可生物降解的PHBV和PLA聚合物制备的微球作为布洛芬的延长释放系统:体外药物释放和体内评估

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In this study, poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) and poly(l-lactide) (PLA) microspheres containing ibuprofen were prepared with the aim of prolonging the drug release. The oil-in-water (O/W) emulsion solvent evaporation technique was used, varying the polymer ratio. All formulations provided spherical particles with drug crystals on the surface and a porous and rough polymeric matrix when PHBV was used and smooth external surface when prepared with PLA. The in vitro dissolution profiles show that the formulation containing PHBV/PLA at the proportion of 30/70 presented the best results in terms of prolonging the ibuprofen release. The analysis of the concentration of ibuprofen in the blood of rats showed that maximum levels were achieved at between one and two hours after administration of the immediate-release form (pure drug), while the prolonged microspheres led to a small amount of the drug being released within the first two hours and reached the maximum level after six hours of administration. It was concluded that it is possible to prolong the release of ibuprofen through its incorporation into PHBV/PLA microspheres.
机译:在这项研究中,以延长布洛芬的释放为目的,制备了含布洛芬的聚(羟基丁酸酯-共-羟基戊酸酯)(PHBV)和聚(1-丙交酯)(PLA)微球。使用水包油(O / W)乳液溶剂蒸发技术,改变了聚合物的比例。当使用PHBV时,所有配方均提供在表面具有药物晶体的球形颗粒和多孔且粗糙的聚合物基质,而在用PLA制备时则提供光滑的外表面。体外溶出曲线显示,以延长布洛芬释放的比例,以30/70的比例包含PHBV / PLA的制剂表现出最好的结果。对大鼠血液中布洛芬浓度的分析表明,在施用速释形式(纯药物)后的一到两个小时内达到了最高水平,而延长的微球体导致少量的在最初的两个小时内释放,并在给药六个小时后达到最高水平。结论是,通过将布洛芬掺入PHBV / PLA微球中可以延长布洛芬的释放。

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