首页> 外文期刊>International Journal of Pharmaceutics >Biodegradable drug-eluting pellets provide steady and sustainable cisplatin release in the intrapleural cavity: In vivo and in vitro studies
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Biodegradable drug-eluting pellets provide steady and sustainable cisplatin release in the intrapleural cavity: In vivo and in vitro studies

机译:可生物降解的药物洗脱药丸可在胸膜腔内提供稳定且可持续的顺铂释放:体内和体外研究

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The purpose of this study is to develop biodegradable drug-eluting pellets to provide a sustainable delivery of cisplatin intrapleurally. Poly(D,L)-lactide-co-glycolide (PLGA) (LA: GA= 50: 50) copolymer and cisplatin were mixed, compressed, and sintered to construct biodegradable pellets and placed in phosphate-buffered saline to test the characteristics of in vitro release. In vivo, equal amounts of cisplatin (10 mg/kg) were introduced into rabbit pleural cavities either by free form (Gr1) or pellets form (Gr2). Cisplatin concentrations in the collected pleural effusion and blood were measured and compared by repeated measurement ANOVA. In vitro, approximately 5% of the cisplatin was released in the first day while the rest was gradually released in the following 50 days. In vivo, the cisplatin level in the pleural fluid was equally high during the first 2 days but dropped quickly in Gr1 while remaining high in Gr2 for 18 days, the difference was statistically significant (P < 0.001) In contrast, the plasma cisplatin level was 10 times significantly higher in Gr1 than in Gr2 (P < 0.001), which resulted in two early deaths of rabbits. Thus we concluded that our biodegradable pellets could achieve high and steady cisplatin release in the pleural cavity. This novel drug delivery system may have the potential to serve as an adjuvant treatment for malignant pleural lesion. (C) 2015 Elsevier B.V. All rights reserved.
机译:这项研究的目的是开发可生物降解的药物洗脱药丸,以可持续地在胸膜内递送顺铂。将聚(D,L)-丙交酯-乙交酯(PLGA)(LA:GA = 50:50)共聚物和顺铂进行混合,压缩和烧结,以构建可生物降解的颗粒,然后放入磷酸盐缓冲盐水中以测试其特性体外释放。在体内,通过游离形式(Gr1)或颗粒形式(Gr2)将等量的顺铂(10 mg / kg)引入兔胸膜腔。测量并在收集的胸腔积液和血液中的顺铂浓度,并通过重复测量ANOVA进行比较。在体外,大约5%的顺铂在第一天被释放,其余的则在接下来的50天内逐渐释放。在体内,胸水中的顺铂水平在最初的2天中同样较高,但在Gr1中迅速下降,而在Gr2中则保持18天较高,差异具有统计学意义(P <0.001)。 Gr1的含量比Gr2的含量高10倍(P <0.001),从而导致了两只兔子的早期死亡。因此,我们得出的结论是,我们的可生物降解药丸可以在胸膜腔内实现高而稳定的顺铂释放。这种新颖的药物递送系统可能具有作为恶性胸膜病变的辅助治疗的潜力。 (C)2015 Elsevier B.V.保留所有权利。

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