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首页> 外文期刊>Frontiers in Pharmacology >Preparation, Evaluation and Bioavailability Studies of Eudragit Coated PLGA Nanoparticles for Sustained Release of Eluxadoline for the Treatment of Irritable Bowel Syndrome
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Preparation, Evaluation and Bioavailability Studies of Eudragit Coated PLGA Nanoparticles for Sustained Release of Eluxadoline for the Treatment of Irritable Bowel Syndrome

机译:Eudragit包衣的PLGA纳米粒子的制备,评价和生物利用度,用于Eluxadoline的持续释放,用于治疗肠易激综合征。

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Eluxadoline is a newly approved orally administered drug used for the treatment of Irritable Bowel Syndrome with Diarrhea. It is reported as a poorly water-soluble drug due to which its dissolution rate and oral bioavailability are very poor. In this work, various plain PLGA nanoparticles (NPs) (F1–F4) were prepared and optimized based on particle size, PDI, zeta potential and percent drug entrapment efficiency (EE). The developed plain NPs (F1–F4) showed average particle size ranging from 260.19 to 279.76 nm with smooth surface and EE of 17.83–56.29%. The optimized plain NPs (F3) had particle size of 273.76 ± 7.25 nm with a low PDI value 0.327, zeta potential - 30.63 ± 2.47 mV and % EE of 56.29 ± 2.56%. The optimized F3 NPs was further submitted for enteric coating using Eudragit S100 polymer and evaluated in terms of particles characterization, in vitro release and pharmacokinetic studies in rats. The bioavailability of plain and coated nanaoparticles were enhanced by 6.8- and 18.5-fold, respectively, compared to normal suspension. These results revealed that the developed coated NPs could be used for its oral delivery for an effective treatment of Irritable Bowel Syndrome with Diarrhea.
机译:Eluxadoline是一种新批准的口服药物,用于治疗腹泻型肠易激综合症。据报道它是水溶性差的药物,由于其溶解速度和口服生物利用度非常差。在这项工作中,制备了各种普通的PLGA纳米颗粒(NP)(F1-F4),并根据粒径,PDI,ζ电位和药物截留效率(EE)进行了优化。发达的普通纳米颗粒(F1-F4)的平均粒径范围为260.19至279.76 nm,表面光滑,EE为17.83-56.29%。优化的普通NP(F3)的粒径为273.76±7.25 nm,PDI值低,为0.327,ζ电势为30.63±2.47 mV,%EE为56.29±2.56%。将优化的F3 NPs进一步使用Eudragit S100聚合物进行肠溶衣,并根据大鼠的颗粒表征,体外释放和药代动力学研究进行评估。与正常悬浮液相比,普通纳米颗粒和包覆纳米颗粒的生物利用度分别提高了6.8倍和18.5倍。这些结果表明,开发的包被的NP可用于其口服递送,以有效治疗腹泻型肠易激综合症。

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