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The Preparation and Evaluation of Water-Soluble SKLB610 Nanosuspensions with Improved Bioavailability

机译:具有更高生物利用度的水溶性SKLB610纳米悬浮液的制备和评价

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摘要

The aim of the study was to investigate the potential of nanosuspension to enhance the bioavailability of SKLB610 (Biopharmaceutical Classification System class II drug), a bioactive anticancer compound synthesized in our labs. SKLB610 nanosuspensions were prepared using wet media milling. Physicochemical characteristics of the nanosuspensions were evaluated, including particle size and distribution, dissolution, transmission electron microscopy, atomic force microscopy, thermogravimetric analysis, and X-ray powder diffractometry. The dissolution rate of SKLB610 was greatly improved in nanosuspensions, compared to crude SKLB610. Pharmacokinetic studies in rats demonstrated that the oral bioavailability of SKLB610 in nanosuspension (89.4%) was 2.6-fold higher than in coarse suspension (34.1%). Stabilizer type, milling time, and milling speed had a significant effect on particle size of the SKLB610 nanosuspensions. Nanosuspensions effectively improved the dissolution rate and bioavailability of the water-insoluble drug SKLB610 by reducing the compound particle size to the nanoscale and employing a proper formulation.
机译:该研究的目的是研究纳米悬浮液增强我们实验室合成的生物活性抗癌化合物SKLB610(生物药物分类系统II类药物)的生物利用度的潜力。使用湿介质研磨制备SKLB610纳米悬浮液。评价了纳米悬浮液的理化特性,包括粒径和分布,溶解度,透射电子显微镜,原子力显微镜,热重分析和X射线粉末衍射法。与粗制SKLB610相比,纳米悬浮液中SKLB610的溶解速度大大提高。在大鼠中进行的药代动力学研究表明,纳米悬浮液(89.4%)中SKLB610的口服生物利用度比粗悬浮液(34.1%)高2.6倍。稳定剂的类型,研磨时间和研磨速度对SKLB610纳米悬浮液的粒径有重要影响。纳米悬浮液通过将化合物的粒径减小至纳米级并采用适当的配方,有效地提高了水不溶性药物SKLB610的溶出度和生物利用度。

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