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Thiolated chitosan nanoparticles for enhancing oral absorption of docetaxel: preparation in vitro and ex vivo evaluation

机译:硫醇化壳聚糖纳米颗粒可增强多西紫杉醇的口服吸收:制备体外和离体评估

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摘要

The aim of this study was to prepare and evaluate mucoadhesive core-shell nanoparticles based on copolymerization of thiolated chitosan coated on poly methyl methacrylate cores as a carrier for oral delivery of docetaxel. Docetaxel-loaded nanoparticles with various concentrations were prepared via a radical emulsion polymerization method using cerium ammonium nitrate as an initiator. The physicochemical properties of the obtained nanoparticles were characterized by: dynamic light-scattering analysis for their mean size, size distribution, and zeta potential; scanning electron microscopy and transmission electron microscopy for surface morphology; and differential scanning calorimetry analysis for confirmation of molecular dispersity of docetaxel in the nanoparticles. Nanoparticles were spherical with mean diameter below 200 nm, polydispersity of below 0.15, and positive zeta potential values. The entrapment efficiency of the nanoparticles was approximately 90%. In vitro release studies showed a sustained release characteristic for 10 days after a burst release at the beginning. Ex vivo studies showed a significant increase in the transportation of docetaxel from intestinal membrane of rat when formulated as nanoparticles. Cellular uptake of nanoparticles was investigated using fluoresceinamine-loaded nanoparticles. Docetaxel nanoparticles showed a high cytotoxicity effect in the Caco-2 and MCF-7 cell lines after 72 hours. It can be concluded that by combining the advantages of both thiolated polymers and colloidal particles, these nanoparticles can be proposed as a drug carrier system for mucosal delivery of hydrophobic drugs.
机译:这项研究的目的是基于涂覆在聚甲基丙烯酸甲酯核芯上的巯基化壳聚糖的共聚作用,以制备和评估粘膜粘附性核壳纳米颗粒,该载体作为多西紫杉醇的口服载体。通过自由基乳液聚合法,使用硝酸铈铵作为引发剂,制备了具有各种浓度的多西他赛的纳米颗粒。获得的纳米颗粒的理化特性的特征在于:动态光散射分析其平均尺寸,尺寸分布和ζ电势;扫描电子显微镜和透射电子显微镜的表面形态;和差示扫描量热法分析证实多西他赛在纳米颗粒中的分子分散性。纳米颗粒是球形的,平均直径低于200 nm,多分散度低于0.15,且ζ电势值为正。纳米颗粒的包封率约为90%。体外释放研究显示,在爆发性释放开始后的10天内具有持续释放特性。体外研究表明,当制成纳米颗粒时,多西紫杉醇从大鼠肠膜的转运明显增加。使用装载荧光素胺的纳米颗粒研究了纳米颗粒的细胞摄取。 72小时后,多西他赛纳米颗粒在Caco-2和MCF-7细胞系中显示出高细胞毒性作用。可以得出结论,通过结合硫醇化聚合物和胶体颗粒的优点,这些纳米颗粒可以作为疏水性药物的粘膜递送的药物载体系统。

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