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首页> 外文期刊>Journal of Polymers and the Environment >In Vitro and In Vivo Evaluation of Oral Disintegrating Nanofiber and Thin-Film Contains Hyperbranched Chitosan/Donepezil for Active Drug Delivery
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In Vitro and In Vivo Evaluation of Oral Disintegrating Nanofiber and Thin-Film Contains Hyperbranched Chitosan/Donepezil for Active Drug Delivery

机译:体外和体内口腔崩解纳米纤维和薄膜的评估含有超胆囊壳聚糖/多奈哌齐,用于活性药物递送

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摘要

Hyperbranched chitosan (HPCN) has been synthesized from the polycondensation route and transformed into an oral thin film (HCTF) and nanofiber (HCNF) formulation with the addition of donepezil drug. Chitosan blended hyperbranched polyester (HBPE) prepared and formulated as a nanofiber (CNHPN) and thin film (CNHPF). Both carried out to process for the treatment of Alzheimer's disease. Higher thermal stability and porous surface with fiber diameter (110 to 115 nm) observed for hyperbranched nanofiber formulations. Faster disintegration (15 s) of nanofiber (HCNF 2) achieved in vitro drug release about 97.03% of drugs with an interval of 45 min. In vivo animal model studies demonstrated that plasma absorbing maximum concentration (C-max ) as 18.94 ng/mL for CNHPN 2 formulation at the lowest time-bound (3.3 h). The total are under curve [AUC((0-infinity))] of hyperbranched chitosan has faster absorption rate (978.1 ng/mL) than marketed formulation (132.05 ng/mL). These results suggested that chitosan blended/hyperbranched chitosan nanofiber formulation is good alternative with commercial formulations for the treatment of Alzheimer's disease.
机译:已经从缩聚途径合成了超胆囊壳聚糖(HPCN),并通过添加多奈哌齐药物转化成口腔薄膜(HCTF)和纳米纤维(HCNF)制剂。壳聚糖混合超支化聚酯(HBPE)制备并配制为纳米纤维(CNHPN)和薄膜(CNHPF)。两者都进行了治疗阿尔茨海默病的过程。对于超支化纳米纤维制剂,观察到具有纤维直径(110至115nm)的较高的热稳定性和多孔表面。更快的崩解(15秒)纳米纤维(HCNF 2)的体外药物释放约97.03%的药物,间隔45分钟。在体内动物模型研究中,在最低时间结合(3.3h)下,等离子体吸收最大浓度(C-max)为18.94ng / ml的CNHPN 2制剂。超支化壳聚糖的总曲线[AUC((0-无穷大)]具有比市场化制剂更快的吸收率(978.1ng / ml)(132.05ng / ml)。这些结果表明,壳聚糖混合/超支化壳聚糖纳米纤维制剂是具有用于治疗阿尔茨海默病的商业制剂的替代品。

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