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设计和评价口腔贴膜作为经粘膜给奥丹西酮的儿科给药剂型。

Design and evaluation of buccal films as paediatric dosage form for transmucosal delivery of ondansetron.

机构信息

Department of Pharmacy and Biotechnology, University of Bologna, Via San Donato 19/2, 40127 Bologna, Italy.

PolyCrystalLine srl, Via F.S. Fabri 127/1, 40059 Medicina, Bologna, Italy.

出版信息

Eur J Pharm Biopharm. 2016 Aug;105:115-21. doi: 10.1016/j.ejpb.2016.05.026. Epub 2016 Jun 4.

Abstract

In the process of implementation and innovation of paediatric dosage forms, buccal films for transmucosal administration of drug represent one of the most interesting approach. In fact, films are able to provide an extended duration of activity allowing minimal dosage and frequency and offer an exact and flexible dose, associated with ease of handling. The objective of the present study was to develop polymeric films for the sustained release of ondansetron hydrochloride, a selective inhibitor of 5-HT3 receptors indicated in paediatrics for the prevention and treatment of nausea and vomiting caused by cytotoxic chemotherapy or radiotherapy and postoperatively. Films were prepared by casting and drying of aqueous solutions containing different weight ratios of hydroxypropylmethylcellulose (HPMC) with chitosan (CH) or sodium hyaluronate (HA) or gelatin (GEL) and characterized for their physico-chemical and functional properties. The presence of HA, GEL and CH did not improve the mucoadhesive properties of HPMC film. The inclusion of GEL and CH in HPMC film increased in vitro drug release with respect to the inclusion of HA, although films containing HA showed the highest water uptake. Moreover in agreement with the release behaviour, the inclusion of CH and GEL provided higher drug permeation through porcine buccal mucosa with respect to HPMC film and ensured linear permeation profiles of drug.

摘要

在儿科剂型的实施和创新过程中,经粘膜给药的颊膜是最有趣的方法之一。事实上,薄膜能够提供延长的作用持续时间,允许最小剂量和频率,并提供精确和灵活的剂量,与易于处理相关联。本研究的目的是开发盐酸昂丹司琼的聚合物薄膜,盐酸昂丹司琼是一种 5-HT3 受体的选择性抑制剂,适用于儿科,用于预防和治疗细胞毒性化疗或放疗引起的恶心和呕吐以及术后。通过浇注和干燥含有不同重量比羟丙基甲基纤维素(HPMC)与壳聚糖(CH)或透明质酸钠(HA)或明胶(GEL)的水溶液来制备薄膜,并对其物理化学和功能性质进行了表征。HA、GEL 和 CH 的存在并没有改善 HPMC 薄膜的粘膜粘附性能。与 HA 相比,GEL 和 CH 包含在 HPMC 薄膜中增加了体外药物释放,尽管含有 HA 的薄膜显示出最高的吸水率。此外,与释放行为一致,CH 和 GEL 的包含提供了通过猪颊粘膜的更高药物渗透,与 HPMC 薄膜相比,并确保药物的线性渗透曲线。

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