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重新审视氯硝柳胺制剂方法——药物再定位的途径。

Revisiting Niclosamide Formulation Approaches - a Pathway Toward Drug Repositioning.

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, 10 000, Croatia.

Department of Pharmaceutical Technology, Institute of Pharmacy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, 6020, Austria.

出版信息

Drug Des Devel Ther. 2024 Sep 17;18:4153-4182. doi: 10.2147/DDDT.S473178. eCollection 2024.

Abstract

Niclosamide (NIC), an anthelmintic drug, has garnered recent attention for its potential as an antiviral, antibacterial, and chemotherapeutic agent, among other applications. Repurposing NIC presents a current trend, offering significant time and cost savings compared to developing entirely new therapeutic chemical entities. However, its drawback lies in poor solubility, resulting in notably low oral bioavailability. This review consolidates efforts to overcome this limitation by summarizing twelve categories of formulations, spanning derivatives, amorphous solid dispersions, co-crystals, nanocrystals, micelles, nanohybrids, lipid nanoparticles and emulsions, cyclodextrins, polymeric nanoparticles, dry powders for inhalation, 3D printlets, and nanofibers. These formulations cover oral, injectable, inhalable and potentially (trans)dermal routes of administration. Additionally, we present a comprehensive overview of NIC characteristics, including physico-chemical properties, metabolism, safety, and pharmacokinetics. Moreover, we identify gaps in formulation and administration pathways that warrant further investigation to address NIC poor bioavailability.

摘要

尼氯硝唑(NIC)是一种驱虫药,最近因其在抗病毒、抗菌和化疗等方面的潜力而备受关注。尼氯硝唑的重新定位是当前的一个趋势,与开发全新的治疗性化学实体相比,可显著节省时间和成本。然而,它的缺点是溶解度差,导致口服生物利用度明显较低。本综述通过总结十二类制剂来克服这一限制,这些制剂涵盖了衍生物、无定形固体分散体、共晶、纳米晶体、胶束、纳米杂化、脂质纳米粒和乳液、环糊精、聚合物纳米粒、吸入干粉、3D 打印小丸和纳米纤维。这些制剂涵盖了口服、注射、吸入和潜在(经)皮途径的给药方式。此外,我们还全面介绍了 NIC 的特性,包括物理化学性质、代谢、安全性和药代动力学。此外,我们确定了制剂和给药途径方面的差距,这些差距需要进一步研究来解决 NIC 生物利用度差的问题。

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