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阿苯达唑和甲苯咪唑新型口服制剂的制备、理化性质表征以及对旋毛虫的体内外活性。

Preparation, Physicochemical Characterization and In Vitro and In Vivo Activity Against Heligmosomoides polygyrus of Novel Oral Formulations of Albendazole and Mebendazole.

机构信息

Swiss Tropical and Public Health Institute, Socinstrasse 57, P.O. Box CH-4002, Basel, Switzerland; University of Basel, Petersplatz 1, P.O. Box CH-4001, Basel, Switzerland.

IQUIR-CONICET, Suipacha 570, S2002LRK, Rosario, Argentina.

出版信息

J Pharm Sci. 2020 May;109(5):1819-1826. doi: 10.1016/j.xphs.2020.02.002. Epub 2020 Feb 15.

DOI:10.1016/j.xphs.2020.02.002
PMID:32070702
Abstract

Albendazole (ABZ) and mebendazole (MBZ) are the 2 most commonly used drugs in the treatment of soil-transmitted helminth infections in humans, but their performance is hampered by low solubility and physicochemical properties. We developed different formulations (β-cyclodextrin inclusion complexes, chitosan-based microcrystals (CH), and polyvinyl alcohol and polysorbate 80-based nanoparticles [P80]) of ABZ and MBZ with an improved in vitro solubility profile and tested their activities in vitro and in vivo against the hookworm Heligmosomoides polygyrus. We found that all formulations tested showed a faster and higher dissolution level and were more active than the standard drugs. When compared to ABZ, ABZ-P80 revealed the highest improvement in terms of solubility increase (4-fold increase) and in vivo activity (an ED of 7.0 mg/kg for ABZ and of 4.1 mg/kg for ABZ-P80). Although the activity of MBZ was in all cases lower than ABZ, the improved formulations of MBZ performed better than standard MBZ, where MBZ-CH showed a significantly higher in vivo activity (ED of 8.02 mg/kg vs. an ED of 203 mg/kg for MBZ). In this work, we identified MBZ-CH and ABZ-P80 formulations as lead formulations hence further studies should be conducted.

摘要

阿苯达唑(ABZ)和甲苯达唑(MBZ)是治疗人体土壤传播性蠕虫感染最常用的两种药物,但由于溶解度低和物理化学性质差,其疗效受到限制。我们开发了 ABZ 和 MBZ 的不同制剂(β-环糊精包合物、壳聚糖基微晶(CH)和聚乙烯醇和聚山梨醇 80 基纳米粒[P80]),具有改善的体外溶解度特征,并在体外和体内测试了它们对钩虫 Heligmosomoides polygyrus 的活性。我们发现,所有测试的制剂都表现出更快和更高的溶解水平,并且比标准药物更有效。与 ABZ 相比,ABZ-P80 在溶解度增加(增加 4 倍)和体内活性方面表现出最高的改善(ABZ 的 ED 为 7.0 mg/kg,ABZ-P80 的 ED 为 4.1 mg/kg)。虽然 MBZ 的活性在所有情况下均低于 ABZ,但 MBZ 的改良制剂的性能优于标准 MBZ,其中 MBZ-CH 显示出更高的体内活性(ED 为 8.02 mg/kg,而 MBZ 的 ED 为 203 mg/kg)。在这项工作中,我们确定了 MBZ-CH 和 ABZ-P80 制剂作为先导制剂,因此应进一步开展研究。

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