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盐酸多非利特及其环糊精包合物的肝毒性、光毒性和光敏性的比较评价。

Comparative evaluation of the hepatotoxicity, phototoxicity and photosensitizing potential of dronedarone hydrochloride and its cyclodextrin-based inclusion complexes.

机构信息

Postgraduate Program in Pharmaceutical Sciences, Universidade Federal de Santa Maria, Av. Roraima 1000, 97105-900, Santa Maria, RS, Brazil.

出版信息

Photochem Photobiol Sci. 2019 Jun 12;18(6):1565-1575. doi: 10.1039/c8pp00559a.

DOI:10.1039/c8pp00559a
PMID:31037283
Abstract

In this study, the hepatotoxicity, phototoxicity and photosensitizing potential of free dronedarone (DRO) and its inclusion complexes with β-cyclodextrin (β-CD) and 2-hydroxypropyl-β-cyclodextrin (HP-β-CD), prepared by different methods, were investigated by using in vitro cell-based approaches. The results of the 3T3 NRU phototoxicity assay showed that free DRO and the CD-based inclusion complexes did not present any substantial phototoxic potential. The photosensitizing potential was assessed by using THP-1 cells and IL-8 as a biomarker, and the experimental data confirmed that both the free drug and the inclusion complexes are likely to cause skin photosensitization, as they were able to induce IL-8 release after irradiation. Nevertheless, the inclusion complexes obtained by kneading followed by spray-drying induced a lower IL-8 release and also presented a smaller stimulation index in comparison with free DRO, suggesting a reduction in the photosensitizing potential. Finally, the free drug and inclusion complexes were also tested for hepatotoxicity using HepG2 cells. Even though lower IC50 values were found for the inclusion complexes prepared by kneading followed by spray-drying, there was no significant difference, indicating that the complexation of dronedarone did not induce hepatotoxicity. Overall, the obtained data confirmed that the inclusion complexes prepared by kneading followed by spray-drying, especially those based on HP-β-CD, appeared to be the most promising formulations and, therefore, could be encouragingly explored in the development of novel pharmaceutical dosage forms containing DRO, presumably with reduced side effects and improved safety profile.

摘要

在这项研究中,通过体外基于细胞的方法研究了游离决奈达隆(DRO)及其与β-环糊精(β-CD)和 2-羟丙基-β-环糊精(HP-β-CD)的包合物的肝毒性、光毒性和光敏化潜力,这些包合物是通过不同的方法制备的。3T3 NRU 光毒性测定的结果表明,游离 DRO 和基于 CD 的包合物复合物没有表现出任何实质性的光毒性潜力。通过 THP-1 细胞和白细胞介素-8(IL-8)作为生物标志物评估光敏化潜力,实验数据证实,游离药物和包合物复合物都可能引起皮肤光敏化,因为它们在照射后能够诱导 IL-8 释放。然而,通过捏合随后喷雾干燥获得的包合物诱导的 IL-8 释放较低,并且与游离 DRO 相比具有较小的刺激指数,表明光敏化潜力降低。最后,还使用 HepG2 细胞测试了游离药物和包合物复合物的肝毒性。尽管通过捏合随后喷雾干燥制备的包合物的 IC50 值较低,但没有显著差异,表明决奈达隆的络合没有引起肝毒性。总体而言,获得的数据证实,通过捏合随后喷雾干燥制备的包合物,特别是基于 HP-β-CD 的包合物,似乎是最有前途的制剂,因此可以在含有 DRO 的新型药物剂型的开发中令人鼓舞地探索,可能具有降低的副作用和改善的安全性。

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