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大麻二酚及其环糊精包合物对肿瘤细胞系的生物物理研究和体外效应

Biophysical Studies and In Vitro Effects of Tumor Cell Lines of Cannabidiol and Its Cyclodextrin Inclusion Complexes.

作者信息

Hatziagapiou Kyriaki, Bethanis Kostas, Koniari Eleni, Christoforides Elias, Nikola Olti, Andreou Athena, Mantzou Aimilia, Chrousos George P, Kanaka-Gantenbein Christina, Lambrou George I

机构信息

Choremeio Research Laboratory, First Department of Pediatrics, National and Kapodistrian University of Athens, Thivon & Levadeias 8, 11527 Athens, Greece.

Division of Endocrinology, First Department of Pediatrics, Metabolism, and Diabetes, National and Kapodistrian University of Athens, Thivon & Levadeias 8, 11527 Athens, Greece.

出版信息

Pharmaceutics. 2022 Mar 26;14(4):706. doi: 10.3390/pharmaceutics14040706.

Abstract

Phytocannabinoids possess anticancer properties, as established in vitro and in vivo. However, they are characterized by high lipophilicity. To improve the properties of cannabidiol (CBD), such as solubility, stability, and bioavailability, CBD inclusion complexes with cyclodextrins (CDs) might be employed, offering targeted, faster, and prolonged CBD release. The aim of the present study is to investigate the in vitro effects of CBD and its inclusion complexes in randomly methylated -CD (RM--CD) and 2-hyroxypropyl--CD (HP--CD). The enhanced solubility of CBD upon complexation with CDs was examined by phase solubility study, and the structure of the inclusion complexes of CBD in 2,6-di-O-methyl--CD (DM--CD) and 2,3,6-tri-O-methyl--CD (TM--CD) was determined by X-ray crystallography. The structural investigation was complemented by molecular dynamics simulations. The cytotoxicity of CBD and its complexes with RM--CD and HP--CD was tested on two cell lines, the A172 glioblastoma and TE671 rhabdomyosarcoma cell lines. Methylated -CDs exhibited the best inclusion ability for CBD. A dose-dependent effect of CBD on both cancer cell lines and improved efficacy of the CBD-CDs complexes were verified. Thus, cannabinoids may be considered in future clinical trials beyond their palliative use as possible inhibitors of cancer growth.

摘要

植物大麻素具有抗癌特性,这已在体外和体内得到证实。然而,它们具有高亲脂性的特点。为了改善大麻二酚(CBD)的性质,如溶解度、稳定性和生物利用度,可以采用CBD与环糊精(CDs)的包合物,实现有针对性、更快且持续时间更长的CBD释放。本研究的目的是研究CBD及其与随机甲基化-β-CD(RM-β-CD)和2-羟丙基-β-CD(HP-β-CD)形成的包合物的体外作用。通过相溶解度研究考察了CBD与CDs络合后溶解度的提高情况,并通过X射线晶体学确定了CBD在2,6-二-O-甲基-β-CD(DM-β-CD)和2,3,6-三-O-甲基-β-CD(TM-β-CD)中的包合物结构。通过分子动力学模拟对结构研究进行了补充。在两种细胞系,即A172胶质母细胞瘤细胞系和TE671横纹肌肉瘤细胞系上测试了CBD及其与RM-β-CD和HP-β-CD形成的复合物的细胞毒性。甲基化-β-CDs对CBD表现出最佳的包合能力。证实了CBD对两种癌细胞系均有剂量依赖性作用,且CBD-CD复合物的疗效有所提高。因此,大麻素在未来的临床试验中,除了作为姑息治疗药物外,还可作为癌症生长的潜在抑制剂加以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad6b/9027293/27be0b593c3a/pharmaceutics-14-00706-g001.jpg

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