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Enhancing ovarian cancer conventional chemotherapy through the combination with cannabidiol loaded microparticles

大麻酚 紫杉醇 药理学 卵巢癌 医学 化学 佐剂 化疗 癌症 外科 内科学 大麻 精神科
作者
Ana Isabel Fraguas‐Sánchez,Ana Fernández-Carballido,Florence Delié,Marie Cohen,Cristina Martín‐Sabroso,Delia Mezzanzanica,Mariangela Figini,Alessandro Satta,Ana Isabel Torres‐Suárez
出处
期刊:European Journal of Pharmaceutics and Biopharmaceutics [Elsevier BV]
卷期号:154: 246-258 被引量:27
标识
DOI:10.1016/j.ejpb.2020.07.008
摘要

In this work, we evaluated, for the first time, the antitumor effect of cannabidiol (CBD) as monotherapy and in combination with conventional chemotherapeutics in ovarian cancer and developed PLGA-microparticles as CBD carriers to optimize its anticancer activity. Spherical microparticles, with a mean particle size around 25 µm and high entrapment efficiency were obtained. Microparticles elaborated with a CBD:polymer ratio of 10:100 were selected due to the most suitable release profile with a zero-order CBD release (14.13 ± 0.17 μg/day/10 mg Mps) for 40 days. The single administration of this formulation showed an in vitro extended antitumor activity for at least 10 days and an in ovo antitumor efficacy comparable to that of CBD in solution after daily topical administration (≈1.5-fold reduction in tumor growth vs control). The use of CBD in combination with paclitaxel (PTX) was really effective. The best treatment schedule was the pre + co-administration of CBD (10 µM) with PTX. Using this protocol, the single administration of microparticles was even more effective than the daily administration of CBD in solution, achieving a ≈10- and 8- fold reduction in PTX IC50 respectively. This protocol was also effective in ovo. While PTX conducted to a 1.5-fold tumor growth inhibition, its combination with both CBD in solution (daily administered) and 10-Mps (single administration) showed a 2-fold decrease. These results show the promising potential of CBD-Mps administered in combination with PTX for ovarian cancer treatment, since it would allow to reduce the administered dose of this antineoplastic drug maintaining the same efficacy and, as a consequence, reducing PTX adverse effects.

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