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注意金属类药物候选物的水溶行为。

Note of Caution for the Aqueous Behaviour of Metal-Based Drug Candidates.

机构信息

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005, Paris, France.

INRS-Centre Armand-Frappier Santé Biotechnologie, Organometallic Chemistry Laboratory for the Design of Catalysts and Therapeutics, Université du Québec, 531 boul. des Prairies Laval, Québec, H7V 1B7, Canada.

出版信息

ChemMedChem. 2020 Feb 17;15(4):345-348. doi: 10.1002/cmdc.201900677. Epub 2020 Jan 21.

DOI:10.1002/cmdc.201900677
PMID:31840945
Abstract

Poor aqueous solubility is one of the recurrent drawbacks of many compounds in medicinal chemistry. To overcome this limitation, the dilution of drug candidates from stock solutions of an organic solvent is common practice. However, the precise characterisation of these compounds in aqueous solutions is often neglected, leading to some uncertainties regarding the nature of the actual active species. In this communication, we demonstrate that two ruthenium complexes previously reported by our group for their chemotherapeutic potential against cancer, namely Ru(DIP) (sq) and Ru(DIP) (3-methoxysq), where DIP is 4,7-diphenyl-1,10-phenanthroline, sq=semiquinonate and 3-methoxysq=3-methoxysemiquinonate, form colloids in water-DMSO (1 % v/v) mixtures that are invisible to the naked eyes. Ru(DIP) (3-methoxysq) was found to form a highly stable and monodispersed colloid with nanoaggregates of ∼25 nm. In contrast, Ru(DIP) (sq) was found to form large reticulates of mostly spherical aggregates which size was found to increase over time. The difference in size and shape distribution of drug candidates is of tremendous significance as the study of their biological activity might be severely affected. Overall, we strongly believe that these observations should be taken into account by the scientific community working on the development of metal-based drugs with poor water solubility.

摘要

水溶性差是许多药物化学中化合物的常见缺陷之一。为了克服这一限制,将候选药物从有机溶剂的储备溶液中稀释是常见的做法。然而,通常会忽略这些化合物在水溶液中的精确特征,这导致了对实际活性物质性质的一些不确定性。在本通讯中,我们证明了我们小组先前报道的两种具有抗癌化疗潜力的钌配合物,即[Ru(DIP)(sq)](PF )和[Ru(DIP)(3-甲氧基sq)](PF ),其中 DIP 是 4,7-二苯基-1,10-菲咯啉,sq 是半醌,3-甲氧基sq 是 3-甲氧基半醌,在水-DMSO(1%v/v)混合物中形成肉眼不可见的胶体。发现[Ru(DIP)(3-甲氧基sq)](PF )形成了高度稳定且单分散的胶体,具有约 25nm 的纳米聚集体。相比之下,发现[Ru(DIP)(sq)](PF )形成了主要为球形聚集体的大网,其大小随着时间的推移而增加。候选药物的尺寸和形状分布的差异具有巨大的意义,因为它们的生物活性研究可能会受到严重影响。总的来说,我们坚信,从事开发水溶性差的金属基药物的科学界应该考虑到这些观察结果。

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