Sene Saad, McLane Joshua, Schaub Nicholas, Bégu Sylvie, Hubert Mutin P, Ligon Lee, Gilbert Ryan J, Laurencin Danielle
Institut Charles Gerhardt de Montpellier, UMR 5253, CNRS-UM-ENSCM, Place E. Bataillon, CC1701, 34095 Montpellier cedex 05, France.
J Mater Chem B. 2016 Jan 14;4(2):257-272. doi: 10.1039/c5tb02258d. Epub 2015 Dec 9.
Benzoxaboroles are a family of organoboron molecules, which have been finding over the past few years an increasing number of biological applications, notably for the design of new drugs. Given that these molecules are still relatively new in the biomedical context, very few investigations regarding their formulation have been reported to date. Here, a complete study on the formulation of benzoxaboroles in a biopolymer, poly-l-lactic acid (PLLA), is reported. The incorporation of two small benzoxaboroles, namely the simplest benzoxaborole molecule (BBzx) and the antifungal drug tavaborole (AN2690), inside PLLA films was investigated. Different variations in the film composition and texture were looked into, by performing a heat-treatment on the PLLA films, or by preparing PLLA-PEO (polyethylene oxide) blends or PLLA-LDH (layered double hydroxide) composites. In each case, the impact of these changes in formulation on the local environment of the benzoxaboroles in the material (as determined by multinuclear solid state NMR), and on the kinetics of release in physiological media were analyzed, showing that a variety of release profiles could be achieved. Finally, cellular assays were carried out looking at the migration of MDA-MB-231 cancer cells. These tests revealed for the first time that benzoxaboroles like AN2690 and BBzx inhibited the migration of these cells. Moreover, the molecules incorporated in the films were found to remain active, and their effect on cancer cells was directly related to the release kinetics from the films. All in all, PLLA-based materials appear as highly versatile and attractive matrices for formulating benzoxaborole-based drugs.
苯并硼唑是一类有机硼分子,在过去几年中,其生物学应用越来越多,特别是在新药设计方面。鉴于这些分子在生物医学领域仍相对较新,迄今为止,关于其制剂的研究报道很少。在此,我们报道了一项关于苯并硼唑在生物聚合物聚左旋乳酸(PLLA)中的制剂的完整研究。研究了两种小分子苯并硼唑,即最简单的苯并硼唑分子(BBzx)和抗真菌药物他伏硼唑(AN2690)在PLLA薄膜中的掺入情况。通过对PLLA薄膜进行热处理,或制备PLLA-PEO(聚环氧乙烷)共混物或PLLA-LDH(层状双氢氧化物)复合材料,研究了薄膜组成和质地的不同变化。在每种情况下,分析了这些制剂变化对材料中苯并硼唑局部环境(通过多核固态核磁共振确定)以及在生理介质中释放动力学的影响,结果表明可以实现多种释放曲线。最后,进行了细胞实验,观察MDA-MB-231癌细胞的迁移情况。这些测试首次表明,像AN2690和BBzx这样的苯并硼唑能抑制这些细胞的迁移。此外,发现掺入薄膜中的分子仍具有活性,它们对癌细胞的作用与从薄膜中的释放动力学直接相关。总之,基于PLLA的材料似乎是用于配制苯并硼唑类药物的高度通用且有吸引力的基质。