Shin Dae Hwan, Kwon Glen S
Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI, United States.
Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI, United States.
Int J Pharm. 2017 Feb 25;518(1-2):307-311. doi: 10.1016/j.ijpharm.2017.01.006. Epub 2017 Jan 3.
Epothilones are microtubule inhibitors that are promising alternatives to paclitaxel due to enhanced anticancer efficacy. While epothilones are slightly more water soluble than paclitaxel and more active against paclitaxel-resistant cells, they still require formulation with Cremophor EL and/or cosolvents and drug resistance still limits therapeutic efficacy. In this report, we showed that the combinational treatment of epothilone B (EpoB), 17-N-allylamino-17-demethoxygeldanamycin (17-AAG, Hsp90 inhibitor), and rapamycin (mTOR inhibitor) displays strong anticancer activity in vitro and in vivo. To address the poor water solubility of this 3 drug-combination, they were co-loaded into poly(ethylene glycol)-block-poly(d,l-lactic acid) (PEG-b-PLA) micelles, and the 3-in-1 loaded PEG-b-PLA micelle (m-EAR) was characterized in terms of drug loading efficiency, particle size, release kinetics. The m-EAR achieved high levels of all three drugs in water; formed micelles with hydrodynamic diameters at ca. 30nm and released the drugs in a sustained manner in vitro at rates slower than individually loaded PEG-b-PLA micelles. In A549-derived xenograft mice, m-EAR (2.0, 15.0, and 7.5mg/kg) caused tumor regression after four weekly injections, whereas EpoB alone (2.0mg/kg) was the same as control. No severe changes in body weight relative to PBS control were observed, attesting to the safety of m-EAR. Collectively, these results suggest that m-EAR provides a simple, but effective and safe EpoB-based combination nanomedicine for cancer therapy.
埃坡霉素是微管抑制剂,因其增强的抗癌功效而有望成为紫杉醇的替代物。虽然埃坡霉素的水溶性比紫杉醇略高,且对紫杉醇耐药细胞更具活性,但它们仍需要与聚氧乙烯蓖麻油和/或助溶剂配制成制剂,而且耐药性仍然限制了治疗效果。在本报告中,我们表明埃坡霉素B(EpoB)、17-N-烯丙基氨基-17-去甲氧基格尔德霉素(17-AAG,热休克蛋白90抑制剂)和雷帕霉素(mTOR抑制剂)的联合治疗在体外和体内均显示出强大的抗癌活性。为了解决这种三联药物组合水溶性差的问题,将它们共载入聚(乙二醇)-嵌段-聚(d,l-乳酸)(PEG-b-PLA)胶束中,并对载有三种药物的PEG-b-PLA胶束(m-EAR)的载药效率、粒径、释放动力学进行了表征。m-EAR在水中实现了三种药物的高载量;形成的胶束流体动力学直径约为30nm,并且在体外以比单独载入的PEG-b-PLA胶束更慢的速率持续释放药物。在A549衍生的异种移植小鼠中,每周注射四次后,m-EAR(2.0、15.0和7.5mg/kg)导致肿瘤消退,而单独使用EpoB(2.0mg/kg)与对照组相同。相对于PBS对照组,未观察到体重有严重变化,证明了m-EAR的安全性。总体而言,这些结果表明m-EAR为癌症治疗提供了一种简单但有效且安全的基于EpoB的联合纳米药物。