Ramasamy Thiruganesh, Kim Jeong Hwan, Choi Ju Yeon, Tran Tuan Hiep, Choi Han-Gon, Yong Chul Soon, Kim Jong Oh
College of Pharmacy, Yeungnam University, 214-1, Dae-dong, Gyeongsan 712-749, South Korea.
J Mater Chem B. 2014 Oct 7;2(37):6324-6333. doi: 10.1039/c4tb00867g. Epub 2014 Aug 12.
The co-encapsulation of two or more drugs in the same carrier affords synergistic therapeutic effects and enhanced therapeutic potency. For this, polyethylene oxide-b-polyacrylic acid di-block polymer based-smart pH-sensitive di-block polyelectrolyte complex (PEC) micelles were designed to encapsulate mitoxantrone (MTX) and doxorubicin (DOX) with high payload capacity and precise drug ratio. Three molar ratios (MTX/DOX: 2 : 1, 1 : 1, 1 : 2) of the drug-loaded PECs were prepared with high payload capacity and evaluated for various physicochemical characteristics. The dual drug combination exhibited a synergistic cytotoxic activity against both sensitive (MCF-7 and A-549) and resistant cancer cell lines (MDA-MB-231), unlike the individual drugs. Dual drug-loaded nanosystems (MTX/DOX-M) prolonged the blood circulation of drugs, and a synergic ratio was maintained throughout the study period. MTX/DOX-M exhibited superior therapeutic efficacy in xenograft models; by contrast, the free drug cocktail caused a significant loss of body weight in mice. Taken together, our results suggest that PEC micelles have great potential as nano-scaled therapeutic delivery systems for combination chemotherapy.
将两种或更多种药物共包封于同一载体中可产生协同治疗效果并增强治疗效力。为此,设计了基于聚环氧乙烷-b-聚丙烯酸二嵌段聚合物的智能pH敏感二嵌段聚电解质复合物(PEC)胶束,以高载药量和精确的药物比例包封米托蒽醌(MTX)和阿霉素(DOX)。制备了三种摩尔比(MTX/DOX:2∶1、1∶1、1∶2)的载药PEC,其具有高载药量,并对其各种物理化学特性进行了评估。与单一药物不同,这种双药组合对敏感癌细胞系(MCF-7和A-549)和耐药癌细胞系(MDA-MB-231)均表现出协同细胞毒性活性。双载药纳米系统(MTX/DOX-M)延长了药物的血液循环时间,并且在整个研究期间都保持了协同比例。MTX/DOX-M在异种移植模型中表现出优异的治疗效果;相比之下,游离药物混合物导致小鼠体重显著下降。综上所述,我们的结果表明,PEC胶束作为联合化疗的纳米级治疗递送系统具有巨大潜力。