Yan Guoqing, Wang Jun, Qin Jiejie, Hu Liefeng, Zhang Panpan, Wang Xin, Tang Rupei
Engineering Research Center for Biomedical Materials, School of Life Science, Anhui University, 111 Jiulong Road, Hefei, Anhui Province, 230601, P. R. China.
Macromol Biosci. 2017 Jul;17(7). doi: 10.1002/mabi.201600503. Epub 2017 Mar 29.
To compare the chemotherapeutic efficacy determined by extra- and intracellular drug release strategies, poly(ortho ester amide)-based drug carriers (POEAd-C) with well-defined main-chain lengths, are successfully constructed by a facile method. POEAd-C3-doxorubicin (DOX) can be rapidly dissolved to release drug at tumoral extracellular pH (6.5-7.2), while POEAd-C6-DOX can rapidly release drug following gradual swelling at intracellular pH (5.0-6.0). In vitro cytotoxicity shows that POEAd-C3-DOX exhibits more toxic effect on tumor cells than POEAd-C6-DOX at extracellular pH, but POEAd-C6-DOX has stronger tumor penetration and inhibition in vitro and in vivo tumor models. So, POEAd-C6-DOX with the intracellular drug release strategy has stronger overall chemotherapeutic efficacy than POEAd-C3-DOX with extracellular drug release strategy. It is envisioned that these poly(ortho ester amides) can have great potential as drug carriers for efficient chemotherapy with further optimization.
为了比较通过细胞外和细胞内药物释放策略确定的化疗效果,采用简便方法成功构建了具有明确主链长度的聚(原酸酯酰胺)基药物载体(POEAd-C)。POEAd-C3-阿霉素(DOX)在肿瘤细胞外pH值(6.5 - 7.2)下可迅速溶解以释放药物,而POEAd-C6-DOX在细胞内pH值(5.0 - 6.0)下逐渐溶胀后可迅速释放药物。体外细胞毒性表明,在细胞外pH值下,POEAd-C3-DOX对肿瘤细胞的毒性作用比POEAd-C6-DOX更强,但POEAd-C6-DOX在体外和体内肿瘤模型中具有更强的肿瘤穿透能力和抑制作用。因此,采用细胞内药物释放策略的POEAd-C6-DOX比采用细胞外药物释放策略的POEAd-C3-DOX具有更强的整体化疗效果。可以设想,这些聚(原酸酯酰胺)经过进一步优化后作为高效化疗药物载体具有巨大潜力。