Li Weinan, Sun Jialin, Zhang Xiaoyu, Jia Li, Qiao Mingxi, Zhao Xiuli, Hu Haiyang, Chen Dawei, Wang Yanhong
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
School of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Pharmaceutics. 2020 Jan 30;12(2):111. doi: 10.3390/pharmaceutics12020111.
PEG-poly(β-amino ester) (PEG-PBAE), which is an effective pH-responsive copolymer, was mainly synthesized by Michael step polymerization. Thioridazine (Thz), which was reported to selectively eliminate cancer stem cells (CSCs), was loaded into PEG-PBAE micelles (PPM) prepared by self-assembly at low concentrations. The critical micelle concentrations (CMC) of PPM in water were 2.49 μg/mL. The pH-responsive PBAE segment was soluble due to protonated tertiary amine groups when the pH decreased below pH 6.8, but it was insoluble at pH 7.4. The Thz-loaded PEG-PBAE micelle (Thz/PPM) exhibited a spherical shape, and the drug loading was 15.5%. In vitro release of Thz/PPM showed that this pH-sensitivity triggered the rapid release of encapsulated Thz in a weakly acidic environment. The in vitro cytotoxicity and cellular uptake of various formulations at pH 7.4 and 5.5 were evaluated on the mammospheres (MS), which were sorted by MCF-7 human breast cancer cell lines and identified to be a CD44/CD24 phenotype. The results of the cytotoxicity assay showed that blank micelles were nontoxic and Thz/PPM exhibited a similar anti-CSC effect on MS compared to Thz solution. Stronger fluorescence signal of Coumarin-6 (C6) was observed in MS treated by C6-loaded PPM (C6/PPM) at pH 5.5. The tumor inhibition rate and tumor weight of the free DOX and Thz/PPM groups were significantly different from those of the other groups, which free DOX and Thz/PPM effectively suppressed breast tumor growth in vivo. The above experimental results showed that Thz/PPM is an ideal and effective pH-responsive drug delivery carrier to a targeted therapy of CSCs.
聚乙二醇-聚(β-氨基酯)(PEG-PBAE)是一种有效的pH响应共聚物,主要通过迈克尔逐步聚合反应合成。据报道,能够选择性消除癌症干细胞(CSCs)的硫利达嗪(Thz),以低浓度负载到通过自组装制备的PEG-PBAE胶束(PPM)中。PPM在水中的临界胶束浓度(CMC)为2.49μg/mL。当pH值降至6.8以下时,pH响应性的PBAE链段由于叔胺基团质子化而可溶,但在pH 7.4时不溶。负载Thz的PEG-PBAE胶束(Thz/PPM)呈球形,载药量为15.5%。Thz/PPM的体外释放表明,这种pH敏感性在弱酸性环境中引发了包封的Thz的快速释放。在由MCF-7人乳腺癌细胞系分选并鉴定为CD44/CD24表型的乳腺球(MS)上,评估了pH 7.4和5.5时各种制剂的体外细胞毒性和细胞摄取。细胞毒性试验结果表明,空白胶束无毒,与Thz溶液相比,Thz/PPM对MS表现出相似的抗CSC作用。在pH 5.5时,负载香豆素-6(C6)的PPM(C6/PPM)处理的MS中观察到更强的C6荧光信号。游离阿霉素(DOX)组和Thz/PPM组的肿瘤抑制率和肿瘤重量与其他组有显著差异,游离DOX和Thz/PPM在体内有效抑制乳腺肿瘤生长。上述实验结果表明,Thz/PPM是用于CSCs靶向治疗的理想且有效的pH响应药物递送载体。