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Synthesis and Characterization of pH-Responsive PEG-Poly(β-Amino Ester) Block Copolymer Micelles as Drug Carriers to Eliminate Cancer Stem Cells

机译:pH响应的PEG-聚(β-氨基酯)嵌段共聚物胶束作为药物载体消除癌症干细胞的合成与表征

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摘要

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.
机译:PEG-聚(β-氨基酯)(PEG-PBAE)是一种有效的pH响应共聚物,主要是通过迈克尔逐步聚合法合成的。据报道,噻哒嗪(Thz)可选择性消除癌症干细胞(CSC),将其装入低浓度自组装制备的PEG-PBAE胶束(PPM)中。水中PPM的临界胶束浓度(CMC)为2.49μg/ mL。当pH降至pH 6.8以下时,由于质子化的叔胺基,pH响应的PBAE片段可溶,但在pH 7.4时不溶。载有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敏感性触发了在弱酸性环境中胶囊化Thz的快速释放。在乳球(MS)上评估了pH 7.4和5.5下各种制剂的体外细胞毒性和细胞摄取,该乳球通过MCF-7人乳腺癌细胞系分类,并鉴定为CD44 / CD24表型。细胞毒性试验的结果表明,空白的胶束无毒,与Thz溶液相比,Thz / PPM对MS表现出相似的抗CSC作用。在pH 5.5的C6加载的PPM(C6 / PPM)处理的MS中观察到了香豆素6(C6)较强的荧光信号。游离DOX和Thz / PPM组的肿瘤抑制率和肿瘤重量与其他组显着不同,游离DOX和Thz / PPM有效地抑制了体内乳腺癌的生长。以上实验结果表明,Thz / PPM是针对CSC靶向治疗的理想且有效的pH响应药物递送载体。

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