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基于氟化双子两亲聚合物的氧化还原响应载体用于联合癌症治疗。

Redox-responsive carrier based on fluorinated gemini amphiphilic polymer for combinational cancer therapy.

机构信息

Key Laboratory of Leather Chemistry and Engineering, Ministry of Education, National Engineering Research Center of Clean Technology in Leather Industry, Sichuan University, Chengdu 610065, PR China.

Key Laboratory of Leather Chemistry and Engineering, Ministry of Education, National Engineering Research Center of Clean Technology in Leather Industry, Sichuan University, Chengdu 610065, PR China.

出版信息

Colloids Surf B Biointerfaces. 2022 Aug;216:112551. doi: 10.1016/j.colsurfb.2022.112551. Epub 2022 May 9.

Abstract

Polymeric micelle has emerged as an efficient implement to overcome the shortcomings of conventional cancer chemotherapy due to its superior solubility of hydrophobic drugs and less side effects of drugs. However, insufficient dilution resistance and ordinary therapeutic effect severely restrict the further translation of current drug-loaded polymeric micelles. Here, we showed that well-defined G-Fn (n = 5, 9, 13) polymeric micelles possessed excellent capabilities as a drug carrier in light of high drug loading content, high stability and precise drug release combined with wonderful endocytosis efficiency to tumors. The representative G-F13 exhibited an excellent dilution resistance, outstanding high drug loading content (22 wt%) and drug loading efficiency (82%), which might be attributed to the extremely low critical micelle concentration conferred by its special Gemini structure and the superhydrophobicity of the fluorocarbon chain. Furthermore, the "cross-linked" internal fluoride membrane consisted of the two chains of the Gemini structure made G-F13 stable even after 24 h of incubation in 10% fetal bovine serum (FBS). The camptothecin (CPT) release was selectively triggered by glutathione (GSH) and HO, reaching 75% and 85% after 24 h respectively, in which only 15% of drugs leak under physiological conditions. The CCK-8 assays of Hela cells showed that CPT-loaded G-F13 micelles had high cell compatibility (200 μg/mL, 93% cell viability, 48 h) and high cancer cytotoxicity (IC50 0.1 μg/mL). Notably, a tenfold lower dosage of loaded CPT had an higher tumor growth inhibition than the free CPT. This result was attributed to the combined treatment of fluorinated drug carriers were more likely to penetrate the cell membrane to enter tumor cells, the cytotoxicity of selenic acid generated after the oxidation of G-F13 and the large amounts of CPT after redox release. Excellent physical and chemical properties as well as good therapeutic effects reveal that G-F13 can act as a promising drug carrier to widely use in cancer chemotherapy.

摘要

高分子胶束作为一种有效的手段克服了传统癌症化疗的缺点,因为它具有优越的疏水性药物的溶解度和更少的药物副作用。然而,不足的稀释抗性和普通的治疗效果严重限制了当前载药高分子胶束的进一步转化。在这里,我们表明,具有良好定义的 G-Fn(n=5、9、13)高分子胶束具有作为药物载体的优异能力,因为它们具有高载药含量、高稳定性和精确的药物释放,以及对肿瘤的出色内吞效率。代表性的 G-F13 表现出优异的稀释抗性、出色的高载药含量(22wt%)和载药效率(82%),这可能归因于其特殊的双子结构赋予的极低临界胶束浓度和氟碳链的超疏水性。此外,由双子结构的两条链构成的“交联”内部氟化物膜使 G-F13 即使在 10%胎牛血清(FBS)孵育 24 小时后也保持稳定。喜树碱(CPT)的释放被谷胱甘肽(GSH)和 HO 选择性触发,分别在 24 小时后达到 75%和 85%,而在生理条件下只有 15%的药物泄漏。Hela 细胞的 CCK-8 测定表明,载喜树碱的 G-F13 胶束具有高细胞相容性(200μg/mL,48 小时后 93%细胞活力)和高抗癌细胞毒性(IC50 0.1μg/mL)。值得注意的是,载药 CPT 的十倍低剂量具有比游离 CPT 更高的肿瘤生长抑制作用。这一结果归因于氟化物药物载体的联合治疗更有可能穿透细胞膜进入肿瘤细胞,G-F13 氧化后生成的亚硒酸和大量还原释放后的 CPT 的细胞毒性。优异的物理化学性质和良好的治疗效果表明,G-F13 可以作为一种有前途的药物载体广泛应用于癌症化疗。

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