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首页> 外文期刊>Pharmaceutical research >Multifunctional tumor-targeting nanocarriers based on hyaluronic acid-mediated and pH-sensitive properties for efficient delivery of docetaxel
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Multifunctional tumor-targeting nanocarriers based on hyaluronic acid-mediated and pH-sensitive properties for efficient delivery of docetaxel

机译:基于透明质酸介导和pH敏感特性的多功能靶向肿瘤纳米载体,可有效递送多西他赛

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Purpose: The objective of this work was to develop a multifunctional tumor-targeting nanocarrier based on the mechanism of CD44-mediated endocytosis and pH-induced drug release to improve the therapeutic efficacy of docetaxel (DTX). Methods: Hyaluronic acid-coated docetaxel-loaded cholesteryl hemisuccinate vesicles (HA-CHEMS vesicles) were prepared. The physiochemical properties and pH-dependent drug release of HA-CHEMS vesicles were evaluated. The HA-CHEMS vesicles were investigated for CD44-mediated internalization and in vitro cell viability using MCF-7,A549 and L929 cells.In addition,tissue distribution as well as antitumor efficacy was also evaluated in MCF-7 tumor-bearing mouse model. Results: The particle size and zeta potential of HA-CHEMS vesicles were 131.4 ± 6.2 nm and -13.3 ± 0.04 mV,respectively. The in vitro drug release results demonstrated a pH-responsive drug release under different pH conditions. In vitro cell viability tests suggested that the encapsulation of DTX in HA-CHEMS vesicles led to more than 51.6-fold and 46.3-fold improved growth inhibition in MCF-7 and A549 cell lines,respectively compared to Taxotere?. From the cell uptake studies,the coumarin 6-loaded HA-CHEMS vesicles enhanced intracellular fluorescent intensity in the CD44-overexpressing cell line (MCF-7). Biodistribution studies revealed selective accumulation of HA-CHEMS vesicles in the MCF-7 bearing BalB/c nude mice as a result of passive accumulation and active targeting (CD44-mediated endocytosis). Compared to Taxotere?,HA-CHEMS vesicles exhibited higher antitumor activity by reducing tumor volume (P < 0.05) and drug toxicity,demonstrating the success of the multifunctional targeting delivery. Conclusions: This work corresponds to the preparation of a multifunctional tumor-targeted delivery system. Our investigation shows that hyaluronan-bearing docetaxel-loaded cholesteryl hemisuccinate vesicles (HA-CHEMS vesicles) is a highly promising therapeutic system,leading to tumor regression after intravenous administration without visible toxicity.
机译:目的:这项工作的目的是基于CD44介导的内吞作用和pH诱导的药物释放机制,开发一种多功能的靶向肿瘤的纳米载体,以提高多西他赛(DTX)的治疗效果。方法:制备透明质酸涂层的多西他赛负载的胆固醇半琥珀酸酯囊泡(HA-CHEMS囊泡)。评价了HA-CHEMS囊泡的理化性质和pH依赖性药物释放。使用MCF-7,A549和L929细胞研究了HA-CHEMS囊泡的CD44介导的内在化和体外细胞存活力。此外,还对MCF-7荷瘤小鼠模型的组织分布和抗肿瘤功效进行了评估。结果:HA-CHEMS囊泡的粒径和Zeta电位分别为131.4±6.2 nm和-13.3±0.04 mV。体外药物释放结果表明在不同的pH条件下pH响应药物释放。体外细胞生存力测试表明,与Taxotere?相比,DTX在HA-CHEMS囊泡中的封装导致MCF-7和A549细胞系的生长抑制分别提高了51.6倍和46.3倍。从细胞摄取研究来看,加载了香豆素6的HA-CHEMS囊泡增强了CD44过表达细胞系(MCF-7)的细胞内荧光强度。生物分布研究表明,由于被动积累和主动靶向(CD44介导的胞吞作用),MCF-7携带BalB / c裸鼠体内的HA-CHEMS囊泡选择性积累。与紫杉醇相比,HA-CHEMS囊泡通过减少肿瘤体积(P <0.05)和药物毒性表现出更高的抗肿瘤活性,证明了多功能靶向递送的成功。结论:这项工作对应于多功能肿瘤靶向递送系统的制备。我们的研究表明,带有透明质酸的多西他赛负载的胆固醇半琥珀酸酯囊泡(HA-CHEMS囊泡)是一种很有前途的治疗系统,在静脉内给药后导致肿瘤消退而无明显毒性。

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