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A Novel Monomethoxy Polyethylene Glycol–Polylactic Acid Polymeric Micelles with Higher Loading Capacity for Docetaxel and Well-Reconstitution Characteristics and Its Anti-metastasis Study

机译:多西他赛具有较高载量和良好重构特性的新型单甲氧基聚乙二醇-聚乳酸聚合物胶束及其抗转移性研究

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Docetaxel (DTX) is hydrophobic, and its available formulations (Taxotere? & Duopafei?) require Tween80 and ethanol vehicle to allow parental administration. DTX-loaded poly( D , L -lactide)- b -polyethylene glycol–methoxy (mPEG- b -PDLLA) polymeric micelle (PM) is a Tween80-free formulation of DTX, which has been extensively studied but rarely involved with industrialization issues. In this work, novel DTX-PM with improved loading capacity and well-reconsitution ability was developed. The freeze-dried DTX-PM was analyzed by HPLC, transmission electron microscopy (TEM) and dynamic light scattering (DLS) to determine the DTX loading, micelle morphology and size respectively. The in vitro cytotoxic activity of DTX-PM in 4T1 cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and the corresponding in vivo study was assessed in BALB/c mice bearing 4T1 tumor through intravenous administration. The DTX-loading and efficiency into the micelles were 20.74±1.23% and 93.7±1.03% respectively, which was much higher than ever reported PM. The DTX-PM was spherical with a mean particle size of 16.62±0.31?nm, which suggested that they were able to selectively accumulate in solid tumors by enhanced permeability and retention (EPR) effect. Another important characteristic of DTX-PM is the long term storage and reuses as aqueous injection solution. Many kinds of lyoprotectants were also investigated and dextrose was found to an excellent one. Compared with Duopafei?, DTX-PM showed better cytotoxicity and anti-metastasis ability against 4T1 cells in vitro and in vivo . In conclusion, DTX-PM significantly enhanced drug-loading capacity of DTX and had well-reconsitution ability, which could be a promising drug delivery system for clinic.
机译:多西紫杉醇(DTX)是疏水性的,其可用的制剂(Taxotere?&Duopafei?)需要Tween80和乙醇载体以允许父母给药。载有DTX的聚(D,L-丙交酯)-b-聚乙二醇-甲氧基(mPEG- b -PDLLA)聚合物胶束(PM)是不含Tween80的DTX制剂,已广泛研究,但很少涉及工业化问题。在这项工作中,开发了具有改善的负载能力和良好重构能力的新型DTX-PM。通过HPLC,透射电子显微镜(TEM)和动态光散射(DLS)分析冷冻干燥的DTX-PM,分别测定DTX负载量,胶束形态和大小。 DTX-PM在4T1细胞中的体外细胞毒性活性通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)分析进行了评估,相应的体内研究在BALB / c通过静脉内给药携带4T1肿瘤的小鼠。胶束中DTX的负载量和效率分别为20.74±1.23%和93.7±1.03%,远高于以往报道的PM。 DTX-PM为球形,平均粒径为16.62±0.31?nm,这表明它们能够通过增强的通透性和保留(EPR)效应选择性地在实体瘤中蓄积。 DTX-PM的另一个重要特性是可以长期储存并作为注射用水重新使用。还研究了多种冻干保护剂,发现葡萄糖是一种极好的。与Duopafei?相比,DTX-PM在体外和体内对4T1细胞表现出更好的细胞毒性和抗转移能力。总之,DTX-PM显着增强了DTX的载药能力,并具有良好的重构能力,这可能是临床上有希望的药物输送系统。

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