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首页> 外文期刊>RSC Advances >cRGDyK-modified camretastain A4-loaded graphene oxide nanosheets for targeted anticancer drug delivery
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cRGDyK-modified camretastain A4-loaded graphene oxide nanosheets for targeted anticancer drug delivery

机译:cRGDyK修饰的camretastain A4负载的氧化石墨烯纳米片用于靶向抗癌药物的递送

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摘要

Functionalized graphene oxide (CGO-cRGDyK/POLO) nanosheets were designed and developed for targeted drug delivery to integrin expression. The anticancer drug cambretastain A4 (CA4) was conjugated onto the CGO-cRGDyK/POLO nanosheets. The tumor targeting ligands, cyclic arginine-glycine-aspartic acid-tyrosine-lysine pentapeptides (cRGDyK), were conjugated to carboxylated graphene oxide (CGO) nanosheets, and poloxamer 188 (POLO) was rendered to make the CGO-cRGDyK nanosheets stable. The CGO-cRGDyK/POLO nanosheets exhibited good cytocompatibility, high CA4-loading capacity (0.6872 +/- 0.0121 mg mg(-1)) via pi-pi stacking or hydrophobic interactions, and controlled release in vitro. The MTT assays showed that the CGO-cRGDyK nanosheets had greater antitumor effects on Hela cells than CGO/POLO nanosheets but lower cytotoxicity on the L02 cells than free CA4. In addition, the cellular uptake of CGO-cRGDyK/POLO nanosheets was increased significantly in human umbilical vein endothelial cells (the integrins-overexpressed cells) compared to the normal L02 cells. Thus, the CGO-cRGDyK/POLO nanosheets are an appealing platform for cancer chemotherapy.
机译:设计并开发了功能化的氧化石墨烯(CGO-cRGDyK / POLO)纳米片,用于靶向药物递送至整联蛋白表达。将抗癌药cambretastain A4(CA4)偶联到CGO-cRGDyK / POLO纳米片上。将肿瘤靶向配体环状精氨酸-甘氨酸-天冬氨酸-酪氨酸-赖氨酸五肽(cRGDyK)偶联到羧化氧化石墨烯(CGO)纳米片上,并制备泊洛沙姆188(POLO)以使CGO-cRGDyK纳米片稳定。 CGO-cRGDyK / POLO纳米片通过pi-pi堆积或疏水相互作用表现出良好的细胞相容性,高CA4负载量(0.6872 +/- 0.0121 mg mg(-1))和体外控制释放。 MTT分析表明,CGO-cRGDyK纳米片对Hela细胞的抗肿瘤作用比CGO / POLO纳米片大,但对L02细胞的细胞毒性则低于游离CA4。另外,与正常的L02细胞相比,在人脐静脉内皮细胞(整联蛋白过表达的细胞)中,CGO-cRGDyK / POLO纳米片的细胞摄取显着增加。因此,CGO-cRGDyK / POLO纳米片是用于癌症化学疗法的吸引人的平台。

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