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'One-pot' synthesis of multifunctional GSH-CdTe quantum dots for targeted drug delivery

机译:多功能GSH-CdTe量子点的“一锅法”合成,用于靶向药物递送

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摘要

A novel quantum dots-based multifunctional nanovehicle (DOX-QD-PEG-FA) was designed for targeted drug delivery, fluorescent imaging, tracking, and cancer therapy, in which the GSH- CdTe quantum dots play a key role in imaging and drug delivery. To exert curative effects, the antineoplastic drug doxorubicin hydrochloride (DOX) was loaded on the GSH-CdTe quantum dots through a condensation reaction. Meanwhile, a polyethylene glycol (PEG) shell was introduced to wrap the DOX-QD, thus stabilizing the structure and preventing clearance and drug release during systemic circulation. To actively target cancer cells and prevent the nanovehicles from being absorbed by normal cells, the nanoparticles were further decorated with folic acid (FA), allowing them to target HeLa cells that express the FA receptor. The multifunctional DOX-QD-PEG-FA conjugates were simply prepared using the 'one pot' method. In vitro study demonstrated that this simple, multifunctional nanovehicle can deliver DOX to the targeted cancer cells and localize the nanoparticles. After reaching the tumor cells, the FA on the DOX-QD-PEG surface allowed folate receptor recognition and increased the drug concentration to realize a higher curative effect. This novel, multifunctional DOX-QD-PEG-FA system shows great potential for tumor imaging, targeting, and therapy.
机译:一种新型的基于量子点的多功能纳米车辆(DOX-QD-PEG-FA)被设计用于靶向药物输送,荧光成像,跟踪和癌症治疗,其中GSH-CdTe量子点在成像和药物输送中起关键作用。为了发挥疗效,将抗肿瘤药盐酸阿霉素(DOX)通过缩合反应加载到GSH-CdTe量子点上。同时,引入了聚乙二醇(PEG)外壳包裹DOX-QD,从而稳定了结构并防止了全身循环过程中的清除和药物释放。为了主动靶向癌细胞并防止纳米载体被正常细胞吸收,将纳米颗粒进一步用叶酸(FA)修饰,使其靶向表达FA受体的HeLa细胞。多功能DOX-QD-PEG-FA共轭物使用“一锅法”简单地制备。体外研究表明,这种简单的多功能纳米载体可以将DOX递送至目标癌细胞并定位纳米颗粒。到达肿瘤细胞后,DOX-QD-PEG表面的FA可以识别叶酸受体并增加药物浓度以实现更高的疗效。这种新颖的多功能DOX-QD-PEG-FA系统显示出在肿瘤成像,靶向和治疗方面的巨大潜力。

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