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用于药物递送和生物成像的诊疗一体化脂质体-纳米颗粒杂化物

Theranostic Liposome-Nanoparticle Hybrids for Drug Delivery and Bioimaging.

作者信息

Seleci Muharrem, Ag Seleci Didem, Scheper Thomas, Stahl Frank

机构信息

Institute of Technical Chemistry, Leibniz University of Hanover, Callinstr. 5, 30167 Hanover, Germany.

出版信息

Int J Mol Sci. 2017 Jul 2;18(7):1415. doi: 10.3390/ijms18071415.

DOI:10.3390/ijms18071415
PMID:28671589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5535907/
Abstract

Advanced theranostic nanomedicine is a multifunctional approach which combines the diagnosis and effective therapy of diseased tissues. Here, we investigated the preparation, characterization and in vitro evaluation of theranostic liposomes. As is known, liposome-quantum dot (L-QD) hybrid vesicles are promising nanoconstructs for cell imaging and liposomal-topotecan (L-TPT) enhances the efficiency of TPT by providing protection against systemic clearance and allowing extended time for it to accumulate in tumors. In the present study, hydrophobic CdSe/ZnS QD and TPT were located in the bilayer membrane and inner core of liposomes, respectively. Dynamic light scattering (DLS), zeta potential (ζ) measurements and fluorescence/absorption spectroscopy were performed to determine the vesicle size, charge and spectroscopic properties of the liposomes. Moreover, drug release was studied under neutral and acidic pH conditions. Fluorescence microscopy and flow cytometry analysis were used to examine the cellular uptake and intracellular distribution of the TPT-loaded L-QD formulation. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was utilized to investigate the in vitro cytotoxicity of the formulations on HeLa cells. According to the results, the TPT-loaded L-QD hybrid has adequate physicochemical properties and is a promising multifunctional delivery vehicle which is capable of a simultaneous co-delivery of therapeutic and diagnostic agents.

摘要

先进的治疗诊断纳米药物是一种将患病组织的诊断与有效治疗相结合的多功能方法。在此,我们研究了治疗诊断脂质体的制备、表征及体外评价。众所周知,脂质体-量子点(L-QD)混合囊泡是用于细胞成像的有前景的纳米结构,且脂质体-拓扑替康(L-TPT)通过提供针对全身清除的保护并延长其在肿瘤中积累的时间来提高TPT的效率。在本研究中,疏水性CdSe/ZnS量子点和TPT分别位于脂质体的双层膜和内核中。进行动态光散射(DLS)、zeta电位(ζ)测量以及荧光/吸收光谱分析以确定脂质体的囊泡大小、电荷和光谱性质。此外,还研究了在中性和酸性pH条件下的药物释放。使用荧光显微镜和流式细胞术分析来检测负载TPT的L-QD制剂的细胞摄取和细胞内分布。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法研究该制剂对HeLa细胞的体外细胞毒性。根据结果,负载TPT的L-QD复合物具有足够的物理化学性质,是一种有前景的多功能递送载体,能够同时共递送治疗剂和诊断剂。

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