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Lipid composition has significant effect on targeted drug delivery properties of NGR-modified liposomes

机译:脂质组合物对NGR修饰脂质体的靶向药物递送特性具有重大影响

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摘要

The Asn-Gly-Arg (NGR) motif has previously been demonstrated to specifically bind to CD13, which is selectively overexpressed in tumor vasculature and some tumor cells (e.g. HT1080). It was reported that NGR-modified stealth liposomes (NGR-SL) could be prepared with different lipid composition, such as 1,2-dipalmitoyl-sn-glycero-phosphatidylcholine (DPPC), hydrogenated soy posphatidylcholine (HSPC) and soy posphatidylcholine (SPC). In the present study, NGR-modified liposomes were prepared with DPPC, HSPC, SPC or the mixture of HSPC and SPC. The resultant liposomes with different lipid composition were compared in terms of cell uptake, antitumor efficacy and targeted drug delivery efficiency using HT1080 tumor model. It was found that NGR-SL composed of the mixture of HSPC and SPC was able to improve targeted drug delivery efficiency to tumor producing the most significant antitumor activity. Collectively, the NGR-modified liposomes composed of the mixture of HSPC and SPC are promising carriers for the treatment of tumor. Besides NGR ligand, lipid composition could also significantly affect the targeted delivery efficiency to the tumor.
机译:先前已证明,Asn-Gly-Arg(NGR)基序与CD13特异性结合,而CD13在肿瘤脉管系统和某些肿瘤细胞(例如HT1080)中选择性过表达。据报道,NGR修饰的隐形脂质体(NGR-SL)可以用不同的脂质成分制备,例如1,2-二棕榈酰-sn-甘油磷脂酰胆碱(DPPC),氢化大豆磷脂酰胆碱(HSPC)和大豆磷脂酰胆碱(SPC) )。在本研究中,用DPPC,HSPC,SPC或HSPC和SPC的混合物制备了NGR修饰的脂质体。使用HT1080肿瘤模型,比较了具有不同脂质组成的所得脂质体的细胞摄取,抗肿瘤功效和靶向药物递送效率。发现由HSPC和SPC的混合物组成的NGR-SL能够提高靶向药物向肿瘤的递送效率,产生最显着的抗肿瘤活性。总的来说,由HSPC和SPC的混合物组成的NGR修饰脂质体是有望用于治疗肿瘤的载体。除NGR配体外,脂质成分还可显着影响靶向肿瘤的递送效率。

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