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小分子肽修饰的纳米结构脂质载体在体内的分布和对 EGFR 过表达肿瘤的靶向作用。

Small peptide-modified nanostructured lipid carriers distribution and targeting to EGFR-overexpressing tumor in vivo.

机构信息

School of Pharmacy, Shenyang Pharmaceutical University , Shenyang , P. R. China.

出版信息

Artif Cells Nanomed Biotechnol. 2014 Jun;42(3):161-6. doi: 10.3109/21691401.2013.801848. Epub 2013 Jun 3.

Abstract

Ala-Glu-Tyr-Leu-Arg (AEYLR) was identified as a small peptide ligand targeting epidermal growth factor receptors (EGFR) in vitro in our previous study. The in vivo targeting ability of AEYLR and AEYLR-conjugated nanostructured lipid carriers (NLC) was studied in this paper. Near-infrared fluorescent (NIFR) dye 1,1'-dioctadecyltetramethyl indotricarbocyanine iodide (DiR)-loaded and AEYLR-modified NLC (A-D-NLC) were prepared. The average diameter, zeta potential, coupling efficiency between AEYLR and NLC and the amount of DiR released from A-D-NLC were used to evaluate their in vivo characteristics. AEYLR was labeled by Cy7 and A549 xenograft tumor-bearing mice model were establish. The in vivo distribution in tumor-bearing mice of A-D-NLC and Cy7-AEYLR was examined using NIRF imaging experiments at different times post-injection. AEYLR and AEYLR-conjugated NLC showed obvious targeting to A549 xenograft tumor compared with the control group. These results suggested that AEYLR-modified NLC could be considered as a promising targeted delivery system for combination cancer chemotherapy to improve therapeutic efficacy and to minimize adverse effects.

摘要

在我们之前的研究中,Ala-Glu-Tyr-Leu-Arg(AEYLR)被鉴定为一种在体外靶向表皮生长因子受体(EGFR)的小肽配体。本文研究了 AEYLR 和 AEYLR 缀合的纳米结构脂质载体(NLC)的体内靶向能力。制备了近红外荧光(NIFR)染料 1,1'-二辛基四甲基吲哚三碳氰化碘(DiR)负载和 AEYLR 修饰的 NLC(A-D-NLC)。使用平均直径、zeta 电位、AEYLR 与 NLC 的偶联效率以及 A-D-NLC 中 DiR 的释放量来评估它们的体内特性。用 Cy7 标记 AEYLR,并建立 A549 异种移植肿瘤荷瘤小鼠模型。在注射后不同时间点使用 NIRF 成像实验检查 A-D-NLC 和 Cy7-AEYLR 在荷瘤小鼠体内的分布。与对照组相比,AEYLR 和 AEYLR 缀合的 NLC 对 A549 异种移植肿瘤具有明显的靶向作用。这些结果表明,AEYLR 修饰的 NLC 可以被认为是一种有前途的联合癌症化疗的靶向递送系统,以提高治疗效果并最小化不良反应。

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