糖基化聚合物胶束中的吲哚菁绿是绘制前哨淋巴结和乳腺癌图谱的潜在图像剂†。

Nicole Lecot, Marcelo Fernández-Lomónaco, Hugo Cerecetto, Juan Pablo Gambini, Pablo Cabral and Romina Glisoni
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引用次数: 0

摘要

吲哚菁绿(ICG)是一种经美国食品及药物管理局(FDA)批准的近红外(NIR)染料,在图像引导手术(IGS)和 IGS 支持的前哨淋巴结活检(SNLB)绘图等技术中用作医学诊断的造影剂。然而,它在临床应用中存在许多缺点:(i) 在溶液中会自我聚集;(ii) 靶向性差;(iii) 由于会被肝脏快速吸收,因此在体内的半衰期较短。在此,为了克服这些障碍,我们利用基于两亲性线性和支链嵌段聚环氧乙烷-聚环氧丙烷(PEO-PPO)共聚物(Pluronic® 和 Tetronic®)的聚合物胶束(PMs)来稳定和载体化 ICG,并定向靶向乳腺癌组织。聚甲基丙烯酸酯具有独特的性能,因此具有多种优势,例如可以用各种受体靶向配体修饰其表面,而且其纳米级尺寸适合利用增强的渗透性和保留(EPR)效应进行癌症诊断。在这项工作中,我们在原始 F127 和 T1307 及其葡萄糖基化衍生物(分别为 F127-Glu 和 T1307-Glu)中制备了 ICG。这些体系的流体力学直径(19-27 nm)小于 30 nm,Z 电位为中等负值(直到 -10 mV),即使在冻干和复溶后(温度分别为 25 和 37 °C)在水中的稳定性也令人满意。特别是,T1307-Glu PMs 中的 ICG 显示出最大的溶解度和出色的封装效率(100%),由于在淋巴结(LN)和肿瘤中的高特异性和有效捕获,其体内摄取量可能很大。这项工作中展示的所有结果表明,ICG 负载 PMs 有可能用作 IGS、SLNB 和乳腺癌成像的图像探针剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Indocyanine green within glycosylated polymeric micelles as potential image agents to map sentinel lymph nodes and breast cancer†

Indocyanine green within glycosylated polymeric micelles as potential image agents to map sentinel lymph nodes and breast cancer†

Indocyanine green (ICG) is an FDA-approved near-infrared (NIR) dye used as a contrast agent for medical diagnosis in such techniques as image-guided surgery (IGS) and IGS-supported mapping for sentinel lymph node biopsy (SNLB). However, there are numerous disadvantages to its use in clinical applications: (i) self-aggregation in solution, (ii) poor targeting and (iii) short half-life in vivo, due to the rapid uptake by the liver. Herein, to overcome these obstacles, we utilized polymeric micelles (PMs) based on the amphiphilic linear and branched block poly(ethylene oxide)–poly(propylene oxide) (PEO–PPO) copolymers (Pluronic® and Tetronic®) for ICG stabilization, vehicleization and to directionally target breast cancer tissues. Because of their singular properties, PMs offer several advantages such as the ability to modify their surfaces with a variety of receptor-targeting ligands and their nano-scale size, which is suitable for taking advantage of the enhanced permeability and retention (EPR) effect for cancer diagnosis. In this work, we prepared ICG within pristine F127 and T1307 and their glucosylated derivatives (F127-Glu and T1307-Glu, respectively). These systems have a sub-30 nm-nanosized hydrodynamic diameter (19–27 nm), moderate negative Z-potentials (until −10 mV), and satisfactory stability in water even after lyophilisation and reconstitution, at 25 and 37 °C, respectively. Particularly, ICG within T1307-Glu PMs displayed maximum solubility and excellent encapsulation efficiency (100%), with a potentially large in vivo uptake according to high specificity and efficacious capture in lymph nodes (LNs) and tumors. All the results presented in this work, indicate that ICG-loaded PMs can potentially be used as image probe agents for IGS, SLNB and breast cancer imaging.

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