基于与肿瘤靶向肽和/或细胞穿透肽共轭的 HPMA 共聚物的胶质母细胞瘤肿瘤荧光可视化增强新策略

View Pub Date : 2024-04-24 DOI:10.1002/viw.20230116
Eliška Grosmanová, R. Pola, M. Filipová, M. Henry, Jean-Luc Coll, T. Etrych
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摘要

纳米聚合物系统通常被用作药物和造影剂的载体,以增加循环时间和溶解度,并减少可能出现的副作用。由于增强的渗透性和滞留(EPR)效应,这些纳米药物通常会在肿瘤组织中积聚。不过,除了活性物质外,聚合物载体上还可以附着一个靶向基团,以进一步增加肿瘤积累和特异性。本研究选择了寡肽序列 RGD 来靶向肿瘤血管和某些肿瘤细胞上过度表达的 αvβ3 整合素。研究人员制备了一组含有荧光染料和不同结构(线性、环状、支链)RGD 肽的聚合物共轭物,用于肿瘤诊断,未来可能应用于导航手术。与仅因 EPR 效应而积累的非靶向对照组相比,最有希望的候选靶向荧光纳米探针在胶质母细胞瘤肿瘤中的积累增加了 35%。然而,作为一种抗血管生成治疗方法,使用聚合物结合的改良西仑吉肽并未显示出抑制血管生成的有益效果。
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Novel strategies for enhanced fluorescence visualization of glioblastoma tumors based on HPMA copolymers conjugated with tumor targeting and/or cell‐penetrating peptides
Nano‐sized polymer systems are often used as carriers for drugs and contrast agents to increase circulation time and solubility and to reduce possible side effects. These nanomedicines usually accumulate in tumor tissue due to the enhanced permeability and retention (EPR) effect. However, a targeting group may be attached to the polymer carrier in addition to the active substance to further increase tumor accumulation and specificity. In this study, the oligopeptide sequence RGD was chosen to target αvβ3 integrins overexpressed in the tumor vasculature and on some tumor cells. A set of polymer conjugates bearing a fluorescent dye and RGD peptide of different structures (linear, cyclic, branched) was prepared for use in tumor diagnosis, with a potential future application in navigated surgery. The accumulation of the most promising candidate, a targeted fluorescent nanoprobe, increased by 35% in glioblastoma tumors compared to the non‐targeted control, which accumulated only due to the EPR effect. However, the administration of a polymer‐bound modified cilengitide as an antiangiogenic treatment did not show a beneficial effect in the suppression of angiogenesis.
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