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荧光聚合物纳米复合材料作为通过调节ERBB4用于胶质瘤治疗的新型载药和靶向递送纳米载体

Fluorescent Polymer Nanocomposites as Novel Drug-Loading and Targeted Delivery Nanocarriers for Glioma Therapy by Modulating ERBB4.

作者信息

Li Jian, Lv Hui-Qing, Wu Fei, Li Xue-En

机构信息

Department of Neurosurgery, Qilu Hospital of Shandong University, Jinan, Shandong, China.

Department of Neurosurgery, Heze Third People's Hospital, Heze, Shandong, China.

出版信息

J Fluoresc. 2024 Dec 18. doi: 10.1007/s10895-024-04078-w.

Abstract

Gliomas are the most common type of tumor in the human central nervous system, characterized by high aggressiveness, elevated mortality, and poor prognosis. Therefore, developing new therapeutic strategies is crucial for improving glioma treatment. Temozolomide (TMZ) is widely used in glioma therapy due to its excellent ability to penetrate the blood-brain barrier. In this study, we synthesized HA-PEG@ICG using hyaluronic acid (HA) and polyethylene glycol (PEG), modified with the fluorescent compound indocyanine green (ICG), and thoroughly characterized the product's structure. Subsequently, compound 1 and TMZ were co-loaded onto this carrier to construct a synergistic drug delivery system (HA-PEG@ICG@1@TMZ). Additionally, we evaluated the inhibitory effects and mechanisms of HA-PEG@ICG@1@TMZ on glioma cell proliferation. Our study lays the foundation for further exploration of TMZ-based therapies for glioma treatment.

摘要

神经胶质瘤是人类中枢神经系统中最常见的肿瘤类型,其特点是侵袭性强、死亡率高且预后差。因此,开发新的治疗策略对于改善神经胶质瘤的治疗至关重要。替莫唑胺(TMZ)因其出色的血脑屏障穿透能力而被广泛用于神经胶质瘤治疗。在本研究中,我们使用透明质酸(HA)和聚乙二醇(PEG)合成了HA-PEG@ICG,并使用荧光化合物吲哚菁绿(ICG)进行修饰,对产物结构进行了全面表征。随后,将化合物1和TMZ共负载到该载体上,构建了一种协同给药系统(HA-PEG@ICG@1@TMZ)。此外,我们评估了HA-PEG@ICG@1@TMZ对神经胶质瘤细胞增殖的抑制作用及其机制。我们的研究为进一步探索基于TMZ的神经胶质瘤治疗方法奠定了基础。

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