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多功能聚合物胶束增强的芬顿反应用于肿瘤消融。

Multifunctional Polymeric Micelles with Amplified Fenton Reaction for Tumor Ablation.

机构信息

CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering , University of Science and Technology of China , Hefei 230026 , Anhui , China.

Department of Pharmacology , Xinhua University of Anhui , Hefei 230088 , Anhui , China.

出版信息

Biomacromolecules. 2018 Jun 11;19(6):1990-1998. doi: 10.1021/acs.biomac.7b01777. Epub 2018 Feb 20.

Abstract

Relative to normal cells, tumor cells lack adequate capability of reactive oxygen scavenging. Thus, tumor cells can be selectively killed by increasing the concentration of reactive oxygen species in tumor tissue. In this report, we construct an integrated multifunctional polymeric nanoparticle which can selectively improve hydrogen peroxide (HO) levels in tumor tissue and convert them into more active hydroxyl radicals by Fenton reaction. First, the diblock copolymers containing polyethylene glycol (PEG) and poly(glutamic acid) modified by β-cyclodextrin (β-CD) were synthesized. The block copolymer, ferrocenecarboxylic acid hexadecyl ester (DFc), and ascorbyl palmitate (PA) were coassembled in aqueous solution to obtain stable core-shell micelles through the inclusion complexation between β-CD moieties in the block copolymer and ferrocene (Fc) groups from DFc. After intravenous injection, the particles achieved significant accumulation in tumor tissue where ascorbic acid at the pharmacological concentration promotes the production of HO, and subsequently Fenton reaction was catalyzed by Fc groups to produce hydroxyl radicals to efficiently kill cancer cells and suppress tumor growth. The micellar systems possess great potentials toward cancer therapy through synergistic HO production and conversion into hydroxyl radicals specifically in tumor tissue.

摘要

与正常细胞相比,肿瘤细胞缺乏足够的活性氧清除能力。因此,可以通过增加肿瘤组织中活性氧物种的浓度来选择性地杀死肿瘤细胞。在本报告中,我们构建了一种集成的多功能聚合物纳米粒子,该粒子可以通过芬顿反应选择性地提高肿瘤组织中过氧化氢(HO)的浓度,并将其转化为更活跃的羟基自由基。首先,合成了含有聚乙二醇(PEG)和β-环糊精(β-CD)修饰的聚谷氨酸(PGA)的两亲性嵌段共聚物。将嵌段共聚物、二茂铁羧酸十六酯(DFc)和抗坏血酸棕榈酸酯(PA)共组装在水溶液中,通过嵌段共聚物中β-CD 部分与 DFc 中的二茂铁(Fc)基团之间的包合作用,得到稳定的核壳型胶束。静脉注射后,这些粒子在肿瘤组织中实现了显著的积累,在肿瘤组织中,药理浓度的抗坏血酸促进了 HO 的产生,随后 Fc 基团催化芬顿反应产生羟基自由基,有效地杀死癌细胞并抑制肿瘤生长。通过协同产生 HO 并将其转化为特定于肿瘤组织的羟基自由基,胶束系统在癌症治疗方面具有巨大的潜力。

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