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单次注射后,用于重复和增强声动力治疗的热触发原位壳聚糖凝胶化系统。

Thermo-Triggered In Situ Chitosan-Based Gelation System for Repeated and Enhanced Sonodynamic Therapy Post a Single Injection.

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon Based Functional Materials & Devices, Soochow University, Suzhou, Jiangsu, 215123, China.

出版信息

Adv Healthc Mater. 2021 Feb;10(3):e2001208. doi: 10.1002/adhm.202001208. Epub 2020 Nov 25.

Abstract

Sonodynamic therapy (SDT) by utilizing ultrasonic waves triggers the generation of reactive oxygen species (ROS) with the help of sonosensitizers to destruct deep-seated tumors has attracted great attention. However, the efficacy of SDT may not be robust enough due to the insufficient oxygen supply within solid tumors. Additionally, repeated injections and treatments, which are often required to achieve the optimal therapeutic responses, may cause additional side effects and patient incompliance. Herein, a thermo-triggered in situ hydrogel system is developed in which catalase (CAT) conjugated with sonosensitizer meso-tetra (4-carboxyphenyl) porphine (TCPP) is mixed into chitosan (CS) and beta-glycerol phosphate disodium (GP) to form the precursor solution. After injection of the precursor solution into tumors, the in situ sol-gel transformation will occur as triggered by the body temperature, resulting in the localized tumor retention of TCPP-CAT. The locally restrained TCPP-CAT not only produces ROS under ultrasonic treatment, but also sustainably reverses the oxygen-deficient status in solid tumors by triggering the O generation from the decomposition of endogenous H O , further promoting the efficacy of SDT. As a result, the repeated SDT after a single dose injection of such a hydrogel can offer robust treatment effects to effectively eradicate tumors.

摘要

声动力学疗法(SDT)利用超声波在声敏剂的帮助下触发活性氧(ROS)的产生,以破坏深部肿瘤,引起了极大的关注。然而,由于实体瘤内氧气供应不足,SDT 的疗效可能不够强大。此外,为了达到最佳的治疗效果,通常需要重复注射和治疗,这可能会引起额外的副作用和患者不配合。在此,开发了一种热触发原位水凝胶系统,其中将过氧化氢酶(CAT)与声敏剂meso-四(4-羧基苯基)卟啉(TCPP)偶联,并混入壳聚糖(CS)和β-甘油磷酸二钠(GP)中,形成前体溶液。将前体溶液注射到肿瘤中后,体温触发原位溶胶-凝胶转化,导致 TCPP-CAT 在局部肿瘤中的保留。局部受限的 TCPP-CAT 不仅在超声处理下产生 ROS,还通过触发内源性 H 2 O 2 的分解产生 O 2 来持续逆转实体瘤中的缺氧状态,进一步促进 SDT 的疗效。因此,单次注射这种水凝胶后重复进行 SDT 可以提供强大的治疗效果,有效地根除肿瘤。

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