一种pH响应性超分子水凝胶,包封CuMnS纳米酶催化剂,用于肿瘤的协同光热光动力化学动力学治疗。

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Anqin Dong, Shiwei Huang, Zhiyi Qian, Sicheng Xu, Weizhong Yuan and Bing Wang
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引用次数: 0

摘要

传统的癌症疗法已不能满足目前对癌症精准治疗和个性化治疗的需求,开发新的治疗方式和研究新的联合抗肿瘤机制至关重要。因此,设计并合成了以己二酸二酰肼(ADH)为pH响应中心连接甲氧基聚乙二醇(mPEG)和肉桂醛(CA)的两亲性前药聚合物链,该聚合物链可以在水溶液中自组装成PAC胶束。基于α-环糊精(α-CD)与PAC胶束的主客体相互作用,形成了超分子水凝胶。采用溶剂热法制备了聚醚酰亚胺(PEI)修饰的铜锰硫化物纳米酶催化剂(PCMS NPs),该催化剂可均匀分散在水凝胶中形成复合超分子水凝胶(PCMS@PAC/α-CD凝胶)。在酸性肿瘤环境下,pH响应性腙键被破坏,导致CA的缓慢释放和过氧化氢(H2O2)水平的扩增。PCMS NPs具有过氧化物酶(POD)样活性和过氧化氢酶(CAT)样活性,可将H2O2转化为羟基自由基(*OH)和氧(O2)以缓解肿瘤内缺氧并诱导细胞凋亡,同时发挥谷胱甘肽氧化酶(GPX)样活性消耗谷胱甘肽(GSH)以进一步增强化学动力学治疗(CDT)的效果。在近红外光(NIR)照射下,PCMS NPs表现出优异的光热转换性能,可以快速将肿瘤细胞的温度提高到42°C以上进行光热治疗(PTT),并通过发挥氧化酶(OXD)样活性将O2转化为超氧化物阴离子(*O2-)进行光动力治疗(PDT)。通过体外和体内实验证明PCMS@PAC/α-CD凝胶对癌症细胞具有较高的细胞毒性,可有效抑制肿瘤生长,具有在生物医学和智能材料领域的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A pH-responsive supramolecular hydrogel encapsulating a CuMnS nanoenzyme catalyst for synergistic photothermal–photodynamic–chemodynamic therapy of tumours†

A pH-responsive supramolecular hydrogel encapsulating a CuMnS nanoenzyme catalyst for synergistic photothermal–photodynamic–chemodynamic therapy of tumours†

Traditional cancer therapies no longer meet the current demand for cancer precision therapy and personalized treatment and it's essential to develop new therapeutic modalities as well as to investigate new combination anti-tumor mechanisms. Therefore, amphiphilic prodrug polymer chains linking methoxy poly(ethylene glycol) (mPEG) and cinnamaldehyde (CA) with adipic acid dihydrazide (ADH) as the pH-responsive center were designed and synthesized, which could self-assemble into PAC micelles in aqueous solution. A supramolecular hydrogel was formed based on the host–guest interaction between α-cyclodextrin (α-CD) and PAC micelles. Polyetherimide (PEI) modified copper manganese sulfide nanoenzyme catalysts (PCMS NPs) were prepared by a solvothermal method, which could be uniformly dispersed in the hydrogel to form a composite supramolecular hydrogel (PCMS@PAC/α-CD Gel). Under an acidic tumor environment, pH-responsive hydrazone bonds were broken, resulting in the slow release of CA and the amplification of hydrogen peroxide (H2O2) levels. PCMS NPs exerted peroxidase (POD)-like activity and catalase (CAT)-like activity, which could convert H2O2 into hydroxyl radicals (˙OH) and oxygen (O2) to alleviate intra-tumor hypoxia and induce apoptosis, while exerting glutathione oxidase (GPX)-like activity to consume glutathione (GSH) to further enhance the effect of chemodynamic therapy (CDT). Under near-infrared light (NIR) irradiation, PCMS NPs exhibited an excellent photothermal conversion performance, which could rapidly increase the temperature of tumor cells to above 42 °C for photothermal therapy (PTT) and convert O2 to a superoxide anion (˙O2) by exerting oxidase (OXD)-like activity for photodynamic therapy (PDT). It was demonstrated by in vitro and in vivo experiments that the PCMS@PAC/α-CD Gel was highly cytotoxic to cancer cells and could effectively inhibit tumor growth, indicating the potential for applications in the fields of biomedicine and smart materials.

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来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
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