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瓜尔胶改性上转换纳米复合材料通过酶响应药物释放和近红外触发光动力疗法治疗结直肠癌。

Guar gum modified upconversion nanocomposites for colorectal cancer treatment through enzyme-responsive drug release and NIR-triggered photodynamic therapy.

机构信息

Department of Chemistry, National Institute of Technology, Rourkela. Odisha-769008, India.

出版信息

Nanotechnology. 2019 Aug 2;30(31):315102. doi: 10.1088/1361-6528/ab116e. Epub 2019 Mar 20.

DOI:10.1088/1361-6528/ab116e
PMID:30893650
Abstract

Multimodal therapeutic approach towards colorectal cancer (CRC) holds great promise. There is, however, no convincing strategy reported to date that employs a multimodal strategy in CRC treatment. The present study reports an intense green-emitting core-shell photoluminescent upconversion (CSGU) nanocrystal engineered to synergistically perform photodynamic and enzyme-triggered delivery of the chemotherapeutic agent for an enhanced therapeutic outcome on HT-29 colon carcinoma cells in vitro. The photodynamic activity is achieved by the energy transfer between CSGU and the chemically conjugated Rose Bengal (RB) molecules that are further protected by a mesoporous silica (MS) layer. The chemical assay demonstrates a remarkable FRET mediated generation of O under NIR (980 nm) excitation. The outermost MS layer of the nanoplatform is utilized for the loading of the 5FU anticancer drug, which is further capped with a guar gum (GG) polysaccharide polymer. The release of the 5FU is specifically triggered by the degradation of the GG cap by specific enzymes secreted from colonic microflora, which otherwise showed 'zero-release behavior' in the absence of any enzymatic trigger in various simulated gastro-intestinal (GI) conditions. Furthermore, the enhanced therapeutic efficacy of the nanoplatform (CSGUR-MSGG/5FU) was evaluated through in vitro studies using HT-29 CRC cell lines by various biochemical and microscopic assays by the simultaneous triggering effect of colonic enzyme and 980 nm laser excitation. In addition, the strong visible emission from the nanoplatform has been utilized for NIR-induced cellular bioimaging.

摘要

多模态治疗方法在结直肠癌(CRC)中具有广阔的应用前景。然而,目前尚未报道任何令人信服的策略,能够在 CRC 治疗中采用多模态策略。本研究报告了一种强烈的绿色发射核壳光致上转换(CSGU)纳米晶体,该纳米晶体经过精心设计,可协同进行光动力和酶触发的化疗药物递送,从而在体外对 HT-29 结肠癌细胞产生增强的治疗效果。光动力活性是通过 CSGU 和化学偶联的孟加拉玫瑰红(RB)分子之间的能量转移实现的,这些 RB 分子进一步被介孔硅(MS)层保护。化学分析表明,在近红外(980nm)激发下,通过 FRET 介导可以显著生成 O。纳米平台的最外层 MS 层用于负载 5FU 抗癌药物,然后用瓜尔胶(GG)多糖聚合物进行封端。只有在结肠微生物群分泌的特定酶的作用下,GG 帽才会发生降解,从而触发 5FU 的释放,否则在各种模拟胃肠(GI)条件下,在没有任何酶触发的情况下,会表现出“零释放行为”。此外,通过使用 HT-29 CRC 细胞系进行的各种生化和显微镜检测,通过结肠酶和 980nm 激光激发的同时触发作用,评估了纳米平台(CSGUR-MSGG/5FU)的增强治疗效果。此外,纳米平台的强可见光发射已被用于近红外诱导的细胞生物成像。

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