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含亚甲蓝光敏药物的蛋白纳米笼的细胞摄取和光动力活性。

Cellular uptake and photodynamic activity of protein nanocages containing methylene blue photosensitizing drug.

机构信息

Department of Biomedical Engineering, Duke University, Durham, NC, USA.

出版信息

Photochem Photobiol. 2010 May-Jun;86(3):662-6. doi: 10.1111/j.1751-1097.2009.00696.x. Epub 2010 Jan 27.

Abstract

This study reports that photosensitizers encapsulated in supramolecular protein cages can be internalized by tumor cells and can deliver singlet oxygen intracellularly for photodynamic therapy (PDT). As an alternative to other polymeric and/or inorganic nanocarriers and nanoconjugates, which may also deliver photosensitizers to the inside of the target cells, protein nanocages provide a unique vehicle of biological origin for the intracellular delivery of photosensitizing molecules for PDT by protecting the photosensitizers from reactive biomolecules in the cell membranes, and yet providing a coherent, critical mass of destructive power (by way of singlet oxygen) upon specific light irradiation for photodynamic therapy of tumor cells. As a model, we demonstrated the successful encapsulation of methylene blue (MB) in apoferritin via a dissociation-reassembly process controlled by pH. The resulting MB-containing apoferritin nanocages show a positive effect on singlet oxygen production, and cytotoxic effects on MCF-7 human breast adenocarcinoma cells when irradiated at the appropriate wavelength (i.e. 633 nm).

摘要

本研究报告称,封装在超分子蛋白质笼中的光敏剂可以被肿瘤细胞内吞,并可以将单线态氧递送至细胞内用于光动力疗法(PDT)。与其他可能将光敏剂递送至靶细胞内部的聚合和/或无机纳米载体和纳米缀合物相比,蛋白质纳米笼为通过保护光敏剂免受细胞膜中反应性生物分子的侵害,同时在特定光照射下提供一致的、关键的破坏能力(通过单线态氧),从而为 PDT 提供了一种独特的生物来源的载体,用于光敏化分子的细胞内递药。作为一个模型,我们通过 pH 控制的解离-组装过程成功地将亚甲蓝(MB)封装在脱铁铁蛋白中。所得的含 MB 的脱铁铁蛋白纳米笼在适当波长(即 633nm)照射下对单线态氧的产生和 MCF-7 人乳腺癌细胞的细胞毒性均有积极影响。

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