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智能人血清白蛋白纳米药物具有自我放大的叶酸受体靶向能力,用于慢性髓性白血病治疗。

Smart Human-Serum-Albumin-As O Nanodrug with Self-Amplified Folate Receptor-Targeting Ability for Chronic Myeloid Leukemia Treatment.

机构信息

Molecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, College of Life Sciences, Aptamer Engineering Center of Hunan Province, Hunan University, Changsha, 410082, China.

Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha, 410008, China.

出版信息

Angew Chem Int Ed Engl. 2017 Aug 28;56(36):10845-10849. doi: 10.1002/anie.201701366. Epub 2017 Aug 4.

Abstract

Arsenic trioxide (ATO, As O ) is currently used to treat acute promyelocytic leukemia. However, expanding its use to include high-dose treatment of other cancers is severely hampered by serious side effects on healthy organs. To address these limitations, we loaded ATO onto folate (FA)-labeled human serum albumin (HSA) pretreated with glutathione (GSH) based on the low pH- and GSH-sensitive arsenic-sulfur bond, and we termed the resulting smart nanodrug as FA-HSA-ATO. FA-HSA-ATO could specifically recognize folate receptor-β-positive (FRβ+) chronic myeloid leukemia (CML) cells, resulting in more intracellular accumulation of ATO. Furthermore, the nanodrug could upregulate FRβ expression in CML cancer cells and xenograft tumor model, facilitating even more recruitment and uptake of FRβ-targeting drugs. In vitro and in vivo experiments indicate that the nanodrug significantly alleviates side effects and improves therapeutic efficacy of ATO on CML and xenograft tumor model.

摘要

三氧化二砷(ATO,As2O3)目前用于治疗急性早幼粒细胞白血病。然而,由于对健康器官的严重副作用,将其用途扩展到包括高剂量治疗其他癌症受到严重阻碍。为了解决这些限制,我们根据低 pH 值和 GSH 敏感的砷-硫键,将 ATO 装载到叶酸(FA)标记的经谷胱甘肽(GSH)预处理的人血清白蛋白(HSA)上,并将所得智能纳米药物命名为 FA-HSA-ATO。FA-HSA-ATO 可以特异性识别叶酸受体-β阳性(FRβ+)慢性髓系白血病(CML)细胞,导致 ATO 的更多细胞内积累。此外,该纳米药物可以上调 CML 癌细胞和异种移植肿瘤模型中的 FRβ 表达,从而更有利于募集和摄取 FRβ 靶向药物。体外和体内实验表明,该纳米药物显著减轻了 ATO 对 CML 和异种移植肿瘤模型的副作用并提高了其治疗效果。

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