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负载一氧化碳释放分子-2(CORM-2)的叶酸标记蛋白纳米乳剂可提高荷皮下A20淋巴瘤肿瘤小鼠的存活率。

Folic acid-tagged protein nanoemulsions loaded with CORM-2 enhance the survival of mice bearing subcutaneous A20 lymphoma tumors.

作者信息

Loureiro Ana, Bernardes Gonçalo J L, Shimanovich Ulyana, Sárria Marisa P, Nogueira Eugénia, Preto Ana, Gomes Andreia C, Cavaco-Paulo Artur

机构信息

CEB-Centre of Biological Engineering, University of Minho, Campus of Gualtar, Braga, Portugal; CBMA (Centre of Molecular and Environmental Biology), University of Minho, Campus of Gualtar, Braga, Portugal.

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, United Kingdom; Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal.

出版信息

Nanomedicine. 2015 Jul;11(5):1077-83. doi: 10.1016/j.nano.2015.02.022. Epub 2015 Mar 16.

Abstract

UNLABELLED

Folic Acid (FA)-tagged protein nanoemulsions were found to be preferentially internalized on B-cell lymphoma cell line (A20 cell line), which, for the first time, is reported to express folate receptor (FR)-alpha. Carbon monoxide releasing molecule-2 (CORM-2) was incorporated in the oil phase of the initial formulation. FA-functionalized nanoemulsions loaded with CORM-2 exhibited a considerable antitumor effect and an increased survival of BALB/c mice bearing subcutaneous A20 lymphoma tumors. The developed nanoemulsions also demonstrated to be well tolerated by these immunocompetent mice. Thus, the results obtained in this study demonstrate that FA-tagged protein nanoemulsions can be successfully used in cancer therapy, with the important ability to delivery drugs intracellularly.

FROM THE CLINICAL EDITOR

In this research, the authors developed folic acid tagged nanoemulsions containing a carbon monoxide releasing protein molecule for targeted cancer cell treatment. In-vitro and in-vivo experiments showed efficacy against B-cell lymphoma cells. The same nanocarrier platform could be applied to other tumor cells expressing folate receptors on the cell surface.

摘要

未标记

发现叶酸(FA)标记的蛋白质纳米乳剂优先被B细胞淋巴瘤细胞系(A20细胞系)内化,首次报道该细胞系表达叶酸受体(FR)-α。一氧化碳释放分子-2(CORM-2)被掺入初始制剂的油相中。负载CORM-2的FA功能化纳米乳剂表现出相当大的抗肿瘤作用,并提高了携带皮下A20淋巴瘤肿瘤的BALB/c小鼠的存活率。所开发的纳米乳剂也被证明能被这些具有免疫活性的小鼠很好地耐受。因此,本研究获得的结果表明,FA标记的蛋白质纳米乳剂可成功用于癌症治疗,并具有将药物递送至细胞内的重要能力。

临床编辑评论

在本研究中,作者开发了含有一氧化碳释放蛋白分子的叶酸标记纳米乳剂用于靶向癌细胞治疗。体外和体内实验显示对B细胞淋巴瘤细胞有效。相同的纳米载体平台可应用于其他在细胞表面表达叶酸受体的肿瘤细胞。

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