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使用锚定在生物连接体上的生物源金纳米颗粒,通过叶酸介导的阿霉素突触递送。

Folic acid mediated synaphic delivery of doxorubicin using biogenic gold nanoparticles anchored to biological linkers.

作者信息

Pandey Sunil, Oza Goldie, Mewada Ashmi, Shah Ritu, Thakur Mukeshchand, Sharon Madhuri

机构信息

N. Shankaran Nair Research Institute for Nanotechnology and Bionanotechnology, Ambernath, MS, India.

出版信息

J Mater Chem B. 2013 Mar 7;1(9):1361-1370. doi: 10.1039/c2tb00168c. Epub 2013 Jan 25.

Abstract

Azadirachta indica as a biological sink for fabrication of gold nanoparticles (GNPs) and its applications in efficient delivery of doxorubicin (DOX) are presented here. Sucrose density gradient centrifugation was used to isolate the spherical GNPs of <50 nm from the mixture (containing both spherical and non-spherical) of nanoparticles synthesized using leaves of A. indica at inherent pH (6.14). The stability of GNPs due to the biological capping agents was scrutinised by measuring the flocculation parameter which was found to be in the range of 0-0.65. On the surface of these capped GNPs, doxorubicin was attached along with activated folic acid (FA) as navigational molecules for targeted drug delivery. Attachments were verified using FTIR which confirmed the formation of non-covalent interactions. The GNPs-FA-DOX complex was found be non-toxic for normal cells and considerably toxic for HeLa cells. The drug loading capacity of the GNPs was found to 93%. Doxorubicin release kinetics using GNPs followed 1 order at pH 5.3 which is ideal for solid tumor targeting.

摘要

本文介绍了印楝作为制备金纳米颗粒(GNPs)的生物载体及其在阿霉素(DOX)高效递送中的应用。使用蔗糖密度梯度离心法从在固有pH值(6.14)下用印楝叶合成的纳米颗粒混合物(包含球形和非球形)中分离出直径小于50 nm的球形GNPs。通过测量絮凝参数来研究生物封端剂对GNPs稳定性的影响,发现絮凝参数在0 - 0.65范围内。在这些封端的GNPs表面,阿霉素与活化叶酸(FA)一起附着,作为靶向药物递送的导航分子。使用傅里叶变换红外光谱(FTIR)对附着情况进行了验证,证实形成了非共价相互作用。发现GNPs - FA - DOX复合物对正常细胞无毒,对HeLa细胞有显著毒性。GNPs的载药能力为93%。使用GNPs时,阿霉素在pH 5.3下的释放动力学符合一级动力学,这对于实体瘤靶向是理想的。

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