锚定在磁铁矿纳米颗粒表面的 L-半胱氨酸的抗氧化作用

Tatiane Britos , Nicole Santana , Maria Lucia Schumacher , Emerson Barbosa , Ariane de Espindola , Camila Chagas , Fernando L.A. Fonseca , Fabio F. Ferreira , Paula S. Haddad
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摘要

本研究探讨了锚定在超顺磁性氧化铁纳米粒子(SPIONs)(主要是磁铁矿(Fe3O4))上的 L-半胱氨酸(L-Cys)分子的合成、表征和评估,以开发潜在的药物递送应用。Fe3O4纳米粒子是通过共沉淀获得的,并用L-Cys进行了功能化处理,以提高生物相容性和抗氧化活性。为了优化功能化过程,研究人员通过改变反应时间和质量比例,研究了半胱氨酸到胱氨酸的二聚反应。样品通过粉末 X 射线衍射(PXRD)、傅立叶变换红外光谱(FTIR)和拉曼光谱、透射电子显微镜(TEM)和磁性曲线进行表征。这些结果证实,L-Cys 分子通过其羧酸基团锚定在纳米粒子表面,分散的纳米粒子中存在游离的 SH 基团。然而,在固态下,L-Cys 二聚化会形成胱氨酸晶体结构,导致没有自由 SH 基团。这种纳米粒子具有磁铁矿结构,平均结晶尺寸为 (8.7±0.8) nm,具有超顺磁性。体外生物检测表明,L-半胱氨酸在纳米粒子表面具有抗氧化作用。
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Antioxidant action of L-cysteine anchored on the surface of magnetite nanoparticles

This study addresses the synthesis, characterization, and evaluation of L-Cysteine (L-Cys) molecules anchored on superparamagnetic iron oxide nanoparticles (SPIONs), mainly magnetite (Fe3O4), for potential drug delivery applications. Fe3O4 nanoparticles are obtained via co-precipitation and functionalized with L-Cys to improve biocompatibility and antioxidant activity. To optimize the functionalization process, the dimerization of cysteine to cystine is investigated by varying the reaction time and mass proportions. The samples are characterized by powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) and Raman spectroscopies, transmission electron microscopy (TEM), and magnetic curves. These results confirm that L-Cys molecules are anchored on the nanoparticle surface through their carboxylate groups, with free SH groups present in the dispersed nanoparticles. However, in the solid state, L-Cys dimerization leads to a cystine crystal structure, resulting in no free SH groups. The nanoparticles have a magnetite structure with an average crystallite size of (8.7±0.8) nm and superparamagnetic behavior. In vitro biological assays show the antioxidant effect of L-Cysteine on the surface of the nanoparticles.

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