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研究氮化硼纳米结构与美法仑抗卵巢癌药物的吸附作用及细胞毒性。

Studying Adsorption and Cellular Toxicity of Boron Nitride Nanostructure versus Melphalan Anti-ovarian Cancer Drug.

作者信息

Fu Min, Tayebee Reza, Saberi Satar, Nourbakhsh Narjes, Esmaeili Effat, Maleki Behrooz, Vatanpour Hamid R

机构信息

Department of Pharmacy Intravenous Admixture Services, Weifang People's Hospital, Weifang, Shandong, China.

Department of Chemistry, School of Sciences, Hakim Sabzevari University, Sabzevar, 96179-76487, Iran.

出版信息

Curr Mol Med. 2021;21(8):698-705. doi: 10.2174/1566524021666210111104428.

Abstract

BACKGROUND

Inclusion of anticancer drugs into biocompatible nanoparticulate carriers decreases the general toxicity and improves the efficacy of clinical treatments due to the reduction of soluble circulating free drugs.

METHODS

In addition, removal of emerging drug contaminants from wastewaters is a necessity that should be seriously attended. Boron nitride (BN) is a choice in drug delivery because of its many surprising properties. Here, boron nitride nanoparticles are prepared, characterized by Fourier-transform infrared spectroscopy (FT-IR) and x-ray diffraction (XRD) and used in the delivery of melphalan anti-cancer drug.

RESULTS

Then, density functional theory (DFT) calculations are carried out to study the adsorption of this drug on the surface of pure boron nitride fullerene via familiar hybrid functionals B3LYP and B3PW91. In addition, the polarizable continuum model (PCM) calculations show that BN is stable in water.

CONCLUSION

Finally, the in vitro cellular toxicity and viability of BN nanoparticles was examined on ES-2 cancer cells. The inhibitory dose IC50 of the material confirmed acceptable cytotoxicity and nanoparticles affected the average growth of the ES-2 cancer cells.

摘要

背景

将抗癌药物纳入生物相容性纳米颗粒载体中,由于可溶性循环游离药物的减少,可降低总体毒性并提高临床治疗效果。

方法

此外,去除废水中新出现的药物污染物是一项必须认真对待的必要任务。氮化硼(BN)因其许多惊人特性而成为药物递送的一种选择。在此,制备了氮化硼纳米颗粒,通过傅里叶变换红外光谱(FT-IR)和X射线衍射(XRD)对其进行表征,并将其用于美法仑抗癌药物的递送。

结果

然后,通过熟悉的杂化泛函B3LYP和B3PW91进行密度泛函理论(DFT)计算,以研究该药物在纯氮化硼富勒烯表面的吸附。此外,极化连续介质模型(PCM)计算表明BN在水中是稳定的。

结论

最后,检测了BN纳米颗粒对ES-2癌细胞的体外细胞毒性和活力。该材料的抑制剂量IC50证实了可接受的细胞毒性,且纳米颗粒影响了ES-2癌细胞的平均生长。

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