抗癌药物负载ZnO纳米粒子的光学带隙和晶体尺寸研究

Deepak Kumar, Samanwita Pal
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引用次数: 2

摘要

本研究旨在开发和表征氧化锌纳米颗粒作为各种抗癌药物的载体,即5-氟尿嘧啶(5-FU),阿霉素(DOX)和柔红霉素(DNR)。采用标准沉淀法制备ZnO纳米颗粒。利用紫外-可见漫反射光谱(DRS)分析测量了ZnO的带隙,结果表明载药后ZnO的带隙减小。利用x射线衍射(XRD)分析了负载ZnO纳米粒子的晶粒尺寸。载药后ZnO纳米颗粒的晶粒尺寸增大。两种方法都证实了药物分子在ZnO表面的吸附。本研究旨在开发和表征氧化锌纳米颗粒作为各种抗癌药物的载体,即5-氟尿嘧啶(5-FU),阿霉素(DOX)和柔红霉素(DNR)。采用标准沉淀法制备ZnO纳米颗粒。利用紫外-可见漫反射光谱(DRS)分析测量了ZnO的带隙,结果表明载药后ZnO的带隙减小。利用x射线衍射(XRD)分析了负载ZnO纳米粒子的晶粒尺寸。载药后ZnO纳米颗粒的晶粒尺寸增大。两种方法都证实了药物分子在ZnO表面的吸附。
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Optical band gap and crystallite size investigations of anticancer drug loaded ZnO nanoparticles
The present study aims at the development and characterization of zinc oxide (ZnO) nanoparticles as a carrier for various anti-cancerous drugs viz. 5-Fluorouracil (5-FU), Doxorubicin (DOX) and Daunorubicin (DNR). ZnO nanoparticles were prepared by standard precipitation method. The measurement of optical band gap using UV-Visible Diffuse Reflectance Spectroscopy (DRS) analysis reveals the lowering of ZnO band gap after the drug loading. Crystallite size of free and drug loaded ZnO nanoparticles were determined using X-ray Diffraction (XRD) analysis. The crystallite size of ZnO nanoparticles increases after the drug loading. Both the techniques confirm the adsorption of drug molecules on ZnO surface.The present study aims at the development and characterization of zinc oxide (ZnO) nanoparticles as a carrier for various anti-cancerous drugs viz. 5-Fluorouracil (5-FU), Doxorubicin (DOX) and Daunorubicin (DNR). ZnO nanoparticles were prepared by standard precipitation method. The measurement of optical band gap using UV-Visible Diffuse Reflectance Spectroscopy (DRS) analysis reveals the lowering of ZnO band gap after the drug loading. Crystallite size of free and drug loaded ZnO nanoparticles were determined using X-ray Diffraction (XRD) analysis. The crystallite size of ZnO nanoparticles increases after the drug loading. Both the techniques confirm the adsorption of drug molecules on ZnO surface.
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