Biocompatible Protein (IgG) Modified Up-conversion Nanoparticles (NaGdF4: Yb3+, Er3+) Deposited by Matrix Assisted Pulsed Laser Evaporation (MAPLE)

Songlin Yang, W. H. Tse, Jin Zhang
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Abstract

In this study, up-conversion nanoparticles (NaGdF4: Yb3+, Er3+) with/without Immunoglobulin G (IgG) modification were produced by a one-pot synthesis method. The average size of the UCNPs is 50 ± 5 nm. Following that, the up-conversion nanoparticles with/without IgG modification were deposited on the culture dish with glass bottom Matrix assisted pulsed laser evaporation (MAPLE) technique. Nd:YAG laser (Ȝ = 532 nm, IJfwhm § 200μs, Ȟ = 10 Hz) was applied in this deposition. The antibody-modified nanoparticles deposited on the bottom of culture dish by MAPLE process are characterized by energy-dispersive X-ray spectroscopy (SEMEDS) and Fourier transform infrared spectroscopy (FT-IR). In addition, human umbilical vein endothelial cells (HUVECs) are cultured on the culture dish with the deposition of up-conversion nanoparticles with/without antibody, IgG. No toxic effect is imposed on cells. The results of this work indicate the deposition of antibody-modified nanoparticles on the bottom of culture dish by MAPLE could provide more possibilities for cell culture.
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基质辅助脉冲激光蒸发(MAPLE)制备生物相容性蛋白(IgG)修饰的上转换纳米粒子(NaGdF4: Yb3+, Er3+)
本研究采用一锅法合成了免疫球蛋白G (IgG)修饰/不修饰的上转换纳米粒子(NaGdF4: Yb3+, Er3+)。UCNPs的平均尺寸为50±5 nm。随后,采用玻璃底基质辅助脉冲激光蒸发(MAPLE)技术将IgG修饰或未修饰的上转化纳米颗粒沉积在培养皿上。采用Nd:YAG激光(Ȝ = 532 nm, IJfwhm§200μs, Ȟ = 10 Hz)进行沉积。利用能谱x射线能谱(SEMEDS)和傅里叶变换红外光谱(FT-IR)对MAPLE工艺沉积在培养皿底部的抗体修饰纳米颗粒进行了表征。此外,在培养皿上培养人脐静脉内皮细胞(HUVECs),沉积有/不含抗体IgG的上转化纳米颗粒。对细胞没有毒性作用。本研究结果表明,用MAPLE在培养皿底部沉积抗体修饰的纳米颗粒可以为细胞培养提供更多的可能性。
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