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半胱氨酸封端的硫化锌纳米粒子作为荧光探针在核酸测定中的制备与应用

Preparation and application of cysteine-capped ZnS nanoparticles as fluorescence probe in the determination of nucleic acids.

作者信息

Li Yongxin, Chen Jinlong, Zhu Changqin, Wang Lun, Zhao Danhua, Zhuo Shujuan, Wu Yuqin

机构信息

College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241000, PR China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2004 Jul;60(8-9):1719-24. doi: 10.1016/j.saa.2003.09.012.

Abstract

Cysteine-capped ZnS nanometer-sized fluorescent particles were produced by a colloidal aqueous synthesis. The functionalized nanoparticles are water-soluble and suitable for biological application. A synchronous fluorescence method has been developed for the rapid determination of DNA with functionalized nano-ZnS as a fluorescence probe, based on the synchronous fluorescence enhancement of cysteine-capped nano-ZnS in the presence of DNA. When Deltalambda =190 nm, maximum synchronous fluorescence is produced at 267 nm at pH 5.12. Under optimum conditions, the synchronous fluorescence intensity is proportional to the concentration of nucleic acids in the range 0.1-1.2 microg ml(-1) for calf thymus DNA, 0.1-0.6 microg ml(-1) for fish sperm DNA. The corresponding detection limit is 32.9 ng ml(-1) for calf thymus DNA and 24.6 ng ml(-1) for fish sperm DNA. This method is simple, inexpensive, rapid and sensitive. The recovery and relative standard deviation are satisfactory.

摘要

通过胶体水相合成法制备了半胱氨酸包覆的硫化锌纳米级荧光颗粒。功能化纳米颗粒具有水溶性,适用于生物应用。基于在DNA存在下半胱氨酸包覆的纳米硫化锌同步荧光增强现象,开发了一种以功能化纳米硫化锌作为荧光探针快速测定DNA的同步荧光方法。当Δλ = 190 nm时,在pH 5.12条件下,267 nm处产生最大同步荧光。在最佳条件下,对于小牛胸腺DNA,同步荧光强度在0.1 - 1.2 μg ml⁻¹范围内与核酸浓度成正比;对于鱼精DNA,在0.1 - 0.6 μg ml⁻¹范围内成正比。小牛胸腺DNA和鱼精DNA的相应检测限分别为32.9 ng ml⁻¹和24.6 ng ml⁻¹。该方法简单、廉价、快速且灵敏。回收率和相对标准偏差令人满意。

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