Key Laboratory of Colloid and Interface Chemistry (Shandong University), Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
J Fluoresc. 2010 Jul;20(4):843-50. doi: 10.1007/s10895-010-0627-z. Epub 2010 Mar 4.
It is found that silver nanoparticles (AgNPs) can further enhance the fluorescence intensity of curcumin (CU)-cetyltrimethylammonium bromide (CTAB)-nucleic acids and improve its anti-photobleaching activity. Under optimum conditions, the enhanced fluorescence intensity is proportion to the concentration of nucleic acids in the range of 2.0 x 10(-8)-1.0 x 10(-6) g mL(-1) for fish sperm DNA (fsDNA), 2.0 x 10(-8)-1.0 x 10(-6) g mL(-1) for calf thymus DNA (ctDNA), 1.0 x 10(-8)-1.0 x 10(-6) g mL(-1) for yeast RNA (yRNA), and their detection limits (S/N = 3) are 8.0 ng mL(-1), 10.5 ng mL(-1) and 5.8 ng mL(-1), respectively. This method is used for determining the concentration of DNA in actual sample with satisfactory results. The interaction mechanism is also studied.
研究发现,银纳米粒子(AgNPs)可以进一步增强姜黄素(CU)-十六烷基三甲基溴化铵(CTAB)-核酸的荧光强度,并提高其抗光漂白活性。在最佳条件下,增强的荧光强度与核酸的浓度成正比,在鱼精 DNA(fsDNA)的 2.0×10^(-8)-1.0×10^(-6)g/mL 范围内,小牛胸腺 DNA(ctDNA)的 2.0×10^(-8)-1.0×10^(-6)g/mL 范围内,酵母 RNA(yRNA)的 1.0×10^(-8)-1.0×10^(-6)g/mL 范围内,其检测限(S/N=3)分别为 8.0ng/mL、10.5ng/mL 和 5.8ng/mL。该方法用于测定实际样品中 DNA 的浓度,结果令人满意。还研究了相互作用机制。