EA 3452 Cibles thérapeutiques, formulation et expertise préclinique du médicament, Faculty of Pharmacy, Nancy-University, Nancy Cedex, France.
Talanta. 2011 Feb 15;83(5):1780-3. doi: 10.1016/j.talanta.2010.12.005. Epub 2010 Dec 13.
A simple spectrophotocolorimetric method devoted to the measurement of gold content in nanoparticles (NPs) was developed. It includes two steps: (i) metal gold NPs (Au NPs) are oxidized into the AuCl(4)(-) anion using a 5×10(-2) M HCl-1.5×10(-2) M NaCl-7×10(-4) M Br(2) solution, next (ii) AuCl(4)(-) concentration is measured using a spectrophotometric assay based on the reaction of AuCl(4)(-) with the cationic form of Rhodamine B to give a violet ion pair complex. This latter is extracted with diisopropyl ether and the absorbance of the organic complex is measured at 565 nm. The method is linear in the range 6-29 μM of AuCl(4)(-) with a limit of detection of 4.5μM. The analytical method was optimized with respect of bromine excess to obtain complete Au NPs oxidation. The method was applied to two types of Au NPs currently under investigation: citrate-stabilized Au NPs and Au NPs capped with dihydrolipoic acid (Au@DHLA). Both the gold content of Au NPs and the concentration of NPs (using NP diameter measured by transmission electron microscopy) have been calculated.
一种简单的分光光度比色法,用于测量纳米粒子(NPs)中的金含量。它包括两个步骤:(i)使用 5×10(-2)M HCl-1.5×10(-2)M NaCl-7×10(-4)M Br(2)溶液将金属金纳米粒子(Au NPs)氧化成 AuCl(4)(-)阴离子,接下来(ii)使用分光光度法测量 AuCl(4)(-)的浓度,该方法基于 AuCl(4)(-)与罗丹明 B 的阳离子形式的反应,生成紫色离子对络合物。该络合物用二异丙醚萃取,并在 565nm 处测量有机络合物的吸光度。该方法在 6-29 μM 的 AuCl(4)(-)范围内呈线性,检出限为 4.5μM。该方法针对获得完全 Au NPs 氧化的溴过量进行了优化。该方法已应用于两种正在研究的 Au NPs:柠檬酸稳定的 Au NPs 和用二氢硫辛酸(Au@DHLA)封端的 Au NPs。已经计算了 Au NPs 的金含量和 NPs 的浓度(使用透射电子显微镜测量的 NP 直径)。