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Paper-Based Device for Rapid Visualization of NADH Based on Dissolution of Gold Nanoparticles

机译:基于金纳米颗粒溶解的纸质NADH快速可视化装置

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摘要

We describe a paper-based device that enables rapid and sensitive room-temperature detection of dihydronicotinamide adenine dinucleotide (NADH) via a colorimetric readout and demonstrate its value for monitoring NAD(+)-driven enzymatic reactions. Our system is based on NADH-mediated inhibition of gold nanoparticle (AuNPs) dissolution in a Au3+-cetyltrimethylammonium bromide (CTAB) solution. We fabricated a device consisting of a mixed cellulose ester paper featuring a wax-encircled, AuNP-coated film atop a cotton absorbent layer sandwiched between two plastic cover layers. In the absence of NADH, the Au3+-CTAB complex dissolves the AuNP layer completely, generating a white color in the test zone. In the presence of NADH, Au3+ is rapidly reduced to Au+, greatly decreasing the dissolution of AuNPs and yielding a red color that becomes stronger at increasing concentrations of NADH. This device exploits capillary force-assisted vertical diffusion, allowing us to apply a 25 mu L sample to a surface-confined test zone to achieve a detection limit of 12.5 mu M NADH. We used the enzyme glucose dehydrogenase as a model to demonstrate that our paper-based device can monitor NAD(+)-driven biochemical processes with and without selective dehydrogenase inhibitors by naked-eye observation within 4 min at room temperature in a small sample volume. We believe that our paper-based device could offer a valuable and low-cost analytical tool for monitoring NAD(+)-associated enzymatic reactions and screening for dehydrogenase inhibitors in a variety of testing contexts.
机译:我们描述了一种基于纸的设备,该设备能够通过比色读数快速,灵敏地在室温下检测二氢烟碱酰胺腺嘌呤二核苷酸(NADH),并证明其可用于监测NAD(+)驱动的酶促反应。我们的系统基于NADH介导的金纳米颗粒(AuNPs)在Au3 +-乙酰基三甲基溴化铵(CTAB)溶液中的溶解抑制。我们制造了一种设备,该设备由混合纤维素酯纸组成,其特征在于,在夹在两个塑料覆盖层之间的棉花吸收层上,有一层蜡环绕的AuNP涂层膜。在不存在NADH的情况下,Au3 + -CTAB络合物完全溶解AuNP层,在测试区域中产生白色。在存在NADH的情况下,Au3 +迅速还原为Au +,大大降低了AuNPs的溶解,并产生红色,在增加NADH浓度时变红。该设备利用毛细管力辅助的垂直扩散,使我们可以将25μL样品施加到表面受限的测试区域,以达到12.5μM NADH的检测限。我们使用酶葡萄糖脱氢酶作为模型来证明我们的纸质设备可以在室温下4分钟内肉眼观察少量样品,从而监测有无选择性脱氢酶抑制剂的NAD(+)驱动的生化过程。我们相信,我们的纸质设备可以为各种NAD(+)相关的​​酶促反应监测和筛选脱氢酶抑制剂提供各种有价值的低成本分析工具。

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