Highlights<'/> A simple and facile paper-based colorimetric assay for detection of free hydrogen sulflde in prostate cancer cells
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A simple and facile paper-based colorimetric assay for detection of free hydrogen sulflde in prostate cancer cells

机译:一种基于纸的简单简便的比色测定法,用于检测前列腺癌细胞中的游离硫化氢

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HighlightsWe introduce a simple and facile colorimetric paper sensor for H2S detection in cancer cells.A silver- and Nafion-embedded PVP membrane was coated onto detection zone on paper.Thein vitroanalytical performance of H2S sensing paper was evaluated.This paper assay can detect the difference in endogenous H2S between LNCaP and PC-3 cells.The result was consistent with western blot analysis and the methylene blue assay.AbstractIn this study, we introduce a new paper-based colorimetric assay fabricated with the 96-well microplate format for cell culture for sensing H2S gas in live cancer cells. The H2S sensing zones on the paper were coated with a polyvinylpyrrolidone (PVP) membrane containing silver/Nafion. The principle of colorimetric detection for free H2S gas is reaction of silver in the coating zones with sulfide to form Ag2S, which is brown in color. First, we optimized the composition of the coating membrane on the paper, including the mixing ratio between PVP and Nafion and the AgNO3concentration. Next, we examined the sensing performance of the paper assay in the form of sensitivity, selectivity reproducibility, and long-term stability using a known concentration of Na2S standard solution in phosphate buffered saline (PBS) at room temperature (RT) and in cell culture media at 37°C in a 5% CO2incubator. Our paper assay for H2S detection showed good sensitivity (2.51 color intensity/μM Na2S in PBS, R2=0.9967 at RT; 1.15 color intensity/μM Na2S in cell culture media, R2=0.9933 at 37°C in incubator), high selectivity, excellent reproducibility (relative standard deviation 2.4%), and high stability over 1 month, as well as a limit of detection of 1.4μM Na2S in PBS. Finally, we successfully measured the difference in endogenous H2S concentration between live LNCaP and PC-3 cells, which show different expression of H2S producing enzymes, using this paper-based colorimetric assay. The results were concordant with those of conventional methylene blue assay and western blot analysis. In summary, our paper assay using silver/Nafion-containing PVP membranes is a simple, facile, and reliable tool for the detection of H2S without complicated sample processing or labor-intensive bioanalytical methods We expect that this paper assay could be easily applied to study H2S signaling and pathophysiology in cancer biology, as well as cancer diagnosis and therapeutics.
机译: 突出显示 < ce:list-item id = “ lsti0005 ”> 我们介绍了一种简单易用的方法比色纸传感器,用于检测癌细胞中的H 2 S。 涂有银和Nafion嵌入的PVP膜 H 2 分析性能 S感测纸。 < / ce:list-item> 本文的检测方法可以检测LNCaP和PC-3细胞之间内源性H 2 S的差异。 The结果与蛋白质印迹分析和亚甲基蓝测定结果一致。 < / ce:abstract> 摘要 在此研究中,我们介绍了一篇新论文- 96孔微孔板形式制备的用于细胞培养的比色测定法,用于检测活菌中的H 2 S气体细胞。在纸上的H 2 -ce 2 in传感区涂有含银/ Nafion的聚乙烯吡咯烷酮(PVP)膜。游离H 2 S气体的比色检测原理是镀层中的银与硫化物反应形成Ag 2 S,它是棕色的。首先,我们优化了纸上涂膜的组成,包括PVP和Nafion之间的混合比例以及AgNO 3 的浓度。接下来,我们使用已知浓度的Na 2 以灵敏度,选择性重现性和长期稳定性的形式检查了纸质检测的传感性能。在室温(RT)的磷酸盐缓冲液(PBS)和37°C的细胞培养基中的5%CO 2 培养箱中的S标准溶液。我们的H 2 S检测纸质检测显示出良好的灵敏度(2.51色强度/μMNa 2 < / ce:inf> S在PBS中,RT时R 2 = 0.9967; 1.15色强度/μMNa 2 S在细胞培养基中,R 2 = 0.9933在37°C的培养箱中),高选择性,出色的重现性(相对标准偏差为2.4%),在1个月内具有很高的稳定性,并且在PBS中的检出限为1.4μMNa 2 S。最后,我们成功地测量了活LNCaP和PC-3细胞之间内源性H 2 S浓度的差异,这些差异显示了H 2 S产生酶,使用这种基于纸张的比色测定法。结果与常规亚甲基蓝测定和蛋白质印迹分析的结果一致。总而言之,我们使用含银/ Nafion的PVP膜进行的纸样分析是一种简单,便捷且可靠的工具,可轻松检测H 2 S样品处理或劳动密集型的生物分析方法我们希望本文的分析方法可以轻松地用于研究H 2 S信号传导和癌症生物学中的病理生理学作为癌症的诊断和治疗方法。

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