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A rapid and sensitive assessment of the toxicity of oxygenated polycyclic aromatic hydrocarbons (OPAHs), widely distributed persistent organic pollutants in the environment, is crucial for human health. In this study, using high-performance liquid chromatography, the separation and detection of four purines, xanthine (X), guanine (G), adenine (A), and hypoxanthine (HX) in cells were performed. The aim was to evaluate the cytotoxicity of three OPAHs, namely 1,4-benzoquinone (1,4-BQ), 1,2-naphthoquinone (1,2-NQ) and 9,10-phenanthrenequinone (9,10-PQ), with higher environmental concentrations, from the perspective of purine nucleotide metabolism in human skin fibroblast cells (HFF-1). The results revealed that the levels of G and A were low in HFF-1 cells, while the levels of HX and X showed a dose-response relationship with persistent organic pollutants concentration. With increased concentration of the three persistent organic pollutants, the purine metabolism in HFF-1 cells weakened, and the impact of the three persistent organic pollutants on purine metabolism in cells was in the order of 9,10-PQ > 1,4-BQ > 1,2-NQ. This study provided valuable insights into the toxic mechanisms of 1,4-BQ, 1,2-NQ and 9,10-PQ, contributing to the formulation of relevant protective measures and the safeguarding of human health. [ABSTRACT FROM AUTHOR]

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• Developing a mini paper-based device to detect fluorene cytotoxicity in 10 µL sample. • The MWCNTs/μ-PAD allowed a sampling volume of 10.0 μL, which is 50.0 times less than the sampling volume required with a conventional electrode (500 μL). • This device is comparable to the MTT method in fluorene cytotoxicity analysis. Developing a cost-effective and simple micro-analysis tool has long been an important objective in the toxicological detection of fluorene. In this study, a disposable paper-based micro-analysis device (μ-PAD) was designed using graphite doped with multi-walled carbon nanotubes (MWCNTs) to hand draw the electrode (MWCNTs/μ-PAD). We investigated the feasibility of the designed MWCNTs/μ-PAD as a cell-sensing platform using voltammetry measurements. Its application for evaluating the cytotoxicity of fluorene was studied based on the electrochemical determination of human breast cancer cells induced by fluorene. The results showed a dose-dependent toxicity effect of fluorene on cellular activity. The measurements were comparable with those obtained using a methyl-thiazolyl-tetrazolium assay. The detection limit of the MWCNTs/μ-PAD for human breast cancer cells was as low as 4.00 × 103 cells·mL−1 owing to the enhanced catalytic activity of the MWCNTs. Notably, the MWCNTs/μ-PAD—which had a diameter of 7.00 mm—allowed a sampling volume of 10.0 μL, which is 50.0 times less than the sampling volume required with a conventional electrode (500 μL). Advantages such as the simplicity of manufacture, low consumption, low cost, rapid detection, and disposability, suggest that the MWCNTs/μ-PAD could provide new opportunities and directions for in vitro microanalysis. [ABSTRACT FROM AUTHOR]

An in situ electrochemical method was used to assess the cytotoxicity of chlorophenols using human breast cancer (MCF-7) and cervical carcinoma (HeLa) cells as models. On treatment with different chlorophenols, the electrochemical responses of the selected cells, resulting from the oxidation of guanine and xanthine in the cytoplasm, indicated the cell viability. In addition, the in situ in vitro electrochemical method was further compared with the traditional MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assays. Although similar cytotoxicity data were obtained from both methods, the effective concentrations of chlorophenols that inhibited 50% cell growth (EC 50 values) from the electrochemical method were only slightly lower than those from the MTT assay. These results indicate that the in situ in vitro electrochemical method paves a simple, rapid, strongly responsive, and label-free way to the cytotoxicity assessment of different chlorophenol pollutants. [ABSTRACT FROM AUTHOR]

Cell viability and cytotoxicity is one of the most important toxicology indicators. In this study, an electrochemical method for detecting cell viability and cytotoxicity was discussed with the intracellular small molecule metabolite purines as indexes. The electrochemical behaviors of Balb/c 3T3, CHO, PC-12 and V79 cell suspensions were studies by cyclic voltammetry, and cell viability and cytotoxicity of four cell lines were compared by electrochemical, cell counting, 3-(4,5-dimethyl-2-Thiazyl)-2, 5-diphenyl-2H-tetrazolium bromide (MTT) and trypan blue exclusion methods. Four cell lines all showed an oxidation peak derived from mixture of xanthine and guanine at about 0.7 V. Using intracellular xanthine and guanine as index, the electrochemical method could not only describe the cell growth curves of four cell lines, but also reflect the changes of cell viability at various phases of the cell growth prior to the counting method. Compared with MTT, cell counting and trypan blue staining methods, the electrochemical method could detect the cytotoxicity of carcinogen earlier and more sensitively. The electrochemical method could track the change of intracellular xanthine and guanine contents, and used it as index to detect cell viability and cytotoxicity at the molecular level without markers, showing greater advantages over the method with apparent cell proliferation as the endpoint. [ABSTRACT FROM AUTHOR]