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Biocompatible Electrochemical Sensor Based on Platinum-Nickel Alloy Nanoparticles for In Situ Monitoring of Hydrogen Sulfide in Breast Cancer Cells

Hydrogen sulfide (H(2)S), an endogenous gasotransmitter, is produced in mammalian systems and is closely associated with pathological and physiological functions. Nevertheless, the complete conversion of H(2)S is still unpredictable owing to the limited number of sensors for accurate and quantitativ...

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Detalles Bibliográficos
Autores principales: Panda, Asit Kumar, Keerthi, Murugan, Sakthivel, Rajalakshmi, Dhawan, Udesh, Liu, Xinke, Chung, Ren-Jei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781777/
https://www.ncbi.nlm.nih.gov/pubmed/35055275
http://dx.doi.org/10.3390/nano12020258
Descripción
Sumario:Hydrogen sulfide (H(2)S), an endogenous gasotransmitter, is produced in mammalian systems and is closely associated with pathological and physiological functions. Nevertheless, the complete conversion of H(2)S is still unpredictable owing to the limited number of sensors for accurate and quantitative detection of H(2)S in biological samples. In this study, we constructed a disposable electrochemical sensor based on PtNi alloy nanoparticles (PtNi NPs) for sensitive and specific in situ monitoring of H(2)S released by human breast cancer cells. PtNi alloy NPs with an average size of 5.6 nm were prepared by a simple hydrothermal approach. The conversion of different forms of sulfides (e.g., H(2)S, HS(−), and S(2−)) under various physiological conditions hindered the direct detection of H(2)S in live cells. PtNi NPs catalyze the electrochemical oxidation of H(2)S in a neutral phosphate buffer (PB, pH 7.0). The PtNi-based sensing platform demonstrated a linear detection range of 0.013–1031 µM and the limit of detection was 0.004 µM (S/N = 3). Moreover, the PtNi sensor exhibited a sensitivity of 0.323 μA μM(−1) cm(−2). In addition, the stability, repeatability, reproducibility, and anti-interference ability of the PtNi sensor exhibited satisfactory results. The PtNi sensor was able to successfully quantify H(2)S in pond water, urine, and saliva samples. Finally, the biocompatible PtNi electrode was effectively employed for the real-time quantification of H(2)S released from breast cancer cells and mouse fibroblasts.