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Alula, Melisew Tadele; Karamchand, Leshern; Hendricks, Nicolette R.; Blackburn, Jonathan M.
Analytica chimica acta, 05/2018, Letnik: 1007Journal Article
Urinary creatinine concentration is a critical physiological parameter that enables reliable assessment of patient renal function and diagnosis of a broad spectrum of diseases. In this study, a simple and inexpensive sensor comprising monodisperse, citrate-capped silver nanoparticles (cc-AgNPs) was developed, which enabled rapid, sensitive and selective quantitation of creatinine directly in unprocessed urine. The mechanism of this sensor entails the creatinine-mediated aggregation of the cc-AgNPs (within 1 min) under alkaline conditions (pH 12). This is attributed to the tautomerization of creatinine to its amino anionic species at alkaline pH, which cross-link the cc-AgNPs via hydrogen bond networks with the negatively charged citrate caps. Creatinine elicited visibly-discernable color changes of the cc-AgNPs colloids in a concentration-dependent manner up to 10 μM. UV-visible spectroscopic analyses of the cc-AgNPs revealed that creatinine elicited a concentration-dependent decrease in intensity of the localized surface plasmon resonance (LSPR) band centered around 403 nm, with a concomitant increase in intensity of the red-shifted LSPR band at 670 nm. This observation denotes a creatinine-mediated increase in cc-AgNP particle size via aggregation, as confirmed by transmission electron microscopy analysis. The cc-AgNP sensor exhibited a linear correlation between the A670/A403 extinction ratio and creatinine concentration range of 0–4.2 μM in aqueous solutions (R2 = 0.996), and a low detection limit of 53.4 nM. Hence, the simplicity, short assay time, and high sensitivity and selectivity of our cc-AgNP sensor affirms its utility as a creatinine monitoring assay for low-resource, point-of-care settings. Display omitted •A colorimetric, LSPR citrate-capped AgNPs (cc-AgNPs) sensor capable of selective quantitation of creatinine was developed.•Creatinine induced concentration-dependent aggregation of cc-AgNPs at pH 12.•Inorganic ions and organic molecules present in urine do not interfere with cc-AgNPs-assay of creatinine.•The A670/A403 extinction ratio of cc-AgNPs increased linearly in aqueous creatinine concentration range of 0–4.2 μM.•A nanomolar urinary creatinine limit of detection (66 nM) was achieved with the cc-AgNPs assay.
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