2024
DOI: 10.1016/j.sintl.2023.100253
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Diagnostic methods employing kidney biomarkers clinching biosensors as promising tools

Neelam Yadav,
Jagriti Narang,
Anil Kumar Chhillar
et al.
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Cited by 2 publications
(3 citation statements)
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“…A significant increase in NIR emission and absorption was seen upon the reaction of FDOCl-22 and HOCl (Figure 4B); hence, drug-induced AKI was linked to the HOCl level. Additionally, it was determined that the use of NIRF and PA imaging made the initial stages of drug-induced kidney failure screening possible by gathering data from in vivo imaging of AKI mice (Figure 4C), fluorescent images of the kidney of a series of mice intraperitoneally injected with cisplatin of varying concentrations (0, 10, 20, and 40 mg/kg) for different time periods (12,24,48, and 72 h) and then intravenously injected with FDOCl-22 (200 μL × 0.5 mM) (left), and average fluorescence intensity output of the groups (right) (Figure 4D), comparing results of biosensor detection with available detection kits (Figure 4E), and in vivo PA imaging of cisplatin-induced AKI mice (Figure 4F). 46 By utilizing the receptor-mediated binding and retention effect in conjunction with enzyme-triggered fluorescence activation, Weng et al developed a multichannel activatable NIRF probe (1-DPA2) for the in situ detection of AKI (Figure 5A).…”
Section: Multicolor Fluorescent Probes For Imaging Of the Progression...mentioning
confidence: 99%
See 2 more Smart Citations
“…A significant increase in NIR emission and absorption was seen upon the reaction of FDOCl-22 and HOCl (Figure 4B); hence, drug-induced AKI was linked to the HOCl level. Additionally, it was determined that the use of NIRF and PA imaging made the initial stages of drug-induced kidney failure screening possible by gathering data from in vivo imaging of AKI mice (Figure 4C), fluorescent images of the kidney of a series of mice intraperitoneally injected with cisplatin of varying concentrations (0, 10, 20, and 40 mg/kg) for different time periods (12,24,48, and 72 h) and then intravenously injected with FDOCl-22 (200 μL × 0.5 mM) (left), and average fluorescence intensity output of the groups (right) (Figure 4D), comparing results of biosensor detection with available detection kits (Figure 4E), and in vivo PA imaging of cisplatin-induced AKI mice (Figure 4F). 46 By utilizing the receptor-mediated binding and retention effect in conjunction with enzyme-triggered fluorescence activation, Weng et al developed a multichannel activatable NIRF probe (1-DPA2) for the in situ detection of AKI (Figure 5A).…”
Section: Multicolor Fluorescent Probes For Imaging Of the Progression...mentioning
confidence: 99%
“…Measuring such biomarkers early on may also offer a way to quickly predict an AKI occurrence, 11 given that certain biomarkers, such as stress biomarkers, neutrophil gelatinase-associated lipocalin (NGAL), and kidney injury molecule-1 (KIM-1), have been demonstrated to be released directly in response to kidney injury. 12,13…”
Section: Introductionmentioning
confidence: 99%
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