2020
DOI: 10.1557/mrc.2020.75
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Biofunctionalized nanodot zirconia-based efficient biosensing platform for noninvasive oral cancer detection

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Cited by 11 publications
(6 citation statements)
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“…(5) Immunohistochemistry . Dewaxing Paraffin sections of 4 thickness were sequentially placed in 100% xylene (a) and 100% xylene (b) at 37°C for 15 min each The slices were sequentially placed in 100% ethanol-100% ethanol-95% ethanol-80% ethanol-70% ethanol-plus % ethanol for 2 minutes each The slices were soaked in double-distilled water for 2 minutes and repeated 3 times [ 15 ] (ii) Antigen Retrieval After dewaxing, the samples were placed in 3% H 2 O, treated at room temperature for 15 minutes, and then soaked in double-distilled water for 2 minutes, repeating 3 times Preheat the 0.1 m citric acid solution in the microwave for 3 minutes, quickly put the slices into the sodium citrate solution, and continue to boil for 15 to 20 minutes (iii) Serum Blocking The samples were cooled for 30 minutes and then soaked in double-distilled water for 2 minutes, repeating 3 times After the double-distilled water on the tissue evaporated, immediately add serum-containing peroxidase blocking agent to block, and incubate at 37°C for 30 minutes (iv) Antibody Incubation Incubate with primary antibody, incubate at 37°C for 30 minutes, discard the blocking solution, add TNF- α or IL-6 antibody, and incubate at 4°C overnight After incubation with the secondary antibody, after recovering the primary antibody, the samples were washed three times with PBS for 5 minutes each time. After washing, biotinylated rabbit anti-goat secondary antibody was added and incubated at room temperature for 15 minutes (v) Color Rendering …”
Section: Methodsmentioning
confidence: 99%
“…(5) Immunohistochemistry . Dewaxing Paraffin sections of 4 thickness were sequentially placed in 100% xylene (a) and 100% xylene (b) at 37°C for 15 min each The slices were sequentially placed in 100% ethanol-100% ethanol-95% ethanol-80% ethanol-70% ethanol-plus % ethanol for 2 minutes each The slices were soaked in double-distilled water for 2 minutes and repeated 3 times [ 15 ] (ii) Antigen Retrieval After dewaxing, the samples were placed in 3% H 2 O, treated at room temperature for 15 minutes, and then soaked in double-distilled water for 2 minutes, repeating 3 times Preheat the 0.1 m citric acid solution in the microwave for 3 minutes, quickly put the slices into the sodium citrate solution, and continue to boil for 15 to 20 minutes (iii) Serum Blocking The samples were cooled for 30 minutes and then soaked in double-distilled water for 2 minutes, repeating 3 times After the double-distilled water on the tissue evaporated, immediately add serum-containing peroxidase blocking agent to block, and incubate at 37°C for 30 minutes (iv) Antibody Incubation Incubate with primary antibody, incubate at 37°C for 30 minutes, discard the blocking solution, add TNF- α or IL-6 antibody, and incubate at 4°C overnight After incubation with the secondary antibody, after recovering the primary antibody, the samples were washed three times with PBS for 5 minutes each time. After washing, biotinylated rabbit anti-goat secondary antibody was added and incubated at room temperature for 15 minutes (v) Color Rendering …”
Section: Methodsmentioning
confidence: 99%
“…Clark and Lyon et al presented the concept of enzyme biosensors utilizing enzyme electrodes for the first time in 1962 (Clark et al, 2021). Horseradish, polyphenol oxidase, tyrosinase, lactate oxidase, peroxidase, alcohol dehydrogenase, cytochrome, glucose oxidase, and glutamate dehydrogenase are all often utilized in the construction of enzymatic biosensors (Kumar et al, 2020).…”
Section: Electrochemical Enzyme Biosensing Of Oral Diseasesmentioning
confidence: 99%
“…Different NPs (ZrO 2 , nHfO 2 , and TiO 2 ) have been electrophoretically deposited onto APTES treated ITO coated glass electrode followed by conjugation with mAb‐anti‐CYFRA‐21‐1 and BSA as the blocking agent. (Kumar et al, 2015, 2020; Kumar, Kumar, et al, 2016; Kumar, Kumar, & Sharma, 2018). The measurements were performed in PBS buffer at pH 7 containing [Fe(CN) 6 ] 3−/4− as the electrolyte species.…”
Section: Nano‐biosensors: a Step Towards Advanced Detection Platformsmentioning
confidence: 99%
“…Different NPs (ZrO 2 , nHfO 2 , and TiO 2 ) have been electrophoretically deposited onto APTES treated ITO coated glass electrode followed by conjugation with mAb-anti-CYFRA-21-1 and BSA as the blocking agent. (Kumar et al, 2015(Kumar et al, , 2020 F I G U R E 1 3 (a) Amplified signal generation via nano-ELISA method for detection of oral cancer-specific biomarker and (b) graphical representation of nanosensor-based microfluidic approach for sensitive detection of oral cancer biomarker Kumar, Kumar, & Sharma, 2018). The measurements were performed in PBS buffer at pH 7 containing [Fe(CN) 6 ] 3À/4À as the electrolyte species.…”
Section: Electrochemical Nano-biosensormentioning
confidence: 99%