Up－Regulated miR-224-5p Can Target the Expression of Neuritin in Hearing Loss

Objective: This study screened the differentially expressed miRNAs in the mouse cochlea during hearing loss and explored the relationship between miR-224-5p and Neuritin.Methods: The combination of kanamycin sulfate and furosemide was used to establish a mouse hearing loss model. High-throughput sequencing was used to screen the differentially expressed miRNAs during hearing loss. qRT-PCR was used to identify the expression of differential miRNAs in hearing loss. Western Blot was used to detect the expression of Neuritin protein. Luciferase was used to identify the binding site of miRNA and Neuritin.Results: The expression of miR-224-5p in the mouse cochlea increased during hearing loss (p<0.05). MiR-224-5p mimics can reduce Neuritin protein expression in 293T cells (p<0.05). MiR-224-5p can specifically bind to Neuritin (p<0.05).Conclusion: The expression of miR-224-5p increases in hearing loss and targets the expression of Neuritin

PCN-222@g-C3N4 cathodic materials for “signal-off” photoelectrochemical sensing of kanamycin sulfate

The PCN-222@g-C3N4 was firstly used as a photoelectrically active material for the detection of kanamycin sulfate; The sensor has lower detection limit and the broad detection range for kanamycin sulfate.

Carbon dots derived from kanamycin sulfate with antibacterial activity and selectivity for Cr6+ detection

Schematic of the synthetic route for fluorescent CDs-Kan and the applications in the Antibacterial, bioimaging and detection of Cr6+.

Validation of TLC-contact bioautography and TLC-densitometry methods for simultaneous limit test of streptomycin sulfate and kanamycin sulfate residues in fresh fish meat

A simple, sensitive, and accurate TLC method was combined and validated for a simultaneous limit test of streptomycin sulfate and kanamycin sulfate residues in fresh fish meat. The optimum mobile phase was 10% potassium dihydrogen phosphate. TLC-contact bioautography used Staphylococcus aureus ATCC 29737 as a test organism. For TLC-densitometry, analyte spots were detected using 1% w/v ninhydrin in ethanol and maximum absorbance at 400 nm. TLC-contact bioautography and TLC-densitometry methods were validated according to USP guidelines for the limit test with respect to selectivity and limit of detection (LOD) added with the accuracy of a recovery test of streptomycin sulfate and kanamycin sulfate in fresh fish samples was developed and validated. The result of LOD from the TLC-contact bioautography method for streptomycin sulfate and kanamycin sulfate were obtained 0.7028 μg and 0.8032 μg, respectively. Meanwhile, LOD of the TLC-densitometry method for streptomycin sulfate and kanamycin sulfate were obtained 0.0631 μg and 0.0685 μg, respectively. In this study, TLC-contact bioautography method showed better results than TLC-densitometry. TLC-contact bioautography appears a good choice for the simultaneous limit test of streptomycin sulfate and kanamycin sulfate residues in fresh fish samples.