Abstract: The present invention provides a liver hypothermic machine perfusion preservation device and a method. The device includes a perfusion loop and a controller, wherein the perfusion loop includes a main pump, a main reservoir, an auxiliary pump and an auxiliary reservoir. The main pump is connected to an inlet of the main reservoir and configured to pump a perfusate from an organ cassette into the main reservoir; an outlet of the main reservoir is connected to a portal vein and a hepatic artery of a liver, and the main reservoir is configured to supply the perfusate to the portal vein and the hepatic artery; and the auxiliary reservoir and the auxiliary pump provide an additional hepatic artery perfusion flow path. According to the present invention, for a poor internal environment of the hepatic artery, the main reservoir and the auxiliary reservoir cooperate with each other to carry out perfusion, so that the perfusion efficiency and effect of the hepatic artery can be improved.

Abstract: The present invention discloses a fluorescent probe for detecting a sulfenated protein, which has good stability and can specifically quantitatively detect a sulfenated protein in complex biological samples, and has a good detection ability of signal-to-noise ratios, is highly sensitive, and has excellent selectivity, thereby realizing specific detection of sulfhydryl sulfenation modification of intracellular proteins.

Abstract: The present invention discloses a fluorescent probe for detecting a sulfenated protein, having the following structural general formula (I). The fluorescent probe has good stability and can be preserved for long-term use. The fluorescent probe is highly sensitive to its environment, having no strong fluorescence in a hydrophilic environment, and producing strong fluorescence only after reaction with a sulfenated protein such that a fluorophore is in a hydrophobic environment in the protein structure, and thus is able to develop in situ in cells the sulfhydryl sulfenated protein. Furthermore, the fluorescent probe has good water solubility and a relatively large absorption-emission wavelength difference, and can be paired with a tryptophan residue in a protein to produce a fluorescence resonance energy transfer (FRET) effect in an extracellular buffer solution detection system, effectively avoiding interference of excitation light and emitted light in protein samples.

Abstract: A method for simultaneously measuring the activities of multiple kinds of enzymes in single channel through concimitantly monitoring multiple wavelength absorbances is claimed; based on linear additivity of absorbances and the isoabsorbance wavelengths of chromogenic substrates and their chromogenic products, both the principles for the combination of chromogenic substrates required for simultaneously measuring the activities of multiple kinds of enzymes in single channel through concimitantly monitoring multiple wavelength absorbances and an approach for data processing to eliminate the interference of the overlapped absorbances are developed, kinetic analysis of reaction curves via numerical integration eliminates the interference of all substrates and products and estimates the maximal reaction rates of the enzymes to be measured, giving the linear ranges and the limits of quantification for simultaneously measuring the activities of multiple kinds of enzymes in single channel comparable to those by separa

Abstract: A method for simultaneously measuring the activities of multiple kinds of enzymes in single channel through concimitantly monitoring multiple wavelength absorbances is claimed; based on linear additivity of absorbances and the isoabsorbance wavelengths of chromogenic substrates and their chromogenic products, both the principles for the combination of chromogenic substrates required for simultaneously measuring the activities of multiple kinds of enzymes in single channel through concimitantly monitoring multiple wavelength absorbances and an approach for data processing to eliminate the interference of the overlapped absorbances are developed, kinetic analysis of reaction curves via numerical integration eliminates the interference of all substrates and products and estimates the maximal reaction rates of the enzymes to be measured, giving the linear ranges and the limits of quantification for simultaneously measuring the activities of multiple kinds of enzymes in single channel comparable to those by separa