Use of iminophenazine compounds as rabies virus inhibitors
A rabies virus and compound technology, applied in the field of medicine, can solve the problems of high price, difficulty in wide use, and high price of immunoglobulin
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Embodiment 1
[0071] Embodiment 1. Construction of pseudovirus
[0072] 1.1 Antiviral Drug Screening Principle Based on Pseudovirus
[0073] For an enveloped virus (eg, rabies virus), the process of cell entry is determined by its envelope protein, since the envelope is responsible for recognizing receptors on the surface of target cells and initiating the process of adsorption and penetration. Furthermore, the phenotypic mixing that occurs when two viruses co-infect a cell suggests that the envelope of one virus can be integrated on the particle surface of a different virus. Based on the above two points, a new technology—pseudovirus technology has been developed in the study of the process of virus invasion into cells and its tissue tropism and receptors.
[0074] The current pseudovirus refers to a retrovirus that can integrate the envelope glycoprotein of another different type of virus to form an envelope with an exogenous virus, and the genome maintains the genomic characteristics ...
Embodiment 2
[0092] Embodiment 2.RV-07 is to the evaluation of the inhibitory activity of rabies pseudovirus
[0093] In this embodiment, the rabies virus inhibitory activity of RV-07 (clofazimine national standard product, provided by the China National Institutes for Food and Drug Control Standard Material) was evaluated by using the rabies pseudovirus as described above.
[0094] Since the pseudovirus backbone plasmid pSG3Δenv.cmvFluc used in the present invention is derived from HIV, in order to exclude the possibility that the drug inhibits the pseudovirus by preventing the reverse transcription process of the backbone HIV, the present invention utilizes the rabies pseudovirus primary screening drug while utilizing A chimeric pseudovirus containing vesicular stomatitis virus (VSV) membrane protein was re-screened to exclude false positives. Calculate the ratio of the drug to the 50% inhibitory concentration (IC50) of the VSV membrane protein chimeric pseudovirus and the rabies virus m...
Embodiment 3
[0107] Cytotoxicity evaluation of embodiment 3.RV-07
[0108] In this embodiment, the influence of RV-07 (the national standard product of clofazimine, provided by the China Institute for Food and Drug Control Standard Materials) on cell viability was evaluated through the quantitative determination of ATP. The detection principle is as follows:
[0109] ATP is an indicator of metabolism in living cells, using CellTiter- Luminescence method cell viability detection kit, through the quantitative determination of ATP to detect the number of living cells in the culture after the action of drugs and cells, the cell lysis and the luminescent signal produced are proportional to the amount of ATP present, and the amount of ATP is directly related to the culture Proportional to the number of cells in . The 50% cytotoxic concentration (CC50) of the drug was calculated by the effect of the drug on the ATP luminescent signal in the cells. Calculate the ratio of the 50% cytotoxic conce...
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