Lotion and use thereof
A technology of lotion and conditioner, which is applied in the field of medicine, can solve the problems of female reproductive system flora imbalance, loss, underwear pollution, etc., and achieve the effect of comprehensively regulating the microecological balance of the vagina or skin
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Embodiment 1
[0070] Embodiment 1 group to embodiment 7 groups of lotions.
[0071] Test method: HPV infection specimen preparation: The specimens taken from the outpatient clinic of the hospital (the HPV type is HPV16, HPV18 and HPV52 mixed types, belonging to the high-risk mucosal type) collected from the outpatient clinic of the hospital were collected into a centrifuge tube, weighed 30 mg, and mixed with glass. Homogenize with a mixer, add 5ml of normal saline, and make a 6mg / ml in vitro suspension for later use.
[0072] Sample processing method: use a pipette gun to draw 50 μl of sample solution and 50 μl of specimen suspension into a 15ml centrifuge tube, shake evenly, so that the sample and specimen can fully interact, culture in a 37°C water bath, and treat the specimen for 1 day , 3 days, 5 days, and 7 days later, one group was taken for the following test.
[0073] Extraction of HPV-DNA: Take out the sample-treated sample suspension from the water bath, and extract DNA according...
Embodiment 7
[0095] Table 7 embodiment 7 products are to the MIC and MBC of standard bacterial strain
[0096]
[0097] As can be seen from the above table, the lotion of the present invention is effective to the selected Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus epidermidis, Proteus vulgaris, Streptococcus faecalis, Neisseria gonorrhoeae selected by the test. Both the marked strains and the clinical reference strains of Gardnerella vaginalis have obvious inhibitory and inactivation effects, and their MBC is 2 to 4 times that of the MIC.
Embodiment 4
[0098] Embodiment 4: anti-herpes virus effect
[0099] Experimental cells and viruses: human liver cancer Hep-2 cells and HSV-II virus were provided by the Institute of Virology, School of Medicine, Wuhan University.
[0100] Test animals: female clean-grade Kunming mice, weighing 17±1g.
[0101] (1) Anti-virus test method: take 0.8×10 5 / mL concentration of Hep-2 cells, added to a 24-well plate, 37 ° C, 5% CO 2 Culture in the incubator for 24 hours, after the cells grow into a single layer, discard the supernatant, add 1000TCID 50 / mL of HSV-II, 0.1mL / well, 37°C, 5% CO 2 , adsorbed for 90min, discarded the supernatant, added drug-containing maintenance solution to be tested, and repeated 4 wells for each drug. 37°C, 5% CO 2 After culturing for 33 hours, the virus inhibition rate was detected by MTT method.
[0102] Inhibition rate = (average OD value of drug-dosed wells - average OD value of solvent wells) × 100% / average OD value of solvent wells.
[0103] Test results...
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