Inhibitor Lo-isohexyl for resisting virulence of staphylococcus aureus and formation of biofilms, and application of inhibitor Lo-isohexyl
A staphylococcus and biofilm technology, applied in the direction of local antibacterial agents, medical preparations containing active ingredients, antibacterial drugs, etc., can solve problems such as chronic infection, limited selection of clinical antibacterial drugs, and reduce the sensitivity of antibacterial drugs. Strong inhibitory activity, inhibitory effect on virulence and biofilm formation
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Embodiment 1
[0039] Lo-isohexyl was prepared using the following steps:
[0040]
[0041] The desloratadine reactant (I) is dissolved in an organic solvent, and triethylamine is used as an acid-binding agent, and an organic solution having a reactant (III) is added, wherein the reactant (I) and the reactant (III ) in a molar ratio of 1:1 to 1.5, the two were mixed, stirred and reacted at -5°C to obtain a reaction solution containing Lo-isohexyl. Wherein organic solvent can be a kind of in dichloromethane, chloroform, acetone, acetonitrile, tetrahydrofuran, DMF, pyridine or toluene. Wherein the reactant (III) is obtained through a conventional synthesis reaction.
[0042] After the reaction, the reaction liquid was poured into cold water, fully shaken and separated into layers, the organic layer was extracted, and washed three times with water continuously. The organic layer was dried and set aside. Then filter and evaporate the solvent under reduced pressure to obtain the compound Lo-i...
Embodiment 2
[0044] The compound Lo-isohexyl inhibits the biofilm formation experiment of Staphylococcus aureus.
[0045] Detection of biofilm formation of strains: Staphylococcus aureus strains were cultured overnight in TSB medium at 37°C and 220 rpm / min for 10-12 hours. Dilute the bacterial solution 1:200 (with or without Lo-isohexyl) with TSBG medium (TSB medium + 0.5% glucose), add 200ul per well to a 96-well plate (Costar 3599), and set 3 replicate wells for each strain , and cultured statically at 37°C for 24h. Discard the supernatant, wash with PBS 3 times (200ul / well / time), dry at room temperature, add methanol for fixation for 15min (200ul / well), discard methanol and add 100ul of 0.5% crystal violet staining solution to each well after drying at room temperature. Stain at room temperature for 10 minutes, gently elute the crystal violet staining solution under clean water until the running water is colorless, dry at room temperature and read OD on a microplate reader 570 value. ...
Embodiment 3
[0049] Compound Lo-isohexyl inhibits aureus pigment production and hemolytic activity of Staphylococcus aureus.
[0050] Detection of golden yellow pigment of bacterial strains: cultured with TSB medium at 37° C. for 48 hours (with or without Lo-isohexyl), centrifuged 3 ml of bacterial culture and washed twice with 0.01 M phosphate buffered saline (PBS). After washing the cell pellet with PBS, discard the supernatant, add 300ul methanol (100%) to the cell pellet, pipette the resuspended bacteria solution, shake for 5 minutes after resuspension, centrifuge (12000r / min, centrifuge for 1-2 minutes), and then Aspirate the supernatant extract into a clean EP tube, then add 300-350ul methanol (100%) to the cell pellet, repeat 2 times, suck out the extract each time, and finally extract these 3 times together After mixing about 1ml of the solution thoroughly, take 200ul and add it to a 96-well plate (three duplicate wells), and measure the OD450 value on a microplate reader. The abo...
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