Ruthenium complex and nanometer silver composite hydrotalcite type nanometer material and preparation method and application thereof
A technology of ruthenium complexes and nanomaterials, applied in the field of ruthenium complexes combined with nano-silver composite hydrotalcite-type nanomaterials and its preparation, can solve problems such as ineffective and slow antibacterial drug treatment
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Embodiment 1
[0076] The preparation of embodiment 1 Ag-Ru / LDH material
[0077] 1) Preparation of Mg-Al / LDH by co-precipitation method
[0078] Take Mg(NO 3 ) 2 ·6H 2 O (10.26g, 0.04mol), Al(NO 3 ) 3 9H 2 O (7.53g, 0.02mol) and 55mL deCO 2 Add ultrapure water into a 100mL flask, protect it with nitrogen, adjust the pH of the above mixed solution to 9 with 2M NaOH, and react at 75°C for 24h, keep the pH constant throughout the reaction process, after the reaction, centrifuge at 5000rpm for 5min The precipitate was collected, rinsed three times with ultrapure water, and then dried in vacuum at 60°C for 24 h.
[0079] 2)[Ru(H 2 dcbpy) 3 ] Cl 2 (hereinafter referred to as "Tris-Ru") preparation: under nitrogen atmosphere, 4,4'-dicarboxylic acid-2,2'-bipyridine 754mg (3.09mmol) and ruthenium trichloride trihydrate 261mg (1mmol) were dissolved in 60mL N,N-dimethylformamide (DMF), reflux at 160°C for 3h. Add 12mL of 0.5M NaOH to reflux for 4h, concentrate to 10mL, cool to room tempera...
Embodiment 2
[0089] The bactericidal activity of embodiment 2 Ag-Ru / LDH
[0090] 1. Culture medium preparation:
[0091] Luria-Bertani medium (LB medium), its formula is: 1% NaCl, 1% Tryptone, 0.5% Yeastextract.
[0092] Another double-concentration LB medium was prepared, denoted as: 2×LB, used as a dilution material, and its formula was: 2% NaCl, 2% Tryptone, 1% Yeast extract.
[0093] Prepare 1L of LB medium and 100mL of 2×LB according to the above formula, and distribute them into 10mL test tubes and 25mL Erlenmeyer flasks respectively, with 4mL in test tubes and 10mL in Erlenmeyer flasks. Sterilize at 121°C and 0.15MPa for 15 minutes, cool to room temperature, and set aside.
[0094] Second, the recovery of bacteria
[0095] Take out the frozen Escherichia coli and Staphylococcus aureus from the refrigerator at minus 80°C, put them on the ice box to thaw, take 20 μL of the bacteria solution and inoculate them into 25 mL Erlenmeyer flasks, and cultivate to the OD of the bacteria sol...
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