Ag/ZIF-8 anti-bacterial agent and preparation method thereof
A technology of ZIF-8 and antibacterial agent, which is applied in the field of Ag/ZIF-8 nano-bacteriostatic agent and its preparation, can solve problems such as easy aggregation of silver nanoparticles, poor stability, and limited antibacterial effect, and achieve good stability, The effect of mild synthetic conditions and broad antibacterial spectrum
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Embodiment 1
[0030] Embodiment 1 adopts impregnation-reduction method to prepare Ag / ZIF-8 nano antibacterial agent
[0031] S1. Synthesis of ZIF-8
[0032] Take 125mL deionized water and add it to the Erlenmeyer flask, add 1.88g Zn(NO 3 )·6H 2 O, 1.2665g CTAB, 2.1425g histidine were ultrasonically dissolved to obtain liquid A;
[0033] Take 125mL of deionized water and add it to another Erlenmeyer flask, add 4.074g of 2-methylimidazole and 6.8565ml of triethylamine for ultrasonic dissolution to obtain liquid B;
[0034] Pour liquid B into liquid A, stir and reflux for 7 hours at a temperature of 20-60°C. The volume ratio of methanol: deionized water = 1:1 was used to centrifuge and wash 3 times, and then refluxed 3 times with methanol, 40min each time, and centrifugally dried to obtain white powder ZIF-8.
[0035] Synthesis of S2.Ag / ZIF-8
[0036] Take 4ml of methanol and add to the Erlenmeyer flask, add 0.5g of ZIF-8, 0.01g of AgNO 3 React for 2 hours, then gradually add 89 mg of so...
Embodiment 2
[0038] Ag / ZIF-8 prepared in the embodiment 1 is evaluated by shake flask method to the bacteriostatic effect of Staphylococcus aureus (Gram-positive bacteria) and Escherichia coli (Gram-negative bacteria), test result is as follows image 3 shown.
[0039] Staphylococcus aureus and Escherichia coli were cultured in LB (Luria-Bertani) broth at 37°C for 12 hours. Disperse 0-12mgAg / ZIF-8 into 40ml LB liquid medium respectively, add 400μL concentration of 10 8 CFU / ml of Staphylococcus aureus and E. coli suspension. Bacterial growth rate was measured by monitoring the optical density at 600 nm while incubating at 37°C. image 3 (a) is the antibacterial effect of Staphylococcus aureus, image 3 (b) is the antibacterial effect of Escherichia coli; it can be clearly seen from the figure that after adding Ag / ZIF-8 to the liquid medium, the growth rate of bacteria can be significantly reduced.
Embodiment 3
[0041] The Ag / ZIF-8 nanometer bacteriostatic agent prepared in the plate method evaluation embodiment 1 is to the bacteriostasis of escherichia coli (gram-negative bacterium) and Bacillus subtilis (gram-positive bacterium), test result is as follows Figure 4 shown.
[0042] Disperse 0-12mgAg / ZIF-8 nanomaterials into 40ml agar medium, and then 50μL concentration of 10 5 The bacterial suspension of CFU / ml was evenly spread on the agar plate, and then cultured at 37° C. for 12 hours, and the number of bacterial colonies was observed. Figure 4 (a) is Escherichia coli plate antibacterial effect, Figure 4 (b) is the antibacterial effect of Bacillus subtilis plate. From Figure 4 It can be clearly seen that Ag / ZIF-8 has significant antibacterial effect on both Gram-positive bacteria and Gram-negative bacteria, and the antibacterial effect is more obvious with the increase of Ag / ZIF-8 concentration. It can be seen that Ag / ZIF-8 has broad-spectrum antibacterial activity.
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