Inorganic-organic hybrid keggin-type polyoxometalate complex, its preparation method and its application in antibacterial
A technology of polyoxometalates and organic hybridization, which is applied in organic chemistry, antibacterial drugs, organic active ingredients, etc., can solve the problems of instability of pure inorganic substances, limit cell penetration, etc., and achieve good bactericidal effect Effect
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Embodiment 1
[0035] A preparation method of an inorganic-organic hybrid Keggin-type polyoxometalate complex, comprising the following steps:
[0036] The Co(NO 3 ) 2 ·6H 2 O (0.189 g, 1.3 mmol), Na 2 MoO 4 ·2H 2 O (0.48 g, 2.0 mmol), EDTMP (0.35 g, 0.8 mmol), and 2-acetylpyrazine thiosemicarbazide (0.097 g, 0.5 mmol) were added to 60 mL of water and methanol (2:1 by volume) In the mixed solvent, stir for 40 minutes until the dissolution is complete, adjust the pH value between 2.5 and 3.0 with dilute hydrochloric acid, then transfer it to a reaction flask, put it in a polytetrafluoroethylene liner, keep it at 130 ° C for 3 days, and cool it. At room temperature, washed with water and air-dried to obtain black quadrilateral crystals, which are composites.
[0037] The above-mentioned inorganic-organic hybrid Keggin-type polyoxometalate belongs to the monoclinic crystal system, C2 / c space group, whose unit cell parameters are: a = 29.1829(13) Å, b = 16.5031(7) Å, c = 18.9095(9) Å...
Embodiment 2
[0047] Antibacterial effect evaluation method 1 Disc diffusion method:
[0048] Taking DMSO as blank control group, the antibacterial activity of this material was studied by agar plate test. The complexes were diluted with DMSO in gradients (1 mg / mL, 0.5 mg / mL, 0.25 mg / mL, 0.125 mg / mL, 0.0625 mg / mL, 0.03125 mg / mL…) prior to testing. All materials used during testing were autoclaved and nutrient agar plates (NA) were sterilized by UV radiation for 1 hour. will 10 7 CFU / mL of Staphylococcus aureus ( S. aureus ), Bacillus subtilis ( B. subtilis ) and 10 6 CFU / mL of Escherichia coli ( E. coli ) and Agrobacterium tumefaciens ( A. tumefaciens) were evenly coated on the nutrient agar (NA) plate, and then punched, and the prepared complexes were sucked into the agar plate holes in turn, then sealed, and the culture was incubated at 37 ° C for 16 hours. , and finally, the size of the zone of inhibition (ZOI) of all samples was measured, and the optical images were recorded...
Embodiment 3
[0054] Time Kill Experiment Evaluation 2 Colony Forming Unit (CFU) Method:
[0055] The bactericidal ability of the complex was studied by plate coating culture method. Serial dilutions of E. coli and S. aureus solutions to 10 5 CFU / mL, and prepare a 1 mg / mL complex solution. Equal volumes of inoculated bacterial solution and complex solution were incubated at 37°C for different times. The bacterial solution without complexes was used as a control experiment. The mixed solution incubated at different times was evenly spread on nutrient agar (NA) plates. The assay was repeated three times and incubated in a constant temperature incubator at 37°C for 16 hours. The experiment continued until few colonies were observed. The experimental results show that Figure 9 and 10 . Bacterial cell survival rate (%) = (the number of colonies in the experimental group / the number of colonies in the control group) × 100%.
[0056] Figure 9 and Figure 10 The complex pairs of the pres...
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