The invention discloses a preparation method of a 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster comparable with
vancomycin and an application of the 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster in infection, and the 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster is used for treating methicillin-resistant
staphylococcus aureus. The result shows that the 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster can be adsorbed on the surface of
bacteria, down-regulate a Na < + > / H < + >
transporter on a
cell membrane, influence the potential of the
cell membrane, reduce the activity of bacterial
ATPase synthetase and the generation of ATP, and finally show the effect of killing the
bacteria. The 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster is good in antibacterial stability, low in
cytotoxicity and good in
blood compatibility, and in a rat
wound infection model experiment, the gold nanocluster has a relatively remarkable
curative effect of promoting
wound healing, is mainly characterized by reduction of local
inflammation, increase of generation of blood vessels and collagenous fibers, down-regulation of
inflammatory factors and the like, and can be used for preparing a
drug for treating
wound healing. And no obvious
side effect is observed during the
treatment period. The 2-sulfydryl-1, 3, 4-thiadiazole-gold nanocluster can be used as a material comparable to
vancomycin and used for treating infection caused by methicillin-resistant
staphylococcus aureus.