Logo image
Nitazoxanide-Gold Nanoparticles Combat Carbapenem-Resistant Enterobacteriaceae via Membrane Disruption and Oxidative Stress
期刊文章

Nitazoxanide-Gold Nanoparticles Combat Carbapenem-Resistant Enterobacteriaceae via Membrane Disruption and Oxidative Stress

Zhuocheng Yao, Jia Zhang, Panjie Hu, Juan Pan, Endian Sun, Haifeng Liu, Zeyong Zhong, Tieli Zhou, Chunquan XuZai-Fu Yao
ACS infectious diseases, 卷.12(3), 頁碼.1122-1134
13/03/2026
PMID: 41655259
Web of Science ID: WOS:001685257100001

摘要

Animals Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Carbapenem-Resistant Enterobacteriaceae - drug effects Cell Membrane - drug effects Enterobacteriaceae Infections - drug therapy Enterobacteriaceae Infections - microbiology Gold - chemistry Metal Nanoparticles - chemistry Mice Microbial Sensitivity Tests Nitro Compounds Oxidative Stress - drug effects Reactive Oxygen Species - metabolism Thiazoles - administration & dosage Thiazoles - chemistry Thiazoles - pharmacology
Carbapenem-resistant Enterobacteriaceae (CRE) pose a serious global health threat due to the ineffectiveness of conventional antibiotics, highlighting the need for new therapeutic strategies. This study explores the potential of nitazoxanide (NTZ), a clinically approved broad-spectrum antiparasitic drug, functionalized onto gold nanoparticles (AuNPs) as an antibacterial approach against CRE. NTZ_AuNPs were synthesized using a one-pot method, and their antibacterial efficacy was assessed through antimicrobial susceptibility testing, bacterial growth analysis, and electron microscopy. Biosafety was evaluated through hemolysis assays and murine models. The NTZ_AuNPs showed significant bactericidal activity against CRE, with MICs ranging from 4 to 8 μg/mL, and exhibited favorable biocompatibility. Mechanistic investigations revealed that NTZ_AuNPs disrupt bacterial membranes, enhance outer membrane permeability, and infiltrate the intracellular environment. Additionally, NTZ_AuNPs increase reactive oxygen species (ROS) levels and impair bacterial ATP synthesis, suggesting a dual mechanism involving membrane disruption and oxidative stress. In a mouse model of abdominal infection, NTZ_AuNPs reduced bacterial burden and improved survival rates. These results validate the potential of NTZ_AuNPs as an effective, low-toxicity treatment for CRE infections, offering a promising alternative to traditional antibiotics.

相關連結

指標

1 檢視次數

詳細資料

Logo image