4.8 Article

Antibiotic-loaded reactive oxygen species-responsive nanomedicine for effective management of chronic bacterial prostatitis

期刊

ACTA BIOMATERIALIA
卷 143, 期 -, 页码 471-486

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2022.02.044

关键词

Chronic bacterial prostatitis; Cefpodoxime proxetil; Reactive oxygen species; Nanomedicines; Targeted therapy; Chronic bacterial prostatitis; Cefpodoxime proxetil; Reactive oxygen species; Nanomedicines; Targeted therapy

资金

  1. National Natural Science Foundation of China [82070779]
  2. Key Support Object of Army Medical University [410301060191]

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The study fabricated cefpodoxime proxetil (CPD)-loaded nanoparticles for targeted treatment of chronic bacterial prostatitis, which demonstrated efficient eradication of bacteria, relief of pain, and reduction of proinflammatory cytokine expression in prostate tissues.
Chronic bacterial prostatitis (CBP) occurs frequently in the male population and significantly influences quality of life. Antibiotics are the main strategy for managing chronic bacterial prostatitis; however, most antibiotics have low efficacy due to their poor penetration of prostate tissues. To overcome this challenge, we fabricated cefpodoxime proxetil (CPD)-loaded reactive oxygen species (ROS)-responsive nanoparticles (NPs) for targeted treatment of CBP. These NPs were modified with folic acid (FA) and could be effectively internalized by bacteria-infected macrophages and prostatic epithelial cells because of the high expression of folate receptors (FRs) in these cells. In vitro cellular assays demonstrated that the CPD-loaded nanomedicine can obviously reduce proinflammatory cytokine expression in cells since the nanomedicine can efficiently eradicate cellular bacteria. In vivo imaging results verified that FA-modified nanomedicines can penetrate the prostatic epithelium and accumulate in the glandular lumen because FRs overexpression was also observed in the prostate tissues of CBP mice. Animal experiments demonstrated that FAmodified nanomedicine can remarkably relieve pelvic pain in CBP mice and dramatically decrease proinflammatory cytokine expression in prostate tissues via eradication of bacteria and scavenging of ROS. Our results provide a new strategy to deliver antibiotics for targeted therapy of CBP.

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