已发表论文

纳米系统作为对抗金黄色葡萄球菌感染的有效方法的综述

 

Authors Zhou KX, Li C, Chen DM, Pan YH, Tao YF, Qu W, Liu ZL, Wang XF, Xie SY

Received 2 April 2018

Accepted for publication 24 July 2018

Published 9 November 2018 Volume 2018:13 Pages 7333—7347

DOI https://doi.org/10.2147/IJN.S169935

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 2

Editor who approved publication: Dr Linlin Sun

Abstract: Staphylococcus aureus  (Saureus ) is an important zoonotic bacteria and hazardous for the health of human beings and livestock globally. The characteristics like biofilm forming, facultative intracellular survival, and growing resistance of Saureus  pose a great challenge to its use in therapy. Nanoparticles are considered as a promising way to overcome the infections’ therapeutic problems caused by Saureus . In this paper, the present progress and challenges of nanoparticles in the treatment of Saureus  infection are focused on stepwise. First, the survival and infection mechanism of Saureus  are analyzed. Second, the treatment challenges posed by Saureus  are provided, which is followed by the third step including the advantages of nanoparticles in improving the penetration and accumulation ability of their payload antibiotics into cell, inhibiting Saureus  biofilm formation, and enhancing the antibacterial activity against resistant isolates. Finally, the challenges and future perspective of nanoparticles for Saureus  infection therapy are introduced. This review will help the readers to realize that the nanosystems can effectively fight against the Saureus  infection by inhibiting biofilm formation, enhancing intracellular delivery, and improving activity against methicillin-resistant Saureus  and small colony variant phenotypes as well as aim to help researchers looking for more efficient nanosystems to combat the Saureus  infections.
Keywords: Staphylococcus aureus , infection mechanism, resistance, antibiotics, nanoparticles




Figure 1 The schematic diagram of Staphylococcus aureus permeabilization into cell membrane via β-toxin and δ-toxin.