The development of a novel ultrashort antimicrobial peptide nanoparticles with potent antimicrobial effect

被引:7
|
作者
Salama, Ali [1 ]
机构
[1] Middle East Univ, Fac Pharm, Amman, Jordan
关键词
antibiotics; peptides; nanoparticles; chitosan; MRSA; DRUG-DELIVERY;
D O I
10.3897/pharmacia.69.e81954
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Conventional antibiotics are facing significant microbial resistance, which has recently reached previously unnoticed critical levels. As a result of this situation, a large proportion of antimicrobial agents currently used in the clinic have significantly reduced therapeutic potential. Antimicrobial peptides (AMPS) may offer the medical community an alternative strategy to traditional antibiotics in the fight against microbial resistance. Current research efforts arc focused on developing technologies that may reduce AMP toxicity while retaining their potent antimicrobial activity and possibly improving their delivery. The ionotropic gelation method was used to encapsulate a novel in-house designed potent ultrashort antimicrobial peptide (USAMP) into chitosan-based nanoparticles (CS-NPs) in this study. WRWRWR -CS-NPs were tested for antibacterial kinetics against two strains of Staphylococcus aureus for four days, and the developed WRWRWR -CS-NPs showed a 3-log decrease in the number of colonies when compared to CS-NP and a 5-log decrease when compared to control bacteria. Loaded WRWRWR into CS-NPs could represent an innovative approach to develop delivery systems based on NPs technology for achieving potent antimicrobial effects against multi-drug resistant and biofilm forming bacteria with negligible systemic toxicity and reduced synthetic costs that are obstructing the clinical development of AMPs generally.
引用
收藏
页码:255 / 260
页数:6
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