Synergistic antimicrobial nanocomposite: Protamine-loaded PVP-capped silver nanoparticles for combating multidrug-resistant infections

抗菌剂 Zeta电位 化学 银纳米粒子 铜绿假单胞菌 金黄色葡萄球菌 体内 微生物学 最小抑制浓度 体外 细菌生长 硝酸银 鱼精蛋白 大肠杆菌 抗菌活性 药品 纳米颗粒 抗生素耐药性 抗药性 菌落形成单位 纳米技术 效力 细菌 琼脂扩散试验 双胍
作者
Mohammad Jaafreh,Walhan Alshaer,Mahmoud Alkawareek,Zalına Zaharı,Shrouq Alsotari,Dana A. Alqudah,Hazem Choukaife,Manal A. Abbas,Yasser Bustanji,Mulham Alfatama
出处
期刊:Asian Journal of Pharmaceutical Sciences [Elsevier BV]
卷期号:21 (3): 101160-101160
标识
DOI:10.1016/j.ajps.2026.101160
摘要

The emergence of multidrug-resistant (MDR) bacterial infections has become a critical global health concern, driving the urgent need for innovative therapeutic strategies beyond conventional antibiotics. In this study, we developed a novel nanotherapeutic platform comprising protamine-loaded poly(N-vinyl-2-pyrrolidone)-stabilized silver nanoparticles (PVP-AgNPs) designed to enhance antimicrobial efficacy while improving biocompatibility. AgNPs were synthesized via chemical reduction using silver nitrate and sodium borohydride, with PVP serving as a stabilizing and capping agent. Protamine sulfate, a cationic antimicrobial peptide, was subsequently incorporated to exploit its strong affinity for bacterial membranes and synergistic bactericidal effects. The resulting nanoparticles exhibited spherical morphology with an average diameter of 70.96 ± 0.27 nm, a PDI of 0.25 ± 0.002, a zeta potential of +10.4 ± 0.15 mV, and a protamine loading efficiency of 66.2% ± 3.2%, indicating excellent colloidal stability and drug incorporation. In vitro antimicrobial testing demonstrated a two- to four-fold reduction in minimum inhibitory concentration values compared to blank PVP–AgNPs and free protamine, with disk diffusion assays confirming significantly enhanced activity against both Gram-positive ( Staphylococcus aureus ) and Gram-negative ( Escherichia coli, Pseudomonas aeruginosa ) bacteria. Furthermore, in vivo evaluation using a murine wound infection model showed effective bacterial clearance, accelerated wound closure, and improved tissue regeneration. These findings demonstrate that protamine-loaded PVP-AgNPs offer multimodal antibacterial activity, enhanced cytocompatibility, and the potential to overcome resistance mechanisms. Collectively, this work introduces a promising nanotherapeutic strategy for managing MDR infections and promoting wound healing, with significant implications for future biomedical applications.
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