Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, University of Lagos, Lagos, Nigeria.
Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, University of Lagos, Lagos, Nigeria.
Int J Biol Macromol. 2024 Oct;277(Pt 3):134484. doi: 10.1016/j.ijbiomac.2024.134484. Epub 2024 Aug 3.
Given the escalating prevalence of drug-resistant wounds, there is a justified imperative to explore innovative and more efficacious therapies that diverge from conventional, ineffective wound healing approaches. This research has introduced a strategy to address multi-drug resistant (MDR) Pseudomonas aeruginosa infections in a chronic wound model, employing MDR-specific phage Pɸ-Mi-Pa loaded onto mucoadhesive electrospun scaffolds. A cocktail of three isolates of P. aeruginosa-specific lytic phages, Pɸ-Mi-Pa 51, Pɸ-Mi-Pa 120, and Pɸ-Mi-Pa 133 were incorporated into varying ratios of fabricated PCL-PVP polymer. These formulations were assessed for their therapeutic efficacy in achieving bacterial clearance in P. aeruginosa-induced wound infections. The study encompassed biological characterization through in vivo wound healing assessments, histology, and histomorphometry. Additionally, morphological, mechanical, and chemical analyses were conducted on the fabricated PCL-PVP electrospun nanofibrous scaffolds. Three clonal differences of the MDR P. aeruginosa-specific phages (Pɸ-Mi-Pa 51, Pɸ-Mi-Pa 120, and Pɸ-Mi-Pa 133) produced lytic activity and were seen to produce distinct and clear zones of inhibition against MDR P. aeruginosa strains Pa 051, Pa 120 and Pa 133 respectively. The average porosity of the nanofibrous scaffolds PB 1, PB 2, PB 3, and PB 4 were 12.2 ± 0.3 %, 22.1 ± 0.7 %, 31.1 ± 2.4 %, 28.0 ± 0.8 % respectively. In vitro cumulative release of MDR-specific phage Pɸ-Mi-Pa from the mucoadhesive electrospun nanofibrous scaffolds was found to be 70.91 % ± 1.02 % after 12 h of incubation after an initial release of 42.8 % ± 3.01 % after 1 h. Results from the in vivo wound healing study revealed a substantial reduction in wound size, with formulations PB 2 and PB 3 exhibiting the most significant reduction in wound size, demonstrating statistically significant results on day 5 (100 % ± 31.4 %). These findings underscore the potential of bacteriophage-loaded electrospun PCL-PVP nanofibrous scaffolds for treating drug-resistant wounds, generating tissue substitutes, and overcoming certain limitations associated with conventional wound care matrices.
鉴于耐药性伤口的流行率不断上升,探索创新且更有效的治疗方法已成为当务之急,这些方法与传统的无效伤口愈合方法不同。本研究提出了一种在慢性伤口模型中解决多药耐药(MDR)铜绿假单胞菌感染的策略,该策略使用负载有多药耐药特异性噬菌体 Pɸ-Mi-Pa 的粘膜粘附性静电纺丝支架。三种铜绿假单胞菌特异性裂解噬菌体 Pɸ-Mi-Pa 51、Pɸ-Mi-Pa 120 和 Pɸ-Mi-Pa 133 的混合物以不同比例掺入到 PCL-PVP 聚合物中。评估了这些配方在实现铜绿假单胞菌诱导的伤口感染中清除细菌的治疗效果。该研究通过体内伤口愈合评估、组织学和组织形态计量学进行了生物学特征描述。此外,还对制备的 PCL-PVP 静电纺丝纳米纤维支架进行了形态、机械和化学分析。三种多药耐药铜绿假单胞菌特异性噬菌体(Pɸ-Mi-Pa 51、Pɸ-Mi-Pa 120 和 Pɸ-Mi-Pa 133)的克隆差异产生了裂解活性,并且针对多药耐药铜绿假单胞菌菌株 Pa 051、Pa 120 和 Pa 133 分别产生了明显且清晰的抑制区。纳米纤维支架 PB1、PB2、PB3 和 PB4 的平均孔隙率分别为 12.2±0.3%、22.1±0.7%、31.1±2.4%、28.0±0.8%。在体外,负载多药耐药特异性噬菌体 Pɸ-Mi-Pa 的粘膜粘附性静电纺丝纳米纤维支架在孵育 12 小时后的累积释放率为 70.91%±1.02%,在孵育 1 小时后的初始释放率为 42.8%±3.01%。体内伤口愈合研究的结果表明,伤口面积显著减小,其中配方 PB2 和 PB3 表现出最小的伤口面积减小,在第 5 天(100%±31.4%)时显示出统计学上的显著结果。这些发现强调了负载噬菌体的静电纺丝 PCL-PVP 纳米纤维支架在治疗耐药性伤口、生成组织替代物以及克服传统伤口护理基质相关的某些局限性方面的潜力。