Lim Young H, Tiemann Kristin M, Heo Gyu Seong, Wagers Patrick O, Rezenom Yohannes H, Zhang Shiyi, Zhang Fuwu, Youngs Wiley J, Hunstad David A, Wooley Karen L
Departments of Chemistry, Chemical Engineering, and Materials Science and Engineering, and Laboratory for Synthetic-Biologic Interactions, Texas A&M University , P.O. Box 30012, 3255 TAMU, College Station, Texas 77842, United States.
ACS Nano. 2015 Feb 24;9(2):1995-2008. doi: 10.1021/nn507046h. Epub 2015 Jan 26.
The development of well-defined polymeric nanoparticles (NPs) as delivery carriers for antimicrobials targeting human infectious diseases requires rational design of the polymer template, an efficient synthetic approach, and fundamental understanding of the developed NPs, e.g., drug loading/release, particle stability, and other characteristics. Herein, we developed and evaluated the in vitro antimicrobial activity of silver-bearing, fully biodegradable and functional polymeric NPs. A series of degradable polymeric nanoparticles (dNPs), composed of phosphoester and L-lactide and designed specifically for silver loading into the hydrophilic shell and/or the hydrophobic core, were prepared as potential delivery carriers for three different types of silver-based antimicrobials-silver acetate or one of two silver carbene complexes (SCCs). Silver-loading capacities of the dNPs were not influenced by the hydrophilic block chain length, loading site (i.e., core or shell), or type of silver compound, but optimization of the silver feed ratio was crucial to maximize the silver loading capacity of dNPs, up to ca. 12% (w/w). The release kinetics of silver-bearing dNPs revealed 50% release at ca. 2.5-5.5 h depending on the type of silver compound. In addition, we undertook a comprehensive evaluation of the rates of hydrolytic or enzymatic degradability and performed structural characterization of the degradation products. Interestingly, packaging of the SCCs in the dNP-based delivery system improved minimum inhibitory concentrations up to 70%, compared with the SCCs alone, as measured in vitro against 10 contemporary epidemic strains of Staphylococcus aureus and eight uropathogenic strains of Escherichia coli. We conclude that these dNP-based delivery systems may be beneficial for direct epithelial treatment and/or prevention of ubiquitous bacterial infections, including those of the skin and urinary tract.
开发明确的聚合物纳米颗粒(NPs)作为针对人类传染病的抗菌药物递送载体,需要对聚合物模板进行合理设计、采用高效的合成方法,并对所开发的纳米颗粒有基本的了解,例如药物负载/释放、颗粒稳定性及其他特性。在此,我们开发并评估了含银、完全可生物降解且具有功能性的聚合物纳米颗粒的体外抗菌活性。制备了一系列由磷酸酯和L-丙交酯组成的可降解聚合物纳米颗粒(dNPs),这些纳米颗粒专门设计用于将银负载到亲水性壳层和/或疏水性核中,作为三种不同类型银基抗菌剂(醋酸银或两种卡宾银配合物(SCCs)之一)的潜在递送载体。dNPs的银负载能力不受亲水性嵌段链长度、负载位点(即核或壳)或银化合物类型的影响,但优化银进料比对于最大化dNPs的银负载能力至关重要,最高可达约12%(w/w)。含银dNPs的释放动力学显示,根据银化合物类型,在约2.5 - 5.5小时时释放50%。此外,我们对水解或酶促降解速率进行了全面评估,并对降解产物进行了结构表征。有趣的是,与单独的SCCs相比,在基于dNP的递送系统中包装SCCs可使对10种当代流行的金黄色葡萄球菌菌株和8种尿路致病性大肠杆菌菌株的体外最小抑菌浓度提高多达70%。我们得出结论,这些基于dNP的递送系统可能有利于直接上皮治疗和/或预防普遍存在的细菌感染,包括皮肤和泌尿系统的感染。