Subramaniam Santhni, Thomas Nicky, Gustafsson Hanna, Jambhrunkar Manasi, Kidd Stephen P, Prestidge Clive A
School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA 5000, Australia.
ARC Centre of Excellence in Convergent Bio-Nano Science & Technology, University of South Australia, Mawson Lakes, SA 5095, Australia.
Antibiotics (Basel). 2019 Apr 11;8(2):39. doi: 10.3390/antibiotics8020039.
Infectious diseases remain a major burden in today's world, causing high mortality rates and significant economic losses, with >9 million deaths per year predicted by 2030. Invasion of host cells by intracellular bacteria poses treatment challenges due to the poor permeation of antimicrobials into the infected cells. To overcome these limitations, mesoporous silica nanoparticles (MSNP) loaded with the antibiotic rifampicin were investigated as a nanocarrier system for the treatment of intracellular bacterial infection with specific interest in the influence of particle size on treatment efficiency. An intracellular infection model was established using small colony variants (SCV) of in macrophages to systemically evaluate the efficacy of rifampicin-loaded MSNP against the pathogen as compared to a rifampicin solution. As hypothesized, the superior uptake of MSNP by macrophages resulted in an enhanced treatment efficacy of the encapsulated rifampicin as compared to free antibiotic. This study provides a potential platform to improve the performance of currently available antibiotics against intracellular infections.
传染病在当今世界仍然是一个重大负担,导致高死亡率和巨大经济损失,预计到2030年每年死亡人数将超过900万。细胞内细菌侵入宿主细胞给治疗带来了挑战,因为抗菌药物难以渗透到受感染的细胞中。为了克服这些限制,研究了负载抗生素利福平的介孔二氧化硅纳米颗粒(MSNP)作为一种纳米载体系统,用于治疗细胞内细菌感染,并特别关注粒径对治疗效果的影响。使用巨噬细胞中的小菌落变体(SCV)建立了细胞内感染模型,以系统地评估负载利福平的MSNP与利福平溶液相比对病原体的疗效。正如所假设的那样,与游离抗生素相比,巨噬细胞对MSNP的摄取优势导致包封的利福平治疗效果增强。这项研究提供了一个潜在的平台,以提高目前可用抗生素对细胞内感染的治疗性能。