Nanomedicine for intracellular therapy

被引:23
|
作者
Ranjan, Ashish [1 ]
Pothayee, Nikorn [2 ]
Seleem, Mohamed N. [3 ]
Boyle, Stephen M. [4 ]
Kasimanickam, Ramanathan [5 ]
Riffle, Judy S. [2 ]
Sriranganathan, Nammalwar [4 ]
机构
[1] NIH, Dept Radiol & Imaging Sci, Bethesda, MD 20892 USA
[2] Virginia Tech, Macromol & Interfaces Inst, Blacksburg, VA USA
[3] Purdue Univ, Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[4] Virginia Tech, Dept Biomed Sci & Pathobiol, Blacksburg, VA USA
[5] Washington State Univ, Pullman, WA 99164 USA
关键词
intracelluar infection; drug delivery; nanoparticle; ENTERICA SEROVAR TYPHIMURIUM; CORE-SHELL NANOSTRUCTURES; LIPOSOME-ENCAPSULATED GENTAMICIN; AMPICILLIN-LOADED NANOPARTICLES; PH-SENSITIVE LIPOSOMES; SALMONELLA-ENTERICA; IN-VIVO; LISTERIOLYSIN-O; ANTIBACTERIAL EFFICACY; INFECTION MODEL;
D O I
10.1111/j.1574-6968.2012.02566.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Intracellular pathogens like Salmonella evade host phagocytic killing by various mechanisms. Classical antimicrobial therapy requires multiple dosages and frequent administration of drugs for a long duration. Intracellular delivery of antimicrobials using nanoparticle may effectively devise therapies for bacterial infections. This review will address the mechanisms used by Salmonella to avoid host pathogenic killing, reasons for therapeutic failure and advances in nanoparticle drug delivery technology for efficient intracellular bacterial clearance.
引用
收藏
页码:1 / 9
页数:9
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