Recent Developments in Drug Delivery for Treatment of Tuberculosis by Targeting Macrophages

被引:13
作者
Gairola, Anirudh [1 ]
Benjamin, Aaron [2 ]
Weatherston, Joshua D. [1 ]
Cirillo, Jeffrey D. [2 ]
Wu, Hung-Jen [1 ]
机构
[1] Texas A&M Univ, Dept Chem Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Hlth Sci Ctr, Dept Microbial Pathogenesis & Immunol, Bryan, TX 77807 USA
基金
美国国家卫生研究院;
关键词
drug delivery; macrophage targeting; nanocarrier; nanomedicine; tuberculosis; SOLID LIPID NANOPARTICLES; HOST-DIRECTED THERAPY; TUFTSIN-BEARING LIPOSOMES; T-CELL RECOGNITION; IN-VIVO EFFICACY; MYCOBACTERIUM-TUBERCULOSIS; ALVEOLAR MACROPHAGES; IRON ACQUISITION; PARTICLE-SIZE; ANTITUBERCULOSIS DRUG;
D O I
10.1002/adtp.202100193
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tuberculosis (TB) is among the greatest public health and safety concerns in the 21st century Mycobacterium tuberculosis, which causes TB, infects alveolar macrophages and uses these cells as one of its primary sites of replication. The current TB treatment regimen, which consists of chemotherapy involving a combination of 3-4 antimicrobials for a duration of 6-12 months, is marked with significant side effects, toxicity, and poor compliance. Targeted drug delivery offers a strategy that can overcome many of the problems of current TB treatment by specifically targeting infected macrophages. Recent advances in nanotechnology and material science have opened an avenue to explore drug carriers that actively and passively target macrophages. This approach can increase the drug penetration into macrophages by using ligands on the nanocarrier that interact with specific receptors for macrophages. This review encompasses the recent development of drug carriers specifically targeting macrophages actively and passively. Future directions and challenges associated with development of effective TB treatment are also discussed.
引用
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页数:25
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