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- W2000710967 endingPage "167" @default.
- W2000710967 startingPage "159" @default.
- W2000710967 abstract "For the successful treatment of pulmonary tuberculosis, drugs need to penetrate complex lung lesions and permeate the mycobacterial cell wall in order to reach their intracellular targets. However, most currently used anti-tuberculosis drugs were introduced into clinical use without considering the pharmacokinetic and pharmacodynamic properties that influence drug distribution, and this has contributed to the long duration and limited success of current therapies. In this Progress article, I describe new methods to quantify and image drug distribution in infected lung tissue and in mycobacterial cells, and I explore how this technology could be used to design optimized multidrug regimens." @default.
- W2000710967 created "2016-06-24" @default.
- W2000710967 creator A5007366821 @default.
- W2000710967 date "2014-02-03" @default.
- W2000710967 modified "2023-10-05" @default.
- W2000710967 title "The path of anti-tuberculosis drugs: from blood to lesions to mycobacterial cells" @default.
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- W2000710967 doi "https://doi.org/10.1038/nrmicro3200" @default.
- W2000710967 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4341982" @default.
- W2000710967 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24487820" @default.
- W2000710967 hasPublicationYear "2014" @default.
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