2019
DOI: 10.1016/j.cca.2019.01.023
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Advances in antifungal drug measurement by liquid chromatography-mass spectrometry

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Cited by 20 publications
(8 citation statements)
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“…Since there are few fungal-specific targets, antifungal drug discovery is problematic and leads to the emergence of resistant fungi. In addition to intrinsic antifungal resistance (e.g., multidrug-resistant Candida auris), there are many other mechanisms that fungi use to resist drug therapy that have been described in the literature (Nett and Andes, 2016;Robbins et al, 2016;Perfect, 2017;Zheng and Wang, 2019;Howard et al, 2020).…”
Section: Natural Products With Antifungal Activitymentioning
confidence: 99%
“…Since there are few fungal-specific targets, antifungal drug discovery is problematic and leads to the emergence of resistant fungi. In addition to intrinsic antifungal resistance (e.g., multidrug-resistant Candida auris), there are many other mechanisms that fungi use to resist drug therapy that have been described in the literature (Nett and Andes, 2016;Robbins et al, 2016;Perfect, 2017;Zheng and Wang, 2019;Howard et al, 2020).…”
Section: Natural Products With Antifungal Activitymentioning
confidence: 99%
“…Some antifungal drugs represent ideal candidates for TDM [92]: itraconazole, voriconazole and posaconazole among azoles and 5-flucytosine among antimetabolites. They are characterized by high inter-and intra-patient variability in blood concentration, absorption, distribution, metabolism, elimination, genetic polymorphism, drug-drug interaction and narrow therapeutic index [93]. PK data for voriconazole and posaconazole already exist for adult patients, but they are not available for pediatric and neonatal patients [94], given the wide differences in volume distribution, clearance and other PK parameters, especially in neonatal age [92].…”
Section: Tdm and Antifungalsmentioning
confidence: 99%
“…As a result of the high toxicity of most antifungal drugs, one needs to ensure that drug exposure at the site of infection is adequate while toxicity to the host is minimized. Many antifungal drugs exhibit great inter- and intra-individual variability in blood concentrations due to variable absorption, metabolism, elimination, non-linear pharmacokinetics, drug–drug interactions, and cytochrome P450 polymorphisms [ 7 ]. TDM can be used for tailoring medications to achieve exposures associated with a high probability of therapeutic success, decrease treatment-related toxicity, and help prevent the emergence of antifungal resistance due to subtherapeutic drug exposures.…”
Section: Antifungal Drugsmentioning
confidence: 99%
“…There are five main classes of antifungal drugs: polyenes, flucytosine, allylamines, azoles, and echinocandins [ 7 ]. TDM is especially justified for flucytosine and triazoles due to their large inter- and intra-individual pharmacokinetic variability and their high tendency for drug–drug interactions.…”
Section: Antifungal Drugsmentioning
confidence: 99%
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