Unambiguous determination of farnesol and tyrosol in vaginal fluid using fast and sensitive UHPLC-MS/MS method
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, validační studie
Grantová podpora
CZ.02.1.01/0.0/0.0/15_003/0000465
Ministerstvo Školství, Mládeže a Tělovýchovy
15-29225A
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
32468279
DOI
10.1007/s00216-020-02699-1
PII: 10.1007/s00216-020-02699-1
Knihovny.cz E-zdroje
- Klíčová slova
- Candida albicans, Farnesol, Microextraction, Quorum sensing, Tyrosol, UHPLC-MS/MS,
- MeSH
- Candida albicans izolace a purifikace MeSH
- dospělí MeSH
- farnesol analýza MeSH
- fenethylalkohol analogy a deriváty analýza MeSH
- lidé středního věku MeSH
- lidé MeSH
- limita detekce MeSH
- mladý dospělý MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vagina chemie mikrobiologie MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- validační studie MeSH
- Názvy látek
- 4-hydroxyphenylethanol MeSH Prohlížeč
- farnesol MeSH
- fenethylalkohol MeSH
The new ultra-high performance liquid chromatography method with tandem mass spectrometry detection (UHPLC-MS/MS) has been optimized to allow fast, selective, and high-throughput analysis of two Candida albicans quorum sensing molecules (QSM), farnesol and tyrosol. The problem of the presence of the interference in the samples and system was successfully solved by careful optimization of chromatographic conditions. Charged hybrid stationary phase modified with pentafluorophenyl group and optimized gradient elution provided adequate separation selectivity and peak shapes. The impurity was identified as dibutyl phthalate and had the same m/z ions as farnesol leading to an important interference on selected reaction monitoring channel. Two different types of biological matrices originating from vaginal fluid, supernatant and sediment, were analysed. Micro-solid phase extraction in pipette tips was optimized for the selective isolation of QSM from the supernatant. The insufficient retention of farnesol on the extraction sorbent was improved when 1% of organic solvent was added prior to extraction, while the retention of tyrosol was only possible when using combined C8 and polymer sorbent type. Strong retention of farnesol had to be solved by increasing elution solvent strength and volume up to 600 μL. However, this approach did not allow the pretreatment of sediment samples due to the sorbent clogging. Therefore, our previously developed protein precipitation method was modified and validated to analyse the sediments. New developed UHPLC-MS/MS method provided suitable accuracy and precision for the determination of QSM in vaginal fluid while using only 50 μL sample volume and two different sample preparation methods.
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