Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography-Hybrid Ion Trap-Time of Flight Mass Spectrometry.
Chromatography, High Pressure Liquid
/ methods
Chromatography, Liquid
/ methods
Cyclic Nucleotide Phosphodiesterases, Type 5
/ metabolism
Dietary Supplements
/ analysis
Drug Contamination
Mass Spectrometry
/ methods
Phosphodiesterase 5 Inhibitors
/ analysis
Sildenafil Citrate
/ analogs & derivatives
Tadalafil
/ analogs & derivatives
Tandem Mass Spectrometry
/ methods
Vardenafil Dihydrochloride
/ analogs & derivatives
analogs
dietary supplements
high-performance liquid chromatography
hybrid ion trap–time of flight mass spectrometry
phosphodiesterase-5 inhibitors
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
12 Jun 2020
12 Jun 2020
Historique:
received:
22
05
2020
revised:
09
06
2020
accepted:
09
06
2020
entrez:
18
6
2020
pubmed:
18
6
2020
medline:
17
2
2021
Statut:
epublish
Résumé
An accurate and reliable method based on ion trap-time of flight mass spectrometry (IT-TOF MS) was developed for screening phosphodiesterase-5 inhibitors, including sildenafil, vardenafil, and tadalafil, and their analogs in dietary supplements. Various parameters affecting liquid chromatographic separation and IT-TOF detection were investigated, and the optimal conditions were determined. The separation was achieved on a reversed-phase column under gradient elution using acetonitrile and water containing 0.2% acetic acid at a flow rate of 0.2 mL/min. The chromatographic eluents were directly ionized in the IT-TOF system equipped with an electrospray ion source operating in the positive ion mode. The proposed screening method was validated by assessing its linearity, precision, and accuracy. Sequential tandem MS was conducted to obtain structural information of the references, and the fragmentation mechanism of each reference was proposed for providing spectral insight for newly synthesized analogs. Structural information, including accurate masses of both parent and fragment ions, was incorporated into the MS
Identifiants
pubmed: 32545673
pii: molecules25122734
doi: 10.3390/molecules25122734
pmc: PMC7355528
pii:
doi:
Substances chimiques
Phosphodiesterase 5 Inhibitors
0
Vardenafil Dihydrochloride
5O8R96XMH7
Tadalafil
742SXX0ICT
Sildenafil Citrate
BW9B0ZE037
Cyclic Nucleotide Phosphodiesterases, Type 5
EC 3.1.4.35
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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