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Analysis of highly polar marine biotoxins in seawater by hydrophilic interaction liquid chromatography coupled to high resolution mass spectrometry.

ABSTRACT: The monitoring of marine biotoxins (MBTs) in seawater is presented as an alternative strategy to determine their presence and the possible implications in the ecosystem. For this, an analytical method based on hydrophilic interaction liquid chromatography coupled to high resolution mass spectrometry (HILIC-HRMS) has been developed to identify and quantify some hydrophilic MBTs in seawater: saxitoxin (STX), decarbamoyl-saxitoxin (dcSTX), neosaxitoxin (NeoSTX), gonaytoxin-2,3 (GTX-2,3) and tetrodotoxin (TTX), which are responsible of gastrointestinal and central nervous system distress in humans when are consumed via seafood. Particulate and filtrate portion were analyzed separately in order to characterize the extracellular toxins dissolved in the water and those present in the particulate. Ultrasound assisted solid-liquid extraction with methanol was used for the isolation of the MBTs from particulate and solid phase extraction using silica cartridges for the filtrate. Extraction procedure was the most critical step during the analytical method due to the high polarity of the toxins and the absolute recoveries obtained ranged from 15 to 47 % in the filtrate and 26 to 71 % in the particulate portions. Limits of detection of the method ranged from 0.5 to 5 µg/L in the filtrate portion and from 3.1 to 62 µg/L in the particulate portion.•Saxitoxins and tetrodotoxins have been analysed by using HILIC-HRMS.•UAE with methanol and SPE with silica cartridges have been employed for the extractions of the polar MBTs from seawater.

SUBMITTER: Bosch-Orea C

PROVIDER: S-EPMC8374475 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Peptide retention prediction using hydrophilic interaction liquid chromatography coupled to mass spectrometry.

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| S-EPMC5539142 | biostudies-literature

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Project description:Hemp seed oil is well known for its nutraceutical, cosmetic and pharmaceutical properties due to a perfectly balanced content of omega 3 and omega 6 polyunsaturated fatty acids. Its importance for human health is reflected by the success on the market of organic goods in recent years. However, it is of utmost importance to consider that its healthy properties are strictly related to its chemical composition, which varies depending not only on the manufacturing method, but also on the hemp variety employed. In the present work, we analyzed the chemical profile of ten commercially available organic hemp seed oils. Their cannabinoid profile was evaluated by a liquid chromatography method coupled to high-resolution mass spectrometry. Besides tetrahydrocannabinol and cannabidiol, other 30 cannabinoids were identified for the first time in hemp seed oil. The results obtained were processed according to an untargeted metabolomics approach. The multivariate statistical analysis showed highly significant differences in the chemical composition and, in particular, in the cannabinoid content of the hemp oils under investigation.

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| S-EPMC4987396 | biostudies-literature

Hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry method for quantification of five phospholipid classes in various matrices

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| S-EPMC10894851 | biostudies-literature

Simultaneous determination of ribonucleoside and deoxyribonucleoside triphosphates in biological samples by hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry.

Project description:Information about the intracellular concentration of dNTPs and NTPs is important for studies of the mechanisms of DNA replication and repair, but the low concentration of dNTPs and their chemical similarity to NTPs present a challenge for their measurement. Here, we describe a new rapid and sensitive method utilizing hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry for the simultaneous determination of dNTPs and NTPs in biological samples. The developed method showed linearity (R2 > 0.99) in wide concentration ranges and could accurately quantify dNTPs and NTPs at low pmol levels. The intra-day and inter-day precision were below 13%, and the relative recovery was between 92% and 108%. In comparison with other chromatographic methods, the current method has shorter analysis times and simpler sample pre-treatment steps, and it utilizes an ion-pair-free mobile phase that enhances mass-spectrometric detection. Using this method, we determined dNTP and NTP concentrations in actively dividing and quiescent mouse fibroblasts.

| S-EPMC6009580 | biostudies-literature

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