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A mussel (Mytilus edulis) tissue certified reference material for the marine biotoxins azaspiracids

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1522-7189(199905/06)7:3<99::aid-nt46>3.0.co;2-lopenalex-snapshot
Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland
inferredcites →https://doi.org/10.1002/anie.200460695openalex-snapshot
Structural Revision and Total Synthesis of Azaspiracid‐1, Part 1: Intelligence Gathering and Tentative Proposal
inferredcites →https://doi.org/10.1002/rcm.3385openalex-snapshot
Discovery of new analogs of the marine biotoxin azaspiracid in blue mussels ( Mytilus edulis ) by ultra‐performance liquid chromatography/tandem mass spectrometry
inferredcites →https://doi.org/10.1002/rcm.863openalex-snapshot
Studies on azaspiracid biotoxins. II. Mass spectral behavior and structural elucidation of azaspiracid analogs
inferredcites →https://doi.org/10.1007/978-3-662-05173-3_17openalex-snapshot
Uncertainty calculations in the certification of reference materials. 2. Homogeneity study
inferredcites →https://doi.org/10.1007/bf00322529openalex-snapshot
Reference materials for domoic acid, a marine neurotoxin
inferredcites →https://doi.org/10.1007/s00216-006-0792-8openalex-snapshot
Fit-for-purpose shellfish reference materials for internal and external quality control in the analysis of phycotoxins
inferredcites →https://doi.org/10.1007/s00216-006-0833-3openalex-snapshot
Effect of addition of antibiotics and an antioxidant on the stability of tissue reference materials for domoic acid, the amnesic shellfish poison
inferredcites →https://doi.org/10.1007/s00216-006-0935-yopenalex-snapshot
Feasibility of gamma irradiation as a stabilisation technique in the preparation of tissue reference materials for a range of shellfish toxins
inferredcites →https://doi.org/10.1007/s00216-006-1104-zopenalex-snapshot
Freeze-drying for the stabilisation of shellfish toxins in mussel tissue (Mytilus edulis) reference materials
inferredcites →https://doi.org/10.1007/s00216-008-2221-7openalex-snapshot
LC-MS-MS aboard ship: tandem mass spectrometry in the search for phycotoxins and novel toxigenic plankton from the North Sea
inferredcites →https://doi.org/10.1007/s00216-010-3886-2openalex-snapshot
In-house validation of a liquid chromatography tandem mass spectrometry method for the analysis of lipophilic marine toxins in shellfish using matrix-matched calibration
inferredcites →https://doi.org/10.1007/s00216-010-4161-2openalex-snapshot
The preparation of certified calibration solutions for azaspiracid-1, -2, and -3, potent marine biotoxins found in shellfish
inferredcites →https://doi.org/10.1007/s00216-011-4787-8openalex-snapshot
A mussel tissue certified reference material for multiple phycotoxins. Part 3: homogeneity and stability
inferredcites →https://doi.org/10.1007/s00216-011-4803-zopenalex-snapshot
A mussel tissue certified reference material for multiple phycotoxins. Part 2: liquid chromatography–mass spectrometry, sample extraction and quantitation procedures
inferredcites →https://doi.org/10.1007/s00216-013-7273-7openalex-snapshot
A feasibility study into the production of a freeze-dried oyster reference material for paralytic shellfish poisoning toxins
inferredcites →https://doi.org/10.1007/s002160050699openalex-snapshot
A synopsis of different approaches to the certification of reference materials
inferredcites →https://doi.org/10.1007/s007690000238openalex-snapshot
Uncertainty calculations in the certification of reference materials. 2. Homogeneity study
inferredcites →https://doi.org/10.1007/s007690000292openalex-snapshot
Uncertainty calculations in the certification of reference materials
inferredcites →https://doi.org/10.1016/j.chroma.2010.09.020openalex-snapshot
Strategies for the elimination of matrix effects in the liquid chromatography tandem mass spectrometry analysis of the lipophilic toxins okadaic acid and azaspiracid-1 in molluscan shellfish
inferredcites →https://doi.org/10.1016/j.chroma.2011.09.017openalex-snapshot
Derivatization of azaspiracid biotoxins for analysis by liquid chromatography with fluorescence detection
inferredcites →https://doi.org/10.1016/j.hal.2011.06.010openalex-snapshot
The role of Azadinium spinosum (Dinophyceae) in the production of azaspiracid shellfish poisoning in mussels
inferredcites →https://doi.org/10.1016/j.jbbm.2006.06.005openalex-snapshot
Matrix solid phase dispersion (MSPD)
inferredcites →https://doi.org/10.1016/j.jbbm.2006.07.007openalex-snapshot
Matrix solid-phase dispersion as a valuable tool for extracting contaminants from foodstuffs
inferredcites →https://doi.org/10.1016/j.toxicon.2005.03.010openalex-snapshot
Tissue distribution, effects of cooking and parameters affecting the extraction of azaspiracids from mussels, Mytilus edulis, prior to analysis by liquid chromatography coupled to mass spectrometry
inferredcites →https://doi.org/10.1016/j.toxicon.2007.08.008openalex-snapshot
Structural confirmation and occurrence of azaspiracids in Scandinavian brown crabs (Cancer pagurus)
inferredcites →https://doi.org/10.1016/j.toxicon.2008.02.016openalex-snapshot
Azaspiracid: First evidence of protein binding in shellfish
inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.008openalex-snapshot
Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin
inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.015openalex-snapshot
Performance of the EU-harmonised mouse bioassay for lipophilic toxins for the detection of azaspiracids in naturally contaminated mussel (Mytilus edulis) hepatopancreas tissue homogenates characterised by liquid chromatography coupled to tandem mass spectrometry
inferredcites →https://doi.org/10.1016/j.toxicon.2012.04.351openalex-snapshot
Azaspiracid accumulation, detoxification and biotransformation in blue mussels (Mytilus edulis) experimentally fed Azadinium spinosum
inferredcites →https://doi.org/10.1016/s0021-9673(01)01429-7openalex-snapshot
Matrix effect and correction by standard addition in quantitative liquid chromatographic–mass spectrometric analysis of diarrhetic shellfish poisoning toxins
inferredcites →https://doi.org/10.1016/s0041-0101(00)00144-6openalex-snapshot
Protein phosphatase inhibition assay adapted for determination of total DSP in contaminated mussels
inferredcites →https://doi.org/10.1016/s0041-0101(02)00082-xopenalex-snapshot
First evidence of an extensive northern European distribution of azaspiracid poisoning (AZP) toxins in shellfish
inferredcites →https://doi.org/10.1016/s0041-0101(02)00288-xopenalex-snapshot
Detection of five new hydroxyl analogues of azaspiracids in shellfish using multiple tandem mass spectrometry
inferredcites →https://doi.org/10.1016/s0041-0101(03)00105-3openalex-snapshot
The first identification of azaspiracids in shellfish from France and Spain
inferredcites →https://doi.org/10.1021/ac048385hopenalex-snapshot
Quantitative 1H NMR with External Standards: Use in Preparation of Calibration Solutions for Algal Toxins and Other Natural Products
inferredcites →https://doi.org/10.1021/ac801506dopenalex-snapshot
Evaluation of Various pH and Temperature Conditions on the Stability of Azaspiracids and Their Importance in Preparative Isolation and Toxicological Studies
inferredcites →https://doi.org/10.1021/es020246zopenalex-snapshot
Geographical, Temporal, and Species Variation of the Polyether Toxins, Azaspiracids, in Shellfish
inferredcites →https://doi.org/10.1021/ja066971hopenalex-snapshot
Antibodies with Broad Specificity to Azaspiracids by Use of Synthetic Haptens
inferredcites →https://doi.org/10.1021/ja981413ropenalex-snapshot
Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis
inferredcites →https://doi.org/10.1021/jf8025138openalex-snapshot
Formation of Azaspiracids-3, -4, -6, and -9 via Decarboxylation of Carboxyazaspiracid Metabolites from Shellfish
inferredcites →https://doi.org/10.1021/tx400434bopenalex-snapshot
Epimers of Azaspiracids: Isolation, Structural Elucidation, Relative LC-MS Response, and in Vitro Toxicity of 37-epi-Azaspiracid-1
inferredcites →https://doi.org/10.1080/02652030802008601openalex-snapshot
Approaches to the evaluation of matrix effects in the liquid chromatography-mass spectrometry (LC-MS) analysis of three regulated lipophilic toxin groups in mussel matrix (Mytilus edulis)
inferredcites →https://doi.org/10.1080/09670260802578534openalex-snapshot
Azadinium spinosumgen. et sp. nov. (Dinophyceae) identified as a primary producer of azaspiracid toxins
inferredcites →https://doi.org/10.1271/bbb.65.740openalex-snapshot
Structures of Azaspiracid Analogs, Azaspiracid-4 and Azaspiracid-5, Causative Toxins of Azaspiracid Poisoning in Europe
inferredcites →https://doi.org/10.2983/0730-8000(2006)25[1067:fdoaim]2.0.co;2openalex-snapshot
FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA
inferredcites →https://doi.org/10.3390/md11061815openalex-snapshot
Diarrhetic Shellfish Toxins and Other Lipophilic Toxins of Human Health Concern in Washington State
inferredcites →https://doi.org/10.3390/md6020039openalex-snapshot
Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4076676openalex-extracted
inferred← citeshttps://doi.org/10.2139/ssrn.4671924openalex-extracted
Assessing Escherichia Coli and Coliform Bacteria in Mussel Mytella Strigata (Hanley, 1843) Collected in Tangub Misamis Occidental and Baroy Lanao Del Norte
inferred← citeshttps://doi.org/10.1002/9781118994672.ch2openalex-snapshot
Detection and Surveillance of Harmful Algal Bloom Species and Toxins
inferred← citeshttps://doi.org/10.1002/ange.201711006openalex-snapshot
Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
inferred← citeshttps://doi.org/10.1002/anie.201711006openalex-snapshot
Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
inferred← citeshttps://doi.org/10.1002/rcm.7918openalex-snapshot
Relative molar response of lipophilic marine algal toxins in liquid chromatography/electrospray ionization mass spectrometry
inferred← citeshttps://doi.org/10.1007/s00216-016-0004-0openalex-snapshot
A mussel tissue certified reference material for multiple phycotoxins. Part 4: certification
inferred← citeshttps://doi.org/10.1007/s00216-017-0507-3openalex-snapshot
Hydrophilic interaction liquid chromatography-tandem mass spectrometry for quantitation of paralytic shellfish toxins: validation and application to reference materials
inferred← citeshttps://doi.org/10.1007/s00216-020-03133-2openalex-snapshot
A mussel tissue certified reference material for multiple phycotoxins. Part 5: profiling by liquid chromatography–high-resolution mass spectrometry
inferred← citeshttps://doi.org/10.1007/s00216-023-04788-3openalex-snapshot
Sample pooling and incurred samples improve analytical throughput and quality control of lipophilic phycotoxins screening in bivalve mollusks
inferred← citeshttps://doi.org/10.1007/s00216-023-04794-5openalex-snapshot
Production and certification of BOTS-1: bovine muscle–certified reference material for incurred veterinary drug residues
inferred← citeshttps://doi.org/10.1007/s00216-023-04868-4openalex-snapshot
Preparation of 18O-labelled azaspiracids for accurate quantitation using liquid chromatography–mass spectrometry
inferred← citeshttps://doi.org/10.1007/s00216-026-06697-7openalex-snapshot
Caribbean ciguatoxin (C-CTX) reference materials: feasibility studies for calibration solutions and fish tissue matrix materials
inferred← citeshttps://doi.org/10.1016/j.aca.2022.339622openalex-snapshot
Non-target analysis and stability assessment of reference materials using liquid chromatography‒high-resolution mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.08.064openalex-snapshot
High resolution mass spectrometry for quantitative analysis and untargeted screening of algal toxins in mussels and passive samplers
inferred← citeshttps://doi.org/10.1016/j.foodchem.2019.05.031openalex-snapshot
Reversed-phase/weak anion exchange magnetic mesoporous microspheres for removal of matrix effects in lipophilic marine biotoxins analysis by ultrahigh-performance liquid chromatography coupled to tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.jchromb.2022.123360openalex-snapshot
Preparation and characterization of an immunoaffinity column for the selective extraction of azaspiracids
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.03.182openalex-snapshot
Analytical approaches for the determination of personal care products and evaluation of their occurrence in marine organisms
inferred← citeshttps://doi.org/10.1016/j.toxcx.2020.100059openalex-snapshot
Fatty acid esters of azaspiracids identified in mussels (Mytilus edulis) using liquid chromatography-high resolution mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.toxicon.2017.12.040openalex-snapshot
Accumulation and transformation of azaspiracids in scallops ( Chlamys farreri ) and mussels ( Mytilus galloprovincialis ) fed with Azadinium poporum, and response of antioxidant enzymes
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c03831openalex-snapshot
In Vitro Metabolism of Azaspiracids 1–3 with a Hepatopancreatic Fraction from Blue Mussels (Mytilus edulis)
inferred← citeshttps://doi.org/10.1021/acs.jafc.8b00346openalex-snapshot
Selective Extraction and Purification of Azaspiracids from Blue Mussels (Mytilus edulis) Using Boric Acid Gel
inferred← citeshttps://doi.org/10.1080/00032719.2023.2237143openalex-snapshot
Novel Coffee Certified Reference Material for Ochratoxin A, B, and C
inferred← citeshttps://doi.org/10.3390/md22020079openalex-snapshot
Current Research Status of Azaspiracids
inferred← citeshttps://doi.org/10.3390/toxins13080510openalex-snapshot
Identification of 24-O-β-d-Glycosides and 7-Deoxy-Analogues of Okadaic Acid and Dinophysistoxin-1 and -2 in Extracts from Dinophysis Blooms, Dinophysis and Prorocentrum Cultures, and Shellfish in Europe, North America and Australasia
inferred← citeshttps://doi.org/10.3390/toxins13110823openalex-snapshot
A Generic LC-HRMS Screening Method for Marine and Freshwater Phycotoxins in Fish, Shellfish, Water, and Supplements
inferred← citeshttps://doi.org/10.3390/toxins15020103openalex-snapshot
Contribution of Mass Spectrometry to the Advances in Risk Characterization of Marine Biotoxins: Towards the Characterization of Metabolites Implied in Human Intoxications
inferred← citeshttps://doi.org/10.4224/crm.2011.aza-mus.200603openalex-snapshot
AZA-Mus: Mussel Tissue Certified Reference Material for Azaspiracids
inferred← citeshttps://doi.org/10.4224/crm.2016.fdmt1.20070717openalex-snapshot
FDMT1: Freeze-dried Mussel Tissue Certified Reference Material for Multiple Marine Toxins
inferred← citeshttps://doi.org/10.70675/69490d6eze46cz491dza5b5zfecd3ff89a66openalex-snapshot
Modèles originaux du système intestinal humain pour l'étude du danger des phycotoxines
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