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1.
Food Chem Toxicol ; 141: 111386, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32376337

ABSTRACT

Paralytic shellfish poisoning (PSP) episodes cause important economic impacts due to closure of shellfish production areas in order to protect human health. These closures, if are frequent and persistent, can seriously affect shellfish producers and the seafood industry, among others. In this study, we have developed an alternative processing method for bivalves with PSP content above the legal limit, which allows reducing toxicity to acceptable levels. A modification of the PSP detoxifying procedure stablished by Decision 96/77/EC of the European Union in Acanthocardia tuberculata, was developed and implemented for PSP elimination in other bivalves species. The procedure was applied to 6 batches of mussels, 2 batches of clams and 2 batches of scallops, achieving detoxification rates of around 85%. A viable industrial protocol which allows the transformation of a product at risk into a safe product was developed. Although a significant reduction was obtained, in a sample circa 9000 µg STX diHCl equiv/kg, the final toxin level in these highly toxic mussels did not fall below the European limit. The processing protocol described may be applied efficiently to mussels, clams and scallops and it may be a major solution to counteract the closure of shellfish harvesting areas, especially if persistent.


Subject(s)
Marine Toxins/isolation & purification , Shellfish Poisoning/metabolism , Shellfish/analysis , Animals , Marine Toxins/metabolism , Shellfish/classification , Species Specificity
2.
Mar Environ Res ; 133: 6-14, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29174400

ABSTRACT

Rapid and cost-effective methods to monitor the presence of diarrhetic shellfish poisoning (DSP) toxins in seawater samples in an easy and reliable manner are required to protect human health and avoid economic losses to shellfish industry. Immunoassays for the detection of okadaic acid (OA) and dinophysistoxin-1 and dinophysistoxin-2 are developed by immobilising OA on self-assembled monothiols or dithiols in an ordered and oriented way, providing an effective limit of detection of ∼1 ng OA equiv./mL seawater. The immunoassays are applied to the analysis of the particulate fraction of seawater samples from two Catalan harbours (NW Mediterranean) and samples collected periodically from the Galician Rias (E Atlantic), as well as a reference mussel sample. Results are in agreement with LC-MS/MS and the certified values. OA concentration in seawater correlates with Dinophysis cell abundance, with a 1-2 weeks lag. The immunoassays provide powerful high-throughput analytical methods potentially applicable as alternative monitoring tools.


Subject(s)
Environmental Monitoring/methods , Immunoassay , Marine Toxins/analysis , Okadaic Acid/analysis , Animals , Bivalvia , Humans , Seawater/chemistry , Shellfish , Shellfish Poisoning
3.
Talanta ; 84(3): 859-66, 2011 May 15.
Article in English | MEDLINE | ID: mdl-21482294

ABSTRACT

Solid-phase extraction (SPE) combined with liquid chromatography electrospray mass spectrometry (LC-(ESI)MS) was used to determine 16 non-ionic and anionic surfactants in different environmental water samples at ng L(-1) levels. The proposed method is sensitive and simple and has good linear range and detection limits (less than 50 ng L(-1)) for most compound classes. The effect of ion suppression was studied in aqueous matrices from several treatment plants-including urban and industrial wastewater treatment plants (WWTPs), drinking-water treatment plants (DWTPs) and seawater desalination plants (SWDPs)-and it was considered when quantifying our samples. In addition, conventional treatments and tertiary treatments that use advanced membrane technologies, such as ultrafiltration (UF) and reverse osmosis (RO) were evaluated in order to determine their efficiency in eliminating these compounds. The concentrations of non-ionic surfactants in the raw waters studied ranged from 0.2 to 100 µg L(-1). In effluents, the concentrations ranged from 0.1 to 5 µg L(-1), which reflects consistent elimination. Anionic surfactants were present in all waters studied at higher levels. Levels up to 3900µgL(-1) of linear alkylbenzene sulfonates (LASs) and 32,000 µg L(-1) of alkyl ethoxysulfates (AESs) were detected in urban WWTP influents, while levels up to 25 µg L(-1) of LASs and 114 µg L(-1) of AESs were found in drinking-water and desalination treatment plants. The results indicate that conventional processes alone are not sufficient to completely remove the studied surfactants from waste streams. Tertiary treatments that use advanced membrane technologies such as UF and RO can further reduce the amount of target compounds in the effluent water.


Subject(s)
Environmental Pollutants/analysis , Surface-Active Agents/analysis , Chromatography, Liquid , Mass Spectrometry , Reference Standards , Solid Phase Extraction
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