Multiplexed fluorescence immunoassay combined with magnetic separation using upconversion nanoparticles as multicolor labels for the simultaneous detection of tyramine and histamine in food samples
ANALYTICA CHIMICA ACTA
Authors: Zhang, Biao; Sheng, Wei; Liu, Yue; Huang, Na; Zhang, Wanli; Wang, Shuo
Abstract
We have developed an upconversion nanoparticles (UCNPs) based fluorescence immunoassay for simultaneously detecting tyramine and histamine in foods. The anti-tyramine and anti-histamine antibody were linked to NaYF4Yb, Tm (emission at 483 nm) and NaYF4Yb, Er (emission at 550 nm) UCNPs as multicolor signal probe, respectively. The tyramine and histamine coating antigen were connected to magnetic microspheres as capture probe, respectively. Base on a competitive format, capture probes compete with analytes to combine corresponding signal probes. Under excitation at 980 nm, the formed competitive immune-complex fluorescent signal at 483 and 550 nm indicates concentration of tyramine and histamine, respectively. This immunoassay has detection linear from 0.5 to 100 mu g L-1 with limit of detection (LOD) of 0.1 mu g L-1 for tyramine, and 0.1-100 mu g L-1 with LOD of 0.01 mu g L-1 for histamine, respectively. This multiplexed analysis format has potential applications for rapid, efficient detecting multiple food risk factors. (C) 2020 Elsevier B.V. All rights reserved.
Quetiapine and other antipsychotics combined with opioids in legal autopsy cases: A random finding or cause of fatal outcome?
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
Authors: Andersen, Freja Drost; Simonsen, Ulf; Andersen, Charlotte Uggerhoj
Abstract
Opioid poisoning is a frequent cause of death in drug addicts and occurs with opioid treatment. Quetiapine is often found in forensic autopsies and may increase the risk of fatal opioid poisoning by enhancing sedation, respiratory depression, hypotension and QT prolongation. We systematically searched for studies of acute toxicity of quetiapine or other antipsychotics combined with morphine or methadone. Case reports describing toxicity of quetiapine combined with morphine or methadone were also included. We retrieved one human study that observed pharmacokinetic interaction between quetiapine and methadone, and 16 other human studies. Fourteen investigated the combination of droperidol and morphine in treatment doses, and some indicated an additive sedative effect. Five animal studies with acepromazine in combination with morphine or methadone were located and indicated an additive effect on sedation and hypotension. Six forensic case reports in which death could have been caused solely by quetiapine, the opioid, or other drugs were found. Thus, acute toxicity of quetiapine combined with morphine or methadone has not been studied. Because of quetiapine's effects on alpha-adrenoceptors, muscarinic and histamine receptors, human ether-a-go-go-channels and methadone kinetics, we suggest further research to clarify if the indicated additive effects of opioids and droperidol or acepromazine are also true for quetiapine.