Explore the vast range of titles available.

Codeine is derived from morphine, an opioid analgesic, and has weaker analgesic and sedative effects than the parent molecule. This weak opioid is commonly used in combination with other drugs for over-the-counter cough relief medication. Due to the psychoactive properties of opioid drugs, the easily obtained codeine often becomes subject to misuse. Codeine misuse has emerged as a concerning public health issue due to its associated adverse effects such as headache, nausea, vomiting, and hemorrhage. Thus, it is very important to develop reliable analytical techniques to detect codeine for both quality control of pharmaceutical formulations and identifying drug misuse in the community. This review aims to provide critical outlooks on analytical methods applicable to the determination of codeine.

Hair analysis for drugs has become extensively used for forensic investigation in recent years. To best interpret hair drug content in post-mortem conditions, the extent of external contamination by biological fluids, such as blood, must be taken into account to avoid false positive results. The present study evaluated opiates and opioids incorporation into hair from blood containing different concentrations of morphine (MOR), 6-mono-acetyl morphine (6-AM), codeine (COD), dihydrocodeine (DHC), tramadol (TRA), oxycodone (OXY), methadone (MET), 2-ethylidene-1,5-dimethyl-3,3- diphenyl pyrrolidine (EDDP), buprenorphine (BUP) and norbuprenorphine (NBUP). The hair strands contaminated by brief soaking into blood were stored at room temperature (RT) or at 4°C during 6 hours, 1, 3, 7 or 14 days. After decontamination by extensive washing, we show that all opiates and opioids were incorporated into hair within a few hours at RT and 4°C, without significant changes over time. The concentrations of opiates and opioids in hair reached the cut-off levels established by the Society of Hair Testing (SoHT) for therapeutic (MET, COD), or toxic or lethal (all other molecules) blood concentrations. The metabolite to parent drug concentration ratios were determined for NBUP/BUP, MOR/6-AM and EDDP/MET and could be helpful as indicators of blood external contamination. •Opiates and opioids incorporate deeply into hair after short exposure to blood.•No influence of temperature of storage on opiates and opioids integration into hair.•Avoid analyzing hair samples contaminated with blood containing opiates and opioids.•Metabolite to parent drug ratio could be helpful as indicator of hair contamination.

The use of natural materials as precursors for synthesizing sorptive phases can reduce the environmental impact of the sample preparation step. In this article, two natural materials, i.e., cellulose and humic acids, are combined, resulting in a porous and flat sorptive phase that combines hydrophobic and cation exchange interactions. The simple preparation, with low reagent consumption, and the high production capacity make this process affordable. The performance of the humic acid–coated paper has been studied towards three basic drugs (cocaine, codeine, and methadone), and it has allowed the determination of the targets in saliva by direct infusion tandem mass spectrometry. The simultaneous extraction of many samples and the rapid analysis (2 min) provide a high sample throughput. The resulting method has been validated following the International Conference on Harmonization (ICH) M10 validation guide. Working at the optimum conditions, the linear range was established from 5 to 500 μg·L −1 and the detection limits were established at 1.5 μg·L −1 for all the analytes. At the LOQ, the inter-day precision and intra-day precision, expressed as relative standard deviation, were better than 13.6% and 17.9%, respectively. For low/mid/high quality controls, the inter-day precision and intra-day precision were better than 11.8% and 9.1%, respectively. The accuracy, calculated as relative recovery, was in the range of 83.8–106.1%. Several samples from patients under treatment with codeine-containing prescriptions were finally analyzed. Graphical Abstract

Insects on corpses could be a useful tool for the detection of exogenous substances such as drugs of abuse. The identification of exogenous substances in carrion insects is critical for proper estimation of the postmortem interval. It also provides information about the deceased person that may prove useful for forensic purposes. High-performance liquid chromatography coupled with Fourier transform mass spectrometry is a highly sensitive analytical technique that can identify substances even at very low concentrations, such as in the case of searching for exogenous substances in larvae. In this paper, a method is proposed for the identification of morphine, codeine, methadone, 6-monoacetylmorphine (6-MAM) and 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in the larvae of Lucilia sericata, a common carrion fly widely distributed in temperate areas of the world. The larvae, which were reared on a pig meat substrate, were killed once they reached their third stage by immersion in hot water at 80 °C and aliquoted into 400 mg samples. The samples were fortified with 5 ng of morphine, methadone and codeine. After solid-phase extraction, the samples were processed with a liquid chromatograph coupled to a Fourier transform mass spectrometer. This qualitative method has been validated and tested on larvae from a real case. The results lead to the correct identification of morphine, codeine, methadone and their metabolites. This method could prove useful in cases where toxicological analysis must be conducted on highly decomposed human remains, where biological matrices are very limited. Furthermore, it could help the forensic pathologist to better estimate the time of death, as the growth cycle of carrion insects can undergo changes if exogenous substances are taken.

Date-rape drugs include many medicines and street drugs that are administered to unaware victims, who are subsequently sexually assaulted (or robbed) while under their influence. Due to drug-induced amnesia, reporting is often delayed, making toxicological analysis crucial evidence. Blood and urine are suitable for most analyses up to 1–4 days after drug administration. Sweat may provide a longer detection time, however, commercial sweat patches are not usually available at police stations where victims report such crimes. Therefore, we evaluated the utility of generally available wound dressings to collect sweat for drug analysis in forensic applications. Various dressings were tested, and results were compared with urine analyses. The detection of drugs was performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Drugs were detected in dressings for a few days when they were no longer present in urine. Drug concentrations varied depending on the body location of the dressing and were higher in dressings worn over several days. After single doses, pseudoephedrine and codeine were detectable for at least 9 days, and dextromethorphan for up to 3 days. The drug concentrations were within the ranges of 2–83 ng/dressing for pseudoephedrine, 2–74 ng/dressing for codeine, and 1–16 ng/dressing for dextromethorphan. This work has demonstrated that wound dressings can be used for sweat collection and may serve as a valuable supplement to urine toxicology in drug-facilitated sexual assault cases or other forensic cases where several days have elapsed since the incident. This approach may increase the detectability of the crimes in question. •Wound dressings can be used for sweat collection as supplement to urine toxicology.•Sweat detection windows are longer than for urine.•Drug concentrations varied in dressings applied to different body parts.•Drug concentrations were higher in dressings worn for multiple days.•This approach may increase the detectability of drug-facilitated crimes.

An electroanalytical method based on disposable screen-printed carbon electrodes modified with non-toxic carbonaceous nanodots is proposed as a reliable and effective device for codeine determination in biological fluids and soft drinks. Graphene quantum dots (GQDs), carbon quantum dots (CQDs) and carbon nanodots (CNDs) were evaluated as electrode modifiers for the determination of the drug. The electroactive areas of the modified electrodes were assessed by cyclic voltammetry using potassium ferricyanide. Results demonstrated that GQDs provided the best analytical response for codeine, displaying an intense and well-defined anodic wave approximately 0.9 V vs reference electrode. The method exhibits an acceptable linear dynamic range, low limits of detection and quantification (0.21 and 0.73 µM, respectively), and satisfactory precision (below 3.9% expressed as relative standard deviation (RSD)) in saliva. Only the analysis of biofluids requires a simple extraction protocol. The feasibility and applicability of this novel approach were assessed by determining codeine in different matrices, with recoveries ranging from 69 to 112%. This cost-effective, simple, easily miniaturised and portable method was applied not only to biofluids but also for the direct detection of codeine in soft drinks combined with a codeine-enriched syrup, a medication that is being used to adulterate beverages, particularly at specific events (drinking and nightclub parties). There is no need for any sample treatment, demonstrating its versatility in analysing beverages for potential adulteration as well. Graphical abstract

Water-based studies have come into prominence for illegal substance monitoring. There are limited studies on the detection of these substances in the surface waters as opposed to wastewater. This study aims to evaluate amphetamine, benzoylecgonine, cocaine, codeine, 3,4-methylenedioxy-N-methylamphetamine, morphine, and 11-nor-Δ9- tetrahydrocannabinol-9-carboxylic acid in the Küçük Menderes (KM) River at four different stations during three different periods and assess the environmental risks. Environmental risk assessment of psychoactive substances based on the calculation of Risk Quotients (RQ) were evaluated. RQ values for amphetamine and benzoylecgonine were < 0.01 at all sampling points during all sampling periods, indicating little risk for aquatic life. Cocaine was found as environmentally high risk (RQ > 1) based on its RQ values of 1.22 and 1.37 at KM-01 and KM-02 sampling points. This research is the first report to investigate the presence of psychoactive substances and define the environmental risks of these substances in Türkiye.

The analysis of opioids, cocaine, and metabolites from blood serum is a routine task in forensic laboratories. Commonly, the employed methods include many manual or partly automated steps like protein precipitation, dilution, solid phase extraction, evaporation, and derivatization preceding a gas chromatography (GC)/mass spectrometry (MS) or liquid chromatography (LC)/MS analysis. In this study, a comprehensively automated method was developed from a validated, partly automated routine method. This was possible by replicating method parameters on the automated system. Only marginal optimization of parameters was necessary. The automation relying on an x-y-z robot after manual protein precipitation includes the solid phase extraction, evaporation of the eluate, derivatization (silylation with N -methyl- N -trimethylsilyltrifluoroacetamide, MSTFA), and injection into a GC/MS. A quantitative analysis of almost 170 authentic serum samples and more than 50 authentic samples of other matrices like urine, different tissues, and heart blood on cocaine, benzoylecgonine, methadone, morphine, codeine, 6-monoacetylmorphine, dihydrocodeine, and 7-aminoflunitrazepam was conducted with both methods proving that the analytical results are equivalent even near the limits of quantification (low ng/ml range). To our best knowledge, this application is the first one reported in the literature employing this sample preparation system.

•Tissue distribution of codeine and metabolites in codeine-related deaths is presented.•Concentrations were lower in brain, fat, muscle and vitreous fluid than in blood.•In brain, the active moieties morphine and M6G were morphine, and M3G>M6G>morphine. In matrices other than blood, the concentration pattern was similar, although in a less systematic fashion. Measured concentrations were generally lower in matrices other than blood, especially in brain and fat, and in particular for the glucuronides (C6G, M3G and M6G) and, to some extent, morphine. In brain tissue, the presumed active moieties morphine and M6G were both below the LLOQ (0.0080mg/L and 0.058mg/L, respectively) in a majority of cases. In general, there was a large variability in both measured concentrations and calculated blood/tissue concentration ratios. There was also a large variability in calculated ratios of morphine to codeine, C6G to codeine and norcodeine to codeine in all matrices, and CYP2D6 genotype was not a reliable predictor of these ratios. The different blood/tissue concentration ratios showed no systematic relationship with the post-mortem interval. No coherent degradation or formation patterns for codeine, morphine, M3G and M6G were observed upon reanalysis in peripheral blood after storage.

•Mag-CNTs/d-µSPE/GC-MS was validated for opiates analysis from poppy seed tea.•Brews from small quantity seed may provide little to no euphoric or analgesic effects.•Majority of opiates were extracted in the first brew.•Opiates produced after the initial brew were minimal to prolong desirable effects.•Adverse or lethal effects could be reached if moderate amount of seeds were used for brewing. With tightening enforcement and restrictions amid the opioid epidemic, poppy seed tea is consumed as an alternative to mitigate the withdrawal symptoms or as a home remedy to relieve pain and stress. Previously published studies suggested the potential danger of consuming tea brewed with a moderate to a large amount of poppy seed. In this study, the effects of small quantity and repeat brewing on opiate concentrations were evaluated. A dispersive-micro solid phase extraction facilitated by magnetic carbon nanotubes (Mag-CNTs/d-µSPE) was developed, optimized, successfully validated, and applied to ten poppy seed tea samples using gas chromatography-mass spectrometry (GC-MS) analysis. A total of ten poppy seed samples were evaluated in this work. Two grams of bulk poppy seeds were brewed with 6 mL of heated and acidified DI water three times. The brewed tea samples were subjected to the validated Mag-CNTs/d-µSPE/GC-MS analysis. The total mean opiate concentrations obtained from three brews were 1.1–1926, 20.2–311, and 9.0–100 mg/kg for morphine, codeine, and thebaine, respectively. The total opiate yields obtained from the small quantity brewing, i.e., 6 g seed in 18 mL tea, in this study may provide minimal analgesic and euphoric effects. Over 80% of the total opiate yield was extracted in the first brew with acidified deionized water from the 10 min brewing period, and opiate yields from the second and third brew were minimal. However, potential overdose could occur for some tea samples when scaled up to the starter quantity of seed suggested for new users.