Analysis of drugs including illicit and new psychoactive substances in oral fluids by gas chromatography-drift tube ion mobility spectrometry.

In this study, a gas chromatograph (GC) has been coupled to a drift tube ion mobility spectrometer (IMS) in order to develop an analytical procedure for the determination of psychoactive substances in oral fluids. Working parameters, including the GC-IMS interface ones, were adjusted in order to obtain sensitive and robust signals. A volume of 500 µL of oral fluid was extracted with 250 µL chloroform and, after centrifugation, were injected into the GC-IMS system. Amphetamine, methylone, α-PVP, ketamine, lidocaine, MPHP, cocaine, THJ-2201, and 5F-ADB were employed as model compounds, providing limits of detection from 6 to 15 µg L-1 and recoveries from 70 to 115% for field oral fluids spiked with target analytes at 250, 500, and 600 µg L-1. Moreover, two oral fluid certified reference materials were analysed by the proposed GC-IMS based methodology with obtained relative percentage errors lower than 8.4%, being the proposed GC-IMS procedure a reliable, selective, and sensitive technique for the determination of psychoactive substances in oral fluids.

Dual mixed-mode poly (vinylpyridine-co-methacrylic acid-co-ethylene glycol dimethacrylate)-based sorbent for acidic and basic drug extraction from oral fluid samples.

In this study, a dual mixed-mode polymer sorbent was prepared via one-step thermally initiated polymerization of 4-vinylpyridine (VP), methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) for the solid-phase extraction (SPE) of basic and acidic drugs. The use of VP and MAA as ionizable functional monomers allowed the tailoring of ion-exchange and hydrophobic features of the polymer. The obtained polymer was characterized by Fourier-transform infrared spectroscopy and scanning electron microscopy. Next, the retention behavior of dual mixed-mode polymer towards basic and acidic drugs was investigated. Moreover, the practical capability of this novel material was tested for the extraction of relevant drugs such as cocaine, 3-methylmethcathinone, and diazepam in oral fluid samples. Recovery values (at different spiked levels in blank oral fluid samples), ranging from 69 to 99%, and limits of detection (LODs), between 0.10 and 0.25 µg L-1, were obtained.

Skin Permeation of Hazardous Compounds of Tobacco Smoke in Presence of Antipollution Cosmetics.

Negative health effects of active and passive smokers have been widely described, but the effect of tobacco smoke on the skin has been less explored. In this study, an analytical methodology has been developed to evaluate the dermal permeation of hazardous compounds present in tobacco smoke, using an exposition chamber to simulate finite and infinite smoking conditions, in vitro vertical Franz diffusion cells, and Strat-M® membranes as human skin simulants. Moreover, the antipollution effect of three cosmetics has been evaluated, showing a significant efficacy to reduce dermal permeation of hazardous tobacco-smoke compounds such as of nicotine and aromatic hydrocarbons.

Direct and fast determination of polychlorinated biphenyls in contaminated soils and sediments by thermal desorption-gas chromatography-tandem mass spectrometry.

A direct procedure based on thermal desorption-gas chromatography-tandem mass spectrometry (TD-GC-MS-MS) was developed for the fast extraction of seven polychlorinated biphenyls (PCBs) from sediments and soils. PCBs were directly extracted, from 20 to 75 mg of sample, without any chemical pre-treatment or use of organic solvents, after the addition of 10 µL internal standard (PCB 195) in acetone. Sample treatment was totally automated. PCBs were extracted at 250 °C for 20 min, using a helium flow and the PCBs were trapped in a cryogenic Tenax trap at -10 °C. After that, analytes were directly desorbed at 270 °C and introduced to the GC-MS-MS system. Recoveries were established using spiked soil and sediment from 2.5 to 50 ng g-1, obtaining values from 74 to 127%. The limits of quantification were from 1.0 to 1.7 ng g-1 for soil and from 0.3 to 0.4 ng g-1 for sediments, respectively. Precision, assessed as the relative standard deviation (RSD), was lower than 8 and 11% for sediment and soil analysis, respectively, except for PCB-28 in soil samples which provided a RSD of 18%. Certified reference material and field samples were analysed by the proposed TD-GC-MS-MS method. Results were compared by a paired samples Student's t-test with those obtained by a reference extraction procedure based on pressurized solvent extraction, followed by stir bar sorptive extraction, being statistically comparable (α = 0.05). A comprehensive greenmetric evaluation of the proposed method was carried out, having the TD extraction a negligible environmental impact as compared to conventional extraction procedures.

Development of immunosorbents for the analysis of forchlorfenuron in fruit juices by ion mobility spectrometry.

The advantages of using smart materials as immunosorbents in the analysis of complex matrices by ion mobility spectrometry (IMS) have been highlighted in this study. A novel analytical method has been proposed for the sensitive, selective, and fast determination of residues of the plant growth regulator forchlorfenuron in fruit juices. Three different monoclonal antibodies (s3#22, p2#21, and p6#41) were employed for the production of immunosorbents, based on Sepharose gel beads, which were characterized in terms of loading capacity, solvent resistance, and repeatability for its use in solid-phase extraction (SPE). Immunosorbents that were prepared with antibody p6#44 provided the best performance, with a loading capacity of 0.97 µg, a 10% (v/v) 2-propanol tolerance, and a reusability of at least eight uses. The SPE procedure involved the use of a column with 0.15 g Sepharose beads, containing 0.5 mg antibody, which was loaded to 20 mL of the sample, washed with 2 mL of water plus 2 mL of 10% (v/v) 2-propanol, and eluted with 2 mL of 2-propanol. The cleaned extract was directly analyzed by IMS, giving a limit of detection of 2 µg L-1 with a relative standard deviation of 7.6%. Trueness was assessed by the analysis of blank grape and kiwifruit juice samples spiked with forchlorfenuron concentrations from 10 to 400 µg L-1, with recoveries from 80 to 115%. The analytical performance of the proposed immunosorbent was compared with conventional extraction and cleanup methods, such as QuEChERS and C18-based SPE, giving the cleanest extracts for accurate determinations of forchlorfenuron by IMS. Graphical abstract ᅟ.

Comprehensive analysis of airborne pesticides using hard cap espresso extraction-liquid chromatography-high-resolution mass spectrometry.

A hard cap espresso extraction procedure has been developed to recover airborne pesticides in particulate matter trapped in filters. This extraction step was made for 20s at 72°C and 19bar using 50mL of 20% (v/v) acetonitrile in water. After that, based on NaCl salting out, extracts were concentrated 22 times and analysed by ultra-high performance liquid chromatography - high resolution mass spectrometry. 35 pesticides were evaluated, as a proof of concept, being validated the whole methodology and compared the extraction method with that based on microwave assisted extraction for 20min. In short, the method avoids cross-contamination of samples, it is relatively fast and consumes only 10mL acetonitrile and 8g NaCl per sample; thus, offering a low cost and green alternatively to available methods based on pressurized solvent extraction or microwave-assisted treatment.

Hard cap espresso extraction-stir bar preconcentration of polychlorinated biphenyls in soil and sediments.

A Nespresso© hard cap espresso machine has been employed for the quantitative extraction of polychlorinated biphenyls (PCBs) from sediments and soils. Sample extraction was performed from five grams of sample in less than 40 s, with 200 mL ethanol 40% (v/v) in water and PCBs were concentrated using stir bar sorptive extraction (SBSE) and determined by thermal desorption-gas chromatography-tandem mass spectrometry (TD-GC-MS-MS). Eleven PCB congeners (28, 52, 77, 80, 81, 101, 118, 138, 153,169, and 180) were determined in soils and sediments with limits of quantification in the 0.03-0.08 ng g-1 range. Extraction efficiency was established by the analysis of soil samples spiked with the studied PCBs at concentrations from 0.1 to 10.0 ng g-1, obtaining quantitative recoveries from 81 to 120% and an adequate precision with relative standard deviations lower than 20%. Certified reference materials and natural samples were analyzed by the proposed hard cap espresso extraction and results were compared with those provided by a reference procedure based on pressurized solvent extraction, obtaining statistically comparable results. Therefore, the use of a hard cap espresso machine in tandem with SBSE and TD-GC-MS-MS allowed a simple, sensitive and quantitative determination of PCBs.

Ion mobility spectrometry evaluation of cocaine occupational exposure in forensic laboratories.

An approach, based on ion mobility spectrometry (IMS) has been developed for the control of cocaine in air of the breathing zone of operators, in laboratory surfaces and in nasal mucus of employees to evaluate cocaine exposure in a forensic laboratory. The analytical methodology has been validated in terms of accuracy, precision and limits of detection and results obtained were statistically comparable with those obtained by liquid chromatography. Cocaine concentration in laboratory air increases from 100 ± 35 ng m(-3) of a normal day to 10,000 ng m(-3) during the manipulation of cocaine seizures. The occupational exposure limit (OEL) for cocaine has not been established which difficult the evaluation of the health effects of continuous exposition to very small doses of cocaine. Cocaine was also found in almost all the analyzed sample surfaces and also was found in nasal mucus of the police officers that were present during the manipulation of cocaine seizures without using a face mask. In summary, cocaine concentrations could present a health hazard to the employees and therefore warrants remediation and some modifications of the manipulation operations have been proposed.

Capillary liquid chromatography with off-line mid-IR and Raman micro-spectroscopic detection: analysis of chlorinated pesticides at ppb levels.

A flow-through microdispenser was used as a solvent elimination interface, allowing vibrational spectroscopic detection in capillary liquid chromatography in addition to standard UV detection. Using a flow-through microdispenser, robust and stable deposition of picoliter-sized droplets on a CaF(2) plate window was achieved. The CaF(2) window was placed on a thermostated sample holder (80 degrees C) mounted on a computerized x, y stage for achieving fast solvent evaporation and enabling recording of the chromatogram as a trace of deposited material. The dried residues that were formed had diameters of a few tens of micrometers and were analysed by mid-IR and Raman micro-spectroscopy. Conditions were optimized for high sensitivity of measurement and maintaining chromatographic resolution during the deposition step. Due to the destruction-free character of Raman and FTIR spectroscopy, these techniques could be applied sequentially to interrogate the same deposits. To test the usefulness of the methodology for environmental analysis, the determination and unambiguous identification of chlorinated pesticides (chlortoluron, diuron, atrazine, and terbuthylazine) in river water was used as an example, obtaining limits of identification of 2 ng analyte on-column and precision of approximately 10% RSD. The application of the developed method to spiked real river samples demonstrated the identification power of the proposed method as, in addition to the four previously studied pesticides, two additional pesticides (simazine and isoproturon) could also be detected and identified.

Univariate near infrared methods for determination of pesticides in agrochemicals.

It has been developed a general strategy for the determination of pesticides in agrochemicals by Fourier transform near infrared (FT-NIR) spectroscopy. The methodology is based on previous extraction of the active principles through sonication with acetonitrile and direct determination by transmission measurements, using glass vials as measurement cells and univariate calibration at selected wavenumbers as a function of the pesticide to be analyzed. Chlorsulfuron, metamitron, iprodione, pirimicarb, procymidone and tricyclazole were used as test molecules and data obtained by FT-NIR for 20 samples containing one of these active principles compare well with those found by reference liquid chromatography (HPLC) procedures. In short, FT-NIR provides relative standard deviations between 0.04 and 0.7% and limit of detection values ranging from 0.004 to 0.17 mg g(-1) with recovery values between 96.4 and 100.5%. On the other hand, FT-NIR offers a 10 times faster methodology than chromatography ones and an environmentally friendly alternative which reduces the reagent consumption to 1 mL acetonitrile per sample.