Handheld SERS coupled with QuEChERs for the sensitive analysis of multiple pesticides in basmati rice

Pesticides are a safety issue globally and cause serious concerns for the environment, wildlife and human health. The handheld detection of four pesticide residues widely used in Basmati rice production using surface-enhanced Raman spectroscopy (SERS) is reported. Different SERS substrates were synthesised and their plasmonic and Raman scattering properties evaluated. Using this approach, detection limits for pesticide residues were achieved within the range of 5 ppb-75 ppb, in solvent. Various extraction techniques were assessed to recover pesticide residues from spiked Basmati rice. Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERs) acetate extraction was applied and characteristic spectral data for each pesticide was obtained from the spiked matrix and analysed using handheld-SERS. This approach allowed detection limits within the matrix conditions to be markedly improved, due to the rapid aggregation of nanogold caused by the extraction medium. Thus, detection limits for three out of four pesticides were detectable below the Maximum Residue Limits (MRLs) of 10 ppb in Basmati rice. Furthermore, the multiplexing performance of handheld-SERS was assessed in solvent and matrix conditions. This study highlights the great potential of handheld-SERS for the rapid on-site detection of pesticide residues in rice and other commodities.

Determination of long distance transport of Cs+, Co2+ and Zn2+ ions in vascular plants by autoradiography and gamma-spectrometry

Heavy metals and radionuclides can enter the food chain via cereals and vegetables grown in contaminated soils. In the case of microelements such as zinc, studies have not focused only to assessing its environmental risk, but also to enhancing its uptake by plants as an important growth-limiting factor. In our study, digitalized autoradiograms of whole plants of celery (Apium graveolens L.), tobacco (Nicotiana tabacum L.) and sunflower (Helianthus annuus L.) grown in hydroponic nutrient media spiked with 137CsCl, 60CoCl2 and 65ZnCl2 were used for quantitative determination of uptake, long-distance transport and distribution of Cs+, Co2+ and Zn2+ ions in plant tissues. Results from autoradiography and gammaspectrometry of plants showed, that cesium was translocated to aboveground part of the plants with the shoot-to-root ratio 1.0 : 0.6. On the contrary, cobalt and zinc were more immobilized in roots, with the shoot-to-root ratio up to 1.0 : 3.8. The highest concentration of cesium, cobalt and zinc, expressed in specific radioactivity per unit of leaf surface (Bq/cm2) was found in top, rapidly growing leaves, the lowest concentration in the oldest leaves in low position. Detection limits 3, 2 and 14 Bq/cm2 by using X-ray film for 137Cs, 60Co and 65Zn, respectively were obtained. These data correspond to detection limits 10.5 pg Cs+/cm2, 7.2 pg Co2+/cm2 and 785 pg Zn2+/cm2 at specific radioactivity of commercially available 137CsCl, 60CoCl2 and 65ZnCl2. Resolutions 1-2 mm was sufficient for visualization of metal uptake and distribution in roots, stalks, leaves and leaf venation. Obtained data are part of quantitative study of uptake and translocation of both low level-radioactive contamination in plants and microelements applied as fertilizers.

Determination of the content of impurity elements in a sample of high purity India by the method of radiochemical neutron activation analysis

The present article is devoted to the development of a method for neutron activation analysis of a microimpurity composition of high-purity indium with the radiochemical separation of indium radionuclides from radionuclides of the determined elements by extraction chromatography in the system tributyl phosphate (TBP) - solutions of hydrobromic acid (HBr). Neutron activation analysis (NAA) has a special place among the physical methods for determining the trace composition of high-purity substances. Low detection limits, the possibility of simultaneous determination of a large number of impurity elements from one sample, no correction for the control experiment, the possibility of using inactive carriers in separating traces of radionuclides of impurity elements from matrix elements ensured the widespread use of NAA in the analysis of highly pure substances. The developed technique allows separating matrix radionuclides from radionuclides of impurity elements with high efficiency and determination of 28 impurity elements in high-purity indium with detection limits of 0.7 ppm to 0.05 ppb.

Improving Planet Detection with Disk Modeling: Keck/NIRC2 Imaging of the HD 34282 Single-armed Protoplanetary Disk

Formed in protoplanetary disks around young stars, giant planets can leave observational features such as spirals and gaps in their natal disks through planet–disk interactions. Although such features can indicate the existence of giant planets, protoplanetary disk signals can overwhelm the innate luminosity of planets. Therefore, in order to image planets that are embedded in disks, it is necessary to remove the contamination from the disks to reveal the planets possibly hiding within their natal environments. We observe and directly model the detected disk in the Keck/NIRC2 vortex coronagraph L′-band observations of the single-armed protoplanetary disk around HD 34282. Despite a nondetection of companions for HD 34282, this direct disk modeling improves planet detection sensitivity by up to a factor of 2 in flux ratio and ∼10 M Jupiter in mass. This suggests that performing disk modeling can improve directly imaged planet detection limits in systems with visible scattered light disks, and can help to better constrain the occurrence rates of self-luminous planets in these systems.

Spectrofluorimetric Determination of Some N. Containing Medicines Using Rhodamine 6G as a Chromogenic Reagent

A sensitive spectrofluorimetric method has been developed for the analysis of some medicines containing primary, secondary, and tertiary amino groups, namely Diclofenac (DIC), Domperidone (DOM), Famotidine (FAM), and Propranolol (PRO), in their pure and medicinal forms. The method is based on the quenching of the fluorescence intensity of rhodamine 6G (R6G) through the formation of ion-pair complexes between the above medicines and the R-6G reagent, which is measured at 552 nm after excitation at 402 nm. The calibration graphs were rectilinear in the concentration ranges of 0.10- 9.00, 0.05-15.00, 0.10-14.0 and 0.05-5.00 µg mL-1 for above medicines respectively. The recovery (%) values were ranged between 99.45%- 100.97%. The detection limits ranged in the concentration of 0.243-0.754 µg/mL, and the limits of quantitation were 0.806- 2.420 µgmL-1 for all drugs. The method was successfully applied for the determination of these drugs in their pharmaceutical preparations.

UiO-66 Selective Enrichment Integrated with Thermal Desorption GC-MS for Detection of Benzene Homologues in Ambient Air

In this study, UiO-66 was selected as sorbent media packed in the tube to selectively enrich trace levels of benzene homologues such as benzene, toluene, and xylene (BTX) in ambient air prior to thermal desorption (TD)-GC-MS determination. A series of experiments were conducted to obtain the optimal TD conditions. The results indicated that the optimal TD parameters were as follows: desorption temperature of 180°C, desorption flow rate of 50 mL min−1, and desorption time of 30 min. Furthermore, the method based on UiO-66 enrichment integrated with TD-GC-MS for trace levels of BTX was successfully developed. It exhibited a good linearity (R2 > 0.99) in the range of 50–1000 ng, except for p, m-xylene in the range of 100–2000 ng, and achieved the recovery of 69.4–101.3%, and the relative standard deviation of 3.8–6.4%. The detection limits of BTX were 1.6–4.0 ng; according to 10 L of sampling volume, the method detection limits would be in the range of 0.16–0.40 µg m−3. Additionally, the method was successfully applied to determine BTX in indoor air and showed good selectivity and sensitivity. In summary, the findings in this work revealed that UiO-66 was an attractive adsorbent for selective enrichment trace levels of BTX compounds in ambient air, which was favorable for the subsequent detection by TD-GC-MS.

Efficiency of the Stool-PCR Test Targeting NADH Dehydrogenase (Nad) Subunits for Detection of Opisthorchis viverrini Eggs

Opisthorchis viverrini infection is the major parasitic infection problem in Southeast Asian countries, and long-term infection will lead to cholangiocarcinoma (CCA), the bile duct cancer. The early diagnosis of O. viverrini infection may interrupt the progression of the opisthorchiasis and other related illnesses, especially CCA. The current diagnostic procedure is stool examination by microscope-based methods such as direct smear and concentration techniques but it is limited by low parasite egg numbers. The molecular diagnosis prompts the chance to evaluate the light infection with low number of parasite eggs but is currently inconvenient for routine use due to special equipment requirement and unstable sensitivities. Our present study aims to establish the efficiency of OvNad subunits, the mitochondrial gene, for introducing as a potential diagnostic target by conventional PCR, the cheapest and easiest molecular procedure. A total of 166 stool samples were investigated microscopically by the PBS-ethyl acetate concentration technique (PECT); 75 samples were O. viverrini positive with 28 samples that were positive with single parasite (hookworm, A. lumbricoides, S. stercoralis, Taenia spp., and T. trichiura), 11 samples were with mixed infection, and 52 samples were without parasite detection. The detection limits of OvNad subunits were evaluated in artificially spiked samples containing 0, 1, 5, 10, 20, 50, and 100 Ov-eggs. The result suggested that the best detection efficacy was of OvNad5 that had exact detection limits at only 5 eggs. In the PCR amplification of OvNad subunits, there exist 100% specificities with varied sensitivities from 64%, 88%, 80%, and 100% of OvNad1, OvNad2, OvNad4, and OvNad5, respectively. OvNad subunits were amplified specifically without cross reactivity with the other collected parasites. Our study established that OvNad subunits, especially OvNad5, are the potent candidates for PCR amplification of stool containing Ov-eggs with high confidential sensitivity, specificity, PPV, and NPV even in the light infection that would be a benefit for developing as a routine diagnosis of O. viverrini infection.