Dhananjay Kumar Tewary

Development and applications of single-drop microextraction for pesticide residue analysis: A review.

Single-drop microextraction (SDME) has become more popular than other microextraction techniques because it is simple, cost-effective, easy to operate and nearly solvent-free. The technique has been employed successfully for trace analysis in environmental, biomedical and food applications. In view of the increasingly stringent regulatory limits for many pesticides, which are below the LOD of the existing instruments, SDME may provide a cost-effective solution for reducing the LOD of pesticides. The present review focuses on recent development in SDME technique, and its application coupled with various analytical techniques, such as GC-MS, GC and HPLC for pesticide residue analysis in different matrices. The advantages, limitations and outlook on the future of SDME technique for its wider applications are also discussed.

Larvicidal and structure-activity studies of natural phenylpropanoids and their semisynthetic derivatives against the tobacco armyworm Spodoptera litura (Fab.) (Lepidoptera: Noctuidae).

The larvicidal activity of 18 phenylpropanoids, 1–18, including phenylpropenoate, phenylpropenal, phenylpropene, and their semisynthetic analogues, were evaluated against the tobacco armyworm, Spodoptera litura (Fab.), to identify promising structures with insecticidal activity. Amongst various phenylpropanoids, isosafrole, a phenylpropene, showed the best activity, with an LC50 value of 0.6 μg/leaf cm2, followed by its hydrogenated derivative dihydrosafrole (LC50=2.7 μg/leaf cm2). The overall larvicidal activity of various phenylpropene derivatives was observed in the following order: isosafrole (6)>dihydrosafrole (16)>safrole (12)>anethole (4)>methyl eugenol (11)>eugenol (13)>β‐asarone (8)>dihydroasarone (18)>dihydroanethole (15). Dihydrosafrole might be a promising compound, although presenting a lower larvicidal activity than isosafrole, because of its better stability and resistance to oxidative degradation (due to the removal of the extremely reactive olefinic bond) in comparison to isosafrole. Such structure–activity relationship studies promote the identification of lead structures from natural sources for the development of larvicidal products against S. litura and related insect pests.

Chemical composition and larvicidal activities of the Himalayan cedar, Cedrus deodara essential oil and its fractions against the diamondback moth, Plutella xylostella

Abstract Plants and plant-derived materials play an extremely important role in pest management programs. Essential oil from wood chips of Himalayan Cedar, Cedrus deodara (Roxburgh) Don (Pinales: Pinaceae), was obtained by hydrodistillation and fractionated to pentane and acetonitrile from which himachalenes and atlantones enriched fractions were isolated. A total of forty compounds were identified from these fractions using GC and GC-MS analyses. Essential oils and fractions were evaluated for insecticidal activities against second instars of the diamondback moth, Plutella xylostella L. (Lepidoptera: Yponomeutidae), using a leaf dip method. All samples showed promising larvicidal activity against larvae of P. xylostella. The pentane fraction was the most toxic with a LC50 value of 287 µg/ml. The himachalenes enriched fraction was more toxic (LC50 = 362 µg/ml) than the atlantones enriched fraction (LC50 = 365 µg/ml). LC50 of crude oil was 425 µg/ml and acetonitrile fraction was LC50 = 815 µg/ml. The major constituents, himachalenes and atlantones, likely accounted for the insecticidal action. Present bioassay results revealed the potential for essential oil and different constituents of C. deodara as botanical larvicides for their use in pest management.

Analytical Method for Determination of Organochlorine Pesticides in Tea Brews using Single-Drop Microextraction with GC-ECD

The single drop microextraction method was developed for the determination of ten organochlorine pesticides in tea brews using gas chromatograph-electron capture detector. The optimized parameters for effective extraction required a 2 μL drop of n-hexane at the tip of a microsyringe immersed in 5 mL of a diluted tea brew sample for 25 min and stirred at 600 rpm. The limit of detection in the range of 0.01 to 0.025 μg/L, with relative standard deviation of repeatability and reproducibility, was in the range of 1–10 and 8–24%. The relationship of the measured signal was a linear function (>0.9863) of concentration and the recovery method ranged from 92–116%. The single drop microextraction method showed the advantage of being easy to operate, low consumption of organic solvent, and high extraction efficiency.