Chitra Srivastava

Nanosulfur: A Potent Fungicide Against Food Pathogen, Aspergillus niger

Elemental sulfur (S0), man’s oldest eco‐friendly fungicide for curing fungal infections in plants and animals, is registered in India as a non‐systemic and contact fungicide. However due to its high volume requirement, Indian agrochemical industry and farmers could not effectively use this product till date. We hypothesize that intelligent nanoscience applications might increase the visibility of nanosulfur in Indian agriculture as a potent and eco‐safe fungicide. Sulfur nanoparticles (NPs) were synthesized bottom‐up via a liquid synthesis method with average particle size in the range of 50–80 nm and the shapes of the NPs were spherical. A comparative study of elemental and nano‐sulfur produced has been tested against facultative fungal food pathogen, Aspergillus niger. Results showed that nanosulfur is more efficacious than its elemental form.

Bio-efficacy evaluation of nanoformulations of β-cyfluthrin against Callosobruchus maculatus (Coleoptera: Bruchidae)

In the present investigation, bioefficacy of developed β-cyfluthrin formulations, utilizing laboratory synthesized poly(ethylene glycols) based amphiphilic copolymers, were evaluated against Callosobruchus maculatus (Coleoptera: Bruchidae). The bioefficacy data indicated that the formulations developed by utilizing polymers having PEG – 1500 (3c) and PEG – 2000 (3d) as the hydrophilic segment showed greater efficacy after 14 days as evident from EC50 values (2.2 and 1.58 mg L−1 respectively). Also, release from the commercial SC formulation was faster than developed formulations as the commercial formulation had the lowest EC50 value on the first day (0.51 mg L−1). The mean EC50 of the commercial formulation against C. maculatus was quite high as compared to those of developed formulations. The results suggest that depending upon the polymer matrix used, the application rate of β-cyfluthrin can be optimized to achieve insect control at the desired level and period. The results described in this paper are promising and provide a comparison of developed formulations with the commercial one showing an earlier degradation of β-cyfluthrin in the latter and relatively prolonged activity in the former.

Development of pyridalyl nanocapsule suspension for efficient management of tomato fruit and shoot borer (Helicoverpa armigera)

The objective of this study was to evaluate in vitro the insecticidal activity of pyridalyl nanosuspension in comparison to technical material and commercial formulation against larvae of Helicoverpa armigera. Suspension of pyridalyl nanocapsules was prepared, for reducing its dose of application. Compatibility of pyridalyl with sodium alginate was ascertained and a formulation was obtained by optimizing various parameters. Average micelle size of different formulations was around 138 nm and size of pyridalyl was less than 100 nm. Spherical shape and nanosize of capsules was confirmed by Transmission electron microscopy. Zeta potential of optimized formulation was found to be about (−)20 ± 1 Mv indicating acceptable range for expressing physical stability of the nano-capsules. The pyridalyl nanosuspension insecticidal activity increased remarkably, with LC50 values of 40 μg mL−1 in comparison to LC50 values of technical material (90 μg mL−1) and commercial product (250 μg mL−1). Bioassay results by leaf dip method showed that nanoformulation is 2.26 and 6.25 times more effective against H. armigera as stomach poison than the technical product and commercial formulation respectively. By topical method, the LC50 values obtained were 80, 150, and 250 μg mL−1 for nanoformulation, technical material, and commercial formulation, respectively, proving our hypothesis. Pyridalyl nanocapsule suspension performed effectively than technical material and commercial product against tomato fruit and shoot borer (Helicoverpa armigera), showing that insecticide load to the environment can be reduced by using nanoformulations.

Synthesis of novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects.

Novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones have been synthesized in high yields by treatment of the corresponding oxo analogs with Lawessons reagent. The structure has been confirmed by X-ray analysis. The compounds were tested for in vitro antifungal activity against Rhizoctonia bataticola, Sclerotium rolfsii, Fusarium oxysporum and Alternaria porii. The compounds exhibited moderate to good activity against all pathogens. Insecticidal activity of these compounds against Spodoptera litura was observed to be comparable to commercial pyrethroid insecticide, cypermethrin. The urease inhibitory activity has also been studied.

Suitability of Nano-sulphur for Biorational Management of Powdery mildew of Okra (Abelmoschus esculentus Moench) caused by Erysiphe cichoracearum

New nano-sulphur synthesized at IARI and three other commercial products namely commercial sulphur (Merck), commercial nano-sulphur (M K Impex, Canada) and Sulphur 80 WP (Corel Insecticide) were evaluated in vitro for fungicidal efficacy at 1000 ppm against Erysiphe cichoracearum of okra. All the sulphur fungicides significantly reduced the germination of conidia of E. cichoracearum as compared to control. Least conidial germination was recorded in IARI nano-sulphur (4.56%) followed by Canadian nanosulphur (14.17%), Merck sulphur (15.53%), sulphur 80 WP (15.97%) and control (23.09%). Non-germinated conidia count was also high in case of IARI nanosulphur followed by Canadian nano-sulphur, Merck sulphur and Sulphur 80WP. Apart from inhibition of conidial germination, cleistothecial appendages were also disrupted in contact with nano-sulphur and the cleistothecia became sterile. The study proved that IARI nano-sulphur is more effective than the commercial formulations and could be applied at lower amount for controlling powdery mildew disease for its better efficacy.

Effect Sulfur and ZnO Nanoparticles on Stress Physiology and Plant (Vignaradiata) Nutrition

Phytotoxic and agro beneficial properties of antimicrobially efficient Sulfur nanoparticles (SNPs) and ZnO nanoparticles (ZNPs) were evaluated on Mung (Vigna radiata). Mung seeds were germinated with an increasing concentration gradient of nanoparticles. The extent of phtotoxicity were assessed depending upon the effect of used nanoparticles on physical factors (relative root and shoot length, dry weight and area of leaves), photosynthetic pigments (chlorophyll, carotene and xanthophyll content) and mitochondrial stress indicator level (thiol), A simultaneous study was undertaken to understand the effect of SNPs and ZNPs on overall plant growth and nutrition. The nutritive values of nanoparticles were determined in terms of total lipid and protein content. All the aforementioned biochemical assays were performed in triplicate for statistical viability.

Insecticidal and antifeedant activities of clerodane diterpenoids isolated from the Indian bhant tree, Clerodendron infortunatum, against the cotton bollworm, Helicoverpa armigera

Abstract The Indian bhant tree, Clerodendron infortunatum L. (Lamialus: Lamiaceae), is a well-known medicinal plant, but little information about its bioefficacy against agricultural pests exists. This scarcity was addressed in the present study, in which dried leaves of C. infortunatum were subjected to extraction with hexane and methanol and then partitioned using different solvents of varying polarity. In a preliminary bioassay, the antifeedant effects of the crude extracts and fractions were tested on a highly polyphagous pest, the cotton bollworm, Helicoverpa armigera Hübner (Lepidoptera: Noctuidae), using the no-choice test method with cabbage leaf discs. The methanol fraction resulted in maximum antifeedant activity. This fraction was further subjected to crystallization and column chromatography in order to isolate the compounds responsible for the activity. Three pure compounds were isolated and identified as clerodin (CL), 15-methoxy-14, 15-dihydroclerodin (MD), and 15-hydroxy-14, 15-dihyroclerodin (HD). The antifeedant activity of these compounds was studied using a choice as well as a no-choice test method with 24 and 48 hr observation periods. Insecticidal activity was measured using the topical application method at 0.5, 1, 1.5, 2, 2.5, and 3% concentrations, and data were recorded 24, 48, and 72 hr after treatment. In the no-choice test conditions, compounds CL and MD showed significantly higher antifeedant activity compared to the key ingredient in many commercial pesticides, azadirachtin, at its highest concentration. Compound HD also showed very good antifeedant activity, which did not differ significantly from that of azadirachtin. In the choice test conditions, all three compounds and azadirachtin showed 100% antifeedant activity at the highest concentration. Antifeedant Index (AI50) values of CL, MD, and HD were 6, 6, and 8 ppm in choice tests, and increased to 8, 9, and 11 ppm in the no-choice tests, respectively. Insecticidal activity of the isolated compounds was not significant compared to the control condition, even at the highest con-concentrations of the compounds. These results suggest that extracts of C. infortunatum have very good antifeedant effects against H. armigera due to the presence of specific compounds. These compounds could be utilized in the development of new biopesticides.

Synthesis and bioefficacy evaluation of new 3-substituted-3,4-dihydro-1,3-benzoxazines

A new series of 1, 3-Benzoxazines were synthesized, characterized (1H NMR and 13C NMR) and evaluated for their pesticidal activity. Six new 3-alkyl-3, 4-dihydro-4-methyl-2H-1, 3-benzoxazines (1-6) were prepared by hydroxymethylation of secondary amines with formaldehyde in 65–68% yields. These compounds were screened for there IGR activity against Spodoptera litura and for antifungal fungal activity in vitro against Sclerotium rolfsii ITCC 6181 by poisoned food technique. Insect Growth Regulatory (IGR) activity against Spodoptera litura showed that compound 3-Nonyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines was most effective as IGR with larval GI50 of 1.863 μ g/Insect. Compounds 3-Octyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines and 3-Decyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines were effective IGRs. Antifungal screening revealed that compound 3-Dodecyl-3, 4-dihydro-4-methyl-2H-1,3-benzoxazines, was highly effective against Sclerotium rolfsii with LC50 value 31.7 mg L−1 comparable with commercial fungicide Hexaconazole (LC50 1.27 mg L−1). Also compounds 3-Nonyl-3, 4-dihydro-4-methyl-2H-1,3-benzoxazines and 3-Decyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines displayed promising fungitoxicity. The results described in this paper are promising and provides new array of synthetic chemicals to be utilized as pesticides.

Synthesis and pesticidal activity of new N-alkyl-N-[1-(2-hydroxyphenyl) ethyl]amines

A series of novel N-alkyl-N-[1-(2-hydroxyphenyl) ethyl]amines were synthesized as potential new agents to control pests. Their structures were confirmed on the basis of IR, NMR and elemental analyses. Six new N-alkyl-N-[1-(2-hydroxyphenyl) ethyl]amines were prepared by reduction of corresponding Schiff bases using sodium borohydride in 80–87 % yields. These compounds were tested for their antifungal activity against two pathogenic fungi viz., Rhizoctonia bataticola ITCC 0482 and Sclerotium rolfsii ITCC 5226 and for insecticidal activity against insects of stored grain pest Callosobruchus analis. Fungicidal bioassay revealed that compound N-Decyl-N-[1-(2-hydroxyphenyl)ethyl]amine, was highly effective against R. bataticola (ED50 6.86 mg L−1) which was comparable with that of commercial fungicide hexaconazole (ED50 6.35 mg L−1). Also compounds N-Heptyl-N-[1-(2-hydroxyphenyl)ethyl]amine, N-Octyl-N-[1-(2-hydroxyphenyl)ethyl]amine and N-Nonyl-N-[1-(2-hydroxyphenyl)ethyl]amine displayed promising fungitoxicity against same pathogen. However, compound N-Heptyl-N-[1-(2-hydroxyphenyl)ethyl]amine was also found to be effective against S. rolfsii (ED50 4.92 mg L−1 as against 1.27 mg L−1 for hexaconazole). Compound N-Hexyl-N-[1-(2-hydroxyphenyl)ethyl]amine was most effective as insecticide followed by compound N-Octyl-N-[1-(2-hydroxyphenyl)ethyl]amine. LC50 values for these compounds were 155.0 and 275.0 mg L−1 respectively as against 36.70 mg L−1 for commercial insecticide dichlorovos. The results obtained from bioassays indicate that this class of compounds can be utilized for the design of new substances endowed with pesticidal activities.

Sensitive and rapid determination of elemental nanosulfur/sulfur by liquid chromatography

In order to identify the most suitable method for the estimation of nanosulfur for studying its residue dynamics, the present work was taken up. HPLC and GC methods were explored for its analysis. A comparative study of the existing analytical methods for the quality control of nanosulfur was undertaken. UV spectrophotometry and HPLC methods were superior with lower LOD when compared to GC-MS, which was not satisfactory due to breakage of catenated S20 into S6 and S8 . The method has been validated by analyzing various nanosulfur formulations of known concentrations. The recovery of the UV and HPLC methods ranged from 80.71 to 109.51% and 82.31 to 109.84%, respectively. The LOD of UV, GC-MS, and HPLC is 4, 20, and 1 ppm, respectively. The retention time of sulfur was 13.77 (HPLC), 2.89 (ultra high performance liquid chromatography), and 12.715 + 21.524 min (GC-MS). The method was successfully utilized for estimating sulfur in natural samples such as water from a sulfur hot spring and wastewater. The method has been validated by following the method recommended by the American Society for Testing and Materials. The HPLC method emerged as the best analytical method for the estimation of elemental sulfur.