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Research Article
 

Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats



Nahed Fawzy Abdel-Aziz, Ahmed Mohamed El-Bakry, Nadia Said Metwally, Elham Ahmed Sammour and Abdel Razik Hussein Farrag
 
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ABSTRACT

Background and Objective: Insecticides were broadly utilized to suppress particular species of insects; it contaminates crop products, groundwater, soil and the environment, health risks to humans. This research intended to study the physico-chemical properties of some prepared green-based formulations namely, Laury, Orego and Rosa compared with a commercial formulation (Pestban), as well as, their efficiency in both laboratory and field against Spodoptera littoralis. The biochemical and histopathological alterations after treating with these formulations were also examined. Materials and Methods: Three types of formulations were naturally prepared using mineral and vegetable oils. Physical and chemical characteristics of the tested formulations were determined. The insecticidal efficiency under laboratory and semi-field conditions was evaluated, the toxicological studies were also investigated and statistical analysis using one-way analysis of variance, the LC50 and LC90 values were calculated using SPSS version 21.0. Results: Rosa was the most potent with LC90 value of 2.54%, followed by Laury and Orego with 3.78 and 6.18%, respectively. All tested natural based formulations were less toxic to the larvae than the reference insecticide, Pestban. Concerning the semi-field evaluation, the effectiveness of the tested formulations was similar to the laboratory studies, where they ranked descending as, Rosa, Laury and Orego. The side effects of the green-based formulations on liver and kidney of male rats were safe, whether, chemically or histopathologically, while, Pestban revealed adverse effects. Conclusion: The prepared green-based formulations have potential effects against S. littoralis. The toxicological studies demonstrated no evidence of toxicity and no biochemical changes in both liver and kidney biomarkers.

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  How to cite this article:

Nahed Fawzy Abdel-Aziz, Ahmed Mohamed El-Bakry, Nadia Said Metwally, Elham Ahmed Sammour and Abdel Razik Hussein Farrag, 2018. Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats. Asian Journal of Crop Science, 10: 198-206.

DOI: 10.3923/ajcs.2018.198.206

URL: https://scialert.net/abstract/?doi=ajcs.2018.198.206
 
Received: September 16, 2018; Accepted: November 02, 2018; Published: December 03, 2018


Copyright: © 2018. This is an open access article distributed under the terms of the creative commons attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

INTRODUCTION

Cotton is the most utilized natural fiber worldwide, hence considered as an important item of the textile industry. In 2017, the worldwide production of cotton totaled 120.86 million bales. India, China and the United States produce more than half of the global yield1.

The Egyptian cotton leafworm, S. littoralis (Boisd.), is a fertile and highly polyphagous insect. It is regarded as a major pest of great economic prominence in several countries where it attacks a wide spectrum of host plants. It is one of the most devastating insects invading cotton plants. This insect causes an intense decrease in cotton yield and quality2-4.

It has been recently clarified that pest species could easily evolve resistance to many synthetic pesticides presently marketed5-6. In addition, the injurious impacts of synthetic pesticides on both the environment and human health have been displayed7-10. Therefore, there is an increasing interest toward replacement tools for eco-friendly pest control11-13.

A pesticide formulation is a composition of active and inert substances, which represents an end-use pesticide product. Pesticides are formulated for making them safer and easier to handle, where most pesticide active ingredients, in pure (technical grade) model are not appropriate for the application. In their concentrated form, some are excessively toxic, most do not mingle well with water, some are unstable and the others are difficult (or unsafe) to handle, convey or store. To assure the quality of the formulations, the physico-chemical exams on formulations must be implemented.

The attempts to discover new natural products with potential for pest control, this study led to examine the insecticidal efficiency of some natural based formulations against S. littoralis, as well as their side effects on the experimental animals.

MATERIALS AND METHODS

All experiments were accomplished for 10 months of the years 2017 and 2018 under semi-field conditions and The Laboratories of Pests and Plant Protection, Therapeutic Chemistry, Pathology Departments of National Research Centre (NRC), Dokki-Cairo, Egypt.

Insect: A laboratory strain of S. littoralis (Boisd.) (Lepidoptera: Noctuidae) was reared on castor leaves according to Eldefrawi et al.14 under controlled conditions (25±2°C and 65±5% R.H.) in the laboratory.

Preparation of the tested essential oils: The air parts of bay laurel (Laurus nobilis), sweet marjoram (Origanum majorana) and rosemary (Rosmarinus officinalis) were dried and pulverized. The essential oils were isolated after hydro-distillation for 4 h in a steam distillation using a Clevenger apparatus.

Preparation of the tested formulated compounds: Three types of formulations were naturally prepared and namely as follow:

Laury (20% EC): The formulation was prepared by mixing bay laurel oil (20%) in appropriate amounts of emulsifier (10%) and natural solvent (mineral (20%) and vegetable (50%) oils)
Orego (35% W/O/W): The compound was prepared by mixing oregano oil (35%) with appropriate amounts of sodium salicylate (6.5%) and two different emulsifiers (6%) in water (52.5%)
Rosa (15% EW): The formulation was prepared by mixing rosemary essential oil (15%) with methyl salicylate (wintergreen oil) (6.5%) appropriate amounts of emulsifier (4%) and mineral oil (6.5%) in water (68%)

Physico-chemical properties of the tested formulations
Emulsion stability test: To prepare standard hard water, anhydrous calcium chloride (0.304 g) and magnesium chloride hexahydrate (0.139 g) were dissolved in distilled water and completed15 to 1 L.

The emulsion stability test was carried out according to WHO specifications16. Into a 250 mL beaker having an internal diameter of 6-6.5 cm, 75-80 mL of hard water were poured. The beaker contents were stirred with a glass rod and then completed to 100 mL by addition of the tested water. The beaker contents are poured immediately into a clean, dry, graduated 100 mL cylinder. The cylinder was kept at 30-31°C for 1 h and examined for any free oil or creaming separation. The volume of free oil, cream or solid matter, if any, should not transcend 2 mL.

Foam test: The emulsion stability test was carried out also to measure the foam amounts formed on the emulsion surface in the cylinder after 5 min. The foam layer should not exceed 5 mL for passing the test.

pH test: The test was carried out according to CIPAC specifications15. About 1 g of the tested formulation was weighed and transferred to measuring cylinder (100 mL) containing about 50 mL distilled water. The cylinder was made up to 100 mL and shook vigorously for 1 min and then it was allowed to settle. The pH of the supernatant liquid was measured.

Insecticidal activity of the tested formulations against Spodoptera littoralis
Laboratory experiments: Dipping technique was carried out as described by Shepard17. Leaves of castor bean were soaked for 5 sec in a series of concentrations of each formulation. The leaves were placed in Petri-dishes with 10 larvae of 4th instar larvae. Four replicates were carried out for each treatment. Larvae in control treatment were fed on leaves treated only with water. The mortality percentages were recorded after 24 h of treatment. The mortality data were subjected to Probit analysis to obtain the LC50 and LC90 values18.

Semi-field experiments: The planting of cotton plant was done using pots (20 cm diam.) under field conditions. The three formulations, Laury, Orego and Rosa, as well as a reference commercial insecticide (Pestban 48% EC) were sprayed with LC90 concentrations multiplied five times. Ten replicates of pots were used for each treatment. Control was treated with water only. The sprayed cotton leaves were randomly selected among the various replicates of the treatments after zero, 1, 3, 5 and 10 days of the treatment. The collected samples were transferred to the laboratory, where the larvae of cotton leafworm were subjected to the treated leaves. Four replicates were used for each treatment. After treatments, 10 larvae were placed in Petri dishes for 2 days. The survivor larvae were fed on untreated castor leaves until pupation. Cumulative mortalities were calculated at the end of each testing time and corrected according to Abbott19.

Toxicological studies
Animals: Male albino rats (Rattus norvegicus) weighing 100±5 g were obtained from the Animal Breeding House of the National Research Centre (NRC). Rats were kept in polypropylene cages, with free access to standard pellet diet and water, 12 h light/dark cycle, 22±2°C temperature and 48% relative humidity in the laboratory. The rats were acclimatized for 1 week before the start of the experiment. All the rats were kept according to the guidelines and welfare regarding animal protection in Animal Breeding House of NRC which approved by NRC Local Ethical Review Committee and were conducted in accordance with “the Guide for the Care and Use of Laboratory Animals”20.

Experimental design: Rats were divided into five-groups, five rats of each. Group 1 was received distilled water (1 mL/rat) and served as a control. The remaining four groups (2, 3, 4 and 5) received LC90 concentrations of the tested formulations for 15 consecutive days.

Biochemical effects: At the end of the experiment, rats were fasted overnight and blood samples were collected by puncturing the retero-orbital venous plexus of the animals with a fine sterilized glass capillary. The collected blood was left to clot in clean dry tubes and centrifuged at 3000 rpm for 10 min at 4°C using Heraeus Labofuge 400R (Kendro Laboratory Products GmbH, Germany) to obtain the sera. Serum samples were stored at -20°C in the deep freezer until analysis. The serum was used to determine some biochemical measurements such as the aminotransaminase enzymes (AST, ALT) activities21 and total bilirubin (TB)22 for liver functions. The methods employed in the assay of kidney functions of urea23 and creatinine levels24.

Histopathological examination: The treated rats were sacrificed at the end of the experiment, samples from liver and kidney fixed in alcoholic Bouin׳s solution for 24 h and washed, few drops of lithium carbonate were used to wash out the picric acid from the material. The samples were dehydrated in standard alcoholic series and cleared in xylol before embedding in paraffin wax, sectioned at the thickness of 2-3 microns and stained according to the technique of Conn25, using Delafield's Haematoxylin and Eosin. The tissues were examined under light microscopy for histological evolution.

Statistical analysis: Statistical analysis were carried out to determine the differences between treatments and days after spraying by using one-way analysis of variance (ANOVA) Costat26 and Duncan's multiple range test27 was applied at 5% probability level. The concentration-mortality data were subjected to Probit analysis to calculate the LC50 and LC90 values using the Statistical Package for the Social Sciences SPSS28 software program. The values of LC50 were considered significantly different if the 95% confidence limits did not overlap.

RESULTS

Physico-chemical properties of the tested formulations: The results of emulsion stability, foam formation and pH of Laury, Orego and Rosa natural prepared formulations, as well as Pestban commercial formulation were exhibited in Table 1. All the tested formulations traversed the emulsion stability. Rosa formulation did not record any separation layers. In the same trend, Pestban traversed the emulsion stability, as there were not any observed separation layers. Each of the prepared and commercial formulations passed the foam formation. Orego did not record any foam layers. The pH of Laury, Orego and Rosa, natural prepared formulations were around 7, while the pH of Pestban was 3.8.

Laboratory evaluation of the tested formulations: The LC50 and LC90 (%) values of the tested natural based formulations along with Pestban commercial formulation against the 4th instar larvae of S. littoralis were given in Table 2. Rosa was the most effective with LC50 value of 1.28%, followed by Laury and Orego with 2.17 and 2.5%, respectively. The corresponding values of LC90 were 2.54, 3.78 and 6.18%, respectively. Pestban was more efficient than the examined essential oil formulations against the larvae.

Semi-field evaluation of the tested formulations: Semi-field application was determined to study initial, residual effect and persistence of Laury, Orego and Rosa compared with Pestban as a reference insecticide against 4th larval instar of S. littoralis. Data were tabulated in Table 3. As for the natural formulations, Rosa caused the highest mortality at the initial kill (zero time), followed by Laury, while, Orego was the least in this respect. There was not any natural based formulation recorded 100% mortality at zero time.

With regard to the aforementioned results, the efficiency of all tested compounds decreased gradually after spray. The activity of all essential oil formulations against S. littoralis was lower than Pestban after zero and one day from application, while the efficiency after 3 and 5 days were not significantly different with Rosa. The mortality of Rosa continued until 5 days after treatment as Pestban, while the mortality of Laury and Orego lasted for 3 and 1 days after application, respectively.

Side effects of the tested compounds on rats
Effects on liver and kidney functions: The biochemical analysis of serum of male rats exposed to green-based formulations showed insignificant changes of all the tested liver (AST, ALT, TB) and kidney (Creatinine, Urea) dysfunction biomarkers compared with the control. While Pestban induced hepatotoxicity reflected by elevating the previous serum parameter levels (Table 4).

Histopathological changes
Liver: As exhibited in Fig. 1a, liver sections from control rats showed a normal structure of the hepatic lobules which formed the structural units of the liver; each was consisted of cords of hepatocytes and blood sinusoids in between, with a well-preserved cytoplasm and well-defined nucleus and nucleoli. Rats that treated with Laury, Orego and Rosa essential oil formulations showed a normal structure of the hepatic lobules and hepatocytes (Fig. 1b-d), respectively. While, rats daily given an oral dose of Pestban showed necrosis of liver cells and dilated blood sinusoids (arrow) (Fig. 1e), focal necrosis associated with inflammatory infiltration (Fig. 1f) and temperate lymphocyte infiltration in the portal and periportal areas (green arrow) (Fig. 1g) associated with dilated and congested veins (asterisk), some pyknotic nuclei were observed (red arrow).

Kidney: Histological examination of control of rat kidney showed the normal structure of renal corpuscles (asterisk) and renal tubules, proximal convoluted tubules (red arrow) and distal convoluted tubules (green arrow) (Fig. 2a). Animals treated with Laury, Orego and Rosa showed normal renal corpuscle and renal tubules, proximal convoluted tubules and distal convoluted tubules (Fig. 2b-d), respectively.

Table 1:Physico-chemical properties of the tested formulations
Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats

Table 2: Toxicity of the tested essential oil formulations against 4th instar larvae of Spodoptera littoralis
Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats
aConcentrations trigger 50% mortality after 24 h of treatment, bSlope of concentration mortality regression line, cIntercept of regression line and dChi-square value

Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats
Fig. 1(a-g): Sections of liver from (a) Control, (b) Laury, (c) Orego, (d) Rosa and (e-g) Pestban formulations (H and E stain-X150)

Table 3: Mortality percentages of 4th instar larvae of Spodoptera littoralis treated with essential oil formulations
Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats
LSD0.05 least significant difference at 0.05 level of probability. Averages accompanied by the same letter in a column are not significantly different at p<0.05

On the other hand, rats treated with Pestban showed some cellular debris in the dilated interstitial space (blue arrow) and the urinary spaces appeared with dilatation (green arrow) (Fig. 2e), inflammatory infiltration in the interstitial distances (Fig. 2f), moreover, the renal corpuscles exhibited congestion, hyper-cellularity (asterisk) and wide urinary spaces (green arrow) and the cells of the renal tubules demonstrated many degenerative changes with pyknotic nuclei (red arrow).

Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats
Fig. 2(a-f): Sections of kidney from (a) Control, (b) Laury, (c) Orego, (d) Rosa and (e-f) Pestban formulations (H and E stain-X150)

Table 4: Levels of some markers of hepatic-renal functions in serum of rats
Image for - Insecticidal Efficiency of Some Green-based Formulations on Spodoptera littoralis and their Side Effects on Albino Rats
AST: Aspartate transaminase, ALT: Alanine transaminase, TB: Total bilirubin, LSD0.05 least significant difference at 0.05 level of probability. Each value is a mean of five rats±SD, values superscripted with same alphabets in the same column are not significantly different at p<0.05

DISCUSSION

The effectiveness of different types of green-based formulations was assessed on Spodoptera littoralis. The results of the physical and chemical characteristics of the tested formulations revealed that the volume of cream layer did not traverse 2 mL, the volume of cream layer, if any, should not exceed16 2 mL. In addition, the foam layers formed did not exceed 5 mL, the limit of foam layer volume should not surpass16 5 mL, therefor all the green formulations passed each of the emulsion stability and foam formation. This implied that the examined formulations could be applied in the field without any separation or foam problems. The pH of the natural prepared formulations were near seven. Our results matched with Halcomb29, who reported that a safe pH of spray solution is within range of 4.5-7.0. A chemical reaction occurs for many utilized pesticides in the existence of water that own pH value higher than 7 (alkaline hydrolysis), thus it lowers the potency of the pesticide’s active ingredient30. The pH affects also on each of the penetration of spray solutions via the cuticle and the leaf surface through the phytotoxicity.

The current study demonstrated that all the tested formulations exhibited a toxic effect to Spodoptera littoralis. Pavela31 evaluated the efficiency of various essential oils against S. littoralis larvae. Twenty essential oils were highly effective to the 3rd instar larvae. Our results were in agreement with Priyanka and Srivastava32, who evaluated some essential oils against 3rd instar larvae of Spodoptera litura. Essential oils were evaluated at 1 and 2% concentrations. The mortality was between 6.66-100%.

The evolution of eco-friendly biopesticides in order to control agricultural pests is an important defiance currently. Essential oils were considered as a valuable alternative for insect control agents33-34. The mortality of the green based formulations showed that there was not any formulation investigated 100% mortality at zero time; so the obtained mortalities might be optimized by increasing the fold of LC90 applied concentrations. Abbassy et al.35 revealed the toxicity effect of Majorana hortensis against S. littoralis with LC50 value of 3.14 g L1 in a residual film technique. Souguir et al.36 evaluated the toxicity of some essential oils against 3rd larval instar of S. littoralis. All essential oils showed a toxic effect on the larvae. Data obtained by Ali and Ibrahim37 exhibited the insecticidal activity of camphor oil against fourth instar larvae of S. littoralis with LC50 value of 163.1 mg mL1. In addition, Abdelgaleil and El-Sabrout38 studied the insecticidal potency of Artemisia monosperma, Callistemon viminals, Citrus aurantifolia Swingle and Cupressus macrocarpa essential oils contra 4th instar larvae of S. littoralis. Data revealed that A. monosperma and C. macrocarpa were the most efficient.

The noxious effects of insecticides on human and their ecosystem are a critical problem worldwide, so several researchers try to find out new compounds, particularly from natural sources such as essential oils as green insecticides.

The results of the green formulations on the biochemical parameters revealed insignificant changes in all tested liver and kidney biochemical parameters, while Pestban caused perturbation of these biomarkers. The liver is the mean organ in the body has a crucial function in xenobiotic detoxification. It is the primary target of toxic xenobiotic and their metabolites. Therefore, alterations in liver function biomarkers are typically used as biomarkers for liver toxicity and damage39,40. It has been mentioned that the increase in the activity of liver enzymes can be attributed to cell injury41, hepatotoxicity and change in proteins biosynthesis. ALT, AST and TB are important indicators of liver damage in clinical findings. These enzymes are secreted into the blood in hepatocellular injury and their levels increase. The remarked increase in the levels of aminotransferase (ALT and AST) as well as TB, is the major diagnostic symptoms of liver diseases40. Because of the kidney’s high blood flow, its capability to concentrate chemicals and the existence of renal xenobiotic metabolizing enzymes, the kidney may also be a site of toxicity of xenobiotics40.

Previous studies demonstrated that essential oils had no significant changes in activities of liver and kidney functions42-44.

Histopathological studies have been broadly utilized as biomarkers for the toxicological inquiries, in addition, pesticide toxicities45,46. It had been reported that organophosphate insecticides were known to occur several histopathological alterations in the liver tissues47,48.

CONCLUSION

The efficiency of the tested green-based formulations had promising effects against S. littoralis in each laboratory and semi-field evaluation. In addition, their side effects revealed that they are harmless on tested animals, hence on humans chemically and histopathologically. Further studies of these formulations should be investigated under field conditions.

SIGNIFICANCE STATEMENT

The present research was investigated to prepare some green-based formulations to combat Egyptian cotton leafworm, S. littoralis. The tested natural formulations revealed a promising insecticidal efficiency. The green-based formulations also revealed no adverse effects on experimental animals. The prepared formulations could be deemed as a good alternative and safe method for controlling S. littoralis than the conventional insecticides.

ACKNOWLEDGMENT

This study was funded by the National Research Centre, Egypt, Project No. 11030140.

REFERENCES

  1. The Statistics Portal, 2017. Cotton-statistics and facts. https://www.statista.com/topics/1542/cotton/.


  2. El-Sheikh, E.S.A. and M.M. Aamir, 2011. Comparative effectiveness and field persistence of insect growth regulators on a field strain of the cotton leafworm, Spodoptera littoralis, Boisd (Lepidoptera: Noctuidae). Crop Prot., 30: 645-650.
    CrossRef  |  Direct Link  |  


  3. Abouelghar, G.E., H. Sakr, H.A. Ammar, A. Yousef and M. Nassar, 2013. Sublethal effects of spinosad (Tracer®) on the cotton leafworm (Lepidoptera: Noctuidae). J. Plant Prot. Res., 53: 275-284.
    CrossRef  |  Direct Link  |  


  4. Alfazairy, A.A., A.M. El-Ahwany, E.A. Mohamed, H.A. Zaghloul and E.R. El-Helow, 2013. Microbial control of the cotton leafworm Spodoptera littoralis (Boisd.) by Egyptian Bacillus thuringiensis isolates. Folia Microbiol., 58: 155-162.
    CrossRef  |  Direct Link  |  


  5. Nasr, H.M., M.E. Badawy and E.I. Rabea, 2010. Toxicity and biochemical study of two insect growth regulators, buprofezin and pyriproxyfen, on cotton leafworm Spodoptera littoralis. Pest. Biochem. Physiol., 98: 198-205.
    CrossRef  |  Direct Link  |  


  6. Pineda, S., A.M. Mart─▒nez, J.I. Figueroa, M.I. Schneider and P.D. Estal et al., 2009. Influence of azadirachtin and methoxyfenozide on life parameters of Spodoptera littoralis (Lepidoptera: Noctuidae). J. Econ. Entomol., 102: 1490-1496.
    CrossRef  |  PubMed  |  Direct Link  |  


  7. Pimentel, D., 2005. Environmental and economic costs of the application of pesticides primarily in the United States. Environ. Dev. Sustainability, 7: 229-252.
    CrossRef  |  Direct Link  |  


  8. Sharpe, R.M. and D.S. Irvine, 2004. How strong is the evidence of a link between environmental chemicals and adverse effects on human reproductive health? Br. Med. J., 328: 447-451.
    CrossRef  |  Direct Link  |  


  9. Aktar, M.W., D. Sengupta and A. Chowdhury, 2009. Impact of pesticides use in agriculture: Their benefits and hazards. Interdisciplin. Toxicol., 2: 1-12.
    CrossRef  |  Direct Link  |  


  10. Nicolopoulou-Stamati, P., S. Maipas, C. Kotampasi, P. Stamatis and L. Hens, 2016. Chemical pesticides and human health: The urgent need for a new concept in agriculture. Front. Public Health, Vol. 4.
    CrossRef  |  Direct Link  |  


  11. Salem, H.A., N.F. Abdel-Aziz, E.A. Sammour and A.M. El-Bakry, 2016. Semi-field evaluation of some natural clean insecticides from essential oils on armored and soft scale insects (Homoptera: Diaspididae and Coccidae) infesting mango plants. Int. J. Chemtech Res., 9: 87-97.


  12. Benelli, G., A. Canale, C. Toniolo, A. Higuchi, K. Murugan, R. Pavela and M. Nicoletti, 2017. Neem (Azadirachta indica): Towards the ideal insecticide? Natl. Prod. Res., 31: 369-386.
    CrossRef  |  Direct Link  |  


  13. El-Bakry, A.M., N.F. Abdel-Aziz and E.A. Sammour, 2018. Impact of Lavandula officinalis, inert dusts and their formulations on Sitophilus oryzae. Agric. Eng. Int.: CIGR J., 19: 166-173.
    Direct Link  |  


  14. Eldefrawi, M.E., A. Toppozada, N. Mansour and M. Zeid, 1964. Toxicological studies on the Egyptian cotton leafworm, Prodenia litura. I. Susceptibility of different larval instars of Prodenia to insecticides. J. Econ. Entomol., 57: 591-593.
    CrossRef  |  Direct Link  |  


  15. Dobrat, W. and A. Martijn, 1995. CIPAC Handbook Volume G: Analysis of Technical and Formulated Pesticides. Collaborative International Pesticides Analytical Council Ltd., Harpenden, UK


  16. WHO., 1979. Specifications for Pesticides Used in Public Health: Insecticides, Molluscicides, Repellents, Methods. 1st Edn., World Health Organization, Geneva


  17. Shepard, H., 1958. Methods of Testing Chemicals on Insects. Vol. 1. Burgess Publishing Company, Minneapolis


  18. Finney, D., 1971. Probit Analysis Cambridge. Cambridge University Press, UK


  19. Abbott, W.S., 1925. A method of computing the effectiveness of an insecticide. J. Econ. Entomol., 18: 265-267.
    CrossRef  |  Direct Link  |  


  20. NRC., 2010. Guide for the Care and Use of Laboratory Animals. 8th Edn., National Academies Press, Washington, DC., USA., ISBN-13: 9780309186636, Pages: 211


  21. Reitman, S. and S. Frankel, 1957. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am. J. Clin. Pathol., 28: 56-63.
    CrossRef  |  PubMed  |  Direct Link  |  


  22. Young, D.S., L.C. Pestaner and V. Gibberman, 1975. Effects of drugs on clinical laboratory tests. Clin. Chem., 21: 1D-432D.
    PubMed  |  Direct Link  |  


  23. Coulombe, J.J. and L. Favreau, 1963. A new simple semimicro method for colorimetric determination of urea. Clin. Chem., 9: 102-108.
    PubMed  |  Direct Link  |  


  24. Husdan, H. and A. Rapoport, 1968. Estimation of creatinine by the jaffe reaction: A comparison of three methods. Clin. Chem., 14: 222-238.
    PubMed  |  Direct Link  |  


  25. Conn, H.J., 1960. Staining Procedures Used by the Biological Stain Commission. Williams and Wilkins, USA


  26. CoStat, 2005. Microcomputer Program Analysis Version 6.303. Cohort Software, Monterey, CA., USA


  27. Duncan, D.B., 1955. Multiple range and multiple F tests. Biometrics, 11: 1-42.
    CrossRef  |  Direct Link  |  


  28. SPSS., 2012. SPSS Statistical Package for Windows. Version 21.0. Statistical Package for the Social Sciences, Chicago, IL., USA


  29. Halcomb, M., 2012. The pH of the spray water is very important. The University of Tennesse. https://extension.tennessee.edu/mtnpi/Documents/handouts/General/pH_of_Spray_Water.pdf.


  30. Fishel, F., 2002. Effects of water pH on the stability of pesticides. Integrated Pest Management MU Guide. University of Missouri, Columbia.


  31. Pavela, R., 2005. Insecticidal activity of some essential oils against larvae of Spodoptera littoralis. Fitoterapia, 76: 691-696.
    CrossRef  |  Direct Link  |  


  32. Priyanka, B. and R.P. Srivastava, 2012. Larvicidal and growth regulatory activities of some essential oils against Asian army worm, Spodoptera litura (Fab.). J. Biopestic., 5: 186-190.
    Direct Link  |  


  33. Govindarajan, M., A. Jebanesan and T. Pushpanathan, 2008. Larvicidal and ovicidal activity of Cassia fistula Linn. leaf extract against filarial and malarial vector mosquitoes. Parasitol. Res., 102: 289-292.
    CrossRef  |  PubMed  |  Direct Link  |  


  34. Cetin, B., S. Cakmakci and R. Cakmakci, 2010. The investigation of antimicrobial activity of thyme and oregano essential oils. Turk. J. Agric. Forest., 35: 145-154 .
    CrossRef  |  


  35. Abbassy, M.A., S.A.M. Abdelgaleil and R.Y.A. Rabie, 2009. Insecticidal and synergistic effects of Majorana hortensis essential oil and some of its major constituents. Entomol. Exp. Applicata, 131: 225-232.
    CrossRef  |  Direct Link  |  


  36. Souguir, S., I. Chaieb, Z.B. Cheikh and A. Laarif, 2013. Insecticidal activities of essential oils from some cultivated aromatic plants against Spodoptera littoralis (Boisd). J. Plant Protect. Res., 53: 388-391.
    CrossRef  |  Direct Link  |  


  37. Ali, A.M. and A.M. Ibrahim, 2018. Castor and camphor essential oils alter hemocyte populations and induce biochemical changes in larvae of Spodoptera littoralis (Boisduval) (Lepidoptera: Noctuidae). J. Asia-Pac. Entomol., 21: 631-637.
    CrossRef  |  Direct Link  |  


  38. Abdelgaleil, S.A.M. and A.M. El-Sabrout, 2018. Anti-nutritional, antifeedant, growth-disrupting and insecticidal effects of four plant essential oils on Spodoptera littoralis (Lepidoptera: Noctuidae). J. Crop Prot., 7: 135-150.
    Direct Link  |  


  39. Mossa, A.T.H., E.S. Swelam and S.M.M. Mohafrasha, 2015. Sub-chronic exposure to fipronil induced oxidative stress, biochemical and histopathological changes in the liver and kidney of male albino rats. Toxicol. Rep., 2: 775-784.
    CrossRef  |  Direct Link  |  


  40. Hodgson, E., 2010. Metabolism of Pesticides. In: Haye's Handbook of Pesticide Toxicology, Krieger, R. (Eds.). 3rd Edn., Academic Press, UK., pp: 893-921


  41. Elgengaihi, S., A.T.H. Mossa, A.A. Refaie and D. Aboubaker, 2016. Hepatoprotective efficacy of Cichorium intybus L. extract against carbon tetrachloride-induced liver damage in rats. J. Dietary Suppl., 13: 570-584.
    CrossRef  |  Direct Link  |  


  42. Mossa, A.T.H., N.A.H. Abdelfattah and S.M.M. Mohafrash, 2017. Nanoemulsion of camphor (Eucalyptus globulus) essential oil, formulation, characterization and insecticidal activity against wheat weevil, Sitophilus granarius. Asian J. Crop Sci., 9: 50-62.
    CrossRef  |  Direct Link  |  


  43. Ghaly, M.H., A.A. Elghoneimy, H.K. Mohamed and M.F. Ali, 2017. Biochemical and histopathological effects of dietary supplementation of Nigella sativa and Mentha piperita oils to broilers. J. Adv. Vet. Res., 7: 7-15.
    Direct Link  |  


  44. Macedo, I.T.F., C.M.L. Bevilaqua, L.M.B. de Oliveira, A.L.F. Camurca-Vasconcelos and L.S. Vieira et al., 2010. Anthelmintic effect of eucalyptus staigeriana essential oil against goat gastrointestinal nematodes. Vet. Parasitol., 173: 93-98.
    CrossRef  |  PubMed  |  Direct Link  |  


  45. Uzun, F.G., S. Kalender, D. Durak, F. Demir and Y. Kalender, 2009. Malathion-induced testicular toxicity in male rats and the protective effect of vitamins C and E. Food Chem. Toxicol., 47: 1903-1908.
    CrossRef  |  PubMed  |  Direct Link  |  


  46. Uzun, F.G. and Y. Kalender, 2013. Chlorpyrifos induced hepatotoxic and hematologic changes in rats: The role of quercetin and catechin. Food Chem. Toxicol., 55: 549-556.
    CrossRef  |  PubMed  |  Direct Link  |  


  47. Yehia, M.A.H., S.G. El-Banna and A.B. Okab, 2007. Diazinon toxicity affects histophysiological and biochemical parameters in rabbits. Exp. Toxicol. Pathol., 59: 215-225.
    CrossRef  |  Direct Link  |  


  48. Selmi, S., K. Rtibi, D. Grami, H. Sebai and L. Marzouki, 2018. Malathion, an organophosphate insecticide, provokes metabolic, histopathologic and molecular disorders in liver and kidney in prepubertal male mice. Toxicol. Rep., 5: 189-195.
    CrossRef  |  Direct Link  |  


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