141 Toxicity assay to single dosis and to repeated dosis of humanized ACMT1HT by endovenous route in CENP:SPRD rats

Abstract Background Powders and extracts of Piper guineense seeds and leaves were assessed for insecticidal activities against Callosobruchus maculatus in the laboratory at temperature and relative humidity of 29.6 °C and 75.9%, respectively. Bioactive compounds in P. guineense leaves and seeds were also investigated. The powders were tested at rates 1.0, 2.0 and 4.0 g/20 g cowpea seeds while extracts were tested at 1.0, 2.0 and 3.0%. Results Results of contact toxicity assay of the seed powder caused 100% adult mortality at 96 h post-treatment period whereas leaf powder evoked 90% adult mortality within the same period at concentration of 1.0 g/20 g cowpea seeds. Low adult emergence was observed on cowpea seeds treated with 1 g of seed powder with percentage adult emergence of 10.0% and inhibition rate (IR) of 97.5%. Beetle Perforation Index (BPI) obtained from treated cowpea seeds was significantly different (P < 0.05) from BPI of untreated seeds. Extracts of P. guineense seed were more toxic than seed powder. Piper guineense seed extract caused 87.5% adult mortality of C. maculatus while leaf extract caused 70.0% adult mortality within 24 h of infestation at concentration of 1%. Progeny development of C. maculatus was completely inhibited in cowpea treated with 2% and 3% leaf and seed extracts of P. guineense. β-Pinene was the most abundant active compound in P. guineense seed (55.6%) and leaf (48.4%). β-Phellandrene occurred 38.2% in seeds while Ocimene had the least value of 0.2% in seed and 0.5% in leaf. Conclusion The study showed that P. guineense seed powder and extracts were more effective than leaf powder and extract. Utilization of plant products as alternative to synthetic insecticides in protecting cowpea seeds against C. maculatus should be encouraged for enhanced food safety and security. Piper guineense is used as spice and medicine and interestingly safe for human use.

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Chromatic intervention and biocompatibility assay for biosurfactant derived from Balanites aegyptiaca (L.) Del

Scientific Reports ◽

10.1038/s41598-021-83573-7 ◽

2021 ◽

Vol 11 (1) ◽

Author(s):

Vishal Panchariya ◽

Vishal Bhati ◽

Harishkumar Madhyastha ◽

Radha Madhyastha ◽

Jagdish Prasad ◽

...

Keyword(s):

Hydrogen Peroxide ◽

Skin Fibroblast ◽

Mouse Skin ◽

Fibroblast Cells ◽

Toxicity Assay ◽

Balanites Aegyptiaca ◽

Hemolysis Assay ◽

Full Factorial ◽

Human Rbcs

AbstractExtraction of biosurfactants from plants is advantageous than from microbes. The properties and robustness of biosurfactant derived from the mesocarp of Balanites aegyptiaca have been reported. However, the dark brown property of biosurfactant and lack of knowledge of its biocompatibility limits its scope. In the present work, the decolorization protocol for this biosurfactant was optimized using hydrogen peroxide. The hemolytic potential and biocompatibility based on cell toxicity and proliferation were also investigated. This study is the first report on the decolorization and toxicity assay of this biosurfactant. For decolorization of biosurfactant, 34 full factorial design was used, and the data were subjected to ANOVA. Results indicate that 1.5% of hydrogen peroxide can decolorize the biosurfactant most efficiently at 40 °C in 70 min at pH 7. Mitochondrial reductase (MTT) and reactive oxygen species (ROS) assays on M5S mouse skin fibroblast cells revealed that decolorized biosurfactant up to 50 µg/mL for 6 h had no significant toxic effect. Hemolysis assay showed ~ 2.5% hemolysis of human RBCs, indicating the nontoxic effect of this biosurfactant. The present work established a decolorization protocol making the biosurfactant chromatically acceptable. Biocompatibility assays confirm its safer use as observed by experiments on M5S skin fibroblast cells under in vitro conditions.

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Virgin Coconut (Cocos nucifera) Oil Attenuates Rotenone-Induced Toxicity in Fruit Flies (Drosophila melanogaster)

Journal of Basic and Social Pharmacy Research ◽

10.52968/27458357 ◽

2021 ◽

Vol 2 (1) ◽

pp. 26-37

Author(s):

O.O. Dosumu ◽

◽

E.N. Akang ◽

O.K. Idowu ◽

G.J. Adeyemi

Keyword(s):

Drosophila Melanogaster ◽

Cocos Nucifera ◽

Coconut Oil ◽

Redox Status ◽

Fruit Flies ◽

Dependent Manner ◽

Toxicity Assay ◽

Behavioural Test ◽

Locomotor Deficits ◽

Dose Dependent

Background: Parkinson's disease (PD) is a multifactorial neurodegenerative disease with pathogenic mechanisms traceable to oxidative damage and mitochondrial dysfunction. Rotenone, a chemical compound commonly found in pesticides, has been found to inhibit mitochondrial complex-I and initiate PD-like symptoms in mammals and several invertebrates. Virgin Coconut Oil (VCNO) obtained from the coconut fruit has been found to possess anti-oxidative and anti-inflammatory properties. Objectives: The present study evaluated the effect of VCNO on rotenone-induced Parkinsonism in fruit flies- Drosophila melanogaster (D. melanogaster). Methods: Canton special (CS) strains of D. melanogaster, aged between 1 to 3 days were orally exposed for 7 days to 0, 250, 500 and 750 μM rotenone diet for toxicity assay, and 0, 2.5, 5 and 10 % w/w VCNO diet for longevity assay. Thereafter, 5 % VCNO diet was selected for evaluation against 500 μM rotenone. Subsequently, behavioural test (negative geotaxis), markers for redox status and enzyme activities were evaluated. Results: The results showed that rotenone induced toxicity in the flies, while VCNO increased the lifespan of D. melanogaster in a dose-dependent manner. In addition, VCNO ameliorated rotenone-induced locomotor deficits, elevated MDA, as well as the depleted GSH levels. It also mitigated the inhibited activities of SOD, CAT and ATPase in the flies. Conclusions: VCNO protected D. melanogaster against rotenone-induced toxicity by extending longevity, preventing locomotor deficits and reducing oxidative stress.

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The Mouse Oocyte Toxicity Assay

Short-Term Bioassays in the Analysis of Complex Environmental Mixtures III ◽

10.1007/978-1-4613-3611-2_16 ◽

1983 ◽

pp. 245-255 ◽

Cited By ~ 2

Author(s):

James S. Felton ◽

R. Lowry Dobson

Keyword(s):

Mouse Oocyte ◽

Toxicity Assay

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Toxicity of Insecticide-Contaminated Soil Used in the Treatment of Cotton Seeds to Bees

Journal of Agricultural Science ◽

10.5539/jas.v10n10p189 ◽

2018 ◽

Vol 10 (10) ◽

pp. 189 ◽

Cited By ~ 1

Author(s):

Ellen P. de Souza ◽

Paulo E. Degrande ◽

Rosalia Azambuja ◽

Rafael A. da Silva ◽

Valter V. Alves Junior

Keyword(s):

Mortality Rate ◽

Surface Soil ◽

Control Group ◽

Soil Dust ◽

Control Groups ◽

Toxicity Assay ◽

Chemical Residues ◽

Cotton Plants ◽

Cotton Seeds ◽

And Control

Insecticide-treated cotton seeds can pose risks to Apis mellifera Linnaeus, 1758 populations during crop establishment if chemical residues reach these insects near agricultural fields via dust drift produced during planting. However, the treatment of seeds with insecticides is essential to protect cotton plants from damage caused by pests, including thrips and aphids. Thus, the aim of this study was to evaluate the toxic effects (acute toxicity) of soil dust from cotton fields planted with insecticide-treated seeds on A. mellifera adults using a toxicity assay developed in the laboratory. Forager honeybees were maintained in 700-ml plastic cages with 7 g of surface soil where insecticide-treated cotton seeds were sown (270 g a.i. clothianidin, 270 g a.i. imidacloprid, 210 g a.i. thiamethoxam, and 75 g a.i. fipronil/100 kg of seeds, and an untreated group). Ten bees were placed in each cage. The experimental design was randomized, with five treatments and twelve replicates. The mortality rate was evaluated during the entire assay. Data were transformed to x + 0.5  and compared with a regression analysis and contrast test. The linear regression model revealed a significant relationship between bee mortality and exposure time. The mortality rate gradually increased as time progressed in all treatments and the control group. The contrast test did not reveal significant differences between the insecticide and control groups. Thus, residues of the products tested, thiamethoxam, clothianidin, imidacloprid, and fipronil, did not influence the mortality of A. mellifera adults as a result of exposure to soil contaminated with insecticide-treated seeds.

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Cost-Effective Fabrication, Antibacterial Application and Cell Viability Studies of Modified Nonwoven Cotton Fabric

10.21203/rs.3.rs-160131/v1 ◽

2021 ◽

Author(s):

Rahat Nawaz ◽

Sayed Tayyab Raza Naqvi ◽

Batool Fatima ◽

Nazia Zulfiqar ◽

Muhammad Umer Farooq ◽

...

Keyword(s):

Cotton Fabric ◽

Biomedical Applications ◽

Active Sites ◽

Food Packaging ◽

Low Cost ◽

Bacterial Species ◽

Enterobacter Aerogenes ◽

Cost Effective ◽

Bacterial Strains ◽

Toxicity Assay

Abstract Nonwoven cotton fabric has been fabricated and designed for antibacterial applications using low cost and ecofriendly precursors. The treatment of fabric with alkali leads to formation of active sites. The surfaces were dip coated with silver nanaoparticles and chitosan. The surface was chlorinated in next step to transform amide (N-H) groups in chitosan into N-halamine (N-Cl). The modified and unmodified surfaces of the nonwoven cotton fabric have been characterized by FTIR, SEM, and XRD. The active chlorine loading is measured with iodine/ sodium thiosulphate. The antimicrobial activity and cell toxicity assay were carried out with and without modifications of nonwoven cotton fabric. The antimicrobial efficacies of loaded fabric were evaluated against four bacterial species (Micrococcus lutes, Staphylococcus aurea, Enterobacter aerogenes, and E.coli). It was found that modified fabric exhibited superior efficiency against gram-positive and gram-negative bacterial strains as compared to their bulk counterparts upon exposure without destroying and affecting fabric nature. The overall process is economical for commercial purposes. The modified fabric can be used for antimicrobial, health, and food packaging industries, and in other biomedical applications.

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