This study examined variables that influence the acid-extraction of pectin from Steam Distillated Orange Peels using two different acids; an organic acid (citric acid) and a mineral one (sulfuric acid). The effects of these acids on extraction of pectin were investigated by response surface methodology. Extraction parameters which are employed in this study are temperature of extraction (X1: 50
Sensitivity tests were performed according to the World Health Organization protocol (WHO) for three essential oils (Citrus aurantium (bitter orange) Citrus sinensis (orange) and Pistacia lentiscus) and four chemical insecticides (Malathion Temephos Fenthion and Fenitrothion) used as a positive controls. Essential oils have shown an interesting larvicidal activity against Culex pipiens, with an interesting lethal doses (LD50= 35 ppm and LD90=70 ppm) in the case of Citrus aurantium essential oils and (LD50= 64 ppm and LD90 = 120 ppm) using Citrus sinensis while the LD50 and LD90 were, respectively, in the case of Pistacia lentiscus 62ppm and 160ppm. Chemical insecticides, used as a positive control, showed a significant larvicidal activity. The larvicidal activity of essential oils could have a great interest in the domain of vector control. This is because of problems caused by the use of chemical insecticides (environmental pollution, resistance, hazards to human health).
Introduction: Methanol is a commonly used organic solvent that, because of its toxicity, can cause metabolic acidosis, neurologic sequelae, and even death, when ingested. It is a constituent of many commercially available industrial solvents and of poorly adulterated alcoholic beverages. The management of acute human methanol intoxication needs methanol dosage. The aim of our study is to validate a method in the order to determinate the amount of blood methanol, using gas chromatography with flame ionization detection (FID), after a Headspace sampling. Methods: We used butanol as an internal standard. The validation procedure was performed according to the guidelines of the French Society of Analytical Toxicology and the French Committee of Accreditation (COFRAC; LABGTA04). Results: Our method is specific and linear at the range amount from 0g/L to 1 g/L. the coefficient of correlation was 0.99868. The intra- and inter-day precision and relative bias were less than 15 %. The limit of detection was 0.060 g/L. In the same conditions, limit of quantification was 0.09 g/L. The storage's and transport's samples were at +4
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