Detection method for residual quantity of phoxim in animal tissue
A detection method and animal tissue technology, which can be used in measurement devices, instruments, scientific instruments, etc., can solve the problems of complex operation process, long detection time, large sampling volume, etc., and achieve accurate detection results, short detection time, and easy operation. Effect
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Embodiment 1
[0027] Determination method of phoxim residues in animal liver tissue
[0028] (l) Materials and equipment:
[0029] The animal species is SD rats. Pesticides adopt phoxim standard substance (chromatographically pure, Sigma company product, number: 14816-18-3), methanol (chromatographically pure, Sigma company product, number: 67-56-1), dichloromethane (analytical pure, Tianjin Fuyu products).
[0030] The high-performance liquid chromatograph is a product of WATERS Company in the United States (WATERS 6000), including a WATERS2487 ultraviolet detector; the chromatographic column ODSC18 is a product of PG instruments Ltd.
[0031] (2) Administration and sampling:
[0032] The conventional feeding method was adopted, and the poisoning was carried out by oral gavage at 8:00 a.m. every day. Soybean oil was used as the solvent, the poisoning dose was 0.5 mL, and the poisoning concentration was 180 mg / kg·BW. Weigh once a day to adjust the feeding amount. Once a day, 7 days a w...
Embodiment 2
[0054] Determination of phoxim residues in jejunum tissue after removal of intestinal contents
[0055] The conventional feeding method was adopted, and the poisoning was carried out by oral gavage at 8:00 a.m. every day. Soybean oil was used as the solvent, the poisoning dose was 0.5 mL, and the poisoning concentration was 180 mg / kg·BW. Weigh once a day to adjust the feeding amount. Once a day, 7 days a week, for a total of 30 days. After feeding, the rats were put back into the cages, with free access to water and food. On the 30th day of the rat experiment, blood was collected and slaughtered for laboratory analysis. The jejunal tissue samples were washed with normal saline and placed in sample bags, labeled and stored in a -20°C refrigerator.
[0056] Take 0.10 g of SD rat jejunum tissue sample, grind it thoroughly in liquid nitrogen, transfer it to a mortar containing 1.5-2.0 g of diatomaceous earth / magnesium trisilicate and continue grinding. Fold the two pieces of r...
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