Pratheeshkumar N, Chandran M, Beevi S Naseema, Mathew Thomas Biju, George Thomas, Paul Ambily, Xavier George, Ravi K Prathibha, Kumar S Visal, Rajith R
Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli, Tamil Nadu, 627012, India.
Department of Chemistry, Vivekananda College, Agasteeswaram, Kanyakumari, Tamil Nadu, India.
Environ Monit Assess. 2016 Jan;188(1):53. doi: 10.1007/s10661-015-5058-5. Epub 2015 Dec 22.
Dissipation behaviour of the chloronicotinyl insecticide, imidacloprid (Tatamida 17.8 % SL), in fresh and cured cardamom capsules was studied following application at doses 20 and 40 g a.i. ha(-1) in a cardamom plantation of Indian Cardamom Hills (ICH), Idukki, Kerala, India. A single-laboratory ultra performance liquid chromatography mass spectrometry (UPLC-MS/MS) method was developed and validated for the estimation of imidacloprid and its six metabolites (5-hydroxy, olefin, guanidine, urea, 6-chloronicotinic acid and nitrosimine) in fresh and cured cardamom. At the lower dose, the initial deposits of total imidacloprid residues were 1.91 and 7.23 μg g(-1), respectively, in fresh and cured cardamom. At the higher dose, the initial residues were 3.94 and 14.72 μg g(-1), respectively, in fresh and cured capsules. The residues dissipated below the quantitation level of 0.01 μg g(-1) after 21 and 28 days at lower dose and after 28 days for both at higher dose. The half-lives of imidacloprid in fresh and cured cardamom were 4.02 and 3.63 days, respectively, at lower dose and 3.61 days for both at higher dose. The waiting periods of imidacloprid on fresh and cured cardamom at lower and higher doses were 21.40, 27.10, 23.85 and 30.70 days, respectively. The mean processing factor of imidacloprid was 3.96 at 20 g a.i. ha(-1). Amongst metabolites of imidacloprid, urea had maximum residues in fresh and cured cardamom followed by 5-hydroxy and guanidine. Other metabolites such as 6-chloronicotinic acid, olefin and nitrosimine were not detected either in fresh or cured cardamom.
在印度喀拉拉邦伊杜基的印度小豆蔻山(ICH)的小豆蔻种植园中,以20克和40克有效成分·公顷⁻¹的剂量施用后,研究了氯代烟碱类杀虫剂吡虫啉(17.8%悬浮剂塔塔米达)在新鲜和干燥小豆蔻荚中的消解行为。建立并验证了一种单实验室超高效液相色谱-质谱联用(UPLC-MS/MS)方法,用于测定新鲜和干燥小豆蔻中吡虫啉及其六种代谢物(5-羟基、烯烃、胍、尿素、6-氯烟酸和亚硝基胺)。在较低剂量下,新鲜和干燥小豆蔻中吡虫啉总残留的初始沉积量分别为1.91和7.23微克·克⁻¹。在较高剂量下,新鲜和干燥荚中的初始残留量分别为3.94和14.72微克·克⁻¹。在较低剂量下,21天和28天后残留量降至0.01微克·克⁻¹的定量限以下;在较高剂量下,28天后两者残留量均降至该水平以下。在较低剂量下,吡虫啉在新鲜和干燥小豆蔻中的半衰期分别为4.02天和3.63天;在较高剂量下,两者的半衰期均为3.61天。在较低和较高剂量下,吡虫啉在新鲜和干燥小豆蔻上的安全间隔期分别为21.40天、27.10天、23.85天和30.70天。在20克有效成分·公顷⁻¹剂量下,吡虫啉的平均加工因子为3.96。在吡虫啉的代谢物中,尿素在新鲜和干燥小豆蔻中的残留量最高,其次是5-羟基和胍。在新鲜或干燥小豆蔻中均未检测到其他代谢物,如6-氯烟酸、烯烃和亚硝基胺。