Alvinerie M, Sutra J F, Capela D, Galtier P, Fernandez-Suarez A, Horne E, O'Keeffe M
Laboratoire de Pharmacologie-Toxicologie, INRA, Toulouse, France.
Analyst. 1996 Oct;121(10):1469-72. doi: 10.1039/an9962101469.
An HPLC method has been developed for the determination of moxidectin in bovine tissues. The extraction and clean-up procedure is based on the matrix solid-phase dispersion technique. Control and moxidectin-fortified bovine tissue samples (0.25 g) are blended with octadecyl (C18 end-capped) packing material. A column made from the C18-bovine tissue blend is washed with hexane (2 ml); when all the hexane has eluted, an Alumina-B SPE cartridge is attached below the C18-tissue column and, after washing, moxidectin is eluted with methanol (6 ml). Moxidectin is derivatized and determined by HPLC with fluorescence detection. The recovery from fortified samples was greater than 80% in the concentration range 1-100 ng g-1 of tissue. This method permits the determination of moxidectin at levels as low as 1 ng g-1 (1 ppb).
已开发出一种用于测定牛组织中莫西菌素的高效液相色谱法。提取和净化程序基于基质固相分散技术。将对照和添加了莫西菌素的牛组织样品(0.25 g)与十八烷基(封端的C18)填充材料混合。用己烷(2 ml)冲洗由C18 - 牛组织混合物制成的柱子;当所有己烷洗脱后,在C18 - 组织柱下方连接一个氧化铝 - B固相萃取柱,冲洗后,用甲醇(6 ml)洗脱莫西菌素。莫西菌素经衍生化后通过高效液相色谱 - 荧光检测法进行测定。在组织浓度范围为1 - 100 ng g-1时,加标样品的回收率大于80%。该方法能够测定低至1 ng g-1(1 ppb)水平的莫西菌素。