Ault J A, Spurgeon T E, Gillard D S, Mallinson E T
J Assoc Off Anal Chem. 1985 Sep-Oct;68(5):941-4.
A validation of a previously studied method for determining organochlorine residues in poultry fat was conducted to extend the usefulness of the method to beef and swine fats. The validation samples consisted of 16 materials all analyzed in duplicate. Fortification levels ranged from 0.02 to 1.2 ppm for alpha-BHC, lindane, cis- and trans-chlordane, octachlor epoxide, o,p'- and p,p'-DDT, p,p'-DDE, p,p'-TDE, hexachlorobenzene, heptachlor epoxide, dieldrin, endrin, methoxychlor, mirex, and toxaphene. The average recovery was 101% with a range of 79-113%, not including toxaphene. The ranges of coefficients of variation were CVo = 0-23.37% and CVx = 3.74-26.19%. The results were comparable to the previous collaborative study of the same method for poultry fat. The extended method has been adopted official first action.
为了将一种先前研究的测定家禽脂肪中有机氯残留量的方法的适用范围扩展到牛肉和猪脂肪,对该方法进行了验证。验证样本包括16种材料,均进行了重复分析。α-六六六、林丹、顺式和反式氯丹、八氯环氧丙烷、o,p'-滴滴涕和p,p'-滴滴涕、p,p'-滴滴伊、p,p'-滴滴滴、六氯苯、七氯环氧丙烷、狄氏剂、异狄氏剂、甲氧滴滴涕、灭蚁灵和毒杀芬的加标水平范围为0.02至1.2 ppm。除毒杀芬外,平均回收率为101%,范围为79 - 113%。变异系数范围为CVo = 0 - 23.37%和CVx = 3.74 - 26.19%。结果与先前对家禽脂肪相同方法的协同研究结果相当。该扩展方法已被正式首次采用。