Food safety and quality
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网络版“:食品和家畜中的一部分兽药残留”

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本数据库保存了关于JECFA推荐的兽药最高残留量的最近信息。粮农组织第41号食品和营养文件公布的所有专题文章电子版均可提供。这些专题文章仅有英文, 虽然数据库某些部分、询问页和背景资料有英文、法文、西班牙文、阿拉伯文和中文。

兽药 Levamisole
功能分类 Antiparasitic
最新评价 1994
食品添加剂和污染物联合专家委员会 42
每日允许摄入量 0-6 µg/kg bw
每日允许摄入量状况 Full
残留量专题文集  
残留标示物 Parent drug
建议的最高残留限量
CattleFat10 µg/kgF
CattleKidney10 µg/kgF
CattleLiver100 µg/kgF
CattleMuscle10 µg/kgF
PigFat10 µg/kgF
PigKidney10 µg/kgF
PigLiver100 µg/kgF
PigMuscle10 µg/kgF
PoultryFat10 µg/kgF
PoultryKidney10 µg/kgF
PoultryLiver100 µg/kgF
PoultryMuscle10 µg/kgF
SheepFat10 µg/kgF
SheepKidney10 µg/kgF
SheepLiver100 µg/kgF
SheepMuscle10 µg/kgF
其他说明
评价概要 The following factors were taken into account in estimating the MRLs:
- The ADI
- The parent drug is a suitable marker residue and accounts for 2.4% of the total residues.
- All of the residues in muscle and fat are free residues and are equivalent to parent drug.
- Of the residues in liver, 50% are present in the bound fraction, and 15% of the bound residues are bioavailable.
- The residues in kidney are qualitatively similar to those in liver.
- It is assumed that all bioavailable residues in liver and kidney are equivalent to parent drug.
- The residues are similar in cattle, sheep and pigs.
Because residues at 1-day withdrawal in yolks of eggs laid by hens given the recommended dose were approximately 800 µg/kg, the Committee considered that levamisole should not be used in laying hens and did therefore not reconmend an MRL for eggs. No new data were submitted by the sponsors to support the re-evaluation of levamisole residues in milk. The Committee therefore withdrew the temporary MRL for milk, that was allocated at its thirty-sixth meeting. The sponsors recommend that levamisole should not be used in lactating cows.
If the recommended values are used for the MRLs and account is taken of the factors mentioned above, the theoretical maximum intake of residues of parent drug and its equivalents is 397 µg per day: of which only 14 µg is parent drug.
In view of the inherent variability involved in estimating total levamisole-equivalent residues based on levamisole as the marker residue and the fact that only a small proportion of the total residues is used to estimate the total levamisole equivalents, the Committee considered this value to be approximately the same as the ADI.
TRS 851