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荷斯坦奶牛单次及重复乳房内和非肠道给药后乳汁中庆大霉素的消除情况。

Depletion of gentamicin in the milk of Holstein cows after single and repeated intramammary and parenteral treatments.

作者信息

Pedersoli W M, Jackson J, Frobish R A

机构信息

Division of Animal Research, FDA-CVM, Beltsville, Maryland 20705, USA.

出版信息

J Vet Pharmacol Ther. 1995 Dec;18(6):457-63. doi: 10.1111/j.1365-2885.1995.tb00626.x.

Abstract

Twenty-four healthy Holstein cows, 2.72 +/- 0.64 (mean +/- SD) years old, weighing 603.96 +/- 73.22 kg (mean +/- SD), and representing various levels of milk production, were used to determine the depletion of gentamicin (GT) in milk. The cows had not received antibiotics or other drugs that could interfere with study for at least 60 days before the beginning of the investigation. The cows were divided into six groups (n = 4) and treated with single (treatments A, B and C) or repeated (treatments D, E and F) doses of GT. Cows were acclimated for 7 days before administration of GT and milked twice a day at 12-h intervals (06.00 hours, 18.00 hours) throughout the duration of the study. Control milk samples were obtained after the arrival of the cows and assayed to establish their GT free status. On day 1 of each treatment, a baseline milk sample was collected from the milk produced (06.00 hours) by each cow. A single dose of GT was administered intramammarily (A, i.m.m. left front quarter, 500 mg), intravenously (B, i.v., 5 mg/kg body weight) or intramuscularly (C, i.m., 5 mg/kg body weight). Cows in treatments D (i.m.m., 500 mg), E (i.v., 5 mg/kg body weight) and F (simultaneous i.m.m. 500 mg plus i.v. 5 mg/kg body weight) were treated twice a day for 5 consecutive days just after the morning and evening milkings. Milk samples from individual cows were collected every day after each milking during and after dosing until GT concentration in the milk was below the safe level of < or = 30 ng/mL. The concentration of GT in milk was determined by a high-performance liquid chromatographic procedure. Depletion of GT to a concentration < or = 30 ng/mL occurred at the seventh (84 h), third (36 h), third (36 h), eleventh (132 h) third (36 h) and nineteenth (228 h) post-dosing milking, for cows in treatments A, B, C, D, E and F respectively. The highest mean +/- SEM) concentrations of GT were 14 710 +/- 1213.89, 167.87 +/- 46.94 and 91.62 +/- 14.55 ng/mL measured in the first milking post dosing (12 h) for cows in treatment A, B and C respectively; for cows in treatments D, E and F, during the dosing period, they were 14067.50 +/- 2989.09, 446.07 +/- 100.92, and 22900 +/- 2843.66 ng/mL and occurred at the seventh, third and eighth milking respectively. Because GT is not approved for use in dairy cattle and because of the long depletion time associated with some possible treatments, illegal and extra-label use is likely to cause residues in milk.

摘要

选用24头健康的荷斯坦奶牛,年龄为2.72±0.64(均值±标准差)岁,体重603.96±73.22千克(均值±标准差),代表不同产奶水平,用于测定庆大霉素(GT)在牛奶中的消除情况。在调查开始前至少60天,这些奶牛未接受过抗生素或其他可能干扰研究的药物。将奶牛分为六组(每组n = 4),分别用单次(处理A、B和C)或重复(处理D、E和F)剂量的GT进行处理。在给予GT前,奶牛先适应7天,在整个研究期间,每天间隔12小时(上午6点、下午6点)挤奶两次。在奶牛到达后采集对照牛奶样本并进行检测,以确定其不含GT的状态。在每种处理的第1天,从每头奶牛生产的牛奶(上午6点)中采集一份基线牛奶样本。单次剂量的GT通过乳房内注射(A组,左前乳房象限,500毫克)、静脉注射(B组,静脉注射,5毫克/千克体重)或肌肉注射(C组,肌肉注射,5毫克/千克体重)给药。处理D组(乳房内注射,500毫克)、E组(静脉注射,5毫克/千克体重)和F组(同时乳房内注射500毫克加静脉注射5毫克/千克体重)的奶牛在每天早晚挤奶后连续5天每天治疗两次。在给药期间及给药后,每次挤奶后每天采集每头奶牛的牛奶样本,直至牛奶中GT浓度低于安全水平≤30纳克/毫升。采用高效液相色谱法测定牛奶中GT的浓度。处理A、B、C、D、E和F组的奶牛,在给药后第7次(84小时)、第3次(36小时)、第3次(36小时)、第11次(132小时)、第3次(36小时)和第19次(228小时)挤奶时,GT浓度降至≤30纳克/毫升。处理A、B和C组奶牛在给药后首次挤奶(12小时)时测得的GT最高平均(±标准误)浓度分别为14710±1213.89、167.87±46.94和91.62±14.55纳克/毫升;处理D、E和F组奶牛在给药期间,其最高平均浓度分别为14067.50±2989.09、446.07±100.92和22900±2843.66纳克/毫升,分别出现在第7次、第3次和第8次挤奶时。由于GT未被批准用于奶牛,且一些可能的处理方式导致消除时间较长,非法和超标签使用可能会导致牛奶中出现残留。

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