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Effect of milking frequency and dosing interval on the pharmacokinetics of cephapirin after intramammary infusion in lactating dairy cows

机译:挤奶频率和给药间隔对奶牛泌乳内头孢哌林药代动力学的影响

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摘要

The objective was to determine the effect of milking frequency and dosing interval on pharmacokinetics of cephapirin after intramammary infusion. Six healthy Holstein cows were administered cephapirin (200 mg) into 1 rear mammary gland after each of 2 milkings. Cows were milked twice daily (2×) and dosed at a 12-h interval or 3 times daily (3×) and dosed at an 8- or 16-h interval. A duplicated Latin square design allowed each cow to receive all 3 frequency-dose treatments, with intervening washout periods. Concentrations of cephapirin (CEPH) and desacetylcephapirin (DAC) in milk from the treated glands were determined at each milking after infusion using liquid chromatography-mass spectrometry. Data were fitted using 1- and 2-compartment pharmacokinetic models, as well as a noncompartmental model. Cephapirin was rapidly metabolized to DAC in the mammary gland, with DAC being the predominant agent in milk until 48 h after infusion. Pharmacokinetics of CEPH and DAC were similar for all treatment groups, with a 1-compartment model providing a better fit than a 2-compartment model in most instances. Milking frequency did not affect the length of time that milk CEPH concentration exceeded MIC_(50) or MIC_(90) values (the minimum inhibitory antimicrobial concentration needed to inhibit 50 or 90% of microbial activity, respectively) for common mastitis pathogens, except that cows milked 3× and dosed at a 16-h interval maintained inhibitory concentrations approximately 8 h longer than those dosed at an 8-h interval. Time for milk CEPH concentration to reach the FDA tolerance did not differ among treatment groups [mean ± SD; 68 ± 20, 66 ± 22, and 57 ± 18 h after last treatment for cows treated at 12, 16, and 8 h, respectively]. Mean residence time for CEPH in the mammary gland was linearly and negatively associatedrnwith the volume of milk produced. Calculated CEPH concentration in composite milk from all 4 mammary glands was below the FDA tolerance in all cows by 96 h after the last infusion, which is the labeled withholding time for the preparation used. Our findings suggest that this CEPH preparation, which is labeled for 2 doses 12 h apart, could be administered at a 16-h interval in herds milking 3×, with no significant effect on inhibitory concentrations in milk or withdrawal time; extended withdrawal times would be prudent for cows with very low milk production. Further investigation is needed to determine if milking frequency affects CEPH pharmacokinetics in cows with clinical mastitis.
机译:目的是确定挤奶频率和给药间隔对乳头内输注后头孢氨苄药代动力学的影响。在两次挤奶后,分别对六只健康的荷斯坦奶牛头孢氨苄(200毫克)施予1个后乳腺。母牛每天挤奶两次(2次),间隔为12小时;每天一次,挤奶3次(3次),间隔为8​​或16小时。重复的拉丁方设计使每头奶牛都能接受所有3种频次剂量的治疗,并有中间冲刷期。在每次挤奶后,使用液相色谱-质谱法测定来自处理过的腺体的牛奶中头孢氨苄(CEPH)和去乙酰头孢菌素(DAC)的浓度。使用1室和2室药代动力学模型以及非室模型对数据进行拟合。头孢哌啶在乳腺中迅速代谢为DAC,在输注后48小时内,DAC是牛奶中的主要成分。在所有治疗组中,CEPH和DAC的药代动力学相似,在大多数情况下,一室模型比二室模型更适合。挤奶频率不会影响乳腺CEPH浓度超过常见乳腺炎病原体的MIC_(50)或MIC_(90)值(分别抑制50%或90%的微生物活性所需的最小抑菌浓度)的时间长度,除了以3倍间隔喂奶的母牛,其抑制浓度比以8小时间隔喂奶的抑制浓度长约8小时。各治疗组之间牛奶CEPH浓度达到FDA耐受时间的时间没有差异[平均值±SD;最后一次处理后分别在12、16和8 h处理的母牛分别为68±20、66±22和57±18 h]。 CEPH在乳腺中的平均停留时间与产奶量呈线性负相关。在最后一次输液后的96小时内,所有4头乳腺的复合乳中计算出的CEPH浓度均低于FDA耐受性,这是所用制剂的标记保留时间。我们的研究结果表明,这种CEPH制剂(间隔12小时2剂)被标记,可以在挤奶3倍的情况下每隔16小时施用一次,对牛奶中的抑制浓度或停药时间没有显着影响。对于产奶量非常低的奶牛,延长戒断时间是明智的。需要进一步研究以确定挤奶频率是否会影响患有临床乳腺炎的母牛的CEPH药代动力学。

著录项

  • 来源
    《Journal of dairy science》 |2009年第9期|4262-4275|共14页
  • 作者单位

    Department of Veterinary Clinical Medicine, University of Illinois, Urbana 61802;

    Department of Veterinary Clinical Medicine, University of Illinois, Urbana 61802;

    Rocky Mountain Instrumental Laboratories, Fort Collins, CO 80525;

    Department of Veterinary Clinical Sciences, Purdue University, West Lafayette, IN 47907;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    milking frequency; cephapirin; pharmacokinetics;

    机译:挤奶频率头孢氨苄药代动力学;
  • 入库时间 2022-08-17 23:25:03

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