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绵羊后肢中利多卡因和布比卡因的体内血液、脂肪及肌肉浓度

The in vivo blood, fat and muscle concentrations of lignocaine and bupivacaine in the hindquarters of sheep.

作者信息

Upton R N, Nancarrow C, McLean C F, Mather L E, Runciman W B

机构信息

Department of Anaesthesia and Intensive Care, Flinders University of South Australia, Bedford Park.

出版信息

Xenobiotica. 1991 Jan;21(1):13-22. doi: 10.3109/00498259109039446.

Abstract
  1. A method was developed for sampling muscle and fat from the hindquarters of sheep undergoing spinal anaesthesia. The method was used to measure the concentrations of lignocaine and bupivacaine in the blood, muscle and fat of the hindquarters of sheep during and after 180 min constant-rate infusions of the drugs. 2. For both drugs the muscle drug concentrations were a relatively constant ratio of the simultaneous arterial blood drug concentrations during and after the infusion. 3. There was uptake of both lignocaine and bupivacaine into subcutaneous fat during the infusions. At the end of the infusion the ratio of the fat: arterial blood drug concentrations were 1.54 (SD = 0.57, n = 4) and 3.1 (SD = 1.4, n = 4) for lignocaine and bupivacaine, respectively. 4. The drug concentrations in fat declined relatively slowly after the infusion. The ratio of the fat: arterial blood drug concentrations 180 min after the end of the infusion was 21.5 (SD 4.0, n = 3) and for lignocaine, and 120 min after the end of the infusion was 9.54 (SD 5.2, n = 3) for bupivacaine. 5. It was concluded that the concentrations of lignocaine and bupivacaine in muscle were essentially in equilibrium with the arterial concentrations during and after the infusion. However, the concentrations of lignocaine and bupivacaine in fat were not in equilibrium with the arterial concentrations in the post-infusion period.
摘要
  1. 开发了一种从接受脊髓麻醉的绵羊后躯采集肌肉和脂肪样本的方法。该方法用于测量在180分钟持续输注药物期间及之后绵羊后躯血液、肌肉和脂肪中利多卡因和布比卡因的浓度。2. 对于这两种药物,在输注期间及之后,肌肉中的药物浓度与同时期动脉血中的药物浓度呈相对恒定的比例。3. 在输注过程中,利多卡因和布比卡因均被皮下脂肪摄取。输注结束时,利多卡因和布比卡因的脂肪:动脉血药物浓度比分别为1.54(标准差=0.57,n=4)和3.1(标准差=1.4,n=4)。4. 输注后脂肪中的药物浓度下降相对缓慢。输注结束180分钟后,利多卡因的脂肪:动脉血药物浓度比为21.5(标准差4.0,n=3);输注结束120分钟后,布比卡因的该比例为9.54(标准差5.2,n=3)。5. 得出的结论是,在输注期间及之后,肌肉中利多卡因和布比卡因的浓度与动脉浓度基本处于平衡状态。然而,在输注后阶段,脂肪中利多卡因和布比卡因的浓度与动脉浓度并不平衡。

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