Intramuscular Tacrolimus Pharmacokinetics in a Pediatric Porcine Model for Partial Heart Transplantation.

IF 0.8
Louis Steen, Herra Javed, Eli Contorno, David Irby, John Lowery, Mary Bradley, Kimberly Paige O'Brien, Brian Reemsten, T Konrad Rajab
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Abstract

Objective: The cornerstone of immunosuppression for transplantation is tacrolimus. One of the most reliable routes for administering tacrolimus in porcine models is intramuscular injection. However, the pharmacokinetics of intramuscular tacrolimus in piglets remain unexplored. Here, we close this gap in knowledge to guide intramuscular tacrolimus dosing in pediatric porcine transplant models.

Method: In the dosing trial, piglets (n = 7) underwent partial heart transplantation. Post-operatively, the piglets received immunosuppression with tacrolimus at daily doses between 0.07-0.4mg/kg. In the pharmacokinetic study, piglets (n = 6) underwent external jugular line placement. After a baseline blood draw, 0.25mg/kg of intramuscular tacrolimus was administered, and serial blood draws were performed to determine tacrolimus blood levels. The data was statistically analyzed to determine the pharmacokinetic parameters.

Results: The dosing trial showed that intramuscular tacrolimus daily doses between 0.217-0.421mg/kg most consistently achieved tacrolimus blood levels within the therapeutic window. Therefore, 0.25mg/kg was used for the pharmacokinetic study. This revealed a half-life of 7.7 ± 0.9 hours, an average elimination constant of 0.09 ± 0.01, and an average volume of distribution of 30.9 ± 5.3 liters.

Conclusions: Intramuscular tacrolimus achieves reliable blood levels with a predictable half-life. Despite high peak blood concentrations, a daily dose of 0.25 mg/kg did not result in clinical or laboratory evidence of toxicity.

他克莫司肌内药代动力学在儿童猪部分心脏移植模型中的应用。
目的:他克莫司是移植免疫抑制的基础。在猪模型中给药他克莫司最可靠的途径之一是肌肉注射。然而,肌注他克莫司在仔猪体内的药代动力学尚未研究。在这里,我们缩小了这方面的知识差距,以指导小儿猪移植模型中肌肉注射他克莫司的剂量。方法:在给药试验中,7头仔猪进行部分心脏移植。术后给予他克莫司免疫抑制,日剂量为0.07 ~ 0.4mg/kg。在药代动力学研究中,仔猪(n = 6)接受颈外静脉置管。基线抽血后,给予0.25mg/kg肌注他克莫司,并连续抽血测定他克莫司血药水平。对数据进行统计分析,确定药代动力学参数。结果:给药试验表明,他克莫司肌注日剂量在0.217-0.421mg/kg之间最能在治疗窗内达到他克莫司血药水平。因此,采用0.25mg/kg进行药代动力学研究。其半衰期为7.7±0.9小时,平均消除常数为0.09±0.01,平均分布容积为30.9±5.3升。结论:肌注他克莫司可达到可靠的血药浓度和可预测的半衰期。尽管血药浓度峰值很高,但每日剂量为0.25 mg/kg并未产生临床或实验室毒性证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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