Louis Steen, Herra Javed, Eli Contorno, David Irby, John Lowery, Mary Bradley, Kimberly Paige O'Brien, Brian Reemsten, T Konrad Rajab
{"title":"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。","authors":"Louis Steen, Herra Javed, Eli Contorno, David Irby, John Lowery, Mary Bradley, Kimberly Paige O'Brien, Brian Reemsten, T Konrad Rajab","doi":"10.1016/j.transproceed.2025.07.030","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Method: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":94258,"journal":{"name":"Transplantation proceedings","volume":" ","pages":""},"PeriodicalIF":0.8000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450072/pdf/","citationCount":"0","resultStr":"{\"title\":\"Intramuscular Tacrolimus Pharmacokinetics in a Pediatric Porcine Model for Partial Heart Transplantation.\",\"authors\":\"Louis Steen, Herra Javed, Eli Contorno, David Irby, John Lowery, Mary Bradley, Kimberly Paige O'Brien, Brian Reemsten, T Konrad Rajab\",\"doi\":\"10.1016/j.transproceed.2025.07.030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>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.</p><p><strong>Method: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>\",\"PeriodicalId\":94258,\"journal\":{\"name\":\"Transplantation proceedings\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450072/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transplantation proceedings\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.transproceed.2025.07.030\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.transproceed.2025.07.030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Intramuscular Tacrolimus Pharmacokinetics in a Pediatric Porcine Model for Partial Heart Transplantation.
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.