{"title":"肌肉注射阿莫西林对小牛犊炎的药代动力学研究及模型建立。","authors":"Morgane Moustaghfir, Bernadette Espana, Karine Hauray, Rémi Charretier, Abdessalem Hammed, Vanessa Louzier, Jean-Yves Madec, Marisa Haenni, Agnese Lupo, Caroline Prouillac","doi":"10.1111/jvp.70016","DOIUrl":null,"url":null,"abstract":"<p><p>The objective of this study was to estimate plasma pharmacokinetic parameters for amoxicillin (AMX) in calves (n = 7) suffering from omphalitis after a single intramuscular (IM) administration of 8.75 mg/kg of amoxicillin and clavulanic acid (AMC) (7 mg/kg of AMX and 1.75 mg/kg of clavulanic acid). Plasma samples were collected over 6 h. AMX concentrations were measured via liquid chromatography/mass spectrometry (LC-MS/MS). A non-compartmental analysis was first used to determine pharmacokinetic parameters; then a population pharmacokinetic and a Monte Carlo simulation were performed on a hypothetical herd of 1000 calves. After a single IM administration, we observed a correlation between Cl and V<sub>d</sub> and a high variability of PK parameters among individuals. Maximum plasma concentration was between 1.22 and 5.99 μg/mL and T<sub>max</sub> was between 0.75 and 2 h. The plasma concentration values of AMX fit to a one-compartment model with linear elimination and administration by extravascular route with a zero-order process (duration Tk0) with a lag time (Tlag). Results showed that the plasma concentration never reached 4 mg/L, which is the breakpoint of AMX-susceptible Escherichia coli or Pasteurella spp. isolates, even after simulation of repeated administration.</p>","PeriodicalId":17596,"journal":{"name":"Journal of veterinary pharmacology and therapeutics","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pharmacokinetics Study and Modelling of Amoxicillin After Intramuscular Administration in Veal Calves Suffering From Omphalitis.\",\"authors\":\"Morgane Moustaghfir, Bernadette Espana, Karine Hauray, Rémi Charretier, Abdessalem Hammed, Vanessa Louzier, Jean-Yves Madec, Marisa Haenni, Agnese Lupo, Caroline Prouillac\",\"doi\":\"10.1111/jvp.70016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The objective of this study was to estimate plasma pharmacokinetic parameters for amoxicillin (AMX) in calves (n = 7) suffering from omphalitis after a single intramuscular (IM) administration of 8.75 mg/kg of amoxicillin and clavulanic acid (AMC) (7 mg/kg of AMX and 1.75 mg/kg of clavulanic acid). Plasma samples were collected over 6 h. AMX concentrations were measured via liquid chromatography/mass spectrometry (LC-MS/MS). A non-compartmental analysis was first used to determine pharmacokinetic parameters; then a population pharmacokinetic and a Monte Carlo simulation were performed on a hypothetical herd of 1000 calves. After a single IM administration, we observed a correlation between Cl and V<sub>d</sub> and a high variability of PK parameters among individuals. Maximum plasma concentration was between 1.22 and 5.99 μg/mL and T<sub>max</sub> was between 0.75 and 2 h. The plasma concentration values of AMX fit to a one-compartment model with linear elimination and administration by extravascular route with a zero-order process (duration Tk0) with a lag time (Tlag). Results showed that the plasma concentration never reached 4 mg/L, which is the breakpoint of AMX-susceptible Escherichia coli or Pasteurella spp. isolates, even after simulation of repeated administration.</p>\",\"PeriodicalId\":17596,\"journal\":{\"name\":\"Journal of veterinary pharmacology and therapeutics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of veterinary pharmacology and therapeutics\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1111/jvp.70016\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of veterinary pharmacology and therapeutics","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/jvp.70016","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Pharmacokinetics Study and Modelling of Amoxicillin After Intramuscular Administration in Veal Calves Suffering From Omphalitis.
The objective of this study was to estimate plasma pharmacokinetic parameters for amoxicillin (AMX) in calves (n = 7) suffering from omphalitis after a single intramuscular (IM) administration of 8.75 mg/kg of amoxicillin and clavulanic acid (AMC) (7 mg/kg of AMX and 1.75 mg/kg of clavulanic acid). Plasma samples were collected over 6 h. AMX concentrations were measured via liquid chromatography/mass spectrometry (LC-MS/MS). A non-compartmental analysis was first used to determine pharmacokinetic parameters; then a population pharmacokinetic and a Monte Carlo simulation were performed on a hypothetical herd of 1000 calves. After a single IM administration, we observed a correlation between Cl and Vd and a high variability of PK parameters among individuals. Maximum plasma concentration was between 1.22 and 5.99 μg/mL and Tmax was between 0.75 and 2 h. The plasma concentration values of AMX fit to a one-compartment model with linear elimination and administration by extravascular route with a zero-order process (duration Tk0) with a lag time (Tlag). Results showed that the plasma concentration never reached 4 mg/L, which is the breakpoint of AMX-susceptible Escherichia coli or Pasteurella spp. isolates, even after simulation of repeated administration.
期刊介绍:
The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.