Differential salivary disposition of linezolid and its two major metabolites (PNU-142300 and PNU-142586) after a single dose in healthy adults.

IF 4.1 2区 医学 Q1 INFECTIOUS DISEASES
Yasuhiro Tsuji, Hitoshi Kawasuji, Tomona Yamada, Fumihiro Kurosaki, Naoki Oikawa, Makito Kaneda, Takahiko Aoyama, Taketo Uchiyama, Yoshihiro Yamamoto
{"title":"Differential salivary disposition of linezolid and its two major metabolites (PNU-142300 and PNU-142586) after a single dose in healthy adults.","authors":"Yasuhiro Tsuji, Hitoshi Kawasuji, Tomona Yamada, Fumihiro Kurosaki, Naoki Oikawa, Makito Kaneda, Takahiko Aoyama, Taketo Uchiyama, Yoshihiro Yamamoto","doi":"10.1093/jac/dkag280","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Salivary therapeutic drug monitoring of linezolid has been proposed as a non-invasive alternative to blood sampling for pharmacokinetic assessment. However, the salivary disposition and pharmacokinetics of the two major linezolid metabolites, PNU-142300 and PNU-142586, have not been characterized.</p><p><strong>Objective: </strong>To evaluate the salivary disposition and serum protein binding of PNU-142300 and PNU-142586 using pharmacokinetic analysis.</p><p><strong>Methods: </strong>In this exploratory study, six healthy adult volunteers received a single intravenous dose of linezolid. Serial blood and saliva samples were collected for 10 h after dosing. The total and protein-unbound concentrations of linezolid and its two major metabolites, PNU-142300 and PNU-142586, were quantified using validated high-performance liquid chromatography methods.</p><p><strong>Results: </strong>Linezolid was consistently quantifiable in saliva, and its salivary concentration-time profile closely followed that of protein-unbound serum exposure. PNU-142300 and PNU-142586 were readily quantifiable in blood but remained below the lower limit of quantification in saliva in all participants at all sampling time points.</p><p><strong>Conclusions: </strong>Under the conditions studied, linezolid was quantifiable in saliva, whereas its two major metabolites were not, indicating different salivary disposition profiles for the parent drug and its metabolites. Salivary concentrations were consistent with protein-unbound serum exposure to linezolid under the conditions studied, whereas exposure to PNU-142300 and PNU-142586 could not be assessed using saliva and required blood-based measurements in the present study.</p>","PeriodicalId":14969,"journal":{"name":"Journal of Antimicrobial Chemotherapy","volume":"81 9","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2026-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Antimicrobial Chemotherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jac/dkag280","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Salivary therapeutic drug monitoring of linezolid has been proposed as a non-invasive alternative to blood sampling for pharmacokinetic assessment. However, the salivary disposition and pharmacokinetics of the two major linezolid metabolites, PNU-142300 and PNU-142586, have not been characterized.

Objective: To evaluate the salivary disposition and serum protein binding of PNU-142300 and PNU-142586 using pharmacokinetic analysis.

Methods: In this exploratory study, six healthy adult volunteers received a single intravenous dose of linezolid. Serial blood and saliva samples were collected for 10 h after dosing. The total and protein-unbound concentrations of linezolid and its two major metabolites, PNU-142300 and PNU-142586, were quantified using validated high-performance liquid chromatography methods.

Results: Linezolid was consistently quantifiable in saliva, and its salivary concentration-time profile closely followed that of protein-unbound serum exposure. PNU-142300 and PNU-142586 were readily quantifiable in blood but remained below the lower limit of quantification in saliva in all participants at all sampling time points.

Conclusions: Under the conditions studied, linezolid was quantifiable in saliva, whereas its two major metabolites were not, indicating different salivary disposition profiles for the parent drug and its metabolites. Salivary concentrations were consistent with protein-unbound serum exposure to linezolid under the conditions studied, whereas exposure to PNU-142300 and PNU-142586 could not be assessed using saliva and required blood-based measurements in the present study.

健康成人单次给药后利奈唑胺及其两种主要代谢物(PNU-142300和PNU-142586)唾液分布的差异
背景:利奈唑胺的唾液治疗药物监测已被提议作为一种非侵入性的替代血液取样进行药代动力学评估。然而,两种主要利奈唑胺代谢物PNU-142300和PNU-142586的唾液分布和药代动力学尚未被表征。目的:应用药动学分析评价PNU-142300和PNU-142586的唾液分布和血清蛋白结合。方法:在这项探索性研究中,6名健康成人志愿者接受单次静脉注射利奈唑胺。给药后10小时连续采集血液和唾液样本。采用高效液相色谱法对利奈唑胺及其两种主要代谢物PNU-142300和PNU-142586的总浓度和蛋白非结合浓度进行定量分析。结果:利奈唑胺在唾液中具有一致性的定量,其唾液浓度-时间曲线与蛋白非结合血清暴露密切相关。PNU-142300和PNU-142586在血液中很容易定量,但在所有采样时间点,所有参与者的唾液中仍低于定量的下限。结论:在所研究的条件下,唾液中可以定量检测利奈唑胺,而其两种主要代谢物却不能定量,这表明唾液对母体药物及其代谢物的分布特征不同。在研究条件下,唾液浓度与非蛋白结合血清暴露于利奈唑胺一致,而在本研究中,PNU-142300和PNU-142586暴露不能通过唾液和所需的血液测量来评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书