A Simplified Method for Determining Blood-to-Plasma Ratios in vitro and ex vivo by Matrix Matching with Blank Blood or Plasma.

Xiaomei Zhang, Gary J Jenkins, Kelly E Desino, Jinrong Liu, Mary Larsen, David M Stresser
{"title":"A Simplified Method for Determining Blood-to-Plasma Ratios <i>in vitro</i> and <i>ex vivo</i> by Matrix Matching with Blank Blood or Plasma.","authors":"Xiaomei Zhang, Gary J Jenkins, Kelly E Desino, Jinrong Liu, Mary Larsen, David M Stresser","doi":"10.2174/2949681016666230817150551","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This work describes a simplified, 96-well plate method for determining the blood-to-plasma concentration ratio (BP ratio) for small molecules.</p><p><strong>Methods: </strong>The need for calibration curves was eliminated using a matrix-matching approach in which blood samples were mixed with blank plasma and plasma samples were mixed with blank blood. As a result, both blood- and plasma-origin samples shared an equivalent matrix ahead of bioanalysis. In the <i>in vitro</i> assay, identical sample matrices were achieved by using the same source of blank plasma and blood.</p><p><strong>Results: </strong>In humans, a good correlation (R2 = 0.84) was observed between the data obtained in this matrix-matching method and literature values for 11 commercial compounds possessing a wide range of logD values across multiple chemical classes. In addition, this method showed good agreement with <i>in vitro</i> BP ratios for 10 proprietary compounds determined radiometrically (R2 = 0.72) in human and preclinical species. Finally, the <i>in vitro</i> matrix matching method compared favorably to BP ratios determined <i>ex vivo</i> for 13 proprietary and literature compounds (R2 = 0.87) in rat.</p><p><strong>Conclusion: </strong>This method, suitable for <i>in vitro</i> and <i>ex vivo</i> BP ratio determinations, is operationally efficient, robust, and a useful improvement upon previously published methods.</p>","PeriodicalId":72844,"journal":{"name":"Drug metabolism and bioanalysis letters","volume":" ","pages":"113-120"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug metabolism and bioanalysis letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2949681016666230817150551","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: This work describes a simplified, 96-well plate method for determining the blood-to-plasma concentration ratio (BP ratio) for small molecules.

Methods: The need for calibration curves was eliminated using a matrix-matching approach in which blood samples were mixed with blank plasma and plasma samples were mixed with blank blood. As a result, both blood- and plasma-origin samples shared an equivalent matrix ahead of bioanalysis. In the in vitro assay, identical sample matrices were achieved by using the same source of blank plasma and blood.

Results: In humans, a good correlation (R2 = 0.84) was observed between the data obtained in this matrix-matching method and literature values for 11 commercial compounds possessing a wide range of logD values across multiple chemical classes. In addition, this method showed good agreement with in vitro BP ratios for 10 proprietary compounds determined radiometrically (R2 = 0.72) in human and preclinical species. Finally, the in vitro matrix matching method compared favorably to BP ratios determined ex vivo for 13 proprietary and literature compounds (R2 = 0.87) in rat.

Conclusion: This method, suitable for in vitro and ex vivo BP ratio determinations, is operationally efficient, robust, and a useful improvement upon previously published methods.

用空白血或血浆基质匹配法测定体外和离体血浆比的简化方法。
目的:建立一种简便的96孔板测定小分子血浆浓度比(BP ratio)的方法。方法:采用血液样品与空白血浆混合,血浆样品与空白血液混合的矩阵匹配方法,消除了对校准曲线的需要。因此,血液和血浆来源的样本在生物分析之前共享一个等效的基质。在体外实验中,使用相同来源的空白血浆和血液获得相同的样品基质。结果:在人体中,该矩阵匹配方法获得的数据与文献值之间具有良好的相关性(R2 = 0.84),其中11种商业化合物在多个化学类别中具有广泛的logD值。此外,该方法与人类和临床前物种中10种专有化合物的体外BP比(R2 = 0.72)具有良好的一致性。最后,体外基质匹配法与13种专利和文献化合物在大鼠体内测定的BP比(R2 = 0.87)比较有利。结论:该方法适用于体外和离体BP比的测定,操作简便,稳健性好,是对已有方法的有益改进。
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
1.60
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信