An investigation of the comparability of commercially sourced plasma and pharmaceutical study plasma, using total protein concentration

被引:0
|
作者
Felgate, Clive [1 ]
Spooner, Neil [1 ]
Calloway, Robert [1 ]
机构
[1] GlaxoSmithKline, David Jack Ctr, Res & Dev, Pk Rd, Ware SG12 0DP, Herts, England
关键词
control blood plasma; endogenous; method validation; preanalytics; CLINICAL-CHEMISTRY; SERUM; ANTIBODY; VALIDATION; STABILITY; PATIENT; BLOOD; IMMUNOASSAYS; INTERFERENCE; COAGULATION;
D O I
10.4155/bio.15.248
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Control blood plasma is regularly used in bioanalysis, biomarkers and proteomics, and is often obtained from commercial sources. It has always been assumed that this plasma will be comparable to plasma drawn during a drug development study. Results: When compared using total protein concentrations, plasma from only one species (dog) demonstrated statistical comparability, plasma from all other species tested (human, rabbit, mouse and rat) shows a statistically significant difference. Conclusion: If endogenous components of blood plasma are being measured, or if an assay technique does not significantly limit matrix effects, any assay controls should be prepared using control plasma from the drug development site, or using commercial plasma that has been screened against drug development site plasma.
引用
收藏
页码:311 / 321
页数:11
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