Related Experiment Video
Updated: Feb 8, 2026

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
Direct comparison of LC-MS/MS and RIA methods for the pharmacokinetics assessment of human insulin in preclinical
Shiqi Dong1,2, Yuan Gu2, Guangli Wei2
1School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Abstract:
Insulin is an effective therapeutic for diabetes, and the level of insulin in vivo is directly related to the health of diabetic patients. Traditionally, the concentrations of insulin in vivo are determined by the radioimmunoassay (RIA) method. In this study, we developed an LC-MS/MS method for the quantification of human insulin in dog plasma and directly compared the RIA and LC-MS/MS methods. Our LC-MS/MS method exhibited superior accuracy, efficiency and cost-effective for the pharmacokinetic (PK) assessment of human insulin. The LC-MS/MS method can quantitate human insulin and canine insulin simultaneously without cross-reactivity, making the analysis more efficient. The LLOQ of our LC-MS/MS method was 38.5 pg/mL, which was necessary to fully describe the PK profiles of endogenous and exogenous insulin in vivo. The direct comparison of PK data obtained from the two methods demonstrated that LC-MS/MS could be an alternative to the RIA method and should be widely used for the quantification of insulin drugs, especially in preclinical studies.
Related Concept Videos
Preclinical Development: Overview
Pharmacokinetic Models: Comparison and Selection Criterion
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.
Direct-Acting Cholinergic Agonists: Pharmacokinetics
Measurement of Bioavailability: Pharmacokinetic Methods
The Sense of Self: Reflected Self-Appraisal and Social Comparison
Development of Analytical Methods

