Determination of in vitro human whole blood-to-plasma ratio of THJ-018 utilizing gas chromatography-Mass spectrometry.
Autor: | Kumar S; Department of Forensic Sciences, College of Criminal Justice, Naif Arab University for Security Sciences, Riyadh, Saudi Arabia., Khleel Alkhibery RN; Department of Forensic Sciences, College of Criminal Justice, Naif Arab University for Security Sciences, Riyadh, Saudi Arabia., Bakdash A; Department of Forensic Sciences, College of Criminal Justice, Naif Arab University for Security Sciences, Riyadh, Saudi Arabia., Mohamed Abdelhady MS; Riyadh Poisons Control & Medical Forensic Chemistry Center, Kaab Ibn Al Harith, Ar Rawdah, Riyadh, Saudi Arabia; Egyptian Drug Authority, National Organizations for Drug Control and Research (NODCAR), Giza, Egypt. |
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Jazyk: | angličtina |
Zdroj: | Indian journal of pharmacology [Indian J Pharmacol] 2021 Jan-Feb; Vol. 53 (1), pp. 13-18. |
DOI: | 10.4103/ijp.IJP_668_19 |
Abstrakt: | Objectives: This study was aimed to determine in vitro human whole blood-to-plasma ratio (K Materials and Methods: The samples (human blood) were sprayed with THJ-018 and an internal standard and extracted using solid-phase extraction. THJ-018 was determined in the final extracts by GC/MS. Results: The value for K Conclusion: The data analysis supports the proposition that the ratio of the plasma to whole blood concentrations (1.56) is a suitable parameter characterizing THJ-018 distribution in whole blood. For toxicological analysis, it would be best to refrain from converting any drug concentration measured in whole blood to that anticipated in plasma or serum; however, toxic and therapeutic concentrations should be determined for the individual specimens collected. Competing Interests: None |
Databáze: | MEDLINE |
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