Highly sensitive simultaneous quantification of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid in human plasma using ultra‐high‐performance liquid chromatography coupled with tandem mass spectrometry. Issue 10 (11th March 2022)
- Record Type:
- Journal Article
- Title:
- Highly sensitive simultaneous quantification of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid in human plasma using ultra‐high‐performance liquid chromatography coupled with tandem mass spectrometry. Issue 10 (11th March 2022)
- Main Title:
- Highly sensitive simultaneous quantification of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid in human plasma using ultra‐high‐performance liquid chromatography coupled with tandem mass spectrometry
- Authors:
- Oda, Ayako
Suzuki, Yosuke
Sato, Banri
Sato, Haruki
Tanaka, Ryota
Ono, Hiroyuki
Ando, Tadasuke
Shin, Toshitaka
Mimata, Hiromitsu
Itoh, Hiroki
Ohno, Keiko - Abstract:
- Abstract : Indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid are uremic toxins that accumulate in renal failure and have been reported to decrease the activities of the drug‐metabolizing enzyme cytochrome P450 3A and the drug transporter organic anion transporting polypeptides 1B, respectively. In this study, we established and validated an assay for simultaneous quantification of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid in human plasma. The samples were pretreated by solid‐phase extraction, and measured by ultra‐high‐performance liquid chromatography–tandem mass spectrometry. The validation results for this assay were within the acceptable limits recommended by the US Food and Drug Administration, with a lower limit of quantitation of 0.05 μg/mL for both indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid. Recovery rates of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid corrected by internal standard were 100.7–101.9 and 100.2–101.3%, respectively. Matrix effects of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid corrected by internal standard were 101.1–105.5 and 97.0–103.8%, respectively. The validated assay was used to analyze indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid concentrations in the plasma samples of healthy volunteers and patients with chronic kidney disease. All the measured plasma indoxyl sulfate andAbstract : Indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid are uremic toxins that accumulate in renal failure and have been reported to decrease the activities of the drug‐metabolizing enzyme cytochrome P450 3A and the drug transporter organic anion transporting polypeptides 1B, respectively. In this study, we established and validated an assay for simultaneous quantification of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid in human plasma. The samples were pretreated by solid‐phase extraction, and measured by ultra‐high‐performance liquid chromatography–tandem mass spectrometry. The validation results for this assay were within the acceptable limits recommended by the US Food and Drug Administration, with a lower limit of quantitation of 0.05 μg/mL for both indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid. Recovery rates of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid corrected by internal standard were 100.7–101.9 and 100.2–101.3%, respectively. Matrix effects of indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid corrected by internal standard were 101.1–105.5 and 97.0–103.8%, respectively. The validated assay was used to analyze indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid concentrations in the plasma samples of healthy volunteers and patients with chronic kidney disease. All the measured plasma indoxyl sulfate and 3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acid concentrations were within the calibration ranges. This novel method may contribute to predicting the activities of drug‐metabolizing enzymes and drug transporters in individual patients. … (more)
- Is Part Of:
- Journal of separation science. Volume 45:Issue 10(2022)
- Journal:
- Journal of separation science
- Issue:
- Volume 45:Issue 10(2022)
- Issue Display:
- Volume 45, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 45
- Issue:
- 10
- Issue Sort Value:
- 2022-0045-0010-0000
- Page Start:
- 1672
- Page End:
- 1682
- Publication Date:
- 2022-03-11
- Subjects:
- chronic kidney disease -- cytochrome P450 3A -- drug transporter -- indoxyl sulfate -- mass spectrometry
Separation (Technology) -- Periodicals
Chromatographic analysis -- Periodicals
543.089 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-9314 ↗
http://www.interscience.wiley.com/jpages/1615-9306 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jssc.202100950 ↗
- Languages:
- English
- ISSNs:
- 1615-9306
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5063.880000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21569.xml