Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique

Background: Ruboxistaurin (RBX) used to treat retinopathy in diabetic patients which caused by microvascular damage and leakage which contributes to visual loss. There are no published studies on the use of liquid chromatography-tandem mass spectrometry for development and validation of a simple, se...

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Main Authors: Bushra T. AlQuadeib, Fadilah S. Aleanizy, Fulwah Y. Alqahtani, Rehab A. Alshammari, Amal Aldarwesh, Ibrahim Alsarra
Format: Article
Language:English
Published: Springer 2023-04-01
Series:Saudi Pharmaceutical Journal
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Online Access:http://www.sciencedirect.com/science/article/pii/S1319016423000373
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author Bushra T. AlQuadeib
Fadilah S. Aleanizy
Fulwah Y. Alqahtani
Rehab A. Alshammari
Amal Aldarwesh
Ibrahim Alsarra
author_facet Bushra T. AlQuadeib
Fadilah S. Aleanizy
Fulwah Y. Alqahtani
Rehab A. Alshammari
Amal Aldarwesh
Ibrahim Alsarra
author_sort Bushra T. AlQuadeib
collection DOAJ
description Background: Ruboxistaurin (RBX) used to treat retinopathy in diabetic patients which caused by microvascular damage and leakage which contributes to visual loss. There are no published studies on the use of liquid chromatography-tandem mass spectrometry for development and validation of a simple, sensitive, and accurate method for measuring RBX in rat plasma. Method: Chromatographic separation of RBX was achieved using ultra-performance liquid chromatography. Multiple-reaction monitoring quantification used RBX [M + H] + ion at m/z 469.18 and daughter ions at m/z 84, 58.12, and 98.10. Atorvastatin was used as internal standard (IS), has a single daughter ion, and was identified using m/z 559.6 → 249.9. Validation of the liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for RBX in rat plasma for linearity (greater than0.997) was carried out at 25–1000 ng/mL. Results: In rat plasma, the accuracy was within 3.4%, and the intra- and inter-day precision was within 11.8%. Stability, recovery, and matrix effect were all within acceptable limits. The drug retention time (0.85 ± 0.03 min) was remarkably short. Conclusion: The method developed in the current study is suitable to quantify RBX in plasma or bulk doses.
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spelling doaj-art-2b2712f1e9d74fb88e4cdeaffb7893882025-08-20T03:54:43ZengSpringerSaudi Pharmaceutical Journal1319-01642023-04-0131454755310.1016/j.jsps.2023.02.007Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS techniqueBushra T. AlQuadeib0Fadilah S. Aleanizy1Fulwah Y. Alqahtani2Rehab A. Alshammari3Amal Aldarwesh4Ibrahim Alsarra5Department of Pharmaceutics, College of Pharmacy, King Saud University, Saudi Arabia, P.O. Box 84428, Riyadh 11671, Saudi Arabia; Corresponding author.Department of Pharmaceutics, College of Pharmacy, King Saud University, Saudi Arabia, P.O. Box 84428, Riyadh 11671, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Saudi Arabia, P.O. Box 84428, Riyadh 11671, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Saudi Arabia, P.O. Box 84428, Riyadh 11671, Saudi ArabiaDepartment of Optometry, College of Applied Medical Sciences, King Saud University, P.O. 11671, Riyadh 11671, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Saudi Arabia, P.O. Box 84428, Riyadh 11671, Saudi ArabiaBackground: Ruboxistaurin (RBX) used to treat retinopathy in diabetic patients which caused by microvascular damage and leakage which contributes to visual loss. There are no published studies on the use of liquid chromatography-tandem mass spectrometry for development and validation of a simple, sensitive, and accurate method for measuring RBX in rat plasma. Method: Chromatographic separation of RBX was achieved using ultra-performance liquid chromatography. Multiple-reaction monitoring quantification used RBX [M + H] + ion at m/z 469.18 and daughter ions at m/z 84, 58.12, and 98.10. Atorvastatin was used as internal standard (IS), has a single daughter ion, and was identified using m/z 559.6 → 249.9. Validation of the liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for RBX in rat plasma for linearity (greater than0.997) was carried out at 25–1000 ng/mL. Results: In rat plasma, the accuracy was within 3.4%, and the intra- and inter-day precision was within 11.8%. Stability, recovery, and matrix effect were all within acceptable limits. The drug retention time (0.85 ± 0.03 min) was remarkably short. Conclusion: The method developed in the current study is suitable to quantify RBX in plasma or bulk doses.http://www.sciencedirect.com/science/article/pii/S1319016423000373RuboxistaurinValidationLC-MS/MSPlasmaRat
spellingShingle Bushra T. AlQuadeib
Fadilah S. Aleanizy
Fulwah Y. Alqahtani
Rehab A. Alshammari
Amal Aldarwesh
Ibrahim Alsarra
Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
Saudi Pharmaceutical Journal
Ruboxistaurin
Validation
LC-MS/MS
Plasma
Rat
title Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
title_full Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
title_fullStr Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
title_full_unstemmed Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
title_short Determination of Ruboxistaurin analysis in rat plasma utilizing LC–MS/MS technique
title_sort determination of ruboxistaurin analysis in rat plasma utilizing lc ms ms technique
topic Ruboxistaurin
Validation
LC-MS/MS
Plasma
Rat
url http://www.sciencedirect.com/science/article/pii/S1319016423000373
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