US FDA-validated green GC–MS method for analysis of gabapentin, tramadol and/or amitriptyline mixtures in biological fluids

Author:

Naguib Ibrahim A12ORCID,Ali Nesma A3ORCID,Elroby Fadwa A4ORCID,El Ghobashy Mohamed R56ORCID,Abdallah Fatma F2ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia

2. Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Beni-Suef University, Alshaheed Shehata Ahmad Hegazy St., 62514, Beni-Suef, Egypt

3. Toxicology Laboratory, Forensic Medicine Authority, Ministry of Justice, 11647, Cairo, Egypt

4. Forensic Medicine Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt

5. Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt

6. Faculty of Pharmacy, October 6 University, October 6 City, Giza, Egypt

Abstract

Background: Mixtures of gabapentin, tramadol and/or amitriptyline are usually recommended for treatment of neuropathic pain. Materials & methods/results: A novel GC–MS/MS method was developed to assess the studied mixture whether in pure forms or human biological fluids (plasma/urine). The chromatographic detection was performed using MS detector applying the selected ion-monitoring mode. An (Agilent, CA, USA) GC–MS with triple axis single quadrupole detector unit was used for the analysis equipped with HP-5MS (5% phenyl methyl siloxane) column. Helium was the carrier gas and positive electron impact ionization mode was applied. Conclusion: The developed method was able to assess the mixture components simultaneously within six minutes. Validation of the method was assured according to US FDA guidelines and Eco-Scale assessment.

Funder

Taif University

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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