A Novel Stability Indicating High Performance Liquid Chromatography Method for Lysergic Acid Diethylamide
Mahima Bansal1, Estelle Miller1, Rachael Sumner1
1School of Pharmacy, Faculty of Medical and Health Sciences, The University of Auckland, 85 Park Road, Grafton, Auckland 1023, New Zealand.
Accurate quantification of lysergic acid diethylamide (LSD) microdosing is crucial for safety. A new HPLC method precisely measures LSD, revealing significant discrepancies in illicit samples and highlighting user risks.
Area of Science:
- Analytical Chemistry
- Pharmacology
- Forensic Science
Background:
- Microdosing lysergic acid diethylamide (LSD) shows therapeutic potential, necessitating reliable quantification and stability assessment.
- Current analytical methods for LSD microdosing lack high throughput and speed, posing challenges for research and safety.
- Accurate LSD quantification is vital for both pharmaceutical development and assessing illicitly sourced microdosing products.
Purpose of the Study:
- To develop a robust, stability-indicating, isocratic reverse-phase-high performance liquid chromatography (RP-HPLC) method for precise LSD quantification.
- To ensure the developed method can separate LSD from its primary degradation product, iso-LSD.
- To validate the method according to International Conference on Harmonization (ICH) guidelines for reliable analytical performance.
Main Methods:
- Development of an isocratic RP-HPLC method for LSD quantification.
- Validation of the method for specificity, linearity, accuracy, precision, LOD, LOQ, and robustness under ICH guidelines.
- Application of the method to analyze LSD content in community-sourced illicit microdosing samples.
Main Results:
- A robust and stability-indicating RP-HPLC method for accurate LSD quantification was successfully developed.
- The method demonstrated high specificity, separating LSD from its degradation product, iso-LSD.
- Analysis of illicit microdosing samples revealed significant discrepancies between estimated and actual LSD concentrations, indicating potential risks to users.
Conclusions:
- The developed RP-HPLC method provides accurate and precise quantification of LSD, essential for quality control in pharmaceutical and illicit formulations.
- The method's ability to detect LSD in the presence of degradants ensures reliability under various stress conditions.
- Findings underscore the critical need for reliable analytical methods to ensure the safety and quality of LSD microdosing products, particularly those sourced illicitly.
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