Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines

Methamphetamine hydrochloride is one of the most widely used illicit drugs in the Philippines. In this study, we describe the application of cluster analysis of trace impurities in the profiling of the seized methamphetamine drug samples. Thirty milligrams of a homogenized drug sample were dissolved...

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Main Authors: Dayrit, Fabian M, Dumlao, Morphy C
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Published: Archīum Ateneo 2004
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Online Access:https://archium.ateneo.edu/chemistry-faculty-pubs/101
https://www.sciencedirect.com/science/article/pii/S0379073804001318
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spelling ph-ateneo-arc.chemistry-faculty-pubs-11002020-07-25T04:16:20Z Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines Dayrit, Fabian M Dumlao, Morphy C Methamphetamine hydrochloride is one of the most widely used illicit drugs in the Philippines. In this study, we describe the application of cluster analysis of trace impurities in the profiling of the seized methamphetamine drug samples. Thirty milligrams of a homogenized drug sample were dissolved in 1 mL of pH 10.5 buffer solution and extracted with ethyl acetate containing three internal standards. The trace impurities were identified using gas chromatography–mass spectrometry (GC–MS) and quantified by gas chromatography with a flame ionization detector (GC–FID). Following previously reported methodologies, 30 impurity peaks were selected from the GC–FID chromatograms. The peak areas and retention times were referenced to the internal standards. The peak areas of the selected peaks were then grouped for cluster analysis. In order to check for consistency of clustering, two further cluster analyses were performed using 40 and 50 impurity peaks. Changes in clustering were observed in going from 30 to 40 impurity peaks, while analyses using 40 and 50 impurity peaks gave similar results. Thus, for the seized drug samples used in this study, cluster analysis using at least 40 impurity peaks showed better consistency of clustering as compared to analysis using 30 peaks only. Ten of the impurity peaks were identified, of which four were identified for the first time in methamphetamine drug samples. These are p-bromotoluene, N-benzyl amphetamine, N-ethyl amphetamine, and N-ethyl methamphetamine. The presence of phenyl-2-propanone (P2P), N,N-dimethyl amphetamine, and N-formyl amphetamine is indicative that these casework samples were synthesized using the Leuckart method. 2004-01-01T08:00:00Z text https://archium.ateneo.edu/chemistry-faculty-pubs/101 https://www.sciencedirect.com/science/article/pii/S0379073804001318 Chemistry Faculty Publications Archīum Ateneo Methamphetamine hydrochloride Profiling of drug impurities Cluster analysis Chemistry Organic Chemistry
institution Ateneo De Manila University
building Ateneo De Manila University Library
country Philippines
collection archium.Ateneo Institutional Repository
topic Methamphetamine hydrochloride
Profiling of drug impurities
Cluster analysis
Chemistry
Organic Chemistry
spellingShingle Methamphetamine hydrochloride
Profiling of drug impurities
Cluster analysis
Chemistry
Organic Chemistry
Dayrit, Fabian M
Dumlao, Morphy C
Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
description Methamphetamine hydrochloride is one of the most widely used illicit drugs in the Philippines. In this study, we describe the application of cluster analysis of trace impurities in the profiling of the seized methamphetamine drug samples. Thirty milligrams of a homogenized drug sample were dissolved in 1 mL of pH 10.5 buffer solution and extracted with ethyl acetate containing three internal standards. The trace impurities were identified using gas chromatography–mass spectrometry (GC–MS) and quantified by gas chromatography with a flame ionization detector (GC–FID). Following previously reported methodologies, 30 impurity peaks were selected from the GC–FID chromatograms. The peak areas and retention times were referenced to the internal standards. The peak areas of the selected peaks were then grouped for cluster analysis. In order to check for consistency of clustering, two further cluster analyses were performed using 40 and 50 impurity peaks. Changes in clustering were observed in going from 30 to 40 impurity peaks, while analyses using 40 and 50 impurity peaks gave similar results. Thus, for the seized drug samples used in this study, cluster analysis using at least 40 impurity peaks showed better consistency of clustering as compared to analysis using 30 peaks only. Ten of the impurity peaks were identified, of which four were identified for the first time in methamphetamine drug samples. These are p-bromotoluene, N-benzyl amphetamine, N-ethyl amphetamine, and N-ethyl methamphetamine. The presence of phenyl-2-propanone (P2P), N,N-dimethyl amphetamine, and N-formyl amphetamine is indicative that these casework samples were synthesized using the Leuckart method.
format text
author Dayrit, Fabian M
Dumlao, Morphy C
author_facet Dayrit, Fabian M
Dumlao, Morphy C
author_sort Dayrit, Fabian M
title Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
title_short Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
title_full Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
title_fullStr Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
title_full_unstemmed Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines
title_sort impurity profiling of methamphetamine hydrochloride drugs seized in the philippines
publisher Archīum Ateneo
publishDate 2004
url https://archium.ateneo.edu/chemistry-faculty-pubs/101
https://www.sciencedirect.com/science/article/pii/S0379073804001318
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