NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines

In the frame of increasingly stringent quality assessment required by the regulators, the pharmaceutical industry has to face increasingly sophisticated counterfeiting practices. Counterfeits based on deliberate copying of processes or on the infringement of current patents for generic medicines are...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of pharmaceutical sciences 2013-02, Vol.48 (3), p.464-473
Hauptverfasser: Remaud, Gérald S., Bussy, Ugo, Lees, Michèle, Thomas, Freddy, Desmurs, Jean-Roger, Jamin, Eric, Silvestre, Virginie, Akoka, Serge
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 473
container_issue 3
container_start_page 464
container_title European journal of pharmaceutical sciences
container_volume 48
creator Remaud, Gérald S.
Bussy, Ugo
Lees, Michèle
Thomas, Freddy
Desmurs, Jean-Roger
Jamin, Eric
Silvestre, Virginie
Akoka, Serge
description In the frame of increasingly stringent quality assessment required by the regulators, the pharmaceutical industry has to face increasingly sophisticated counterfeiting practices. Counterfeits based on deliberate copying of processes or on the infringement of current patents for generic medicines are not straightforward to detect, unless the molecular probe is the active molecule itself. In this context, impurity profiling is limited. A tool based on the determination of intramolecular isotopic profiles has been developed to provide manufacturers of APIs (Active Pharmaceutical Ingredients) with a new solution to meet this double requirement. Stable isotope analyses by NMR gives direct access to site-specific isotope content at natural abundance. In this report, it is shown how both 2H and 13C NMR spectrometry can provide complementary and valuable information that could be applied to link APIs to their manufacturing source. Isotopic 13C NMR offers additional benefits over 2H NMR in using robust adiabatic polarization transfer methods, leading to a tremendous reduction in experimental time. Two approaches are illustrated. Firstly, the use of 2H and single pulse 13C NMR spectra obtained on 20 commercial ibuprofen samples from different origins show that this combined strategy leads to (i) a unique intramolecular isotope identification and (ii) a preliminary classification of the samples according to the synthetic pathways of the main industrial processes. An approach employing polarization transfer methods applied to 11 commercial naproxen samples, for which 2H and single pulse 13C NMR spectra are not exploitable and/or are not accessible in reasonable time. The relative and partial intramolecular 13C distribution obtained on naproxen by applying this methodology is sufficiently informative to allow the same conclusions as for ibuprofen. The additional benefits that these approaches should bring to API manufacturers are discussed.
doi_str_mv 10.1016/j.ejps.2012.12.009
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1615257971</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0928098712004836</els_id><sourcerecordid>1615257971</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-a6d05d86ee7598ea3184a02b78d4f2c07b2fb2df1bc37355c1d8d778c2b3574b3</originalsourceid><addsrcrecordid>eNp9kc9u1DAQxi1ERZfCC3BAPnLJMnY2sYO4rKoClfoHIThbjjNpvSRxsJ1KfRpelYm2cEQayZb9m-_TzMfYGwFbAaJ-f9jiYU5bCUJuqQCaZ2wjtGoKUBKesw00UhfQaHXKXqZ0AIBaK3jBTmUpawlVvWG_b66_8TSjyzGMmOMj9ynkMHvHez_dYZyjnzLdPvA9zyEMvA-R53vko52W3rq8RIzHx2jdTyL53mX_gPzrvY2jdbhk7-zAL6e7iJ3HKSfekxlP2cZVmZQyRm-HRAarK8Ejkc5PmF6xk55-8PXTecZ-fLr4fv6luLr9fHm-vyrcTspc2LqDqtM1oqoajbYUemdBtkp3u146UK3sW9n1onWlKqvKiU53Smkn27JSu7Y8Y--OunMMvxZM2Yw-ORwGO2FYkhG1qGSlGiUIlUfUxZBSxN7QjkYbH40AswZjDmYNxqzBGCoKhprePukvLQ33r-VvEgR8PAJIUz54jCY5WpajRURKx3TB_0__D9_Wo3U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1615257971</pqid></control><display><type>article</type><title>NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Remaud, Gérald S. ; Bussy, Ugo ; Lees, Michèle ; Thomas, Freddy ; Desmurs, Jean-Roger ; Jamin, Eric ; Silvestre, Virginie ; Akoka, Serge</creator><creatorcontrib>Remaud, Gérald S. ; Bussy, Ugo ; Lees, Michèle ; Thomas, Freddy ; Desmurs, Jean-Roger ; Jamin, Eric ; Silvestre, Virginie ; Akoka, Serge</creatorcontrib><description>In the frame of increasingly stringent quality assessment required by the regulators, the pharmaceutical industry has to face increasingly sophisticated counterfeiting practices. Counterfeits based on deliberate copying of processes or on the infringement of current patents for generic medicines are not straightforward to detect, unless the molecular probe is the active molecule itself. In this context, impurity profiling is limited. A tool based on the determination of intramolecular isotopic profiles has been developed to provide manufacturers of APIs (Active Pharmaceutical Ingredients) with a new solution to meet this double requirement. Stable isotope analyses by NMR gives direct access to site-specific isotope content at natural abundance. In this report, it is shown how both 2H and 13C NMR spectrometry can provide complementary and valuable information that could be applied to link APIs to their manufacturing source. Isotopic 13C NMR offers additional benefits over 2H NMR in using robust adiabatic polarization transfer methods, leading to a tremendous reduction in experimental time. Two approaches are illustrated. Firstly, the use of 2H and single pulse 13C NMR spectra obtained on 20 commercial ibuprofen samples from different origins show that this combined strategy leads to (i) a unique intramolecular isotope identification and (ii) a preliminary classification of the samples according to the synthetic pathways of the main industrial processes. An approach employing polarization transfer methods applied to 11 commercial naproxen samples, for which 2H and single pulse 13C NMR spectra are not exploitable and/or are not accessible in reasonable time. The relative and partial intramolecular 13C distribution obtained on naproxen by applying this methodology is sufficiently informative to allow the same conclusions as for ibuprofen. The additional benefits that these approaches should bring to API manufacturers are discussed.</description><identifier>ISSN: 0928-0987</identifier><identifier>EISSN: 1879-0720</identifier><identifier>DOI: 10.1016/j.ejps.2012.12.009</identifier><identifier>PMID: 23262056</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Active Pharmaceutical Ingredient starting materials (API-SMs) ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Anti-Inflammatory Agents, Non-Steroidal - economics ; Carbon Isotopes ; Chemistry, Pharmaceutical ; Counterfeit Drugs - chemistry ; Counterfeiting ; Deuterium ; Fraud - prevention &amp; control ; Ibuprofen ; Ibuprofen - chemistry ; Ibuprofen - economics ; Isotope profile ; Isotopic NMR ; Magnetic Resonance Spectroscopy ; Naproxen ; Naproxen - chemistry ; Naproxen - economics ; Principal Component Analysis ; Quality Control ; Technology, Pharmaceutical</subject><ispartof>European journal of pharmaceutical sciences, 2013-02, Vol.48 (3), p.464-473</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-a6d05d86ee7598ea3184a02b78d4f2c07b2fb2df1bc37355c1d8d778c2b3574b3</citedby><cites>FETCH-LOGICAL-c422t-a6d05d86ee7598ea3184a02b78d4f2c07b2fb2df1bc37355c1d8d778c2b3574b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0928098712004836$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23262056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Remaud, Gérald S.</creatorcontrib><creatorcontrib>Bussy, Ugo</creatorcontrib><creatorcontrib>Lees, Michèle</creatorcontrib><creatorcontrib>Thomas, Freddy</creatorcontrib><creatorcontrib>Desmurs, Jean-Roger</creatorcontrib><creatorcontrib>Jamin, Eric</creatorcontrib><creatorcontrib>Silvestre, Virginie</creatorcontrib><creatorcontrib>Akoka, Serge</creatorcontrib><title>NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines</title><title>European journal of pharmaceutical sciences</title><addtitle>Eur J Pharm Sci</addtitle><description>In the frame of increasingly stringent quality assessment required by the regulators, the pharmaceutical industry has to face increasingly sophisticated counterfeiting practices. Counterfeits based on deliberate copying of processes or on the infringement of current patents for generic medicines are not straightforward to detect, unless the molecular probe is the active molecule itself. In this context, impurity profiling is limited. A tool based on the determination of intramolecular isotopic profiles has been developed to provide manufacturers of APIs (Active Pharmaceutical Ingredients) with a new solution to meet this double requirement. Stable isotope analyses by NMR gives direct access to site-specific isotope content at natural abundance. In this report, it is shown how both 2H and 13C NMR spectrometry can provide complementary and valuable information that could be applied to link APIs to their manufacturing source. Isotopic 13C NMR offers additional benefits over 2H NMR in using robust adiabatic polarization transfer methods, leading to a tremendous reduction in experimental time. Two approaches are illustrated. Firstly, the use of 2H and single pulse 13C NMR spectra obtained on 20 commercial ibuprofen samples from different origins show that this combined strategy leads to (i) a unique intramolecular isotope identification and (ii) a preliminary classification of the samples according to the synthetic pathways of the main industrial processes. An approach employing polarization transfer methods applied to 11 commercial naproxen samples, for which 2H and single pulse 13C NMR spectra are not exploitable and/or are not accessible in reasonable time. The relative and partial intramolecular 13C distribution obtained on naproxen by applying this methodology is sufficiently informative to allow the same conclusions as for ibuprofen. The additional benefits that these approaches should bring to API manufacturers are discussed.</description><subject>Active Pharmaceutical Ingredient starting materials (API-SMs)</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - economics</subject><subject>Carbon Isotopes</subject><subject>Chemistry, Pharmaceutical</subject><subject>Counterfeit Drugs - chemistry</subject><subject>Counterfeiting</subject><subject>Deuterium</subject><subject>Fraud - prevention &amp; control</subject><subject>Ibuprofen</subject><subject>Ibuprofen - chemistry</subject><subject>Ibuprofen - economics</subject><subject>Isotope profile</subject><subject>Isotopic NMR</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Naproxen</subject><subject>Naproxen - chemistry</subject><subject>Naproxen - economics</subject><subject>Principal Component Analysis</subject><subject>Quality Control</subject><subject>Technology, Pharmaceutical</subject><issn>0928-0987</issn><issn>1879-0720</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9u1DAQxi1ERZfCC3BAPnLJMnY2sYO4rKoClfoHIThbjjNpvSRxsJ1KfRpelYm2cEQayZb9m-_TzMfYGwFbAaJ-f9jiYU5bCUJuqQCaZ2wjtGoKUBKesw00UhfQaHXKXqZ0AIBaK3jBTmUpawlVvWG_b66_8TSjyzGMmOMj9ynkMHvHez_dYZyjnzLdPvA9zyEMvA-R53vko52W3rq8RIzHx2jdTyL53mX_gPzrvY2jdbhk7-zAL6e7iJ3HKSfekxlP2cZVmZQyRm-HRAarK8Ejkc5PmF6xk55-8PXTecZ-fLr4fv6luLr9fHm-vyrcTspc2LqDqtM1oqoajbYUemdBtkp3u146UK3sW9n1onWlKqvKiU53Smkn27JSu7Y8Y--OunMMvxZM2Yw-ORwGO2FYkhG1qGSlGiUIlUfUxZBSxN7QjkYbH40AswZjDmYNxqzBGCoKhprePukvLQ33r-VvEgR8PAJIUz54jCY5WpajRURKx3TB_0__D9_Wo3U</recordid><startdate>20130214</startdate><enddate>20130214</enddate><creator>Remaud, Gérald S.</creator><creator>Bussy, Ugo</creator><creator>Lees, Michèle</creator><creator>Thomas, Freddy</creator><creator>Desmurs, Jean-Roger</creator><creator>Jamin, Eric</creator><creator>Silvestre, Virginie</creator><creator>Akoka, Serge</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130214</creationdate><title>NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines</title><author>Remaud, Gérald S. ; Bussy, Ugo ; Lees, Michèle ; Thomas, Freddy ; Desmurs, Jean-Roger ; Jamin, Eric ; Silvestre, Virginie ; Akoka, Serge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-a6d05d86ee7598ea3184a02b78d4f2c07b2fb2df1bc37355c1d8d778c2b3574b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Active Pharmaceutical Ingredient starting materials (API-SMs)</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - economics</topic><topic>Carbon Isotopes</topic><topic>Chemistry, Pharmaceutical</topic><topic>Counterfeit Drugs - chemistry</topic><topic>Counterfeiting</topic><topic>Deuterium</topic><topic>Fraud - prevention &amp; control</topic><topic>Ibuprofen</topic><topic>Ibuprofen - chemistry</topic><topic>Ibuprofen - economics</topic><topic>Isotope profile</topic><topic>Isotopic NMR</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Naproxen</topic><topic>Naproxen - chemistry</topic><topic>Naproxen - economics</topic><topic>Principal Component Analysis</topic><topic>Quality Control</topic><topic>Technology, Pharmaceutical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Remaud, Gérald S.</creatorcontrib><creatorcontrib>Bussy, Ugo</creatorcontrib><creatorcontrib>Lees, Michèle</creatorcontrib><creatorcontrib>Thomas, Freddy</creatorcontrib><creatorcontrib>Desmurs, Jean-Roger</creatorcontrib><creatorcontrib>Jamin, Eric</creatorcontrib><creatorcontrib>Silvestre, Virginie</creatorcontrib><creatorcontrib>Akoka, Serge</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Remaud, Gérald S.</au><au>Bussy, Ugo</au><au>Lees, Michèle</au><au>Thomas, Freddy</au><au>Desmurs, Jean-Roger</au><au>Jamin, Eric</au><au>Silvestre, Virginie</au><au>Akoka, Serge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines</atitle><jtitle>European journal of pharmaceutical sciences</jtitle><addtitle>Eur J Pharm Sci</addtitle><date>2013-02-14</date><risdate>2013</risdate><volume>48</volume><issue>3</issue><spage>464</spage><epage>473</epage><pages>464-473</pages><issn>0928-0987</issn><eissn>1879-0720</eissn><abstract>In the frame of increasingly stringent quality assessment required by the regulators, the pharmaceutical industry has to face increasingly sophisticated counterfeiting practices. Counterfeits based on deliberate copying of processes or on the infringement of current patents for generic medicines are not straightforward to detect, unless the molecular probe is the active molecule itself. In this context, impurity profiling is limited. A tool based on the determination of intramolecular isotopic profiles has been developed to provide manufacturers of APIs (Active Pharmaceutical Ingredients) with a new solution to meet this double requirement. Stable isotope analyses by NMR gives direct access to site-specific isotope content at natural abundance. In this report, it is shown how both 2H and 13C NMR spectrometry can provide complementary and valuable information that could be applied to link APIs to their manufacturing source. Isotopic 13C NMR offers additional benefits over 2H NMR in using robust adiabatic polarization transfer methods, leading to a tremendous reduction in experimental time. Two approaches are illustrated. Firstly, the use of 2H and single pulse 13C NMR spectra obtained on 20 commercial ibuprofen samples from different origins show that this combined strategy leads to (i) a unique intramolecular isotope identification and (ii) a preliminary classification of the samples according to the synthetic pathways of the main industrial processes. An approach employing polarization transfer methods applied to 11 commercial naproxen samples, for which 2H and single pulse 13C NMR spectra are not exploitable and/or are not accessible in reasonable time. The relative and partial intramolecular 13C distribution obtained on naproxen by applying this methodology is sufficiently informative to allow the same conclusions as for ibuprofen. The additional benefits that these approaches should bring to API manufacturers are discussed.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23262056</pmid><doi>10.1016/j.ejps.2012.12.009</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0928-0987
ispartof European journal of pharmaceutical sciences, 2013-02, Vol.48 (3), p.464-473
issn 0928-0987
1879-0720
language eng
recordid cdi_proquest_miscellaneous_1615257971
source MEDLINE; Elsevier ScienceDirect Journals
subjects Active Pharmaceutical Ingredient starting materials (API-SMs)
Anti-Inflammatory Agents, Non-Steroidal - chemistry
Anti-Inflammatory Agents, Non-Steroidal - economics
Carbon Isotopes
Chemistry, Pharmaceutical
Counterfeit Drugs - chemistry
Counterfeiting
Deuterium
Fraud - prevention & control
Ibuprofen
Ibuprofen - chemistry
Ibuprofen - economics
Isotope profile
Isotopic NMR
Magnetic Resonance Spectroscopy
Naproxen
Naproxen - chemistry
Naproxen - economics
Principal Component Analysis
Quality Control
Technology, Pharmaceutical
title NMR spectrometry isotopic fingerprinting: A tool for the manufacturer for tracking Active Pharmaceutical Ingredients from starting materials to final medicines
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T05%3A41%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=NMR%20spectrometry%20isotopic%20fingerprinting:%20A%20tool%20for%20the%20manufacturer%20for%20tracking%20Active%20Pharmaceutical%20Ingredients%20from%20starting%20materials%20to%20final%20medicines&rft.jtitle=European%20journal%20of%20pharmaceutical%20sciences&rft.au=Remaud,%20G%C3%A9rald%20S.&rft.date=2013-02-14&rft.volume=48&rft.issue=3&rft.spage=464&rft.epage=473&rft.pages=464-473&rft.issn=0928-0987&rft.eissn=1879-0720&rft_id=info:doi/10.1016/j.ejps.2012.12.009&rft_dat=%3Cproquest_cross%3E1615257971%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1615257971&rft_id=info:pmid/23262056&rft_els_id=S0928098712004836&rfr_iscdi=true