Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir
[Display omitted] This study compares the performance of a reference method of HPLC to Raman spectroscopy (RS) for the analytical quality control (AQC) of therapeutic objects. We assessed a model consisting of a widely used antiviral drug, i.e., ganciclovir, which was compounded in a medical device...
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| Veröffentlicht in: | International journal of pharmaceutics 2014-10, Vol.474 (1-2), p.193-201 |
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| container_title | International journal of pharmaceutics |
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| creator | Amin, Alexandre Bourget, Philippe Vidal, Fabrice Ader, Flavie |
| description | [Display omitted]
This study compares the performance of a reference method of HPLC to Raman spectroscopy (RS) for the analytical quality control (AQC) of therapeutic objects. We assessed a model consisting of a widely used antiviral drug, i.e., ganciclovir, which was compounded in a medical device and then transferred in a vacuum glass vial prior to analyses. As the aim of the alternative RS method is to replace the destructive, time-consuming HPLC method, requiring sample preparation, it needs to be demonstrated that RS performs at least as good as the HPLC method. Therefore, the two methods were validated by calculating the accuracy profile and provided excellent results for the analytical validation key criteria, i.e., trueness, precision and accuracy, ranging from 0.8 to 10mg/mL. The Spearman and Kendall correlation tests (p-value |
| doi_str_mv | 10.1016/j.ijpharm.2014.08.028 |
| format | Article |
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This study compares the performance of a reference method of HPLC to Raman spectroscopy (RS) for the analytical quality control (AQC) of therapeutic objects. We assessed a model consisting of a widely used antiviral drug, i.e., ganciclovir, which was compounded in a medical device and then transferred in a vacuum glass vial prior to analyses. As the aim of the alternative RS method is to replace the destructive, time-consuming HPLC method, requiring sample preparation, it needs to be demonstrated that RS performs at least as good as the HPLC method. Therefore, the two methods were validated by calculating the accuracy profile and provided excellent results for the analytical validation key criteria, i.e., trueness, precision and accuracy, ranging from 0.8 to 10mg/mL. The Spearman and Kendall correlation tests (p-value<1.10–15) and the statistical studies performed on the graphs confirm a strong correlation in the results between RS and the standard HPLC under the experimental conditions. These results confirmed the potential of this option for future applications, owing to its analytical and practical quality and its contributions to the safety of the medication circuit. This method also greatly contributes to the protection of caregivers and their working environment.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2014.08.028</identifier><identifier>PMID: 25148728</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Analytical quality control ; Antiviral Agents - chemistry ; Chromatography, High Pressure Liquid ; Ganciclovir ; Ganciclovir - chemistry ; Hospital environment ; HPLC ; Quality Control ; Raman spectroscopy ; Safety ; Spectrum Analysis, Raman</subject><ispartof>International journal of pharmaceutics, 2014-10, Vol.474 (1-2), p.193-201</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-878ab232999afec7a18ea4e3fc37ab27b45a80eecfd6666f553af1ef22a3aae03</citedby><cites>FETCH-LOGICAL-c365t-878ab232999afec7a18ea4e3fc37ab27b45a80eecfd6666f553af1ef22a3aae03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpharm.2014.08.028$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25148728$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Amin, Alexandre</creatorcontrib><creatorcontrib>Bourget, Philippe</creatorcontrib><creatorcontrib>Vidal, Fabrice</creatorcontrib><creatorcontrib>Ader, Flavie</creatorcontrib><title>Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
This study compares the performance of a reference method of HPLC to Raman spectroscopy (RS) for the analytical quality control (AQC) of therapeutic objects. We assessed a model consisting of a widely used antiviral drug, i.e., ganciclovir, which was compounded in a medical device and then transferred in a vacuum glass vial prior to analyses. As the aim of the alternative RS method is to replace the destructive, time-consuming HPLC method, requiring sample preparation, it needs to be demonstrated that RS performs at least as good as the HPLC method. Therefore, the two methods were validated by calculating the accuracy profile and provided excellent results for the analytical validation key criteria, i.e., trueness, precision and accuracy, ranging from 0.8 to 10mg/mL. The Spearman and Kendall correlation tests (p-value<1.10–15) and the statistical studies performed on the graphs confirm a strong correlation in the results between RS and the standard HPLC under the experimental conditions. These results confirmed the potential of this option for future applications, owing to its analytical and practical quality and its contributions to the safety of the medication circuit. This method also greatly contributes to the protection of caregivers and their working environment.</description><subject>Analytical quality control</subject><subject>Antiviral Agents - chemistry</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Ganciclovir</subject><subject>Ganciclovir - chemistry</subject><subject>Hospital environment</subject><subject>HPLC</subject><subject>Quality Control</subject><subject>Raman spectroscopy</subject><subject>Safety</subject><subject>Spectrum Analysis, Raman</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEuLFDEQgIMo7rj6E5QcvXSbR6eTPoksvmBBWPQcatIVJ0N3ku10L8y_N8OMXq1LQdVXVdRHyFvOWs54_-HYhmM-wDK3gvGuZaZlwjwjO260bGSn--dkx6Q2jeJa3pBXpRwZY73g8iW5EYp3RguzI-4hbWuISCHnKThYQ4o0efoAM0RaMrp1ScWlfKIh0vWA9HGDKawn6lKsrekMH1LJYYWp1uactjjiSH9DdMFN6Sksr8kLD1PBN9d8S359-fzz7ltz_-Pr97tP942TvVobow3shRTDMIBHp4EbhA6ld1LXht53CgxDdH7sa3ilJHiOXgiQAMjkLXl_2ZuX9LhhWe0cisNpgohpK5arXnXDYPhQUXVBXf2uLOhtXsIMy8lyZs9-7dFe_dqzX8uMrX7r3LvriW0_4_hv6q_QCny8AFgffQq42OICRodjWKpLO6bwnxN_AKj_keM</recordid><startdate>20141020</startdate><enddate>20141020</enddate><creator>Amin, Alexandre</creator><creator>Bourget, Philippe</creator><creator>Vidal, Fabrice</creator><creator>Ader, Flavie</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>20141020</creationdate><title>Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir</title><author>Amin, Alexandre ; Bourget, Philippe ; Vidal, Fabrice ; Ader, Flavie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-878ab232999afec7a18ea4e3fc37ab27b45a80eecfd6666f553af1ef22a3aae03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical quality control</topic><topic>Antiviral Agents - chemistry</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Ganciclovir</topic><topic>Ganciclovir - chemistry</topic><topic>Hospital environment</topic><topic>HPLC</topic><topic>Quality Control</topic><topic>Raman spectroscopy</topic><topic>Safety</topic><topic>Spectrum Analysis, Raman</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amin, Alexandre</creatorcontrib><creatorcontrib>Bourget, Philippe</creatorcontrib><creatorcontrib>Vidal, Fabrice</creatorcontrib><creatorcontrib>Ader, Flavie</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>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amin, Alexandre</au><au>Bourget, Philippe</au><au>Vidal, Fabrice</au><au>Ader, Flavie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2014-10-20</date><risdate>2014</risdate><volume>474</volume><issue>1-2</issue><spage>193</spage><epage>201</epage><pages>193-201</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
This study compares the performance of a reference method of HPLC to Raman spectroscopy (RS) for the analytical quality control (AQC) of therapeutic objects. We assessed a model consisting of a widely used antiviral drug, i.e., ganciclovir, which was compounded in a medical device and then transferred in a vacuum glass vial prior to analyses. As the aim of the alternative RS method is to replace the destructive, time-consuming HPLC method, requiring sample preparation, it needs to be demonstrated that RS performs at least as good as the HPLC method. Therefore, the two methods were validated by calculating the accuracy profile and provided excellent results for the analytical validation key criteria, i.e., trueness, precision and accuracy, ranging from 0.8 to 10mg/mL. The Spearman and Kendall correlation tests (p-value<1.10–15) and the statistical studies performed on the graphs confirm a strong correlation in the results between RS and the standard HPLC under the experimental conditions. These results confirmed the potential of this option for future applications, owing to its analytical and practical quality and its contributions to the safety of the medication circuit. This method also greatly contributes to the protection of caregivers and their working environment.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25148728</pmid><doi>10.1016/j.ijpharm.2014.08.028</doi><tpages>9</tpages></addata></record> |
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| source | MEDLINE; Elsevier ScienceDirect Journals |
| subjects | Analytical quality control Antiviral Agents - chemistry Chromatography, High Pressure Liquid Ganciclovir Ganciclovir - chemistry Hospital environment HPLC Quality Control Raman spectroscopy Safety Spectrum Analysis, Raman |
| title | Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir |
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