Validated HPLC determination of 4-dimethylaminoantipyrine in different suppository bases
Suppositories are important tools for individual therapy, especially in paediatrics, and an instrumental assay method has become necessary for the quality control of dosage units. The aim of this work was to develop a rapid, effective high-performance liquid chromatography method to assay aminophena...
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Veröffentlicht in: | Indian journal of pharmaceutical sciences 2014-01, Vol.76 (1), p.31-37 |
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description | Suppositories are important tools for individual therapy, especially in paediatrics, and an instrumental assay method has become necessary for the quality control of dosage units. The aim of this work was to develop a rapid, effective high-performance liquid chromatography method to assay aminophenazone in extemporaneous suppositories prepared with two different suppository bases, adeps solidus and massa macrogoli. With a novel sample preparation method developed by the authors, 4-dimethylaminoantipyrine was determined in these suppository bases with 95-105% recovery. The measurements were carried out on a Shimadzu Prominence ultra high-performance liquid chromatography system equipped with a 20 ΅l sample loop. The separation was achieved on a Hypersil ODS column, with methanol, sodium acetate buffer (pH 5.5±0.05, 0.05 M, 60:40, v/v) as the mobile phase at a flow rate of 1.5 ml/min. The chromatograms were acquired at 253 nm. The chromatographic method was fully validated in accordance with current guidelines. The presented data demonstrate the successful development of a rapid, efficient and robust sample preparation and high-performance liquid chromatography method for the routine quality control of the dosage units of suppositories containing 4-dimethylaminoantipyrine. |
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The aim of this work was to develop a rapid, effective high-performance liquid chromatography method to assay aminophenazone in extemporaneous suppositories prepared with two different suppository bases, adeps solidus and massa macrogoli. With a novel sample preparation method developed by the authors, 4-dimethylaminoantipyrine was determined in these suppository bases with 95-105% recovery. The measurements were carried out on a Shimadzu Prominence ultra high-performance liquid chromatography system equipped with a 20 ΅l sample loop. The separation was achieved on a Hypersil ODS column, with methanol, sodium acetate buffer (pH 5.5±0.05, 0.05 M, 60:40, v/v) as the mobile phase at a flow rate of 1.5 ml/min. The chromatograms were acquired at 253 nm. The chromatographic method was fully validated in accordance with current guidelines. The presented data demonstrate the successful development of a rapid, efficient and robust sample preparation and high-performance liquid chromatography method for the routine quality control of the dosage units of suppositories containing 4-dimethylaminoantipyrine.</description><identifier>ISSN: 0250-474X</identifier><identifier>EISSN: 1998-3743</identifier><identifier>PMID: 24799736</identifier><language>eng</language><publisher>India: Medknow Publications</publisher><subject>Antipyrine ; Chromatography ; Colleges & universities ; Drug dosages ; High performance liquid chromatography ; Methods ; Pharmaceutical sciences ; Pharmacy ; Properties ; Research Paper ; Retention ; Suppositories ; Symmetry ; Technological change</subject><ispartof>Indian journal of pharmaceutical sciences, 2014-01, Vol.76 (1), p.31-37</ispartof><rights>COPYRIGHT 2014 Medknow Publications and Media Pvt. 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The aim of this work was to develop a rapid, effective high-performance liquid chromatography method to assay aminophenazone in extemporaneous suppositories prepared with two different suppository bases, adeps solidus and massa macrogoli. With a novel sample preparation method developed by the authors, 4-dimethylaminoantipyrine was determined in these suppository bases with 95-105% recovery. The measurements were carried out on a Shimadzu Prominence ultra high-performance liquid chromatography system equipped with a 20 ΅l sample loop. The separation was achieved on a Hypersil ODS column, with methanol, sodium acetate buffer (pH 5.5±0.05, 0.05 M, 60:40, v/v) as the mobile phase at a flow rate of 1.5 ml/min. The chromatograms were acquired at 253 nm. The chromatographic method was fully validated in accordance with current guidelines. The presented data demonstrate the successful development of a rapid, efficient and robust sample preparation and high-performance liquid chromatography method for the routine quality control of the dosage units of suppositories containing 4-dimethylaminoantipyrine.</description><subject>Antipyrine</subject><subject>Chromatography</subject><subject>Colleges & universities</subject><subject>Drug dosages</subject><subject>High performance liquid chromatography</subject><subject>Methods</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacy</subject><subject>Properties</subject><subject>Research Paper</subject><subject>Retention</subject><subject>Suppositories</subject><subject>Symmetry</subject><subject>Technological change</subject><issn>0250-474X</issn><issn>1998-3743</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNptkVFrFTEQhRdR7LX6F2TBF19Wkp3sZvMilIta4YI-qPQtZJPJbdpssia7vdx_b9TWWpFAAme-nJnDPKo2VIihAc7gcbUhbUcaxtnFSfUs5ytCQLTAn1YnLeNCcOg31cU35Z1RC5r6_PNuWxtcME0uqMXFUEdbs8a4CZfLo1dFjiosbj4mF7B2oTbOWkwYljqv8xyzW2I61qPKmJ9XT6zyGV_cvqfV1_fvvmzPm92nDx-3Z7tmD4JhQ8uoA9Bh7Iax5YJp0OWmAoixzAr-SxjGUkbgyirdUU5a05FeazGihtPq7W_feR0nNLoMk5SXc3KTSkcZlZMPK8Fdyn28kYwQ3nZQDF7fGqT4fcW8yMlljd6rgHHNknYtFbQdel7QV_-gV3FNocQrFGXQ0UGIe2qvPEoXbCx99U9TeQY9DKwnnBbqzX-ocgxOTseA1hX9wYeXfwf9k_Bul_dBDtGXJeZrvx4wycJeh3iQQOXdruEHDueqyQ</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Kalmár, E</creator><creator>Kormányos, B</creator><creator>Szakonyi, G</creator><creator>Dombi, G</creator><general>Medknow Publications</general><general>Medknow Publications and Media Pvt. 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The aim of this work was to develop a rapid, effective high-performance liquid chromatography method to assay aminophenazone in extemporaneous suppositories prepared with two different suppository bases, adeps solidus and massa macrogoli. With a novel sample preparation method developed by the authors, 4-dimethylaminoantipyrine was determined in these suppository bases with 95-105% recovery. The measurements were carried out on a Shimadzu Prominence ultra high-performance liquid chromatography system equipped with a 20 ΅l sample loop. The separation was achieved on a Hypersil ODS column, with methanol, sodium acetate buffer (pH 5.5±0.05, 0.05 M, 60:40, v/v) as the mobile phase at a flow rate of 1.5 ml/min. The chromatograms were acquired at 253 nm. The chromatographic method was fully validated in accordance with current guidelines. The presented data demonstrate the successful development of a rapid, efficient and robust sample preparation and high-performance liquid chromatography method for the routine quality control of the dosage units of suppositories containing 4-dimethylaminoantipyrine.</abstract><cop>India</cop><pub>Medknow Publications</pub><pmid>24799736</pmid><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; PubMed Central |
subjects | Antipyrine Chromatography Colleges & universities Drug dosages High performance liquid chromatography Methods Pharmaceutical sciences Pharmacy Properties Research Paper Retention Suppositories Symmetry Technological change |
title | Validated HPLC determination of 4-dimethylaminoantipyrine in different suppository bases |
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