Nefopam Hydrochloride Degradation Kinetics in Solution
A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of nefopam hydrochloride and its degradation products under accelerated degradation conditions. The degradation kinetics of nefopam hydrochloride in aqueous solutions over a pH range...
Gespeichert in:
Veröffentlicht in: | Journal of pharmaceutical sciences 1990-01, Vol.79 (1), p.48-52 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 52 |
---|---|
container_issue | 1 |
container_start_page | 48 |
container_title | Journal of pharmaceutical sciences |
container_volume | 79 |
creator | Tu, Yu-Hsing Wang, Da-Peng Allen, Loyd V. |
description | A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of nefopam hydrochloride and its degradation products under accelerated degradation conditions. The degradation kinetics of nefopam hydrochloride in aqueous solutions over a pH range of 1.18 to 9.94 at 90 ± 0.2°C was studied. The degradation of nefopam hydrochloride was found to follow apparent first-order kinetics. The pH–rate profile shows that maximum stability of nefopam hydrochloride was obtained at pH 5.2–5.4. No general acid or base catalysis from acetate, phosphate, or borate buffer species was observed. The catalytic rate constants on the protonated nefopam imposed by hydrogen ion and water was determined to be 7.16 × 10−6 M−1 sec−1, and 4.54 × 10−9 sec−1, respectively. The pKa of nefopam hydrochloride in aqueous solution was determined to be 8.98 ± 0.33 (n = 3) at 25 ± 0.2°C by the spectrophotometric method. The catalytic rate constant of hydroxyl ion on the degradation of nefopam in either protonated or nonprotonated form was determined to be 6.63 × 10−6 M−1 sec−1 and 4.06 × 10−6 M−1 sec−1, respectively. A smaller effect of hydroxyl ion on the degradation of nonprotonated than on the degradation of protonated nefopam was observed.
The salt effect on the degradation of nefopam hydrochloride in pH 3.11 and pH 7.26 solutions obeyed the modified Debye-Huckel equation well; however, the observed ZAZB values (1.54 for pH 3.11 and −1.21 for pH 7.26 solutions) deviated slightly from the theoretical values (1.0 for pH 3.11 and −1.0 for pH 7.26 solutions) due to the high ionic strength (μ = 0.05 to 0.9) of the solutions. The temperature effect study shows an activation energy of 19.04 kcal/mol of the degradation of nefopam hydrochloride in a pH 3.11 solution with a constant ionic strength of 0.5. No significant effect of UV irradiation (254 nm) at a distance of 30 cm and intensity of 150 μwatt/cm2 on the degradation of nefopam hydrochloride in pH 3.11 solution at 25 ± 0.2°C was found when compared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol 400 in the pH 3.11 nefopam hydrochloride solution shows an increase in its stability at 90 ± 0.2 °C. |
doi_str_mv | 10.1002/jps.2600790112 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79673613</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022354915481481</els_id><sourcerecordid>79673613</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4562-6313ce798bdf8573840f87a70763fc19ba0d987eaa27885cbbc2aa90b4829ab13</originalsourceid><addsrcrecordid>eNqFkEtvEzEUhS0EKqFlyw5pFojdpNee-LVEAdKXWkJ5LC2P5w64TMbBngD593U0USoWiNWV7v3OOfYh5AWFKQVgp3frNGUCQGqglD0iE8oZlAKofEwmGWBlxWf6KXmW0h0ACOD8iByxilZcigkR19iGtV0VZ9smBve9C9E3WLzFb9E2dvChLy59j4N3qfB9cRu6zW55Qp60tkv4fD-Pyef37z7Nz8qrm8X5_M1V6WZcsFLkGIdSq7ppFZeVmkGrpJUgRdU6qmsLjVYSrWVSKe7q2jFrNdQzxbStaXVMXo--6xh-bjANZuWTw66zPYZNMlILWQlaZXA6gi6GlCK2Zh39ysatoWB2RZlclHkoKgte7p039QqbA75vJt9f7e82Odu10fbOpwOWYzMGGdMj9tt3uP1PqLn4cPvXE8pR69OAfw5aG3_s7CU3X68XZjln9Mty8dEsM69GHnPjvzxGk5zH3mHjI7rBNMH_67f3nhah-w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79673613</pqid></control><display><type>article</type><title>Nefopam Hydrochloride Degradation Kinetics in Solution</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Alma/SFX Local Collection</source><creator>Tu, Yu-Hsing ; Wang, Da-Peng ; Allen, Loyd V.</creator><creatorcontrib>Tu, Yu-Hsing ; Wang, Da-Peng ; Allen, Loyd V.</creatorcontrib><description>A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of nefopam hydrochloride and its degradation products under accelerated degradation conditions. The degradation kinetics of nefopam hydrochloride in aqueous solutions over a pH range of 1.18 to 9.94 at 90 ± 0.2°C was studied. The degradation of nefopam hydrochloride was found to follow apparent first-order kinetics. The pH–rate profile shows that maximum stability of nefopam hydrochloride was obtained at pH 5.2–5.4. No general acid or base catalysis from acetate, phosphate, or borate buffer species was observed. The catalytic rate constants on the protonated nefopam imposed by hydrogen ion and water was determined to be 7.16 × 10−6 M−1 sec−1, and 4.54 × 10−9 sec−1, respectively. The pKa of nefopam hydrochloride in aqueous solution was determined to be 8.98 ± 0.33 (n = 3) at 25 ± 0.2°C by the spectrophotometric method. The catalytic rate constant of hydroxyl ion on the degradation of nefopam in either protonated or nonprotonated form was determined to be 6.63 × 10−6 M−1 sec−1 and 4.06 × 10−6 M−1 sec−1, respectively. A smaller effect of hydroxyl ion on the degradation of nonprotonated than on the degradation of protonated nefopam was observed.
The salt effect on the degradation of nefopam hydrochloride in pH 3.11 and pH 7.26 solutions obeyed the modified Debye-Huckel equation well; however, the observed ZAZB values (1.54 for pH 3.11 and −1.21 for pH 7.26 solutions) deviated slightly from the theoretical values (1.0 for pH 3.11 and −1.0 for pH 7.26 solutions) due to the high ionic strength (μ = 0.05 to 0.9) of the solutions. The temperature effect study shows an activation energy of 19.04 kcal/mol of the degradation of nefopam hydrochloride in a pH 3.11 solution with a constant ionic strength of 0.5. No significant effect of UV irradiation (254 nm) at a distance of 30 cm and intensity of 150 μwatt/cm2 on the degradation of nefopam hydrochloride in pH 3.11 solution at 25 ± 0.2°C was found when compared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol 400 in the pH 3.11 nefopam hydrochloride solution shows an increase in its stability at 90 ± 0.2 °C.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600790112</identifier><identifier>PMID: 2313576</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Analgesics ; Biological and medical sciences ; Buffers ; Chromatography, High Pressure Liquid ; Drug Stability ; Hydrogen-Ion Concentration ; Medical sciences ; Nefopam - pharmacokinetics ; Nefopam - radiation effects ; Neuropharmacology ; Oxazocines - pharmacokinetics ; Pharmacology. Drug treatments ; Polyethylene Glycols ; Propylene Glycols ; Solutions ; Solvents ; Temperature ; Ultraviolet Rays</subject><ispartof>Journal of pharmaceutical sciences, 1990-01, Vol.79 (1), p.48-52</ispartof><rights>1990 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4562-6313ce798bdf8573840f87a70763fc19ba0d987eaa27885cbbc2aa90b4829ab13</citedby><cites>FETCH-LOGICAL-c4562-6313ce798bdf8573840f87a70763fc19ba0d987eaa27885cbbc2aa90b4829ab13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600790112$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600790112$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6733570$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2313576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tu, Yu-Hsing</creatorcontrib><creatorcontrib>Wang, Da-Peng</creatorcontrib><creatorcontrib>Allen, Loyd V.</creatorcontrib><title>Nefopam Hydrochloride Degradation Kinetics in Solution</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of nefopam hydrochloride and its degradation products under accelerated degradation conditions. The degradation kinetics of nefopam hydrochloride in aqueous solutions over a pH range of 1.18 to 9.94 at 90 ± 0.2°C was studied. The degradation of nefopam hydrochloride was found to follow apparent first-order kinetics. The pH–rate profile shows that maximum stability of nefopam hydrochloride was obtained at pH 5.2–5.4. No general acid or base catalysis from acetate, phosphate, or borate buffer species was observed. The catalytic rate constants on the protonated nefopam imposed by hydrogen ion and water was determined to be 7.16 × 10−6 M−1 sec−1, and 4.54 × 10−9 sec−1, respectively. The pKa of nefopam hydrochloride in aqueous solution was determined to be 8.98 ± 0.33 (n = 3) at 25 ± 0.2°C by the spectrophotometric method. The catalytic rate constant of hydroxyl ion on the degradation of nefopam in either protonated or nonprotonated form was determined to be 6.63 × 10−6 M−1 sec−1 and 4.06 × 10−6 M−1 sec−1, respectively. A smaller effect of hydroxyl ion on the degradation of nonprotonated than on the degradation of protonated nefopam was observed.
The salt effect on the degradation of nefopam hydrochloride in pH 3.11 and pH 7.26 solutions obeyed the modified Debye-Huckel equation well; however, the observed ZAZB values (1.54 for pH 3.11 and −1.21 for pH 7.26 solutions) deviated slightly from the theoretical values (1.0 for pH 3.11 and −1.0 for pH 7.26 solutions) due to the high ionic strength (μ = 0.05 to 0.9) of the solutions. The temperature effect study shows an activation energy of 19.04 kcal/mol of the degradation of nefopam hydrochloride in a pH 3.11 solution with a constant ionic strength of 0.5. No significant effect of UV irradiation (254 nm) at a distance of 30 cm and intensity of 150 μwatt/cm2 on the degradation of nefopam hydrochloride in pH 3.11 solution at 25 ± 0.2°C was found when compared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol 400 in the pH 3.11 nefopam hydrochloride solution shows an increase in its stability at 90 ± 0.2 °C.</description><subject>Analgesics</subject><subject>Biological and medical sciences</subject><subject>Buffers</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Drug Stability</subject><subject>Hydrogen-Ion Concentration</subject><subject>Medical sciences</subject><subject>Nefopam - pharmacokinetics</subject><subject>Nefopam - radiation effects</subject><subject>Neuropharmacology</subject><subject>Oxazocines - pharmacokinetics</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyethylene Glycols</subject><subject>Propylene Glycols</subject><subject>Solutions</subject><subject>Solvents</subject><subject>Temperature</subject><subject>Ultraviolet Rays</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtvEzEUhS0EKqFlyw5pFojdpNee-LVEAdKXWkJ5LC2P5w64TMbBngD593U0USoWiNWV7v3OOfYh5AWFKQVgp3frNGUCQGqglD0iE8oZlAKofEwmGWBlxWf6KXmW0h0ACOD8iByxilZcigkR19iGtV0VZ9smBve9C9E3WLzFb9E2dvChLy59j4N3qfB9cRu6zW55Qp60tkv4fD-Pyef37z7Nz8qrm8X5_M1V6WZcsFLkGIdSq7ppFZeVmkGrpJUgRdU6qmsLjVYSrWVSKe7q2jFrNdQzxbStaXVMXo--6xh-bjANZuWTw66zPYZNMlILWQlaZXA6gi6GlCK2Zh39ysatoWB2RZlclHkoKgte7p039QqbA75vJt9f7e82Odu10fbOpwOWYzMGGdMj9tt3uP1PqLn4cPvXE8pR69OAfw5aG3_s7CU3X68XZjln9Mty8dEsM69GHnPjvzxGk5zH3mHjI7rBNMH_67f3nhah-w</recordid><startdate>199001</startdate><enddate>199001</enddate><creator>Tu, Yu-Hsing</creator><creator>Wang, Da-Peng</creator><creator>Allen, Loyd V.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>American Pharmaceutical Association</general><scope>BSCLL</scope><scope>IQODW</scope><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>199001</creationdate><title>Nefopam Hydrochloride Degradation Kinetics in Solution</title><author>Tu, Yu-Hsing ; Wang, Da-Peng ; Allen, Loyd V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4562-6313ce798bdf8573840f87a70763fc19ba0d987eaa27885cbbc2aa90b4829ab13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Analgesics</topic><topic>Biological and medical sciences</topic><topic>Buffers</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Drug Stability</topic><topic>Hydrogen-Ion Concentration</topic><topic>Medical sciences</topic><topic>Nefopam - pharmacokinetics</topic><topic>Nefopam - radiation effects</topic><topic>Neuropharmacology</topic><topic>Oxazocines - pharmacokinetics</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyethylene Glycols</topic><topic>Propylene Glycols</topic><topic>Solutions</topic><topic>Solvents</topic><topic>Temperature</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tu, Yu-Hsing</creatorcontrib><creatorcontrib>Wang, Da-Peng</creatorcontrib><creatorcontrib>Allen, Loyd V.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tu, Yu-Hsing</au><au>Wang, Da-Peng</au><au>Allen, Loyd V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nefopam Hydrochloride Degradation Kinetics in Solution</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1990-01</date><risdate>1990</risdate><volume>79</volume><issue>1</issue><spage>48</spage><epage>52</epage><pages>48-52</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of nefopam hydrochloride and its degradation products under accelerated degradation conditions. The degradation kinetics of nefopam hydrochloride in aqueous solutions over a pH range of 1.18 to 9.94 at 90 ± 0.2°C was studied. The degradation of nefopam hydrochloride was found to follow apparent first-order kinetics. The pH–rate profile shows that maximum stability of nefopam hydrochloride was obtained at pH 5.2–5.4. No general acid or base catalysis from acetate, phosphate, or borate buffer species was observed. The catalytic rate constants on the protonated nefopam imposed by hydrogen ion and water was determined to be 7.16 × 10−6 M−1 sec−1, and 4.54 × 10−9 sec−1, respectively. The pKa of nefopam hydrochloride in aqueous solution was determined to be 8.98 ± 0.33 (n = 3) at 25 ± 0.2°C by the spectrophotometric method. The catalytic rate constant of hydroxyl ion on the degradation of nefopam in either protonated or nonprotonated form was determined to be 6.63 × 10−6 M−1 sec−1 and 4.06 × 10−6 M−1 sec−1, respectively. A smaller effect of hydroxyl ion on the degradation of nonprotonated than on the degradation of protonated nefopam was observed.
The salt effect on the degradation of nefopam hydrochloride in pH 3.11 and pH 7.26 solutions obeyed the modified Debye-Huckel equation well; however, the observed ZAZB values (1.54 for pH 3.11 and −1.21 for pH 7.26 solutions) deviated slightly from the theoretical values (1.0 for pH 3.11 and −1.0 for pH 7.26 solutions) due to the high ionic strength (μ = 0.05 to 0.9) of the solutions. The temperature effect study shows an activation energy of 19.04 kcal/mol of the degradation of nefopam hydrochloride in a pH 3.11 solution with a constant ionic strength of 0.5. No significant effect of UV irradiation (254 nm) at a distance of 30 cm and intensity of 150 μwatt/cm2 on the degradation of nefopam hydrochloride in pH 3.11 solution at 25 ± 0.2°C was found when compared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol 400 in the pH 3.11 nefopam hydrochloride solution shows an increase in its stability at 90 ± 0.2 °C.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>2313576</pmid><doi>10.1002/jps.2600790112</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3549 |
ispartof | Journal of pharmaceutical sciences, 1990-01, Vol.79 (1), p.48-52 |
issn | 0022-3549 1520-6017 |
language | eng |
recordid | cdi_proquest_miscellaneous_79673613 |
source | MEDLINE; Access via Wiley Online Library; Alma/SFX Local Collection |
subjects | Analgesics Biological and medical sciences Buffers Chromatography, High Pressure Liquid Drug Stability Hydrogen-Ion Concentration Medical sciences Nefopam - pharmacokinetics Nefopam - radiation effects Neuropharmacology Oxazocines - pharmacokinetics Pharmacology. Drug treatments Polyethylene Glycols Propylene Glycols Solutions Solvents Temperature Ultraviolet Rays |
title | Nefopam Hydrochloride Degradation Kinetics in Solution |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T21%3A16%3A10IST&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=Nefopam%20Hydrochloride%20Degradation%20Kinetics%20in%20Solution&rft.jtitle=Journal%20of%20pharmaceutical%20sciences&rft.au=Tu,%20Yu-Hsing&rft.date=1990-01&rft.volume=79&rft.issue=1&rft.spage=48&rft.epage=52&rft.pages=48-52&rft.issn=0022-3549&rft.eissn=1520-6017&rft.coden=JPMSAE&rft_id=info:doi/10.1002/jps.2600790112&rft_dat=%3Cproquest_cross%3E79673613%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=79673613&rft_id=info:pmid/2313576&rft_els_id=S0022354915481481&rfr_iscdi=true |