Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies
Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water...
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Veröffentlicht in: | Journal of pharmaceutical sciences 1979-07, Vol.68 (7), p.863-866 |
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description | Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid. |
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Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600680720</identifier><identifier>PMID: 458604</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>amorphous and crystalline solids ; Antibiotics-cefoxitin sodium ; Antibiotics—cefoxitin sodium, chemical stability, amorphous and crystalline solids, water content ; Biological Assay ; Cefoxitin - analysis ; Cefoxitin sodium-chemical stability ; Cefoxitin sodium—chemical stability, amorphous and crystalline solids, water content ; Cephalosporins - analysis ; Chemical Phenomena ; chemical stability ; Chemistry, Physical ; Chromatography, High Pressure Liquid ; Chromatography, Thin Layer ; Crystallization ; Drug Stability ; Kinetics ; Solutions ; Spectrophotometry, Ultraviolet ; Stability-cefoxitin sodium ; Stability—cefoxitin sodium, amorphous and crystalline solids, water content ; Time Factors ; water content</subject><ispartof>Journal of pharmaceutical sciences, 1979-07, Vol.68 (7), p.863-866</ispartof><rights>1979 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1979 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4260-21435d0d07ac75935dacf7e64dd80067e1cd534acee303dc72630f9d33e8c9603</citedby><cites>FETCH-LOGICAL-c4260-21435d0d07ac75935dacf7e64dd80067e1cd534acee303dc72630f9d33e8c9603</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.2600680720$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600680720$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/458604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oberholtzer, Earl R.</creatorcontrib><creatorcontrib>Brenner, Gerald S.</creatorcontrib><title>Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid.</description><subject>amorphous and crystalline solids</subject><subject>Antibiotics-cefoxitin sodium</subject><subject>Antibiotics—cefoxitin sodium, chemical stability, amorphous and crystalline solids, water content</subject><subject>Biological Assay</subject><subject>Cefoxitin - analysis</subject><subject>Cefoxitin sodium-chemical stability</subject><subject>Cefoxitin sodium—chemical stability, amorphous and crystalline solids, water content</subject><subject>Cephalosporins - analysis</subject><subject>Chemical Phenomena</subject><subject>chemical stability</subject><subject>Chemistry, Physical</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Chromatography, Thin Layer</subject><subject>Crystallization</subject><subject>Drug Stability</subject><subject>Kinetics</subject><subject>Solutions</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Stability-cefoxitin sodium</subject><subject>Stability—cefoxitin sodium, amorphous and crystalline solids, water content</subject><subject>Time Factors</subject><subject>water content</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtv2zAMxoVi7ZY-rjv1kNNuTmnLsuzdBiN9wegyZEOBXgRVojFmfmSW3Tb_fRU4SLHD0BNJ8McPHz_GPocwCwGii9XazaIEIElBRnDAJqGIIEgglB_YxANRwEWcfWLHzq3AYyDER3YUizSBeMLmOZbtC_XUTJetpaH-6ms19NQ2U93Y7UA2WPa6x2n-G2syupr68ZEq6je-GyyhO2WHpa4cnu3qCft1Of-ZXwfF96ub_FsRmNhbDKIw5sKCBamNFJnvtSklJrG1qXcmMTRW8FgbRA7cGhklHMrMco6pyRLgJ-zLqLvu2r8Dul7V5AxWlW6wHZySsX-Ky9SDsxE0Xetch6Vad1TrbqNCUNvYlI9NvcXmD853ysNjjXaPjzn5dTaun6nCzTti6nax_Ec6GG_J9fiyv9XdH5VILoW6v7tSix9FVuT5g9p6T0cefZJPhJ1yhrAxaKlD0yvb0v--eAVlfJoq</recordid><startdate>197907</startdate><enddate>197907</enddate><creator>Oberholtzer, Earl R.</creator><creator>Brenner, Gerald S.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>197907</creationdate><title>Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies</title><author>Oberholtzer, Earl R. ; Brenner, Gerald S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4260-21435d0d07ac75935dacf7e64dd80067e1cd534acee303dc72630f9d33e8c9603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>amorphous and crystalline solids</topic><topic>Antibiotics-cefoxitin sodium</topic><topic>Antibiotics—cefoxitin sodium, chemical stability, amorphous and crystalline solids, water content</topic><topic>Biological Assay</topic><topic>Cefoxitin - analysis</topic><topic>Cefoxitin sodium-chemical stability</topic><topic>Cefoxitin sodium—chemical stability, amorphous and crystalline solids, water content</topic><topic>Cephalosporins - analysis</topic><topic>Chemical Phenomena</topic><topic>chemical stability</topic><topic>Chemistry, Physical</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Chromatography, Thin Layer</topic><topic>Crystallization</topic><topic>Drug Stability</topic><topic>Kinetics</topic><topic>Solutions</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Stability-cefoxitin sodium</topic><topic>Stability—cefoxitin sodium, amorphous and crystalline solids, water content</topic><topic>Time Factors</topic><topic>water content</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oberholtzer, Earl R.</creatorcontrib><creatorcontrib>Brenner, Gerald S.</creatorcontrib><collection>Istex</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>Oberholtzer, Earl R.</au><au>Brenner, Gerald S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1979-07</date><risdate>1979</risdate><volume>68</volume><issue>7</issue><spage>863</spage><epage>866</epage><pages>863-866</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>458604</pmid><doi>10.1002/jps.2600680720</doi><tpages>4</tpages></addata></record> |
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subjects | amorphous and crystalline solids Antibiotics-cefoxitin sodium Antibiotics—cefoxitin sodium, chemical stability, amorphous and crystalline solids, water content Biological Assay Cefoxitin - analysis Cefoxitin sodium-chemical stability Cefoxitin sodium—chemical stability, amorphous and crystalline solids, water content Cephalosporins - analysis Chemical Phenomena chemical stability Chemistry, Physical Chromatography, High Pressure Liquid Chromatography, Thin Layer Crystallization Drug Stability Kinetics Solutions Spectrophotometry, Ultraviolet Stability-cefoxitin sodium Stability—cefoxitin sodium, amorphous and crystalline solids, water content Time Factors water content |
title | Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies |
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