Influence of isostatic compression on the stability of vancomycin loaded with a calcium phosphate-implantable drug delivery device
It is essential to prevent microbial infections after osteoarticular trauma or prothesis implantation. As an alternative to antibiotic parenteral administration, antibiotic‐loaded biomaterials allow high concentrations to be obtained in situ without systemic toxicity. Although the formulation of bip...
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Veröffentlicht in: | Journal of biomedical materials research 2000-11, Vol.52 (2), p.308-314 |
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description | It is essential to prevent microbial infections after osteoarticular trauma or prothesis implantation. As an alternative to antibiotic parenteral administration, antibiotic‐loaded biomaterials allow high concentrations to be obtained in situ without systemic toxicity. Although the formulation of biphasic calcium‐phosphate (BCP)‐vancomycin granules by isostatic compression has recently been used to produce drug‐delivery devices, the stability of vancomycin needs to be proven. In this study, vancomycin was associated with BCP powders by isostatic compression at 100, 140, or 200 MPa and then extracted or released by a rotating paddle system for 24 h. Vancomycin assays were performed by spectrophotometric and microbiological methods. The results show that all vancomycin associated with the material was recovered after extraction without degradation. Thus, vancomycin was not denaturated after application of 100, 140, or 200 MPa of isostatic compression. The results for vancomycin released from granules compressed at the three pressures were not significantly different (p = .01) whether assays were performed microbiologically or spectrophotometrically, indicating a good correlation between the two methods. This process involving high pressure appears to be a good means of developing drug delivery devices loaded with therapeutic agents without denaturating the components. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 52, 308–314, 2000. |
doi_str_mv | 10.1002/1097-4636(200011)52:2<308::AID-JBM9>3.0.CO;2-6 |
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M. ; Daculsi, G. ; Merle, C.</creator><creatorcontrib>Gautier, H. ; Caillon, J. ; Le Ray, A. M. ; Daculsi, G. ; Merle, C.</creatorcontrib><description>It is essential to prevent microbial infections after osteoarticular trauma or prothesis implantation. As an alternative to antibiotic parenteral administration, antibiotic‐loaded biomaterials allow high concentrations to be obtained in situ without systemic toxicity. Although the formulation of biphasic calcium‐phosphate (BCP)‐vancomycin granules by isostatic compression has recently been used to produce drug‐delivery devices, the stability of vancomycin needs to be proven. In this study, vancomycin was associated with BCP powders by isostatic compression at 100, 140, or 200 MPa and then extracted or released by a rotating paddle system for 24 h. Vancomycin assays were performed by spectrophotometric and microbiological methods. The results show that all vancomycin associated with the material was recovered after extraction without degradation. Thus, vancomycin was not denaturated after application of 100, 140, or 200 MPa of isostatic compression. The results for vancomycin released from granules compressed at the three pressures were not significantly different (p = .01) whether assays were performed microbiologically or spectrophotometrically, indicating a good correlation between the two methods. This process involving high pressure appears to be a good means of developing drug delivery devices loaded with therapeutic agents without denaturating the components. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 52, 308–314, 2000.</description><identifier>ISSN: 0021-9304</identifier><identifier>EISSN: 1097-4636</identifier><identifier>DOI: 10.1002/1097-4636(200011)52:2<308::AID-JBM9>3.0.CO;2-6</identifier><identifier>PMID: 10951369</identifier><identifier>CODEN: JBMRBG</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - chemistry ; Bioassay ; Biocompatible Materials ; Biological and medical sciences ; Biomaterials ; biphasic calcium phosphate ; Calcium compounds ; calcium phosphate ; Calcium Phosphates ; drug delivery device ; Drug Delivery Systems ; Extraction ; High pressure effects ; Humans ; isosatic compression ; Medical sciences ; Microbiology ; Postoperative Complications - prevention & control ; Prosthesis Implantation ; Spectrophotometry ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Technology. 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M.</creatorcontrib><creatorcontrib>Daculsi, G.</creatorcontrib><creatorcontrib>Merle, C.</creatorcontrib><title>Influence of isostatic compression on the stability of vancomycin loaded with a calcium phosphate-implantable drug delivery device</title><title>Journal of biomedical materials research</title><addtitle>J. Biomed. Mater. Res</addtitle><description>It is essential to prevent microbial infections after osteoarticular trauma or prothesis implantation. As an alternative to antibiotic parenteral administration, antibiotic‐loaded biomaterials allow high concentrations to be obtained in situ without systemic toxicity. Although the formulation of biphasic calcium‐phosphate (BCP)‐vancomycin granules by isostatic compression has recently been used to produce drug‐delivery devices, the stability of vancomycin needs to be proven. In this study, vancomycin was associated with BCP powders by isostatic compression at 100, 140, or 200 MPa and then extracted or released by a rotating paddle system for 24 h. Vancomycin assays were performed by spectrophotometric and microbiological methods. The results show that all vancomycin associated with the material was recovered after extraction without degradation. Thus, vancomycin was not denaturated after application of 100, 140, or 200 MPa of isostatic compression. The results for vancomycin released from granules compressed at the three pressures were not significantly different (p = .01) whether assays were performed microbiologically or spectrophotometrically, indicating a good correlation between the two methods. This process involving high pressure appears to be a good means of developing drug delivery devices loaded with therapeutic agents without denaturating the components. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 52, 308–314, 2000.</description><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Bioassay</subject><subject>Biocompatible Materials</subject><subject>Biological and medical sciences</subject><subject>Biomaterials</subject><subject>biphasic calcium phosphate</subject><subject>Calcium compounds</subject><subject>calcium phosphate</subject><subject>Calcium Phosphates</subject><subject>drug delivery device</subject><subject>Drug Delivery Systems</subject><subject>Extraction</subject><subject>High pressure effects</subject><subject>Humans</subject><subject>isosatic compression</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Postoperative Complications - prevention & control</subject><subject>Prosthesis Implantation</subject><subject>Spectrophotometry</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. Equipments</subject><subject>Toxicity</subject><subject>ultraviolet and microbiologic assays</subject><subject>vancomycin</subject><subject>Vancomycin - administration & dosage</subject><subject>Vancomycin - chemistry</subject><issn>0021-9304</issn><issn>1097-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkV2L1DAUhoMo7rj6FyQgiF50zEebNKMI66jruOvMja7ehTQ9dbL2y6adtbf-cjN2GLwQRAjk6zlvDnkQEpTMKSHsGSVKRrHg4gkjhFD6NGEL9oKTdLE4W72O3r_6oF7yOZkvN89ZJG6h2bHgNpqFABopTuITdM_76xCgFKd30UmAEsqFmqGfq7ooB6gt4KbAzje-N72z2DZV24H3rqlxGP0WcLjJXOn6cU_uTB2Q0boal43JIcc3rt9ig60prRsq3G4b325ND5Gr2tLUobgEnHfDV5xD6XbQjWGxcxbuozuFKT08OMyn6NPbNx-X76LLzflqeXYZ2VimKkpMymVmbBanmWBgiYmLQmbE0KKwOUBmuKR5khEpBFcJKJ5kWc5imhrGqUr4KXo85bZd830A3-vKeQtlaA6awWtGY0FjQv8JUilSkioewPUE2q7xvoNCt52rTDdqSvRen97b0HsbetKnE6aZDvq0Dvr0Xp_mmujlJhyLEPjw8PKQVZD_ETf5CsCjA2B8-OmiCxqcP3JS0UTKQG0m6saVMP5HU3_p6fc-JEZTovM9_Dgmmu6bFpLLRH9en-svV2J9EV9daM5_Acp2z_s</recordid><startdate>200011</startdate><enddate>200011</enddate><creator>Gautier, H.</creator><creator>Caillon, J.</creator><creator>Le Ray, A. M.</creator><creator>Daculsi, G.</creator><creator>Merle, C.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley & Sons</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>200011</creationdate><title>Influence of isostatic compression on the stability of vancomycin loaded with a calcium phosphate-implantable drug delivery device</title><author>Gautier, H. ; Caillon, J. ; Le Ray, A. M. ; Daculsi, G. ; Merle, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4789-5a837bacb48b62ec0a4ff7b0a1ffcdeeba371d5b0766395e935bbd2418a231953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Bioassay</topic><topic>Biocompatible Materials</topic><topic>Biological and medical sciences</topic><topic>Biomaterials</topic><topic>biphasic calcium phosphate</topic><topic>Calcium compounds</topic><topic>calcium phosphate</topic><topic>Calcium Phosphates</topic><topic>drug delivery device</topic><topic>Drug Delivery Systems</topic><topic>Extraction</topic><topic>High pressure effects</topic><topic>Humans</topic><topic>isosatic compression</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Postoperative Complications - prevention & control</topic><topic>Prosthesis Implantation</topic><topic>Spectrophotometry</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Technology. Biomaterials. Equipments</topic><topic>Toxicity</topic><topic>ultraviolet and microbiologic assays</topic><topic>vancomycin</topic><topic>Vancomycin - administration & dosage</topic><topic>Vancomycin - chemistry</topic><toplevel>online_resources</toplevel><creatorcontrib>Gautier, H.</creatorcontrib><creatorcontrib>Caillon, J.</creatorcontrib><creatorcontrib>Le Ray, A. M.</creatorcontrib><creatorcontrib>Daculsi, G.</creatorcontrib><creatorcontrib>Merle, C.</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of biomedical materials research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gautier, H.</au><au>Caillon, J.</au><au>Le Ray, A. M.</au><au>Daculsi, G.</au><au>Merle, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of isostatic compression on the stability of vancomycin loaded with a calcium phosphate-implantable drug delivery device</atitle><jtitle>Journal of biomedical materials research</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2000-11</date><risdate>2000</risdate><volume>52</volume><issue>2</issue><spage>308</spage><epage>314</epage><pages>308-314</pages><issn>0021-9304</issn><eissn>1097-4636</eissn><coden>JBMRBG</coden><abstract>It is essential to prevent microbial infections after osteoarticular trauma or prothesis implantation. As an alternative to antibiotic parenteral administration, antibiotic‐loaded biomaterials allow high concentrations to be obtained in situ without systemic toxicity. Although the formulation of biphasic calcium‐phosphate (BCP)‐vancomycin granules by isostatic compression has recently been used to produce drug‐delivery devices, the stability of vancomycin needs to be proven. In this study, vancomycin was associated with BCP powders by isostatic compression at 100, 140, or 200 MPa and then extracted or released by a rotating paddle system for 24 h. Vancomycin assays were performed by spectrophotometric and microbiological methods. The results show that all vancomycin associated with the material was recovered after extraction without degradation. Thus, vancomycin was not denaturated after application of 100, 140, or 200 MPa of isostatic compression. The results for vancomycin released from granules compressed at the three pressures were not significantly different (p = .01) whether assays were performed microbiologically or spectrophotometrically, indicating a good correlation between the two methods. This process involving high pressure appears to be a good means of developing drug delivery devices loaded with therapeutic agents without denaturating the components. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 52, 308–314, 2000.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10951369</pmid><doi>10.1002/1097-4636(200011)52:2<308::AID-JBM9>3.0.CO;2-6</doi><tpages>7</tpages></addata></record> |
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subjects | Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - chemistry Bioassay Biocompatible Materials Biological and medical sciences Biomaterials biphasic calcium phosphate Calcium compounds calcium phosphate Calcium Phosphates drug delivery device Drug Delivery Systems Extraction High pressure effects Humans isosatic compression Medical sciences Microbiology Postoperative Complications - prevention & control Prosthesis Implantation Spectrophotometry Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Technology. Biomaterials. Equipments Toxicity ultraviolet and microbiologic assays vancomycin Vancomycin - administration & dosage Vancomycin - chemistry |
title | Influence of isostatic compression on the stability of vancomycin loaded with a calcium phosphate-implantable drug delivery device |
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