A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis
Osteomyelitis therapy is a long-term and inconvenient procedure for a patient. Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (C...
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description | Osteomyelitis therapy is a long-term and inconvenient procedure for a patient. Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (CPC), called α-TCP/HAP (α-tricalcium phosphate/hydroxyapatite) biphasic cement, was prepared as an antibiotics carrier for osteomyelitis. The developed biphasic cement with a microstructure of α-TCP surrounding the HAP has a fast setting time which will fulfill the clinical demand. The X-ray diffraction and Fourier transform infrared spectrometry analyses showed the final phase to be HAP, the basic bone mineral, after setting for a period of time. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The addition of gentamicin in α-TCP/HAP would delay the transition of α-TCP but would not change the final-phase HAP. The gentamicin-loaded α-TCP/HAP supplies high doses of the antibiotic during the initial 24 hours when they are soaked in phosphate buffer solution (PBS). Thereafter, a slower drug release is produced, supplying minimum inhibitory concentration until the end of the experiment (30 days). Studies of growth inhibition of Staphylococcus aureus and Pseudomonas aeruginosa in culture indicated that gentamicin released after 30 days from α-TCP/HAP biphasic cement retained antibacterial activity. |
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Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (CPC), called α-TCP/HAP (α-tricalcium phosphate/hydroxyapatite) biphasic cement, was prepared as an antibiotics carrier for osteomyelitis. The developed biphasic cement with a microstructure of α-TCP surrounding the HAP has a fast setting time which will fulfill the clinical demand. The X-ray diffraction and Fourier transform infrared spectrometry analyses showed the final phase to be HAP, the basic bone mineral, after setting for a period of time. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The addition of gentamicin in α-TCP/HAP would delay the transition of α-TCP but would not change the final-phase HAP. The gentamicin-loaded α-TCP/HAP supplies high doses of the antibiotic during the initial 24 hours when they are soaked in phosphate buffer solution (PBS). Thereafter, a slower drug release is produced, supplying minimum inhibitory concentration until the end of the experiment (30 days). Studies of growth inhibition of Staphylococcus aureus and Pseudomonas aeruginosa in culture indicated that gentamicin released after 30 days from α-TCP/HAP biphasic cement retained antibacterial activity.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2013/801374</identifier><identifier>PMID: 23662153</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject>Antibacterial activity ; Antibiotics ; Biomedical materials ; Bone cements ; Bone surgery ; Buffer solutions ; Calcium ; Calcium phosphates ; Cement ; Drug delivery systems ; Fourier transforms ; Gentamicin ; Growth inhibition ; Hydroxyapatite ; Infections ; Infrared analysis ; Intravenous administration ; Joint surgery ; Minimum inhibitory concentration ; Orthopedics ; Osteomyelitis ; Scanning electron microscopy ; Spectrometry ; Tricalcium phosphate ; X-ray diffraction</subject><ispartof>Evidence-based complementary and alternative medicine, 2013-01, Vol.2013 (2013), p.1-9</ispartof><rights>Copyright © 2013 Wen-Yu Su et al.</rights><rights>Copyright © 2013 Wen-Yu Su et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2013 Wen-Yu Su et al. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-459beba6a03c6e041a7f7b6095cd978729a2691286b888aeefed3534593434ff3</citedby><cites>FETCH-LOGICAL-c466t-459beba6a03c6e041a7f7b6095cd978729a2691286b888aeefed3534593434ff3</cites><orcidid>0000-0002-6201-2985</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638604/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638604/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23662153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chen, Yueh-Sheng</contributor><contributor>Yueh-Sheng Chen</contributor><creatorcontrib>Su, Wen-Yu</creatorcontrib><creatorcontrib>Chen, Yu-Chun</creatorcontrib><creatorcontrib>Lin, Feng-Huei</creatorcontrib><title>A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>Osteomyelitis therapy is a long-term and inconvenient procedure for a patient. Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (CPC), called α-TCP/HAP (α-tricalcium phosphate/hydroxyapatite) biphasic cement, was prepared as an antibiotics carrier for osteomyelitis. The developed biphasic cement with a microstructure of α-TCP surrounding the HAP has a fast setting time which will fulfill the clinical demand. The X-ray diffraction and Fourier transform infrared spectrometry analyses showed the final phase to be HAP, the basic bone mineral, after setting for a period of time. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The addition of gentamicin in α-TCP/HAP would delay the transition of α-TCP but would not change the final-phase HAP. The gentamicin-loaded α-TCP/HAP supplies high doses of the antibiotic during the initial 24 hours when they are soaked in phosphate buffer solution (PBS). Thereafter, a slower drug release is produced, supplying minimum inhibitory concentration until the end of the experiment (30 days). Studies of growth inhibition of Staphylococcus aureus and Pseudomonas aeruginosa in culture indicated that gentamicin released after 30 days from α-TCP/HAP biphasic cement retained antibacterial activity.</description><subject>Antibacterial activity</subject><subject>Antibiotics</subject><subject>Biomedical materials</subject><subject>Bone cements</subject><subject>Bone surgery</subject><subject>Buffer solutions</subject><subject>Calcium</subject><subject>Calcium phosphates</subject><subject>Cement</subject><subject>Drug delivery systems</subject><subject>Fourier transforms</subject><subject>Gentamicin</subject><subject>Growth inhibition</subject><subject>Hydroxyapatite</subject><subject>Infections</subject><subject>Infrared analysis</subject><subject>Intravenous administration</subject><subject>Joint surgery</subject><subject>Minimum inhibitory concentration</subject><subject>Orthopedics</subject><subject>Osteomyelitis</subject><subject>Scanning electron microscopy</subject><subject>Spectrometry</subject><subject>Tricalcium phosphate</subject><subject>X-ray diffraction</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0c9rFDEUB_AgFvtDT56VgJdiWZtfkx8XoV20CsV6qKCnkMm-uCkzk20y07L_vSlTF_XiJXkknzxe-CL0kpJ3lDbNKSOUn-q6KPEEHVAl6EIwrZ_uavV9Hx2WckMIM0qpZ2ifcSkZbfgB-nGGv8A9vt5uAKeAz-Nm7Ur0eOk6H6cef12nUo9GwEvoYRixK9jhi1q5Pvo4VJhzhIxDyviqjJD6LXRxjOU52guuK_DicT9C3z5-uF5-WlxeXXxenl0uvJByXIjGtNA66Qj3EoigTgXVSmIavzJKK2Yck4YyLVuttQMIsOINr8-44CIEfoTez303U9vDytfRsuvsJsfe5a1NLtq_b4a4tj_TneWSa0lEbXD82CCn2wnKaPtYPHSdGyBNxVLeENoIok2lb_6hN2nKQ_2eZURxZijnrKqTWfmcSskQdsNQYh8isw-R2Tmyql__Of_O_s6ogrczWMdh5e7jf7q9mjFUAsHtsDCGUsZ_AZe5pq8</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Su, Wen-Yu</creator><creator>Chen, Yu-Chun</creator><creator>Lin, Feng-Huei</creator><general>Hindawi Puplishing Corporation</general><general>Hindawi Publishing Corporation</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6201-2985</orcidid></search><sort><creationdate>20130101</creationdate><title>A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis</title><author>Su, Wen-Yu ; Chen, Yu-Chun ; Lin, Feng-Huei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-459beba6a03c6e041a7f7b6095cd978729a2691286b888aeefed3534593434ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antibacterial activity</topic><topic>Antibiotics</topic><topic>Biomedical materials</topic><topic>Bone cements</topic><topic>Bone surgery</topic><topic>Buffer solutions</topic><topic>Calcium</topic><topic>Calcium phosphates</topic><topic>Cement</topic><topic>Drug delivery systems</topic><topic>Fourier transforms</topic><topic>Gentamicin</topic><topic>Growth inhibition</topic><topic>Hydroxyapatite</topic><topic>Infections</topic><topic>Infrared analysis</topic><topic>Intravenous administration</topic><topic>Joint surgery</topic><topic>Minimum inhibitory concentration</topic><topic>Orthopedics</topic><topic>Osteomyelitis</topic><topic>Scanning electron microscopy</topic><topic>Spectrometry</topic><topic>Tricalcium phosphate</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Su, Wen-Yu</creatorcontrib><creatorcontrib>Chen, Yu-Chun</creatorcontrib><creatorcontrib>Lin, Feng-Huei</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Proquest Health & Medical Complete</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Psychology Database (ProQuest)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Wen-Yu</au><au>Chen, Yu-Chun</au><au>Lin, Feng-Huei</au><au>Chen, Yueh-Sheng</au><au>Yueh-Sheng Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>2013</volume><issue>2013</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Osteomyelitis therapy is a long-term and inconvenient procedure for a patient. Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (CPC), called α-TCP/HAP (α-tricalcium phosphate/hydroxyapatite) biphasic cement, was prepared as an antibiotics carrier for osteomyelitis. The developed biphasic cement with a microstructure of α-TCP surrounding the HAP has a fast setting time which will fulfill the clinical demand. The X-ray diffraction and Fourier transform infrared spectrometry analyses showed the final phase to be HAP, the basic bone mineral, after setting for a period of time. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The addition of gentamicin in α-TCP/HAP would delay the transition of α-TCP but would not change the final-phase HAP. The gentamicin-loaded α-TCP/HAP supplies high doses of the antibiotic during the initial 24 hours when they are soaked in phosphate buffer solution (PBS). Thereafter, a slower drug release is produced, supplying minimum inhibitory concentration until the end of the experiment (30 days). Studies of growth inhibition of Staphylococcus aureus and Pseudomonas aeruginosa in culture indicated that gentamicin released after 30 days from α-TCP/HAP biphasic cement retained antibacterial activity.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>23662153</pmid><doi>10.1155/2013/801374</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6201-2985</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibacterial activity Antibiotics Biomedical materials Bone cements Bone surgery Buffer solutions Calcium Calcium phosphates Cement Drug delivery systems Fourier transforms Gentamicin Growth inhibition Hydroxyapatite Infections Infrared analysis Intravenous administration Joint surgery Minimum inhibitory concentration Orthopedics Osteomyelitis Scanning electron microscopy Spectrometry Tricalcium phosphate X-ray diffraction |
title | A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis |
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