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- Publisher Website: 10.1007/s10856-011-4493-2
- Scopus: eid_2-s2.0-84863441856
- PMID: 22095448
- WOS: WOS:000301640800022
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Article: Prolonged release from PLGA/HAp scaffolds containing drug-loaded PLGA/gelatin composite microspheres
Title | Prolonged release from PLGA/HAp scaffolds containing drug-loaded PLGA/gelatin composite microspheres | ||||||
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Authors | |||||||
Issue Date | 2012 | ||||||
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0957-4530 | ||||||
Citation | Journal of Materials Science: Materials in Medicine, 2012, v. 23 n. 2, p. 419-429 How to Cite? | ||||||
Abstract | Porous scaffolds that can prolong the release of bioactive factors are urgently required in bone tissue engineering. In this study, PLGA/gelatin composite microspheres (PGMs) were carefully designed and prepared by entrapping poly(L: -lactide-co-glycolide) (PLGA) microspheres (PMs) in gelatin matrix. By mixing PGMs with PLGA solution directly, drug-loaded PLGA/carbonated hydroxyapatite (HAp)/PGMs composite scaffolds were successfully fabricated. In vitro release of fluorescein isothiocyanate-dextran (FD70S) as a model drug from the scaffolds as well as PMs and PGMs was studied by immersing samples in phosphate buffered saline (pH = 7.4) at 37 degrees C for 32 days. Compared with PMs, PGMs and PLGA/HAp/PGMs scaffolds exhibited slow and steady release behavior with constant release rate and insignificantly original burst release. The swelling of PGMs, diffusion of drugs, and degradation of polymer dominated the release behaviors synergistically. The PLGA/HAp/PGMs scaffold offers a novel option for sequential or simultaneous release of several drugs in terms of bone regeneration. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/157158 | ||||||
ISSN | 2023 Impact Factor: 4.2 2023 SCImago Journal Rankings: 0.651 | ||||||
ISI Accession Number ID |
Funding Information: This work was supported by Natural Science Foundation of China via grant Nos. 30828008 and 51073117 and also by the Scientific Research Foundation of Graduate School of Tianjin University. |
DC Field | Value | Language |
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dc.contributor.author | Tang, G | en_US |
dc.contributor.author | Zhang, H | en_US |
dc.contributor.author | Zhao, Y | en_US |
dc.contributor.author | Li, X | en_US |
dc.contributor.author | Yuan, X | en_US |
dc.contributor.author | Wang, M | en_US |
dc.date.accessioned | 2012-08-08T08:45:35Z | - |
dc.date.available | 2012-08-08T08:45:35Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Journal of Materials Science: Materials in Medicine, 2012, v. 23 n. 2, p. 419-429 | en_US |
dc.identifier.issn | 0957-4530 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/157158 | - |
dc.description.abstract | Porous scaffolds that can prolong the release of bioactive factors are urgently required in bone tissue engineering. In this study, PLGA/gelatin composite microspheres (PGMs) were carefully designed and prepared by entrapping poly(L: -lactide-co-glycolide) (PLGA) microspheres (PMs) in gelatin matrix. By mixing PGMs with PLGA solution directly, drug-loaded PLGA/carbonated hydroxyapatite (HAp)/PGMs composite scaffolds were successfully fabricated. In vitro release of fluorescein isothiocyanate-dextran (FD70S) as a model drug from the scaffolds as well as PMs and PGMs was studied by immersing samples in phosphate buffered saline (pH = 7.4) at 37 degrees C for 32 days. Compared with PMs, PGMs and PLGA/HAp/PGMs scaffolds exhibited slow and steady release behavior with constant release rate and insignificantly original burst release. The swelling of PGMs, diffusion of drugs, and degradation of polymer dominated the release behaviors synergistically. The PLGA/HAp/PGMs scaffold offers a novel option for sequential or simultaneous release of several drugs in terms of bone regeneration. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0957-4530 | en_US |
dc.relation.ispartof | Journal of Materials Science: Materials in Medicine | en_US |
dc.rights | The original publication is available at www.springerlink.com | - |
dc.subject.mesh | Durapatite - chemistry | - |
dc.subject.mesh | Gelatin - chemistry | - |
dc.subject.mesh | Lactic Acid - chemistry | - |
dc.subject.mesh | Microspheres | - |
dc.subject.mesh | Polyglycolic Acid - chemistry | - |
dc.title | Prolonged release from PLGA/HAp scaffolds containing drug-loaded PLGA/gelatin composite microspheres | en_US |
dc.type | Article | en_US |
dc.identifier.email | Yuan, X: yuanxy@tju.edu.cn | en_US |
dc.identifier.email | Wang, M: memwang@hku.hk | - |
dc.identifier.authority | Wang, M=rp00185 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s10856-011-4493-2 | en_US |
dc.identifier.pmid | 22095448 | - |
dc.identifier.scopus | eid_2-s2.0-84863441856 | en_US |
dc.identifier.hkuros | 207521 | - |
dc.identifier.volume | 23 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 419 | en_US |
dc.identifier.epage | 429 | en_US |
dc.identifier.isi | WOS:000301640800022 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Wang, M=15749714100 | en_US |
dc.identifier.scopusauthorid | Yuan, X=7402202655 | en_US |
dc.identifier.scopusauthorid | Li, X=36012686700 | en_US |
dc.identifier.scopusauthorid | Zhao, Y=7406633316 | en_US |
dc.identifier.scopusauthorid | Zhang, H=36071184600 | en_US |
dc.identifier.scopusauthorid | Tang, G=23494188700 | en_US |
dc.identifier.citeulike | 10053218 | - |
dc.identifier.issnl | 0957-4530 | - |