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Article: Biomimetic Mineralization of Fibrillar Collagen with Strontium-doped Hydroxyapatite
Title | Biomimetic Mineralization of Fibrillar Collagen with Strontium-doped Hydroxyapatite |
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Authors | |
Issue Date | 1-Mar-2023 |
Publisher | American Chemical Society |
Citation | ACS Macro Letters, 2023, v. 12, n. 3, p. 408-414 How to Cite? |
Abstract | Fibrillar collagen structures mineralized with hydroxyapatite using the polymer-induced liquid precursor (PILP) process have been explored as synthetic models for studying biomineralization of human hard tissues and have also been applied in the fabrication of scaffolds for hard tissue regeneration. Strontium has important biological functions in bone and has been used as a therapeutic agent for treating diseases that result in bone defects, such as osteoporosis. Here, we developed a strategy to mineralize collagen with Sr-doped hydroxyapatite (HA) using the PILP process. Doping with Sr altered the crystal lattice of HA and inhibited the degree of mineralization in a concentration-dependent manner, but did not affect the unique formation of intrafibrillar minerals using the PILP. The Sr-doped HA nanocrystals were aligned in the [001] direction but did not recapitulate the parallel alignment of the c-axis of pure Ca HA in relation to the collagen fiber long axis. The mimicry of doping Sr in PILP-mineralized collagen can help understand the doping of Sr in natural hard tissues and during treatment. The fibrillary mineralized collagen with Sr-doped HA will be explored in future work as biomimetic and bioactive scaffolds for regeneration of bone and tooth dentin. |
Persistent Identifier | http://hdl.handle.net/10722/328378 |
ISSN | 2023 Impact Factor: 5.1 2023 SCImago Journal Rankings: 1.491 |
DC Field | Value | Language |
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dc.contributor.author | Ye, Z | - |
dc.contributor.author | Qi, YP | - |
dc.contributor.author | Zhang, AQ | - |
dc.contributor.author | Karels, BJ | - |
dc.contributor.author | Aparicio, C | - |
dc.date.accessioned | 2023-06-28T04:43:44Z | - |
dc.date.available | 2023-06-28T04:43:44Z | - |
dc.date.issued | 2023-03-01 | - |
dc.identifier.citation | ACS Macro Letters, 2023, v. 12, n. 3, p. 408-414 | - |
dc.identifier.issn | 2161-1653 | - |
dc.identifier.uri | http://hdl.handle.net/10722/328378 | - |
dc.description.abstract | <p>Fibrillar collagen structures mineralized with hydroxyapatite using the polymer-induced liquid precursor (PILP) process have been explored as synthetic models for studying biomineralization of human hard tissues and have also been applied in the fabrication of scaffolds for hard tissue regeneration. Strontium has important biological functions in bone and has been used as a therapeutic agent for treating diseases that result in bone defects, such as osteoporosis. Here, we developed a strategy to mineralize collagen with Sr-doped hydroxyapatite (HA) using the PILP process. Doping with Sr altered the crystal lattice of HA and inhibited the degree of mineralization in a concentration-dependent manner, but did not affect the unique formation of intrafibrillar minerals using the PILP. The Sr-doped HA nanocrystals were aligned in the [001] direction but did not recapitulate the parallel alignment of the <em>c</em>-axis of pure Ca HA in relation to the collagen fiber long axis. The mimicry of doping Sr in PILP-mineralized collagen can help understand the doping of Sr in natural hard tissues and during treatment. The fibrillary mineralized collagen with Sr-doped HA will be explored in future work as biomimetic and bioactive scaffolds for regeneration of bone and tooth dentin.<br></p> | - |
dc.language | eng | - |
dc.publisher | American Chemical Society | - |
dc.relation.ispartof | ACS Macro Letters | - |
dc.title | Biomimetic Mineralization of Fibrillar Collagen with Strontium-doped Hydroxyapatite | - |
dc.type | Article | - |
dc.identifier.doi | 10.1021/acsmacrolett.3c00039 | - |
dc.identifier.hkuros | 344656 | - |
dc.identifier.volume | 12 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 408 | - |
dc.identifier.epage | 414 | - |
dc.identifier.eissn | 2161-1653 | - |
dc.identifier.issnl | 2161-1653 | - |