Engineered nanostructures within sol-gel bioactive glass for enhanced bioactivity and modulated drug delivery
The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol-gel-derived bioactive...
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Published in | Journal of materials chemistry. B, Materials for biology and medicine Vol. 1; no. 48; pp. 1112 - 1127 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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England
Royal Society of Chemistry
14.12.2022
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Abstract | The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol-gel-derived bioactive glass using P123 as the structure-directing agent. The synthesis of a multicomponent 80SiO
2
-15CaO-5P
2
O
5
bioactive glass material having a hierarchically ordered mesoporous structure with uniformly grown nanocrystals of apatite was achieved through a sono-assisted surfactant-templated sol-gel method. The bulk crystallographic analysis together with microstructural characterizations shows that the nanocrystalline apatite domains are uniformly dispersed as well as embedded along the mesopores. These nanocrystalline domains were found to influence the textural properties. In addition, macroscopic evidence for higher signs of bonelike matrix formation was observed by the biomineralization study in simulated body fluids. Osteostimulatory effects of these glass samples were evident by cultures in a osteogenic and non-osteogenic mediums with human osteosarcoma cells and a higher osteopromotive potential was authenticated by the alkaline phosphatase activity and alizarin red staining. Further, this study shows a new strategy to prolong the drug release period on account of the nanocrystalline phase and hierarchically positioned mesopores, thus making it a better drug delivery matrix as well.
Infusion of apatite nanocrystals into non-crystalline glass matrix was achieved. The nanocrystalline domains are well dispersed and embedded along the hierarchically positioned mesopores. |
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AbstractList | The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol–gel-derived bioactive glass using P123 as the structure-directing agent. The synthesis of a multicomponent 80SiO2–15CaO–5P2O5 bioactive glass material having a hierarchically ordered mesoporous structure with uniformly grown nanocrystals of apatite was achieved through a sono-assisted surfactant-templated sol–gel method. The bulk crystallographic analysis together with microstructural characterizations shows that the nanocrystalline apatite domains are uniformly dispersed as well as embedded along the mesopores. These nanocrystalline domains were found to influence the textural properties. In addition, macroscopic evidence for higher signs of bonelike matrix formation was observed by the biomineralization study in simulated body fluids. Osteostimulatory effects of these glass samples were evident by cultures in a osteogenic and non-osteogenic mediums with human osteosarcoma cells and a higher osteopromotive potential was authenticated by the alkaline phosphatase activity and alizarin red staining. Further, this study shows a new strategy to prolong the drug release period on account of the nanocrystalline phase and hierarchically positioned mesopores, thus making it a better drug delivery matrix as well. The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol-gel-derived bioactive glass using P123 as the structure-directing agent. The synthesis of a multicomponent 80SiO 2 -15CaO-5P 2 O 5 bioactive glass material having a hierarchically ordered mesoporous structure with uniformly grown nanocrystals of apatite was achieved through a sono-assisted surfactant-templated sol-gel method. The bulk crystallographic analysis together with microstructural characterizations shows that the nanocrystalline apatite domains are uniformly dispersed as well as embedded along the mesopores. These nanocrystalline domains were found to influence the textural properties. In addition, macroscopic evidence for higher signs of bonelike matrix formation was observed by the biomineralization study in simulated body fluids. Osteostimulatory effects of these glass samples were evident by cultures in a osteogenic and non-osteogenic mediums with human osteosarcoma cells and a higher osteopromotive potential was authenticated by the alkaline phosphatase activity and alizarin red staining. Further, this study shows a new strategy to prolong the drug release period on account of the nanocrystalline phase and hierarchically positioned mesopores, thus making it a better drug delivery matrix as well. Infusion of apatite nanocrystals into non-crystalline glass matrix was achieved. The nanocrystalline domains are well dispersed and embedded along the hierarchically positioned mesopores. The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol-gel-derived bioactive glass using P123 as the structure-directing agent. The synthesis of a multicomponent 80SiO -15CaO-5P O bioactive glass material having a hierarchically ordered mesoporous structure with uniformly grown nanocrystals of apatite was achieved through a sono-assisted surfactant-templated sol-gel method. The bulk crystallographic analysis together with microstructural characterizations shows that the nanocrystalline apatite domains are uniformly dispersed as well as embedded along the mesopores. These nanocrystalline domains were found to influence the textural properties. In addition, macroscopic evidence for higher signs of bonelike matrix formation was observed by the biomineralization study in simulated body fluids. Osteostimulatory effects of these glass samples were evident by cultures in a osteogenic and non-osteogenic mediums with human osteosarcoma cells and a higher osteopromotive potential was authenticated by the alkaline phosphatase activity and alizarin red staining. Further, this study shows a new strategy to prolong the drug release period on account of the nanocrystalline phase and hierarchically positioned mesopores, thus making it a better drug delivery matrix as well. The engineering of nanocrystalline phase in amorphous oxide materials such as bioactive glass is emerging as a new area of great technological and scientific interest in the field of biomaterials. This study reports for the first time the infusion of apatite nanocrystals in sol–gel-derived bioactive glass using P123 as the structure-directing agent. The synthesis of a multicomponent 80SiO 2 –15CaO–5P 2 O 5 bioactive glass material having a hierarchically ordered mesoporous structure with uniformly grown nanocrystals of apatite was achieved through a sono-assisted surfactant-templated sol–gel method. The bulk crystallographic analysis together with microstructural characterizations shows that the nanocrystalline apatite domains are uniformly dispersed as well as embedded along the mesopores. These nanocrystalline domains were found to influence the textural properties. In addition, macroscopic evidence for higher signs of bonelike matrix formation was observed by the biomineralization study in simulated body fluids. Osteostimulatory effects of these glass samples were evident by cultures in a osteogenic and non-osteogenic mediums with human osteosarcoma cells and a higher osteopromotive potential was authenticated by the alkaline phosphatase activity and alizarin red staining. Further, this study shows a new strategy to prolong the drug release period on account of the nanocrystalline phase and hierarchically positioned mesopores, thus making it a better drug delivery matrix as well. |
Author | Dhara, Santanu Mukundan, Lakshmi M Kumar, Nikhil Chattopadhyay, Santanu Nirmal, Remya |
AuthorAffiliation | Rubber Technology Center Division of Toxicology School of Medical Science and Technology Sree Chitra Tirunal Institute for Medical Sciences & Technology Indian Institute of Technology Kharagpur |
AuthorAffiliation_xml | – name: Rubber Technology Center – name: Sree Chitra Tirunal Institute for Medical Sciences & Technology – name: School of Medical Science and Technology – name: Division of Toxicology – name: Indian Institute of Technology Kharagpur |
Author_xml | – sequence: 1 givenname: Lakshmi M surname: Mukundan fullname: Mukundan, Lakshmi M – sequence: 2 givenname: Remya surname: Nirmal fullname: Nirmal, Remya – sequence: 3 givenname: Nikhil surname: Kumar fullname: Kumar, Nikhil – sequence: 4 givenname: Santanu surname: Dhara fullname: Dhara, Santanu – sequence: 5 givenname: Santanu surname: Chattopadhyay fullname: Chattopadhyay, Santanu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36468610$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Alizarin Alkaline phosphatase Amorphous materials Apatite Apatites Biocompatible Materials - chemistry Bioglass Biological activity Biomaterials Biomedical materials Body fluids Crystallography Crystals Domains Drug delivery Drug Delivery Systems Glass - chemistry Humans Mineralization Nanocrystals Nanoparticles - chemistry Osteosarcoma Osteosarcoma cells Sol-gel processes |
Title | Engineered nanostructures within sol-gel bioactive glass for enhanced bioactivity and modulated drug delivery |
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