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Packaging biological cargoes in mesoporous materials: opportunities for drug delivery

Introduction: Confinement of biomolecules in structured nanoporous materials offers several desirable features ranging from chemical and thermal stability, to resistance to degradation from the external environment. A new generation of mesoporous materials presents exciting new possibilities for the...

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Autores principales: Siefker, Justin, Karande, Pankaj, Coppens, Marc-Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245185/
https://www.ncbi.nlm.nih.gov/pubmed/25016923
http://dx.doi.org/10.1517/17425247.2014.938636
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author Siefker, Justin
Karande, Pankaj
Coppens, Marc-Olivier
author_facet Siefker, Justin
Karande, Pankaj
Coppens, Marc-Olivier
author_sort Siefker, Justin
collection PubMed
description Introduction: Confinement of biomolecules in structured nanoporous materials offers several desirable features ranging from chemical and thermal stability, to resistance to degradation from the external environment. A new generation of mesoporous materials presents exciting new possibilities for the formulation and controlled release of biological agents. Such materials address niche applications in enteral and parenteral delivery of biologics, such as peptides, polypeptides, enzymes and proteins for use as therapeutics, imaging agents, biosensors, and adjuvants. Areas covered: Mesoporous silica Santa Barbara Amorphous-15 (SBA-15), with its unique, tunable pore diameter, and easily functionalized surface, provides a representative example of this new generation of materials. Here, we review recent advances in the design and synthesis of nanostructured mesoporous materials, focusing on SBA-15, and highlight opportunities for the delivery of biological agents to various organ and tissue compartments. Expert opinion: The SBA-15 platform provides a delivery carrier that is inherently separated from the active biologic due to distinct intra and extra-particle environments. This permits the SBA-15 platform to not require direct modification of the active biological therapeutic. Additionally, this makes the platform universal and allows for its application independent of the desired methods of discovery and development. The SBA-15 platform also directly addresses issues of targeted delivery and controlled release, although future challenges in the implementation of this platform reside in particle design, biocompatibility, and the tunability of the internal and external material properties. Examples illustrating the flexibility in the application of the SBA-15 platform are also discussed.
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spelling pubmed-42451852014-12-08 Packaging biological cargoes in mesoporous materials: opportunities for drug delivery Siefker, Justin Karande, Pankaj Coppens, Marc-Olivier Expert Opin Drug Deliv Reviews Introduction: Confinement of biomolecules in structured nanoporous materials offers several desirable features ranging from chemical and thermal stability, to resistance to degradation from the external environment. A new generation of mesoporous materials presents exciting new possibilities for the formulation and controlled release of biological agents. Such materials address niche applications in enteral and parenteral delivery of biologics, such as peptides, polypeptides, enzymes and proteins for use as therapeutics, imaging agents, biosensors, and adjuvants. Areas covered: Mesoporous silica Santa Barbara Amorphous-15 (SBA-15), with its unique, tunable pore diameter, and easily functionalized surface, provides a representative example of this new generation of materials. Here, we review recent advances in the design and synthesis of nanostructured mesoporous materials, focusing on SBA-15, and highlight opportunities for the delivery of biological agents to various organ and tissue compartments. Expert opinion: The SBA-15 platform provides a delivery carrier that is inherently separated from the active biologic due to distinct intra and extra-particle environments. This permits the SBA-15 platform to not require direct modification of the active biological therapeutic. Additionally, this makes the platform universal and allows for its application independent of the desired methods of discovery and development. The SBA-15 platform also directly addresses issues of targeted delivery and controlled release, although future challenges in the implementation of this platform reside in particle design, biocompatibility, and the tunability of the internal and external material properties. Examples illustrating the flexibility in the application of the SBA-15 platform are also discussed. Taylor & Francis 2014-11-01 2014-07-12 /pmc/articles/PMC4245185/ /pubmed/25016923 http://dx.doi.org/10.1517/17425247.2014.938636 Text en © 2014 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Reviews
Siefker, Justin
Karande, Pankaj
Coppens, Marc-Olivier
Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title_full Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title_fullStr Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title_full_unstemmed Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title_short Packaging biological cargoes in mesoporous materials: opportunities for drug delivery
title_sort packaging biological cargoes in mesoporous materials: opportunities for drug delivery
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245185/
https://www.ncbi.nlm.nih.gov/pubmed/25016923
http://dx.doi.org/10.1517/17425247.2014.938636
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