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Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells
Morphologically discrete nanoarchitectures, which mimic the structural complexity of biological systems, are an increasingly popular design paradigm in the development of new nanomedical technologies. Herein, engineered polymeric stomatocytes are presented as a structural and functional mimic of red...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402394/ https://www.ncbi.nlm.nih.gov/pubmed/30886797 http://dx.doi.org/10.1002/advs.201801678 |
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author | Shao, Jingxin Pijpers, Imke A. B. Cao, Shoupeng Williams, David S. Yan, Xuehai Li, Junbai Abdelmohsen, Loai K. E. A. van Hest, Jan C. M. |
author_facet | Shao, Jingxin Pijpers, Imke A. B. Cao, Shoupeng Williams, David S. Yan, Xuehai Li, Junbai Abdelmohsen, Loai K. E. A. van Hest, Jan C. M. |
author_sort | Shao, Jingxin |
collection | PubMed |
description | Morphologically discrete nanoarchitectures, which mimic the structural complexity of biological systems, are an increasingly popular design paradigm in the development of new nanomedical technologies. Herein, engineered polymeric stomatocytes are presented as a structural and functional mimic of red blood cells (RBCs) with multifunctional therapeutic features. Stomatocytes, comprising biodegradable poly(ethylene glycol)‐block‐poly(D,L‐lactide), possess an oblate‐like morphology reminiscent of RBCs. This unique dual‐compartmentalized structure is augmented via encapsulation of multifunctional cargo (oxygen‐binding hemoglobin and the photosensitizer chlorin e6). Furthermore, stomatocytes are decorated with a cell membrane isolated from erythrocytes to ensure that the surface characteristics matched those of RBCs. In vivo biodistribution data reveal that both the uncoated and coated nano‐RBCs have long circulation times in mice, with the membrane‐coated ones outperforming the uncoated stomatoctyes. The capacity of nano‐RBCs to transport oxygen and create oxygen radicals upon exposure to light is effectively explored toward photodynamic therapy, using 2D and 3D tumor models; addressing the challenge presented by cancer‐induced hypoxia. The morphological and functional control demonstrated by this synthetic nanosystem, coupled with indications of therapeutic efficacy, constitutes a highly promising platform for future clinical application. |
format | Online Article Text |
id | pubmed-6402394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64023942019-03-18 Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells Shao, Jingxin Pijpers, Imke A. B. Cao, Shoupeng Williams, David S. Yan, Xuehai Li, Junbai Abdelmohsen, Loai K. E. A. van Hest, Jan C. M. Adv Sci (Weinh) Communications Morphologically discrete nanoarchitectures, which mimic the structural complexity of biological systems, are an increasingly popular design paradigm in the development of new nanomedical technologies. Herein, engineered polymeric stomatocytes are presented as a structural and functional mimic of red blood cells (RBCs) with multifunctional therapeutic features. Stomatocytes, comprising biodegradable poly(ethylene glycol)‐block‐poly(D,L‐lactide), possess an oblate‐like morphology reminiscent of RBCs. This unique dual‐compartmentalized structure is augmented via encapsulation of multifunctional cargo (oxygen‐binding hemoglobin and the photosensitizer chlorin e6). Furthermore, stomatocytes are decorated with a cell membrane isolated from erythrocytes to ensure that the surface characteristics matched those of RBCs. In vivo biodistribution data reveal that both the uncoated and coated nano‐RBCs have long circulation times in mice, with the membrane‐coated ones outperforming the uncoated stomatoctyes. The capacity of nano‐RBCs to transport oxygen and create oxygen radicals upon exposure to light is effectively explored toward photodynamic therapy, using 2D and 3D tumor models; addressing the challenge presented by cancer‐induced hypoxia. The morphological and functional control demonstrated by this synthetic nanosystem, coupled with indications of therapeutic efficacy, constitutes a highly promising platform for future clinical application. John Wiley and Sons Inc. 2019-01-19 /pmc/articles/PMC6402394/ /pubmed/30886797 http://dx.doi.org/10.1002/advs.201801678 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Shao, Jingxin Pijpers, Imke A. B. Cao, Shoupeng Williams, David S. Yan, Xuehai Li, Junbai Abdelmohsen, Loai K. E. A. van Hest, Jan C. M. Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title | Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title_full | Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title_fullStr | Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title_full_unstemmed | Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title_short | Biomorphic Engineering of Multifunctional Polylactide Stomatocytes toward Therapeutic Nano‐Red Blood Cells |
title_sort | biomorphic engineering of multifunctional polylactide stomatocytes toward therapeutic nano‐red blood cells |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402394/ https://www.ncbi.nlm.nih.gov/pubmed/30886797 http://dx.doi.org/10.1002/advs.201801678 |
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