Multifunctional metal-organic framework heterostructures for enhanced cancer therapy
Metal-organic frameworks (MOFs) are an emerging class of molecular crystalline materials built from metal ions or clusters bridged by organic linkers. By taking advantage of their synthetic tunability and structural regularity, MOFs can hierarchically integrate nanoparticles and/or biomolecules into...
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Published in | Chemical Society reviews Vol. 5; no. 2; pp. 1188 - 1218 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
21.01.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Metal-organic frameworks (MOFs) are an emerging class of molecular crystalline materials built from metal ions or clusters bridged by organic linkers. By taking advantage of their synthetic tunability and structural regularity, MOFs can hierarchically integrate nanoparticles and/or biomolecules into a single framework to enable multifunctions. The MOF-protected heterostructures not only enhance the catalytic capacity of nanoparticle components but also retain the biological activity of biomolecules in an intracellular microenvironment. Therefore, the multifunctional MOF heterostructures have great advantages over single components in cancer therapy. In this review, we comprehensively summarize the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy within the last five years. The functions of MOF heterostructures with a controlled size can be regulated by designing various functional ligands and
in situ
growth/postmodification of nanoparticles and/or biomolecules. The advances in the application of multifunctional MOF heterostructures are also explored for enhanced cancer therapies involving photodynamic therapy, photothermal therapy, chemotherapy, radiotherapy, immunotherapy, and theranostics. The remaining challenges and future opportunities in this field, in terms of precisely localized assembly, maximizing composite properties, and processing new techniques, are also presented. The introduction of multiple components into one crystalline MOF provides a promising approach to design all-in-one theranostics in clinical treatments.
We review the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy. |
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Bibliography: | Lei Zhang received her BS degree from Nanjing Normal University in 2009, MS degree from Xiamen University in 2012, and PhD degree from Nanjing University in 2015, and then became a Humboldt scholar at University of Munich in 2018. Her research interests include biofunctionalization and self-assembly of nanomaterials for biosensing, cellular imaging and cancer therapy. Jianping Lei received his PhD degree from the Department of Chemistry at Kanazawa University (Japan) in 2004, and pursued postdoc training at Stanford University (USA) in 2005. He is now a university distinguished professor at Nanjing University (China). His research interests include design and functionalization of MOF nanostructures for biosensing and enhanced therapy. He has authored/co-authored over 170 peer-reviewed papers and the total citations exceed 8600 (H-index of 56). Jintong Liu received her BS degree from Jilin University in 2013 and PhD degree from Nanjing University in 2018, and then became an assistant professor at Nanjing Agricultural University in 2018. Her research interests include functionalization and self-assembly of MOF hybrids for cellular imaging and cancer therapy. Jing Huang received her BS degree from the Dalian University of Technology in 2017, and her MS degree from Nanjing University in 2020. Her research interests include design and self-assembly of MOF hybrids for the detection of cellular biomolecules and construction of a theranostic system. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 0306-0012 1460-4744 1460-4744 |
DOI: | 10.1039/d0cs00178c |