A novel fabricated material with divergent chemical handles based on UiO-66 and used for targeted photodynamic therapy
A unique zirconium-based framework named N -UiO-66-NH , which can be used as a fabricated material to achieve the dual functional chemical modification of UiO-66, was synthesized and demonstrated. This work offers a facile and selective covalent post-synthetic modification of UiO-66 by different che...
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Veröffentlicht in: | Journal of materials chemistry. B, Materials for biology and medicine Materials for biology and medicine, 2017-08, Vol.5 (31), p.6227-6232 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A unique zirconium-based framework named N
-UiO-66-NH
, which can be used as a fabricated material to achieve the dual functional chemical modification of UiO-66, was synthesized and demonstrated. This work offers a facile and selective covalent post-synthetic modification of UiO-66 by different chemical reactions related to azide- and amino-groups, respectively. Using N
-UiO-66-NH
as a fabricated material, a newly dual functionalized MOF named E-UiO-66-Pc, in which a carboxyl substituted zinc phthalocyanine (Pc) and Erlotinib (E) were employed as a photosensitizer and targeting moiety, was designed and synthesized via amidation and click chemistry, respectively. The photochemical properties, tumor specificity and anticancer activity of E-UiO-66-Pc were investigated. We further demonstrated that it is viable to achieve facile and selective covalent post-synthetic modification of N
-UiO-66-NH
with Pc and E and obtained a series of functionalized UiO-66 nanomaterials. The Pc-containing UiO-66 nanomaterials exhibit high photodynamic activity, and the Erlotinib-containing UiO-66 nanomaterials show obvious dark cytotoxicity and high selective affinity to cancer cells. E-UiO-66-Pc reveals cooperative photodynamic and targeted anticancer activity. To the best of our knowledge, this is the only example of UiO-66 with two different chemical handles (-NH
and -N
) anchoring to different functional molecules via amidation and click chemistry, respectively. |
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ISSN: | 2050-750X 2050-7518 |
DOI: | 10.1039/c7tb01295k |