Green Synthesis of Cyclodextrin-Based Metal–Organic Frameworks through the Seed-Mediated Method for the Encapsulation of Hydrophobic Molecules
Metal–organic frameworks (MOFs) are attracting considerable attention as a result of their unique structural properties, such as a high surface area, highly porous topology, and tunable size and shape, which enable them to have potential applications as a new class of carriers for functional agent o...
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Published in | Journal of agricultural and food chemistry Vol. 66; no. 16; pp. 4244 - 4250 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
25.04.2018
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Abstract | Metal–organic frameworks (MOFs) are attracting considerable attention as a result of their unique structural properties, such as a high surface area, highly porous topology, and tunable size and shape, which enable them to have potential applications as a new class of carriers for functional agent or drug delivery. However, most of the MOFs and the polymers used are not pharmaceutically acceptable. For the first time, this study successfully conducted the rapid synthesis of cyclodextrin metal–organic frameworks (CD-MOFs) through a facile and green seed-mediated method. The size control, crystal structure, and thermal properties of CD-MOFs with and without seeds were investigated. When 1 mg/mL seed was added, the size of γ-CD-MOF crystals decreased from 6.2 ± 0.8 to 1.8 ± 0.4 μm. The CD-MOFs synthesized though the seed-mediated method had higher crystallinity and thermal stability than those that were not. Furthermore, the CD-MOFs could encapsulate hydrophobic molecules, such as Nile red (NR), which was chosen as a model, and the interaction mechanism between γ-CD-MOFs and NR was investigated. Results showed the formation of a 1:1 complex between NR and CD-MOFs, demonstrating the potential of these polymers as carriers for hydrophobic drug delivery applications. |
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AbstractList | Metal–organic frameworks (MOFs) are attracting considerable attention as a result of their unique structural properties, such as a high surface area, highly porous topology, and tunable size and shape, which enable them to have potential applications as a new class of carriers for functional agent or drug delivery. However, most of the MOFs and the polymers used are not pharmaceutically acceptable. For the first time, this study successfully conducted the rapid synthesis of cyclodextrin metal–organic frameworks (CD-MOFs) through a facile and green seed-mediated method. The size control, crystal structure, and thermal properties of CD-MOFs with and without seeds were investigated. When 1 mg/mL seed was added, the size of γ-CD-MOF crystals decreased from 6.2 ± 0.8 to 1.8 ± 0.4 μm. The CD-MOFs synthesized though the seed-mediated method had higher crystallinity and thermal stability than those that were not. Furthermore, the CD-MOFs could encapsulate hydrophobic molecules, such as Nile red (NR), which was chosen as a model, and the interaction mechanism between γ-CD-MOFs and NR was investigated. Results showed the formation of a 1:1 complex between NR and CD-MOFs, demonstrating the potential of these polymers as carriers for hydrophobic drug delivery applications. Metal-organic frameworks (MOFs) are attracting considerable attention as a result of their unique structural properties, such as a high surface area, highly porous topology, and tunable size and shape, which enable them to have potential applications as a new class of carriers for functional agent or drug delivery. However, most of the MOFs and the polymers used are not pharmaceutically acceptable. For the first time, this study successfully conducted the rapid synthesis of cyclodextrin metal-organic frameworks (CD-MOFs) through a facile and green seed-mediated method. The size control, crystal structure, and thermal properties of CD-MOFs with and without seeds were investigated. When 1 mg/mL seed was added, the size of γ-CD-MOF crystals decreased from 6.2 ± 0.8 to 1.8 ± 0.4 μm. The CD-MOFs synthesized though the seed-mediated method had higher crystallinity and thermal stability than those that were not. Furthermore, the CD-MOFs could encapsulate hydrophobic molecules, such as Nile red (NR), which was chosen as a model, and the interaction mechanism between γ-CD-MOFs and NR was investigated. Results showed the formation of a 1:1 complex between NR and CD-MOFs, demonstrating the potential of these polymers as carriers for hydrophobic drug delivery applications.Metal-organic frameworks (MOFs) are attracting considerable attention as a result of their unique structural properties, such as a high surface area, highly porous topology, and tunable size and shape, which enable them to have potential applications as a new class of carriers for functional agent or drug delivery. However, most of the MOFs and the polymers used are not pharmaceutically acceptable. For the first time, this study successfully conducted the rapid synthesis of cyclodextrin metal-organic frameworks (CD-MOFs) through a facile and green seed-mediated method. The size control, crystal structure, and thermal properties of CD-MOFs with and without seeds were investigated. When 1 mg/mL seed was added, the size of γ-CD-MOF crystals decreased from 6.2 ± 0.8 to 1.8 ± 0.4 μm. The CD-MOFs synthesized though the seed-mediated method had higher crystallinity and thermal stability than those that were not. Furthermore, the CD-MOFs could encapsulate hydrophobic molecules, such as Nile red (NR), which was chosen as a model, and the interaction mechanism between γ-CD-MOFs and NR was investigated. Results showed the formation of a 1:1 complex between NR and CD-MOFs, demonstrating the potential of these polymers as carriers for hydrophobic drug delivery applications. |
Author | Xu, Xueming Qin, Yang Jin, Zhengyu Wang, Jinpeng Qiu, Chao Fan, Haoran |
AuthorAffiliation | State Key Laboratory of Food Science and Technology Synergetic Innovation Center of Food Safety and Nutrition School of Food Science and Technology |
AuthorAffiliation_xml | – name: School of Food Science and Technology – name: State Key Laboratory of Food Science and Technology – name: Synergetic Innovation Center of Food Safety and Nutrition |
Author_xml | – sequence: 1 givenname: Chao surname: Qiu fullname: Qiu, Chao – sequence: 2 givenname: Jinpeng surname: Wang fullname: Wang, Jinpeng – sequence: 3 givenname: Yang surname: Qin fullname: Qin, Yang – sequence: 4 givenname: Haoran surname: Fan fullname: Fan, Haoran – sequence: 5 givenname: Xueming surname: Xu fullname: Xu, Xueming – sequence: 6 givenname: Zhengyu orcidid: 0000-0001-6880-9955 surname: Jin fullname: Jin, Zhengyu email: fpcenter@jiangnan.edu.cn |
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Cites_doi | 10.1021/ja0740364 10.1021/cr200256v 10.1039/b807080f 10.1016/j.ijbiomac.2012.09.030 10.1016/j.ijpharm.2012.06.055 10.1021/acs.cgd.6b01658 10.1021/la0101200 10.1016/j.foodchem.2016.06.013 10.1016/j.jphotobiol.2013.06.005 10.1039/C6NR07593B 10.1016/j.molstruc.2015.08.020 10.1016/j.cbpa.2009.12.012 10.1016/j.ccr.2014.10.008 10.1039/c2tb00366j 10.1002/anie.201204919 10.1039/C4NR03095H 10.1016/j.foodchem.2014.04.068 10.1007/s10847-017-0715-7 10.1016/j.carbpol.2014.12.070 10.1007/s10847-008-9522-5 10.1016/j.inoche.2014.02.022 10.1016/j.chroma.2017.01.062 10.1016/j.aca.2015.07.029 10.1021/ic201396m 10.1039/C7GC01078H 10.1016/j.foodchem.2016.11.009 10.1021/acs.jafc.7b03465 10.1002/anie.200906560 10.1016/j.ijpharm.2016.09.029 10.1016/j.carbpol.2008.04.043 10.1039/C2DT32479B 10.1007/s10450-015-9691-7 10.1021/jacs.6b01414 |
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SubjectTerms | coordination polymers crystal structure crystals cyclodextrins drug delivery systems drugs encapsulation hydrophobicity seeds surface area thermal stability topology |
Title | Green Synthesis of Cyclodextrin-Based Metal–Organic Frameworks through the Seed-Mediated Method for the Encapsulation of Hydrophobic Molecules |
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