Flower-shaped covalent organic framework synthesis and its anticancer drug delivery application

被引:2
|
作者
Anbazhagan, Rajeshkumar [1 ,2 ]
Van Dinh, Thi Thuy [1 ]
Krishnamoorthi, Rajakumari [1 ,2 ]
Thankachan, Darieo [3 ]
Tsai, Hsieh-Chih [1 ,2 ,4 ]
Chang, Yen-Hsiang [5 ,6 ]
Yang, Jen-Ming [5 ,6 ,7 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Grad Inst Appl Sci & Technol, Taipei 106, Taiwan
[2] Natl Taiwan Univ Sci & Technol, Adv Membrane Mat Ctr, Taipei 106, Taiwan
[3] Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, Taipei 106, Taiwan
[4] Chung Yuan Christian Univ, R&D Ctr Membrane Technol, Taoyuan 320, Taiwan
[5] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan 333, Taiwan
[6] Chang Gung Mem Hosp, Dept Gen Dent, Taoyuan 333, Taiwan
[7] Innovat Life & Technol CO LTD, 53 Ln 447,Sec 1,Wenhua 3rd Rd, New Taipei City 244015, Taiwan
关键词
Covalent organic framework (COFs); Imine nitrogen protonation; Hyaluronic acid (HA); Drug delivery; HYALURONIC-ACID; NANOPARTICLES; CRYSTALLINE; NANOSHEETS; CARRIERS;
D O I
10.1016/j.matchemphys.2023.128612
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Fabrication of covalent organic frameworks (COFs) at room temperature is necessary due to their easy preparation, practical scale-up, and low cost to overcome the limitations of solvothermal and high-temperature synthesis. Herein, we fabricated flower-shaped COFs (FSCOFs) that were synthesized in various ratios of orthoxylene and butanol mixture solvents. The FSCOFs exhibited excellent crystallinity with a pore size of approximately 10 nm, which was confirmed by PXRD and BET measurements. To utilize the FSCOFs as a drug carrier, doxorubicin (DOX) was loaded, followed by encapsulation of hyaluronic acid to increase the colloidal stability of FSCOFs in a physiological environment (FSCOFs-DOX-HA). The encapsulation efficiency and the drug loading capacity of FSCOFs-DOX-HA were 21.23 % and 29.82 %, respectively. Moreover, 92 % and 59 % of DOX is released in acidic environments and elevated GSH environments, proving the sensitivity of the FSCOFs as carriers. The excellent drug release mechanism of FSCOFs-HA-DOX is demonstrated by FSCOFs imine nitrogen protonation under acidic environment confirmed by its zeta potential changes under various physiological environments. The designed FSCOFs-DOX-HA was demonstrated to be a pH-sensitive drug carrier to deliver anticancer drugs into cancer cells. The MTT and drug internalization data demonstrated sustained DOX release from FSCOFs-DOX-HA. Finally, the real-time fluorescence demonstrates the effectiveness of the FSCOFs-DOX-HA upon cellular uptake and release of the anticancer drug. Thus, the FSCOFs system reported here opens a new path in COF research for drug carrier systems.
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页数:10
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