期刊
JOURNAL OF POROUS MATERIALS
卷 28, 期 2, 页码 641-649出版社
SPRINGER
DOI: 10.1007/s10934-020-01027-3
关键词
Drug delivery; Zn-2(BDC)(2)DABCO; Imatinib mesylate; Hydrolytic decomposition; Zn-MOF; Encapsulation
资金
- Science and Research Branch, Islamic Azad University
Mesoporous Zn-2(BDC)(2)(DABCO)-MOF synthesized via ball-milling effectively encapsulated small molecules of Imatinib mesylate, showing rapid drug release upon hydrolytic decomposition in dissolution media under in vitro conditions.
Mesoporous Zn-2(BDC)(2)(DABCO)-MOF (BDC = 1,4-benzenedicarboxilic acid, and DABCO = diazabicyclooctane) was synthesized via ball-milling and employed as a good and efficient platform for targeted drug delivery. Imatinib mesylate (IM) was encapsulated in Zn-MOF and IM@Zn-MOF characterized using different technique including X-ray powder diffraction, field emission scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, inductively coupled plasma, Brunauer-Emmett-Teller surface area analysis. The result showed that small molecules of the IM successfully were encapsulated inside of the Zn-MOF. Releasing of drug-loaded Zn-MOF was studied by UV-vis spectroscopy at 240 nm at in vitro condition in HCl (0.1N) and PBS buffer. Rapid release of IM occurs upon hydrolytic decomposition of MOF in dissolution media.
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