Porous metal–organic-framework MIL-100(Fe) as a nanoscale platform for sustainable release of tetracycline
Seyed Dariush Taherzade
School of Chemistry, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.
I was Born in 1990 and achieved my B.Sc. degree in applied chemistry in 2013. I finished my M.Sc. in Inorganic chemistry in 2015 and my thesis was "Synthesis of nanostructured supramolecular compounds from Mn(II) metal ion and their application in the synthesis of nano-metal oxides". I have initiated my Ph.D. in inorganic chemistry since 2015. My research area is the application of MOF and coordination polymers in drug delivery and bioinorganic systems. I am very enthusiastic about collaboration with other scientists around the world especially those who involved in biochemistry, biology, and nanobiotechnology.My email: D.taherzade@ut.ac.ir
Abstract
Tetracyclines are a group of broad-spectrum antibiotics used in the treatment of infections of urinary and respiratory tract [1]. Nanoscale porous MIL-100 is a great platform for delivery of broad types of drugs like... [ view full abstract ]
Tetracyclines are a group of broad-spectrum antibiotics used in the treatment of infections of urinary and respiratory tract [1]. Nanoscale porous MIL-100 is a great platform for delivery of broad types of drugs like doxorubicin, ibuprofen and etc [2, 3]. In current research nano MIL-100 was synthesized via Horcajada, et al. method [2]. Sample characterizations carried out with FT-IR, XRD, BET and SEM. Tetracycline (TC) was loaded on MIL-100 in the ratio of 1:3 and the nano-drug-carrier abbreviated as TC@Mil-100. FT-IR spectra confirmed the loading of the drug into the carrier framework. XRD pattern of TC@MIL-100 indicated no pattern of TC. On the other hand, BET analysis showed a 66 percent decrease in available pores and the free surface decreased to 801 Cm3g-1, so it can be concluded that the drug is well dispersed into the nano-pores of MIL-100. The release of TC from MOF was investigated in Simulated Gastric Fluid (SGF) media during 48 hours via UV analysis and it was observed that 96 percent of the drug was sustain released which is an unprecedented amount in comparison with other methods[4]. The results demonstrated the substantially enhanced release of tetracycline as a very slightly soluble drug.
1. Chopra, I. and M. Roberts, Tetracycline antibiotics: mode of action, applications, molecular biology, and epidemiology of bacterial resistance. Microbiology and molecular biology reviews, 2001. 65(2): p. 232-260.
2. Horcajada, P., et al., Porous metal-organic-framework nanoscale carriers as a potential platform for drug delivery and imaging. Nature materials, 2010. 9(2): p. 172-178.
3. Agostoni, V., et al., Impact of phosphorylation on the encapsulation of nucleoside analogues within porous iron (III) metal–organic framework MIL-100 (Fe) nanoparticles. Journal of Materials Chemistry B, 2013. 1(34): p. 4231-4242.
4. Xie, J.F., et al. In Vitro Release Characterization of Tetracycline Hydrochloride from PLGA/Tetracycline Hydrochloride Electrospun Nanofiber Mats. in Advanced Materials Research. 2013. Trans Tech Publ.
Corresponding author: janet_soleimannejad@khayam.ut.ac.ir
Authors
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Seyed Dariush Taherzade
(School of Chemistry, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.)
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Aliakbar Tarlani
(Chemistry & Chemical Engineering Research Center of Iran (CCERCI), Pajoohesh Blvd., km 17, Karaj Hwy, P.O. Box 14968-13151, Tehran, Iran.)
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Janet Soleimannejad
(School of Chemistry, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.)
Topic Area
Targeted drug delivery and Nanocarriers
Session
PS1 » Poster Session & Sponsors Exhibition (13:30 - Wednesday, 28th September, Patio 25)
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