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dc.contributor.authorAhmed, Ahmed H.S
dc.contributor.authorKarami, Abdollah
dc.contributor.authorSabouni, Rana
dc.contributor.authorHusseini, Ghaleb
dc.contributor.authorPaul, Vinod
dc.date.accessioned2024-04-22T08:28:10Z
dc.date.available2024-04-22T08:28:10Z
dc.date.issued2021
dc.identifier.citationAhmed Ahmed, Abdollah Karami, Rana Sabouni, Ghaleb A. Husseini, Vinod Paul, pH and ultrasound dual-responsive drug delivery system based on PEG–folate-functionalized Iron-based metal–organic framework for targeted doxorubicin delivery, Colloids and Surfaces A: Physicochemical and Engineering Aspects, Volume 626, 2021, 127062, ISSN 0927-7757, https://doi.org/10.1016/j.colsurfa.2021.127062.en_US
dc.identifier.issn0927-7757
dc.identifier.urihttp://hdl.handle.net/11073/25517
dc.description.abstractIn recent years, the use of metal–organic frameworks (MOFs) as drug nanocarriers has gained attention because of their extraordinary physical and chemical properties. In this work, dual-responsive iron-based MOFs were synthesized via the microwave-assisted method using FeCl₃.6 (H₂O) as the metal cluster and 2-aminoterephthalic acid (NH₂-BDC) as the organic linker (namely NH₂-Fe-BDC) and loaded with the anti-cancer drug doxorubicin (DOX). The DOX-loaded MOFs were further functionalized with polyethylene glycol-folate (PEG–FA), yielding PEG–FA-NH₂-Fe-BDC. The folate moiety is used to specifically target several cancers overexpressing the folate receptor (FR). These nanoparticles were characterized using Fourier-Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA), and Dynamic Light Scattering (DLS). The FTIR confirmed the PEG–FA conjugation to the MOFs, while the XRD patterns confirmed the crystallinity of the nanoparticles. TGA results demonstrated the thermal stability of the MOFs. Moreover, the DLS analysis showed that regular MOFs had a particle diameter of 577 nm, while the PEG–FA-functionalized MOF had a particle diameter of 461 nm, which demonstrates the improved colloidal stability of the functionalized MOF. The DOX encapsulation efficiency was determined to be approximately 97%, while the encapsulation capacity was around 14.5 wt%. Furthermore, the in-vitro release profiles were studied under different pH values (5.3 and 7.4) with and without low-frequency ultrasound (LFUS, at 40 kHz). The results confirmed the sonosensitivity of the nanovehicles, with US-triggered release efficiency reaching up to 90% after 280 min (at a pH of 5.3). The MTT study revealed that these nanocarriers are non-toxic at lower concentrations. Their toxicity increases at higher concentrations. Furthermore, the cellular uptake was investigated via flow cytometry, and the results showed that the conjugation of the PEG-FA moiety to the MOF’s surface significantly enhanced uptake by cancer cells. Accordingly, this study showed the pH/US dual-responsive capability of NH₂-Fe-BDC and PEG–FA-NH₂-Fe-BDC.en_US
dc.description.sponsorshipAmerican University of Sharjahen_US
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.urihttps://doi.org/10.1016/j.colsurfa.2021.127062en_US
dc.subjectMetal–organic frameworksen_US
dc.subjectDrug deliveryen_US
dc.subjectUltrasounden_US
dc.subjectTriggered releaseen_US
dc.subjectEncapsulation efficiencyen_US
dc.subjectDoxorubicinen_US
dc.subjectNH2-Fe-BDCen_US
dc.titlepH and ultrasound dual-responsive drug delivery system based on PEG–folate-functionalized Iron-based metal–organic framework for targeted doxorubicin deliveryen_US
dc.typeArticleen_US
dc.typePeer-Revieweden_US
dc.typePostprinten_US
dc.identifier.doi10.1016/j.colsurfa.2021.127062


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