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Alginate-polycaprolactone nanoparticles for drug delivery and wound healing applications

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dc.contributor.author Maatouk, Batoul Ibrahim
dc.date.accessioned 2021-09-23T08:56:39Z
dc.date.available 2021-09-23T08:56:39Z
dc.date.issued 2019
dc.date.submitted 2019
dc.identifier.other b25782769
dc.identifier.uri http://hdl.handle.net/10938/23082
dc.description Thesis. M.S. American University of Beirut. Biomedical Engineering Program, 2019. ET:7098
dc.description Advisor : Dr. Rami Mhanna, Assistant Professor, Biomedical Engineering Program ; Co-Advisor : Dr. Ayad Jaffa, Assistant Dean, Chairperson and Professor, Biochemistry and Molecular Genetics ; Committee members : Dr. Jason Ammatoury, Assistant Professor, Biomedical Engineering Program ; Dr. Ali Tehrani, Associate Professor, Bahaa and Walid Bassatne Department of Chemical Engineering and Advanced Energy ; Dr. Yousef Mubarak, Visiting Associate Professor, Bahaa and Walid Bassatne Department of Chemical Engineering and Advanced Energy.
dc.description Includes bibliographical references.
dc.description.abstract Diabetic foot ulcers (DFUs) that are not effectively treated might ultimately lead to partial or complete lower limb amputations; such losses take place every 30 seconds worldwide. DFU’s and related amputations together pose an annual economic burden of up to $15 billion on the global healthcare system. The lack of connective tissue growth factor (CTGF) and insulin-like growth factor (IGF-I) in DFU results in limited matrix deposition and consequently limited tissue repair. In the current thesis, we sought to address the lack of growth factors in DFUs by engineering double emulsion polymeric nanoparticles (NPs) with high affinity and sustained release of CTGF and IGF and study the effect of the synthesized growth factor (GF)-loaded NPs on DFU healing. The double emulsion NPs were made of an alginate (Alg) or the heparin-mimetic alginate sulfate (AlgSulf) core and a polycaprolactone (PCL) shell. The optimal NPs formulation was determined by investigating the effects of sonication time and amplitude, organic solvent evaporation rate and processed volume on the morphology, size, and polydispersity of the NPs using scanning electron microscopy (SEM) and dynamic light scattering (DLS). The protein encapsulation efficiency (EE) and release profile were assessed using bovine serum albumin (BSA) as a model drug via the Lowry protein assay. Toxicity of the synthesized NPs and their effect on signaling pathways were evaluated using trypan blue, MTT and immunoblotting assays. Finally, the effect of NPs on wound healing and the role of RhoA signaling were evaluated using a scratch assay. The results showed that an increase in the sonication time and amplitude which correspond to an increase in the total delivered energy, significantly reduced the NPs diameter to a minimum of 235.5±25 nm. Similarly, increasing the organic solvent evaporation rate by which particles solidify or decreasing the total processed volume caused a significant decrease in the NPs diameter (P=0.002). The highest BSA (EE) based on Alg or
dc.format.extent 1 online resource (xvi, 104 leaves) : illustrations (some color)
dc.language.iso en
dc.subject.classification ET:007098
dc.subject.lcsh Alginates.
dc.subject.lcsh Growth factors.
dc.subject.lcsh Polycaprolactone.
dc.subject.lcsh Wound healing.
dc.subject.lcsh Diabetic neuropathies.
dc.subject.lcsh Nanoparticles.
dc.subject.lcsh Biomedical engineering.
dc.title Alginate-polycaprolactone nanoparticles for drug delivery and wound healing applications
dc.type Thesis
dc.contributor.department Biomedical Engineering Program
dc.contributor.faculty Faculty of Medicine
dc.contributor.faculty Maroun Semaan Faculty of Engineering and Architecture
dc.contributor.institution American University of Beirut.


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