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Harnessing silk fibroin microparticles for metformin delivery: A novel approach to treating corneal neovascularization

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dc.creator ÜNAL, SEDAT
dc.creator ÇALAMAK, SEMİH
dc.creator Kurt, Nihat
dc.creator Demirci, Nazire
dc.creator Çaylı, Yağmur Akdağ
dc.creator KARAKUYU, Nasıf Fatih
dc.creator Bozdağ Pehlivan, Sibel
dc.creator Mendil, Ali Sefa
dc.creator Mokhtare, Behzad
dc.creator Erkan, Eda
dc.creator Çırak, Rumeysa
dc.creator AYTEKİN, EREN
dc.creator Polat, Heybet Kerem
dc.date 2024-06-01T00:00:00Z
dc.date.accessioned 2025-02-25T10:41:16Z
dc.date.available 2025-02-25T10:41:16Z
dc.identifier efafa22f-3c09-4e10-b4ff-1bb4340d868d
dc.identifier 10.1016/j.jddst.2024.105625
dc.identifier https://avesis.sdu.edu.tr/publication/details/efafa22f-3c09-4e10-b4ff-1bb4340d868d/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/101869
dc.description Corneal neovascularization (CV) poses significant challenges in ophthalmology, often leading to impaired vision and discomfort. Silk fibroin microparticles have emerged as promising candidates for drug delivery applications, owing to their biocompatibility, biodegradability, and controlled release characteristics. In the current research, metformin-loaded silk microparticles were developed, and their potential for treating corneal neovascularization was evaluated. Silk microparticles were prepared using silk fibroin and polyvinyl alcohol (PVA) at various weight ratios, facilitating phase separation to create a porous structure conducive to drug loading. Metformin (MT), a widely used antidiabetic agent with potential anti-angiogenic properties, was incorporated into the silk microparticles at different concentrations. The formulation termed TB (0.3 % MT loaded Microparticles) emerged as the most promising candidate was identified through comprehensive in vitro evaluations. In in vitro cytotoxicity studies, it was determined that all formulations provided cell viability above 80%, however, in permeability studies and encapsulation efficiency studies, TB was determined to be more effective than other formulations. TB demonstrated a particle size of approximately 8.9 ± 3.6 μm and an encapsulation efficiency of 96.3 ± 2.1%. In vitro release studies revealed that TB exhibited a burst release of 62% within the initial two days, followed by sustained release over a period of 14 days, consistent with Peppas-Sahlin kinetics. Mathematical modeling further corroborated the diffusion mechanism underlying drug release from TB microparticles. In vivo studies on rats and histochemical analyzes on corneas showed that TB exhibited efficacy comparable to dexamethasone, a standard treatment for CV, despite being administered once daily. Histological analyses of corneal tissues revealed reduced neovascularization and inflammation in the TB-treated group, underscoring its therapeutic potential. Overall, our findings highlight the promise of metformin-loaded silk fibroin microparticles as a novel therapeutic approach for managing CV, offering sustained drug release and enhanced efficacy in treating this challenging ocular condition.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Harnessing silk fibroin microparticles for metformin delivery: A novel approach to treating corneal neovascularization
dc.type info:eu-repo/semantics/article


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