D
Dilek Keskin
Researcher at Middle East Technical University
Publications - 104
Citations - 2337
Dilek Keskin is an academic researcher from Middle East Technical University. The author has contributed to research in topics: Drug delivery & Medicine. The author has an hindex of 24, co-authored 90 publications receiving 1745 citations.
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Evaluation of sericin/collagen membranes as prospective wound dressing biomaterial
TL;DR: Wound dressing membranes of Sericin and Collagen were prepared by glutaraldehyde cross-linking at S/C and showed stable in water for 4 weeks, however, increasing the proportion of sericin had decreasing effect on the membrane stability.
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Collagen/gold nanoparticle nanocomposites: A potential skin wound healing biomaterial.
Omer Akturk,Kemal Kismet,Ahmet Çınar Yastı,Serdar Kuru,Mehmet Esat Duymus,Feridun Kaya,Muzaffer Caydere,Sema Hucumenoglu,Dilek Keskin +8 more
TL;DR: Overall, their contribution to the enhancement of degradation profiles and mechanical properties, their excellent in vitro biocompatibility, and tendency to accelerate wound healing are encouraging the use of AuNPs in collagen sponges as potent skin substitutes in the future.
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The effectiveness of early rehabilitation in patients with modified radical mastectomy.
TL;DR: Early onset rehabilitation program after modified radical mastectomy provides improvement in shoulder mobility and functional capacity without causing adverse effect in postoperative period.
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Cellulose acetate based 3-dimensional electrospun scaffolds for skin tissue engineering applications.
TL;DR: Results suggest that uncrosslinked CA/PULL (50/50) electrospun scaffolds hold potential for skin tissue engineering applications and are suggested to be cytocompatible as cell carriers.
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Celecoxib-loaded liposomes: effect of cholesterol on encapsulation and in vitro release characteristics.
TL;DR: The results indicated that CLX, without the requirement of modifications to enhance solubilization, can be encapsulated and released from liposomal formulations and may be used to circumvent the low bioavailability and systemic side effects of oral CLX formulations.