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2023
DOI: 10.1016/j.ijbiomac.2023.123819
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Electrospun sandwich-structured of polycaprolactone/gelatin-based nanofibers with controlled release of ceftazidime for wound dressing

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Cited by 13 publications
(5 citation statements)
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“…For instance, Sardareh et al [ 63 ] reported that the incorporation of toxic silver nanoparticles in the PLA/gelatin nanofibers designed for wound dressing application led to inducing a lower level of toxicity on L929 cells. No notable cytotoxic effects on human normal cells were reported when electrospun multilayered mats composed of polycaprolactone/gelatin/polycaprolactone [ 64 ], chitosan (CS)/gelatin (GL) and graphene nanosheet (GNS)-CS/GL nanofibers [ 65 ], and gelatin/PVA nanofibers [ 66 ] were investigated, demonstrating cell proliferation without any signs of necrosis. The good cytotoxicity of a fish gelatin nanofibrous scaffold evaluated based on a cell proliferation study by culturing human dermal fibroblasts (HDFs) was explained due to the hydrophilic surface of nanofibrous fish gelatin, which provides an appropriate environment for the attaching of fibroblast cells [ 67 ].…”
Section: Resultsmentioning
confidence: 99%
“…For instance, Sardareh et al [ 63 ] reported that the incorporation of toxic silver nanoparticles in the PLA/gelatin nanofibers designed for wound dressing application led to inducing a lower level of toxicity on L929 cells. No notable cytotoxic effects on human normal cells were reported when electrospun multilayered mats composed of polycaprolactone/gelatin/polycaprolactone [ 64 ], chitosan (CS)/gelatin (GL) and graphene nanosheet (GNS)-CS/GL nanofibers [ 65 ], and gelatin/PVA nanofibers [ 66 ] were investigated, demonstrating cell proliferation without any signs of necrosis. The good cytotoxicity of a fish gelatin nanofibrous scaffold evaluated based on a cell proliferation study by culturing human dermal fibroblasts (HDFs) was explained due to the hydrophilic surface of nanofibrous fish gelatin, which provides an appropriate environment for the attaching of fibroblast cells [ 67 ].…”
Section: Resultsmentioning
confidence: 99%
“…Given its distinctive membrane-like structure and suitable physical and chemical properties, electrospun fibers are commonly employed as dressings for wound healing. Nezamoleslami et al utilized electrospinning to fabricated sandwich-structured multilayered mats and demonstrated that the controlled release of ceftazidime from the gelatin layer within the mats exhibited potent antibacterial activity without negatively affecting the viability of fibroblast cells [ 28 ]. In order to facilitate bone regeneration, a multilayer electrospun nanofibrous membrane was designed, capable of sequentially releasing MT01 (a single-stranded cytosine-phosphate-guanosine oligodeoxynucleotide) and stromal cell-derived factor 1α (SDF-1α) from the inner and outer layers, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…Cell viability was evaluated by MTT assay . Approximately 10 4 cells were inoculated in each well of a 96-well plate and incubated at 37 °C for 24 h. In the meantime, a propolis-loaded PLGA membrane was incubated in 5 mL of DMEM at 37 °C, shaking for 24 h to release the drug.…”
Section: Methodsmentioning
confidence: 99%
“…Cell viability was evaluated by MTT assay. 36 Approximately 10 4 cells were inoculated in each well of a 96-well plate and incubated at 37 °C for 24 h. In the meantime, a propolis-loaded PLGA membrane was incubated in 5 mL of DMEM at 37 °C, shaking for 24 h to release the drug. Subsequently, released propolis was diluted to the following concentrations: 12.5, 25, 50, 100, and 200 μg/mL, and an appropriate amount of propolis-containing media was added to 100% confluent cells.…”
Section: Methodsmentioning
confidence: 99%