椰子油明胶基薄膜的生产和表征及其潜在的生物医学应用

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL Biomedical materials Pub Date : 2022-05-03 DOI:10.1088/1748-605X/ac6c67
Mehlika Karamanlioglu, Serap Yesilkir-Baydar
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引用次数: 1

摘要

当用作潜在的伤口敷料材料时,研究了椰子油(CO)对明胶基薄膜的影响。关于蛋白质类伤口敷料材料中CO的研究有限。因此,在本研究中,通过溶液浇铸法配制并获得了一种自支撑、连续且均匀的CO掺入明胶基薄膜。还测定了CO对明胶基薄膜理化性能和热性能的影响。此外,通过初步的细胞培养研究,分析了明胶膜中CO对细胞活力和细胞迁移的影响。当将表面活性剂3%(v/w)吐温80掺入20%(w/w)增塑明胶成膜溶液中时,在膜中获得10%(w/w)CO的均匀分散。通过扫描电子显微镜分析,通过相分离观察了CO对明胶基薄膜的影响。不含CO、GE膜的明胶膜的吸水性;和10%(w/w)CO掺入的GE膜GE-CO在水中3小时后分别为320%和210%。傅立叶变换红外光谱分析表明,在GE-CO薄膜中,CO的甘油三酯成分和明胶NH基团之间的氢键增加。差示扫描量热法结果表明,由于GE-CO薄膜的类熔体转变温度和熔融焓的增加,GE-CO膜的结构更加有序。通过XTT测定评估,CO含量也增加了细胞活力,因为当L929细胞培养物与5–100μg ml−1的GE-CO孵育时,细胞活力约为100%。此外,在5–25μg ml−1浓度范围内的GE-CO样品增加了L929细胞的增殖,因为细胞活力显著高于100%活力的细胞培养对照(P<0.05),这也是有效愈合的指标。然而,GE在100–10μg ml−1浓度范围内显著降低L929细胞的活力(P<0.05),在100、75和50μg ml–1浓度下具有毒性,降低了细胞活力的50%。评估体外伤口愈合的划痕试验显示,细胞在24小时后向划痕迁移,这仅在GE-CO样品中表明伤口愈合。这项研究表明,CO可以有效地添加到明胶基薄膜中,用于制备初级伤口敷料生物材料,该生物材料也被证明对轻微伤口具有良好的伤口愈合效果。
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Production and characterization of a coconut oil incorporated gelatin-based film and its potential biomedical application
The influence of coconut oil (CO) on a gelatin-based film was investigated when used as a potential wound dressing material. There is limited study on CO in protein-based wound dressing materials. Therefore, in this study a self-supporting, continuous and homogenous CO incorporated gelatin-based film was formulated and obtained by solution casting method. The influence of CO on physicochemical and thermal properties of gelatin-based film was also determined. Moreover, the effect CO in gelatin films on cell viability and cell migration was analysed with a preliminary cell culture study. Homogenous dispersion of 10% (w/w) CO was obtained in films when 3% (v/w) Tween 80, a surfactant, was incorporated to 20% (w/w) plasticized gelatin film forming solution. Effect of CO on gelatin-based film was observed via phase separation by scanning electron microscopy analysis. Water uptake of gelatin film with no CO, GE film; and 10% (w/w) CO incorporated GE film, GE-CO, were 320% and 210%, respectively, after 3 h in water. Fourier transform infrared spectroscopy analysis showed triglyceride component of CO and increased hydrogen bonding between NH groups of gelatin in GE-CO films. Differential scanning calorimetry results suggested a more ordered structure of GE-CO film due to an increase in melt-like transition temperature and melting enthalpy of GE-CO film. CO content also increased cell viability, assessed by XTT assay since cell viability was approximately 100% when L929 cell culture was incubated with GE-CO of 5–100 μg ml−1. Moreover, GE-CO samples within 5–25 μg ml−1 concentration range, increased proliferation of L929 cells since cell viability was significantly higher than the 100% viable cell culture control (P < 0.05) which is also an indication of efficient healing. However, GE decreased viability of L929 cells significantly at 100–10 μg ml−1 concentration range (P < 0.05) and were toxic at concentrations of 100, 75 and 50 μg ml−1 which decreased ∼50% of the viability of the cells. Scratch Assay to assess in vitro wound healing showed cell migration towards scratch after 24 h as an indication of wound healing only in GE-CO samples. This study showed that, CO could efficiently be added to gelatin-based films for preparation of a primary wound dressing biomaterial which is also demonstrated to have a promising wound healing effect for minor wounds.
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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