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A Comparison of Chitosan Adhesion to KOH and H2O2 Pre-Treated Electrospun Poly(3-Hydroxybutyrate) Nanofibers 壳聚糖与KOH和H2O2预处理静电纺丝聚3-羟基丁酸酯纳米纤维的黏附比较
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-26 DOI: 10.3390/fib11110091
Yansheng Zhou, Daqing Li, Xin Li, Ying Li, Bing Li, Fenglei Zhou
Chitosan coatings could effectively increase the biostability and biocompatibility of biomaterials while maintaining their structural integrity. In this study, electrospun fibrous polyhydroxybutyrate (PHB) membranes were pre-treated with potassium hydroxide (KOH) or hydrogen peroxide (H2O2) and then modified with dopamine (DA) and glutaraldehyde (GA) to improve their adhesion with chitosan (CS). Scanning electron microscopy (SEM), water contact angles (WCA), and Fourier transform infrared spectroscopy (FTIR) were used to demonstrate the successful generation of DA and GA-modified PHB fibers. KOH pre-treated PHB membranes exhibited superior binding efficiency with CS at low concentrations compared to their H2O2 pre-treated counterparts. The thermal analysis demonstrated a considerable decrease in the degradation temperature and crystallinity of KOH pre-treated membranes, with temperatures dropping from 309 °C to 265.5 °C and crystallinity reducing from 100% to 25.59% as CS concentration increased from 0 to 2 w/v%. In comparison, H2O2 pre-treated membranes experienced a mild reduction in degradation temperature, from 309 °C to 284.4 °C, and a large decrease in crystallinity from 100% to 43%. UV-vis analysis using Cibacron Brilliant Red 3B-A dye (CBR) indicated similar binding efficiencies at low CS concentrations for both pre-treatments, but decreased stability at higher concentrations for KOH pre-treated membranes. Mechanical testing revealed a considerable increase in Young’s modulus (2 to 14%), toughness (31 to 60%), and ultimate tensile stress (UTS) (14 to 63%) for KOH-treated membranes compared with H2O2 pre-treated membranes as CS concentration increased from 0 to 2 w/v%.
壳聚糖涂层可以有效提高生物材料的生物稳定性和生物相容性,同时保持生物材料的结构完整性。本研究采用氢氧化钾(KOH)或过氧化氢(H2O2)对电纺丝纤维聚羟基丁酸酯(PHB)膜进行预处理,然后用多巴胺(DA)和戊二醛(GA)对其进行改性,以提高其与壳聚糖(CS)的粘附性。利用扫描电镜(SEM)、水接触角(WCA)和傅里叶变换红外光谱(FTIR)验证了DA和ga改性PHB纤维的成功生成。与H2O2预处理的PHB膜相比,KOH预处理的PHB膜在低浓度下与CS的结合效率更高。热分析表明,当CS浓度从0 w/v%增加到2 w/v%时,KOH预处理膜的降解温度和结晶度明显降低,温度从309°C下降到265.5°C,结晶度从100%下降到25.59%。相比之下,H2O2预处理膜的降解温度从309°C轻微降低到284.4°C,结晶度从100%大幅降低到43%。使用Cibacron Brilliant Red 3B-A染料(CBR)进行紫外-可见分析表明,两种预处理方法在低CS浓度下的结合效率相似,但在高浓度KOH预处理膜的稳定性降低。力学测试表明,当CS浓度从0 w/v%增加到2 w/v%时,与H2O2预处理膜相比,koh处理膜的杨氏模量(2 ~ 14%)、韧性(31 ~ 60%)和极限拉伸应力(UTS)(14 ~ 63%)显著增加。
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引用次数: 0
Next-Generation Cellulosic Filaments from Hemp Pulp via Dry-Jet Wet Spinning Using HighPerCell® Technology 使用HighPerCell®技术通过干喷湿纺丝从大麻浆中提取新一代纤维细丝
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-26 DOI: 10.3390/fib11110090
Antje Ota, Marc Philip Vocht, Ronald Beyer, Anne Reboux, Charles Reboux, Frank Hermanutz
Fiber demand of cellulosic fibers is rapidly increasing; however, these fibers are mainly based on the use of wood pulp (WP), which often have long transport times and, consequently, a high CO2 footprint. So, alternative pulps based on non-wood, annual fast-growing plants are an option to cover the demand for raw materials and resources. Herein, we report on the use of a novel developed hemp pulp (HP) for man-made cellulosic fiber filament spinning. Commercial WP was used as a reference material. While HP could be used and directly spun as received without any further pretreatment, an additional step to adjust the degree of polymerization (DP) was needed to use the wood pulp. Continuous filaments were spun using a novel dry-jet wet spinning (HighPerCell® process) technique, which is based on the use of 1-ethyl-3-methylimidazolium octanoate ([C2C1im][Oc]) as a solvent. Via this approach, several thousand meters (12,000 m–15,000 m) of continuous multifilament filaments were spun. The HP pulps showed excellent spinning performance. The novel approach allows the preparation of cellulosic fibers for either technical—with high tensile strength—or textile—possessing a low fibrillation tendency—applications. Textile hemp-based filaments were used for first weaving trials, resulting in a flawless fabric.
纤维素纤维的需求量正在迅速增加;然而,这些纤维主要是基于使用木浆(WP),这往往有很长的运输时间,因此,高二氧化碳足迹。因此,基于非木材、一年生快速生长植物的替代纸浆是满足原材料和资源需求的一种选择。在此,我们报告了一种新开发的大麻浆(HP)用于人造纤维素纤维长丝纺丝。以商用WP作为参考材料。虽然HP可以直接使用,不需要任何进一步的预处理,但要使用木浆需要额外的步骤来调整聚合度(DP)。以1-乙基-3-甲基咪唑辛酸盐([C2C1im][Oc])为溶剂,采用一种新型干喷湿纺(HighPerCell®工艺)技术纺出连续长丝。通过这种方法,可以纺出数千米(12,000 - 15,000米)的连续多丝细丝。HP浆具有良好的纺丝性能。这种新方法可以制备纤维纤维,用于高拉伸强度的技术或具有低纤维性倾向的纺织品。纺织麻基长丝被用于第一次编织试验,结果是一个完美的织物。
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引用次数: 0
Optimization and Dispersion Tailoring of Chalcogenide M-Type Fibers Using a Modified Genetic Algorithm 基于改进遗传算法的硫族m型纤维优化与色散裁剪
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-24 DOI: 10.3390/fib11110089
Nikolay I. Salnikov, Alexey V. Andrianov, Elena A. Anashkina
M-type optical fibers in which a core is surrounded by a thin ring layer with a higher refractive index have attracted increasing attention in recent years. One of their advantageous features is the ability to operate a non-fundamental LP02 mode possessing unusual dispersion properties, namely, a zero-dispersion wavelength (ZDW) shifted to the short wavelength region relative to the material ZDW. The LP02 mode can be selectively excited since it is predominantly localized near the core, while the fundamental LP01 and other higher modes are localized near the ring (for proper fiber parameters). In this paper, we present a comprehensive theoretical analysis of effective dispersion tailoring for the HE12 mode of highly nonlinear chalcogenide glass fibers (for which the LP mode approximation fails due to large refractive index contrasts). We demonstrate fiber designs for which ZDWs can be shifted to the spectral region < 2 μm, which is of great interest for the development of mid-IR supercontinuum sources and frequency-tunable pulse sources with standard near-IR pumping. We obtained the characteristic equation and solved it numerically to find mode fields and dispersion characteristics. We show the possibility of achieving dispersion characteristics of the HE12 mode with one, two, three, and four ZDWs in the wavelength range of 1.5–5.5 μm. We used a modified genetic algorithm (MGA) to design fibers with desired dispersion parameters. In particular, by applying an MGA, we optimized four fiber parameters and constructed a fiber for which HE12 mode dispersion is anomalous in the 1.735–5.155 μm range.
m型光纤是一种纤芯外包有高折射率薄环层的光纤,近年来受到越来越多的关注。它们的优势之一是能够操作具有不同寻常色散特性的非基态LP02模式,即零色散波长(ZDW)相对于材料ZDW转移到短波长区域。LP02模式可以被选择性地激发,因为它主要定位在核心附近,而基本的LP01和其他更高的模式定位在环附近(为了适当的光纤参数)。在本文中,我们提出了一个全面的理论分析,有效色散裁剪的HE12模式的高度非线性硫系玻璃纤维(LP模式近似失败,由于大折射率对比)。我们演示了可以将zdw转移到光谱区域的光纤设计<这对于开发中红外超连续谱源和标准近红外泵浦频率可调脉冲源具有重要意义。得到了特征方程,并对其进行了数值求解,得到了模场和色散特性。我们展示了在1.5-5.5 μm波长范围内使用1、2、3和4个zdw实现HE12模式色散特性的可能性。我们使用改进的遗传算法(MGA)来设计具有理想色散参数的纤维。特别地,我们利用MGA优化了4个光纤参数,构建了在1.735 ~ 5.155 μm范围内HE12模色散异常的光纤。
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引用次数: 0
The Natural Growth of CaCO3 Crystals on Hemp Yarns: A Morphology Analysis and the Mechanical Effects on Composites CaCO3晶体在大麻纱线上的自然生长:形态分析及其对复合材料的力学影响
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-20 DOI: 10.3390/fib11100088
Quentin Drouhet, Romain Barbière, Fabienne Touchard, Laurence Chocinski-Arnault, David Mellier
Plant fibres are promising candidates to replace synthetic fibres in polymer matrix composites. However, there is still an important issue to overcome: the poor quality of adhesion at the fibre/matrix interface. Many surface treatments of plant fibres have been developed, most of them based on non-environmentally friendly processes. In this paper, a 100% natural treatment is proposed. Hemp yarns are immersed in tap water until the natural growth of limestone beads attached to their surface occurs. The morphology analysis reveals that these calcium carbonate crystals have a nanoneedle architecture, with hemp fibres acting as nucleators for these highly ordered coral-like structures. Tensile tests on ±45° woven hemp/epoxy composites show that the presence of CaCO3 beads improves the adhesion quality of the fibre/matrix interface and, therefore, increases Young’s modulus value.
植物纤维是替代合成纤维在聚合物基复合材料中的应用前景广阔。然而,仍然有一个重要的问题需要克服:纤维/基质界面的粘附质量差。已经开发了许多植物纤维的表面处理方法,其中大多数是基于非环境友好的工艺。本文提出了一种100%自然处理方法。大麻纱线浸泡在自来水中,直到附着在其表面的石灰石珠自然生长。形态学分析表明,这些碳酸钙晶体具有纳米针状结构,大麻纤维充当这些高度有序的珊瑚状结构的成核剂。对±45°编织麻/环氧复合材料的拉伸试验表明,CaCO3珠的存在改善了纤维/基体界面的粘附质量,从而提高了杨氏模量值。
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引用次数: 0
Conversion of Animal-Derived Protein By-Products into a New Dual-Layer Nanofiber Biomaterial by Electrospinning Process 静电纺丝法将动物源性蛋白质副产品转化为新型双层纳米纤维生物材料
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-14 DOI: 10.3390/fib11100087
Carmen Gaidău, Maria Râpă, Laura Mihaela Stefan, Ecaterina Matei, Andrei Constantin Berbecaru, Cristian Predescu, Liliana Mititelu-Tartau
The aim of this study was to design a dual-layer wound dressing as a new fibrous biomaterial based on the valorization of animal-derived proteins. The first layer was fabricated by the deposition of poly(ethylene oxide) (PEO) loaded with keratin hydrolysate (KH) via a mono-electrospinning process onto a poly(lactic acid) (PLA) film, which was used as a support. The second layer consisted of encapsulating a bovine collagen hydrolysate (CH) into poly(vinyl pyrrolidone) (PVP) through a coaxial electrospinning process, which was added onto the previous layer. This assemblage was characterized by electronic microscopy for morphology and the controlled release of KH. In vitro biocompatibility was evaluated on the L929 (NCTC) murine fibroblasts using quantitative MTT assay and qualitative cell morphological examination after Giemsa staining. Additionally, in vivo biocompatibility methods were used to assess the impact of the biomaterial on white Swiss mice, including the evaluation of hematological, biochemical, and immunological profiles, as well as its impact on oxidative stress. The results revealed a nanofibrous structure for each layer, and the assembled product demonstrated antioxidant activity, controlled release of KH, a high degree of in vitro biocompatibility, negligible hematological and biochemical changes, and minimal impact of certain specific oxidative stress parameters compared to the use of patches with textile support.
本研究的目的是设计一种基于动物源性蛋白增值的双层伤口敷料作为新型纤维生物材料。第一层是通过单静电纺丝工艺将负载角蛋白水解物(KH)的聚环氧乙烷(PEO)沉积在聚乳酸(PLA)薄膜上,并将其作为支撑材料。第二层是通过同轴静电纺丝工艺将牛胶原蛋白水解物(CH)封装到聚乙烯基吡咯烷酮(PVP)中,并将其添加到前一层。用电子显微镜观察了该组合的形态和KH的控释。采用定量MTT法和吉姆萨染色后的定性细胞形态学检查评价L929 (NCTC)小鼠成纤维细胞的体外生物相容性。此外,采用体内生物相容性方法评估生物材料对瑞士白小鼠的影响,包括血液学、生化和免疫学特征的评估,以及对氧化应激的影响。结果显示,每一层都具有纳米纤维结构,组装后的产品具有抗氧化活性,KH释放可控,体外生物相容性高,血液和生化变化可忽略不计,并且与使用带有纺织品支撑的贴片相比,某些特定氧化应激参数的影响最小。
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引用次数: 0
Optimization of the Alkali-Silane Treatment of Agave lechuguilla Fibers (Ixtle) for Potential Reinforcement in Polymeric Composites 龙舌兰纤维碱硅烷处理在聚合物复合材料中增强性能的优化
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-13 DOI: 10.3390/fib11100086
Noemi Jardon-Maximino, Mariamne Dehonor Gómez, Rolando Villa Moreno, M. D. Baeza-Alvarado, Luis Edmundo Lugo Uribe
Reinforced polymeric composites with natural fibers have garnered significant interest in recent years due to the need for biomass utilization and the requirements of various industries, such as automotive and construction. Among these natural fibers, Agave lechuguilla fiber, commonly known as ixtle (FIx) or Tampico fiber, exhibits important characteristics such as length, high strength, and durability. However, there is limited literature on its conditioning, functionalization, and utilization as a reinforcing material in polymeric composites (CP). This study presents the optimization of the alkali-silane treatment of FIx, identifying the most suitable reaction conditions to enhance their thermal stability, tensile strength, and silane coupling agent (ACSi) grafting on the fiber surface. The chemical treatment with ACSi proved highly effective, resulting in a significant grafting content, which was confirmed through FTIR and SEM–EDS analyses. The high level of functionalization did not compromise the mechanical performance of the fibers, suggesting that functionalized FIx holds great potential as a reinforcing material in CP. These findings open new paths for the sustainable use of Agave lechuguilla fibers, contributing to the development of environmentally friendly and high-performance polymeric composites in various industrial applications.
近年来,由于生物质利用的需要以及汽车和建筑等各个行业的要求,天然纤维增强聚合物复合材料引起了人们的极大兴趣。在这些天然纤维中,龙舌兰纤维,通常被称为ixtle (FIx)或Tampico纤维,具有长度、高强度和耐用性等重要特性。然而,关于其调节、功能化和作为增强材料在聚合物复合材料(CP)中的应用的文献有限。本研究对FIx的碱-硅烷处理进行了优化,确定了最合适的反应条件,以提高其热稳定性、抗拉强度,并在纤维表面接枝硅烷偶联剂(ACSi)。经FTIR和SEM-EDS分析证实,ACSi化学处理非常有效,接枝含量显著。这些发现为龙舌兰纤维的可持续利用开辟了新的途径,有助于在各种工业应用中开发环保型和高性能的聚合物复合材料。
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引用次数: 0
Optimization of Polyvinyl Alcohol-Based Electrospun Fibers with Bioactive or Electroconductive Phases for Tissue-Engineered Scaffolds 具有生物活性或导电相的聚乙烯醇基静电纺丝纤维用于组织工程支架的优化
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-12 DOI: 10.3390/fib11100085
Zeynep Renkler, Iriczalli Cruz Maya, Vincenzo Guarino
The accurate mimicking of the fibrillary structure of the extracellular matrix represents one of the critical aspects of tissue engineering, playing a significant role in cell behavior and functions during the regenerative process. This work proposed the design of PVA-based multi-component membranes as a valuable and highly versatile strategy to support in vitro regeneration of different tissues. PVA can be successfully processed through electrospinning processes, allowing for the integration of other organic/inorganic materials suitable to confer additive bio-functional properties to the fibers to improve their biological response. It was demonstrated that adding polyethylene oxide (PEO) improves fiber processability; moreover, SEM analyses confirmed that blending PVA with PEO or gelatin enables the reduction of fiber size from 1.527 ± 0.66 μm to 0.880 ± 0.30 μm and 0.938 ± 0.245 μm, respectively, also minimizing defect formation. Furthermore, in vitro tests confirmed that gelatin integration allows the formation of bioactive nanofibers with improved biological response in terms of L929 adhesion and proliferation. Lastly, the processability of PVA fibers with conductive phases such as polyvinylpyrrolidone (PVP) or poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) has also been verified. From this perspective, they could be promisingly used to design electroactive composite fibers able to support the regeneration process of electrically stimulated tissues such as nerves or muscles.
准确模拟细胞外基质的原纤维结构是组织工程的一个重要方面,在再生过程中对细胞行为和功能起着重要作用。这项工作提出了pva基多组分膜的设计作为一个有价值的和高度通用的策略来支持不同组织的体外再生。PVA可以通过静电纺丝工艺成功加工,允许其他有机/无机材料的整合,以赋予纤维添加剂的生物功能特性,以改善其生物反应。结果表明,聚乙烯氧化物(PEO)的加入提高了纤维的加工性能;此外,SEM分析证实,PVA与PEO或明胶共混可使纤维尺寸分别从1.527±0.66 μm减小到0.880±0.30 μm和0.938±0.245 μm,也最大限度地减少了缺陷的形成。此外,体外试验证实,明胶整合可以形成具有生物活性的纳米纤维,在L929粘附和增殖方面具有更好的生物反应。最后,还验证了导电相如聚乙烯吡罗烷酮(PVP)或聚(3,4-乙烯二氧噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)的PVA纤维的可加工性。从这个角度来看,它们有望用于设计电活性复合纤维,能够支持电刺激组织(如神经或肌肉)的再生过程。
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引用次数: 0
Numerical Analysis of Dual-Wavelength Tungsten-Tellurite Fiber Raman Lasers with Controllable Mode Switching 可控模式切换双波长钨碲光纤拉曼激光器的数值分析
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-10 DOI: 10.3390/fib11100084
Elena A. Anashkina, Alexey V. Andrianov
Fiber laser sources in the spectral range near 1.7–1.8 μm are in highly demand for a lot of applications. We propose and theoretically investigate a dual-wavelength switchable Raman tungsten-tellurite fiber laser in the 1.7–1.8 µm range which can produce two stable modes at frequencies separated by ~7 THz with a pump at 1.55 µm. The Raman waves shifted by 19.8 THz (mode 1) and 27.5 THz (mode 2) from the pump frequency can be generated near two different maxima of the Raman gain spectrum (gain is higher at 19.8 THz and twice lower at 27.5 THz). We numerically simulate two-mode Raman lasing with allowance for energy transfer from the pump wave to modes 1 and 2, and from mode 1 to mode 2 due to inelastic Raman scattering. Diagrams of generation regimes depending on system parameters are constructed. We demonstrate controlled switching between two modes by changing the pump power. For the same intracavity losses for both Raman modes at relatively low pump powers, only mode 1 is generated. At medium pump power, generation occurs simultaneously in both modes. At relatively high pump power, only mode 2 is generated near the weaker maximum. This effect seems surprising, but a rigorous explanation with allowance for the nonlinear interaction between mode 1 and mode 2 is found. When losses for one of the modes change, switching of the generated regimes is also predicted.
在1.7 ~ 1.8 μm光谱范围内的光纤激光光源有着广泛的应用需求。我们提出并从理论上研究了在1.7 ~ 1.8µm范围内的双波长可切换的钨碲光纤激光器,该激光器在1.55µm的泵浦下,可以在间隔约7太赫兹的频率下产生两个稳定模式。从泵浦频率位移19.8太赫兹(模式1)和27.5太赫兹(模式2)的拉曼波可以在拉曼增益谱的两个不同最大值附近产生(增益在19.8太赫兹时更高,在27.5太赫兹时低两倍)。我们对双模拉曼激光进行了数值模拟,考虑了泵浦波到模式1和模式2的能量传递,以及由于非弹性拉曼散射从模式1到模式2的能量传递。构造了随系统参数变化的发电状态图。我们演示了通过改变泵的功率来控制两种模式之间的切换。在相对较低的泵浦功率下,两种拉曼模式的腔内损耗相同,只产生模1。在中等泵功率时,两种模式同时发电。在较高的泵功率下,在较弱的最大值附近只产生模态2。这种效应似乎令人惊讶,但考虑到模式1和模式2之间的非线性相互作用,发现了一个严格的解释。当其中一个模态的损耗发生变化时,还可以预测产生的状态的切换。
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引用次数: 0
Overcoming Challenges and Limitations Regarding the Atomic Force Microscopy Imaging and Mechanical Characterization of Nanofibers 克服纳米纤维原子力显微镜成像和力学表征的挑战和局限性
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-10-09 DOI: 10.3390/fib11100083
Stylianos Vasileios Kontomaris, Andreas Stylianou, Georgios Chliveros, Anna Malamou
Atomic force microscopy (AFM) is a powerful tool that enables imaging and nanomechanical properties characterization of biological materials. Nanofibers are the structural units of many biological systems and their role in the development of advanced biomaterials is crucial. AFM methods have proven to be effective towards the characterization of fibers with respect to biological and bioengineering applications at the nanoscale. However, both the topographical and mechanical properties’ nanocharacterizations of single fibers using AFM are challenging procedures. In particular, regarding imaging procedures, significant artifacts may arise from tip convolution effects. The geometrical characteristics of the AFM tip and the nanofibers, and the fact that they have similar magnitudes, may lead to significant errors regarding the topographical imaging. In addition, the determination of the mechanical properties of nanofibers is also challenging due to their small dimensions and heterogeneity (i.e., the elastic half-space assumption is not valid in most cases). This review elucidates the origins of errors in characterizing individual nanofibers, while also providing strategies to address limitations in experimental procedures and data processing.
原子力显微镜(AFM)是一种功能强大的工具,可以实现生物材料的成像和纳米力学特性表征。纳米纤维是许多生物系统的结构单元,在先进生物材料的发展中起着至关重要的作用。AFM方法已被证明是有效的表征纤维在纳米尺度上的生物和生物工程应用。然而,利用原子力显微镜对单纤维的形貌和力学性能进行纳米表征是一项具有挑战性的工作。特别是在成像过程中,尖端卷积效应可能会产生明显的伪影。由于AFM针尖和纳米纤维的几何特性,以及它们具有相似的大小,这可能会导致形貌成像的显著误差。此外,由于纳米纤维的小尺寸和非均质性(即弹性半空间假设在大多数情况下不成立),其力学性能的测定也具有挑战性。这篇综述阐明了表征单个纳米纤维错误的起源,同时也提供了解决实验程序和数据处理限制的策略。
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引用次数: 0
Preparation and Characterization of Poliglecaprone-Incorporated Polycaprolactone Composite Fibrous Scaffolds 聚己内酯复合纤维支架的制备与表征
Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2023-09-25 DOI: 10.3390/fib11100082
Felix Tettey, Jaclynn Siler-Dearring, Alexis Moody, Narayan Bhattarai
Electrospun fibrous scaffolds made from polymers such as polycaprolactone (PCL) have been used in drug delivery and tissue engineering for their viscoelasticity, biocompatibility, biodegradability, and tunability. Hydrophobicity and the prolonged degradation of PCL causes inhibition of the natural tissue-remodeling processes. Poliglecaprone (PGC), which consists of PCL and Poly (glycolic acid) (PGA), has better mechanical properties and a shorter degradation time compared to PCL. A blend between PCL and PGC called PPG can give enhanced shared properties for biomedical applications. In this study, we fabricated a blend of PCL and PGC nanofibrous scaffold (PPG) at different ratios of PGC utilizing electrospinning. We studied the physicochemical and biological properties, such as morphology, crystallinity, surface wettability, degradation, surface functionalization, and cellular compatibility. All PPG scaffolds exhibited good uniformity in fiber morphology and improved mechanical properties. The surface wettability and degradation studies confirmed that increasing PGC in the PPG composites increased hydrophilicity and scaffold degradation respectively. Cell viability and cytotoxicity results showed that the scaffold with PGC was more viable and less toxic than the PCL-only scaffolds. PPG fibers were successfully coated with polydopamine (PDA) and collagen to improve degradation, biocompatibility, and bioactivity. The nanofibrous scaffolds synthesized in this study can be utilized for tissue engineering applications such as for regeneration of human articular cartilage regeneration and soft bones.
由聚己内酯(PCL)等聚合物制成的电纺丝纤维支架因其粘弹性、生物相容性、生物可降解性和可调性而被用于药物输送和组织工程。PCL的疏水性和长期降解导致自然组织重塑过程的抑制。聚己甲醚(PGC)是由聚己甲醚(PCL)和聚乙醇酸(PGA)组成,与PCL相比具有更好的力学性能和更短的降解时间。PCL和PGC的混合物称为PPG,可以为生物医学应用提供增强的共享特性。在本研究中,我们利用静电纺丝技术制备了PCL和PGC在不同比例下的共混纳米纤维支架(PPG)。我们研究了其物理化学和生物特性,如形态、结晶度、表面润湿性、降解、表面功能化和细胞相容性。所有PPG支架均表现出良好的纤维形态均匀性和力学性能的改善。表面润湿性和降解研究证实,PPG复合材料中PGC的增加分别提高了亲水性和支架降解能力。细胞活力和细胞毒性结果表明,含PGC的支架比仅含pcl的支架更有活力,毒性更小。PPG纤维成功地包被聚多巴胺(PDA)和胶原蛋白,以改善降解,生物相容性和生物活性。本研究合成的纳米纤维支架可用于人体关节软骨再生和软骨再生等组织工程应用。
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引用次数: 0
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