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Gel dressing based on type I collagen modified with oligourethane and silica for skin wound healing 基于低聚氨基甲酸酯和二氧化硅修饰的I型胶原凝胶敷料用于皮肤伤口愈合
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-28 DOI: 10.1088/1748-605X/ac6b70
Pedro U Muñoz-González, M. C. Lona-Ramos, L. D. Gutiérrez-Verdín, Guadalupe H Luévano-Colmenero, F. Tenorio-Rocha, R. García-Contreras, G. González-García, A. Rosillo-de la Torre, Jorge Delgado, L. Castellano, B. Mendoza-Novelo
Cutaneous wound healing is a complex process that leads the skin reparation with the formation of scar tissue that typically lacks skin appendages. This fact drives us to find new strategies to improve regenerative healing of the skin. This study outlines, the contribution of colloidal silica particles and oligourethane crosslinking on the collagen material properties and the effect on skin wound healing in rats. We characterized the gel properties that are key for in-situ gelation, which is accomplished by the latent reactivity of oligourethane bearing blocked isocyanate groups to crosslink collagen while entrapping silica particles. The swelling/degradation behavior and the elastic modulus of the composite gel were consistent with the modification of collagen type I with oligourethane and silica. On the other hand, these gels were characterized as scaffold for murine macrophages and human stem cells. The application of a composite gel dressing on cutaneous wounds showed a histological appearance of the recovered skin as intact skin; featured by the epidermis, hair follicles, sebaceous glands, subcutaneous adipose layer, and dermis. The results suggest that the collagen-based composite dressings are promising modulators in skin wound healing to achieve a regenerative skin closure with satisfactory functional and aesthetic scars.
皮肤伤口愈合是一个复杂的过程,导致皮肤修复,形成通常缺乏皮肤附属物的疤痕组织。这一事实促使我们寻找新的策略来改善皮肤的再生愈合。本研究概述了胶体二氧化硅颗粒和低聚氨基甲酸酯交联对大鼠胶原材料性能的贡献以及对皮肤伤口愈合的影响。我们表征了原位凝胶化的关键凝胶性质,这是通过含有封闭异氰酸酯基团的低聚氨基甲酸酯在包埋二氧化硅颗粒的同时与胶原交联的潜在反应性来实现的。复合凝胶的溶胀/降解行为和弹性模量与低聚氨基甲酸酯和二氧化硅对I型胶原的改性一致。另一方面,这些凝胶被表征为小鼠巨噬细胞和人类干细胞的支架。复合凝胶敷料在皮肤伤口上的应用显示了恢复的皮肤作为完整皮肤的组织学外观;以表皮、毛囊、皮脂腺、皮下脂肪层和真皮为特征。结果表明,基于胶原的复合敷料是皮肤伤口愈合中有前途的调节剂,可实现再生皮肤闭合,并具有令人满意的功能和美学疤痕。
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引用次数: 5
A simple and scalable 3D printing methodology for generating aligned and extended human and murine skeletal muscle tissues 一种简单且可扩展的3D打印方法,用于生成对齐和扩展的人类和小鼠骨骼肌组织
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-28 DOI: 10.1088/1748-605X/ac6b71
S. Çakal, Carmen Radeke, Juan F Alcala, D. Ellman, Sarkhan Butdayev, D. C. Andersen, K. Calloe, Johan U. Lind
Preclinical biomedical and pharmaceutical research on disease causes, drug targets, and side effects increasingly relies on in vitro models of human tissue. 3D printing offers unique opportunities for generating models of superior physiological accuracy, as well as for automating their fabrication. Towards these goals, we here describe a simple and scalable methodology for generating physiologically relevant models of skeletal muscle. Our approach relies on dual-material micro-extrusion of two types of gelatin hydrogel into patterned soft substrates with locally alternating stiffness. We identify minimally complex patterns capable of guiding the large-scale self-assembly of aligned, extended, and contractile human and murine skeletal myotubes. Interestingly, we find high-resolution patterning is not required, as even patterns with feature sizes of several hundred micrometers is sufficient. Consequently, the procedure is rapid and compatible with any low-cost extrusion-based 3D printer. The generated myotubes easily span several millimeters, and various myotube patterns can be generated in a predictable and reproducible manner. The compliant nature and adjustable thickness of the hydrogel substrates, serves to enable extended culture of contractile myotubes. The method is further readily compatible with standard cell-culturing platforms as well as commercially available electrodes for electrically induced exercise and monitoring of the myotubes.
关于病因、药物靶点和副作用的临床前生物医学和药物研究越来越依赖于人体组织的体外模型。3D打印为生成具有卓越生理精度的模型以及自动化其制造提供了独特的机会。为了实现这些目标,我们在这里描述了一种简单且可扩展的方法,用于生成骨骼肌的生理相关模型。我们的方法依赖于两种类型的明胶水凝胶的双材料微挤出到具有局部交替刚度的图案化软基底中。我们确定了能够引导对齐、延伸和收缩的人类和小鼠骨骼肌管的大规模自组装的最小复杂模式。有趣的是,我们发现不需要高分辨率的图案化,因为即使是具有几百微米特征尺寸的图案也足够了。因此,该过程是快速的,并且与任何低成本的基于挤出的3D打印机兼容。生成的肌管很容易跨越几毫米,并且可以以可预测和可重复的方式生成各种肌管图案。水凝胶基质的顺应性和可调节的厚度有助于延长可收缩肌管的培养。该方法还容易与标准细胞培养平台以及用于电诱导运动和监测肌管的市售电极兼容。
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引用次数: 3
Advances in digital light processing of hydrogels 水凝胶数字光处理研究进展
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-27 DOI: 10.1088/1748-605X/ac6b04
Xingwu Mo, Liliang Ouyang, Zhuo Xiong, Ting Zhang
Hydrogels, three-dimensional (3D) networks of hydrophilic polymers formed in water, are a significant type of soft matter used in fundamental and applied sciences. Hydrogels are of particular interest for biomedical applications, owing to their soft elasticity and good biocompatibility. However, the high water content and soft nature of hydrogels often make it difficult to process them into desirable solid forms. The development of 3D printing (3DP) technologies has provided opportunities for the manufacturing of hydrogels, by adopting a freeform fabrication method. Owing to its high printing speed and resolution, vat photopolymerization 3DP has recently attracted considerable interest for hydrogel fabrication, with digital light processing (DLP) becoming a widespread representative technique. Whilst acknowledging that other types of vat photopolymerization 3DP have also been applied for this purpose, we here only focus on DLP and its derivatives. In this review, we first comprehensively outline the most recent advances in both materials and fabrication, including the adaptation of novel hydrogel systems and advances in processing (e.g. volumetric printing and multimaterial integration). Secondly, we summarize the applications of hydrogel DLP, including regenerative medicine, functional microdevices, and soft robotics. To the best of our knowledge, this is the first time that either of these specific review focuses has been adopted in the literature. More importantly, we discuss the major challenges associated with hydrogel DLP and provide our perspectives on future trends. To summarize, this review aims to aid and inspire other researchers investigatng DLP, photocurable hydrogels, and the research fields related to them.
水凝胶是在水中形成的亲水性聚合物的三维(3D)网络,是一种重要的软物质类型,用于基础科学和应用科学。水凝胶由于其柔软的弹性和良好的生物相容性,在生物医学应用中具有特别的意义。然而,水凝胶的高含水量和软性质往往使其难以加工成理想的固体形式。3D打印(3DP)技术的发展为水凝胶的制造提供了机会,采用了一种自由形状的制造方法。由于其高打印速度和分辨率,还原光聚合3d打印最近引起了水凝胶制造的极大兴趣,数字光处理(DLP)成为一种广泛的代表性技术。虽然承认其他类型的还原光聚合3DP也已用于此目的,但我们在这里只关注DLP及其衍生物。在这篇综述中,我们首先全面概述了材料和制造方面的最新进展,包括新型水凝胶系统的适应和加工方面的进展(例如体积打印和多材料集成)。其次,总结了水凝胶DLP在再生医学、功能微器件、软机器人等领域的应用。据我们所知,这是第一次在文献中采用这两种特定的综述焦点。更重要的是,我们讨论了与水凝胶DLP相关的主要挑战,并提供了我们对未来趋势的看法。综上所述,本文旨在帮助和启发其他研究DLP、光固化水凝胶及其相关研究领域的研究人员。
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引用次数: 5
The additive effects of photobiomodulation and bioactive glasses on enhancing early angiogenesis 光生物调节剂和生物活性玻璃对促进早期血管生成的叠加效应
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-27 DOI: 10.1088/1748-605X/ac6b07
Lidong Huang, W. Gong, Gui-qin Huang, Jingyi Li, Jilin Wu, Yuguang Wang, Yanmei Dong
Bioactive glasses (BG) have been widely utilized as a biomaterial for bone repair. However, the early angiogenesis of BG may be inadequate, which weakens its osteogenic effects in large-sized bone defects and often leads to the failure of bone regeneration. In this study, we explored the effects of photobiomodulation (PBM) combined with BG on early angiogenesis to solve this bottleneck problem of insufficient early angiogenesis. In vitro, human umbilical vein endothelial cells (HUVECs) were cultured with BG extracts and treated with PBM using 1 J cm−2. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, real-time reverse transcription-polymerase chain reaction (real-time RT-PCR) and tubule formation assay were utilized to detect HUVECs’ proliferation, vascular growth factor genes expression and tubules formation. In vivo, bone defects at the femoral metaphysis in Sprague-Dawley rats were treated with BG particulates and PBM at 120 J cm−2. Hematoxylin–eosin staining was used to observe the inflammatory response, tissue formation and biomaterial absorption of bone defects. Immunohistochemical staining was applied to observe the vascular-like structure formation. The in vitro results showed that PBM combined with BG significantly promoted HUVECs’ proliferation, genes expression and mature tubules formation. On days 2, 4 and 7, the mRNA expression of VEGF in BG + PBM group was 2.70-, 2.59- and 3.05-fold higher than control (P< 0.05), and significantly higher than PBM and BG groups (P< 0.05). On days 4 and 7, the bFGF gene expression in BG + PBM group was 2.42- and 1.82-fold higher than control (P< 0.05), and also higher than PBM and BG groups (P< 0.05). Tube formation assay showed that mature tubules were formed in BG + PBM and PBM groups after 4 h, and the number in BG + PBM group was significantly higher than other groups (P< 0.05). In vivo results further confirmed PBM induced early angiogenesis, with more vascular-like structures observed in BG + PBM and PBM groups 2 week post-surgery. With the optimum PBM fluence and BG concentration, PBM combined with BG exerted additive effects on enhancing early angiogenesis.
生物活性玻璃(BG)作为一种用于骨修复的生物材料已被广泛应用。然而,BG的早期血管生成可能不足,这削弱了其在大型骨缺损中的成骨作用,并经常导致骨再生失败。在本研究中,我们探讨了光生物调节(PBM)与BG联合对早期血管生成的影响,以解决早期血管生成不足的瓶颈问题。在体外,用BG提取物培养人脐静脉内皮细胞(HUVECs),并用1 J cm−2的PBM处理。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法、实时逆转录聚合酶链式反应(RT-PCR)法和小管形成法检测HUVECs增殖、血管生长因子基因表达和小管形成。在体内,用BG颗粒和PBM在120 J cm−2下处理Sprague-Dawley大鼠股干骺端的骨缺损。苏木精-伊红染色观察骨缺损的炎症反应、组织形成和生物材料吸收。免疫组化染色观察血管样结构的形成。体外实验结果表明,PBM与BG联合应用可显著促进HUVECs的增殖、基因表达和成熟小管的形成。在第2、4和7天,BG+PBM组VEGF的mRNA表达分别是对照组的2.70、2.59和3.05倍(P<0.05),显著高于PBM和BG组(P<0.05),造管实验显示,BG+PBM和PBM组在4h后形成成熟小管,且BG+PBM组的数量明显高于其他组(P<0.05)。体内结果进一步证实了PBM诱导的早期血管生成,术后2周,BG+PDM和PBM两组观察到更多的血管样结构。在最佳PBM注量和BG浓度下,PBM与BG联合对促进早期血管生成具有加性作用。
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引用次数: 1
Exosomes derived from magnesium ion—stimulated macrophages inhibit angiogenesis 镁离子刺激巨噬细胞衍生的外泌体抑制血管生成
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-27 DOI: 10.1088/1748-605X/ac6b03
R. Hang, Xue Tian, Guangping Qu, Yuyu Zhao, Runhua Yao, Yi Zhang, Wenfa Wei, Xiaohong Yao, P. K. Chu
Angiogenesis, an essential prerequisite to osteogenesis in bone repair and regeneration, can be mediated by immunoregulation of macrophages. Magnesium and its alloys are promising biodegradable bone implant materials and can affect immunoregulation of macrophages by the degradation products (magnesium ions). Nevertheless, the mechanism of macrophage-derived exosomes stimulated by Mg ions in immunoregulation is still not well understood. Herein, 10–50 mM magnesium ions are shown to inhibit the macrophage viability and proliferation in a dose-dependent manner, but a high concentration results in macrophage apoptosis. The exosomes secreted by macrophages from magnesium ion stimulation inhibit angiogenesis of endothelial cells, as manifested by the suppressed cell viability, proliferation, migration, and tube formation, which arise at least partially from exosome-mediated downregulation of endothelial nitric oxide and the vascular endothelial growth factor. The findings reported in this paper suggest that the bio-functionality of biodegradable magnesium alloys must be considered from the perspective of immunoregulation of macrophage-derived exosomes. Our results also suggest potential cancer therapy by inhibiting tumor-associated angiogenesis.
血管生成是骨修复和再生成骨的必要前提,可通过巨噬细胞的免疫调节介导。镁及其合金是一种很有前途的生物可降解骨植入材料,其降解产物(镁离子)可以影响巨噬细胞的免疫调节。然而,巨噬细胞源性外泌体在镁离子刺激下的免疫调节机制尚不清楚。在本研究中,10-50 mM镁离子以剂量依赖的方式抑制巨噬细胞的活力和增殖,但高浓度会导致巨噬细胞凋亡。镁离子刺激巨噬细胞分泌的外泌体抑制内皮细胞的血管生成,表现为细胞活力、增殖、迁移和管形成受到抑制,至少部分原因是外泌体介导的内皮一氧化氮和血管内皮生长因子的下调。本文的研究结果表明,必须从巨噬细胞来源的外泌体的免疫调节角度来考虑可生物降解镁合金的生物功能。我们的研究结果还提示通过抑制肿瘤相关血管生成来治疗癌症。
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引用次数: 0
Cellular studies and sustained drug delivery via nanostructures fabricated on 3D printed porous Neovius lattices of Ti6Al4V ELI Ti6Al4V ELI 3D打印多孔Neovius晶格上制备的纳米结构的细胞研究和持续药物递送
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-21 DOI: 10.1088/1748-605X/ac6922
Sonu Singh, Priya Vashisth, V. Meena, D. Kalyanasundaram
Site-specific drug delivery has the potential to reduce drug dosage by 3- to 5-folds. Given the propensity of drugs used in the treatment of tuberculosis and cancers, the increased drug dosages via oral ingestion for several months to a few years of medication is often detrimental to the health of patients. In this study, the sustained delivery of drugs with multiscale structured novel Neovius lattices was achieved. 3D Neovius open cell lattices (NOCL) with porosities of 40%, 45%, and 50% were fabricated layer-by-layer on the laser bed fusion process. Micron-sized Ti6Al4V ELI powder was used for 3D printing. The Young’s modulus achieved from the novel Neovius lattices were in the range of 1.2–1.6 GPa, which is comparable to human cortical bone and helps to improve implant failure due to the stress shielding effect. To provide sustained drug delivery, nanotubes (NTs) were fabricated on NOCLs via high-voltage anodization. The osteogenic agent icariin was loaded onto the NOCL-NT samples and their release profiles were studied for 7 d. A significantly steady and slow release rate of 0.05% per hour of the drug was achieved using NOCL-NT. In addition, the initial burst release of NOCL-NT was 4 fold lower than that of the open-cell lattices without NTs. Cellular studies using MG63 human osteoblast-like cells were performed to determine their biocompatibility and osteogenesis which were analyzed using Calcein AM staining and Alamar Blue after 1, 5, and 7 d. 3D printed NOCL samples with NTs and with Icariin loaded NTs demonstrated a significant increase in cell proliferation as compared to as printed NOCL samples.
位点特异性药物递送有可能将药物剂量减少3-5倍。考虑到用于治疗结核病和癌症的药物的倾向,通过口服几个月到几年的药物来增加药物剂量往往对患者的健康有害。在这项研究中,利用多尺度结构的新型Neovius晶格实现了药物的持续递送。在激光床融合工艺上逐层制备了孔隙率分别为40%、45%和50%的三维Neovius开孔晶格(NOCL)。微米尺寸的Ti6Al4V ELI粉末用于3D打印。新型Neovius晶格实现的杨氏模量在1.2–1.6 GPa范围内,与人类皮质骨相当,有助于改善因应力屏蔽效应而导致的植入失败。为了提供持续的药物递送,通过高压阳极氧化在NOCL上制备了纳米管。将成骨剂icariin加载到NOCL-NT样品上,并对其释放特性进行7天的研究。使用NOCL-NT实现了药物每小时0.05%的显著稳定和缓慢释放率。此外,NOCL-NT的初始爆发释放比没有NT的开放细胞晶格低4倍。使用MG63人成骨细胞样细胞进行细胞研究,以确定其生物相容性和成骨作用,并在1、5和7天后使用Calcein AM染色和Alamar Blue对其进行分析。与打印的NOCL样品相比,具有NT和负载Icariin的NT的3D打印NOCL样品显示细胞增殖显著增加。
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引用次数: 0
MSC-derived sEV-loaded hyaluronan hydrogel promotes scarless skin healing by immunomodulation in a large skin wound model 在大型皮肤伤口模型中,msc衍生的sev负载透明质酸水凝胶通过免疫调节促进无疤痕皮肤愈合
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-20 DOI: 10.1088/1748-605X/ac68bc
Sen Yang, Hua Jiang, Meng Qian, Guangbo Ji, Yongzhen Wei, Ju He, H. Tian, Qiang Zhao
Designing hydrogel-based constructs capable of adjusting immune cell functions holds promise for skin tissue regeneration. Mesenchymal stem cell (MSC)-derived small extracellular vesicles (sEVs) have attracted increasing attention owing to their anti-inflammatory and proangiogenic effects. Herein, we constructed a biofunctional hydrogel in which MSC-derived sEVs were incorporated into the injectable hyaluronic acid hydrogel, thus endowing the hydrogel with immunomodulatory effects. When implanted onto the wound site in a mouse large skin injury model, this functional hydrogel facilitates wound healing and inhibits scar tissue formation by driving macrophages towards an anti-inflammatory and anti-fibrotic (M2c) phenotype. Further investigation showed that the M2c-like phenotype induced by MSC-derived sEVs markedly inhibited the activation of fibroblasts, which could result in scarless skin wound healing. Taken together, these results suggest that modulation of the immune response is a promising and efficient approach to prevent fibrotic scar formation.
设计能够调节免疫细胞功能的水凝胶结构为皮肤组织再生带来了希望。间充质干细胞(MSC)衍生的小细胞外囊泡(sev)因其抗炎和促血管生成的作用而受到越来越多的关注。在此,我们构建了一种生物功能水凝胶,将msc衍生的sev掺入可注射的透明质酸水凝胶中,从而赋予水凝胶免疫调节作用。当植入小鼠大皮肤损伤模型的伤口部位时,这种功能性水凝胶通过驱动巨噬细胞向抗炎和抗纤维化(M2c)表型发展,促进伤口愈合并抑制疤痕组织形成。进一步研究表明,mscs衍生的sev诱导的m2c样表型显著抑制成纤维细胞的激活,从而导致无疤痕皮肤伤口愈合。综上所述,这些结果表明,调节免疫反应是预防纤维化瘢痕形成的一种有希望和有效的方法。
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引用次数: 13
Corrigendum: Osteogenesis effects of strontium-substituted hydroxyapatite coatings on true bone ceramic surfacesin vitroandin vivo(2018Biomed. Mater.13015018). 更正:锶取代的羟基磷灰石涂层在体外和体内真实骨陶瓷表面上的成骨作用(2018 Biomed.Mater.13 015018)
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-19 DOI: 10.1088/1748-605X/ac64de
Jingfeng Li, Liang Yang, Xiaodong Guo, Wei Cui, Shuyi Yang, Jianping Wang, Yanzhen Qu, Zengwu Shao, Shuyun Xu
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引用次数: 0
Synthetic vascular graft with spatially distinct architecture for rapid biomimetic cell organisation in a perfusion bioreactor 具有空间独特结构的合成血管移植物用于灌注生物反应器中的快速仿生细胞组织
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-12 DOI: 10.1088/1748-605X/ac66b2
P. Michael, Nianji Yang, M. Moore, Miguel Santos, Y. Lam, Annabelle Ward, J. Hung, R. Tan, S. Wise
Access to lab-grown fully functional blood vessels would provide an invaluable resource to vascular medicine. The complex architecture and cellular makeup of native vessels, however, makes this extremely challenging to reproduce in vitro. Bioreactor systems have helped advanced research in this area by replicating many of the physiological conditions necessary for full-scale tissue growth outside of the body. A key element underpinning these technologies are 3D vascular graft templates which serve as temporary scaffolds to direct cell growth into similar cellular architectures observed in native vessels. Grafts further engineered with appropriate physical cues to accommodate the multiple cell types that reside within native vessels may help improve the production efficiency and physiological accuracy of bioreactor-grown vessel substitutes. Here, we engineered two distinct scaffold architectures into an electrospun vascular graft aiming to encourage the spatial organisation of human vascular endothelial cells (hCAECs) in a continuous luminal monolayer, co-cultured with human fibroblasts (hFBs) populating the graft wall. Using an electrospun composite of polycaprolactone and gelatin, we evaluated physical parameters including fibre diameter, fibre alignment, and porosity, that best mimicked the spatial composition and growth of hCAECs and hFBs in native vessels. Upon identifying the optimal scaffold architectures for each cell type, we constructed a custom-designed mandrel that combined these distinct architectures into a single vascular graft during a single electrospinning processing run. When connected to a perfusion bioreactor system, the dual architecture graft spatially oriented hCAECs and hFBs into the graft wall and lumen, respectively, directly from circulation. This biomimetic cell organisation was consistent with positive graft remodelling with significant collagen deposition in the graft wall. These findings demonstrate the influence of architectural cues to direct cell growth within vascular graft templates and the future potential of these approaches to more accurately and efficiency produce blood vessel substitutes in bioreactor systems.
获得实验室培养的功能齐全的血管将为血管医学提供宝贵的资源。然而,天然血管的复杂结构和细胞组成使其在体外繁殖极具挑战性。生物反应器系统通过复制体外全面组织生长所需的许多生理条件,帮助推进了这一领域的研究。支撑这些技术的一个关键因素是3D血管移植模板,它可以作为临时支架,指导细胞生长成在天然血管中观察到的类似细胞结构。利用适当的物理线索进一步改造移植物,以适应存在于天然血管中的多种细胞类型,可能有助于提高生物反应器培养的血管替代品的生产效率和生理准确性。在这里,我们将两种不同的支架结构设计成电纺丝血管移植物,旨在促进人血管内皮细胞(hcaec)在连续的管腔单层中的空间组织,并与填充移植物壁的人成纤维细胞(hFBs)共培养。使用聚己内酯和明胶的电纺丝复合材料,我们评估了包括纤维直径、纤维排列和孔隙率在内的物理参数,这些参数最能模拟hcaec和hFBs在天然血管中的空间组成和生长。在确定每种细胞类型的最佳支架结构后,我们构建了一个定制设计的芯轴,在单次静电纺丝处理过程中将这些不同的结构组合成单个血管移植物。当连接到灌注生物反应器系统时,双结构将空间定向的hcaec和hFBs分别从循环中直接移植物壁和管腔。这种仿生细胞组织与移植物正向重构一致,移植物壁有明显的胶原沉积。这些发现证明了结构线索对血管移植物模板内指导细胞生长的影响,以及这些方法在生物反应器系统中更准确、更有效地产生血管替代品的未来潜力。
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引用次数: 0
Modification of polyether ether ketone for the repairing of bone defects 聚醚醚酮的改性修复骨缺损
IF 4 3区 医学 Q2 Engineering Pub Date : 2022-04-08 DOI: 10.1088/1748-605X/ac65cd
Junfeng Chen, Guangxiu Cao, Linhao Li, Q. Cai, N. Dunne, Xiaoming Li
Bone damage as a consequence of disease or trauma is a common global occurrence. For bone damage treatment—bone implant materials are necessary across three classifications of surgical intervention (i.e. fixation, repair, and replacement). Many types of bone implant materials have been developed to meet the requirements of bone repair. Among them, polyether ether ketone (PEEK) has been considered as one of the next generation of bone implant materials, owing to its advantages related to good biocompatibility, chemical stability, x-ray permeability, elastic modulus comparable to natural bone, as well as the ease of processing and modification. However, as PEEK is a naturally bioinert material, some modification is needed to improve its integration with adjacent bones after implantation. Therefore, it has become a very hot topic of biomaterials research and various strategies for the modification of PEEK including blending, 3D printing, coating, chemical modification and the introduction of bioactive and/or antibacterial substances have been proposed. In this systematic review, the recent advances in modification of PEEK and its application prospect as bone implants are summarized, and the remaining challenges are also discussed.
骨损伤作为疾病或创伤的后果是一个常见的全球事件。对于骨损伤治疗,骨植入材料在三种手术干预中是必需的(即固定、修复和置换)。为了满足骨修复的需要,已经开发出多种类型的骨种植材料。其中聚醚醚酮(PEEK)由于具有良好的生物相容性、化学稳定性、x射线渗透性、弹性模量可与天然骨媲美以及易于加工和修饰等优点,被认为是下一代骨植入材料之一。然而,由于PEEK是一种天然的生物惰性材料,植入后需要进行一些修饰以改善其与邻近骨骼的融合。因此,它已成为生物材料研究的一个非常热门的话题,人们提出了各种对PEEK进行改性的策略,包括共混、3D打印、涂层、化学改性以及引入生物活性和/或抗菌物质。本文综述了近年来PEEK改性材料的研究进展及其作为骨种植体的应用前景,并对其面临的挑战进行了讨论。
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引用次数: 8
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Biomedical materials
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