首页 > 最新文献

Biopolymers最新文献

英文 中文
Nisin-Incorporated Solid Lipid Nanoparticles-Based In Situ Ocular Gel Using Box–Behnken Design for Enhanced Antibacterial Activity: In Vitro-Ex Vivo-In Vivo Analysis 乳链球菌素结合固体脂质纳米颗粒为基础的原位眼凝胶,使用Box-Behnken设计增强抗菌活性:体外-体外-体内-体内分析。
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-24 DOI: 10.1002/bip.70052
Meghanath B. Shete, Vaishnavi Fatangare, Sopan Nangare, Pankaj Jain, Shailesh S. Chalikwar

Microbial ocular infections, namely bacterial conjunctivitis (BC), are a major concern in the biomedical field. Nisin (NIS) is an amphiphilic natural antimicrobial peptide. It showed antibacterial potential against Pseudomonas aeruginosa, which is responsible for BC. Despite this, the application of NIS in pharmaceuticals for the treatment of ocular infections is hindered by several limitations that include poor aqueous solubility and stability. The preference for solid lipid nanoparticles (SLN) shows the aptitude to enhance solubility, bioavailability, etc., of therapeutically active molecules. Therefore, the present research work intends to prepare a thermoresponsive poloxamer 407 (P-407)-based in situ ocular gel of NIS-incorporated SLN using Box Behnken Design (BBD) for improved antibacterial application. Herein, NIS-SLN was formulated with glyceryl monostearate (GMS) and Tween 80 using a HSH-probe sonication method. It resulted in the spherical shape NIS-SLN with the particle size (PS) of 158.8 ± 13.56 nm, zeta potential (ZP) of −22.48 ± 1.86 mV, and drug loading (DL) of 12.8% ± 2.84%. The formulated thermo-responsive in situ gel (ISG) pH, gelling temperature, and viscosity were found to be 7.45 ± 0.02, 36.5°C ± 0.5°C, and 465.5 ± 6.5 cps, respectively, with drug release of 68.65% ± 5.1% over 24 h. Moreover, it shows improved permeation of 66.43% ± 2.6%, which might be because of the nanoscale dimensions of SLN and Tween 80. The formulation demonstrates good stability for 3 months and improved antimicrobial potential against P. aeruginosa compared to pure NIS, possibly owing to sustained release and improved penetration of NIS. Moreover, in vivo experiments demonstrated no irritation of the gel formulation, confirming biocompatibility with the ocular region. In conclusion, the SLN incorporated thermo-responsive P-407-based in situ ocular gel provides the improved potential of NIS. In the future, it will reveal a new horizon for the delivery of NIS and other molecules for ocular disease treatment.

眼部微生物感染,即细菌性结膜炎(BC),是生物医学领域的一个主要问题。Nisin (NIS)是一种两亲性天然抗菌肽。对引起BC的铜绿假单胞菌具有抑菌作用。尽管如此,NIS在治疗眼部感染的药物中的应用受到一些限制,包括水溶性差和稳定性差。对固体脂质纳米颗粒(SLN)的偏爱显示出增强治疗活性分子的溶解度、生物利用度等能力。因此,本研究拟采用Box Behnken Design (BBD)方法制备一种热响应性的波洛沙姆407 (P-407)为基础的ris - SLN原位眼凝胶,以改善抗菌应用。本研究采用hsh探针超声法,用单硬脂酸甘油酯(GMS)和Tween 80配制NIS-SLN。得到粒径为158.8±13.56 nm, ZP为-22.48±1.86 mV,载药量为12.8%±2.84%的球形NIS-SLN。制备的热响应原位凝胶(ISG) pH值为7.45±0.02,胶凝温度为36.5°C±0.5°C,黏度为465.5±6.5 cps, 24 h释药率为68.65%±5.1%。此外,它的渗透率提高了66.43%±2.6%,这可能与SLN和Tween 80的纳米级尺寸有关。与纯NIS相比,该制剂具有3个月的良好稳定性和对铜绿假单胞菌的抗菌潜力,这可能是由于其缓释和提高了NIS的渗透性。此外,体内实验表明,凝胶配方没有刺激,证实了与眼部区域的生物相容性。综上所述,加入热响应性p -407基原位眼凝胶的SLN可提高NIS的潜力。未来,它将为NIS和其他眼部疾病治疗分子的递送提供新的视野。
{"title":"Nisin-Incorporated Solid Lipid Nanoparticles-Based In Situ Ocular Gel Using Box–Behnken Design for Enhanced Antibacterial Activity: In Vitro-Ex Vivo-In Vivo Analysis","authors":"Meghanath B. Shete,&nbsp;Vaishnavi Fatangare,&nbsp;Sopan Nangare,&nbsp;Pankaj Jain,&nbsp;Shailesh S. Chalikwar","doi":"10.1002/bip.70052","DOIUrl":"10.1002/bip.70052","url":null,"abstract":"<div>\u0000 \u0000 <p>Microbial ocular infections, namely bacterial conjunctivitis (BC), are a major concern in the biomedical field. Nisin (NIS) is an amphiphilic natural antimicrobial peptide. It showed antibacterial potential against <i>Pseudomonas aeruginosa</i>, which is responsible for BC. Despite this, the application of NIS in pharmaceuticals for the treatment of ocular infections is hindered by several limitations that include poor aqueous solubility and stability. The preference for solid lipid nanoparticles (SLN) shows the aptitude to enhance solubility, bioavailability, etc., of therapeutically active molecules. Therefore, the present research work intends to prepare a thermoresponsive poloxamer 407 (P-407)-based in situ ocular gel of NIS-incorporated SLN using Box Behnken Design (BBD) for improved antibacterial application. Herein, NIS-SLN was formulated with glyceryl monostearate (GMS) and Tween 80 using a HSH-probe sonication method. It resulted in the spherical shape NIS-SLN with the particle size (PS) of 158.8 ± 13.56 nm, zeta potential (ZP) of −22.48 ± 1.86 mV, and drug loading (DL) of 12.8% ± 2.84%. The formulated thermo-responsive in situ gel (ISG) pH, gelling temperature, and viscosity were found to be 7.45 ± 0.02, 36.5°C ± 0.5°C, and 465.5 ± 6.5 cps, respectively, with drug release of 68.65% ± 5.1% over 24 h. Moreover, it shows improved permeation of 66.43% ± 2.6%, which might be because of the nanoscale dimensions of SLN and Tween 80. The formulation demonstrates good stability for 3 months and improved antimicrobial potential against <i>P. aeruginosa</i> compared to pure NIS, possibly owing to sustained release and improved penetration of NIS. Moreover, in vivo experiments demonstrated no irritation of the gel formulation, confirming biocompatibility with the ocular region. In conclusion, the SLN incorporated thermo-responsive P-407-based in situ ocular gel provides the improved potential of NIS. In the future, it will reveal a new horizon for the delivery of NIS and other molecules for ocular disease treatment.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 6","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145130034","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
On the Rheological Properties and Printability of Sodium Alginate–Carboxymethyl Chitosan Composite Solutions for Tissue Scaffold Printing 海藻酸钠-羧甲基壳聚糖复合溶液的流变性和打印性能研究。
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-24 DOI: 10.1002/bip.70050
Xavier L. Tabil, Tate N. Cao, Xiongbiao Chen

Composites of sodium alginate (Alg) and carboxymethyl chitosan (CMCS) are used to 3D print tissue scaffolds, but the rheological properties and printability of these composites remain underreported, resulting in time-consuming trial-and-error printing. This study investigates these properties to rigorously design the 3D printing process. Dynamic shear tests characterize viscoelastic and frequency-dependent properties, while steady shear tests assess the apparent viscosity and temperature-dependent viscosity. A novel approach based on mass flow rate models guides the printing of two-layer scaffolds for printability analysis. Brightfield microscopy and printability indexes quantify the deviations between printed and designed scaffolds, defined as printability. Results show that Alg predominantly directs the rheological properties. At 4% w/v Alg, the addition of < 3% w/v CMCS reduces elasticity, contrary to the trend where increasing CMCS increases elasticity. CMCS improves the thermal resistance of the composites, while Alg reduces it. Of the composites printed, a 4% w/v Alg + 1% w/v CMCS formulation most accurately replicates the designed scaffold, and adding CMCS improves scaffold printing repeatability by at least threefold compared to Alg-only solutions. These findings provide a framework that informs the preparation and performance of Alg-CMCS composites with tunable properties, advancing scaffold bioprinting for tissue engineering.

海藻酸钠(Alg)和羧甲基壳聚糖(CMCS)复合材料用于3D打印组织支架,但这些复合材料的流变性和可打印性仍然缺乏报道,导致耗时的反复试验打印。本研究通过研究这些特性来严格设计3D打印工艺。动态剪切测试表征粘弹性和频率相关的特性,而稳定剪切测试评估表观粘度和温度相关的粘度。提出了一种基于质量流率模型的双层支架打印可打印性分析方法。明场显微镜和可打印性指标量化打印支架和设计支架之间的偏差,定义为可打印性。结果表明,Alg对其流变特性起主导作用。在4% w/v Alg下,加入
{"title":"On the Rheological Properties and Printability of Sodium Alginate–Carboxymethyl Chitosan Composite Solutions for Tissue Scaffold Printing","authors":"Xavier L. Tabil,&nbsp;Tate N. Cao,&nbsp;Xiongbiao Chen","doi":"10.1002/bip.70050","DOIUrl":"10.1002/bip.70050","url":null,"abstract":"<p>Composites of sodium alginate (Alg) and carboxymethyl chitosan (CMCS) are used to 3D print tissue scaffolds, but the rheological properties and printability of these composites remain underreported, resulting in time-consuming trial-and-error printing. This study investigates these properties to rigorously design the 3D printing process. Dynamic shear tests characterize viscoelastic and frequency-dependent properties, while steady shear tests assess the apparent viscosity and temperature-dependent viscosity. A novel approach based on mass flow rate models guides the printing of two-layer scaffolds for printability analysis. Brightfield microscopy and printability indexes quantify the deviations between printed and designed scaffolds, defined as printability. Results show that Alg predominantly directs the rheological properties. At 4% w/v Alg, the addition of &lt; 3% w/v CMCS reduces elasticity, contrary to the trend where increasing CMCS increases elasticity. CMCS improves the thermal resistance of the composites, while Alg reduces it. Of the composites printed, a 4% w/v Alg + 1% w/v CMCS formulation most accurately replicates the designed scaffold, and adding CMCS improves scaffold printing repeatability by at least threefold compared to Alg-only solutions. These findings provide a framework that informs the preparation and performance of Alg-CMCS composites with tunable properties, advancing scaffold bioprinting for tissue engineering.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 6","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.70050","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145129967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Comparison of Ester- and Ether-Based Bio-TPUs With Regard to Their Resistance to Environmental Influences in Terms of Their Mechanical and Adhesive Properties 酯基和醚基生物tpu在机械性能和粘接性能方面的抗环境影响比较。
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-20 DOI: 10.1002/bip.70051
Marco Klute, Hans-Peter Heim

The demand for bio-based alternatives to fossil-based plastics is growing rapidly due to the increasing environmental awareness of consumers and manufacturers, as well as the goal of carbon-neutral production. There are many promising alternatives that can be obtained from various renewable resources, but their use in series production, especially of technical components, is often hampered by doubts about their usability and, above all, their resistance to environmental influences. The present study is intended to help overcome these obstacles and demonstrate the applicability of bio-based TPUs in multi-component technical parts with high bonding requirements. Different polyester and polyether TPUs were used, and their resistance to elevated temperatures and humidity was compared. Both the mechanical properties and the bond strength in bio-based hard-soft composites were investigated. It was shown that good to very good bond strengths of approximately 2.5–8 N/mm could be achieved depending on the Shore hardness. The formation of adhesive forces depends on both the type of polyol and its proportion in the TPU. While ether-based TPU exhibited higher adhesive bond strengths, the strength increases with a higher proportion of soft segments. After storage tests, a decrease in bond strength was observed, mainly due to thermal aging effects and absorption of water molecules, correlating with the change in mechanical properties.

由于消费者和制造商的环保意识日益提高,以及碳中和生产的目标,对生物基替代品的需求正在迅速增长。从各种可再生资源中可以获得许多有希望的替代品,但它们在批量生产中的使用,特别是技术部件的使用,往往受到对其可用性的怀疑,尤其是对其对环境影响的抵抗力的阻碍。本研究旨在帮助克服这些障碍,并证明生物基tpu在具有高粘合要求的多组件技术部件中的适用性。采用不同的聚酯和聚醚tpu,比较了它们对高温和高湿的耐受性。研究了生物基软硬复合材料的力学性能和结合强度。结果表明,根据邵氏硬度的不同,可以获得约2.5-8 N/mm的良好至非常好的结合强度。粘合力的形成取决于多元醇的种类及其在TPU中的比例。醚基TPU具有较高的粘接强度,软段比例越高,强度越高。储存试验后,粘结强度下降,主要是由于热老化效应和水分子的吸收,与力学性能的变化有关。
{"title":"A Comparison of Ester- and Ether-Based Bio-TPUs With Regard to Their Resistance to Environmental Influences in Terms of Their Mechanical and Adhesive Properties","authors":"Marco Klute,&nbsp;Hans-Peter Heim","doi":"10.1002/bip.70051","DOIUrl":"10.1002/bip.70051","url":null,"abstract":"<p>The demand for bio-based alternatives to fossil-based plastics is growing rapidly due to the increasing environmental awareness of consumers and manufacturers, as well as the goal of carbon-neutral production. There are many promising alternatives that can be obtained from various renewable resources, but their use in series production, especially of technical components, is often hampered by doubts about their usability and, above all, their resistance to environmental influences. The present study is intended to help overcome these obstacles and demonstrate the applicability of bio-based TPUs in multi-component technical parts with high bonding requirements. Different polyester and polyether TPUs were used, and their resistance to elevated temperatures and humidity was compared. Both the mechanical properties and the bond strength in bio-based hard-soft composites were investigated. It was shown that good to very good bond strengths of approximately 2.5–8 N/mm could be achieved depending on the Shore hardness. The formation of adhesive forces depends on both the type of polyol and its proportion in the TPU. While ether-based TPU exhibited higher adhesive bond strengths, the strength increases with a higher proportion of soft segments. After storage tests, a decrease in bond strength was observed, mainly due to thermal aging effects and absorption of water molecules, correlating with the change in mechanical properties.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 6","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.70051","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145090931","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advanced Biomaterial for Dual-Drug Release: A Hydrogel-Microparticle Approach 用于双重药物释放的先进生物材料:水凝胶-微粒方法
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-13 DOI: 10.1002/bip.70049
Jose Gregorio Fontainez Garrido, Newton Andreo Filho, Fabiana Perrechil, Mariana Agostini de Moraes

Advanced biomaterials with dual drug delivery represent a promising strategy to enhance therapeutic outcomes in wound treatment. This work aimed to combine antimicrobial and analgesic actions in a single platform, enabling the simultaneous release of both drugs from an advanced dual-drug delivery system based on a combined hydrogel and microparticle approach. The system was composed of alginate microparticles containing the antibiotic gentamicin incorporated into a gellan gum/collagen hydrogel matrix, in which the local anesthetic bupivacaine was directly loaded. The resulting composite was thoroughly characterized in terms of its morphological, physicochemical, mechanical, rheological, and thermal properties, as well as drug release profiles. The incorporation of microparticles significantly influenced the structural and functional behavior of the hydrogel, particularly at higher microparticle concentrations (50% w/v). Notably, the microparticles played a crucial role in maintaining the hydrogel's integrity in the presence of both drugs and enabled their controlled and simultaneous release, with each exhibiting distinct release kinetics. These findings highlight the potential of this hydrogel and microparticle composite as an advanced material for wound dressings, capable of promoting healing while simultaneously providing localized pain relief.

具有双重给药功能的先进生物材料是提高伤口治疗效果的一种很有前途的策略。这项工作旨在将抗菌和镇痛作用结合在一个平台上,使两种药物能够同时从基于水凝胶和微粒联合方法的先进双药递送系统中释放。该系统由含有抗生素庆大霉素的海藻酸盐微颗粒掺入到结冷胶/胶原蛋白水凝胶基质中,其中直接装载局部麻醉剂布比卡因。所得到的复合材料在形态、物理化学、机械、流变学和热性能以及药物释放谱方面进行了彻底的表征。微粒的掺入显著影响了水凝胶的结构和功能行为,特别是在较高的微粒浓度(50% w/v)下。值得注意的是,在两种药物存在的情况下,微颗粒在维持水凝胶的完整性方面发挥了至关重要的作用,并使它们能够控制和同时释放,每种药物都表现出不同的释放动力学。这些发现突出了这种水凝胶和微粒复合材料作为伤口敷料的先进材料的潜力,能够促进愈合,同时提供局部疼痛缓解。
{"title":"Advanced Biomaterial for Dual-Drug Release: A Hydrogel-Microparticle Approach","authors":"Jose Gregorio Fontainez Garrido,&nbsp;Newton Andreo Filho,&nbsp;Fabiana Perrechil,&nbsp;Mariana Agostini de Moraes","doi":"10.1002/bip.70049","DOIUrl":"https://doi.org/10.1002/bip.70049","url":null,"abstract":"<p>Advanced biomaterials with dual drug delivery represent a promising strategy to enhance therapeutic outcomes in wound treatment. This work aimed to combine antimicrobial and analgesic actions in a single platform, enabling the simultaneous release of both drugs from an advanced dual-drug delivery system based on a combined hydrogel and microparticle approach. The system was composed of alginate microparticles containing the antibiotic gentamicin incorporated into a gellan gum/collagen hydrogel matrix, in which the local anesthetic bupivacaine was directly loaded. The resulting composite was thoroughly characterized in terms of its morphological, physicochemical, mechanical, rheological, and thermal properties, as well as drug release profiles. The incorporation of microparticles significantly influenced the structural and functional behavior of the hydrogel, particularly at higher microparticle concentrations (50% w/v). Notably, the microparticles played a crucial role in maintaining the hydrogel's integrity in the presence of both drugs and enabled their controlled and simultaneous release, with each exhibiting distinct release kinetics. These findings highlight the potential of this hydrogel and microparticle composite as an advanced material for wound dressings, capable of promoting healing while simultaneously providing localized pain relief.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.70049","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145050911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recent Chitosan@Magnetite Adsorbents for the Removal of Heavy Metals and Organic Pollutants From Water 最近Chitosan@Magnetite吸附剂去除水中重金属和有机污染物。
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-12 DOI: 10.1002/bip.70047
Noura N. Eltahan, Hamada H. Abdel-Razik, Fathy M. ElTaweel, Magdy Y. Abdelaal

Chitosan@Magnetite composites have gained significant attention in the field of water purification due to their high capacity to absorb contaminants and their ease of separation using magnets. In this review, we reviewed the latest methods for preparing this material and explained its key properties, particularly its structural shape and the ways of modifying it to be more efficient. One of its most obvious advantages is the increase of surface area, which helps improve absorption. To this end, we mentioned several analytical techniques, such as morphology and structure, to understand how this material works. We also explained how this material can remove heavy metals and organic pollutants from water. Finally, we evaluated its performance in terms of absorption capacity, reaction rate, and its ability to be regenerated and reused, confirming its excellent suitability for practical and sustainable water purification.

Chitosan@Magnetite复合材料在水净化领域受到了极大的关注,因为它们具有高吸收污染物的能力,并且易于使用磁铁分离。本文综述了该材料的最新制备方法,并解释了其关键性能,特别是其结构形状和改进其效率的方法。其最明显的优点之一是增加表面积,这有助于提高吸收。为此,我们提到了几种分析技术,如形态学和结构,以了解这种材料是如何工作的。我们还解释了这种材料如何去除水中的重金属和有机污染物。最后,从吸附能力、反应速率、再生回用能力等方面对其性能进行了评价,证实了其在实际和可持续的水净化中具有良好的适用性。
{"title":"Recent Chitosan@Magnetite Adsorbents for the Removal of Heavy Metals and Organic Pollutants From Water","authors":"Noura N. Eltahan,&nbsp;Hamada H. Abdel-Razik,&nbsp;Fathy M. ElTaweel,&nbsp;Magdy Y. Abdelaal","doi":"10.1002/bip.70047","DOIUrl":"10.1002/bip.70047","url":null,"abstract":"<div>\u0000 \u0000 <p>Chitosan@Magnetite composites have gained significant attention in the field of water purification due to their high capacity to absorb contaminants and their ease of separation using magnets. In this review, we reviewed the latest methods for preparing this material and explained its key properties, particularly its structural shape and the ways of modifying it to be more efficient. One of its most obvious advantages is the increase of surface area, which helps improve absorption. To this end, we mentioned several analytical techniques, such as morphology and structure, to understand how this material works. We also explained how this material can remove heavy metals and organic pollutants from water. Finally, we evaluated its performance in terms of absorption capacity, reaction rate, and its ability to be regenerated and reused, confirming its excellent suitability for practical and sustainable water purification.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145038933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stability of Bioactive Compounds From Argemone platyceras in Sorbitol-Gum Arabic Biopolymer Films: A Food Coating Alternative 山梨醇-阿拉伯山梨醇-树胶生物聚合物薄膜中亚银酮生物活性化合物的稳定性:一种食品涂层替代品
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-08-30 DOI: 10.1002/bip.70048
Daniel Arizmendi-Cotero, Rosa Maria Gómez-Espinosa

A plastic film made from Gum Arabic and sorbitol (BioFilm-EAp) was developed to enhance the stability of bioactive compounds from Argemone platyceras (EAp) and preserve their antimicrobial properties. The EAp compounds identified through spectrophotometric methods in ethanolic extracts of leaves and stems included alkaloids (3320 and 1260 cm−1), flavonoids (1739 cm−1), and phenols (1260 cm−1). Additionally, the extracts demonstrated the ability to inhibit the growth of Escherichia coli and Staphylococcus aureus. The BioFilm, with and without EAp, was characterized through mechanical tests, revealing that films containing EAp were less resistant (1.07–11.82 N) than those without compounds (23.02 N). Furthermore, these properties depended on the concentration of sorbitol. The presence of alkaloids, flavonoids, and phenols in the BioFilm-EAp was assessed qualitatively using a simple and inexpensive methodology based on UV–Vis spectroscopy. The results indicated that these compounds remained stable within the sorbitol-Gum Arabic biopolymer matrix over 21 days. Finally, a sample of grapes was coated with the BioFilm-EAp films through the solution immersion method. This coating preserved the physical parameters of the grapes stored at room temperature, while the active compounds inhibited the growth of microorganisms on the grapes.

以阿拉伯树胶和山梨糖醇为原料制备了一种生物膜(BioFilm-EAp),以提高银尾草(EAp)中生物活性化合物的稳定性并保持其抗菌性能。通过分光光度法在叶和茎的乙醇提取物中鉴定出EAp化合物,包括生物碱(3320和1260 cm−1)、类黄酮(1739 cm−1)和酚(1260 cm−1)。此外,提取物还显示出抑制大肠杆菌和金黄色葡萄球菌生长的能力。通过力学测试对含EAp和不含EAp的BioFilm进行了表征,结果表明,含EAp的BioFilm膜的耐蚀性(1.07-11.82 N)低于不含EAp的膜(23.02 N)。此外,这些性质与山梨醇的浓度有关。生物碱、黄酮类化合物和酚类化合物在BioFilm-EAp中的存在采用一种简单而廉价的基于紫外可见光谱的方法进行定性评估。结果表明,这些化合物在山梨醇-阿拉伯树胶生物聚合物基质中保持稳定超过21天。最后,通过溶液浸泡法将BioFilm-EAp膜包覆在葡萄样品上。这种包膜可以保持葡萄在室温下的物理参数,同时活性化合物可以抑制葡萄上微生物的生长。
{"title":"Stability of Bioactive Compounds From Argemone platyceras in Sorbitol-Gum Arabic Biopolymer Films: A Food Coating Alternative","authors":"Daniel Arizmendi-Cotero,&nbsp;Rosa Maria Gómez-Espinosa","doi":"10.1002/bip.70048","DOIUrl":"https://doi.org/10.1002/bip.70048","url":null,"abstract":"<div>\u0000 \u0000 <p>A plastic film made from Gum Arabic and sorbitol (BioFilm-EAp) was developed to enhance the stability of bioactive compounds from <i>Argemone platyceras</i> (EAp) and preserve their antimicrobial properties. The EAp compounds identified through spectrophotometric methods in ethanolic extracts of leaves and stems included alkaloids (3320 and 1260 cm<sup>−1</sup>), flavonoids (1739 cm<sup>−1</sup>), and phenols (1260 cm<sup>−1</sup>). Additionally, the extracts demonstrated the ability to inhibit the growth of <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>. The BioFilm, with and without EAp, was characterized through mechanical tests, revealing that films containing EAp were less resistant (1.07–11.82 N) than those without compounds (23.02 N). Furthermore, these properties depended on the concentration of sorbitol. The presence of alkaloids, flavonoids, and phenols in the BioFilm-EAp was assessed qualitatively using a simple and inexpensive methodology based on UV–Vis spectroscopy. The results indicated that these compounds remained stable within the sorbitol-Gum Arabic biopolymer matrix over 21 days. Finally, a sample of grapes was coated with the BioFilm-EAp films through the solution immersion method. This coating preserved the physical parameters of the grapes stored at room temperature, while the active compounds inhibited the growth of microorganisms on the grapes.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144918852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of Nano ZnO-Embedded Gelatin/Alginate Bioscaffolds for Potential Skin Tissue Regeneration via Oxidative Stress Modulation and ECM Mimicry 纳米zno包埋明胶/海藻酸盐生物支架通过氧化应激调节和ECM模拟的潜在皮肤组织再生的开发
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-08-23 DOI: 10.1002/bip.70046
Marija M. Babić Radić, Martina Žabčić, Marija Vukomanović, Jasmina Nikodinović-Runić, Dušan Milivojević, Vuk Filipović, Simonida Tomić

Engineering of biomaterials for advanced skin tissue regeneration requires optimization of critical parameters including interconnected porous structure, biomaterial stability, hydrophilicity, biocompatibility, and bioactivity. These features enable the mimicry of the skin tissue microenvironment and support the key phases of the regeneration process, which are crucial for effective tissue repair. Another important requirement for successful skin tissue regeneration is the modulation of oxidative stress, as excessive accumulation of reactive oxygen species (ROS) at the site of the skin lesion can hinder healing and cause chronic inflammation and scarring. To address these challenges, we propose a reductionist therapeutic approach to skin tissue regeneration by developing bio-sourced scaffolds that replicate the native extracellular matrix (ECM), neutralize ROS levels, and actively promote tissue regeneration at both structural and molecular levels. These nano ZnO-embedded gelatin/alginate bioscaffolds were prepared via a simple crosslinking reaction and loaded with carefully selected active agents with antioxidant and skin tissue regenerative potential. Characterization studies of the bioscaffolds confirmed their porous interconnected morphology with tunable porosity (92%–94%), mechanical strength (1.95–3.22 MPa), hydrophilicity, stable adhesion to skin tissue, and ROS-scavenging activity. Additionally, the bioscaffolds demonstrated simultaneous release of quercetin, allantoin, and caffeic acid, and both biocompatibility—in vitro on human fibroblasts (MRC5) and in vivo on Caenorhabditis elegans. Overall, these findings provide valuable insight into the design of multifunctional bioscaffolds as a promising therapeutic platform for skin tissue regeneration application, which simultaneously modulates oxidative stress, replicates ECM architecture, and stimulates the healing cascade, ultimately enhancing skin tissue repair and reducing scarring.

用于高级皮肤组织再生的生物材料工程需要优化关键参数,包括互联多孔结构、生物材料稳定性、亲水性、生物相容性和生物活性。这些特征使皮肤组织微环境的模仿和支持再生过程的关键阶段,这是有效的组织修复的关键。成功的皮肤组织再生的另一个重要要求是氧化应激的调节,因为活性氧(ROS)在皮肤损伤部位的过度积累会阻碍愈合并导致慢性炎症和瘢痕形成。为了解决这些挑战,我们提出了一种还原治疗方法,通过开发生物来源的支架来复制天然细胞外基质(ECM),中和ROS水平,并在结构和分子水平上积极促进组织再生。这些纳米zno包埋的明胶/海藻酸盐生物支架通过简单的交联反应制备,并负载精心挑选的具有抗氧化和皮肤组织再生潜力的活性剂。生物支架的表征研究证实其多孔互联形态具有可调的孔隙率(92%-94%)、机械强度(1.95-3.22 MPa)、亲水性、与皮肤组织的稳定粘附以及清除ros的活性。此外,该生物支架还显示出槲皮素、尿囊素和咖啡酸的同步释放,并且在体外对人成纤维细胞(MRC5)和体内对秀丽隐杆线虫的生物相容性。总的来说,这些发现为多功能生物支架的设计提供了有价值的见解,作为一种有前途的皮肤组织再生治疗平台,它同时调节氧化应激,复制ECM结构,刺激愈合级联,最终增强皮肤组织修复和减少疤痕。
{"title":"Development of Nano ZnO-Embedded Gelatin/Alginate Bioscaffolds for Potential Skin Tissue Regeneration via Oxidative Stress Modulation and ECM Mimicry","authors":"Marija M. Babić Radić,&nbsp;Martina Žabčić,&nbsp;Marija Vukomanović,&nbsp;Jasmina Nikodinović-Runić,&nbsp;Dušan Milivojević,&nbsp;Vuk Filipović,&nbsp;Simonida Tomić","doi":"10.1002/bip.70046","DOIUrl":"https://doi.org/10.1002/bip.70046","url":null,"abstract":"<div>\u0000 \u0000 <p>Engineering of biomaterials for advanced skin tissue regeneration requires optimization of critical parameters including interconnected porous structure, biomaterial stability, hydrophilicity, biocompatibility, and bioactivity. These features enable the mimicry of the skin tissue microenvironment and support the key phases of the regeneration process, which are crucial for effective tissue repair. Another important requirement for successful skin tissue regeneration is the modulation of oxidative stress, as excessive accumulation of reactive oxygen species (ROS) at the site of the skin lesion can hinder healing and cause chronic inflammation and scarring. To address these challenges, we propose a reductionist therapeutic approach to skin tissue regeneration by developing bio-sourced scaffolds that replicate the native extracellular matrix (ECM), neutralize ROS levels, and actively promote tissue regeneration at both structural and molecular levels. These nano ZnO-embedded gelatin/alginate bioscaffolds were prepared via a simple crosslinking reaction and loaded with carefully selected active agents with antioxidant and skin tissue regenerative potential. Characterization studies of the bioscaffolds confirmed their porous interconnected morphology with tunable porosity (92%–94%), mechanical strength (1.95–3.22 MPa), hydrophilicity, stable adhesion to skin tissue, and ROS-scavenging activity. Additionally, the bioscaffolds demonstrated simultaneous release of quercetin, allantoin, and caffeic acid, and both biocompatibility—in vitro on human fibroblasts (MRC5) and in vivo on <i>Caenorhabditis elegans</i>. Overall, these findings provide valuable insight into the design of multifunctional bioscaffolds as a promising therapeutic platform for skin tissue regeneration application, which simultaneously modulates oxidative stress, replicates ECM architecture, and stimulates the healing cascade, ultimately enhancing skin tissue repair and reducing scarring.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144891674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In Vivo Degradation and Local Tissue Response of Experimental Carp Collagen Membranes: Micro-MRI and Histological Analysis 实验鲤鱼胶原膜的体内降解和局部组织反应:显微mri和组织学分析
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-08-18 DOI: 10.1002/bip.70045
Michele Bujda, Tomáš Suchý, Vít Herynek, Jaroslava Dušková, Margit Žaloudková, Luděk Šefc, Karel Klíma, Robert Plachý, René Foltán

Collagen membranes are widely used in tissue and bone engineering, including guided bone regeneration (GBR). For effective and uninterrupted bone healing, a GBR membrane must maintain its functionality for an initial critical period of 4 weeks. A novel carp collagen sponge has already shown promise as a wound coating and vascular graft coating, making it a candidate for GBR applications as well. To enhance the mechanical properties and longevity of GBR membranes, we modified the basic carp collagen membrane with combinations of l-lactide, ε-caprolactone, d,l-lactide, and glycolide in various molar ratios. While traditional methods rely on histological evaluation to assess the degradation pattern and therefore suitability of GBR membranes ex vivo, this study employed micro-MRI as an innovative, noninvasive approach to monitor the in vivo degradation of carp collagen membrane and its polymer-modified variants. Our findings demonstrated that micro-MRI is a reliable and effective method for visualizing collagen membrane degradation in vivo, up to scaffold disintegration. Among the variants tested, collagen GBR membrane coated with d,l-lactide and glycolide in a 50:50 M ratio emerged as the most suitable for GBR purposes. However, since this study was conducted in the subcutaneous tissue of a rat model, further research is required to determine the behavior of carp collagen GBR membrane variants on bony surfaces.

胶原膜广泛应用于组织和骨工程,包括引导骨再生(GBR)。为了有效和不间断的骨愈合,GBR膜必须在最初的关键时期4周内保持其功能。一种新型鲤鱼胶原蛋白海绵已经显示出作为伤口涂层和血管移植涂层的前景,使其成为GBR应用的候选材料。为了提高GBR膜的力学性能和使用寿命,我们将l-丙交酯、ε-己内酯、d、l-丙交酯和甘油酯按不同的摩尔比对碱性鲤鱼胶原膜进行了改性。传统方法依赖于组织学评估来评估GBR膜的体外降解模式和适用性,而本研究采用微mri作为一种创新的、无创的方法来监测鲤鱼胶原膜及其聚合物修饰变体的体内降解。我们的研究结果表明,微mri是一种可靠而有效的方法来观察胶原膜在体内的降解,直到支架解体。在测试的变体中,以50:50 M的比例涂覆d,l-丙交酯和乙醇酸酯的胶原GBR膜最适合GBR用途。然而,由于本研究是在大鼠模型的皮下组织中进行的,因此需要进一步的研究来确定鲤鱼胶原GBR膜变体在骨表面的行为。
{"title":"In Vivo Degradation and Local Tissue Response of Experimental Carp Collagen Membranes: Micro-MRI and Histological Analysis","authors":"Michele Bujda,&nbsp;Tomáš Suchý,&nbsp;Vít Herynek,&nbsp;Jaroslava Dušková,&nbsp;Margit Žaloudková,&nbsp;Luděk Šefc,&nbsp;Karel Klíma,&nbsp;Robert Plachý,&nbsp;René Foltán","doi":"10.1002/bip.70045","DOIUrl":"https://doi.org/10.1002/bip.70045","url":null,"abstract":"<p>Collagen membranes are widely used in tissue and bone engineering, including guided bone regeneration (GBR). For effective and uninterrupted bone healing, a GBR membrane must maintain its functionality for an initial critical period of 4 weeks. A novel carp collagen sponge has already shown promise as a wound coating and vascular graft coating, making it a candidate for GBR applications as well. To enhance the mechanical properties and longevity of GBR membranes, we modified the basic carp collagen membrane with combinations of <span>l</span>-lactide, ε-caprolactone, <span>d</span>,<span>l</span>-lactide, and glycolide in various molar ratios. While traditional methods rely on histological evaluation to assess the degradation pattern and therefore suitability of GBR membranes ex vivo<i>,</i> this study employed micro-MRI as an innovative, noninvasive approach to monitor the in vivo degradation of carp collagen membrane and its polymer-modified variants. Our findings demonstrated that micro-MRI is a reliable and effective method for visualizing collagen membrane degradation in vivo, up to scaffold disintegration. Among the variants tested, collagen GBR membrane coated with <span>d</span>,<span>l</span>-lactide and glycolide in a 50:50 M ratio emerged as the most suitable for GBR purposes. However, since this study was conducted in the subcutaneous tissue of a rat model, further research is required to determine the behavior of carp collagen GBR membrane variants on bony surfaces.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.70045","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144861683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Formulation and Characterization of Cerium Ion Cross-Linked Alginate/PVA Films for Wound Dressing Applications 伤口敷料用铈离子交联海藻酸盐/聚乙烯醇膜的配方和性能
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-08-13 DOI: 10.1002/bip.70043
Nilay Kahya, Nevin Öztekin, Alper Gürarslan

Herein, alginate films doped with cerium(III) carbonate were prepared via the casting method. An acid treatment process was applied to the films for cross-linking by free Ce3+ ions. The incorporation of poly(vinyl) alcohol into the alginate matrix enhanced the film properties. Fourier transform infrared spectroscopy and differential scanning calorimetry analyses confirmed that PVA did not alter the chemical structure of the Ce/Alg films. Analysis of the morphological characteristics of Ce/Alg films using a scanning electron microscope revealed that porosity existed in the films. Cerium-alginate films rapidly swell in PBS (pH = 7.4) and water within 10 min, demonstrating their potential for effective fluid absorption in wound environments. The water vapor permeability test exhibited that the films have the ability to transmit moisture. This present work reports the formulation of cerium(III) cross-linked alginate films and characterization studies of the films. The films are regarded as subject to efficient wound coverage dressings in future studies with their favorable biomaterial properties.

本文采用浇铸法制备了掺杂碳酸铈的海藻酸盐薄膜。采用酸处理工艺对薄膜进行了自由Ce3+交联。在海藻酸盐基质中加入聚乙烯醇增强了膜的性能。傅里叶变换红外光谱和差示扫描量热分析证实,PVA没有改变Ce/Alg薄膜的化学结构。扫描电镜分析了Ce/Alg膜的形态特征,发现膜中存在孔隙。海藻酸铈薄膜在PBS (pH = 7.4)和水中10分钟内迅速膨胀,表明它们在伤口环境中有效吸收液体的潜力。透湿性试验表明,薄膜具有透湿性。本文报道了铈(III)交联藻酸盐薄膜的制备及其表征研究。该膜具有良好的生物材料性能,在未来的研究中被认为是有效的伤口覆盖敷料。
{"title":"Formulation and Characterization of Cerium Ion Cross-Linked Alginate/PVA Films for Wound Dressing Applications","authors":"Nilay Kahya,&nbsp;Nevin Öztekin,&nbsp;Alper Gürarslan","doi":"10.1002/bip.70043","DOIUrl":"https://doi.org/10.1002/bip.70043","url":null,"abstract":"<div>\u0000 \u0000 <p>Herein, alginate films doped with cerium(III) carbonate were prepared via the casting method. An acid treatment process was applied to the films for cross-linking by free Ce<sup>3+</sup> ions. The incorporation of poly(vinyl) alcohol into the alginate matrix enhanced the film properties. Fourier transform infrared spectroscopy and differential scanning calorimetry analyses confirmed that PVA did not alter the chemical structure of the Ce/Alg films. Analysis of the morphological characteristics of Ce/Alg films using a scanning electron microscope revealed that porosity existed in the films. Cerium-alginate films rapidly swell in PBS (pH = 7.4) and water within 10 min, demonstrating their potential for effective fluid absorption in wound environments. The water vapor permeability test exhibited that the films have the ability to transmit moisture. This present work reports the formulation of cerium(III) cross-linked alginate films and characterization studies of the films. The films are regarded as subject to efficient wound coverage dressings in future studies with their favorable biomaterial properties.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144833096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fabrication and Characterization of 3D Printed Polycaprolactone/Baghdadite/Zinc Oxide Nanocomposite Scaffolds for Bone Tissue Engineering 3D打印聚己内酯/巴格达石/氧化锌纳米复合材料骨组织工程支架的制备与表征
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-07-30 DOI: 10.1002/bip.70041
Zahra Safaei, Mojtaba Ansari, Hossein Eslami

Nowadays, the use of 3D printing method in the construction of scaffolds is significantly common for bone tissue engineering applications. Moreover, the addition of nanoparticles and additives can significantly improve the mechanical and biological properties of polymeric scaffolds as polymers alone are not able to show enough performances. In this study, composite scaffolds based on polycaprolactone (PCL) containing different amounts of zinc oxide (ZnO) and Baghdadite (B) nanoparticles were fabricated by 3D printing method as novel combinations for bone tissue engineering. Then, their physical, mechanical, and biological properties were investigated. The scanning electron microscopy (SEM) of the composite showed uniform and porous structures with open porosity. Fourier-transform infrared spectroscopy (FTIR) of the scaffolds confirmed that no reaction occurred between PCL, B, and ZnO nanoparticles during the fabrication of composite scaffolds. The PCL/B/ZnO composite scaffolds showed high compressive strength. They also showed weight loss during 4 weeks, which was related to PCL degradation. The high bioactivity of the composite scaffolds was confirmed by dispersive X-ray analysis (EDS). SEM images showed the formation of calcium phosphate (CaP) layer on scaffolds in simulated body fluid (SBF). Inductively coupled plasma (ICP) analysis confirmed the formation of apatite layer on their surfaces. Based on the results of the (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) (MTT) test, cell proliferation on the scaffolds increased after 72 h, which shows that the scaffolds are biocompatible and non-toxic. SEM images showed that the cells on the surface of PCL-based nanocomposite scaffolds prepared had a suitable density. The results of alizarin red staining showed a significant amount of calcium deposition on the scaffolds. It has been shown that PCL-based nanocomposite scaffolds containing B and ZnO nanoparticles are suitable candidates for use in bone tissue engineering applications as they have suitable mechanical, biological, and physical properties.

目前,在骨组织工程应用中,使用3D打印方法构建支架是非常普遍的。此外,纳米颗粒和添加剂的加入可以显著改善聚合物支架的力学和生物性能,而聚合物本身无法表现出足够的性能。本研究采用3D打印技术制备了含不同氧化锌(ZnO)和Baghdadite (B)纳米颗粒的聚己内酯(PCL)复合支架,作为骨组织工程的新型组合。然后,研究了它们的物理、机械和生物特性。复合材料的扫描电镜(SEM)显示出均匀的多孔结构和开放的孔隙率。傅里叶变换红外光谱(FTIR)证实,在复合支架的制备过程中,PCL、B和ZnO纳米颗粒之间没有发生反应。PCL/B/ZnO复合支架具有较高的抗压强度。他们在4周内也表现出体重减轻,这与PCL降解有关。经x射线色散分析(EDS)证实复合支架具有较高的生物活性。SEM图像显示在模拟体液(SBF)中支架表面形成磷酸钙(CaP)层。电感耦合等离子体(ICP)分析证实其表面形成磷灰石层。根据(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑)(MTT)试验结果,72 h后支架上细胞增殖增强,表明支架具有生物相容性和无毒性。SEM图像显示,所制备的pcl基纳米复合支架表面细胞密度适宜。茜素红染色结果显示支架上有明显的钙沉积。研究表明,含有B和ZnO纳米颗粒的pcl基纳米复合支架具有合适的机械、生物和物理性能,是骨组织工程应用的合适候选者。
{"title":"Fabrication and Characterization of 3D Printed Polycaprolactone/Baghdadite/Zinc Oxide Nanocomposite Scaffolds for Bone Tissue Engineering","authors":"Zahra Safaei,&nbsp;Mojtaba Ansari,&nbsp;Hossein Eslami","doi":"10.1002/bip.70041","DOIUrl":"https://doi.org/10.1002/bip.70041","url":null,"abstract":"<div>\u0000 \u0000 <p>Nowadays, the use of 3D printing method in the construction of scaffolds is significantly common for bone tissue engineering applications. Moreover, the addition of nanoparticles and additives can significantly improve the mechanical and biological properties of polymeric scaffolds as polymers alone are not able to show enough performances. In this study, composite scaffolds based on polycaprolactone (PCL) containing different amounts of zinc oxide (ZnO) and Baghdadite (B) nanoparticles were fabricated by 3D printing method as novel combinations for bone tissue engineering. Then, their physical, mechanical, and biological properties were investigated. The scanning electron microscopy (SEM) of the composite showed uniform and porous structures with open porosity. Fourier-transform infrared spectroscopy (FTIR) of the scaffolds confirmed that no reaction occurred between PCL, B, and ZnO nanoparticles during the fabrication of composite scaffolds. The PCL/B/ZnO composite scaffolds showed high compressive strength. They also showed weight loss during 4 weeks, which was related to PCL degradation. The high bioactivity of the composite scaffolds was confirmed by dispersive X-ray analysis (EDS). SEM images showed the formation of calcium phosphate (CaP) layer on scaffolds in simulated body fluid (SBF). Inductively coupled plasma (ICP) analysis confirmed the formation of apatite layer on their surfaces. Based on the results of the (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) (MTT) test, cell proliferation on the scaffolds increased after 72 h, which shows that the scaffolds are biocompatible and non-toxic. SEM images showed that the cells on the surface of PCL-based nanocomposite scaffolds prepared had a suitable density. The results of alizarin red staining showed a significant amount of calcium deposition on the scaffolds. It has been shown that PCL-based nanocomposite scaffolds containing B and ZnO nanoparticles are suitable candidates for use in bone tissue engineering applications as they have suitable mechanical, biological, and physical properties.</p>\u0000 </div>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"116 5","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144725647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Biopolymers
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1