Pub Date : 2026-01-22DOI: 10.1016/j.carbpol.2026.124996
Congpei Wu , Zhenqi Hu , Jianping Zhang , Chang Tian , Anthony Chun Yin Yuen , Jinlong Zhao
Traditional fluorinated foams (AFFF/FFFP), widely used for liquid fire suppression, suffer from poor thermal stability, re-ignition propensity, and often contain environmentally harmful fluorocarbon surfactants. This study developed an interpenetrating double-network gel foam (IDNGF) using non-fluorinated surfactants (AEG and AOS), gelling agent (CMC-Na and Na₂SiO₃), and crosslinking agent (AlCit). Orthogonal experiments optimized the foam expansion ratio and water retention. The optimal formulation—0.6 wt% AOS/AEG (1:9), 2.2 wt% Na₂SiO₃, 0.14 wt% CMCNa, and 1.0 wt% AlCit—produced homogeneous foams with enhanced thermal stability due to the formation of a CMC–Al3+/silicate double-network structure. Thermogravimetric analysis revealed a significantly higher complete evaporation temperature than conventional FFFP. Reactive forcefield molecular dynamics (ReaxFF-MD) simulations identified orthosilicic acid and aluminum-containing oxides as key pyrolysis products. Fire extinguishing and re-ignition existence experiments demonstrated that IDNGF reduced extinguishing time by 3.6% relative to FFFP while significantly extending the burnback time to 603 s—a 76.3% improvement. These results highlight the potentil of using IDNGF as a high-performance, re-ignition-resistant, and sustainable fire suppression agent.
{"title":"Development of a double-network gel foam based on sodium carboxymethyl cellulose with enhanced extinguishing and re-ignition resistance performance for tank fires","authors":"Congpei Wu , Zhenqi Hu , Jianping Zhang , Chang Tian , Anthony Chun Yin Yuen , Jinlong Zhao","doi":"10.1016/j.carbpol.2026.124996","DOIUrl":"10.1016/j.carbpol.2026.124996","url":null,"abstract":"<div><div>Traditional fluorinated foams (AFFF/FFFP), widely used for liquid fire suppression, suffer from poor thermal stability, re-ignition propensity, and often contain environmentally harmful fluorocarbon surfactants. This study developed an interpenetrating double-network gel foam (IDNGF) using non-fluorinated surfactants (AEG and AOS), gelling agent (CMC-Na and Na₂SiO₃), and crosslinking agent (AlCit). Orthogonal experiments optimized the foam expansion ratio and water retention. The optimal formulation—0.6 wt% AOS/AEG (1:9), 2.2 wt% Na₂SiO₃, 0.14 wt% CMC<img>Na, and 1.0 wt% AlCit—produced homogeneous foams with enhanced thermal stability due to the formation of a CMC–Al<sup>3+</sup>/silicate double-network structure. Thermogravimetric analysis revealed a significantly higher complete evaporation temperature than conventional FFFP. Reactive forcefield molecular dynamics (ReaxFF-MD) simulations identified orthosilicic acid and aluminum-containing oxides as key pyrolysis products. Fire extinguishing and re-ignition existence experiments demonstrated that IDNGF reduced extinguishing time by 3.6% relative to FFFP while significantly extending the burnback time to 603 s—a 76.3% improvement. These results highlight the potentil of using IDNGF as a high-performance, re-ignition-resistant, and sustainable fire suppression agent.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"379 ","pages":"Article 124996"},"PeriodicalIF":12.5,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076550","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124979
Yue Huang , Dekun Meng , Nan Zhang , Huajiang Zhang , Lina Xu , Yunhe Xu , Hanyu Li , Ning Xia , Mohamed Ghamry , Ahmed M. Rayan
The integration of polysaccharides into high internal phase Pickering emulsions (HIPPEs) has been recognized as an innovative approach to improving their stability. To reveal the enhancing mechanisms of gellan gum (GG) on the stability of HIPPEs based on egg yolk granules (EYGs), this study systematically investigated the effect of GG concentration on the molecular structure, interfacial properties, and emulsion stability of EYGs-GG complexes. The results showed that HIPPEs stabilized by EYGs-0.3%GG complex exhibited the highest stability. In this complex, GG bound to the surface of EYGs particles via electrostatic attractions and hydrophobic interactions, leading to a 60.0% higher surface charge and a 59.2% lower surface hydrophobicity compared with those of EYGs particles. While the interaction reduced the penetration of EYGs particles at the oil-water interface, it increased the diffusion rate and molecular rearrangement behavior, facilitating the formation of the stable elastic interfacial film. Moreover, adding 0.3% GG formed denser 3D network structures in the aqueous phase, which inhibited oil droplet coalescence and further enhanced the structural strength of the HIPPEs. These findings provided theoretical insights into the mechanism by which GG enhanced the stability of emulsions based on EYGs, offering a rational design strategy for developing high-performance systems of HIPPEs.
{"title":"Insight into the mechanism of gellan gum enhancing stability of high internal phase Pickering emulsions based on egg yolk granules: Intermolecular interaction and network structure","authors":"Yue Huang , Dekun Meng , Nan Zhang , Huajiang Zhang , Lina Xu , Yunhe Xu , Hanyu Li , Ning Xia , Mohamed Ghamry , Ahmed M. Rayan","doi":"10.1016/j.carbpol.2026.124979","DOIUrl":"10.1016/j.carbpol.2026.124979","url":null,"abstract":"<div><div>The integration of polysaccharides into high internal phase Pickering emulsions (HIPPEs) has been recognized as an innovative approach to improving their stability. To reveal the enhancing mechanisms of gellan gum (GG) on the stability of HIPPEs based on egg yolk granules (EYGs), this study systematically investigated the effect of GG concentration on the molecular structure, interfacial properties, and emulsion stability of EYGs-GG complexes. The results showed that HIPPEs stabilized by EYGs-0.3%GG complex exhibited the highest stability. In this complex, GG bound to the surface of EYGs particles via electrostatic attractions and hydrophobic interactions, leading to a 60.0% higher surface charge and a 59.2% lower surface hydrophobicity compared with those of EYGs particles. While the interaction reduced the penetration of EYGs particles at the oil-water interface, it increased the diffusion rate and molecular rearrangement behavior, facilitating the formation of the stable elastic interfacial film. Moreover, adding 0.3% GG formed denser 3D network structures in the aqueous phase, which inhibited oil droplet coalescence and further enhanced the structural strength of the HIPPEs. These findings provided theoretical insights into the mechanism by which GG enhanced the stability of emulsions based on EYGs, offering a rational design strategy for developing high-performance systems of HIPPEs.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"379 ","pages":"Article 124979"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124981
Jingya Ruan , Ping Zhang , Jiaming Cheng , Lequan Yu , Yijin Wu , Yinuo Zheng , Yi Zhang , Tao Wang
Two glycans, ZJPr2–2-1 and ZJPr3–2-1, were isolated from jujube fruits. Structural analysis revealed ZJPr2–2-1 (7.20 kDa) as a previously unreported pectin featuring main chain of →4)-α-D-GalpA-(1→, →3,4)-α-D-GalpA-(1→, and →3)-α-L-Rhap-(1→, with side chains containing →4)-α-L-Arap-(1→, and t-4-deoxy-L-threo-hex-4-enopyranuronic acid (t-α-L-HexA), as well as two isolated fragments linked to →4)-β-D-GalpA, →4)-α-D-GalpA. Nevertheless, the absence of HMBC correlations precluded the structural elucidation of its connected side chain. Meanwhile, ZJPr3–2-1 was identified as the first plant-derived cyclic α-1,6-glucan heptasaccharide. Both glycans were found to promote M1 macrophage polarization (increased CD86 and decreased CD206 expression), and enhance the production of pro-inflammatory mediators (NO, iNOS, and TNF-α) in RAW264.7 cells. The mechanism was supposed to associated with the direct (ZJPr3–2-1) and indirect (ZJPr2–2-1) activation of the Dectin-1/Syk signaling pathway.
从枣果实中分离得到ZJPr2-2-1和ZJPr3-2-1两个聚糖。结构分析表明,ZJPr2-2-1 (7.20 kDa)是一种未见报道的果胶,其主链为→4)-α- d - galpa -(1→,→3,4)-α- d - galpa -(1→,→3)-α- l - rhap -(1→,和→3)-α- l - rhap -(1→),侧链含有→4)-α- l - arap -(1→,和t-4-脱氧- l -三己-4-烯吡喃醛酸(t-α- l - hexa),以及两个分离片段连接到→4)-β- d - galpa,→4)-α- d - galpa。然而,缺乏HMBC相关性排除了其连接侧链的结构解析。同时,ZJPr3-2-1被鉴定为第一个植物衍生的环α-1,6-葡聚糖七糖。两种聚糖均可促进M1巨噬细胞极化(增加CD86表达,降低CD206表达),并增强RAW264.7细胞中促炎介质(NO、iNOS和TNF-α)的产生。其机制可能与Dectin-1/Syk信号通路的直接(ZJPr3-2-1)和间接(ZJPr2-2-1)激活有关。
{"title":"Structural properties of two glycans in the fruits of jujube and their regulation effect of M1-type and M2-type macrophage","authors":"Jingya Ruan , Ping Zhang , Jiaming Cheng , Lequan Yu , Yijin Wu , Yinuo Zheng , Yi Zhang , Tao Wang","doi":"10.1016/j.carbpol.2026.124981","DOIUrl":"10.1016/j.carbpol.2026.124981","url":null,"abstract":"<div><div>Two glycans, <strong>ZJPr2–2-1</strong> and <strong>ZJPr3–2-1</strong>, were isolated from jujube fruits. Structural analysis revealed <strong>ZJPr2–2-1</strong> (7.20 kDa) as a previously unreported pectin featuring main chain of →4)-<em>α</em>-D-Gal<em>p</em>A-(1→, →3,4)-<em>α</em>-D-Gal<em>p</em>A-(1→, and →3)-<em>α</em>-L-Rha<em>p</em>-(1→, with side chains containing →4)-<em>α</em>-L-Ara<em>p</em>-(1→, and t-4-deoxy-L-<em>threo</em>-hex-4-enopyranuronic acid (t-<em>α</em>-L-HexA), as well as two isolated fragments linked to →4)-<em>β</em>-D-Gal<em>p</em>A, →4)-<em>α</em>-D-Gal<em>p</em>A. Nevertheless, the absence of HMBC correlations precluded the structural elucidation of its connected side chain. Meanwhile, <strong>ZJPr3–2-1</strong> was identified as the first plant-derived cyclic <em>α</em>-1,6-glucan heptasaccharide. Both glycans were found to promote M1 macrophage polarization (increased CD86 and decreased CD206 expression), and enhance the production of pro-inflammatory mediators (NO, iNOS, and TNF-<em>α</em>) in RAW264.7 cells. The mechanism was supposed to associated with the direct (<strong>ZJPr3–2-1</strong>) and indirect (<strong>ZJPr2–2-1</strong>) activation of the Dectin-1/Syk signaling pathway.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"378 ","pages":"Article 124981"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146024204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124984
Mengkun Song , Yongji Ni , Junhui Gao , Xiangjie Li , Yingying Zhang , Yanyan Zhang , Xingli Liu , Huishan Shen , Hua Zhang , Hongwei Wang
This work investigated the evolution of multi-scale structures and physicochemical properties of starch from the break, sizing, reduction and tailing flour mill streams and their influence on Chinese steamed bread quality. The break milling with toothed rollers severely damaged starch granular surface, thinned semi-crystalline lamellae, reduced crystallinity degree and molecular orderliness. As milling progressed from the sizing to the tailing system, intensified mechanical forces induced surface cracks and disrupted lamellar structure. Furthermore, these forces could induce disorganization or amorphization of ordered crystalline, short-range ordered and double-helical structure as milling proceeded from the sizing to the tailing system, with the values of starch relative crystallinity, R1047/1022 and double helices decreased from 22.8% to 18.1%, 0.89 to 0.77, and 40.8% to 36.2%, respectively. The resultant structural disordering enhanced water-starch interactions, thereby markedly increasing the hydration capacity, swelling power and characteristic viscosity of starch, especially for starch from the tailing system. The steamed bread reconstituted with sizing and reduction starches presented a higher specific volume and lower hardness compared to those containing break and tailing starches, which could be attributed to their well-preserved structural stability. The findings provide a theoretical basis for optimizing the wheat flour milling process and regulating steamed bread quality.
{"title":"Mechanistic insights into how wheat flour mill streams affect Chinese steamed bread quality: A perspective from starch multi-scale structure and physicochemical properties","authors":"Mengkun Song , Yongji Ni , Junhui Gao , Xiangjie Li , Yingying Zhang , Yanyan Zhang , Xingli Liu , Huishan Shen , Hua Zhang , Hongwei Wang","doi":"10.1016/j.carbpol.2026.124984","DOIUrl":"10.1016/j.carbpol.2026.124984","url":null,"abstract":"<div><div>This work investigated the evolution of multi-scale structures and physicochemical properties of starch from the break, sizing, reduction and tailing flour mill streams and their influence on Chinese steamed bread quality. The break milling with toothed rollers severely damaged starch granular surface, thinned semi-crystalline lamellae, reduced crystallinity degree and molecular orderliness. As milling progressed from the sizing to the tailing system, intensified mechanical forces induced surface cracks and disrupted lamellar structure. Furthermore, these forces could induce disorganization or amorphization of ordered crystalline, short-range ordered and double-helical structure as milling proceeded from the sizing to the tailing system, with the values of starch relative crystallinity, <em>R</em><sub>1047/1022</sub> and double helices decreased from 22.8% to 18.1%, 0.89 to 0.77, and 40.8% to 36.2%, respectively. The resultant structural disordering enhanced water-starch interactions, thereby markedly increasing the hydration capacity, swelling power and characteristic viscosity of starch, especially for starch from the tailing system. The steamed bread reconstituted with sizing and reduction starches presented a higher specific volume and lower hardness compared to those containing break and tailing starches, which could be attributed to their well-preserved structural stability. The findings provide a theoretical basis for optimizing the wheat flour milling process and regulating steamed bread quality.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"378 ","pages":"Article 124984"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2025.124510
Wen Sun , Changjun Mu , Xu Zhang , Hengchong Shi , Qiuyan Yan , Shifang Luan
{"title":"Corrigendum to “Mussel-inspired polysaccharide-based sponges for hemostasis and bacteria infected wound healing” [Carbohydrate Polymers 295 (2022) 119868]","authors":"Wen Sun , Changjun Mu , Xu Zhang , Hengchong Shi , Qiuyan Yan , Shifang Luan","doi":"10.1016/j.carbpol.2025.124510","DOIUrl":"10.1016/j.carbpol.2025.124510","url":null,"abstract":"","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"377 ","pages":"Article 124510"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146074118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124983
Shanshan Li , Lixin Xia , Shuo Wang , Ruibao Ju , Zi Han , Xiansen Lv , Baoqin Han , Jinhua Chi
Acute liver injury (ALI) caused by acetaminophen (APAP) has a high incidence rate worldwide, and severe cases may cause liver failure or even death. N-acetylcysteine (NAC), as an effective treatment drug approved for clinical application in ALI, has limitations such as a short half-life and the requirement for high-dose injections. Consequently, it is imperative to optimize new administration method of NAC and promote alternative therapeutic strategies for ALI. Herein, hydrogel patches ONC composed of oxidized chondroitin sulfate (OCS) and NAC-grafted CMCS were developed, and their reparative effects on APAP-induced ALI were investigated. ONC hydrogels exhibited excellent biocompatibility and appropriate biodegradability, and favorable hemostatic effects in the liver. In vitro experiments demonstrated that ONC could promote the proliferation and migration of hepatocytes, as well as the angiogenesis of HUVECs. By establishing an APAP-induced ALI model in mice, liver enzymes after ONC hydrogel patches treatment recovered to near-normal levels. Moreover, histological examination, RT-qPCR, and transcriptome sequencing results demonstrated that ONC patches could reduce the expression of inflammatory factors and apoptosis in the liver, while simultaneously activating antioxidant-related signaling pathways, thereby promoting the regeneration and functional repair of damaged tissues. Therefore, ONC hydrogel patches may be a promising alternative strategy for treating ALI.
{"title":"N-acetylcysteine-functionalized biodegradable polysaccharide hydrogel patches for the repair of acute liver injury","authors":"Shanshan Li , Lixin Xia , Shuo Wang , Ruibao Ju , Zi Han , Xiansen Lv , Baoqin Han , Jinhua Chi","doi":"10.1016/j.carbpol.2026.124983","DOIUrl":"10.1016/j.carbpol.2026.124983","url":null,"abstract":"<div><div>Acute liver injury (ALI) caused by acetaminophen (APAP) has a high incidence rate worldwide, and severe cases may cause liver failure or even death. <em>N</em>-acetylcysteine (NAC), as an effective treatment drug approved for clinical application in ALI, has limitations such as a short half-life and the requirement for high-dose injections. Consequently, it is imperative to optimize new administration method of NAC and promote alternative therapeutic strategies for ALI. Herein, hydrogel patches ONC composed of oxidized chondroitin sulfate (OCS) and NAC-grafted CMCS were developed, and their reparative effects on APAP-induced ALI were investigated. ONC hydrogels exhibited excellent biocompatibility and appropriate biodegradability, and favorable hemostatic effects in the liver. In vitro experiments demonstrated that ONC could promote the proliferation and migration of hepatocytes, as well as the angiogenesis of HUVECs. By establishing an APAP-induced ALI model in mice, liver enzymes after ONC hydrogel patches treatment recovered to near-normal levels. Moreover, histological examination, RT-qPCR, and transcriptome sequencing results demonstrated that ONC patches could reduce the expression of inflammatory factors and apoptosis in the liver, while simultaneously activating antioxidant-related signaling pathways, thereby promoting the regeneration and functional repair of damaged tissues. Therefore, ONC hydrogel patches may be a promising alternative strategy for treating ALI.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"379 ","pages":"Article 124983"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124978
Faying Zheng , Xinxin Li , Zhaowei Han , Xuchun Zhu , Pengtao Zhang , Feiyue Ren , Hongzhi Liu
The incorporation of fiber polysaccharides into refined wheat flour enhances its nutritional properties. However, promoting the consumption of high dietary fiber (DF) products is challenging due to the undesirable quality issues. This review examines the potential of incorporating physically modified DF polysaccharides to enhance quality, with a specific focus on their impact on DF structure, dough rheological properties, and the quality of the final product. Different physical modification techniques exert distinct structural fingerprints on DF, each inducing primary effects at different hierarchical levels. Extrusion-induced increases in soluble components were observed to enhance dough extensibility, while ultrasonic and microwave treatments formed surface structures that promoted dough water absorption. Micronization helped maintain gluten network continuity, which in turn improved dough viscoelasticity. Furthermore, improvements in the gluten matrix, gas phase, and the formation of liquid films are considered key mechanisms through which physically modified DF enhances the quality of flour products. Additionally, mechanical stress-induced cell-wall disruption was associated with increased nutrient release from the DF matrix. This study offers theoretical guidance for the quality formation of high DF products, potentially supporting the creation of products that balance nutritional value with sensory appeal.
{"title":"Improvement of dough rheological behavior and overall product quality through incorporation of physically modified dietary fiber polysaccharides: A review","authors":"Faying Zheng , Xinxin Li , Zhaowei Han , Xuchun Zhu , Pengtao Zhang , Feiyue Ren , Hongzhi Liu","doi":"10.1016/j.carbpol.2026.124978","DOIUrl":"10.1016/j.carbpol.2026.124978","url":null,"abstract":"<div><div>The incorporation of fiber polysaccharides into refined wheat flour enhances its nutritional properties. However, promoting the consumption of high dietary fiber (DF) products is challenging due to the undesirable quality issues. This review examines the potential of incorporating physically modified DF polysaccharides to enhance quality, with a specific focus on their impact on DF structure, dough rheological properties, and the quality of the final product. Different physical modification techniques exert distinct structural fingerprints on DF, each inducing primary effects at different hierarchical levels. Extrusion-induced increases in soluble components were observed to enhance dough extensibility, while ultrasonic and microwave treatments formed surface structures that promoted dough water absorption. Micronization helped maintain gluten network continuity, which in turn improved dough viscoelasticity. Furthermore, improvements in the gluten matrix, gas phase, and the formation of liquid films are considered key mechanisms through which physically modified DF enhances the quality of flour products. Additionally, mechanical stress-induced cell-wall disruption was associated with increased nutrient release from the DF matrix. This study offers theoretical guidance for the quality formation of high DF products, potentially supporting the creation of products that balance nutritional value with sensory appeal.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"378 ","pages":"Article 124978"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Edible coleopteran insects are an important source for sustainable protein and generating chitin as a significant waste (exuviae, cuticle residues, and frass), which can be valorized into value-added biopolymers. These side-streams can be diverted for chitin and chitosan production due to their biocompatibility and biodegradability in biomaterial applications which gained attention in recent times. Therefore, this review evaluates various types of chitin and chitosan extractions and their structural characterization suitable for industrial applications. The nutritional and bioactive functionalities of chitin as derived from coleoptera insect side-streams were critically discussed. Furthermore, it also distinguishes the presence of α-, β-, and γ-chitin polymorphic forms exhibited in the coleopterans order with recent research gaps was also discussed herein. Currently, there is no literature review that describes the roles of coleopteran side-streams derived chitin and chitosan. Hence, this review not only underscores the potential for chitin production from coleopteran side-streams but also outlines critical bottlenecks that warrant further investigation in biopolymer chemistry. Moreover, it provides comprehensive recommendations to facilitate the scale-up of chitin and chitosan derived from coleopteran side-streams as an added advantage for new business models.
{"title":"Critical insights into coleopteran insect side-streams derived chitin and chitosan: extraction chemistry, structural features and multifunctional applications","authors":"Divya Karthick Rajan , Durairaj Karthick Rajan , Jayakumar Rajarajeswaran , Nagarajan Revathi , Shubing Zhang , Kannan Mohan , Abirami Ramu Ganesan","doi":"10.1016/j.carbpol.2026.124958","DOIUrl":"10.1016/j.carbpol.2026.124958","url":null,"abstract":"<div><div>Edible coleopteran insects are an important source for sustainable protein and generating chitin as a significant waste (exuviae, cuticle residues, and frass), which can be valorized into value-added biopolymers. These side-streams can be diverted for chitin and chitosan production due to their biocompatibility and biodegradability in biomaterial applications which gained attention in recent times. Therefore, this review evaluates various types of chitin and chitosan extractions and their structural characterization suitable for industrial applications. The nutritional and bioactive functionalities of chitin as derived from coleoptera insect side-streams were critically discussed. Furthermore, it also distinguishes the presence of α-, β-, and γ-chitin polymorphic forms exhibited in the coleopterans order with recent research gaps was also discussed herein. Currently, there is no literature review that describes the roles of coleopteran side-streams derived chitin and chitosan. Hence, this review not only underscores the potential for chitin production from coleopteran side-streams but also outlines critical bottlenecks that warrant further investigation in biopolymer chemistry. Moreover, it provides comprehensive recommendations to facilitate the scale-up of chitin and chitosan derived from coleopteran side-streams as an added advantage for new business models.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"378 ","pages":"Article 124958"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146024274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1016/j.carbpol.2026.124982
Ane García-García , Maialen Goyoaga , Francisco Nuño , Ana Catarina Lopes , Estíbaliz Hernáez-Laviña , Isabel Moreno-Benítez , Jose Luis Vilas-Vilela , Senentxu Lanceros , Leyre Pérez-Álvarez
Despite the increasing interest on self-healing hydrogels in the fabrication of customized scaffolds for tissue engineering applications, their optimal printability is still a challenge due to the weak mechanical stability of dynamic networks. This work presents the first successful extrusion-based 3D-printing of N-succinyl chitosan (S-CHI) and oxidized hyaluronic acid (A-HA). The dynamic hydrogels based on imine bonds formation between S-CHI and A-HA were reinforced with graphene oxide (GO), amino-functionalized GO (GO-NH2), carboxyl-functionalized carbon nanotubes (CNT-COOH), and amino-functionalized CNTs (CNT-NH2) in order to study their effect on the 3D-printability, mechanical, rheological and self-healing properties of the gels. Compression tests, strain sweeps tests and the geometry of the printed scaffolds shown that non-aminolized GO and CNTs strengthen the networks, and improve printability but cause a detrimental effect on the self-recovery capability, unlike amino-functionalized fillers that enhance self-repairing but weaken mechanical strength and printability. The presence of the fillers also delays gelation, particularly in the case of amino functionalized particles. However, electrochemical impedance spectroscopy confirmed that the incorporation of the fillers did not affect the electrical conductivity of the hydrogels. Besides, this study analyses the role of the molecular weight of S-CHI units on the aforementioned properties.
{"title":"Dynamic chitosan-hyaluronic acid hydrogels for extrusion printing: Combined effects of polymer molecular weight and carbon nanofillers","authors":"Ane García-García , Maialen Goyoaga , Francisco Nuño , Ana Catarina Lopes , Estíbaliz Hernáez-Laviña , Isabel Moreno-Benítez , Jose Luis Vilas-Vilela , Senentxu Lanceros , Leyre Pérez-Álvarez","doi":"10.1016/j.carbpol.2026.124982","DOIUrl":"10.1016/j.carbpol.2026.124982","url":null,"abstract":"<div><div>Despite the increasing interest on self-healing hydrogels in the fabrication of customized scaffolds for tissue engineering applications, their optimal printability is still a challenge due to the weak mechanical stability of dynamic networks. This work presents the first successful extrusion-based 3D-printing of <em>N</em>-succinyl chitosan (S-CHI) and oxidized hyaluronic acid (A-HA). The dynamic hydrogels based on imine bonds formation between S-CHI and A-HA were reinforced with graphene oxide (GO), amino-functionalized GO (GO-NH<sub>2</sub>), carboxyl-functionalized carbon nanotubes (CNT-COOH), and amino-functionalized CNTs (CNT-NH<sub>2</sub>) in order to study their effect on the 3D-printability, mechanical, rheological and self-healing properties of the gels. Compression tests, strain sweeps tests and the geometry of the printed scaffolds shown that non-aminolized GO and CNTs strengthen the networks, and improve printability but cause a detrimental effect on the self-recovery capability, unlike amino-functionalized fillers that enhance self-repairing but weaken mechanical strength and printability. The presence of the fillers also delays gelation, particularly in the case of amino functionalized particles. However, electrochemical impedance spectroscopy confirmed that the incorporation of the fillers did not affect the electrical conductivity of the hydrogels. Besides, this study analyses the role of the molecular weight of S-CHI units on the aforementioned properties.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"379 ","pages":"Article 124982"},"PeriodicalIF":12.5,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-20DOI: 10.1016/j.carbpol.2026.124974
Peng Shi , Shibin Wang , Fengjie Ma , Mian Zhang , Hongbo Zeng
The adsorption conformation of guar gum molecules on silica surfaces determines the structural characteristics of the adsorption layer, potentially enabling diverse functionalities in engineering applications. However, the influence of grafted groups on the adsorption characteristics of guar gum remains unclear. The adsorption conformations and morphologies of unmodified ordinary guar gum (GG) and three modified guar gums — hydroxypropyl guar gum (HPG), carboxymethyl guar gum (CMG), and hydroxypropyl trimethylammonium chloride guar gum (HPTCG) — on silica surfaces were investigated via molecular dynamics simulations and AFM topography. The adsorption behavior of four guar gums was investigated by QCM-D experiment. The four guar gums exhibited distinct adsorption conformations: GG formed a mushroom-like structure, HPG adopted a “lying-flat” conformation with moderate folding, CMG presented an “L-shaped” orientation, and HPTCG displayed an upright conformation. AFM adhesion force measurements and chemical calculations indicated that the types and intensities of interactions between the four guar gums and silica surfaces varied. These differences result in different adsorption capacities, diffusion coefficients, adsorption layer stability, and layer structural characteristics of the four guar gums on silica surfaces. The results provide valuable insights for the molecular design of guar gum derivatives and their potential applications in interfacial fields.
{"title":"Effect of grafted groups on adsorption conformation and adsorption behavior of guar gum: insights from molecular interactions","authors":"Peng Shi , Shibin Wang , Fengjie Ma , Mian Zhang , Hongbo Zeng","doi":"10.1016/j.carbpol.2026.124974","DOIUrl":"10.1016/j.carbpol.2026.124974","url":null,"abstract":"<div><div>The adsorption conformation of guar gum molecules on silica surfaces determines the structural characteristics of the adsorption layer, potentially enabling diverse functionalities in engineering applications. However, the influence of grafted groups on the adsorption characteristics of guar gum remains unclear. The adsorption conformations and morphologies of unmodified ordinary guar gum (GG) and three modified guar gums — hydroxypropyl guar gum (HPG), carboxymethyl guar gum (CMG), and hydroxypropyl trimethylammonium chloride guar gum (HPTCG) — on silica surfaces were investigated via molecular dynamics simulations and AFM topography. The adsorption behavior of four guar gums was investigated by QCM-D experiment. The four guar gums exhibited distinct adsorption conformations: GG formed a mushroom-like structure, HPG adopted a “lying-flat” conformation with moderate folding, CMG presented an “L-shaped” orientation, and HPTCG displayed an upright conformation. AFM adhesion force measurements and chemical calculations indicated that the types and intensities of interactions between the four guar gums and silica surfaces varied. These differences result in different adsorption capacities, diffusion coefficients, adsorption layer stability, and layer structural characteristics of the four guar gums on silica surfaces. The results provide valuable insights for the molecular design of guar gum derivatives and their potential applications in interfacial fields.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"378 ","pages":"Article 124974"},"PeriodicalIF":12.5,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146024202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}