Systematic review of multi-mechanistic synergy and multifunctional integration in natural bio-gel design.
Proposed intelligently responsive hydrogel materials based on dynamic bonding and bionic design.
Development of full-cycle wound management systems and standardized manufacturing for clinical translation.
| [1] | Gong A., Yao X. and Lin W. (2020). Dermoscopy image classification based on styleGANs and decision fusion. IEEE Access 8:70640−70650. DOI:10.1109/ACCESS.2020.2986916 |
| [2] | Xi Y. W., Ge J., Wang M., et al. (2020). Bioactive anti-inflammatory, antibacterial, antioxidative silicon-based nanofibrous dressing enables cutaneous tumor photothermo-chemo therapy and infection-induced wound healing. ACS Nano 14:2904−2916. DOI:10.1021/acsnano.9b07173 |
| [3] | Eslahi N., Soleimani F., Lotfi R., et al. (2024). How biomimetic nanofibers advance the realm of cutaneous wound management: The state-of-the-art and future prospects. Prog. Mater. Sci. 145:101293. DOI:10.1016/j.pmatsci.2024.101293 |
| [4] | Lee J., Rabbani C. C., Gao H., et al. (2020). Hair-bearing human skin generated entirely from pluripotent stem cells. Nature 582:399−404. DOI:10.1038/s41586-020-2352-3 |
| [5] | Zeng Z. Y., Zhang J. M., Gao Y. G., et al. (2024). Bioadhesive first-aid patch with rapid hemostasis and high toughness designed for sutureless sealing of acute bleeding wounds. Adv. Healthc. Mater. 14:2403412. DOI:10.1002/adhm.202403412 |
| [6] | Brohi K., Gruen R. L. and Holcomb J. B. (2019). Why are bleeding trauma patients still dying. Intens. Care Med. 45:709−711. DOI:10.1007/s00134-019-05560-x |
| [7] | Fang Y., Guo W., Ni P., et al. (2024). Recent research advances in polysaccharide-based hemostatic materials: A review. Int. J. Biol. Macromol. 271:132559. DOI:10.1016/j.ijbiomac.2024.132559 |
| [8] | Enoch S. and Leaper D. J. (2008). Basic science of wound healing. Surgery (Oxford) 26:31−37. DOI:10.1016/j.mpsur.2007.11.005 |
| [9] | Wang P. H., Huang B. S., Horng H. C., et al. (2018). Wound healing. J. Chin. Med. Assoc. 81:94−101. DOI:10.1016/j.jcma.2017.11.002 |
| [10] | Huang K., Liu W. B., Wei W. Y., et al. (2022). Photothermal hydrogel encapsulating intelligently bacteria-capturing bio-MOF for infectious wound healing. ACS Nano 16:19491−19508. DOI:10.1021/acsnano.2c09593 |
| [11] | Guo S., Ren Y. K., Chang R., et al. (2022). Injectable self-healing adhesive chitosan hydrogel with antioxidative, antibacterial, and hemostatic activities for rapid hemostasis and skin wound healing. ACS Appl. Mater. Interfaces 14:34455−34469. DOI:10.1021/acsami.2c08870 |
| [12] | Jiang S. B., Liu S. Y., Lau S., et al. (2022). Hemostatic biomaterials to halt non-compressible hemorrhage. J. Mater. Chem. B 10:7239−7259. DOI:10.1039/d2tb00546h |
| [13] | Chan L. W., Ching A. L., Liew C. V., et al. (2007). Mechanistic study on hydration and drug release behavior of sodium alginate compacts. Drug Dev. Ind. Pharm. 33:667−676. DOI:10.1080/03639040600943814 |
| [14] | Huang Y., Zhao X., Wang C., et al. (2022). High-strength anti-bacterial composite cryogel for lethal noncompressible hemorrhage hemostasis: Synergistic physical hemostasis and chemical hemostasis. Chem. Eng. J. 427:131977. DOI:10.1016/j.cej.2021.131977 |
| [15] | Peng X., Xu X., Deng Y. R., et al. (2021). Ultrafast self-gelling and wet adhesive powder for acute hemostasis and wound healing. Adv. Funct. Mater. 31: 2102583. DOI:10.1002/adfm.202102583 |
| [16] | Wang Y., Guo Y. C., Liu Y. Q., et al. (2024). Platelet vesicles synergetic with biosynthetic cellulose aerogels for ultra-fast hemostasis and wound healing. Adv. Healthc. Mater. 13. DOI:10.1002/adhm.202304523 |
| [17] | Haining E. J., Cherpokova D., Wolf K., et al. (2017). CLEC-2 contributes to hemostasis independently of classical hemITAM signaling in mice. Blood 130:2224−2228. DOI:10.1182/blood-2017-03-771907 |
| [18] | Jiang D., Houck K. L., Murdiyarso L., et al. (2024). RBCs regulate platelet function and hemostasis under shear conditions through biophysical and biochemical means. Blood 144:1521−1531. DOI:10.1182/blood.2024023887 |
| [19] | Poventud-Fuentes I., Kwon K. W., Seo J., et al. (2021). A human vascular injury-on-a-chip model of hemostasis. Small 17:2004889. DOI:10.1002/smll.202004889 |
| [20] | Wei J. J., Zhang W. T., Mou X. H., et al. (2024). Bioinspired hemostatic and anti-infective armor for wound healing assisted by metal-phenol-polyamine system. Adv. Funct. Mater. 34:2306267. DOI:10.1002/adfm.202306267 |
| [21] | Sakurai Y., Hardy E. T., Ahn B., et al. (2018). A microengineered vascularized bleeding model that integrates the principal components of hemostasis. Nat. Commun. 9:509. DOI:10.1038/s41467-018-02990-x |
| [22] | Xu T., Ji H. F., Xu L., et al. (2023). Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation. Nat. Commun. 14:4875. DOI:10.1038/s41467-023-40646-7 |
| [23] | Zheng C., Liu H., Ginsburg D., et al. (2009). Critical role of calcium in the regulation of the ER-to-Golgi transport of FV and FVIII by the LMAN1-MCFD2 cargo receptor. Blood 114:2140−2140. DOI:10.1182/blood.V114.22.2140.2140 |
| [24] | Zhang X., Yang C., Zeng X., et al. (2024). A bioactive composite sponge based on biomimetic collagen fibril and oxidized alginate for noncompressible hemorrhage and wound healing. Carbohydr. Polym. 343:122409. DOI:10.1016/j.carbpol.2024.122409 |
| [25] | Scales J. T. (1963). Wound healing and the dressing. Br. J. Ind. Med. 20:82−94. DOI:10.1136/oem.20.2.82 |
| [26] | Puthia M., Butrym M., Petrlova J., et al. (2020). A dual-action peptide-containing hydrogel targets wound infection and inflammation. Sci. Transl. Med. 12:eaax6601. DOI:10.1126/scitranslmed.aax6601 |
| [27] | Liang J. H., Ling J. H., Sun D. G., et al. (2024). Dextran-based antibacterial hydrogel dressings for accelerating infected wound healing by reducing inflammation levels. Adv. Healthc. Mater. 13:2400494. DOI:10.1002/adhm.202400494 |
| [28] | Rong L. D., Liu Y., Fan Y., et al. (2023). Injectable nano-composite hydrogels based on hyaluronic acid-chitosan derivatives for simultaneous photothermal-chemo therapy of cancer with anti-inflammatory capacity. Carbohydr. Polym. 310:120721. DOI:10.1016/j.carbpol.2023.120721 |
| [29] | Chang L. M., Chen Y. N., Zhou M., et al. (2024). Photothermal enhanced antibacterial chitosan-based polydopamine composite hydrogel for hemostasis and burn wound repairing. Carbohydr. Polym. 345:122568. DOI:10.1016/j.carbpol.2024.122568 |
| [30] | Zhao X., Liang Y. P., Huang Y., et al. (2020). Physical double-network hydrogel adhesives with rapid shape adaptability, fast self-healing, antioxidant and nir/ph stimulus-responsiveness for multidrug-resistant bacterial infection and removable wound dressing. Adv. Funct. Mater. 30:1910748. DOI:10.1002/adfm.201910748 |
| [31] | Rubio P. A. (1991). Use of semiocclusive, transparent film dressings for surgical wound protection - experience in 3637 cases. Int. Surg. 76:253−254. |
| [32] | Zhang Y. T., Gao X., Tang X. N., et al. (2023). A dual pH- and temperature-responsive hydrogel produced in situ crosslinking of cyclodextrin-cellulose for wound healing. Int. J. Biol. Macromol. 253:126693. DOI:10.1016/j.ijbiomac.2023.126693 |
| [33] | Wang X. Y., Wang Z. P., Fang S., et al. (2021). Injectable Ag nanoclusters-based hydrogel for wound healing via eliminating bacterial infection and promoting tissue regeneration. Chem. Eng. J. 420:127589. DOI:10.1016/j.cej.2020.127589 |
| [34] | Meng W. L., Lin Z., Cheng X., et al. (2024). Thiourea-cation chelation based hydrogel and its application as antibacterial dressing for the repair of diabetic wound. Adv. Funct. Mater. 34:202314202. DOI:10.1002/adfm.202314202 |
| [35] | Song Y. B., Xing J., Ren L., et al. (2023). Preparation of multi-functional quaternary ammonium chitosan/surfactin hydrogel and its application in wound management. Macromol. Biosci. 23:2300166. DOI:10.1002/mabi.202300166 |
| [36] | Du S., Zhou N., Xie G., et al. (2021). Surface-engineered triboelectric nanogenerator patches with drug loading and electrical stimulation capabilities: Toward promoting infected wounds healing. Nano Energy 85:106004. DOI:10.1016/j.nanoen.2021.106004 |
| [37] | Zhu S. L., Dai Q. Y., Yao L. T., et al. (2022). Engineered multifunctional nanocomposite hydrogel dressing to promote vascularization and anti-inflammation by sustained releasing of Mg2+ for diabetic wounds. Compos. Pt. B-Eng. 231:109569. DOI:10.1016/j.compositesb.2021.109569 |
| [38] | Schaly S., Islam P., Abosalha A., et al. (2022). Alginate-Chitosan hydrogel formulations sustain baculovirus delivery and vegfa expression which promotes angiogenesis for wound dressing applications. Pharmaceuticals 15:1382. DOI:10.3390/ph15111382 |
| [39] | Song Y. N., Li S., Chen H. F., et al. (2023). Kaolin-loaded carboxymethyl chitosan/sodium alginate composite sponges for rapid hemostasis. Int. J. Biol. Macromol. 233:123532. DOI:10.1016/j.ijbiomac.2023.123532 |
| [40] | Du X. C., Wu L., Yan H. Y., et al. (2021). Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing. Nat. Commun. 12:4733. DOI:10.1038/s41467-021-24972-2 |
| [41] | Dong L. Z., Zhang W., Ren M., et al. (2023). Moisture-adaptive contractile biopolymer-derived fibers for wound healing promotion. Small 19:2300589. DOI:10.1002/smll.202300589 |
| [42] | Chen Z., Yao J. P., Zhao J. L., et al. (2023). Injectable wound dressing based on carboxymethyl chitosan triple-network hydrogel for effective wound antibacterial and hemostasis. Int. J. Biol. Macromol. 225:1235−1245. DOI:10.1016/j.ijbiomac.2022.11.184 |
| [43] | Pan G. X., Li F. H., He S. H., et al. (2022). Mussel- and barnacle cement proteins-inspired dual-bionic bioadhesive with repeatable wet-tissue adhesion, multimodal self-healing, and antibacterial capability for nonpressing hemostasis and promoted wound healing. Adv. Funct. Mater. 32:2200908. DOI:10.1002/adfm.202200908 |
| [44] | Peng X., Xu X., Deng Y., et al. (2021). Ultrafast self-gelling and wet adhesive powder for acute hemostasis and wound healing. Adv. Funct. Mater. 31:2102583. DOI:10.1002/adfm.202102583 |
| [45] | Tan Z., Li X., Yu C., et al. (2023). A self-gelling powder based on polyacrylic acid/polyacrylamide/quaternate chitosan for rapid hemostasis. Int. J. Biol. Macromol. 232:123449. DOI:10.1016/j.ijbiomac.2023.123449 |
| [46] | Luo Y., Fan L., Liu C., et al. (2022). An injectable, self-healing, electroconductive extracellular matrix-based hydrogel for enhancing tissue repair after traumatic spinal cord injury. Bioact. Mater. 7:98−111. DOI:10.1016/j.bioactmat.2021.05.039 |
| [47] | Asadi N., Pazoki-Toroudi H., Del Bakhshayesh A. R., et al. (2021). Multifunctional hydrogels for wound healing: special focus on biomacromolecular based hydrogels. Int. J. Biol. Macromol. 170:728−750. DOI:10.1016/j.ijbiomac.2020.12.202 |
| [48] | Ni P. X. Z., Ye S., Xiong S. T., et al. (2023). A chitosan-optimized polyethyleneimine/polyacrylic acid multifunctional hydrogel for reducing the risk of ulcerative arterial bleeding. J. Mater. Chem. B 11:5207−5222. DOI:10.1039/d3tb00239j |
| [49] | Lin P., Ma S. H., Wang X. L., et al. (2015). Molecularly engineered dual-crosslinked hydrogel with ultrahigh mechanical strength, toughness, and good self-recovery. Adv. Mater. 27:2054−2059. DOI:10.1002/adma.201405022 |
| [50] | Li Y. Y., Wen X., Li X. R., et al. (2025). Design of super stretchability, rapid self-healing, and self-adhesion hydrogel based on starch for wearable strain sensors. Carbohydr. Polym. 348:122858. DOI:10.1016/j.carbpol.2024.122858 |
| [51] | Qiao Z. W., Lv X. L., He S. H., et al. (2021). A mussel-inspired supramolecular hydrogel with robust tissue anchor for rapid hemostasis of arterial and visceral bleedings. Bioact. Mater. 6:2829−2840. DOI:10.1016/j.bioactmat.2021.01.039 |
| [52] | Ouyang Y. L., Zhao Y. Z., Zheng X. Y., et al. (2023). Rapidly degrading and mussel-inspired multifunctional carboxymethyl chitosan/montmorillonite hydrogel for wound hemostasis. Int. J. Biol. Macromol. 242:124960. DOI:10.1016/j.ijbiomac.2023.124960 |
| [53] | Liang Y. P., He J. H. and Guo B. L. (2021). Functional hydrogels as wound dressing to enhance wound healing. ACS Nano 15:12687−12722. DOI:10.1021/acsnano.1c04206 |
| [54] | Montazerian H., Davoodi E., Baidya A., et al. (2022). Engineered hemostatic biomaterials for sealing wounds. Chem. Rev. 122:12864−12903. DOI:10.1021/acs.chemrev.1c01015 |
| [55] | Guo B. L., Dong R. N., Bang Y. P., et al. (2021). Haemostatic materials for wound healing applications. Nat. Rev. Chem. 5:773−791. DOI:10.1038/s41570-021-00323-z |
| [56] | Chen Y., Wang X., Tao S., et al. (2023). Research advances in smart responsive-hydrogel dressings with potential clinical diabetic wound healing properties. Mil. Med. Res. 10:37. DOI:10.1186/s40779-023-00473-9 |
| [57] | Wang Y., Yang P., Wang Y., et al. (2025). Thrombin‐anchored bacterial cellulose dressing for advanced burn wound care. Adv. Mater. 2025:e20338. DOI:10.1002/adma.202420338 |
| [58] | Fang Y., Zhang L., Chen Y., et al. (2023). Polysaccharides based rapid self-crosslinking and wet tissue adhesive hemostatic powders for effective hemostasis. Carbohydr. Polym. 312:120819. DOI:10.1016/j.carbpol.2023.120819 |
| [59] | Jiang F., Duan Y., Li Q., et al. (2024). Insect chitosan/pullulan/gallium photo-crosslinking hydrogels with multiple bioactivities promote MRSA-infected wound healing. Carbohydr. Polym. 334:122045. DOI:10.1016/j.carbpol.2024.122045 |
| [60] | Sun W., Mu C., Zhang X., et al. (2022). Mussel-inspired polysaccharide-based sponges for hemostasis and bacteria infected wound healing. Carbohydr. Polym. 295:119868. DOI:10.1016/j.carbpol.2022.119868 |
| [61] | Chen J., An X., Xu L., et al. (2024). Adhesive nanoparticle-in-microgel system with ros scavenging capability and hemostatic activity for postoperative adhesion prevention. Small 20:2306598. DOI:10.1002/smll.202306598 |
| [62] | Han K., Bai Q., Wu W., et al. (2021). Gelatin-based adhesive hydrogel with self-healing, hemostasis, and electrical conductivity. Int. J. Biol. Macromol. 183:2142−2151. DOI:10.1016/j.ijbiomac.2021.05.147 |
| [63] | Wang J.-H., Tsai C.-W., Tsai N.-Y., et al. (2021). An injectable, dual crosslinkable hybrid pectin methacrylate (PECMA)/ gelatin methacryloyl (GelMA) hydrogel for skin hemostasis applications. Int. J. Biol. Macromol. 185:441−450. DOI:10.1016/j.ijbiomac.2021.06.162 |
| [64] | Babaluei M., Mojarab Y., Mottaghitalab F., et al. (2024). Conductive hydrogels based on tragacanth and silk fibroin containing dopamine functionalized carboxyl-capped aniline pentamer: merging hemostasis, antibacterial, and anti-oxidant properties into a multifunctional hydrogel for burn wound healing. Int. J. Biol. Macromol. 261:129932. DOI:10.1016/j.ijbiomac.2024.129932 |
| [65] | Han W., Zhou B., Yang K., et al. (2020). Biofilm-inspired adhesive and antibacterial hydrogel with tough tissue integration performance for sealing hemostasis and wound healing. Bioact. Mater. 5:768−778. DOI:10.1016/j.bioactmat.2020.05.008 |
| [66] | Wang Y., Zhang Y., Yang Y.-P., et al. (2024). Versatile dopamine-functionalized hyaluronic acid-recombinant human collagen hydrogel promoting diabetic wound healing via inflammation control and vascularization tissue regeneration. Bioact. Mater. 35:330−345. DOI:10.1016/j.bioactmat.2024.02.010 |
| [67] | Huang L.-J., Lin S.-H., Chen T.-Y., et al. (2024). Chitosan catechol-tannic acid composite hydrogel and cryogel with antimicrobial and hemostatic properties. Int. J. Biol. Macromol. 270:132174. DOI:10.1016/j.ijbiomac.2024.132174 |
| [68] | Du X., Wu L., Yan H., et al. (2021). Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing. Nat. Commun. 12:4733. DOI:10.1038/s41467-021-24972-2 |
| [69] | Leonhardt E. E., Kang N., Hamad M. A., et al. (2019). Absorbable hemostatic hydrogels comprising composites of sacrificial templates and honeycomb-like nanofibrous mats of chitosan. Nat. Commun. 10:2307. DOI:10.1038/s41467-019-10290-1 |
| [70] | Cheng H., Shi W., Feng L., et al. (2021). Facile and green approach towards biomass-derived hydrogel powders with hierarchical micro-nanostructures for ultrafast hemostasis. J. Mater. Chem. B 9:6678−6690. DOI:10.1039/d1tb01477c |
| [71] | Du Y., Chen X., Li L., et al. (2023). Benzeneboronic-alginate/quaternized chitosan-catechol powder with rapid self-gelation, wet adhesion, biodegradation and antibacterial activity for non-compressible hemorrhage control. Carbohydr. Polym. 318:121049. DOI:10.1016/j.carbpol.2023.121049 |
| [72] | Kumar A., Sah D. K., Khanna K., et al. (2023). A calcium and zinc composite alginate hydrogel for pre-hospital hemostasis and wound care. Carbohydr. Polym. 299:120186. DOI:10.1016/j.carbpol.2022.120186 |
| [73] | Li D., Dong X., Liu X., et al. (2024). Cellulose nanofibers embedded chitosan/tannin hydrogel with high antibacterial activity and hemostatic ability for drug-resistant bacterial infected wound healing. Carbohydr. Polym. 329:121687. DOI:10.1016/j.carbpol.2023.121687 |
| [74] | Pan S., Li Y., Tong X., et al. (2023). Strongly-adhesive easily-detachable carboxymethyl cellulose aerogel for noncompressible hemorrhage control. Carbohydr. Polym. 301:120324. DOI:10.1016/j.carbpol.2022.120324 |
| [75] | Sun Z., Chen X., Ma X., et al. (2018). Cellulose/keratin-catechin nanocomposite hydrogel for wound hemostasis. J. Mater. Chem. B 6:6133−6141. DOI:10.1039/c8tb01109e |
| [76] | An S., Jeon E. J., Jeon J., et al. (2019). A serotonin-modified hyaluronic acid hydrogel for multifunctional hemostatic adhesives inspired by a platelet coagulation mediator. Mater. Horiz. 6:1169−1178. DOI:10.1039/c9mh00157c |
| [77] | Cui L., Li J., Guan S., et al. (2022). Injectable multifunctional CMC/HA-DA hydrogel for repairing skin injury. Mater. Today Bio 14. 100257,DOI:10.1016/j.mtbio.2022.100257. |
| [78] | Weng H., Jia W., Li M., et al. (2022). New injectable chitosan-hyaluronic acid based hydrogels for hemostasis and wound healing. Carbohydr. Polym. 294:119767. DOI:10.1016/j.carbpol.2022.119767 |
| [79] | Cui R., Chen F., Zhao Y., et al. (2020). A novel injectable starch-based tissue adhesive for hemostasis. J. Mater. Chem. B 8:8282−8293. DOI:10.1039/d0tb01562h |
| [80] | Tavakoli S., Kharaziha M., Nemati S., et al. (2021). Nanocomposite hydrogel based on carrageenan-coated starch/cellulose nanofibers as a hemorrhage control material. Carbohydr. Polym. 251:117013. DOI:10.1016/j.carbpol.2020.117013 |
| [81] | Choi Y. C., Choi J. S., Jung Y. J., et al. (2014). Human gelatin tissue-adhesive hydrogels prepared by enzyme-mediated biosynthesis of DOPA and Fe3+ ion crosslinking. J. Mater. Chem. B 2:201−209. DOI:10.1039/c3tb20696c |
| [82] | Luo J.-W., Liu C., Wu J.-H., et al. (2019). In situ injectable hyaluronic acid/gelatin hydrogel for hemorrhage control. Mater. Sci. Eng. C 98:628−634. DOI:10.1016/j.msec.2019.01.034 |
| [83] | Wang H., Wang M., Wu J., et al. (2024). Nature-inspired gelatin-based adhesive hydrogel: A rapid and user-friendly solution for hemostatic applications. Adv. Healthc. Mater. 13:2304444. DOI:10.1002/adhm.202304444 |
| [84] | Yan X., Chen Y., Dan N., et al. (2022). A novel thermosensitive growth-promoting collagen fibers composite hemostatic gel. J. Mater. Chem. B 10:4070−4082. DOI:10.1039/d1tb02644e |
| [85] | Liu J., Ding Y., Wang Y., et al. (2024). Enhanced specific surface area and mechanical property of silk nanofibers aerogel for potential hemostasis applications. Int. J. Biol. Macromol. 277:134345. DOI:10.1016/j.ijbiomac.2024.134345 |
| [86] | Si R., Wang Y., Yang Y., et al. (2023). Dynamic dual-crosslinking antibacterial hydrogel with enhanced bio-adhesion and self-healing activities for rapid hemostasis in vitro and in vivo. Mater. Des. 233:112244. DOI:10.1016/j.matdes.2023.112244 |
| [87] | Li H., Shen S., Yu K., et al. (2023). Construction of porous structure-based carboxymethyl chitosan/ sodium alginate/ tea polyphenols for wound dressing. Int. J. Biol. Macromol. 233:123404. DOI:10.1016/j.ijbiomac.2023.123404 |
| [88] | Ma H., Axi Y., Lu Y., et al. (2024). A dual network cross-linked hydrogel with multifunctional Bletilla striata polysaccharide/gelatin/tea polyphenol for wound healing promotion. Int. J. Biol. Macromol. 265:130780. DOI:10.1016/j.ijbiomac.2024.130780 |
| [89] | Wang Z., Lyu T., Xie Q., et al. (2023). Shape-adapted self-gelation hydrogel powder for high-performance hemostasis and wound healing. Appl. Mater. Today 35:101948. DOI:10.1016/j.apmt.2023.101948 |
| [90] | Zhou Z. B., Xiao J. W., Guan S. W., et al. (2022). A hydrogen-bonded antibacterial curdlan-tannic acid hydrogel with an antioxidant and hemostatic function for wound healing. Carbohydr. Polym. 285:119235. DOI:10.1016/j.carbpol.2022.119235 |
| [91] | Ma H. Y., Axi Y., Lu Y. H., et al. (2024). A dual network cross-linked hydrogel with multifunctional Bletilla striata polysaccharide/gelatin/tea polyphenol for wound healing promotion. Int. J. Biol. Macromol. 265:130780. DOI:10.1016/j.ijbiomac.2024.130780 |
| [92] | Wang Y., Zhang Y., Yang Y. P., et al. (2024). Versatile dopamine-functionalized hyaluronic acid-recombinant human collagen hydrogel promoting diabetic wound healing via inflammation control and vascularization tissue regeneration. Bioact. Mater. 35:330−345. DOI:10.1016/j.bioactmat.2024.02.010 |
| [93] | Zhang B., Qiang G., Barta K., et al. (2024). Bio–based polymers from lignin. .Innov. Mater. 2:100062. DOI:10.59717/j.xinn-mater.2024.100062 |
| [94] | Zou C. Y., Lei X. X., Hu J. J., et al. (2022). Multi-crosslinking hydrogels with robust bio-adhesion and pro-coagulant activity for first-aid hemostasis and infected wound healing. Bioact. Mater. 16:388−402. DOI:10.1016/j.bioactmat.2022.02.034 |
| [95] | Fan R., Li H., Aladejana J. T., et al. (2024). Soybean protein "mechanically interlocked" bonding of polysaccharide and MXene to improve the strength and toughness of biomass adhesive. Ind. Crops Prod. 221:119429. DOI:10.1016/j.indcrop.2024.119429 |
| [96] | Ferreira M. O. G., Leite L. L. R., de Lima I. S., et al. (2016). Chitosan hydrogel in combination with nerolidol for healing wounds. Carbohydr. Polym. 152:409−418. DOI:10.1016/j.carbpol.2016.07.037 |
| [97] | Turley J. L., Moran H. B. T., McEntee C. P., et al. (2021). Chitin-derived polymer deacetylation regulates mitochondrial reactive oxygen species dependent cGAS-STING and NLRP3 inflammasome activation. Biomaterials 275:120961. DOI:10.1016/j.biomaterials.2021.120961 |
| [98] | Liu F., Wang L., Zhai X., et al. (2023). A multi-functional double cross-linked chitosan hydrogel with tunable mechanical and antibacterial properties for skin wound dressing. Carbohydr. Polym 322:121344. DOI:10.1016/j.carbpol.2023.121344 |
| [99] | Hu Z., Lu S., Cheng Y., et al. (2018). Investigation of the effects of molecular parameters on the hemostatic properties of chitosan. Molecules 23:3147. DOI:10.3390/molecules23123147 |
| [100] | Klokkevold P. R., Lew D. S., Ellis D. G., et al. (1990). Effect of chitosan on intraoral hemostasis and wound-healing. J. Dent. Res 69:352−352. |
| [101] | Ouyang Y., Zhao Y., Zheng X., et al. (2023). Rapidly degrading and mussel-inspired multifunctional carboxymethyl chitosan/montmorillonite hydrogel for wound hemostasis. Int. J. Biol. Macromol. 242:124960. DOI:10.1016/j.ijbiomac.2023.124960 |
| [102] | Liu X., Hu J., Hu Y., et al. (2025). Multifunctional injectable oxidized sodium alginate/carboxymethyl chitosan hydrogel for rapid hemostasis. Colloid. Surface. B 245:114346. DOI:10.1016/j.colsurfb.2024.114346 |
| [103] | Quadrado R. F. N., Zhai Z., Zavadinack M., et al. (2024). All-polysaccharide, self-healing, pH-sensitive, in situ-forming hydrogel of carboxymethyl chitosan and aldehyde-functionalized hydroxyethyl cellulose. Carbohydr. Polym. 336:122105. DOI:10.1016/j.carbpol.2024.122105 |
| [104] | Ronghua H., Yumin D. and Jianhong Y. (2003). Preparation and anticoagulant activity of carboxybutyrylated hydroxyethyl chitosan sulfates. Carbohydr. Polym. 51:431−438. DOI:10.1016/S0144-8617(02)00208-4 |
| [105] | Peng S., Niu S., Gao Q., et al. (2024). Hydroxypropyl chitosan/ε-poly-l-lysine based injectable and self-healing hydrogels with antimicrobial and hemostatic activity for wound repair. Carbohydr. Polym. 337:122135. DOI:10.1016/j.carbpol.2024.122135 |
| [106] | Zhu C., Zou S., Rao Z., et al. (2017). Preparation and characterization of hydroxypropyl chitosan modified with nisin. Int. J. Biol. Macromol. 105:1017−1024. DOI:10.1016/j.ijbiomac.2017.07.136 |
| [107] | Fan L., Zou S., Ge H., et al. (2016). Preparation and characterization of hydroxypropyl chitosan modified with collagen peptide. Int. J. Biol. Macromol. 93:636−643. DOI:10.1016/j.ijbiomac.2016.07.093 |
| [108] | Hu C., Long L., Cao J., et al. (2021). Dual-crosslinked mussel-inspired smart hydrogels with enhanced antibacterial and angiogenic properties for chronic infected diabetic wound treatment via pH-responsive quick cargo release. Chem. Eng. J. 411:128564. DOI:10.1016/j.cej.2021.128564 |
| [109] | Huang K., Liu W., Wei W., et al. (2022). Photothermal hydrogel encapsulating intelligently bacteria-capturing bio-MOF for infectious wound healing. ACS Nano 16:19491−19508. DOI:10.1021/acsnano.2c09593 |
| [110] | Cao W., Yan J., Liu C., et al. (2020). Preparation and characterization of catechol-grafted chitosan/gelatin/modified chitosan-AgNP blend films. Carbohydr. Polym. 247:116643. DOI:10.1016/j.carbpol.2020.116643 |
| [111] | Hu S., Bi S., Yan D., et al. (2018). Preparation of composite hydroxybutyl chitosan sponge and its role in promoting wound healing. Carbohydr. Polym. 184:154−163. DOI:10.1016/j.carbpol.2017.12.033 |
| [112] | Yuk H., Varela C. E., Nabzdyk C. S., et al. (2019). Dry double-sided tape for adhesion of wet tissues and devices. Nature 575:169−174. DOI:10.1038/s41586-019-1710-5 |
| [113] | Fang Y., Zhang L., Chen Y., et al. (2023). Polysaccharides based rapid self-crosslinking and wet tissue adhesive hemostatic powders for effective hemostasis. Carbohydr. Polym. 312:120819. DOI:10.1016/j.carbpol.2023.120819 |
| [114] | Zhao Y., Xiao A., Wu P., et al. (2021). Fabrication of hydroxypropyl chitosan/soy protein isolate hydrogel for effective hemorrhage control. Tissue Eng. Part A 27:788−795. DOI:10.1089/ten.TEA.2020.0174 |
| [115] | Li S., Li X., Xu Y., et al. (2024). Collagen fibril-like injectable hydrogels from self-assembled nanoparticles for promoting wound healing. Bioact. Mater. 32:149−163. DOI:10.1016/j.bioactmat.2023.09.012 |
| [116] | Zhou Z.-X., Li J., Hu J., et al. (2024). Towards promoting wound healing: a near-infrared light-triggered persistently antibacterial, synergistically hemostatic nanoarchitecture-integrated chitosan hydrogel. Carbohydr. Polym. 329:121783. DOI:10.1016/j.carbpol.2024.121783 |
| [117] | Li H. B., Cheng F., Wei X. J., et al. (2021). Injectable, self-healing, antibacterial, and hemostatic N,O-carboxymethyl chitosan/oxidized chondroitin sulfate composite hydrogel for wound dressing. Mater. Sci. Eng. C 118:111324. DOI:10.1016/j.msec.2020.111324 |
| [118] | Song X., Zhao Y., Liu Y., et al. (2021). Effects of degree of deacetylation on hemostatic performance of partially deacetylated chitin sponges. Carbohydr. Polym. 273:118615. DOI:10.1016/j.carbpol.2021.118615 |
| [119] | Du Y., Chen X., Li L., et al. (2023). Benzeneboronic−alginate/quaternized chitosan−catechol powder with rapid self-gelation, wet adhesion, biodegradation and antibacterial activity for non-compressible hemorrhage control. Carbohydr. Polym. 318:121049. DOI:10.1016/j.carbpol.2023.121049 |
| [120] | Daiyong Y. E., Hong H., Heqing F. U., et al. (2006). Advances in cellulose chemistry. Journal of Chemical Industry and Engineering (China) 57:1782−1791. |
| [121] | Fahim H., Motamedzadegan A., Farahmandfar R., et al. (2023). Surface analysis and thermal behavior of the functionalized cellulose by glutaric anhydride through a solvent-free and catalyst-free process. Int. J. Biol. Macromol. 232:123268. DOI:10.1016/j.ijbiomac.2023.123268 |
| [122] | Liebert T. (2010). Cellulose Solvents – Remarkable History, Bright Future. ACS Symp. Ser. 1033:3−54. DOI:10.1021/bk-2010-1033.ch001 |
| [123] | Sano M., Kojima T. and Naruse T. (2000). Effect of red blood cells on the antitumor activity of oxycellulose. Cancer Biother. Radio. 15:195−200. DOI:10.1089/cbr.2000.15.195 |
| [124] | Tuncel S. and Gokturk T. (1953). Bleeding control by oxycellulose gauze. Tip Fakultesi mecmuasi 16:517−523. |
| [125] | Zhou Y., Fan M., Luo X., et al. (2014). Acidic ionic liquid catalyzed crosslinking of oxycellulose with chitosan for advanced biocomposites. Carbohydr. Polym. 113:108−114. DOI:10.1016/j.carbpol.2014.06.081 |
| [126] | Li S., Li Y., Ding Y., et al. (2022). Chemical modification of nitrocellulose by grafting sodium carboxymethyl. Cellulose 29:8103−8115. DOI:10.1007/s10570-022-04780-7 |
| [127] | Morris E., Pulham C. R. and Morrison C. A. (2023). Structure and properties of nitrocellulose: approaching 200 years of research. RSC Adv. 13:32321−32333. DOI:10.1039/d3ra05457h |
| [128] | Gupta S. K., Deshpande A. P. and Kumar R. (2024). Rheological and dielectric behavior of sodium carboxymethyl cellulose (NaCMC)/Ca2+ and esterified NaCMC/Ca2+ hydrogels: correlating microstructure and dynamics with properties. Carbohydr. Polym. 335:122049. DOI:10.1016/j.carbpol.2024.122049 |
| [129] | Kono H. and Fujita S. (2012). Biodegradable superabsorbent hydrogels derived from cellulose by esterification crosslinking with 1,2,3,4-butanetetracarboxylic dianhydride. Carbohydr. Polym. 87:2582−2588. DOI:10.1016/j.carbpol.2011.11.045 |
| [130] | Wang S., Yu L., Jia X., et al. (2024). Cellulose nanofibril-guided orienting response of supramolecular network enables superstretchable, robust, and antifatigue hydrogel. Innov. Mater. 2:100092. DOI:10.59717/j.xinn-mater.2024.100092 |
| [131] | Cheng H., Yu Q., Chen Q., et al. (2023). Biomass-derived ultrafast cross-linked hydrogels with double dynamic bonds for hemostasis and wound healing. Biomater. Sci. 11:931−948. DOI:10.1039/d2bm00907b |
| [132] | Li D., Dong X., Liu X., et al. (2024). Cellulose nanofibers embedded chitosan/tannin hydrogel with high antibacterial activity and hemostatic ability for drug-resistant bacterial infected wound healing. Carbohydr. Polym. 329:121687. DOI:10.1016/j.carbpol.2023.121687 |
| [133] | Komatsu F., Ghosh P. and Sengupta R. (2021). How I do it: management of venous bleeding from the superior petrosal vein during endoscopic microvascular decompression. ACTA Neurochir. 163:2403−2405. DOI:10.1007/s00701-020-04659-1 |
| [134] | Suchy P., Paprskarova A., Chalupova M., et al. (2020). Composite hemostatic nonwoven textiles based on hyaluronic acid, cellulose, and etamsylate. Materials 13:1627. DOI:10.3390/ma13071627 |
| [135] | Firmino F., Villela-Castro D. and Santos V. L. C. d. G. (2024). Oxidized regenerated cellulose versus calcium alginate in controlling bleeding from malignant wounds: a randomized controlled trial. Cancer Nursing 47:E287−E297. DOI:10.1097/NCC.0000000000001235 |
| [136] | Cao S., Zhang K., Li Q., et al. (2023). Injectable and photothermal antibacterial bacterial cellulose cryogel for rapid hemostasis and repair of irregular and deep skin wounds. Carbohydr. Polym. 320:121239. DOI:10.1016/j.carbpol.2023.121239 |
| [137] | Stiger-Pouvreau V., Bourgougnon N. and Deslandes E. (2016). Chapter 8 - Carbohydrates From Seaweeds. Seaweed in Health and Disease Prevention 2016:223−274. DOI:10.1016/B978-0-12-802772-1.00008-7 |
| [138] | Gilchrist T. and Martin A. M. (1983). Wound treatment with sorbsan — an alginate fibre dressing. Biomaterials 4:317−320. DOI:10.1016/0142-9612(83)90036-4 |
| [139] | Haseef H. M. A., Dinesh S., Prakash J., et al. (2024). Calcium oxide/silica nanocomposite and L. coromandelica bark incorporated κ-carrageenan/sodium alginate hydrogel for rapid hemostasis. Int. J. Biol. Macromol. 254:127951. DOI:10.1016/j.ijbiomac.2023.127951 |
| [140] | Qiao L., Liang Y., Chen J., et al. (2023). Antibacterial conductive self-healing hydrogel wound dressing with dual dynamic bonds promotes infected wound healing. Bioact. Mater. 30:129−141. DOI:10.1016/j.bioactmat.2023.07.015 |
| [141] | Zou C.-Y., Lei X.-X., Hu J.-J., et al. (2022). Multi-crosslinking hydrogels with robust bio-adhesion and pro-coagulant activity for first-aid hemostasis and infected wound healing. Bioact. Mater. 16:388−402. DOI:10.1016/j.bioactmat.2022.02.034 |
| [142] | Sun X., Mao Y. M., Yu Z. Y., et al. (2024). A biomimetic "salting out-alignment-locking" tactic to design strong and tough hydrogel. Adv. Mater. 36:2400084. DOI:10.1002/adma.202400084 |
| [143] | Leng Z. W., Zhu P. C., Wang X. C., et al. (2023). Sebum-membrane-inspired protein-based bioprotonic hydrogel for artificial skin and human-machine merging interface. Adv. Funct. Mater. 33:2211056. DOI:10.1002/adfm.202211056 |
| [144] | Dong Q., Liang X., Chen F. X., et al. (2022). Injectable shape memory hydroxyethyl cellulose/soy protein isolate based composite sponge with antibacterial property for rapid noncompressible hemorrhage and prevention of wound infection. Int. J. Biol. Macromol 217:367−380. DOI:10.1016/j.ijbiomac.2022.07.051 |
| [145] | Yu Y. L., Li P. F., Zhu C. L., et al. (2019). Multifunctional and recyclable photothermally responsive cryogels as efficient platforms for wound healing. Adv. Funct. Mater. 29:1904402. DOI:10.1002/adfm.201904402 |
| [146] | Wang H. Z., Lu B., Zhou J. Y., et al. (2025). Biobased physicochemical reversible dual-cross-linked hydrogel: self-healing, antibacterial, antioxidant, and hemostatic properties for diabetic wound healing. Biomacromolecules 26:2637−2653. DOI:10.1021/acs.biomac.5c00087 |
| [147] | He S. B., Shi L. Y., Yang Z. Q., et al. (2025). Platinum nanozyme embedded in hyaluronate with multifunctional attributes synergistically promoting tracheal fistula healing. Int. J. Biol. Macromol. 287:138337. DOI:10.1016/j.ijbiomac.2024.138337 |
| [148] | Wen N., Li S. S., Jiang H. Z., et al. (2025). Bio-inspired self-healing hydrogel for fast hemostasis and accelerated wound healing of gastric ulcers. Adv. Funct. Mater. 35:2411959. DOI:10.1002/adfm.202411959 |
| [149] | Liu H., Chu H. X., Yuan H. L., et al. (2024). Bioinspired multifunctional self-sensing actuated gradient hydrogel for soft-hard robot remote interaction. Nano-Micro Letters 16:69. DOI:10.1007/s40820-023-01287-z |
| [150] | He J. H., Zhang Z. X., Yang Y. T., et al. (2021). Injectable self-healing adhesive ph-responsive hydrogels accelerate gastric hemostasis and wound healing. Nano-Micro Letters 13:80. DOI:10.1007/s40820-020-00585-0 |
| [151] | Manira M., Anuar K. K., Seet W. T., et al. (2014). Comparison of the effects between animal-derived trypsin and recombinant trypsin on human skin cells proliferation, gene and protein expression. Cell and Tissue Banking 15:41−49. DOI:10.1007/s10561-013-9368-y |
| [152] | Tazawa R., Uchida K., Minehara H., et al. (2020). Poly(POG)n loaded with recombinant human bone morphogenetic protein-2 accelerates new bone formation in a critical-sized bone defect mouse model. J. Orthop. Surg. Res. 15:471. DOI:10.1186/s13018-020-01977-z |
| [153] | Wang Q., Yan H., Yao L., et al. (2024). A highly bioactive THPC-crosslinked recombinant collagen hydrogel implant for aging skin rejuvenation. Int. J. Biol. Macromol. 266:131276. DOI:10.1016/j.ijbiomac.2024.131276 |
| [154] | Yoon J., Zirpel N. K., Park H.-J., et al. (2016). Angiogenic type i collagen extracellular matrix integrated with recombinant bacteriophages displaying vascular endothelial growth factors. Adv. Healthc. Mater. 5:205−212. DOI:10.1002/adhm.201500534 |
| [155] | Chang P., Guo K., Li S. J., et al. (2024). In situ sodium chloride cross-linked fish skin collagen scaffolds for functional hemostasis materials. Small 20:2208001. DOI:10.1002/smll.202208001 |
| [156] | Yan T., Cheng F., Wei X., et al. (2017). Biodegradable collagen sponge reinforced with chitosan/calcium pyrophosphate nanoflowers for rapid hemostasis. Carbohydr. Polym. 170:271−280. DOI:10.1016/j.carbpol.2017.04.080 |
| [157] | Ablat N., Ablimit M., Abudoukadier A., et al. (2023). Liver protection and hemostatic effects of medicinal plant arnebia euchroma (royle) I. M.Johnst extract in a rat model. Journal of Ethnopharmacology 300:115739. DOI:10.1016/j.jep.2022.115739 |
| [158] | Khan R. and Khan M. H. (2013). Use of collagen as a biomaterial: An update. J. Indian Soc. Periodontol. 17:539−542. DOI:10.4103/0972-124X.118333 |
| [159] | Zhao C., Wang H., Sun X., et al. (2024). Non-covalent cross-linking hydrogel: a new method for visceral hemostasis. Gels 10:326. DOI:10.3390/gels10050326 |
| [160] | Yang W., Kang X. Y., Gao X., et al. (2023). Biomimetic natural biopolymer-based wet-tissue adhesive for tough adhesion, seamless sealed, emergency/nonpressing hemostasis, and promoted wound healing. Adv. Funct. Mater. 33:2211340. DOI:10.1002/adfm.202211340 |
| [161] | Chen X. Q., Tang J. B., Dong Y. Q., et al. (2025). A novel hydrogel with inherent antibacterial and hemostatic properties for burn wound healing. Colloid Surface B. 245:114250. DOI:10.1016/j.colsurfb.2024.114250 |
| [162] | Ye W. J., Qin M., Qiu R. M., et al. (2022). Keratin-based wound dressings: from waste to wealth. Int. J. Biol. Macromol. 211:183−197. DOI:10.1016/j.ijbiomac.2022.04.216 |
| [163] | Yang W., Kang X., Gao X., et al. (2022). Biomimetic natural biopolymer‐based wet‐tissue adhesive for tough adhesion, seamless sealed, emergency/nonpressing hemostasis, and promoted wound healing. Adv. Funct. Mater. 33:2211340. DOI:10.1002/adfm.202211340 |
| [164] | Tanrikulu I. C., Dang L., Nelavelli L., et al. (2024). Synthetic collagen hydrogels through symmetric self-assembly of small peptides. Adv. Sci. 11:2303228. DOI:10.1002/advs.202303228 |
| [165] | Tanrikulu I. C., Dang L., Nelavelli L., et al. (2024). Synthetic collagen hydrogels through symmetric self-assembly of small peptides. Adv. Sci. 11:2303228. DOI:10.1002/advs.202303228 |
| [166] | Jenkins H. P. and Clarke J. S. (1945). Gelatin sponge, a new hemostatic substance; studies on absorbability. JAMA Surgery 51:253−261. DOI:10.1001/archsurg.1945.01230040262005 |
| [167] | Huang Y., Zhao X., Zhang Z., et al. (2020). Degradable gelatin-based ipn cryogel hemostat for rapidly stopping deep noncompressible hemorrhage and simultaneously improving wound healing. Chem. Mater. 32:6595−6610. DOI:10.1021/acs.chemmater.0c02030 |
| [168] | Koshy S. T., Ferrante T. C., Lewin S. A., et al. (2014). Injectable, porous, and cell-responsive gelatin cryogels. Biomaterials 35:2477−2487. DOI:10.1016/j.biomaterials.2013.11.044 |
| [169] | Huang Y., Bai L., Yang Y. T., et al. (2022). Biodegradable gelatin/silver nanoparticle composite cryogel with excellent antibacterial and antibiofilm activity and hemostasis for pseudomonas aeruginosa-infected burn wound healing. J. Colloid Interface Sci. 608:2278−2289. DOI:10.1016/j.jcis.2021.10.131 |
| [170] | Zhang X., Zhu Y., Liu W., et al. (2024). Polyvinyl alcohol/chitosan-Fe3+/gelatin/tri-network composite hydrogel wound dressing with effective hemostasis and self-healing properties. Polym. 307:127304. DOI:10.1016/j.polymer.2024.127304 |
| [171] | Luo J., Shi X., Li L., et al. (2021). An injectable and self-healing hydrogel with controlled release of curcumin to repair spinal cord injury. Bioact. Mater. 6:4816−4829. DOI:10.1016/j.bioactmat.2021.05.022 |
| [172] | Wang M., Lin S., Liu M., et al. (2023). An injectable and rapidly degraded carboxymethyl chitosan/polyethylene glycol hydrogel for postoperative antiadhesion. Chem. Eng. J. 463:142283. DOI:10.1016/j.cej.2023.142283 |
| [173] | Wang P., Wu J., Xiao X., et al. (2024). Engineering injectable coassembled hydrogel by photothermal driven chitosan-stabilized MoS2 nanosheets for infected wound healing. ACS Nano 18:26961−26974. DOI:10.1021/acsnano.4c08883 |
| [174] | Singla R. K., Dubey A. K., Garg A., et al. (2019). Natural polyphenols: Chemical classification, definition of classes, subcategories, and structures. J. Aoac Int. 102:1397−1400. DOI:10.1093/jaoac/102.5.1397 |
| [175] | Cao H., Yang L., Tian R., et al. (2022). Versatile polyphenolic platforms in regulating cell biology. Chem. Soc. Rev. 51:4175−4198. DOI:10.1039/d1cs01165k |
| [176] | Cao C. Y., Yang N., Zhao Y., et al. (2021). Biodegradable hydrogel with thermo-response and hemostatic effect for photothermal enhanced anti-infective therapy. Nano Today 39:101165. DOI:10.1016/j.nantod.2021.101165 |
| [177] | Cao X. L., Deng Y. H., Xu Z. Y., et al. (2025). A versatile natural gelatin-based hydrogel for emergency wound treatment through hemostasis, antibacterial, and anti-inflammation. Biofabrication 17:015017. DOI:10.1088/1758-5090/ad89ff |
| [178] | Yi X. T., He J. M., Wei X. J., et al. (2023). A polyphenol and ε-polylysine functionalized bacterial cellulose/PVA multifunctional hydrogel for wound healing. Int. J. Biol. Macromol. 247:125663. DOI:10.1016/j.ijbiomac.2023.125663 |
| [179] | Kang X. C., Guan P. F., Xiao C. R., et al. (2023). Injectable intrinsic photothermal hydrogel bioadhesive with on-demand removability for wound closure and mrsa-infected wound healing. Adv. Healthc. Mater. 12:2203306. DOI:10.1002/adhm.202203306 |
| [180] | Cheng H., Zhang D. D., Wu J., et al. (2023). Interactions between gut microbiota and polyphenols: A mechanistic and metabolomic review. Phytomedicine 119:154979. DOI:10.1016/j.phymed.2023.154979 |
| [181] | Ju J., Jin S. B., Kim S., et al. (2022). Addressing the shortcomings of polyphenol-derived adhesives: Achievement of long shelf life for effective hemostasis. ACS Appl. Mater. Interfaces 14:25115−25125. DOI:10.1021/acsami.2c03930 |
| [182] | Li J., Chen J. and Kirsner R. (2007). Pathophysiology of acute wound healing. Clin. Dermatol. 25:9−18. DOI:10.1016/j.clindermatol.2006.09.007 |
| [183] | Casey G. (1997). The stages of wound healing. Nurs. N. Z. 3:31. |
| [184] | Clark R. A. F., Ashcroft G. S., Spencer M. J., et al. (1996). Re-epithelialization of normal human excisional wounds is associated with a switch from alpha v beta 5 to alpha v beta 6 integrins. Br. J. Dermatol. 135:46−51. DOI:10.1046/j.1365-2133.1996.d01-931.x |
| [185] | Qiu X., Nie L., Liu P., et al. (2024). From hemostasis to proliferation: Accelerating the infected wound healing through a comprehensive repair strategy based on GA/OKGM hydrogel loaded with MXene@TiO2 nanosheets. Biomaterials 308:122548. DOI:10.1016/j.biomaterials.2024.122548 |
| [186] | Chen G., Yu Y., Wu X., et al. (2018). Bioinspired multifunctional hybrid hydrogel promotes wound healing. Adv. Funct. Mater. 28:1801386. DOI:10.1002/adfm.201801386 |
| [187] | Mo Z., Ma Y., Chen W., et al. (2024). Protamine-grafted carboxymethyl chitosan based hydrogel with adhesive and long-term antibacterial properties for hemostasis and skin wound healing. Carbohydr. Polym. 336:122125. DOI:10.1016/j.carbpol.2024.122125 |
| [188] | Wu S., Li Y., Zhou J., et al. (2023). Collagen based hydrogel containing chondroitin sulfate a or c with hemostatic and anti-inflammatory potential. Polym. Bull. 36:69−81. DOI:10.14028/j.cnki.1003-3726.2023.01.006 |
| [189] | Lei H. and Fan D. (2021). Conductive, adaptive, multifunctional hydrogel combined with electrical stimulation for deep wound repair. Chem. Eng. J. 421:129578. DOI:10.1016/j.cej.2021.129578 |
| [190] | Zhao X., Luo J., Huang Y., et al. (2023). Injectable antiswelling and high-strength bioactive hydrogels with a wet adhesion and rapid gelling process to promote sutureless wound closure and scar-free repair of infectious wounds. ACS Nano 17:22015−22034. DOI:10.1021/acsnano.3c08625 |
| [191] | Chen X., Li X., He W., et al. (2023). Rational multivalency construction enables bactericidal effect amplification and dynamic biomaterial design. The Innovation 4:100483. DOI:10.1016/j.xinn.2023.100483 |
| [192] | Liu Y., Zhang J., Jin Y., et al. (2024). Gelatin methacrylate based liquid dressing with antibacterial and hemostasis properties. Colloid Surf. Physicochem. Eng. Asp. 689:133749. DOI:10.1016/j.colsurfa.2024.133749 |
| [193] | Zhu J., Li F., Wang X., et al. (2018). Hyaluronic acid and polyethylene glycol hybrid hydrogel encapsulating nanogel with hemostasis and sustainable antibacterial property for wound healing. ACS Appl. Mater. Interfaces 10:13304−13316. DOI:10.1021/acsami.7b18927 |
| [194] | Ravindra S., Mulaba-Bafubiandi A. F., Rajinikanth V., et al. (2012). Development and characterization of curcumin loaded silver nanoparticle hydrogels for antibacterial and drug delivery applications. J. Inorg. Organomet. P. 22:1254−1262. DOI:10.1007/s10904-012-9734-4 |
| [195] | Zhang J., Hurren C., Lu Z., et al. (2022). pH-sensitive alginate hydrogel for synergistic anti-infection. Int. J. Biol. Macromol. 222:1723−1733. DOI:10.1016/j.ijbiomac.2022.09.234 |
| [196] | Xia S., Liu D., Jiang K., et al. (2024). Photothermal driven BMSCs osteogenesis and M2 macrophage polarization on polydopamine-coated Ti3C2 nanosheets/poly(vinylidene fluoride trifluoroethylene) nanocomposite coatings. Mater. Today Bio. 27:101156. DOI:10.1016/j.mtbio.2024.101156 |
| [197] | Cui Q., Yuan H., Bao X., et al. (2020). Synergistic photodynamic and photothermal antibacterial therapy based on a conjugated polymer nanoparticle-doped hydrogel. ACS Appl. Bio Mater. 3:4436−4443. DOI:10.1021/acsabm.0c00423 |
| [198] | Lee C., Lim K., Kim S. S., et al. (2019). Near infrared light-responsive heat-emitting hemoglobin hydrogels for photothermal cancer therapy. Colloid. Surface. B. 176:156−166. DOI:10.1016/j.colsurfb.2018.12.070 |
| [199] | Yan Q., Long X., Zhang P., et al. (2022). Oxidized bletilla rhizome polysaccharide-based aerogel with synergistic antibiosis and hemostasis for wound healing. Carbohydr. Polym. 293:119696. DOI:10.1016/j.carbpol.2022.119696 |
| [200] | Cao S., Ji P., Hao L., et al. (2025). Self-assembling chitosan based injectable and expandable sponge with antimicrobial property for hemostasis and wound healing. Carbohydr. Polym. 347:122699. DOI:10.1016/j.carbpol.2024.122699 |
| [201] | Gan D., Xu T., Xing W., et al. (2019). Mussel-inspired contact-active antibacterial hydrogel with high cell affinity, toughness, and recoverability. Adv. Funct. Mater. 29:1805964. DOI:10.1002/adfm.201805964 |
| [202] | Kong M., Chen X. G., Xing K., et al. (2010). Antimicrobial properties of chitosan and mode of action: A state of the art review. Int. J. Food Microbiol. 144:51−63. DOI:10.1016/j.ijfoodmicro.2010.09.012 |
| [203] | Rabea E. I., Badawy M. E. T., Stevens C. V., et al. (2003). Chitosan as antimicrobial agent: Applications and mode of action. Biomacromolecules 4:1457−1465. DOI:10.1021/bm034130m |
| [204] | Yang Y., Ao H., Wang Y., et al. (2016) Cytocompatibility with osteogenic cells and enhanced in vivo anti-infection potential of quaternized chitosan-loaded titania nanotubes. Bone Res. 4:140-153. DOI:10.1038/boneres.2016.27. |
| [205] | Yuan H., Li Z., Zhao Q., et al. (2023). Molecular evolution of acceptor-donor-acceptor-type conjugated oligomer nanoparticles for efficient photothermal antimicrobial therapy. Adv. Funct. Mater. 33:2213209. DOI:10.1002/adfm.202213209 |
| [206] | Qi X., Huang Y., You S., et al. (2022). Engineering robust ag-decorated polydopamine nano-photothermal platforms to combat bacterial infection and prompt wound healing. Adv. Sci. 9:2106015. DOI:10.1002/advs.202106015 |
| [207] | Hu D., Li Y., Yuan W., et al. (2025). Bioactive cationic polymer-based hydrogel with Engrailed-1 gene silencing and microenvironment modulation for enhanced scarless diabetic wound healing. Chem. Eng. J. 504:158713. DOI:10.1016/j.cej.2024.158713 |
| [208] | Li Z., Xing X., Zhao C., et al. (2024). A rapid interactive chitosan-based medium with antioxidant and pro-vascularization properties for infected burn wound healing. Carbohydr. Polym. 333:121991. DOI:10.1016/j.carbpol.2024.121991 |
| [209] | Zan X., Yang D., Xiao Y., et al. (2024). Facile general injectable gelatin/metal/tea polyphenol double nanonetworks remodel wound microenvironment and accelerate healing. Adv. Sci. 11:2305405. DOI:10.1002/advs.202305405 |
| [210] | Yeo Y. H., Chathuranga K., Lee J. S., et al. (2022). Multifunctional and thermoresponsive methylcellulose composite hydrogels with photothermal effect. Carbohydr. Polym. 277:118834. DOI:10.1016/j.carbpol.2021.118834 |
| [211] | Chen S., Liu S., Zhang L., et al. (2020). Construction of injectable silk fibroin/polydopamine hydrogel for treatment of spinal cord injury. Chem. Eng. J. 399:125795. DOI:10.1016/j.cej.2020.125795 |
| [212] | Zhao X., Liu R., Tang T., et al. (2024). Promotion and monitor wound healing by anthocyanin enhanced light curing ε-poly-l-lysine hydrogel encapsulated Cu-MOF. Chem. Eng. J. 494:152875. DOI:10.1016/j.cej.2024.152875 |
| [213] | Cunha F., Rajnicek A. M. and McCaig C. D. (2019). Electrical stimulation directs migration, enhances and orients cell division and upregulates the chemokine receptors CXCR4 and CXCR2 in endothelial cells. J. Vasc. Res. 56:39−53. DOI:10.1159/000495311 |
| [214] | Cheah Y. J., Buyong M. R. and Yunus M. H. M. (2021). Wound healing with electrical stimulation technologies: A review. Polymers 13:3790. DOI:10.3390/polym13213790 |
| [215] | Fan W., Yang X., Hu X., et al. (2024). A novel conductive microtubule hydrogel for electrical stimulation of chronic wounds based on biological electrical wires. J. Nanobiotechnology 22:258. DOI:10.1186/s12951-024-02524-2 |
| [216] | Shahemi N. H., Mahat M. M., Asri N. A. N., et al. (2023). Application of conductive hydrogels on spinal cord injury repair: A review. ACS Biomater. Sci. Eng. 9:4045−4085. DOI:10.1021/acsbiomaterials.3c00194 |
| [217] | Dang X., Fu Y. and Wang X. (2024). Versatile biomass-based injectable photothermal hydrogel for integrated regenerative wound healing and skin bioelectronics. Adv. Funct. Mater. 34:2405745. DOI:10.1002/adfm.202405745 |
| [218] | Wei C., Shi W., Zhao C., et al. (2023). Superwetting injectable hydrogel with ultrastrong and fast tissue adhesion for minimally invasive hemostasis. Adv. Healthc. Mater. 12:2201799. DOI:10.1002/adhm.202201799 |
| [219] | Feng W. and Wang Z. (2022). Shear-thinning and self-healing chitosan-graphene oxide hydrogel for hemostasis and wound healing. Carbohydr. Polym. 294:119824. DOI:10.1016/j.carbpol.2022.119824 |
| [220] | Wang S., Liu Y., Wang X., et al. (2024). Modulating macrophage phenotype for accelerated wound healing with chlorogenic acid-loaded nanocomposite hydrogel. J. Control. Release. 369:420−443. DOI:10.1016/j.jconrel.2024.03.054 |
| [221] | Wang S., Chen B., Ouyang L., et al. (2021). A novel stimuli-responsive injectable antibacterial hydrogel to achieve synergetic photothermal/gene-targeted therapy towards uveal melanoma. Adv. Sci. 8:2004721. DOI:10.1002/advs.202004721 |
| [222] | Liang Y., Li M., Yang Y., et al. (2022). pH/glucose dual responsive metformin release hydrogel dressings with adhesion and self-healing via dual-dynamic bonding for athletic diabetic foot wound healing. ACS Nano 16:3194−3207. DOI:10.1021/acsnano.1c11040 |
| Wu S., Liu W., Tang T., et al. (2025). Research progress on the hemostatic mechanism of natural bio-based gel and its application in wound healing. The Innovation Materials 3:100164. https://doi.org/10.59717/j.xinn-mater.2025.100164 |
To request copyright permission to republish or share portions of our works, please visit Copyright Clearance Center's (CCC) Marketplace website at marketplace.copyright.com.
Schematic illustration of wound hemostasis mechanisms
Modification strategies and functional mechanisms of chitosan-based hemostatic gels
Enhanced mechanical engineering of cellulose-based hemostatic hydrogel
Synergistic mechanisms of bacterial cellulose-enhanced hydrogel for mechanical, hemostatic, and antibacterial functions
Adhesion-synergized wound-healing mechanisms and performance validation of modified sodium alginate-based hemostatic hydrogel
Bioinspired engineering and multifunctional synergy of collagen-based hydrogels
Transformation roadmap of hemostatic gel from laboratory to clinical.