Engineering a naturally derived hemostatic sealant for sealing internal organs

Berríos-Torres, 2017, Centers for disease control and prevention guideline for the prevention of surgical site infection, JAMA Surgery, 152, 784, 10.1001/jamasurg.2017.0904 Galanakis, 2011, A review of current hemostatic agents and tissue sealants used in laparoscopic partial nephrectomy, Rev. Urol., 13, 131 Spotnitz, 2008, Hemostats, sealants, and adhesives: components of the surgical toolbox, Transfusion, 48, 1502, 10.1111/j.1537-2995.2008.01703.x Chiara, 2018, A systematic review on the use of topical hemostats in trauma and emergency surgery, BMC Surg., 18, 68, 10.1186/s12893-018-0398-z Sierra, 1993, Fibrin sealant adhesive systems: a review of their chemistry, material properties and clinical applications, J. Biomater. Appl., 7, 309, 10.1177/088532829300700402 Jackson, 2001, Fibrin sealants in surgical practice: an overview, Am. J. Surg., 182, 1s, 10.1016/S0002-9610(01)00770-X Baik, 2010, Development and analysis of a collagen-based hemostatic adhesive, J. Surg. Res., 164, e221, 10.1016/j.jss.2010.08.004 Grabska-Liberek, 2013, [Collagen based dressings in the treatment of wound healing], Pol. Merkur. Lek., 35, 51 Elvin, 2010, A highly elastic tissue sealant based on photopolymerised gelatin, Biomaterials, 31, 8323, 10.1016/j.biomaterials.2010.07.032 Tavafoghi, 2020, Engineering tough, injectable, naturally derived, bioadhesive composite hydrogels, Adv. Healthcare Mater., 9, 10.1002/adhm.201901722 Brown, 2009, Experience with chitosan dressings in a civilian EMS system, J. Emerg. Med., 37, 1, 10.1016/j.jemermed.2007.05.043 Klokkevold, 1999, The effect of chitosan (poly-N-acetyl glucosamine) on lingual hemostasis in heparinized rabbits, J. Oral Maxillofac. Surg., 57, 49, 10.1016/S0278-2391(99)90632-8 Quinn, 1997, A randomized trial comparing octylcyanoacrylate tissue adhesive and sutures in the management of lacerations, JAMA, 277, 1527, 10.1001/jama.1997.03540430039030 Reece, 2001, A prospectus on tissue adhesives, Am. J. Surg., 182, 40s, 10.1016/S0002-9610(01)00742-5 Duarte, 2012, Surgical adhesives: systematic review of the main types and development forecast, Prog. Polym. Sci., 37, 1031, 10.1016/j.progpolymsci.2011.12.003 Singer, 2004, A review of the literature on octylcyanoacrylate tissue adhesive, Am. J. Surg., 187, 238, 10.1016/j.amjsurg.2003.11.017 Edmonson, 2001, Foreign body reactions to dermabond, Am. J. Emerg. Med., 19, 240, 10.1053/ajem.2001.22672 Annabi, 2017, Engineering a sprayable and elastic hydrogel adhesive with antimicrobial properties for wound healing, Biomaterials, 139, 229, 10.1016/j.biomaterials.2017.05.011 Lee, 2007, A reversible wet/dry adhesive inspired by mussels and geckos, Nature, 448, 338, 10.1038/nature05968 Lang, 2014, A blood-resistant surgical glue for minimally invasive repair of vessels and heart defects, Sci. Transl. Med., 6, 10.1126/scitranslmed.3006557 Han, 2017, Tough, self-healable and tissue-adhesive hydrogel with tunable multifunctionality, NPG Asia Mater., 9, e372, 10.1038/am.2017.33 Fuller, 2013, Reduction of intraoperative air leaks with Progel in pulmonary resection: a comprehensive review, J. Cardiothorac. Surg., 8, 90, 10.1186/1749-8090-8-90 Kord Forooshani, 2017, Recent approaches in designing bioadhesive materials inspired by mussel adhesive protein, J. Polym. Sci. Polym. Chem., 55, 9, 10.1002/pola.28368 Lee, 2006, Single-molecule mechanics of mussel adhesion, Proc. Natl. Acad. Sci. Unit. States Am., 103, 12999, 10.1073/pnas.0605552103 Yu, 1999, Role of l-3,4-Dihydroxyphenylalanine in mussel adhesive proteins, J. Am. Chem. Soc., 121, 5825, 10.1021/ja990469y Han, 2016, Polydopamine nanoparticles modulating stimuli-responsive PNIPAM hydrogels with cell/tissue adhesiveness, ACS Appl. Mater. Interfaces, 8, 29088, 10.1021/acsami.6b11043 Lee, 2009, Facile conjugation of biomolecules onto surfaces via mussel adhesive protein inspired coatings, Adv. Mater., 21, 431, 10.1002/adma.200801222 Zhang, 2014, Mussel-inspired hyperbranched poly(amino ester) polymer as strong wet tissue adhesive, Biomaterials, 35, 711, 10.1016/j.biomaterials.2013.10.017 Yang, 2020, Hydrogel adhesion: a supramolecular synergy of chemistry, topology, and mechanics, Adv. Funct. Mater., 30, 10.1002/adfm.201901693 Kim, 2018, Preparation and characterization of dual-crosslinked gelatin hydrogel via Dopa-Fe3+ complexation and fenton reaction, J. Ind. Eng. Chem., 58, 105, 10.1016/j.jiec.2017.09.014 Zhang, 2020, Catechol-functionalized hydrogels: biomimetic design, adhesion mechanism, and biomedical applications, Chem. Soc. Rev., 49, 433, 10.1039/C9CS00285E Quan, 2019, Mussel-inspired catechol-functionalized hydrogels and their medical applications, Molecules, 24, 10.3390/molecules24142586 Pourshahrestani, 2020, Polymeric hydrogel systems as emerging biomaterial platforms to enable hemostasis and wound healing, Adv. Healthcare Mater., 9, 10.1002/adhm.202000905 Behrens, 2014, Hemostatic strategies for traumatic and surgical bleeding, J. Biomed. Mater. Res., 102, 4182, 10.1002/jbm.a.35052 Hong, 2019, A strongly adhesive hemostatic hydrogel for the repair of arterial and heart bleeds, Nat. Commun., 10, 10.1038/s41467-019-10004-7 Ostomel, 2007, Metal oxide surface charge mediated hemostasis, Langmuir, 23, 11233, 10.1021/la701281t Bordes, 2016, Intraoperative anaphylactic reaction: is it the Floseal?, J. Pediatr. Pharmacol. Therapeut., 21, 358, 10.5863/1551-6776-21.4.358 Li, 2015, Gelatin effects on the physicochemical and hemocompatible properties of gelatin/PAAm/laponite nanocomposite hydrogels, ACS Appl. Mater. Interfaces, 7, 18732, 10.1021/acsami.5b05287 Lokhande, 2018, Nanoengineered injectable hydrogels for wound healing application, Acta Biomater., 70, 35, 10.1016/j.actbio.2018.01.045 Golafshan, 2017, Nanohybrid hydrogels of laponite: PVA-Alginate as a potential wound healing material, Carbohydr. Polym., 176, 392, 10.1016/j.carbpol.2017.08.070 Gaharwar, 2014, Shear-thinning nanocomposite hydrogels for the treatment of hemorrhage, ACS Nano, 8, 9833, 10.1021/nn503719n Wang, 2020, A novel double-crosslinking-double-network design for injectable hydrogels with enhanced tissue adhesion and antibacterial capability for wound treatment, Adv. Funct. Mater., 30, 10.1002/adfm.201904156 Jennings, 2017, Controlling chitosan degradation properties in vitro and in vivo, Chitosan Based Biomater., 1, 159, 10.1016/B978-0-08-100230-8.00007-8 Keshavarzi, 2013, Clinical experience with the surgicel family of absorbable hemostats (oxidized regenerated cellulose) in neurosurgical applications: a review, Wounds, 25, 160 Yue, 2017, Structural analysis of photocrosslinkable methacryloyl-modified protein derivatives, Biomaterials, 139, 163, 10.1016/j.biomaterials.2017.04.050 Zhou, 2020, Biodegradable β-cyclodextrin conjugated gelatin methacryloyl microneedle for delivery of water-insoluble drug, Adv. Healthcare Mater., 9, 10.1002/adhm.202000527 Kaneko, 2021, A new aspiration device equipped with a hydro-separator for acute ischemic stroke due to challenging soft and stiff clots, Intervent Neuroradiol. Shih, 2006, Platelet adsorption and hemolytic properties of liquid crystal/composite polymers, Int. J. Pharm., 327, 117, 10.1016/j.ijpharm.2006.07.043 Gowda, 2020, Design of tunable gelatin-dopamine based bioadhesives, Int. J. Biol. Macromol., 164, 1384, 10.1016/j.ijbiomac.2020.07.195 Noshadi, 2017, In vitro and in vivo analysis of visible light crosslinkable gelatin methacryloyl (GelMA) hydrogels, Biomater. Sci., 5, 2093, 10.1039/C7BM00110J Quan, 2019, Mussel-inspired catechol-functionalized hydrogels and their medical applications, Molecules, 24, 10.3390/molecules24142586 Guo, 2018, Development of tannin-inspired antimicrobial bioadhesives, Acta Biomater., 72, 35, 10.1016/j.actbio.2018.03.008 Yadav, 2018, Interpretation of IR and Raman spectra of dopamine neurotransmitter and effect of hydrogen bond in HCl, J. Mol. Struct., 1160, 256, 10.1016/j.molstruc.2018.01.066 Spicer, 2018, Achieving controlled biomolecule–biomaterial conjugation, Chem. Rev., 118, 7702, 10.1021/acs.chemrev.8b00253 Zha, 2020, Conjugation of pea protein isolate via maillard-driven chemistry with saccharide of diverse molecular mass: molecular interactions leading to aggregation or glycation, J. Agric. Food Chem., 68, 10157, 10.1021/acs.jafc.0c04281 Rickman, 2019, Rotation-assisted wet-spinning of UV-cured gelatin fibres and nonwovens, J. Mater. Sci., 54, 10529, 10.1007/s10853-019-03498-5 Cao, 2018, Radical scavenging activities of biomimetic catechol-chitosan films, Biomacromolecules, 19, 3502, 10.1021/acs.biomac.8b00809 Hu, 2020, Polydopamine free radical scavengers, Biomater. Sci., 8, 4940, 10.1039/D0BM01070G Asadi, 2021, Multifunctional hydrogels for wound healing: special focus on biomacromolecular based hydrogels, Int. J. Biol. Macromol., 170, 728, 10.1016/j.ijbiomac.2020.12.202 Montazerian, 2021, Stretchable and bioadhesive gelatin methacryloyl-based hydrogels enabled by in situ dopamine polymerization, ACS Appl. Mater. Interfaces, 13, 40290, 10.1021/acsami.1c10048 Hong, 2016, Supramolecular metallo-bioadhesive for minimally invasive use, Adv. Mater., 28, 8675, 10.1002/adma.201602606 Yavvari, 2017, Injectable, self-healing chimeric catechol-Fe(III) hydrogel for localized combination cancer therapy, ACS Biomater. Sci. Eng., 3, 3404, 10.1021/acsbiomaterials.7b00741 Rahimnejad, 2017, Mussel-inspired hydrogel tissue adhesives for wound closure, RSC Adv., 7, 47380, 10.1039/C7RA06743G Huang, 2017, Ultrasound-mediated self-healing hydrogels based on tunable metal–organic bonding, Biomacromolecules, 18, 1162, 10.1021/acs.biomac.6b01841 Gong, 2017, Injectable dopamine-modified poly(α,β-aspartic acid) nanocomposite hydrogel as bioadhesive drug delivery system, J. Biomed. Mater. Res., 105, 1000, 10.1002/jbm.a.35931 Cheng, 2017, Mussel-inspired multifunctional hydrogel coating for prevention of infections and enhanced osteogenesis, ACS Appl. Mater. Interfaces, 9, 11428, 10.1021/acsami.6b16779 Zhao, 2019, Synthetic poly(vinyl alcohol)–chitosan as a new type of highly efficient hemostatic sponge with blood-triggered swelling and high biocompatibility, J. Mater. Chem. B, 7, 1855, 10.1039/C8TB03181A MacDonald, 2017, An in vivo comparison of the efficacy of hemostatic powders, using two porcine bleeding models, Med. Dev. (Auckl), 10, 273 Zhong, 2021, Mussel-inspired hydrogels as tissue adhesives for hemostasis with fast-forming and self-healing properties, Eur. Polym. J., 148, 10.1016/j.eurpolymj.2021.110361 Mehdizadeh, 2013, Design strategies and applications of tissue bioadhesives, Macromol. Biosci., 13, 271, 10.1002/mabi.201200332 Shin, 2018, Hemostatic swabs containing polydopamine-like catecholamine chitosan-catechol for normal and coagulopathic animal models, ACS Biomater. Sci. Eng., 4, 2314, 10.1021/acsbiomaterials.8b00451 Shin, 2017, Complete prevention of blood loss with self-sealing haemostatic needles, Nat. Mater., 16, 147, 10.1038/nmat4758 Zhao, 2011, Coagulation characteristics of titanium (Ti) salt coagulant compared with aluminum (Al) and iron (Fe) salts, J. Hazard. Mater., 185, 1536, 10.1016/j.jhazmat.2010.10.084 Guo, 2021, Haemostatic materials for wound healing applications, Nat. Rev. Chem., 5, 773, 10.1038/s41570-021-00323-z Ashour, 1987, Use of a 96-well microplate reader for measuring routine enzyme activities, Anal. Biochem., 166, 353, 10.1016/0003-2697(87)90585-9 Zhou, 1999, Blood-compatibility of polyurethane/liquid crystal composite membranes, Biomaterials, 20, 2093, 10.1016/S0142-9612(99)00080-0 Xu, 2018, A hybrid injectable hydrogel from hyperbranched PEG macromer as a stem cell delivery and retention platform for diabetic wound, Healing, 75, 63 Meng, 2017, Model polymer system for investigating the generation of hydrogen peroxide and its biological responses during the crosslinking of mussel adhesive moiety, Acta Biomater., 48, 144, 10.1016/j.actbio.2016.10.016 Meng, 2015, Hydrogen peroxide generation and biocompatibility of hydrogel-bound mussel adhesive moiety, Acta Biomater., 17, 160, 10.1016/j.actbio.2015.02.002 Assmann, 2017, A highly adhesive and naturally derived sealant, Biomaterials, 140, 115, 10.1016/j.biomaterials.2017.06.004 Previte, 2017, Reactive oxygen species are required for driving efficient and sustained aerobic glycolysis during CD4+ T cell activation, PLoS One, 12, 10.1371/journal.pone.0175549 Shin, 2017, Catechol groups enable reactive oxygen species scavenging-mediated suppression of PKD-NFkappaB-IL-8 signaling pathway by chlorogenic and caffeic acids in human intestinal cells, Nutrients, 9, 10.3390/nu9020165 Franchina, 2018, Reactive oxygen species: involvement in T cell signaling and metabolism, Trends Immunol., 39, 489, 10.1016/j.it.2018.01.005 Oskeritzian, 2012, Mast cells and wound healing, Adv. Wound Care, 1, 23, 10.1089/wound.2011.0357