Abstract
The insect industry wherein insects are a novel food is growing, making insect chitin a byproduct. A leading scientist wondered if insects can be an alternative source of chitin from marine arthropods. Chitin can be used to fabricate hydrogels by using a DMAc/LiCl solvent. The current study aims to compare the physicochemical properties of extracted chitin and its hydrogels from different insects as Zophobas morio (ZM), grasshopper (GH), large brown Cicada nymph exoskeleton (CIEXO), and marine sources such as shrimp and crab. Fourier transform infrared spectroscopy, and X-ray diffraction analysis results demonstrated all extracted chitins and their hydrogels to be α-chitin. For both chemical extraction (1 M HCl at 20 °C for 24 h — 1 M NaOH at 90 °C for 5 h) and bleaching (2.5 v/v % sodium hypochlorite at 20 °C for 2 h), CIEXO exhibited the highest yields. Bleaching reduced the crystallinity and molecular weight but increased solubility in DMAc/LiCl over 95% for all samples. Hydrogels were fabricated from all samples; the hydrogelation process increased crystallinity and decreased chloride remanent for the bleaching process. Also, bleached hydrogels exhibited a bigger diameter and a regular surface. Thus, CIEXO-bleached hydrogel showed a viscoelastic behavior comparable to marine sources. CIEXO was shown to be a suitable substitute as a chitin source for hydrogel preparation.
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References
Hou J, Aydemir BE, Dumanli AG (2021) Understanding the structural diversity of chitins as a versatile biomaterial. Phil Trans Royal Soc A: Math, Phys Eng Sci 379:2206. https://doi.org/10.1098/rsta.2020.0331
Ifuku S, Nomura R, Morimoto M, Saimoto H (2011) Preparation of chitin nanofibers from mushrooms. Materials 4(8):1417–1425. https://doi.org/10.3390/ma4081417
Rong J, Lin Y, Sui Z, Wang S, Wei X, Xiao J, Huang D (2019) Amorphous calcium phosphate in the pupal cuticle of Bactrocera dorsalis Hendel (Diptera: Tephritidae): a new discovery for reconsidering the mineralization of the insect cuticle. J Insect Physiol 119:103964. https://doi.org/10.1016/j.jinsphys.2019.103964
Taokaew S, Zhang X, Chuenkaek T, Kobayashi T (2020) Chitin from fermentative extraction of crab shells using okara as a nutrient source and comparative analysis of structural differences from chemically extracted chitin. Biochem Eng J 159:107588. https://doi.org/10.1016/j.bej.2020.107588
Sugumaran M (2009) Complexities of cuticular pigmentation in insects. Pigment Cell Melanoma Res 22(5):523–525. https://doi.org/10.1111/j.1755-148X.2009.00608.x
Gahukar RT (2016) Edible insects farming: efficiency and impact on family livelihood, food security, and environment compared with livestock and crops, in: Insects as sustainable food ingredients: production, processing and food applications. https://doi.org/10.1016/B978-0-12-802856-8.00004-1
Nikkhah A, Van Haute S, Jovanovic V, Jung H, Dewulf J, CirkovicVelickovic T, Ghnimi S (2021) Life cycle assessment of edible insects (Protaetia brevitarsis seulensis larvae) as a future protein and fat source. Sci Rep 11:1. https://doi.org/10.1038/s41598-021-93284-8
Ayieko IA, Onyango M, Ngadze RT, Ayieko MA (2021) Edible insects as new food frontier in the hospitality industry, Front Sustain Food Syst 5. https://doi.org/10.3389/fsufs.2021.693990
Dagevos H (2021) A literature review of consumer research on edible insects: recent evidence and new vistas from 2019 studies. J Insects Food Feed 7(3):249–259. https://doi.org/10.3920/JIFF2020.0052
Errico S, Spagnoletta A, Verardi A, Moliterni S, Dimatteo S, Sangiorgio P (2022) Tenebrio molitor as a source of interesting natural compounds, their recovery processes, biological effects, and safety aspects. Compr Rev Food Sci Food Saf 21(1):148–197. https://doi.org/10.1111/1541-4337.12863
Wu WM, Criddle CS (2021) Characterization of biodegradation of plastics in insect larvae. Methods Enzymol. https://doi.org/10.1016/bs.mie.2020.12.029
Zheng L, Hou Y, Li W, Yang S, Li Q, Yu Z (2013) Exploring the potential of grease from yellow mealworm beetle (Tenebrio molitor) as a novel biodiesel feedstock. Appl Energy 101:618–621. https://doi.org/10.1016/j.apenergy.2012.06.067
Pons P, Puig-Gironès R, Tobella C, Peiris A, Bas JM (2023) Cicada-MET: an efficient ecological monitoring protocol of cicada populations, Front Ecol Evol 11. https://doi.org/10.3389/fevo.2023.1219636
Sajomsang W, Gonil P (2010) Preparation and characterization of α-chitin from cicada sloughs. Mater Sci Eng C 30(3):357–363. https://doi.org/10.1016/j.msec.2009.11.014
Jang MK, Kong BG, Il Jeong Y, Lee CH, Nah JW (2004) Physicochemical characterization of α-chitin, β-chitin, and γ-chitin separated from natural resources. J Polym Sci A Polym Chem 42(14):3423–3432. https://doi.org/10.1002/pola.20176
Handbook of chitin and chitosan, 2020. https://doi.org/10.1016/c2018-0-03015-7
Nguyen KD, Kobayashi T (2020) Chitin hydrogels prepared at various lithium chloride/ N N-dimethylacetamide solutions by water vapor-induced phase inversion. J Chem 2020(1):16. https://doi.org/10.1155/2020/6645351
Wattjes J, Sreekumar S, Richter C, Cord-Landwehr S, Singh R, El Gueddari NE, Moerschbacher BM (2020) Patterns matter part 1: chitosan polymers with non-random patterns of acetylation. React Funct Polym 151:104583. https://doi.org/10.1016/j.reactfunctpolym.2020.104583
Tang H, Zhang L, Hu L, Zhang L (2014) Application of chitin hydrogels for seed germination, seedling growth of rapeseed. J Plant Growth Regul 33(2):195–201. https://doi.org/10.1007/s00344-013-9361-5
Peralta Ramos ML, González JA, Albornoz SG, Pérez CJ, Villanueva ME, Giorgieri SA, Copello GJ (2016) Chitin hydrogel reinforced with TiO2 nanoparticles as an arsenic sorbent. Chem Eng J 285:581–587. https://doi.org/10.1016/j.cej.2015.10.035
Jiang H, Kobayashi T (2017) Ultrasound stimulated release of gallic acid from chitin hydrogel matrix. Mater Sci Eng C 75:478–486. https://doi.org/10.1016/j.msec.2017.02.082
Rinaudo M (2006) Chitin and chitosan: properties and applications. Prog Polym Sci (Oxford) 31(7):63–632. https://doi.org/10.1016/j.progpolymsci.2006.06.001
Lv J, Lv X, Ma M, Oh DH, Jiang Z, Fu X (2023) Chitin and chitin-based biomaterials: a review of advances in processing and food applications. Carbohydr Polym 299:120142. https://doi.org/10.1016/j.carbpol.2022.120142
Dodda JM, Deshmukh K, Bezuidenhout D, Yeh Y-C (2023) Hydrogels: definition, history, classifications, formation, constitutive characteristics, and applications. Multicomponent Hydrogels. https://doi.org/10.1039/bk9781837670055-00001
Grand View Research Inc, Hydrocolloid dressing market size, share & trends analysis report by application (acute wounds, chronic wounds), by end-use (hospitals, specialty clinics), by region (EU, Asia Pacific, North America), and segment forecasts, 2022 - 2030, GVR-4–68039–952–2 (2024) 0–90. https://www.grandviewresearch.com/industry-analysis/hydrocolloid-dressing-market-report/toc. Accessed 17 Apr 2024
DataBridge, Global hydrocolloid dressing market – industry trends and forecast to 2031, (2024) 0–350. https://www.databridgemarketresearch.com/reports/global-hydrocolloid-dressing-market (Accessed April 17, 2024)
Kobayashi T, Carrillo KLT (2015) Fibroblast cell cultivation on wooden pulp cellulose hydrogels for cytocompatibility scaffold method. Pharm Anal Acta 6:10. https://doi.org/10.4172/2153-2435.1000423
Tovar-Carrillo KL, Saucedo-Acuña RA, Ríos-Arana J, Tamayo G, Guzmán-Gastellum DA, Díaz-Torres BA, Nava-Martínez SD, Espinosa-Cristóbal LF, Cuevas-González JC (2020) Synthesis, characterization, and in vitro and in vivo evaluations of cellulose hydrogels enriched with Larrea tridentata for regenerative applications. Biomed Res Int 2020:1–11. https://doi.org/10.1155/2020/1425402
GuangorenaZarzosa GI, Kobayashi T (2023) Insect chitins and hydrogels sourced from Zophobas morio in different lifes stage and their properties. Chem Lett 52(8):674–677. https://doi.org/10.1246/cl.230248
Wu SJ, Pan SK, Bin Wang H, Wu JH (2013) Preparation of chitooligosaccharides from cicada slough and their antibacterial activity. Int J Biol Macromol 62:348–351. https://doi.org/10.1016/j.ijbiomac.2013.09.042
Mol A, Kaya M, Mujtaba M, Akyuz B (2018) Extraction of high thermally stable and nanofibrous chitin from Cicada (Cicadoidea). Entomol Res 48(6):480–489. https://doi.org/10.1111/1748-5967.12299
Poerio A, Girardet T, Petit C, Fleutot S, Jehl JP, Arab-Tehrany E, Mano JF, Cleymand F (2021) Comparison of the physicochemical properties of chitin extracted from cicada orni sloughs harvested in three different years and characterization of the resulting chitosan. Appl Sci (Switzerland) 11(23):11278. https://doi.org/10.3390/app112311278
Machado SSN, da Silva JBA, Nascimento RQ, Lemos PVF, de Assis DJ, Marcelino HR, de Ferreira ES, Cardoso LG, Pereira JD, Santana JS, da Silva MLA, de Souza CO (2024) Insect residues as an alternative and promising source for the extraction of chitin and chitosan. Int J Biol Macromol 254:127773. https://doi.org/10.1016/j.ijbiomac.2023.127773
Smets R, Verbinnen B, Van De Voorde I, Aerts G, Claes J, Van Der Borght M (2020) Sequential extraction and characterisation of lipids, proteins, and chitin from black soldier fly (Hermetia illucens) larvae, prepupae, and pupae. Waste Biomass Valorization 11(12):6455–6466. https://doi.org/10.1007/s12649-019-00924-2
Li K, Tang B, Zhang W, Shi Z, Tu X, Li K, Xu J, Ma J, Liu L, Zhang H (2020) Formation mechanism of bleaching damage for a biopolymer: differences between sodium hypochlorite and hydrogen peroxide bleaching methods for shellac. ACS Omega 5(35):22551–22559. https://doi.org/10.1021/acsomega.0c03178
Ibitoye EB, Lokman IH, Hezmee MNM, Goh YM, Zuki ABZ, Jimoh AA (2018) Extraction and physicochemical characterization of chitin and chitosan isolated from house cricket. Biomed Mater (Bristol) 13(2):025009. https://doi.org/10.1088/1748-605X/aa9dde
Pires CTGVMT, Vilela JAP, Airoldi C (2014) The effect of chitin alkaline deacetylation at different condition on particle properties. Procedia Chem 9:220–225. https://doi.org/10.1016/j.proche.2014.05.026
Kaya M, Baublys V, Can E, Šatkauskienė I, Bitim B, Tubelytė V, Baran T (2014) Comparison of physicochemical properties of chitins isolated from an insect (Melolontha melolontha) and a crustacean species (Oniscus asellus). Zoomorphology 133(3):285–293. https://doi.org/10.1007/s00435-014-0227-6
Wu Q, Mushi NE, Berglund LA (2020) High-strength nanostructured films based on well-preserved α-chitin nanofibrils disintegrated from insect cuticles. Biomacromolecules 21(2):604–612. https://doi.org/10.1021/acs.biomac.9b01342
Minke R, Blackwell J (1978) The structure of α-chitin. J Mol Biol 120(2):167–181. https://doi.org/10.1016/0022-2836(78)90063-3
Hamdan YA, Elouali S, Eladlani N, Lefeuvre B, Oudadesse H, Rhazi M (2023) Investigation on Akis granulifera (Coleoptera, Sahlberg, 1823) as a potential source of chitin and chitosan: extraction, characterization and hydrogel formation. Int J Biol Macromol 252:126292. https://doi.org/10.1016/j.ijbiomac.2023.126292
Triunfo M, Tafi E, Guarnieri A, Salvia R, Scieuzo C, Hahn T, Zibek S, Gagliardini A, Panariello L, Coltelli MB, De Bonis A, Falabella P (2022) Characterization of chitin and chitosan derived from Hermetia illucens, a further step in a circular economy process. Sci Rep 12:1. https://doi.org/10.1038/s41598-022-10423-5
Draczynski Z (2008) Honeybee corpses as an available source of chitin. J Appl Polym Sci 109(3):1974–1981. https://doi.org/10.1002/app.28356
Isobe N, Kaku Y, Okada S, Kawada S, Tanaka K, Fujiwara Y, Nakajima R, Bissessur D, Chen C (2022) Identification of chitin allomorphs in poorly crystalline samples based on the complexation with ethylenediamine. Biomacromolecules 23(10):4220–4229. https://doi.org/10.1021/acs.biomac.2c00714
Yuan F, Zhang XX, Wu K, Li Z, Lin Y, Liang X, Yang Q, Liu T (2023) Damping chitin hydrogels by harnessing insect-cuticle-inspired hierarchical structures. Cell Rep Phys Sci 4(11):101644. https://doi.org/10.1016/j.xcrp.2023.101644
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Guillermo Ignacio Guangorena Zarzosa: Methodology, formal analysis, investigation, and writing — original draft preparation; Takaomi Kobayashi: conceptualization, writing — review and editing, and supervision.
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Highlights
• Chitin extracted from large brown cicada nymph exoskeleton has a superior yield in comparison of other insects and marine sources of chitin.
• Bleaching treatment improves solubility in DMAc/LiCl solvent system, and the resultant gels showed bigger diameter and uniform surface.
• Sodium hypochlorite as bleaching agent leaves chloride remnants which can be removed by the gelation process according to the presented XRF results.
• After gelation, bleached chitin hydrogels crystallinity increased as shown by XRD.
• Insect chitin hydrogels showed a similar viscoelastic property as those from marine sources.
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Zarzosa, G.I.G., Kobayashi, T. Regenerated chitin from insect sources and fabrication of their hydrogel films as an alternative from marine sources. Biomass Conv. Bioref. (2024). https://doi.org/10.1007/s13399-024-05686-z
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DOI: https://doi.org/10.1007/s13399-024-05686-z