KitoZyme (Belgium)

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Title DOI
https://doi.org/10.1038/s41598-019-42257-z Ability of bifidobacteria to metabolize chitin-glucan and its impact on the gut microbiota
https://doi.org/10.1111/j.1468-2494.2008.00470.x Chitin–glucan, a natural cell scaffold for skin moisturization and rejuvenation
https://doi.org/10.1080/19490976.2020.1810530 Metabolite profiling reveals the interaction of chitin-glucan with the gut microbiota
https://doi.org/10.1016/j.jff.2017.01.030 Fate of chitin-glucan in the human gastrointestinal tract as studied in a dynamic gut simulator (SHIME®)
https://doi.org/10.1007/s00217-007-0577-0 Chitosan, chitin-glucan and chitin effects on minerals (iron, lead, cadmium) and organic (ochratoxin A) contaminants in wines
https://doi.org/10.1016/j.actbio.2010.09.013 Long-term in vitro degradation of PDLLA/Bioglass® bone scaffolds in acellular simulated body fluid
https://doi.org/10.1186/s12937-016-0122-8 Single-blind, placebo controlled randomised clinical study of chitosan for body weight reduction
https://doi.org/10.1038/ejcn.2012.121 Chitin-glucan fiber effects on oxidized low-density lipoprotein: a randomized controlled trial
https://doi.org/10.1016/j.actbio.2008.05.021 Controlled release of drugs from multi-component biomaterials
https://doi.org/10.1002/pi.5340 Innovative polyelectrolytes/poly(ionic liquid)s for energy and the environment
https://doi.org/10.1111/jam.12682 Effect of a fungal chitosan preparation onBrettanomyces bruxellensis,a wine contaminant
https://doi.org/10.1016/j.vaccine.2003.11.011 Glycol chitosan improves the efficacy of intranasally administrated replication defective human adenovirus type 5 expressing glycoprotein D of bovine herpesvirus 1
https://doi.org/10.1016/j.joca.2013.04.017 Protective effect of a new biomaterial against the development of experimental osteoarthritis lesions in rabbit: a pilot study evaluating the intra-articular injection of alginate-chitosan beads dispersed in an hydrogel
https://doi.org/10.1371/journal.pone.0128362 Chitosan Enriched Three-Dimensional Matrix Reduces Inflammatory and Catabolic Mediators Production by Human Chondrocytes
https://doi.org/10.3390/nu12092824 Development of a Repertoire and a Food Frequency Questionnaire for Estimating Dietary Fiber Intake Considering Prebiotics: Input from the FiberTAG Project
https://doi.org/10.1016/j.ebiom.2022.104051 Breath volatile metabolome reveals the impact of dietary fibres on the gut microbiota: Proof of concept in healthy volunteers
https://doi.org/10.1080/19490976.2020.1862028 Noninvasive monitoring of fibre fermentation in healthy volunteers by analyzing breath volatile metabolites: lessons from the FiberTAG intervention study
https://doi.org/10.1038/s41598-022-12920-z Chitin-glucan supplementation improved postprandial metabolism and altered gut microbiota in subjects at cardiometabolic risk in a randomized trial
https://doi.org/10.3390/nu13093249 Chitin Glucan Shifts Luminal and Mucosal Microbial Communities, Improve Epithelial Barrier and Modulates Cytokine Production In Vitro
https://doi.org/10.3390/ijms251910732 A Synbiotic Combining Chitin–Glucan and Lactobacillus acidophilus NCFM Induces a Colonic Molecular Signature Soothing Intestinal Pain and Inflammation in an Animal Model of IBS
https://doi.org/10.1016/j.arrct.2025.100516 Post-COVID Rehabilitation Outcomes: A Comparative Cohort Study
https://doi.org/10.1111/nbu.12416 The FiberTAG project: Tagging dietary fibre intake by measuring biomarkers related to the gut microbiota and their interest for health
https://doi.org/10.1016/b978-0-323-02598-0.50135-x Silicone Oils: Physicochemical Properties
https://doi.org/10.4081/ws.2014.4574 Evaluating the impact of a fungal-origin chitosan preparation on Brettanomyces bruxellensis in the context of wine aging
https://doi.org/10.1007/978-3-319-12478-0_14 Polymers in Wound Repair
https://doi.org/10.3748/wjg.v30.i16.2258 Chitin-glucan improves important pathophysiological features of irritable bowel syndrome
https://doi.org/10.20870/oeno-one.2005.39.4.890 Applications and interest of chitin, chitosan and their derivatives in enology
https://doi.org/10.1016/j.fct.2010.06.042 Subchronic (13-week) oral toxicity study in rats with fungal chitin-glucan from Aspergillus niger
https://doi.org/10.4081/ws.4574 Evaluating the impact of a fungal-origin chitosan preparation on Brettanomyces bruxellensis in the context of wine aging
https://doi.org/10.1093/cdn/nzac053.072 Chitin-Glucan Supplementation Altered Gut Microbiota and Improved Postprandial Metabolism in Subjects at Cardiometabolic Risk
https://doi.org/10.1007/978-3-031-24378-3_10 EDGAR: Embedded Detection of Gunshots by AI in Real-time
https://doi.org/10.1016/j.ab.2009.06.013 Development of a procedure to simultaneously isolate RNA, DNA, and proteins from characterizing cells invading or cultured on chitosan scaffolds
https://doi.org/10.1016/j.ab.2009.09.002 Corrigendum to “Development of a procedure to simultaneously isolate RNA, DNA, and proteins from characterizing cells invading or cultured on chitosan scaffolds” [Anal. Biochem. 393 (2009) 145–147]
https://doi.org/10.1016/j.joca.2013.02.150 The intra-articular injection of a new chitosan biomaterial prevents the progression of osteoarthritis in ACLT rabbit model
https://doi.org/10.21203/rs.3.rs-31912/v1 Development of a repertoire and a food frequency questionnaire for estimating dietary fiber intake considering prebiotics: input from the FiberTAG project
Chitin-Glucan, a natural cell scaffold for skin rejuvenation: in vivo safety and efficacy.
Un biopolymère d'origine fongique (chitine glucan) efficace pour le débourbage de moût blanc : essais réalisés au Portugal et en Italie
https://doi.org/10.1017/s0029665120004474 Breath volatile compounds and conjugated polyunsaturated fatty acids as metabolic biomarkers reflecting the interaction between chitin-glucan and the gut microbiota.
https://doi.org/10.1016/j.clnesp.2020.09.278 Identification of new biomarkers reflecting the interaction between chitin-glucan dietary fiber and the gut microbiota in healthy volunteers
https://doi.org/10.1016/j.clnesp.2021.09.352 Identification of the breath-signature of chitin-glucan insoluble fiber in healthy volunteers
https://doi.org/10.1016/j.nupar.2021.12.016 Impact de la supplémentation en chitine-glucane chez le sujet à risque cardiométabolique : focus sur le métabolisme postprandial et le microbiote intestinal
https://doi.org/10.2139/ssrn.3931749 Breath Volatile Metabolome Reveals the Impact of Dietary Fibres on the Gut Microbiota: Proof of Concept in Healthy Volunteers
https://doi.org/10.21203/rs.3.rs-62395/v1 Non-invasive monitoring of fiber fermentation in healthy volunteers by analyzing breath volatile metabolites: lessons from the FiberTAG intervention study
https://doi.org/10.1136/gutjnl-2024-bsg.93 P11 Chitin-glucan improves important pathophysiological features of IBS
https://doi.org/10.4081/ejtm.2025.14060 What matters in rehabilitation: a mixed methods study of critical success factors from the perspectives of patients and healthcare professionals
https://doi.org/10.1183/13993003.congress-2025.pa5799 Influence of Fatigue on Rehabilitation Trajectories of Post-COVID Patients: A Cohort Study
https://doi.org/10.1007/s40520-026-03341-3 The impact of transitional care on geriatric rehabilitation outcomes: prevalence and associated factors of sarcopenia and malnutrition