The Synthesis and Structural Characterization of Bioactive Chitosan Hydrogels from Lobster Shell Waste

  • Fatima Zahoor University of the Punjab, Lahore, Pakistan
  • Hira Tariq University of the Punjab, Lahore, Pakistan
  • Muhammad Kashif University of the Punjab, Lahore, Pakistan
  • Shahmeen Sheikh University of the Punjab, Lahore, Pakistan
  • Saiqa Sattar University of the Punjab, Lahore, Pakistan
  • Hera Naheed Khan University of the Punjab, Lahore, Pakistan
Keywords: antibacterial, antibiofilm, biomaterial, chitosan hydrogel, implant coatings

Abstract

Abstract Views: 19

Background. Chitosan is a biopolymer derived from chitin, a polysaccharide abundantly present in the shells of marine crustaceans. It has good antimicrobial and biomedical applications. Chitosan plays a vital role in the production of hydrogels, which retain significant water-holding capacity and antimicrobial properties, making this biomaterial useful for treatment options, particularly in implant coatings and wound dressings. The current study focuses on the use of lobster shell waste to produce a bioactive, chitosan-based, hydrogel biomaterial with a wide range of biological applications. Lobsters provide a rich source of chitin, while the hydrogels act as carriers of pharmaceutical drugs. After structural characterization, these hydrogels were evaluated for their antibiofilm activity and dental applications.

Objective. The study focuses on the use of lobster shell waste as a source of chitosan hydrogels. Further, it evaluates the antibacterial and antibiofilm potential of the prepared chitosan hydrogels against dental bacterial isolates.

Method. Polysaccharide chitin from lobster shells was isolated by deproteinization, demineralization, and deacetylization to yield chitosan. For hydrogel preparation, the dispersing agent, tween-80, and 2% acetic acid were mixed. Water holding capacity, swelling, and dissolution were monitored for structural evaluation. Agar well diffusion assay was performed against bacterial isolates (Staphylococcus aureus, Bacillus sp., E. coli, and Pseudomonas pneumoneae). Antibiofilm and hemolytic assays were also performed for biofilm and biocompatibility purposes.

Results. Synthesized chitosan hydrogels showed good water retention (51.25%) and swelling (10.45%), with the highest inhibition zone of 22 mm against Staphylococcus aureus, along with strong antibiofilm activity and better biocompatibility. Chitosan hydrogels against dental isolates (DI2, DI5, DI8, DI9) exhibited activity comparable to pyodine, suggesting strain-dependent efficacy of the hydrogel.

Conclusion. The current study suggests chitosan hydrogel as an effective and promising coating material for dental implants

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References

Ali G, Sharma M, Salama ES, Ling Z, Li X. Applications of chitin and chitosan as natural biopolymer: potential sources, pretreatments, and degradation pathways. Biomass Convers Biorefin. 2024;14(4):4567-4581. https://doi.org/10.1007/s13399-022-02684-x

Desai N, Rana D, Salave S, Gupta R, Patel P, Karunakaran B, et al. Chitosan: a potential biopolymer in drug delivery and biomedical applications. Pharmaceutics. 2023;15(4):e1313. https://doi.org/10.3390/pharmaceutics15041313

Affes S, Aranaz I, Acosta N, Heras Á, Nasri M, Maalej H. Physicochemical and biological properties of chitosan derivatives with varying molecular weight produced by chemical depolymerization. Biomass Convers Biorefin. 2024;14(3):4111-4121. https://doi.org/10.1007/s13399-022-02662-3

Faghmous N, Bouzid D, Boumaza M, Touati A, Boyron O. Optimization of chitosan-coated W/O/W multiple emulsion stabilized with Span 80 and Tween 80 using Box–Behnken design. J Dispersion Sci Technol. 2021;42(10):1566-1578. https://doi. org/10.1080/01932691.2020.1774387

Periyannan K, Selvaraj H, Subbu B, Pallikondaperumal M, Karuppiah P, Rajabathar JR, et al. Green fabrication of chitosan from marine crustaceans and mushroom waste: toward sustainable resource utilization. Green Process Synth. 2023;12(1):e20230093. https://doi.org/10.1515/gps-2023-0093

Lu G, Ling K, Zhao P, Xu Z, Deng C, Zheng H, et al. A novel in situ-formed hydrogel wound dressing by the photocross-linking of a chitosan derivative. Wound Repair Regen. 2010;18(1):70-79. https://doi.org/10.1111/j.1524-475X.2009.00557.x

Fasiku VO, Omolo CA, Devnarain N, Ibrahim UH, Rambharose S, Faya M, et al. Chitosan-based hydrogel for the dual delivery of antimicrobial agents against bacterial methicillin-resistant Staphylococcus aureus biofilm-infected wounds. ACS Omega. 2021;6(34):21994-22010. https://doi. org/10.1021/acsomega.1c02547

Stewart PS, Bjarnsholt T. Risk factors for chronic biofilm-related infection associated with implanted medical devices. Clin Microbiol Infect. 2020;26(8):1034-1038. https://doi.org/10.1016/j.cmi.2020.02.027

Colombo APV, Tanner ACR. The role of bacterial biofilms in dental caries and periodontal and peri-implant diseases: a historical perspective. J Dent Res. 2019;98(4):373-385. https://doi.org/10.1177/0022034519830686

Nag M, Lahiri D, Mukherjee D, Banerjee R, Garai S, Sarkar T, et al. Functionalized chitosan nanomaterials: a jammer for quorum sensing. Polymers. 2021;13(15):e2533. https://doi.org/10.3390/polym13152533

Zhou HY, Zhang YP, Zhang WF, Chen XG. Biocompatibility and characteristics of injectable chitosan-based thermosensitive hydrogel for drug delivery. Carbohydr Polym. 2011;83(4):1643-1651. https://doi.org/10.1016/j.carbpol.2010.10.022

Jia Y, Wei Z, Fu W, Huo M, Li F, Zhong C, et al. Biocompatibility evaluation on a bio-hydrogel composed of bacterial cellulose and chitosan. J Biomater Tissue Eng. 2014;4(2):118-125. https://doi.org /10.1166/jbt.2014.1142

Al Hoqani HAS, Noura AS, Hossain MA, Al Sibani MA. Isolation and optimization of the method for industrial production of chitin and chitosan from Omani shrimp shell. Carbohydr Res. 2020;492:e108001. https://doi.org/10.1016/j.carres.2020.108001

Felinto MC, Parra DF, da Silva C, Angerami J, Oliveira M, Lugão A. The swelling behavior of chitosan hydrogels membranes obtained by UV- and γ-radiation. Nucl Instrum Methods Phys Res B. 2007;265(1):418-424. https://doi.org /10.1016/j.nimb.2007.09.025

Ankur G, Harish K. Synthesis and swelling behavior of superabsorbent hydrogels acquired from CMC for efficient drug delivery. Res J Chem Environ. 2018;22:19-26.

Malagoli D. A full-length protocol to test hemolytic activity of palytoxin on human erythrocytes. Invertebr Surviv J. 2007;4(2):92-94.

Castro-Concha LA, Escobedo RM, de Miranda-Ham ML. Measurement of cell viability in in vitro cultures. In: Loyola-Vargas VM, Vázquez-Flota F. eds. Plant Cell Culture Protocols. Springer; 2006:71-76.

Chopra I, Sharad S, Kumar S, et al. A comprehensive review on hydrogels. Curr Drug Deliv. 2021;19(6):658‑675. https://doi.org/10.2174/1567201818666210601155558

Wang Y, Zhang Q, Li H, et al. The synergistic effects of 3‑D porous silk fibroin matrix scaffold properties and hydrodynamic environment in cartilage tissue regeneration. Biomaterials. 2010;31(17):4672‑4681. https://doi.org/10.1016/j.biomaterials.2010.02.006

Published
2026-04-20
How to Cite
Zahoor, F., Tariq, H., Kashif, M., Sheikh, S., Sattar, S., & Khan, H. N. (2026). The Synthesis and Structural Characterization of Bioactive Chitosan Hydrogels from Lobster Shell Waste. BioScientific Review, 8(2), 01-15. https://doi.org/10.32350/bsr.82.01
Section
Research Articles