Novel composite zinc-alginate hydrogels with activated charcoal aimed for potential applications in multifunctional primary wound dressings

Main Article Content

Andrea Osmokrovic
Ivan Jancic
Ivona Jankovic Castvan
Predrag Petrovic
Marina Milenkovic
Bojana Obradovic

Abstract

Composites based on Zn-alginate hydrogels in the form of beads were produced by extrusion of a suspension containing 0.5 % w/w of alginate and 20 % w/w of activated charcoal (AC) with the intent to simultaneously release two active agents, Zn2+ and AC particles, in a physiological-like environment. The obtained composite beads were analyzed by FE-SEM and characterized regarding textural parameters, as well as Zn2+ and AC release kinetics in the physiological saline solution. Zn2+ions were quickly released reaching the equilibrium concentration within the first hour in the contrary to the release of AC particles, which was described by internal diffusion with the apparent diffusion coefficient of approximately 10-13 m2 s-1. Potential functionality of the obtained beads was evaluated regarding antibacterial activity in suspensions of the standard bacterial strain Escherichia coli 25922. The observed strong bactericidal effects were related to the quick release of Zn2+that was not affected by AC. Thus, taking into account results of this study as well as high sorption capacity of alginate hydrogel, efficiency of AC to adsorb malodor and tissue degradation products and positive effects of Zn2+ on wound healing, the obtained composites have shown promising potentials for applications as multifunctional wound dressings.

Article Details

Section

Engineering of Materials - Composites

How to Cite

[1]
A. Osmokrovic, I. Jancic, I. Jankovic Castvan, P. Petrovic, M. Milenkovic, and B. Obradovic, “Novel composite zinc-alginate hydrogels with activated charcoal aimed for potential applications in multifunctional primary wound dressings”, Hem Ind, vol. 73, no. 1, pp. 37–46, Mar. 2019, doi: 10.2298/HEMIND180629003O.

References

Williams K, Griffiths E. Malodorous wounds: causes and treatment. Nurs Residential Care. 1999; 1 (5): 276-285.

Wilson V. Assessment and management of fungating wounds: a review. Br J Community Nurs . 2005; 10 (3): S28-34.

McDonald A, Lesage P. Palliative management of pressure ulcers and malignant wounds in patients with advanced illness. J Palliat Med. 2006; 9 (2): 285–295.

Grocott PA. Review of advances in fungating wound management since EWMA 1991. EWMA J. 2002; 2 (1), 21-24.

Alexander S. Malignant fungating wounds: key symptoms and psychosocial issues. J Wound Care. 2009; 18 (8): 325-329.

Bishop SM, Walker M, Rogers AA, Chen WYJ. Importance of moisture balance at the wound-dressing interface. J Wound Care 2003; 12 (4): 125-128.

Nazarko L. Malignant fungating wounds. Nurs Residential Care. 2006; 8 (9): 402-406.

Landsdown A. Calcium: a potential central regulator in wound healing in the skin. Wound Repair Regen. 2002; 10: 271–285.

Stenvik J, Sletta H, Grimstad O, Pukstad B, Rzan L, Aune R, Strand W, Tondervik A, Torp SH, Skjak-Braek G, Espevik T. Alginates induce differentiation and expression of CXCR7 and CXCL12/SDF-1 in human keratinocytes – the role of calcium. J Biomed Mater Res A. 2012; 100: 2803–2812.

Stojkovskа J, Djurdjevic Z, Jancic I, Bufan B, Milenkovic M, Jankovic R, Miskovic-Stankovic V, Obradovic B. Comparative in vivo evaluation of novel formulations based on alginate and silver nanoparticles for wound treatments, J. Biomater. Appl. 2018; 32 (9): 1197-1211.

Qin Y. Alginate fibres: an overview of the production processes and applications in wound management, Polym Int. 2008; 57: 171–180.

Haase H, Overbeck S, Rink L. Zinc supplementation for the treatment or prevention of disease: current status and future perspectives, Exp. Gerontol. 2008; 43: 394–408.

Leung YH, Chan CMN, Ng AMC, Chan HT, Chiang MWL, Djurisic AB, Ng YH, Jim WY, Guo MY, Leung FCC, Chan WK, Au DTW. Antibacterial activity of ZnO nanoparticles with a modified surface under ambient illumination, Nanotechnology. 2012; 23 (47): 475703.

Vallee B L, Falchuk H. The biochemical basis of zinc physiology, Physiol. Rev. 1993; 73: 79-118.

Eide D. Zinc transporters and the cellular trafficking of zinc. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 2006; 1763 (7): 711-722.

Bafaro E, Liu Y, Xu Y, Dempski RE. The emerging role of zinc transporters in cellular homeostasis and cancer. Signal Transduct Target Ther. 2017; 2: 17029.

Borovansky J, Riley PA. Cytotoxicity of zinc in vitro. Chem. Biol. Interact. 1989; 69: 279–291.

Lipovsky A, Nitzan Y, Gedanken A, Lubart R. Antifungal activity of ZnO nanoparticles—the role of ROS mediated cell injury. Nanotechnology. 2011; 22: 105101.

Atmaca S, Gül K, Cicek R. The effect of zinc on microbial growth Turk. J. Med.Sci. 1998; 28: 595–597.

Padmavathy N, Vijayaraghavan R. Enhanced bioactivity of ZnO nanoparticles—an antimicrobial study. Sci. Technol. Adv. Mater. 2008; 9: 035004.

Zhang L, Jiang Y, Ding Y, Daskalakis N, Jeuken L, Povey M, ONeill AJ, York DW. Mechanistic investigation into antibacterial behaviour of suspensions of ZnO nanoparticles against E. coli. J. Nanopart. Res. 2010; 12: 1625–1636.

Miller LP, McCallan SEA. Toxic action of metal ions to fungus spores. J. Agric.Food Chem. 1957; 5: 116–122.

Lansdown ABG, Path FRC, Mirastschijski U, Stubbs N, Scanion E, Agren MS. Zinc in wound healing; theoretical, experimental and clinical aspects. Wound repair and regeneration. 2007; 15: 2–16.

Lin P-H, Sermersheim M, Li H, Lee PHU, Steinberg SM, Ma J, Zinc in wound healing modulation, Nutrients, 2017; 10 (1).

Cole L. The effect of coupled haemofiltration and adsorption on inflammatory cytokines in an ex vivo model. Nephrology Dialysis Transplantation. 2002; 17 (11): 1950-1956.

Howell C, Sandeman S, Phillips G, Lloyd A, Davies J, Mikhalovsky S, Tennison S, Rawlinson A, Kozynchenko O, Owen H, Gaylor J, Rouse J, Courtney J. The in vitro adsorption of cytokines by polymer-pyrolysed carbon. Biomaterials. 2006; 27 (30): 5286-5291.

Kerihuel J. Effect of activated charcoal dressings on healing outcomes of chronic wounds. Journal of Wound Care. 2010; 19 (5): 208-214.

Naka K, Watarai S, Tana Inoue K, Kodama Y, Oguma K, Yasuda T, Kodama H. Adsorption Effect of Activated Charcoal on Enterohemorrhagic Escherichia coli. Journal of Veterinary Medical Science. 2001; 63 (3): 281-285.

Sandeman S, Howell C, Mikhalovsky S, Phillips G, Lloyd A, Davies J, Tennison S, Rawlinson A, Kozynchenko O. Inflammatory cytokine removal by an activated carbon device in a flowing system. Biomaterials. 2008; 29 (11): 1638-1644.

Atkins P, de Paula, Physical Chemistry, 9th Edition, 2010; Oxford: Oxford University Press.

Rouquerol F, Rouquerol J, Sing K. Adsorption by Powders and Porous Solids. 1975; London: Academic Press.

Barrett E, Joyner L, Halenda P. The Determination of Pore Volume and Area Distributions in Porous Substances. I. Computations from Nitrogen Isotherms. Journal of the American Chemical Society. 1951; 73 (1): 373-380.

Lippens B. Studies on pore systems in catalysts V. The t method. Journal of Catalysis. 1965; 4 (3): 319-323.

Hassan A, Abdel-Mohsen A, Fouda M. Comparative study of calcium alginate, activated carbon, and their composite beads on methylene blue adsorption. Carbohydrate Polymers. 2014; 102: 192-198.

Siepmann J, Siepmann F. Modeling of diffusion controlled drug delivery. Journal of Controlled Release. 2012; 161 (2): 351-362.

Osmokrovic A, Obradovic B. Polymer composites based on alginate and activated charcoal, patent application RS 20150403 (A1), 2015.

Gethin G. The significance of surface pH in chronic wounds, Wounds UK. 2007; 3:52-56.

Chuang J-J, Huang Y-Y, Lo S-H, Hsu T-F, Huang W-Y, Huang S-L, Lin Y-S. Effects of pH on the Shape of Alginate Particles and Its Release Behavior, International Journal of Polymer Science. 2017; Article ID 3902704, 9 pages. https://doi.org/10.1155/2017/3902704.

Malagurski I, Levic S, Pantic M, Matijasevic D, Mitric M, Pavlovic V, Dimitrijevic-Brankovic S. Synthesis and antimicrobial properties of Zn-mineralized alginate nanocomposites, Carbohydrate Polymers. 2017; 165: 313-321.

Madhava Rao M, Chandra Rao GP, Seshaiah K, Choudarz NV, Wang MC. Activated carbon from Ceiba pentandra hulls, an agricultural waste, as an adsorbent in the removal of lead and zinc from aqueous solutions, Waste Management. 2008; 28: 849-858.

Kouakou U, Ello AS, Yapo JA, Trokourey A. Adsorption of iron and zinc on commercial activated carbon. Journal of Environmental Chemistry and Ecotoxicology. 2013; 5 (6): 168-171.

Gyu Parl H, Won Kim T, Yun Chae M, Yoo I-K. Activated carbon-containing alginate adsorbent for the simultaneous removal of heavy metals and toxic organics, Process Biochemistry. 2007; 42: 1371–1377.

Muller G, Winkler Y, Kramer A. Antibacterial activity and endotoxin-binding capacity of Actisorb® Silver 220. Journal of Hospital Infection, 2003; 53 (3): 211-214.

Osmokrovic A, Jancic I, Vunduk J, Petrovic P, Milenkovic M, Obradovic B. Achieving high antimicrobial activity: Composite alginate hydrogel beads releasing activated charcoal with an immobilized active agent. Carbohydrate Polymers. 2018; 196: 279-288.

Aarestrup F, Hasman H. Susceptibility of different bacterial species isolated from food animals to copper sulphate, zinc chloride and antimicrobial substances used for disinfection. Veterinary Microbiology. 2004; 100: 83–89.

Brocklehurst K, Morby A P. Metal-ion tolerance in Escherichia coli: analysis of transcriptional profiles by gene-array technology. Microbiology. 2000; 146: 2277–2282.

Similar Articles

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)

1 2 3 > >>