Antibacterial nanostructures derived from oxidized sodium alginate-ZnO

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Abstract

The present study describes synthesis, characterization and antibacterial application of oxidized sodium alginate (OSA)-zinc oxide (ZnO) hybrid nanostructures (OSA-ZnO). In continuation to our previous study on oxidized guar gum (OGG)-ZnO (OGG-ZnO) nanocomposite, in the present study we have chosen OSA to understand the role of polysaccharide charge type in designing the antibacterial material. The nanomaterial has been characterized using UV–visible, FTIR, XRD, SEM and TEM analyses. The nanostructure has shown crystalline nature having hexagonal phase with preferred (101) orientation, while TEM image indicated that the material has ~6 nm particle size. It exhibited very good antibacterial performance against Bacillus subtilis (B. subtilis), Cellulomonas cellulans (C. cellulans), Staphylococcus typhi (S. typhi), and Escherichia coli (E. coli) bacterial strains, ZOI for B. subtilis, C. cellulans, S. typhi, and E. coli being 22, 18, 19.5 and 18.5 mm respectively. Under identical conditions, pure ZnO showed significantly lower ZOI for the corresponding bacterial strains (14, 12.5, 12 and 13.5 mm respectively), while native SA and OSA did not exhibit any biological activity.

Introduction

These days, nanotechnology has made its special place in the fields of biomedicine and pharmacy. Nanotechnology has been utilized as an alternative antimicrobial strategy to cope with the re-emergence of infectious diseases and to tackle with the antibiotic-resistant bacterial strains [1]. As opposed to micro- or macro-sized metal oxide particles, corresponding nanoparticles show enhanced antimicrobial activity due to their large surface to volume ratio [2]. Now a day's biopolymer modified nanoparticles have attracted attention in the field of nanotechnology [3] as these natural polymers not only reduce the toxicity of the nanoparticles but also they enhance their antimicrobial potential [4].

Zinc oxide is a promising antimicrobial and antitumor material [5,6]. It has been reported to inhibit the adhesion and internalization of enterotoxigenic E. coli bacteria [7]. In addition, ZnO nanoparticles (ZnO-NPs) are known for reducing the attachment and viability of microbes on biomedical surfaces [8]. The particle size has an important role in determining the antibacterial performance of ZnO-NPs [9]. Size control of ZnO-NPs has been accomplished via thermal decomposition of zinc acetate coated on organic additives [10]. Several methods are known for obtaining ZnO-NPs e.g. microwave assisted synthesis [11], sol–gel technique [12], hydrothermal synthesis [13], solution combustion method [14], laser technique [15], mechanochemical synthesis [16], solvothermal process [17], and sonochemical synthesis [18]. The co-precipitation is an inexpensive and environmentally friendly technique which allows room temperature growth and fabrication of the nanoparticles.

SA, sourced from brown marine algae, is an anionic and hydrophilic polysaccharide [19]. It consists of β-d-mannuronic acid (M-unit), and α-l-guluronic acid residues (G-unit) which are arranged as the interspersed blocks of M and G units [20]. The high molecular weight alginate polymers are difficult to degrade through hydrolytic and enzymatic chain breakage; however their oxidation degradation is reported [21]. Hydrogen peroxide is a popular and an environmentally friendly oxidant for oxidizing polysaccharides [[22], [23], [24], [25], [26], [27]]. Polysaccharides may be depolymerized through oxidation while their structures get modified e.g. during cellulose oxidation, high content of ketone groups are introduced [26]. Similarly oxidation of starch by hydrogen peroxide introduces carboxyl and carbonyl groups at the C-6 positions [24]. Hydrogen peroxide oxidizes chitosan to result carboxyl groups and deamination with simultaneous ring-opening [22]. There are only rare reports on the oxidation of SA through H2O2 [28,29].

Owing to high relevance of SA in biomedical field [30,31], it has been chosen for stabilization and binding nano ZnO [32]. In our previous study we have revealed that OGG-ZnO hybrid nanostructures have excellent antibacterial activity against B. subtilis and Salmonella typhi (S. typhi) [33]. In continuation to this study, in present study we have taken OSA instead OGG to understand the effect of polysaccharide charge type in deriving antibacterial nano ZnO.

Section snippets

Materials and instrumentation

Zinc acetate (Qualigens) has been used as zinc oxide (ZnO) precursor. SA (Merck, India) was used as supplied. Hydrogen peroxide solution (30%) and ammonia solution (25%), Merck, India were used. Ethanol (99.9%) was procured from Changshu Yangyum Chemical Company (China). Nutrient agar, peptone, sodium chloride were purchased from HiMedia Laboratories. Beef extract (Loba Chemie) was used. Bacterial strain B. subtilis MTCC 8661 was purchased from IMTECH, Chandigarh, India, whereas all the other

Result and discussion

The chemical structure of SA was altered by H2O2 oxidation in order to increase higher oxidation state functional groups. The oxidation is reported to break the glucoside bonds with the change in the structure of reducing end residues and formation of single bondCOOH groups. Three samples of OSA-ZnO were synthesized by using 30 mL of OSA solution of known concentrations (ranging from 0.5 to 1.5% (w/v)) while concentration of zinc acetate was kept fixed at 0.08 M (Table 1). A schematic diagram for the

Conclusion

SA and OSA proved very productive in producing ZnO nanocomposites in terms of antibacterial activity for both gram positive and gram negative bacterial strains. In contrast to GG, SA did not mask the antibacterial activity. OSA-ZnO was more effective as antibacterial material than SA-ZnO and neat ZnO because of extra defect states in the nanostructures and smaller particle size. Nanocomposite derived from 1% OSA was most effective for all the studied bacterial strains and the most promising

CRediT authorship contribution statement

L.M. Dwivedi: Conceptualization, Investigation, Formal analysis, Writing - original draft. K. Baranwal: Formal analysis, Writing - original draft. S. Gupta: Formal analysis, Writing - original draft. M. Mishra: Investigation, Writing - original draft. S. Sundaram: Formal analysis, Writing - review & editing. V. Singh: Conceptualization, Formal analysis, Writing - original draft, Writing - review & editing.

Acknowledgment

Author thanks MNNIT, Allahabad for XRD facility. MNIT, Jaipur is acknowledged for SEM, TEM and FTIR instrumental facilities. Author Lalit Mohan Dwivedi thanks U.G.C., New Delhi, for the financial support to carry out this work.

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