Received Date: November 21, 2016; Accepted Date: December 27, 2016; Published Date: December 31, 2016
Citation: Vijayalakshmi K, Devi BM, Sudha PN, Venkatesan J, Anil S (2016) Synthesis, Characterization and Applications of Nanochitosan/Sodium Alginate/Microcrystalline Cellulose Film. J Nanomed Nanotechnol 7: 419. doi: 10.4172/2157-7439.1000419
Copyright: © 2016 Vijayalakshmi K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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The antimicrobial potential of the synthesized ternary nanochitosan (NCS)/sodium alginate (SA)/microcrystalline cellulose (MC) (extracted from banana fiber) film in 4:16:1 ratio against Bascillus subtilis and E. coli are reported here. Initially the present work focuses on the synthesis and characterization of ternary nanochitosan (NCS)/sodium alginate (SA)/microcrystalline cellulose (MC) (extracted from banana fiber) film. The prepared NCS/SA/MC film sample was then characterized using advanced analytical techniques such as FT-IR, XRD, TGA, DSC and SEM studies. The obtained results of FT-IR studies clearly indicate that the nanochitosan gets effectively binded with the sodium alginate and the microcrystalline cellulose in the film form. The change in crystallinity and the increased thermal behavior was elucidated from XRD and TGA analysis respectively. The scanning electron microscopic (SEM) studies of NCS/SA/MC film showed that the prepared film has the improved rough surface morphology and fractured structure. The bactericidal action of NCS/SA/MC film determined using Muller Hinton Agar medium on two microbial strains (Escherichia coli and Bacillus subtilis) reveals that the prepared NCS/SA/MC film has the greater potential to kill the microorganisms to a greater extent and hence this NCS/SA/MC film was found to be suggested as the promising material for biomedical applications.
Nanochitosan; Sodium alginate; Microcrystalline cellulose; Antimicrobial activity
Pathogenic bacteria remain a major health concern especially since it is responsible for causing a large number of deaths and hospitalizations each year . Recently one of the major issues and concern for governments around the globe were the antimicrobial resistance inside an extensive variety of infectious agents . It is a public wellbeing menace that influences nations and various fields which, in turn, undermine to the achievements of modern medicine . The synthesis and biocide mpacts of novel compounds were severely studied consequently . In recent years, the risk of infection caused by microorganisms is of major concern in clinical, pharmaceutical areas (drugs, medical devices, odontology, hospital surfaces, etc.) and as well as in the food industries (food packaging, storage, fresh products, etc.). About two million peoples were affected by the bacterial infections in hospitals each year and this was reported according to the centers of disease control and prevention, Department of Health and Human Services, USA . Gram-positive organism including Bacillus subtilis and gram negative bacteria including E. coli, were among the top 10 most frequently isolated organisms which produces too many infectitious diseases to the humans, in severe cases lead to death too.
In order to improve the protection against pathogenic bateria it is ncecessary to introduce the new and effective/efficient antibacterial therapeutics and diagnostics which appears to be highly relevant in health care. At an alarming rate, eventhough we have current treatments such as antibiotics which proved as effective against multidrug-resistant bacteria, the pathogens evolved effective mechanisms to counter the biocidal action of antibiotics . The emergence of resistance to conventional antimicrobials necessitates constant development of newer agents, which can inhibit the growth of resistant organisms. The use of substances with antimicrobial properties to treat the infections is known to have been common practice for at least 2000 years and so a large amount of intensive researches was made by various researchers recently leading to the formation of new materials, which would assure permanent bioactive effects together with complete safety for the people [7,8].
A large group of the studies includes the implementation of nanomaterials and nanotechnologies to create new antibacterial agents that increased effectiveness and efficiency [9,10]. Among the numerous materials having the antimicrobial feature, in the present research work, the three materials namely the nanochitosan, sodium alginate and cellulose extracted from the banana fiber can be highlighted. The biopolymeric chitosan N-deacetylated derivative of chitin isolated from shellfish, crab and shrimp has been reported to exhibit numerous health-related beneficial effects, including strong antimicrobial and antioxidative activities. The chitosan biopolymer has been chosen in this work due to its biodegradable, non antigenic, biocompatible, non toxic nature and the ability of transformation into gels, beads, fibers, colloids, films, flakes, powders, capsules [11,12]. The antibacterial activity of chitosan was mainly influenced by bacterial species, concentration, pH, solvent and molecular mass .
Recently, there have been significant scientific interests to scientists for the chemical modifications of chitosan to increase its applications . The modified chitosan have attracted lots of interest especially regarding its bactericidal property against several types of bacteria . Due to high aspect ratio and surface area, the nano-sized composites (nanoparticles, nanomaterials) are expected to be more effective in penetrating and disrupting bacterial cell membranes. Nano-size materials are able to enhance the physical properties of bulk materials . The large surface area and the smaller size of the nanoparticles have interaction with microbes in a broad range and hence the nanochitosan were selected in this study. Alginate is a copolysaccharide extracted from brown algae consisting of D-mannuronic and L-guluronic acid monomers. By the preferential interaction of calcium ions with the G moieties, alginate forms 3-dimensional ionotropic hydrogel resulting in the production of an inhomogeneous gel . Alginate based products were currently found to be the most popular fibrous products utilized in developing antimicrobial agents releasing systems or dressing materials .
Due to its unique colloidal properties such as suspending, thickening, film forming, stabilizing, gel producing, and emulsion stabilizing properties the alginate has a greater potential to form biopolymer film or coating component . Since the alginate gels exhibit bacteriostatic properties against various microorganisms such as Gram-negative Escherichia coli, Gram-positive Staphylococcus aureus etc., the sodium alginate is utilized in film formation in the present study. The lignocellulosics contribute to their diversity in structure and property  and this was due to large number of reactive groups with the wide range of molecular weight, varying chemical composition. The Banana pseudostem has some special properties relating to various phenomena such as antioxidant, permanent staining of cloth and fibers, antimicrobial and antihemorrhagic properties . In recent years the surface modification of fibers, either natural or synthetic, is highly desired [22-24].
During the last few decades, the microcrystalline cellulose extracted from the various lignocellulosic fibers has received much attention and interest due to its excellent properties such as renewability, biodegradability, biocompatibility, nontoxic and high surface area  suitable for antimicrobial behavior. A new class of soluble cellulosegrafted hyperbranched polymers has been synthesized through facile “hypergrafting” reaction using bis(2-chloroethyl) amine and soluble cellulose tosylates by Deniz Demircan and Baozhong Zhang . Results suggested that the obtained natural cellulosic materials can act as effective polymeric biocides, and may have great potential in various antimicrobial material applications. Hence based on the reports suggested by various authors, the microcrystalline cellulose was extracted from banana fiber and studied for its antimicrobial behavior in blended form in this work. This study addresses the ways of obtaining and using the blended form of nanochitosan and sodium alginate with microcrystalline cellulose extracted from the banana fiber in the form of film in 4:16:1 ratio as antimicrobial agents against gram positive bacteria Bacillus subtilis and gram negative bacteria E. coli due to the problem of resistance of many infectious agents to the usual treatments. The results were investigated.
Chemicals such as the sodium alginate, sodium hypochlorite, oxalic acid and sodium hydroxide were purchased from Nice chemicals Pvt Ltd, India and Central Drug House Pvt Ltd, New Delhi. The solvent glacial acetic acid were obtained from Sisco Research Laboratories Pvt Ltd, Mumbai and the crosslinking agents namely sodium tripolyphosphate, CaCl2.2H2O were procured from Finar chemicals Ltd, Ahmedabad, Nice chemicals PvtLtd, India respectively. In addition, the banana fiber was collected from local farms and the chitosan biopolymer (92% deacetylated) was procured from India Sea Foods, Cochin, Kerala. All the chemicals used in the present research work were of analytical grade.
Extraction of microcrystalline cellulose from banana fiber by steam explosion process
As per the procedure reported by Bibin Mathew cherian and his coworkers , the isolation of microcrystalline cellulose from the banana fiber was done using the steam explosion method. The complete extraction of microcrystalline cellulose from banana fiber was done by the combined chemical (acidic) and mechanical treatments. Initially the steam explosion of the chopped lignocellulosic banana fibers (30 g) with 2% NaOH (fiber to liquor ratio 1:10) solution was carried out in anautoclave at a pressure of 20 lb for a period of 1 h. The steamed alkali treated fibers was then bleached using a mixture of acetic acid and sodium hypochlorite solution, further treated with oxalic acid and stirred mechanically well to extract the cellulose completely with different degrees of crystallinity. The photograph of the prepared four stages of fiber was represented in Figure 1.
Preparation of nanochitosan
In the present work, the nanochitosan was synthesized from the chitosan using sodium tripolyphosphate as a crosslinking agent by ionotropic gelation method as per the procedure reported by Govindarajan and his coworkers . Initially in order to create the homogeneous chitosan solution, about 1 g of chitosan dissolved in 200 ml of 2% acetic acid solution was kept under magnetic stirring process for about 20 min. Then to the above prepared chitosan solution, 0.8 g of sodium tripolyphosphate dissolved in 107 ml of conductivity water was added drop wise and stirred well for about 30 min to reach equilibrium. A milky colored emulsion like appearance of chitosan nanoparticles were formed upon the ionic cross linking between the sodium tripolyphosphate and chitosan solution. After reaching equilibrium, the supersaturated solution was decanted and the thick emulsion of nanochitosan settled at the bottom of beaker was poured into the petri plates and it is allowed to dry for few hours. A photograph of the nanochitosan prepared from chitosan was shown in Figure 2.
Preparation of NCS/SA/MC (4:16:1) film
Ternary biopolymeric film was prepared by mixing the nanochitosan, sodium alginate and microcrystalline cellulose extracted from the banana fiber in certain ratio. Three solutions were prepared: (i) an aqueous 5% nanochitosan solution; (ii) aqueous 20 wt% alginate solution and (iii) aqueous 1.25 wt% micro-crystalline cellulose solution. An emulsion was formed by blending above prepared solutions at 500 rpm for about 30 min. After this process is over the above prepared emulsion was fabricated evenly onto the petri plates, allowed to dry for few hours and these dried films were then soaked in a 0.2 M calcium chloride solution for about 3 hours. Finally the NCS/SA/MC films were rinsed with double distilled water to remove any excess CaCl2 on the film and dried for 24 hours. A photograph of the prepared NCS/SA/ MC film was shown in Figure 3.
Fourier transform infra red spectroscopy studies
The Perkin Elmer 200 FTIR spectrophotometer instrument was utilized in recording the FT-IR spectrum of the prepared samples in the wave number range from 4000 cm-1 to 450 cm-1 during 64 scans, with 2 cm-1 resolution.
X-Ray diffraction studies
The X-ray diffraction patterns of NCS/SA/MC film was measured using X-ray powder diffractometer (XRD- SHIMADUZ XD-D1) with Ni filter Cu Kα radiation source (λ=0.154 nm), set at scan rate=10°/ min, using a voltage of 40 kv and a current of 30 mA.
Thermogravimetric analysis of the prepared samples was performed using SDT Q600 V8.0 Build 95 instrument. The range of temperature used is between 30°C to 750°C with a heating rate of 10°C/min under nitrogen atmosphere.
Differential scanning calorimetric analysis
The DSC studies of the prepared samples were carried out using DSC Q10 V 9.0 Build 275 instrument in the temperature range between 30°C to 350°C with the heating rate of 10°C/min.
Scanning electron microscopic studies
The surface morphology of the prepared samples was examined with the Scanning Electron Microscope (Zeiss EVO 40). The photographs of the various cross sectional morphologies of the NCS/SA/MC film samples were taken at different magnifications.
Two bacterial strains namely Bacillus subtilis - gram positive bacteria and Escherichia coli-gram negative bacteria were utilized to investigate the antibacterial activity of the NCS/SA/MC film by diffusion method using Muller Hinton Agar (MHA) medium. The microorganisms Escherichia coli and Bascillus subtilis were inoculated initially on Muller Hinton Agar (MHA) medium and spread uniformly using sterile spreader in Petri plates. After solidification of the MHA medium, a small amount of the NCS/SA/MC film prepared in 4:16:1 ratio were then placed on different cultured agar plates and the plates were incubated on individual racks for 24 h at 37°C. The evaluation of the antibacterial activities of the prepared samples was done by measuring the diameter of zone of inhibition grown around the samples against the test microorganisms using the ruler.
FT-IR spectral analysis
Fourier transform infrared spectroscopic (FTIR) analysis mainly provides information about the functional properties which correlate functional group and structure of composite blended film .
The FT-IR spectral details of chitosan and nanochitosan was represented in Table 1 and Figure 4. The FT-IR spectral details of pure chitosan (Figure 4a) showed that the hydroxyl (OH) peaks can be assigned at 3454.75 cm-1 and alkyl C–H stretching vibration were identified as doublets at 2923.08/2830.05 cm-1 respectively [30,31]. Strong peaks observed at 1628.87 cm-1, 1540.02 cm-1 and 1421.52 cm-1 showing the presence of C=O stretching (amide-I band) , N-H bending and C-H deformation respectively.
|Responsible groups||Chitosan Waven umbers (cm-1)||Nanochitosan Wave numbers (cm-1)|
|OH stretching and NH stretching||3454.75||3385.92|
|Aliphatic CH stretching in CH2||2923.08||2920.57|
|C=O in 2° Amide||1628.87||1635.20|
Table 1: FT-IR spectral details of chitosan and nanochitosan.
Figure 4b represents the FT-IR spectral details of nanochitosan prepared from the chitosan using ionotropic gelation method. The absorption band obtained at 3385.92 cm-1 attributed to –NH group in chitosan was broadened by the physical interactions with TPP . Strong peaks obtained at 2920.57 cm-1, 2908.57 cm-1, 1635.23 cm- 1, 1510.05 cm-1, 1376.80 cm-1 and 1219.00 cm-1 indicate the presence of asymmetrical and symmetrical stretching in CH2 group, NH3+ stretching, C=O stretching in amides, NH bending, OH in plane bending in alcohols and P=O stretching . The peak obtained at 1163.38 cm−1 indicated the overlapping peak of C–O stretching in polysaccharide and formation of chitosan nanoparticles due to the interaction of ammonium ion and phosphate ion in chitosan nanoparticle molecules .
When compared to pure chitosan, the nanochitosan obtained by ionotropic gelation method showed different bands. The shift of the peak observed at 3454.75 cm-1 corresponding to the presence of NH, OH stretching in chitosan to lower wavenumber (3385.92 cm- 1) in nanochitosan sample indicate that crosslinking had taken place effectively between the sodium tripolyphosphate and the chitosan. This observed results showed that the amide group and NH2 group of chitosan are both slightly crosslinked with a TPP molecule. Also in addition to this, in case of nanochitosan the appearance of some new peaks (1210.00 cm-1 due to P=O stretching) proves the formation of nanoparticles from the chitosan by ionotropic gelation method.
The nanochitosan/sodium alginate/microcrystalline cellulose (4:16:1) ternary film thus prepared were characterized by FTIR spectral studies. Table 2 and Figure 5 represent the FT-IR spectral details of NCS/SA/MC film prepared in 4:16:1 ratio.
|Wave number (cm-1)||Responsible Groups|
|3334.92||O-H stretching in alcohols (Intermolecular H bonded)|
|3275.13||N-H stretching in amines|
|2924.09||Asymmetrical CH stretching in CH2 group|
|1612.49||C=O stretchingin carboxylate ion|
|1423.47||Weak band due to carboxylate ion group|
Table 2: FT-IR spectral details of NCS/SA/MC film.
The FTIR spectrum of NCS/SA/MC film (Figure 5) shows a broad adsorption band at 3583.74 – 3275.13 cm-1 corresponding to the overlapping of –OH stretching and –NH stretching bands . The appearance of peak at 2924.09 cm-1 indicates the presence of aliphatic asymmetrical C-H stretching in methylenic group respectively . The prominent peaks observed at various wave numbers such as 2854.65 cm-1 , 1612.49 cm-1, 1423.47 cm-1, 1153.43 cm-1, 1033.85 cm- 1, 893.04 cm-1 and 821.68 cm-1 was attributed toNH3 + stretching, carbonyl stretching in carboxylate ion, weak band due to carboxylate ion, P=O stretching , C-O-C linkage, C-C stretching and NH wagging respectively.
On comparing the FT-IR spectral details of NCS/SA/MC film with nanochitosan it was observed that after the reaction of nanochitosan with alginate and microcrystalline cellulose in ternary NCS/SA/MC film, the stretching vibration of -OH and -NH2 observed at 3385.92 cm-1 in nanochitosan was shifted to 3334.92 cm-1 and becomes broad , the asymmetrical stretching of NH3+ groups was shifted from 2908.57 cm-1 to 2854.65 cm-1 cm-1 and also a new peak was appeared at 1612.49 cm-1 corresponding to the presence of C=O stretching in carboxylate ion. These observed shifts in the frequencies and the appearance of new peak confirms that the nanochitosan and sodium alginate were effectively binded with the cellulose extracted from banana fiber in the prepared film.
X-ray diffraction studies (XRD)
XRD analysis helps in describing the physical properties of samples in terms of crystalline structure and in addition it also assesses the compatibility of each component material present in the blended films . Table 3, Figure 6a and 6b shows the X-ray diffractogram details and patterns of pure chitosan and nanochitosan.
|Sample||2q values||Degree ofcrystallinity(%)|
|Nanochitosan||28˚ (broad 20˚- 40˚)||4.64|
Table 3: XRD details of chitosan and nanochitosan.
The X-ray diffractogram of chitosan (Figure 6a) had a semi crystalline nature with two main diffraction peaks at around 2θ=10° and 20°. The semi crystalline nature of pure chitosan was confirmed from the appearance of the diffraction peak centered at diffraction angle 2θ-10° and sharp diffraction peak at 20° which are indicative of high degree of crystalline morphology . The chitosan molecule easily form the crystalline regions and this may be due to the presence of plenty of -OH and -NH2 groups in the chitosan structure, which could form stronger inter and intramolecular hydrogen bonds .
The X-ray diffraction pattern of nanochitosan obtained using ionic gelation technique is shown in Figure 6b. The X ray diffractogram of nanochitosan shows a broad peak at around 2=28°. The broadening of the peaks is due to the deformation of the crystalline regions by the increased packing of chitosan chains by ionic crosslinking . The structure of chitosan molecules has certain regularity and as a result of this the chitosan molecules could form crystalline regions very easily but after crosslinking with tripolyphosphate it shows a decrease in crystallinity of chitosan. This could be attributed due to the deformation of the hydrogen bond in original chitosan by the substitution of hydroxyl and amino groups , which efficiently destroyed the regularity of the packing of the original chitosan chains resulting in the formation of amorphous nanochitosan.
From the nature of the broad peak obtained it was concluded that nanochitosan was found to be more amorphous than the pure chitosan. The comparison of XRD results of nanochitosan with pure chitosan reveals that there was a significant shift in the diffraction pattern with a broad amorphous peak in nanochitosan and the obtained results indicated that there was an effective crosslinking, molecular miscibility and also certain interaction takes place between the chitosan with the ionic crosslinking agent. The X-ray diffractogram details of NCS/SA/ MC film prepared in 4:16:1 ratio was represented in Figure 7 and Table 4.
|Sample||2q values||Degree ofcrystallinity(%)|
|NCS/SA/MC film (4:16:1)||14.963˚, 30.098˚, 87.103˚||4.44|
Table 4: XRD details of NCS/SA/MC film.
The X- ray diffractogram details of NCS/SA/MC film (Figure 7) shows peaks at various 2θ values such as 14.963°, 30.098° and 87.103°. Due to the dispersion of the polymer matrix in the NCS/ SA/MC film, certain changes in the degree of crystallinity have been occurred. The less intense peak and less crystalline entity (broad nature-more amorphous) obtained in NCS/SA/MC film might be due to the destruction of the packing of the polymers by the strong interaction which occurred between the nanochitosan, sodium alginate and microcrystalline cellulose polymers . On comparing the XRD details of NCS/SA/MC film with chitosan and nanochitosan, it was observed that the calculated lower degree of crystallinity values suggests that the prepared NCS/SA/MC film has highly amorphous nature suitable for a variety of applications.
Thermogravimetric analysis (TGA)
Thermogravimetric analysis (TGA) is a method of thermal analysis in which changes in physical and chemical properties of materials were measured as a function of increasing temperature (with constant heating rate) or as a function of time . The TGA thermogram details of chitosan was represented in Figure 8.
The TGA thermogram of chitosan presented in Figure 8 shows mainly two major weight losses one before 200° C and another after 270°C in polymer mass. The first one is due to the elimination of water molecules bound to the two polar groups in chitosan and the second one is due to the dehydration of saccharide rings, depolymerisation and decomposition of volatile products . Maximum weight loss occurs at the temperature range of 217°C – 450°C and the residual temperature was found to be 850°C. At the end of the experiment around 69.933% of the chitosan gets disintegrated within 840°C leaving behind 30.067% of the sample as residue showing higher thermal stability.
The TGA thermogram details of nanochitosan (Figure 9) indicate that the first thermal event occurs at temperature range 50-150°C and is accompanied by the weight loss ranging from 8% to 10% which may be due to the loss of residual water present in the sample. The maximum weight loss occuring in nanochitosan after 150°C may be due to the decomposition of polymer matrix . At the end of the experiment nearly 45.63% of the sample remained as residue showing the higher thermal stability of nanochitosan. The increased thermal stability indicates the formation of stronger and stiffer hydrogel network as a result of crosslinking.
Figure 1 shows the TGA thermo gram details of NCS/SA/MC film prepared in 4:16:1 ratio. The TGA curve shows that the weight loss occurs mainly in two stages. The first stage weight loss was mainly due to loss of water because the polysaccharides usually have strong affinity of water and hence may be easily hydrated . The second stage weight loss corresponds to the thermal decomposition of main chain of nanochitosan, sodium alginate and microcrystalline cellulose, vaporization and elimination of volatile product. From Figure 7, it was evident that around 65% of the sample gets disintegrated in the temperature range of 400°C and the linear shallow decrease in weight was observed in the temperature range of 250-400°C. The residual temperature of the sample was found to be 750°C and the amount of sample remained as a residue at the end of the experiment was observed to be 21.11%. The obtained higher amount of residue indicates the highly stable thermal behavior. The comparison of TGA thermogram details of NCS/SA/MC film with pure chitosan and nanochitosan indicate that the NCS/SA/MC film was also found to be thermally more stable and this was confirmed from the observed higher decxomposition termperature and the higher amount of residue remained at the end of the experiment.
Differential scanning calorimtery (DSC) studies
Differential scanning calorimetry (DSC) monitors heat effects associated with phase transitions and chemical reactions as a function of temperature. The DSC thermogram of pure chitosan was shown in Figure 8.
In Figure 8, the broad endothermic peak obtained at 89.04°C and a sharp exothermic peak at 312.26°C showing the crystallization and the melting process of polymer at different temperatures. A wide endothermic peak obtained at 89.04°C is attributed to the elimination of absorbed water and a sharp exothermic peak at 312.26°C is due to the decomposition of chitosan chains . The glass transition temperature of the polymer is observed at 203°C and an exothermic peak obtained at 313.26°C indicating that certain chemical changes had taken place in this temperature range.
The DSC thermogram details of nanochitosan prepared from chitosan by utilizing the ionotropic gelation method was shown in Figure 9. A broad enothermic peak obtained below 80°C is due to the removal of absorbed water and a sharp endothermic peak at 217°C is associated with the breakage of chitosan phosphoric acid cross linkage. The glass transition temperature of the nanochitosan was found to be 205°C and the higher value of glass transition temperature is due to the presence of crosslinking agent .
Figure 10 represents the DSC thermo gram details of NCS/SA/ MC film prepared in 4:16:1 ratio. Two broad endothermic peaks were observed in the temperature range of 80-100°C and 210-260°C. The glass transistion temperature was found to be 145°C. The observation of a single glass transition in the DSC heating curves indicates that nanochitosan, sodium alginate and microcrystalline cellulose are highly compatible. The higher onset temperatures are associated with higher thermal stability . From the obtained higher onset temperature and higher value of glass transition temperature, it was concluded that the NCS/SA/MC film prepared in 4:16:1 ratio was also found to be highly thermally stable.
Scanning electron microscopic (SEM) studies
The scanning electron microscopy (SEM) gives information about the topography, surfaces, structures, morphologies, and forms of materials and composition of the studied material . The SEM micrograph details of the pure chitosan and nanaochitosan was represented in Figures 11 and 12.
The SEM micrograph obtained for the pure chitosan (Figure 11) revealed that the texture is plain without pores having smooth, compact and homogeneous even surface structure with no gross effects .
The SEM micrograph of nanochitosan (Figure 12) revealed the rough surface morphology. The SEM picture of nanochitosan demonstrates the good dispersion of the nanoparticles which are entangled one on the other with a larger exposed surface making the material very suitable for adsorption. Several authors reported that the nanochitosan prepared from chitosan was found to be having the spherical shape , whereas the obtained image reveals that the formation of nanoparticles is not spherical shaped but they are in the rod shaped structure which is a peculiar structure. On comparing the SEM micrograph details of nanochitosan with pure chitosan it was observed that the nanochitosan has relatively rougher surface with uneven structure which exhibited highly amorphous feature.
The surface and cross-sectional morphology of the NCS/SA/MC film prepared in 4:16:1 ratio was shown in Figure 13. The scanning electron micrograph of NCS/SA/MC film prepared in 4:16:1 ratio (Figure 13) shows that the cellulose and nanochitosan were coated uniformly with alginate and also it dispersed in the alginate matrix effectively resulting in a very good rough texture and the interfacial adhesion was evidenced between nanochitosan, sodium alginate and microcrystalline cellulose extracted from the banana fiber. The NCS/ SA/MC film prepared in 4:16:1 ratio showed dense structure at lower magnification and some porosity was detected, although these pores were seen to be closed.
The bioefficacy of the NCS/SA/MC films prepared in 4:16:1 ratio were tested against bacterial strains such as Bascillus subtilis a Gram positive model bacterium and E. coli a Gram negative model bacterium. The zone of inhibition values of the prepared ternary polymeric film against the growth of selected bacteria are given in Table 5 and Figure 14a and 14b. The antibacterial activities of the prepared ternary polymeric NCS/SA/MC film samples prepared in various ratios are predicted from the diameter of zone of inhibhition values measured in mm.
|Organism (Bacteria)||Diameter of zone of Inhibition (mm)|
|NCS/SA/MC film(4:16:1)||Control Ciproflaxicin|
|Bascillus subtilis||15||17.0 ± 0.6|
|E. coli||14||15.4 ± 0.6|
Table 5: Antibacterial activity details of NCS/SA/MC film.
Cationic polyelectrolytes, as well as other molecules with a net positive charge are capable of killing microorganisms . Chitosan is a polycationic material composed of N-acetyl glucosamine and glucosamine units which has antibacterial activity against both gram positive and gram negative bacterial species . The disruption of microbial cell wall by the binding of cationic sites of chitosan to anionic surfaces mainly leads to the cell death .
In recent years, various biological activities of chitosan nanoparticles including immunoenhancing effects , antitumoral, antifungal, and antimicrobial activities  have been reported. The chitosan nanoparticles are successfully being exploited as antimicrobial agents. LiFeng Qi and his coworkers  reported that the nanochitosan exhibited higher antibacterial activity than chitosan itself. Based on the special character of the nanoparticles, the chitosan nanoparticles exhibit higher antibacterial activity than chitosan. The chitosan nanoparticles could be well distributed in bacterial suspension after a slight shock for a nice dispersion and hence the bacteria can adhere to the surface of nanochitosan significantly in short time and thus nanochitosan exhibit antibacterial activity.
The target site of the polycation is the negatively charged surface of the bacterial cell. The polycationic nanochitosan with higher surface charge density interact with the bacteria to a greater degree than chitosan itself. The negatively charged surface of the bacterial cell wall interacts effectively to a greater degree with the polycationic nanochitosan (NH3+) and hinders the growth of the microorganism . Chitosan nano-particles provide higher affinity with bacteria cells for a quantum-size effect, due to the larger surface area of the chitosan nanoparticles, which could be tightly adsorbed onto the surface of the bacteria cells to disrupt the membrane, which would lead to the leakage of intracellular components, thus killing the bacteria cells [61,62].
The potential of chitosan nanoparticles of different sizes evaluated against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) by Aakriti Tyagi and her coworkers concludes that the size heterogeneity of chitosan nanoparticles exhibit potent bacteriocidal activity but does not show cytotoxicity on mammalian cells .
In addition to this it is also identified that the sodium alginate and cellulosic fibers has higher antibacterial activity. Cellulose fibres were found be an ideal matrix for the design of bioactive, biocompatible, and intelligent materials  due to their molecular structure and a large active surface area. Hence based on the reports the NCS/SA/ MC mixture was prepared in the form of film in 4:16:1 ratio and it was tested for the antibacterial activity against two model bacteria namely Bascillus subtilis and E. coli. From the observed higher zone of inhibhition values of NCS/SA/MC film presented in Table 5 and Figures 15-17, it was identified that NCS/SA/MC film prepared in 4:16:1 ratio have higher antibacterial activity towards both Bascillus Subtilis and E. coli. When compared to the gram negative bacteria (E. coli), the NCS/SA/MC film exhibits higher antibacterial activity against Gram-positive bacteria (Bacillus subtilis) and this was due to their different cell walls. In case of gram positive bacterium, the cell wall is fully composed of peptide polyglycogen and since the peptidoglycan layer is composed of networks with plenty of pores it allows the foreign molecules to come into the cell without difficulty. But in case of gramnegative bacterium, since the cell wall is made up of a thin membrane of peptide polyglycogen and an outer membrane constituted of lipopolysaccharide, lipoprotein and phospholipids which is a bilayer, it acts as a potential barrier against foreign molecules to enter into cell wall [65-68].
According to the standard antibacterial test “SNV 195920-1992”, specimens showing more than 1 mm microbial zone inhibition can be considered as good antibacterial agents . In the present study since the NCS/SA/MC film prepared in all ratios shows the inhibitory zone greater than 1 mm it was concluded that NCS/SA/MC film prepared in 4:16:1 ratio acts as good antibacterial agent and effective in killing the microbes.
The strong interaction had taken place effectively between the molecular chains of nanochitosan, sodium alginate and microcrystalline cellulose which may lead to the miscibility at specific ratios of the three components. From FT-IR results it was evident that, in the prepared ternary NCS/SA/MC film, the peaks were observed due to the various functional groups (OH, COO-, NH) present in three added polymeric components. The XRD studies elucidate the highly amorphous nature of the NCS/SA/MC film. The TGA and DSC studies clearly indicate that the prepared film was found to be highly thermally stable and the rough surface morphology was identified from the SEM studies. The results of this study showed the potent anti-microbial effect of NCS/ SA/MC film against Bacillus subtilis and E. coli and hence the NCS/SA/ MC film can be used for future application in antimicrobial therapy.
The authors are thankful to D.K.M College for Women, Vellore, VIT University, Vellore for providing research facilities, co- operation and constant encouragement to carry out the work.