Abdul Wahab Jatoi

Silver coated anionic cellulose nanofiber composites for an efficient antimicrobial activity.

Herein, we report a comparative study of silver coated anionic cellulose nanocomposite before (CMC-Ag) and after (AgNPs/CMC) chemical reduction for antibacterial activity. Cellulose nanofibers were prepared by deacetylation of electrospun cellulose acetate nanofibers, which were then treated with sodium chloroacetate to prepare anionic cellulose nanofibers (CMC). Aqueous AgNO3 solution with different concentrations was employed to produce nanofiber composites. To obtain AgNPs/CMC, the resultant Ag/CMC nanofibers were chemically reduced with NaBH4. The nanocomposites were characterized by FE-SEM, FTIR, XPS and SEM-EDS. Antimicrobiality tests were conducted using S. aureus and Escherichia coli bacteria following standard test method JIS L1902, 2008. The EDS results confirmed higher silver content in CMC-Ag nanofibers than AgNPs/CMC nanofibers. The antimicrobial test and EDS results demonstrated higher silver release (larger halo width) by the former in comparison to later which confers better antimicrobiality by CMC-Ag nanofibers.

Ultrasonic dyeing of cellulose nanofibers.

Textile dyeing assisted by ultrasonic energy has attained a greater interest in recent years. We report ultrasonic dyeing of nanofibers for the very first time. We chose cellulose nanofibers and dyed with two reactive dyes, CI reactive black 5 and CI reactive red 195. The cellulose nanofibers were prepared by electrospinning of cellulose acetate (CA) followed by deacetylation. The FTIR results confirmed complete conversion of CA into cellulose nanofibers. Dyeing parameters optimized were dyeing temperature, dyeing time and dye concentrations for each class of the dye used. Results revealed that the ultrasonic dyeing produced higher color yield (K/S values) than the conventional dyeing. The color fastness test results depicted good dye fixation. SEM analysis evidenced that ultrasonic energy during dyeing do not affect surface morphology of nanofibers. The results conclude successful dyeing of cellulose nanofibers using ultrasonic energy with better color yield and color fastness results than conventional dyeing.

Ultrasonic-assisted deacetylation of cellulose acetate nanofibers: A rapid method to produce cellulose nanofibers.

Herein we report a rapid method for deacetylation of cellulose acetate (CA) nanofibers in order to produce cellulose nanofibers using ultrasonic energy. The CA nanofibers were fabricated via electrospinning thereby treated with NaOH and NaOH/EtOH solutions at various pH levels for 30, 60 and 90min assisted by ultrasonic energy. The nanofiber webs were optimized by degree of deacetylation (DD%) and wicking behavior. The resultant nanofibers were further characterized by FTIR, SEM, WAXD, DSC analysis. The DD% and FTIR results confirmed a complete conversion of CA nanofibers to cellulose nanofibers within 1h with substantial increase of wicking height. Nanofibers morphology under SEM showed slightly swelling and no damage of nanofibers observed by use of ultrasonic energy. The results of ultrasonic-assisted deacetylation are comparable with the conventional deacetylation. Our rapid method offers substantially reduced deacetylation time from 30h to just 1h, thanks to the ultrasonic energy.

Antibacterial efficacy of poly(vinyl alcohol) composite nanofibers embedded with silver-anchored silica nanoparticles

Silver has been widely used as an effective antibacterial agent especially for treating burns and wounds. However, release of silver from materials often arouse side effects due to toxicity of silver towards mammalian cells. Argyria and argyrosis are well known problems of acute toxicity of silver towards human body. Immobilization of silver is an effective approach to reduce silver release. Herein, we present poly(vinyl alcohol) (PVA) composite nanofibers embedded with silver-anchored silica nanoparticles (SSNs) as a novel antibacterial material. Silver nanoparticles anchored on silica nanoparticles were prepared and incorporated into PVA nanofibers to fabricate silver-silica embedded PVA nanofibers (SSN-PVA) by electrospinning. Incorporation of SSNs into PVA was confirmed by TEM and SEM results revealed regular nanofibers whose diameter increased with successive addition of SSNs. The SSN-PVA nanofibers showed significant antibacterial efficacy against both Gram-negative and Gram-positive bacteria. Our research results demonstrated SSN-embedded polymeric nanofibers can open up a promising prospect for the prevention of bacterial infection in diverse biomedical fields including wound dressing.

Ultrasonic-assisted dyeing of Nylon-6 nanofibers

We first time report ultrasonic dyeing of the Nylon 6 nanofibers with two disperse dyes CI Disperse blue 56 and CI Disperse Red 167:1 by utilising ultrasonic energy during dyeing process. The Nylon 6 nanofibers were fabricated via electrospinning and dyed via batchwise method with and without sonication. Results revealed that ultrasonic dyeing produce higher color yield (K/S values) and substantially reduces dyeing time from 60min for conventional dyeing to 30min can be attributed to breakage of dye aggregate, transient cavitation near nanofiber surface and mass transfer within/between nanofibers. Color fastness results exhibited good to very good dye fixation. SEM images exhibit insignificant effect of sonication on morphology of the nanofibers. Our research results demonstrate ultrasonic dyeing as a better dyeing technique for Nylon 6 nanofibers with higher color yield and substantially reduced dyeing time.

Fabrication of silk fibroin based three dimensional scaffolds for tissue engineering

Herein we report successful synthesis of silk fibroin (SF) three dimensional scaffolds (SF 3D-scaffold) from SF sponge and SF nanofibers. Both the nanofibers and sponge were prepared from Bombyx mori fibroin. The SF 3D-scaffold was prepared by electrospinning the fibroin nanofibers over the sponge. Surface morphology was determined by scanning electron microscopy (SEM), while nanofiber diameter and pore size were measured using imageJ software. Effect of spinning time on the pore size and cell adhesion was determined. Average diameter of the SF nanofibers was measured to be 320 nm and pore size was found to reduce with increasing spinning time, such that, for 1 h spinning time pore size was 231 µm and the same for 3.5 h was 4.1 µm. However, the number of pores increased with spinning time. The results confirmed adhesion of MC3T3-E1 cells on the SF sponge, SF nanofibers and SF three dimensional scaffolds. Higher cell adhesion was found on the three dimensional scaffold in comparison to the nanofibers and sponge, possibly due to highly porous structure with very small and numerous pores in the resultant composite; hence more cell adhesion sites. The cell adhesion result confirmed biocompatibility of the SF 3D-scaffold and hence its suitability for applications in tissue engineering.

Deodorant activity of phthalocyanine complex nanofiber

Unpleasant odor is a problem in the modern lifestyle. In order to prevent malodor, we fabricated phthalocyanine combined with nanofibers to prevent unpleasant odor for the first time. Cu-coordinated phthalocyanine was used as an odor preventing agent and methyl mercaptan gas was selected as a model malodorant. This study was conducted with two different polymers, poly(vinyl alcohol) (PVA) and silk. A total of 4 wt% of phthalocyanine was incorporated in the solutions of both polymers, resulting in the successful fabrication of nanofibers. It is notable that the deodorant activity test clearly showed a reduction of methyl mercaptan gas in both phthalocyanine incorporated PVA and silk nanofibers. In addition, the phthalocyanine/silk nanofibers exhibited better deodorant performance in comparison to the phthalocyanine/PVA nanofiber.

Sonication induced effective approach for coloration of compact polyacrylonitrile (PAN) nanofibers

We present our research on dyeability of polyacrylonitrile (PAN) nanofibers following ultrasonic dyeing method. Although PAN has been extensively utilized in textile apparel, sportswear, upholstery and home furnishing, however, coloration of PAN nanofibers has not yet been reported. PAN is a compact fiber while the nanofiber structure makes it more difficult to color PAN nanofibers. PAN is generally dyed with basic dyes and dyeing is carried out in acidic conditions, while the dyeing process takes about two hours at boiling temperature. A systematic study on dyeability of PAN nanofibers will extend its use in textile apparel industry. Thus, we used ultrasonic energy and first time conducted our research on dyeability of electrospun PAN nanofibers using disperse dyes. Dyeing process parameters such as dyeing time, temperatures and concentrations of dyes were optimized. Ultrasonic dyeing of PAN nanofibers was compared with its conventional dyeing as well. Affect of ultrasonic dyeing on the morphology, chemical state, crystallographic structure and mechanical strength of PAN nanofibers has been studied. PAN nanofiber samples were characterized by SEM, FTIR, XRD and tensile strength tests. The results revealed 80 °C and 60 min as optimum temperature and time for ultrasonic dyeing of PAN nanofibers. The ultrasonic dyeing does not affect morphology, chemical and crystalline structure of the PAN nanofibers while it improves their mechanical strength. Our research suggests dyeability of PAN nanofibers with disperse dyes by ultrasonic method and their subsequent use in textile apparels.