Synthesis and Characterization of Florfenicol-silver Nanocomposite and its Antibacterial Activity against some Gram Positive and Gram-negative Bacteria

In this paper, easy, rapid and cheap synthetic method was described for florfenicol-silver nanocomposite by sonochemical method. Florfenicol-silver nanocomposite was characterized based on three classes namely index, identification and morphology class. Index characterization was carried out by zeta sizing, BET surface area and zeta potential. Identification characterization was performed using X-ray diffraction (XRD) and Raman spectrometry. Morphology characterization was done utilizing transmission electron microscope (TEM), scanning electron microscope (SEM) and atomic force microscope (AFM). Characterization results showed zeta sizing of florfenicol was 30.44nm, while florfenicol-silver nanocomposite was 33.5 nm with zeta potential -14.1 and -18, respectively. BET surface area was found to be 13.3, 73.2 and 103.69 m2/g for florfenicol, silver nanoparticles and florfenicol-silver nanocomposite respectively. XRD and Raman charts confirmed the formation of florfenicol-silver nanocomposite without any contamination. TEM, SEM and AFM spectral data illustrated spherical to sub spherical shape of silver nanoparticles on cubic to sheet shape of florfenicol with size less than 50 nm. Antimicrobial activity was screened where the average zone of inhibitions caused by the prepared nanocomposite were 28.3 mm, 24 mm, 27.3 mm and 24 mm compared to 17.7 mm, 16 mm, 18.7 mm and 13.3 mm of the native drug and 13 mm, 10 mm, 14.3 mm and 15 mm of the used positive reference standards against E. coli, Salmonella typhymurium, Staphylococcus aureus and Staph.aureus MRSA respectively.

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 97
Author(s):  
Suresh V. Chinni ◽  
Subash C. B. Gopinath ◽  
Periasamy Anbu ◽  
Neeraj Kumar Fuloria ◽  
Shivkanya Fuloria ◽  
...  

The present study was planned to characterize and analyze the antimicrobial activity of silver nanoparticles (AgNP) biosynthesized using a Coccinia indica leaf (CIL) ethanolic extract. The present study included the preparation of CIL ethanolic extract using the maceration process, which was further used for AgNP biosynthesis by silver nitrate reduction. Biosynthetic AgNPs were characterized using UV–Visible spectrometry, zeta potential analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), and energy-dispersive X-ray (EDX) spectrometry. The biogenic AgNP and CIL extracts were further investigated against different bacterial strains for their antimicrobial activity. The surface plasmon resonance (SPR) signal at 425 nm confirmed AgNP formation. The SEM and TEM data revealed the spherical shape of biogenic AgNPs and size in the range of 8 to 48 nm. The EDX results verified the presence of Ag. The AgNPs displayed a zeta potential of −55.46 mV, suggesting mild AgNP stability. Compared to Gram-positive bacteria, the biogenic AgNPs demonstrated high antibacterial potential against Gram-negative bacteria. Based on the results, the current study concluded that AgNPs based on CIL extract have strong antibacterial potential, and it established that AgNP biosynthesis using CIL ethanol extract is an effective process.


2018 ◽  
Vol 78 (12) ◽  
pp. 2500-2510 ◽  
Author(s):  
Henry H. Mungondori ◽  
Spencer Ramujana ◽  
David M. Katwire ◽  
Raymond T. Taziwa

AbstractThis work investigates the preparation of a magnetically recoverable photocatalytic nanocomposite of maghemite nanoparticles coated with silica and carbon doped titanium dioxide. The novel nanocomposite boasts the advantages of efficient photocatalytic degradation of organic pollutants in water and ease of recovery of the fine particles after water treatment. The photocatalytic nanocomposite was successfully synthesized through a stepwise approach via co-precipitation and sol-gel methods. Characterisation by Fourier transform infrared (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) substantiated the existence of the intended structure of the nanocomposite and the particles were found to be in the size range of 15–22 nm with a quasi-spherical shape. Brunauer–Emmett–Teller (BET) surface area analysis revealed an average surface area of 55.20 m2/g, which is higher than that of commercial TiO2 (Degussa P25, 50.00 m2/g), and an average pore diameter of 8.36 nm. A 5 ppm methylene blue solution was degraded with an efficiency of 96.8% after 3 h of solar irradiation, which was 19.7% greater than using the same photo-catalyst under strict UV light irradiation. Photo-catalysis using these nanoparticles was observed to be very effective. The prepared novel visible light active nanocomposite has great potential for incorporation into water treatment systems because it exhibits good stability and magnetism, as well as high photocatalytic efficiency.


2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Huan-qin Wang ◽  
Ming-bo Zheng ◽  
Jin-hua Chen ◽  
Guang-bin Ji ◽  
Jie-ming Cao

HierarchicalMnO2microfibers were prepared by using cotton as the template andKMnO4as the precursor via an ultrasonic assistance route. The results of scanning electron microscope characterization showed that the concentration ofKMnO4had a significant effect on the morphology ofMnO2microfiber. At low concentration ofKMnO4, the microfiber was composed ofMnO2nanorods with single crystal structure. With increasing the concentration ofKMnO4, the secondary nanostructure ofMnO2microfibers had a transformation from nanorod to nanoparticle. The results ofN2adsorption-desorption analysis indicated thatMnO2microfibers had BET surface area of about 25 m2/g. This synthesis provides a new way to control the secondary nanostructure ofMnO2microfiber by adjusting the concentration of precursor. Furthermore, the mechanism for the replication was proposed and discussed.


2021 ◽  
Vol 16 (12) ◽  
pp. 72-79
Author(s):  
A.K. Keshari ◽  
S. Saxena ◽  
G. Pal ◽  
V. Srivashtav ◽  
R. Srivastav

A green rapid biogenic synthesis of silver nanoparticles (AgNPs) using Catharanthus roseus leaf extract was performed. Synthesized nanoparticles were characterized using UV-Visible, Fourier transform infra-red (FTIR) and X-ray diffraction (XRD). The reduction of silver ions to AgNPs using C. roseus extract was completed within 240 mins. The formation of AgNPs was confirmed by Surface Plasmon Resonance (SPR) at 442 nm using UV-Vis Spectrophotometer and it is characterized by XRD, Transmission electron microscope (TEM) and Scanning electron microscope (SEM). The morphological studies revealed the spherical shape of the particles with sizes ranging from 16-35 nm and Energy dispersive X-ray (EDX) spectrum confirmed the presence of silver along with other elements in the plants metabolite. The extracellular AgNPs synthesis by aqueous leaf extract demonstrates ultra-fast, simple and inexpensive method comparable to other methods. The antioxidant assay of the synthesized AgNPs indicated that they have a strong antioxidant property as compared to the control. Since these compounds are also safe to use and discharged into the environment, the green AgNPs could be considered as an innovative alternative approach for biomedical and nanoscience based industries.


Nanoscale ◽  
2020 ◽  
Vol 12 (41) ◽  
pp. 21344-21358
Author(s):  
Hajo Frerichs ◽  
Eva Pütz ◽  
Felix Pfitzner ◽  
Tobias Reich ◽  
Athanasios Gazanis ◽  
...  

Ce1−xBixO2−δ is an active halogenation catalyst with maximum activity for x ≈ 0.2 due to the effects of zeta-potential and BET surface area. Ce1−xBixO2−δ/polyethersulfone nanocomposites block bacterial biofilm formation of Gram-negative bacteria.


2016 ◽  
Vol 18 (7) ◽  
pp. 2129-2146 ◽  
Author(s):  
Aye Aye Myint ◽  
Hun Wook Lee ◽  
Bumjoon Seo ◽  
Won-Su Son ◽  
Junho Yoon ◽  
...  

Lignin nanoparticles of uniform, small quasi-spherical shape with a relatively high BET surface area (nearly 92 m2 g−1) were synthesized using a facile, one pot technology of a compressed CO2 antisolvent.


2021 ◽  
Vol 10 (4) ◽  
pp. 2646-2654

Green synthesis of silver nanoparticles (Ag NPs) was performed using flower extract of Hemigraphis colorata (H. Colorata). Synthesized nanoparticles were characterized by UV-Visible Spectrophotometer (UV-Vis), Fourier Transform Infrared (FT-IR), Scanning Electron Microscope (SEM), and Transmission Electron Microscope (TEM-SAED). , The crystalline nature of the sample was examined by an X-ray diffraction study (XRD). The UV-Visible spectrum showed surface plasma resonance (SPR) at 360 nm revealed the formation of nanoparticles, SEM and TEM exhibited spherical shape particles with an average size between 10-20 nm. The valuation of the antibacterial and antifungal study revealed its efficiency in killing bacteria and fungi.


2017 ◽  
Vol 3 (1) ◽  
pp. 18 ◽  
Author(s):  
A. Gowthami ◽  
A. Vinoth Kanna ◽  
T. Uma sankari ◽  
Sarmad Moin

In this investigation we report the bioreduction of silver nitrate to silver nanoparticles using the leaves aqueous extract of Alangium lamarckii. The silver nanoparticles were characterized by UVvis spectrophotometer, scanning electron microscope (SEM), DLS-Size and zeta potential analysis showed that the synthesized silver nanoparticles are varied from 60 - 70 nm and have the spherical shape. Further the prospect of protein as a stabilizing material in silver nanoparticles is shown by FTIR analysis and the XRD examination confirms monocrystalline phase of silver with FCC crystal structure. The antimicrobial activity of Ag nanoparticles was investigated against some pathogens. In these assessments, silver nanoparticles (AgNP) can stop microbial growth and even kill microbes, from now confirmed their antimicrobial importance.


2018 ◽  
Vol 18 (3) ◽  
pp. 441
Author(s):  
Wega Trisunaryanti ◽  
Triyono Triyono ◽  
Iip Izul Falah ◽  
Andreas David Siagian ◽  
Muhammad Fajar Marsuki

The synthesis of Ce/mesoporous silica (Ce/MS) and its lifetime determination for the hydrocracking of waste lubricant has been carried out. The MS was synthesized using tetraethyl orthosilicate (TEOS) and gelatin extracted from bovine bone as a template. Cerium was impregnated onto the MS by wet impregnation method using Ce(NO3)3.6H2O. The MS and Ce/MS were then characterized by means of acidity using ammonia base vapor adsorption, Fourier Transform Spectrophotometer (FTIR), Transmission Electron Microscope (TEM), Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer (SEM-EDX), and surface area analyzer (SAA) based on the BET and BJH equation. The Ce/MS catalyst was tested in hydrocracking of waste lubricant in three runs. Lifetime of Ce/MS catalyst was determined using a linear regression of the liquid product yields vs hydrocracking time. The Ce/MS catalyst showed an acidity of 2.79 mmol/g, BJH desorption pore diameter of 3.84 nm, BET surface area of 246.55 m2/g, and total pore volume of 0.44 cm3/g. The yield of liquid product obtained from hydrocracking of waste lubricant using the Ce/MS catalyst for the first, second, and third runs was 21.42, 17.23 and 10.54 wt.%, respectively for 2.5 h per each run. Lifetime of Ce/MS catalyst in hydrocracking of waste lubricant was 12.54 h.


Polymers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 3578
Author(s):  
Mohd Shahrul Nizam Salleh ◽  
Roshafima Rasit Ali ◽  
Kamyar Shameli ◽  
Mohd Yusof Hamzah ◽  
Rafiziana Md Kasmani ◽  
...  

The production of pure silver nanoparticles (Ag-NPs) with unique properties remains a challenge even today. In the present study, the synthesis of silver nanoparticles (Ag-NPs) from natural pullulan (PL) was carried out using a radiation-induced method. It is known that pullulan is regarded as a microbial polysaccharide, which renders it suitable to act as a reducing and stabilizing agent during the production of Ag-NPs. Pullulan-assisted synthesis under gamma irradiation was successfully developed to obtain Ag-NPs, which was characterized by UV-Vis, XRD, TEM, and Zeta potential analysis. Pullulan was used as a stabilizer and template for the growth of silver nanoparticles, while gamma radiation was modified to be selective to reduce silver ions. The formation of Ag-NPs was confirmed using UV–Vis spectra by showing a surface plasmon resonance (SPR) band in the region of 420–435 nm. As observed by TEM images, it can be said that by increasing the radiation dose, the particle size decreases, resulting in a mean diameter of Ag-NPs ranging from 40.97 to 3.98 nm. The XRD analysis confirmed that silver metal structures with a face-centered cubic (FCC) crystal were present, while TEM images showed a spherical shape with smooth edges. XRD also demonstrated that increasing the dose of gamma radiation increases the crystallinity at a high purity of Ag-NPs. As examined by zeta potential, the synthesized Ag-NP/PL was negatively charged with high stability. Ag-NP/PL was then analysed for antimicrobial activity against Staphylococcus aureus, and it was found that it had high antibacterial activity. It is found that the adoption of radiation doses results in a stable and green reduction process for silver nanoparticles.


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