scholarly journals Enrichment of anodic MgO layers with Ag nanoparticles for biomedical applications

2008 ◽  
Vol 20 (1) ◽  
pp. 339-345 ◽  
Author(s):  
B. S. Necula ◽  
L. E. Fratila-Apachitei ◽  
A. Berkani ◽  
I. Apachitei ◽  
J. Duszczyk
2019 ◽  
Vol 8 (1) ◽  
pp. 246-257 ◽  
Author(s):  
Kaleemullah Kalwar ◽  
Ming Shen

Abstract Au@Ag nanoparticles decorated on cellulose paper could be worthful biomedical applications. Electrospinning technique is broadly employed for fabrication of nano and micro size fibers with a variety of biopolymers adding cellulose acetate nanofibers. Evolutions in cellulose research demonstrate that it is an anticipating material for the biomedical application. Nanofibers acquired by electrospinning technique were utilized in various biomedical applications. In this report, electrospinning of cellulose acetate, the solvent choice for cellulose acetate e-spun nanofabrication and decoration of AgNPs including shape and size for antimicrobial activity are argued.


2019 ◽  
Vol 121 ◽  
pp. 707-717 ◽  
Author(s):  
Samir T. Gaballah ◽  
Hossam A. El-Nazer ◽  
Reham A. Abdel-Monem ◽  
Mohamed Azab El-Liethy ◽  
Bahaa A. Hemdan ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Meghana Matur ◽  
Harishkumar Madhyastha ◽  
T. S. Shruthi ◽  
Radha Madhyastha ◽  
S. P. Srinivas ◽  
...  

AbstractThe successful integration of nanoparticles into biomedical applications requires modulation of their surface properties so that the interaction with biological systems is regulated to minimize toxicity for biological function. In the present work, we have engineered bioactive surfaces on gold (Au) and silver (Ag) nanoparticles and subsequently evaluated their interaction with mouse skin fibroblasts and macrophages. The Au and Ag nanoparticles were synthesized using tyrosine, tryptophan, isonicotinylhydrazide, epigallocatechin gallate, and curcumin as reducing and stabilizing agents. The nanoparticles thus prepared showed surface corona and exhibited free radical scavenging and enzyme activities with limited cytotoxicity and genotoxicity. We have thus developed avenues for engineering the surface of nanoparticles for biological applications.


2020 ◽  
Vol 44 (18) ◽  
pp. 7265-7269
Author(s):  
Chuan-Wan Wei ◽  
Xiao-Qing Gong ◽  
Xiao-Juan Wang ◽  
Xin-Zhi Yang ◽  
Shu-Qin Gao ◽  
...  

A new hybrid hydrogel was constructed by in situ forming Ag NPs within the 3D network of a hydrogel that exhibits both excellent injectability and broad antibacterial activities, which makes it a potential candidate for various biomedical applications.


2019 ◽  
Vol 6 (1) ◽  
pp. 680-689 ◽  
Author(s):  
Xinglu Jiang ◽  
Xiaobo Fan ◽  
Wei Xu ◽  
Rui Zhang ◽  
Guoqiu Wu

Author(s):  
T. L. Hayes

Biomedical applications of the scanning electron microscope (SEM) have increased in number quite rapidly over the last several years. Studies have been made of cells, whole mount tissue, sectioned tissue, particles, human chromosomes, microorganisms, dental enamel and skeletal material. Many of the advantages of using this instrument for such investigations come from its ability to produce images that are high in information content. Information about the chemical make-up of the specimen, its electrical properties and its three dimensional architecture all may be represented in such images. Since the biological system is distinctive in its chemistry and often spatially scaled to the resolving power of the SEM, these images are particularly useful in biomedical research.In any form of microscopy there are two parameters that together determine the usefulness of the image. One parameter is the size of the volume being studied or resolving power of the instrument and the other is the amount of information about this volume that is displayed in the image. Both parameters are important in describing the performance of a microscope. The light microscope image, for example, is rich in information content (chemical, spatial, living specimen, etc.) but is very limited in resolving power.


Author(s):  
Philippe Fragu

The identification, localization and quantification of intracellular chemical elements is an area of scientific endeavour which has not ceased to develop over the past 30 years. Secondary Ion Mass Spectrometry (SIMS) microscopy is widely used for elemental localization problems in geochemistry, metallurgy and electronics. Although the first commercial instruments were available in 1968, biological applications have been gradual as investigators have systematically examined the potential source of artefacts inherent in the method and sought to develop strategies for the analysis of soft biological material with a lateral resolution equivalent to that of the light microscope. In 1992, the prospects offered by this technique are even more encouraging as prototypes of new ion probes appear capable of achieving the ultimate goal, namely the quantitative analysis of micron and submicron regions. The purpose of this review is to underline the requirements for biomedical applications of SIMS microscopy.Sample preparation methodology should preserve both the structural and the chemical integrity of the tissue.


Author(s):  
J. D. Shelburne ◽  
Peter Ingram ◽  
Victor L. Roggli ◽  
Ann LeFurgey

At present most medical microprobe analysis is conducted on insoluble particulates such as asbestos fibers in lung tissue. Cryotechniques are not necessary for this type of specimen. Insoluble particulates can be processed conventionally. Nevertheless, it is important to emphasize that conventional processing is unacceptable for specimens in which electrolyte distributions in tissues are sought. It is necessary to flash-freeze in order to preserve the integrity of electrolyte distributions at the subcellular and cellular level. Ideally, biopsies should be flash-frozen in the operating room rather than being frozen several minutes later in a histology laboratory. Electrolytes will move during such a long delay. While flammable cryogens such as propane obviously cannot be used in an operating room, liquid nitrogen-cooled slam-freezing devices or guns may be permitted, and are the best way to achieve an artifact-free, accurate tissue sample which truly reflects the in vivo state. Unfortunately, the importance of cryofixation is often not understood. Investigators bring tissue samples fixed in glutaraldehyde to a microprobe laboratory with a request for microprobe analysis for electrolytes.


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