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      A Review on Green Synthesis of Nanoparticles and Their Diverse Biomedical and Environmental Applications

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          Abstract

          In recent times, metal oxide nanoparticles (NPs) have been regarded as having important commercial utility. However, the potential toxicity of these nanomaterials has also been a crucial research concern. In this regard, an important solution for ensuring lower toxicity levels and thereby facilitating an unhindered application in human consumer products is the green synthesis of these particles. Although a naïve approach, the biological synthesis of metal oxide NPs using microorganisms and plant extracts opens up immense prospects for the production of biocompatible and cost-effective particles with potential applications in the healthcare sector. An important area that calls for attention is cancer therapy and the intervention of nanotechnology to improve existing therapeutic practices. Metal oxide NPs have been identified as therapeutic agents with an extended half-life and therapeutic index and have also been reported to have lesser immunogenic properties. Currently, biosynthesized metal oxide NPs are the subject of considerable research and analysis for the early detection and treatment of tumors, but their performance in clinical experiments is yet to be determined. The present review provides a comprehensive account of recent research on the biosynthesis of metal oxide NPs, including mechanistic insights into biological production machinery, the latest reports on biogenesis, the properties of biosynthesized NPs, and directions for further improvement. In particular, scientific reports on the properties and applications of nanoparticles of the oxides of titanium, cerium, selenium, zinc, iron, and copper have been highlighted. This review discusses the significance of the green synthesis of metal oxide nanoparticles, with respect to therapeutically based pharmaceutical applications as well as energy and environmental applications, using various novel approaches including one-minute sonochemical synthesis that are capable of responding to various stimuli such as radiation, heat, and pH. This study will provide new insight into novel methods that are cost-effective and pollution free, assisted by the biodegradation of biomass.

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          Macrophage Polarization in Inflammatory Diseases

          Diversity and plasticity are two hallmarks of macrophages. M1 macrophages (classically activated macrophages) are pro-inflammatory and have a central role in host defense against infection, while M2 macrophages (alternatively activated macrophages) are associated with responses to anti-inflammatory reactions and tissue remodeling, and they represent two terminals of the full spectrum of macrophage activation. Transformation of different phenotypes of macrophages regulates the initiation, development, and cessation of inflammatory diseases. Here we reviewed the characters and functions of macrophage polarization in infection, atherosclerosis, obesity, tumor, asthma, and sepsis, and proposed that targeting macrophage polarization and skewing their phenotype to adapt to the microenvironment might hold great promise for the treatment of inflammatory diseases.
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            Memory CD8(+) T cells use cell-intrinsic lipolysis to support the metabolic programming necessary for development.

            Generation of CD8(+) memory T cells requires metabolic reprogramming that is characterized by enhanced mitochondrial fatty-acid oxidation (FAO). However, where the fatty acids (FA) that fuel this process come from remains unclear. While CD8(+) memory T cells engage FAO to a greater extent, we found that they acquired substantially fewer long-chain FA from their external environment than CD8(+) effector T (Teff) cells. Rather than using extracellular FA directly, memory T cells used extracellular glucose to support FAO and oxidative phosphorylation (OXPHOS), suggesting that lipids must be synthesized to generate the substrates needed for FAO. We have demonstrated that memory T cells rely on cell intrinsic expression of the lysosomal hydrolase LAL (lysosomal acid lipase) to mobilize FA for FAO and memory T cell development. Our observations link LAL to metabolic reprogramming in lymphocytes and show that cell intrinsic lipolysis is deterministic for memory T cell fate. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Zinc oxide nanoparticles for selective destruction of tumor cells and potential for drug delivery applications.

              Metal oxide nanoparticles, including zinc oxide, are versatile platforms for biomedical applications and therapeutic intervention. There is an urgent need to develop new classes of anticancer agents, and recent studies demonstrate that ZnO nanomaterials hold considerable promise. This review analyzes the biomedical applications of metal oxide and ZnO nanomaterials under development at the experimental, preclinical and clinical levels. A discussion regarding the advantages, approaches and limitations surrounding the use of metal oxide nanoparticles for cancer applications and drug delivery is presented. The scope of this article is focused on ZnO, and other metal oxide nanomaterial systems, and their proposed mechanisms of cytotoxic action, as well as current approaches to improve their targeting and cytotoxicity against cancer cells. This review aims to give an overview of ZnO nanomaterials in biomedical applications. Through a better understanding of the mechanisms of action and cellular consequences resulting from nanoparticles interactions with cells, the inherent toxicity and selectivity of ZnO nanoparticles against cancer may be improved further to make them attractive new anticancer agents.
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                Author and article information

                Contributors
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                Journal
                CATACJ
                Catalysts
                Catalysts
                MDPI AG
                2073-4344
                May 2022
                April 20 2022
                : 12
                : 5
                : 459
                Article
                10.3390/catal12050459
                72bb7fdd-c393-4f96-bb38-8017b146b45c
                © 2022

                https://creativecommons.org/licenses/by/4.0/

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