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Nanoparticulate Antibiotic Systems as Antibacterial Agents and Antibiotic Delivery Platforms to Fight Infections

机译:纳米颗粒抗生素系统作为抗菌剂和抗生素的递送平台,以对抗感染

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摘要

Today’s human society, product of decades of progress in all fields of knowledge, would have been unimaginable without the discovery of antibiotics and more generally of antimicrobials. However, from the beginning, the scientific community was aware that microorganisms through various strategies were able to hinder and render vain antibiotic action. Common examples are the phenomena of persistence, tolerance, and resistance, up to the creation of the feared bacterial biofilms. Antibiotics are a precious but equally labile resource that must be preserved but at the same time reinforced to safeguard their effectiveness. Nanoparticulate systems such as nanobactericides, with their inherent antibacterial activity, and nanocarriers, which operate as drug delivery systems for conventional antibiotics, are innovative therapies made available by nanotechnology. Inorganic nanoparticles are effective both as nanobactericides (AgNPs, ZnONPs, and TiO2NPs) and as nanocarriers (AgNPs, AuNPs, ZnONPs, and TiO2NPs) against sensitive and multi-drug-resistant bacterial strains. Liposomes are among the most studied and flexible antibiotic delivery platforms: conventional liposomes allow passive targeting at the mononuclear phagocytic system (MPS); “stealth” liposomes prevent macrophage uptake so as to eradicate infections in tissues and organs outside MPS; thanks to their positive charge, cationic liposomes interact preferentially with bacterial and biofilm surfaces, acting as innate antibacterials as well as drug delivery systems (DDS); fusogenic liposomes have fluid bilayers that promote fusion with microbial membranes; and finally, ligand-targeted liposomes provide active targeting at infection sites. Dendrimers are among the most recent and attractive nanoparticulate systems, thanks to their multibranched nanoarchitecture, which equipped them with multiple active sites for loading antibiotics and also interacting with bacteria. Finally, nanoantibiotics represent a new hopeful generation of antibiotic candidates capable of increasing or even restoring the clinical efficacy of “old” antibiotics rendered useless by the resistance phenomena.
机译:今天的人类社会,在所有知识领域的数十年进步的产品,在没有发现抗生素的情况下难以想象,更常见的抗菌剂。然而,从一开始,科学界意识到通过各种策略的微生物能够阻碍和造成抗生素的行动。常见的例子是持久性,耐受性和抗性的现象,达到恐惧的细菌生物膜的产生。抗生素是一种珍贵但同样的不稳定的资源,必须保存,但同时加强了维护其有效性。纳米颗粒系统如纳米杆菌,具有其固有的抗菌活性和纳米载体,其作为常规抗生素的药物递送系统操作,是纳米技术提供的创新性疗法。无机纳米颗粒作为纳米杆菌(AgNP,ZnONP和TiO 2NP)和作为纳米载体(AgNP,AUNP,ZnONP和TiO 2NPS)的纳米杆菌剂(AgNP,AuNP,ZnONP和TiO 2N)有效抗敏感性和多毒性的细菌菌株。脂质体是最熟练的和柔性抗生素递送平台中的:常规脂质体允许在单核吞噬系统(MPS)处被动靶向; “隐形”脂质体可防止巨噬细胞吸收,以在国会议员外面消除组织和器官中的感染;由于它们的正电荷,阳离子脂质体优先与细菌和生物膜表面相互作用,作为先天抗菌以及药物递送系统(DDS);致致沉膜脂质体具有促进与微生物膜融合的流体双层玻璃;最后,配体靶向脂质体在感染部位提供活性靶向。由于它们的多刺山纳米建筑,树枝状大分子是最近且有吸引力的纳米颗粒系统,该系统配备了多个活性位点,用于加载抗生素并与细菌相互作用。最后,纳米尼杀虫剂代表了一种能够增加甚至恢复因抗性现象而无用的“老”抗生素的临床疗效的抗生素候选者的新的充满希望的抗生素候选者。

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