Review of Gold Nanoparticles: Synthesis, Properties, Shapes, Cellular Uptake, Targeting, Release Mechanisms and Applications in Drug Delivery and Therapy.

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Joel Georgeous, Nour AlSawaftah, Waad H Abuwatfa, Ghaleb A Husseini
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引用次数: 0

Abstract

The remarkable versatility of gold nanoparticles (AuNPs) makes them innovative agents across various fields, including drug delivery, biosensing, catalysis, bioimaging, and vaccine development. This paper provides a detailed review of the important role of AuNPs in drug delivery and therapeutics. We begin by exploring traditional drug delivery systems (DDS), highlighting the role of nanoparticles in revolutionizing drug delivery techniques. We then describe the unique and intriguing properties of AuNPs that make them exceptional for drug delivery. Their shapes, functionalization, drug-loading bonds, targeting mechanisms, release mechanisms, therapeutic effects, and cellular uptake methods are discussed, along with relevant examples from the literature. Lastly, we present the drug delivery applications of AuNPs across various medical domains, including cancer, cardiovascular diseases, ocular diseases, and diabetes, with a focus on in vitro and in vivo cancer research.

金纳米颗粒综述:金纳米粒子:合成、性质、形状、细胞吸收、靶向、释放机制以及在药物输送和治疗中的应用》。
金纳米粒子(AuNPs)具有卓越的多功能性,使其成为药物输送、生物传感、催化、生物成像和疫苗开发等各个领域的创新药剂。本文详细综述了 AuNPs 在给药和治疗中的重要作用。我们首先探讨了传统的给药系统 (DDS),强调了纳米粒子在给药技术革命中的作用。然后,我们介绍了 AuNPs 独特而有趣的特性,这些特性使其在药物递送方面独树一帜。我们讨论了 AuNPs 的形状、官能化、药物负载键、靶向机制、释放机制、治疗效果和细胞摄取方法,并列举了文献中的相关实例。最后,我们介绍了 AuNPs 在癌症、心血管疾病、眼部疾病和糖尿病等各个医学领域的药物递送应用,重点是体外和体内癌症研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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