Active Targeting Gold Nanoparticle for Chemotherapy Drug Delivery: A Review

Q4 Pharmacology, Toxicology and Pharmaceutics Infarma Pharmaceutical Sciences Pub Date : 2021-11-30 DOI:10.34172/ps.2021.75
A. Gumala, Sutriyo Sutriyo
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引用次数: 2

Abstract

Objective Active targeting strategy in chemotherapy drug delivery aims to improve the therapeutic outcomes and minimise the side effects of chemotherapeutics. This review discusses utilising ligands attached to gold nanoparticles (AuNPs) along with several specific ligands attached to AuNPs for active targeting in chemotherapy drug delivery. Key finding Antibodies, peptides, vitamins, DNA, polysaccharides, aptamers, and hormones showed active-targeting abilities as ligands attached to AuNPs. Active-targeting AuNPs enhanced cellular uptake and cytotoxicity in a specific cancer cell in vitro while reducing tumor growth in vivo by improving the photothermal, photodynamic and chemotherapy effects. Active-targeting ligands increased the internalization of AuNPs loaded onto the specific tumour site and minimised the accumulation in the normal site. Conclusion AuNPs with active-targeting ligands such as antibodies, peptides, vitamins, DNA polysaccharides, aptamers, and hormones can improve the therapeutic outcomes of chemotherapeutics and can attenuate the toxicity effect in normal cells. For further research and development, researchers should be addressing AuNP characterization, drug–ligand disposition, active-targeting AuNP quantification, and target-AuNPs pertinence concerning the desired therapeutic outcomes.
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活性靶向金纳米颗粒用于化疗药物递送:综述
目的主动靶向给药策略旨在提高化疗药物的治疗效果,减少化疗药物的副作用。本文综述了利用金纳米颗粒(AuNPs)配体以及几种特定的AuNPs配体在化疗药物递送中的主动靶向作用。抗体、多肽、维生素、DNA、多糖、适体和激素作为附着在aunp上的配体显示出活性靶向能力。活性靶向AuNPs在体外增强特定癌细胞的细胞摄取和细胞毒性,同时通过改善光热、光动力和化疗效应,在体内降低肿瘤生长。活性靶向配体增加了装载到特定肿瘤部位的aunp的内化,并将正常部位的积累降至最低。结论含有抗体、多肽、维生素、DNA多糖、适体体和激素等活性靶向配体的AuNPs可改善化疗药物的治疗效果,并可减轻对正常细胞的毒性作用。为了进一步的研究和发展,研究人员应该解决AuNP的表征,药物配体配置,活性靶向AuNP的量化,以及与预期治疗结果相关的目标-AuNP的相关性。
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来源期刊
CiteScore
0.10
自引率
0.00%
发文量
17
审稿时长
10 weeks
期刊最新文献
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