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Surface Functionalization of Gold Nanoparticles for Targeting the Tumor Microenvironment to Improve Antitumor Efficiency
被引:18
|作者:
Tan, Kin Fai
[1
]
In, Lionel Lian Aun
[2
]
Kumar, Palanirajan Vijayaraj
[1
]
机构:
[1] UCSI Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Kuala Lumpur 56000, Malaysia
[2] UCSI Univ, Fac Appl Sci, Dept Biotechnol, Kuala Lumpur 56000, Malaysia
关键词:
gold nanoparticle;
tumor microenvironment;
passive transport;
tumor vessel normalization;
active transport;
hypoxic tumor microenvironment;
acidic tumor microenvironment;
BREAST-CANCER CELLS;
EPITHELIAL-MESENCHYMAL TRANSITION;
PLASMONIC PHOTOTHERMAL THERAPY;
TIRAPAZAMINE PLUS CISPLATIN;
VIVO PHOTODYNAMIC THERAPY;
ANTI-ANGIOGENIC THERAPY;
ENHANCED DRUG-DELIVERY;
IN-VIVO;
CELLULAR UPTAKE;
ERYTHROCYTE-MEMBRANE;
D O I:
10.1021/acsabm.3c00202
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Gold nanoparticles (AuNPs) have undergone significant research for their use in the treatment of cancer. Numerous researchers have established their potent antitumor properties, which have greatly impacted the treatment of cancer. AuNPs have been used in four primary anticancer treatment modalities, namely radiation, photothermal therapy, photodynamic therapy, and chemotherapy. However, the ability of AuNPs to destroy cancer is lacking and can even harm healthy cells without the right direction to transport them to the tumor microenvironment. Consequently, a suitable targeting technique is needed. Based on the distinct features of the human tumor microenvironment, this review discusses four different targeting strategies that target the four key features of the tumor microenvironment, including abnormal vasculature, overexpression of specific receptors, an acidic microenvironment, and a hypoxic microenvironment, to direct surface-functionalized AuNPs to the tumor microenvironment and increase antitumor efficacies. In addition, some current completed or ongoing clinical trials of AuNPs will also be discussed below to further reinforce the concept of using AuNPs in anticancer therapy.
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页码:2944 / 2981
页数:38
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