Lipid-based nanoparticle technologies for liver targeting

被引:145
作者
Boettger, Roland [1 ]
Pauli, Griffin [1 ]
Chao, Po-Han [1 ]
Al Fayez, Nojoud [1 ]
Hohenwarter, Lukas [1 ]
Li, Shyh-Dar [1 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, 2405 Wesbrook Mall, Vancouver, BC V6T 1Z3, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Lipid nanoparticle; Liver targeting; Liposome; Solid lipid nanoparticles; Niosome; Liver fibrosis; Hepatitis; Hepatocellular carcinoma; HEPATIC STELLATE CELLS; CALCIUM-PHOSPHATE NANOPARTICLES; FUCOSE-CONTAINING GLYCOPROTEINS; B-VIRUS INFECTION; IN-VIVO; HEPATOCELLULAR-CARCINOMA; DRUG-DELIVERY; ASIALOGLYCOPROTEIN RECEPTOR; SIRNA DELIVERY; RAT-LIVER;
D O I
10.1016/j.addr.2020.06.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liver diseases such as hepatitis, cirrhosis, and hepatocellular carcinoma are global health problems accounting for approximately 800 million cases and over 2 million deaths per year worldwide. Major drawbacks of standard pharmacological therapies are the inability to deliver a sufficient concentration of a therapeutic agent to the diseased liver, and nonspecific drug delivery leading to undesirable systemic side effects. Additionally, depending on the specific liver disease, drug delivery to a subset of liver cells is required. In recent years, lipid nanoparticles have been developed to passively and actively target drugs to the liver. The success of this approach has been highlighted by the FDA-approval of the first liver-targeting lipid nanoparticle, ONPATTRO, in 2018 and many other promising candidate technologies are expected to follow. This review summarizes recent developments of various lipid-based liver-targeting technologies, namely solid-lipid nanoparticles, liposomes, niosomes and micelles, and discusses the challenges and future perspectives in this field. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 101
页数:23
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