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核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

Ligand-based targeted therapy: a novel strategy for hepatocellular carcinoma.

作者信息

Li Min, Zhang Weiyue, Wang Birong, Gao Yang, Song Zifang, Zheng Qi Chang

机构信息

Department of Hepatobiliary Surgery, Union Hospital.

The First Clinic Institute, Tongji Medical College, Huazhong University of Science and Technology.

出版信息

Int J Nanomedicine. 2016 Oct 31;11:5645-5669. doi: 10.2147/IJN.S115727. eCollection 2016.


DOI:10.2147/IJN.S115727
PMID:27920520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5127222/
Abstract

Hepatocellular carcinoma (HCC) is the most common primary liver cancer with high morbidity and mortality worldwide. Chemotherapy is recommended to patients with intermediate or advanced stage cancer. However, the conventional chemotherapy yields low desired response rates due to multidrug resistance, fast clearance rate, nonspecific delivery, severe side effects, low drug concentration in cancer cells, and so on. Nanoparticle-mediated targeted drug delivery system can surmount the aforementioned obstacles through enhanced permeability and retention effect and active targeting as a novel approach of therapeutics for HCC in recent years. The active targeting is triggered by ligands on the delivery system, which recognize with and internalize into hepatoma cells with high specificity and efficiency. This review focuses on the latest targeted delivery systems for HCC and summarizes the ligands that can enhance the capacity of active targeting, to provide some insight into future research in nanomedicine for HCC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/cd748d7c6a86/ijn-11-5645Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/964249dcaed1/ijn-11-5645Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/e817d46654a1/ijn-11-5645Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/475468e54ddd/ijn-11-5645Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/88787697b81f/ijn-11-5645Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/08a08cb78551/ijn-11-5645Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/cd748d7c6a86/ijn-11-5645Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/964249dcaed1/ijn-11-5645Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/e817d46654a1/ijn-11-5645Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/475468e54ddd/ijn-11-5645Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/88787697b81f/ijn-11-5645Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/08a08cb78551/ijn-11-5645Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d76a/5127222/cd748d7c6a86/ijn-11-5645Fig6.jpg

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本文引用的文献

[1]
Biotin-decorated fluorescent silica nanoparticles with aggregation-induced emission characteristics: fabrication, cytotoxicity and biological applications.

J Mater Chem B. 2013-2-7

[2]
Lactobionic acid and carboxymethyl chitosan functionalized graphene oxide nanocomposites as targeted anticancer drug delivery systems.

Carbohydr Polym. 2016-6-6

[3]
Emerging roles of FGF signaling in hepatocellular carcinoma.

Transl Cancer Res. 2016-2

[4]
Novel gold nanoparticles coated with somatostatin as a potential delivery system for targeting somatostatin receptors.

Drug Dev Ind Pharm. 2016-11

[5]
Dextran based nanosized carrier for the controlled and targeted delivery of curcumin to liver cancer cells.

Int J Biol Macromol. 2016-3-21

[6]
iRGD decorated lipid-polymer hybrid nanoparticles for targeted co-delivery of doxorubicin and sorafenib to enhance anti-hepatocellular carcinoma efficacy.

Nanomedicine. 2016-7

[7]
Asialoglycoprotein receptor-magnetic dual targeting nanoparticles for delivery of RASSF1A to hepatocellular carcinoma.

Sci Rep. 2016-2-26

[8]
Enhanced immunotherapy of SM5-1 in hepatocellular carcinoma by conjugating with gold nanoparticles and its in vivo bioluminescence tomographic evaluation.

Biomaterials. 2016-5

[9]
Stepwise pH-responsive nanoparticles containing charge-reversible pullulan-based shells and poly(β-amino ester)/poly(lactic-co-glycolic acid) cores as carriers of anticancer drugs for combination therapy on hepatocellular carcinoma.

J Control Release. 2016-3-28

[10]
Codelivery of Doxorubicin and shAkt1 by Poly(ethylenimine)-Glycyrrhetinic Acid Nanoparticles To Induce Autophagy-Mediated Liver Cancer Combination Therapy.

Mol Pharm. 2016-4-4

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