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核心技术专利:CN118964589B侵权必究
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Developing Actively Targeted Nanoparticles to Fight Cancer: Focus on Italian Research.

作者信息

Argenziano Monica, Arpicco Silvia, Brusa Paola, Cavalli Roberta, Chirio Daniela, Dosio Franco, Gallarate Marina, Peira Elena, Stella Barbara, Ugazio Elena

机构信息

Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy.

出版信息

Pharmaceutics. 2021 Sep 22;13(10):1538. doi: 10.3390/pharmaceutics13101538.


DOI:10.3390/pharmaceutics13101538
PMID:34683830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8540327/
Abstract

Active targeting is a valuable and promising approach with which to enhance the therapeutic efficacy of nanodelivery systems, and the development of tumor-targeted nanoparticles has therefore attracted much research attention. In this field, the research carried out in Italian Pharmaceutical Technology academic groups has been focused on the development of actively targeted nanosystems using a multidisciplinary approach. To highlight these efforts, this review reports a thorough description of the last 10 years of Italian research results on the development of actively targeted nanoparticles to direct drugs towards different receptors that are overexpressed on cancer cells or in the tumor microenvironment. In particular, the review discusses polymeric nanocarriers, liposomes, lipoplexes, niosomes, solid lipid nanoparticles, squalene nanoassemblies and nanobubbles. For each nanocarrier, the main ligands, conjugation strategies and target receptors are described. The literature indicates that polymeric nanoparticles and liposomes stand out as key tools for improving specific drug delivery to the site of action. In addition, solid lipid nanoparticles, squalene nanoparticles and nanobubbles have also been successfully proposed. Taken together, these strategies all offer many platforms for the design of nanocarriers that are suitable for future clinical translation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/30afe70ae6df/pharmaceutics-13-01538-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/e62d53d09dd5/pharmaceutics-13-01538-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/f3bd72ab1cf6/pharmaceutics-13-01538-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/30afe70ae6df/pharmaceutics-13-01538-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/e62d53d09dd5/pharmaceutics-13-01538-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/f3bd72ab1cf6/pharmaceutics-13-01538-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9699/8540327/30afe70ae6df/pharmaceutics-13-01538-g003.jpg

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[5]
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[6]
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[7]
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[8]
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本文引用的文献

[1]
Advanced and Innovative Nano-Systems for Anticancer Targeted Drug Delivery.

Pharmaceutics. 2021-7-27

[2]
Combining Dextran Conjugates with Stimuli-Responsive and Folate-Targeting Activity: A New Class of Multifunctional Nanoparticles for Cancer Therapy.

Nanomaterials (Basel). 2021-4-25

[3]
A New Bevacizumab Carrier for Intravitreal Administration: Focus on Stability.

Pharmaceutics. 2021-4-15

[4]
Cancer Nanopharmaceuticals: Physicochemical Characterization and In Vitro/In Vivo Applications.

Cancers (Basel). 2021-4-15

[5]
Antibodies Targeting the Transferrin Receptor 1 (TfR1) as Direct Anti-cancer Agents.

Front Immunol. 2021-3-17

[6]
Ligand decorated biodegradable nanomedicine in the treatment of cancer.

Pharmacol Res. 2021-5

[7]
Dual-Targeted Hyaluronic Acid/Albumin Micelle-Like Nanoparticles for the Vectorization of Doxorubicin.

Pharmaceutics. 2021-2-26

[8]
LinTT1 peptide-functionalized liposomes for targeted breast cancer therapy.

Int J Pharm. 2021-3-15

[9]
Glutamate-urea-based PSMA-targeted PLGA nanoparticles for prostate cancer delivery of docetaxel.

Pharm Dev Technol. 2021-4

[10]
Strategies for cancer gene-delivery improvement by non-viral vectors.

Int J Pharm. 2021-3-1

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