Development of core–shell structured nanoparticle for sequential release of tariquidar and docetaxel to overcome multi drug-resistant cancer-Reference-Cited by-同舟云学术

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Development of core–shell structured nanoparticle for sequential release of tariquidar and docetaxel to overcome multi drug-resistant cancer

Published:2023-11-29 Issue:1 Volume:54 Page:61-75
ISSN:2093-5552
Container-title:Journal of Pharmaceutical Investigation
language:en
Short-container-title:J. Pharm. Investig.

Author:

Jung Hyun Min,Kim Chang Hyun,Seo Jo-Eun,Goo Yoon Tae,Hong Sun Ho,Kang Myung Joo,Lee Sangkil,Choi Young Wook

Funder

National Research Foundation of Korea

Chung-Ang University

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Pharmaceutical Science

Link

https://link.springer.com/content/pdf/10.1007/s40005-023-00645-8.pdf

Reference39 articles.

1. Cipolla D, Wu H, Gonda I, Eastman S, Redelmeier T et al (2014) Modifying the release properties of liposomes toward personalized medicine. J Pharm Sci 103:1851–1862

2. Fang J, Nakamura H, Maeda H (2011) The EPR effect: unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect. Adv Drug Deliv Rev 63:136–151

3. Guo Y, He W, Yang S, Zhao D, Li Z et al (2017) Co-delivery of docetaxel and verapamil by reduction-sensitive PEG-PLGA-SS-DTX conjugate micelles to reverse the multi-drug resistance of breast cancer. Colloids Surf B 151:119–127

4. Herbst RS, Khuri FR (2003) Mode of action of docetaxel–a basis for combination with novel anticancer agents. Cancer Treat Rev 29:407–415

5. Jang MH, Kim CH, Yoon HY, Sung SW, Goh MS et al (2019) Steric stabilization of RIPL peptide-conjugated liposomes and in vitro assessment. J Pharm Investig 49:115–125

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