Surfactant-free amorphous solid dispersion with high dissolution for bioavailability enhancement of hydrophobic drugs: a case of quercetin-Reference-Cited by-同舟云学术

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Surfactant-free amorphous solid dispersion with high dissolution for bioavailability enhancement of hydrophobic drugs: a case of quercetin

Published:2021-01-02 Issue:1 Volume:47 Page:153-162
ISSN:0363-9045
Container-title:Drug Development and Industrial Pharmacy
language:en
Short-container-title:Drug Development and Industrial Pharmacy

Author:

Han Jiawei¹²,Tong Meng¹,Li Shukun¹,Yu Xiangyu¹,Hu Ziqi¹,Zhang Quan³,Xu Runze³,Wang Jing¹

Affiliation:

1. Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China

2. School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China

3. School of Pharmacy, China Pharmaceutical University, Nanjing, China

Funder

National Natural Science Foundation of China

Nanjing University of Chinese Medicine

Postgraduate Research & Practice Innovation Program of Jiangsu Province

Publisher

Informa UK Limited

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03639045.2020.1862173

Reference52 articles.

1. Advances in coamorphous drug delivery systems

2. On the role of salt formation and structural similarity of co-formers in co-amorphous drug delivery systems

3. Characterization of in vitro and in vivo bioactivity of a ferulic acid-2-Hydroxypropyl-β-cyclodextrin inclusion complex

4. Conception of nanosized hybrid liposome/poloxamer particles to thicken the interior core of liposomes and delay hydrophilic drug delivery

5. High-temperature stable plasmonic and cavity resonances in metal nanoparticle-decorated silicon nanopillars for strong broadband absorption in photothermal applications

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