Controlling the burst release of amorphous drug–polysaccharide nanoparticle complex via crosslinking of the polysaccharide chains
High-payload amorphous drug–polysaccharide nanoparticle complex (or nanoplex in short) represents a new class of supersaturating drug delivery systems intended for bioavailability enhancement of poorly-soluble drugs. Not unlike other nanoscale amorphous formulations, the nanoplex exhibits fast disso...
Saved in:
Main Authors: | Nguyen, Minh-Hiep, Tran, The-Thien, Hadinoto, Kunn |
---|---|
Other Authors: | School of Chemical and Biomedical Engineering |
Format: | Article |
Language: | English |
Published: |
2016
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/82276 http://hdl.handle.net/10220/41174 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Identification of an exogenic metabolite and extraction of Polysaccharides from mushrooms
by: Ocampo, John Lester R., et al.
Published: (2012) -
Carboxymethyl cellulose is a superior polyanion to dextran sulfate in stabilizing and enhancing the solubility of amorphous drug-polyelectrolyte nanoparticle complex
by: Dong, Bingxue, et al.
Published: (2020) -
Millifluidic synthesis of amorphous drug-polysaccharide nanoparticle complex with tunable size intended for supersaturating drug delivery applications
by: Tran, The-Thien, et al.
Published: (2016) -
Immunomodulatory properties of polysaccharide-protein complex from lycium barbarum L.
by: CHEN ZHISONG
Published: (2010) -
In vitro study on entrapment of lipids within polysaccharide gel from fruit-hulls of Durian
by: Chutima Tippayakul
Published: (2009)