Enhancement of iodinin solubility by encapsulation into cyclodextrin nanoparticles

Phenazine is known to regroup planar nitrogen-containing heterocyclic compounds. It was used here to enhance the bioavailability of the biologically important compound iodinin, which is near insoluble in aqueous solutions. Its water solubility has led to the development of new formulations using div...

Full description

Saved in:
Bibliographic Details
Main Authors: Anthony Prandina (Author), Lars Herfindal (Author), Sylvie Radix (Author), Pål Rongved (Author), Stein O. Døskeland (Author), Marc Le Borgne (Author), Florent Perret (Author)
Format: Book
Published: Taylor & Francis Group, 2018-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_f8efd2d694984d28a404868dc1bc4ce7
042 |a dc 
100 1 0 |a Anthony Prandina  |e author 
700 1 0 |a Lars Herfindal  |e author 
700 1 0 |a Sylvie Radix  |e author 
700 1 0 |a Pål Rongved  |e author 
700 1 0 |a Stein O. Døskeland  |e author 
700 1 0 |a Marc Le Borgne  |e author 
700 1 0 |a Florent Perret  |e author 
245 0 0 |a Enhancement of iodinin solubility by encapsulation into cyclodextrin nanoparticles 
260 |b Taylor & Francis Group,   |c 2018-01-01T00:00:00Z. 
500 |a 1475-6366 
500 |a 1475-6374 
500 |a 10.1080/14756366.2017.1421638 
520 |a Phenazine is known to regroup planar nitrogen-containing heterocyclic compounds. It was used here to enhance the bioavailability of the biologically important compound iodinin, which is near insoluble in aqueous solutions. Its water solubility has led to the development of new formulations using diverse amphiphilic α-cyclodextrins (CDs). With the per-[6-desoxy-6-(3-perfluorohexylpropanethio)-2,3-di-O-methyl]-α-CD, we succeeded to get iodinin-loaded nanoformulations with good parameters such as a size of 97.9 nm, 62% encapsulation efficiency and efficient control release. The study presents an interesting alternative to optimizing the water solubility of iodinin by chemical modifications of iodinin. 
546 |a EN 
690 |a Iodinin 
690 |a solubility 
690 |a amphiphilic α-cyclodextrin 
690 |a nanoparticles 
690 |a encapsulation 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 370-375 (2018) 
787 0 |n http://dx.doi.org/10.1080/14756366.2017.1421638 
787 0 |n https://doaj.org/toc/1475-6366 
787 0 |n https://doaj.org/toc/1475-6374 
856 4 1 |u https://doaj.org/article/f8efd2d694984d28a404868dc1bc4ce7  |z Connect to this object online.