Stabilized R -α-Lipoic Acid by Encapsulation Using Cyclodextrins

Author:

Ikuta Naoko,Terao Keiji,Matsugo Seiichi

Publisher

Elsevier

Reference21 articles.

1. The plasma pharmacokinetics of R-(+)-lipoic acid administered as sodium R-(+)-lipoate to healthy human subjects;Carlson;Altern. Med. Rev.,2007

2. Structural analysis of crystalline R(+)-α-lipoic acid-α-cyclodextrin complex based on microscopic and spectroscopic studies;Ikuta;Int. J. Mol. Sci.,2015

3. NMR studies of inclusion complexes formed by (R)-α-lipoic acid with α-, β-, and γ-cyclodextrins;Ikeda;Bull. Chem. Soc. Jpn.,2015

4. Bioavailability of an R-α-lipoic acid/-cyclodextrin complex in healthy volunteers;Ikuta;Int. J. Mol. Sci.,2016

5. Analysis of the enhanced stability of R(+)-alpha lipoic acid by the complex formation with cyclodextrins;Ikuta;Int. J. Mol. Sci.,2013

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