| Literature DB >> 27803494 |
Kazuaki Kishita1, Kayo Ibaraki, Shoko Itakura, Yumi Yamasaki, Naoko Nishikata, Kenji Yamamoto, Masataka Shimizu, Kazuo Nishiyama, Masao Yamasaki.
Abstract
Conjugated linoleic acid (CLA) has several beneficial biological properties. Specifically, trans10, cis12-CLA, one of the CLA isomers, has strong physiologic activity against cancer and obesity. However, compared with cis9, trans11-CLA, a naturally occurring CLA isomer, trans10, cis12-CLA tends to be easily metabolized. Therefore, to make efficient use of its biological properties, it is necessary to overcome the rapid clearance of trans10, cis12-CLA from the blood. Here, we employed premix membrane emulsification to prepare two oil-in-water CLA microemulsions (CLA-ME), 100 nm CLA-ME and 200 nm CLA-ME, and investigated their pharmacokinetics in a mouse model. We report that 100 nm CLA-ME contributed to the concentration of blood CLA for longer than 200 nm CLA-ME, indicating that small CLA microparticles were more suitable for maintaining blood trans10, cis12-CLA levels in vivo. However, both CLA-ME could be hardly detected in blood and other tissues 24 h after administration, suggesting that additional strategies for prolonging CLA-ME half-life are required.Entities:
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Year: 2016 PMID: 27803494 DOI: 10.5650/jos.ess16099
Source DB: PubMed Journal: J Oleo Sci ISSN: 1345-8957 Impact factor: 1.601