TY - JOUR
T1 - High performance optical resolution with liposome immobilized hydrogel
AU - Ishigami, Takaaki
AU - Sugita, Kazuma
AU - Suga, Keishi
AU - Okamoto, Yukihiro
AU - Umakoshi, Hiroshi
N1 - Funding Information:
We thank Dr. Toshinori Shimanouchi (Graduate School of Environmental Science, Okayama University) for his constructive comments. This research was supported by a Japan Society for the Promotion of Science (JSPS) Grant-in-Aid for JSPS Fellows (No. 13J03878 ), the Funding Program for Next Generation World-Leading Researchers of the Council for Science and Technology Policy ( GR066 ), and a JSPS Grant-in-Aid for Scientific Research A (No. 26249116 ). One of the authors (T.I.) expresses his gratitude for Japan Society for the Promotion of Science (JSPS) scholarships. Furthermore, Y.O. acknowledges the Multidisciplinary Research Laboratory System in Osaka University and a Grant-in-Aid for Scientific Research on Innovative Areas “Nanomedicine Molecular Science” (No. 2306) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - We prepared liposome immobilized hydrogels (LI-gels) for analysis and separation of chiral molecules, to overcome the drawbacks of liposomes such as low stability, and difficulties with handling and isolation from sample solutions. The amounts of liposomes in the hydrogels were larger than those in other solid matrices reported previously. The liposome morphology was intact, and its original properties, such as fluidity and phase transition behaviors, were preserved. We investigated the chiral recognition performance of the LI-gel, as described in our previous paper. Our results indicate that the enantioselectivity of the LI-gel was higher than those of conventional methods and of the liposomes alone. Our prepared LI-gel therefore overcomes the drawbacks of liposomes, and has potential applications in analysis and separation, including chiral separation.
AB - We prepared liposome immobilized hydrogels (LI-gels) for analysis and separation of chiral molecules, to overcome the drawbacks of liposomes such as low stability, and difficulties with handling and isolation from sample solutions. The amounts of liposomes in the hydrogels were larger than those in other solid matrices reported previously. The liposome morphology was intact, and its original properties, such as fluidity and phase transition behaviors, were preserved. We investigated the chiral recognition performance of the LI-gel, as described in our previous paper. Our results indicate that the enantioselectivity of the LI-gel was higher than those of conventional methods and of the liposomes alone. Our prepared LI-gel therefore overcomes the drawbacks of liposomes, and has potential applications in analysis and separation, including chiral separation.
KW - Hydrogel
KW - Liposome
KW - Optical resolution
KW - Tryptophan
UR - http://www.scopus.com/inward/record.url?scp=84942235066&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84942235066&partnerID=8YFLogxK
U2 - 10.1016/j.colsurfb.2015.09.009
DO - 10.1016/j.colsurfb.2015.09.009
M3 - Article
C2 - 26406591
AN - SCOPUS:84942235066
SN - 0927-7765
VL - 136
SP - 256
EP - 261
JO - Colloids and Surfaces B: Biointerfaces
JF - Colloids and Surfaces B: Biointerfaces
ER -