<P>A new pentacosadiynoyl cyclosophoraose (P-Cys) was synthesized using a biosourced cyclooligosac-charide with intrinsic complexation capacity. NOESY analysis revealed that switchable molecular behavior of pentacosadiynoyl moiety attached to P-...
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https://www.riss.kr/link?id=A107642386
2016
-
학술저널
195-203(9쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>A new pentacosadiynoyl cyclosophoraose (P-Cys) was synthesized using a biosourced cyclooligosac-charide with intrinsic complexation capacity. NOESY analysis revealed that switchable molecular behavior of pentacosadiynoyl moiety attached to P-...
<P>A new pentacosadiynoyl cyclosophoraose (P-Cys) was synthesized using a biosourced cyclooligosac-charide with intrinsic complexation capacity. NOESY analysis revealed that switchable molecular behavior of pentacosadiynoyl moiety attached to P-Cys was dependent on the external lipophilicity. Both encapsulation by cyclosophoraose and switchable emulsification by pentacosadiynoyl moiety in P-Cys make it possible to finely formulate a nanoemulsion state for an external hydrophobic guest molecule like Sudan III. Various physicochemical properties of the emulsions of P-Cys were investigated using TEM and DLS. The results indicate that P-Cys is a useful potential platform for the encapsulating emulsification of bioactive molecules for cosmetic and pharmaceutical applications. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.</P>
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