2015 Fiscal Year Final Research Report
Precision Synthesis of Block Glycopolymers for DDS Carrier targeting Macrophages
Project/Area Number |
25410126
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Polymer chemistry
|
Research Institution | University of Yamanashi |
Principal Investigator |
OBATA Makoto 山梨大学, 総合研究部, 准教授 (70343267)
|
Co-Investigator(Kenkyū-buntansha) |
HIROHARA Shiho 宇部工業高等専門学校, 物質工学科, 准教授 (70413804)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Keywords | 糖質高分子 / 精密重合 / ドラッグデリバリーシステム |
Outline of Final Research Achievements |
We have studied synthetic strategy of block copolymers consisting glycopolymer as a hydrophilic segment to develop drug deliver system for immune cells such as macrophages and dendritic cells. We designed two types of block copolymers. One contains poly(lactic acid) as a hydrophobic segments for hydrophobic drug delivery, and the other has poly(L-lysine) as a cationic segments for nucleic acid delivery. We found that coupling method and bifunctional initiator method are promising strategies for synthesis of amphiphilic and cationic block glyco-copolymers, respectively. It should be noted that glycopolymer segments must have stability against acid hydrolysis for use in cationic block copolymer having poly(L-lysine). In addition, we demonstrate an enhanced cellular uptake of glycopolymer presenting mannose by RAW264.7 cells, showing targeting ability of glycopolymers.
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Free Research Field |
高分子合成化学
|