| 研究生: |
何怡瑱 Yi- Chan Ho |
|---|---|
| 論文名稱: |
三團聯聚合物(PF-127)和磷脂質間交互作用力量測和微脂粒穩定度之探討 The study of interaction of PEO-PPO-PEO copolymer (PF-127) with phospholipid and comparison of physical stability of liposomes |
| 指導教授: |
陳文逸
Wen-yih Chen |
| 口試委員: | |
| 學位類別: |
碩士 Master |
| 系所名稱: |
工學院 - 化學工程與材料工程學系 Department of Chemical & Materials Engineering |
| 畢業學年度: | 89 |
| 語文別: | 中文 |
| 論文頁數: | 89 |
| 中文關鍵詞: | 界面 、磷脂質 、單分子層 、微脂粒 |
| 外文關鍵詞: | interface, phospholipid, monolayer, liposome |
| 相關次數: | 點閱:10 下載:0 |
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本研究主要探討25 下,DMPC/PF-127(重量比為34:4、34:14和34:34)之Gibbs’吸附單分子層和PF-127分子吸附於三種不同單分子層(DMPC、DMPC/Vit-E及DMPC/cholesterol)的氣/液界面行為。首先就DMPC/PF-127 Gibbs’吸附單分子層系統而言,主要進行平衡表面張力量測和表面壓-每分子佔據面積等溫線(Π-A isotherm)的實驗。在所得的結果中,平衡表面張力隨著 PF-127添加量的增加呈現正比的線性關係。配合Gibbs表面過剩濃度關係式,可得表面過剩濃度和分子佔據面積。混合單分子層表面壓-每分子佔據面積的量測中,隨著PF-127添加量的增加,等溫線向右平移且有相變區(liquid-expanded transition liquid-condensed)的發生。
PF-127分子吸附在DMPC、DMPC/Vit-E、DMPC/ cholesterol三種不同單分子層的行為,則是藉由量測表面壓隨時間的變化的量測和表面壓-每分子佔據面積等溫線來進行研究。PF-127吸附在DMPC單分子層系統中,不同起始表面壓之表面壓隨時間變化的結果顯示,平衡表面壓與PF-127添加量呈正比關係。對於DMPC/Vit-E和DMPC/cholesterol混合單分子層系統,平衡表面壓的範圍分別是從 15.8∼28.3mN/m和 20.3~27.7mN/m,顯示添加維他命E和膽固醇改變分子間排列距離,使PF-127吸附於單分子層的表面壓產生差異。PF-127吸附平衡後之Π-A等溫線的結果顯示:(1)等溫線中有相變區的發生;(2)曲線向右平移,表示PF-127分子可能吸附或嵌入單分子層中,但因吸附的不夠緊或嵌入的不深,在高表面壓時,PF-127易被擠出單分子層中。此與微脂粒DSC實驗中,無論是嵌入法或吸附法都不影響相轉移溫度,推測PF-127嵌入脂質雙層不深是相符的。
This study investigated the behavior of mixed DMPC/PF-127 Gibbs’ adsorption monolayers (the weight ratio are 34: 4 , 34:14 and 34:34)and the PF-127 absorbed on different monolayers(the composition are DMPC, DMPC/Vit-E and DMPC/cholesterol)at the air/liquid interface at 25 . For mixed DMPC/PF-127 adsorption monolayers system at the air/water interface, the measurements of equilibrium surface tensions and surface pressure-area per molecule(Π-A) isotherms were carried out. The results of the mixed monolayer, the equilibrium surface tensions increased with the PF-127 concentration. But the excess of surface concentration is non- linear. TheΠ-A isotherms of the behavior of mixed DMPC/PF-127 monolayers indicate that the addition of the PF-127increased the shift percentages and the transition phases were obviously.
The behavior of the PF-127 adsorbed on different monolayers were investigated from the measurements of the change of surface pressure with time andΠ-A isotherms. In the PF-127 adsorption of monolayer systems, the equilibrium adsorption surface pressure increased with the PF-127 concentration and the initial surface pressure. The behavior of PF-127 adsorbed on DMPC/Vit-E and DMPC/cholesterol mixed monolayers, the ranges of equilibrium adsorption surface pressures are 15.8~28.3mN/m and 20.3~27.7mN/m, indicated that the addition of α-tocopherol and cholesterol change the distance of mixed monolayers. TheΠ-A isotherms of the PF-127 adsorbed to balance indicate that the transition phases were carried out and the PF-127 might be insert or absorb to monolayers. However, at higher surface pressure, the PF-127 molecules are squeezed into the subphase. From the DSC (differential Scanning Calorimetry ) experiments of liposome, the change of temperatures of phase transition regardless of the PF-127 incorporated or adsorbed to liposomes, which suggest the PF-127 does not insert or absorb deeply. Finally, the results obtained in this study support that the PF-127 can be readily absorbed or inserted onto liposome, providing steric barrier , preventing the fusion or aggregation of liposomes.
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