郑俊民, 顾学裘, 张尔志, 杨红. 多相脂质体(139)不同温度下的1HNMR谱变化和13CNMR谱T1的研究J. 药学学报, 1985, 20(1): 67-70.
引用本文: 郑俊民, 顾学裘, 张尔志, 杨红. 多相脂质体(139)不同温度下的1HNMR谱变化和13CNMR谱T1的研究J. 药学学报, 1985, 20(1): 67-70.
ZHENG Jun-Min, GU Xue-Qiu, ZHANG Er-Zhi , Yang Hong, . STUDIES ON 1H-NMR CHANGE AT DIFFERENT TEMPERATURES AND 13C-NMR T1 OF POLYPHASE (139)J. Acta Pharmaceutica Sinica, 1985, 20(1): 67-70.
Citation: ZHENG Jun-Min, GU Xue-Qiu, ZHANG Er-Zhi , Yang Hong, . STUDIES ON 1H-NMR CHANGE AT DIFFERENT TEMPERATURES AND 13C-NMR T1 OF POLYPHASE (139)J. Acta Pharmaceutica Sinica, 1985, 20(1): 67-70.

多相脂质体(139)不同温度下的1HNMR谱变化和13CNMR谱T1的研究

STUDIES ON 1H-NMR CHANGE AT DIFFERENT TEMPERATURES AND 13C-NMR T1 OF POLYPHASE (139)

  • 摘要: 应用FT-NMR观察多相脂质体(139)不同温度下的1HNMR谱的变化显示:78~90℃之间,谱线有突变,升至108℃后再冷至室温,振摇,谱线复原。添加兼性大分子化合物,磷脂的亲水端和疏水端的质子峰峰形变矮变宽。其~(18)CNMR的弛豫时间T1:端甲基为0.90,酰头基为0.60,说明多相脂质体(139)比大豆磷脂双分子层的流动性变小,酰头基的自由度增加。

     

    Abstract: The polyphase liposome (139) was made of soybean lecithin, cholesterol, tween, span, PVP and a vegetable constituent. Its technological characteristics were investigated by means of 1HNMR at different temperatures. It was found that two distinct high resonances for—CH3(0.88) and—(CH2)n—(1.27)appeareal from 78° to 90℃ in the upfield region of the 1HNMR spectrum of liposomes in deuterowater. This shows that the liposome preparation produces phase change at temperatures above 78℃. However, when the preparation was cooled to room temperature, the spectrum returned to its original pattern. So the injectable preparation may be subjected to steam sterilization for large scale production.The addition of amphipathic compounds broadened the resonances of terminal methyl group, methylene group and headgroup of lecithin. When 13CNMR spectra cf polyphase liposome (139) were observed, we found that the relaxation time of 13carbon nuclei T1 increased along the alkyl chains towards the terminal methyl group. When comparisons were made between liposomes and lecithin, a smaller T1 value of the terminal methyl group and a larger T1 value of—N(CH3)3 group were obtained for the former. This indicates that the terminal methyl group is less mobile and the—N(CH3)3 group has a higher degree of mobility compared with the lecithin in H2OAll the measurements were performed on Jeol-FX60 QNMR.

     

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