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Cholesterol Protects Phosphatidylcholine Liposomes from N,N-dimethyl-l-dodecanamine N-oxide Influence

机译:胆固醇保护磷脂酰胆碱脂质体免受N,N-二甲基-1-十二烷胺N-氧化物的影响

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摘要

The interaction of N,N-dimethyl-l-dodecanamine N-oxide (C12NO) with egg yolk phosphatidylcholine (EYPC) liposomes containing cholesterol (CHOL) was studied. The perturbation of CHOL-EYPC bilayers in unilamellar liposomes (ULL) was observed by the leakage of fluorescence probe calcein. Weak leakage is observed at low surfactant concentration c(C12NO) (minimal perturbation of the bilayer) followed by an intensive leakage at a middle c(C12NO) (creation of pores). No change in fluorescence intensity was measured at high c(C12NO) (calcein totally released from liposomes). The higher CHOL amount in the bilayer, the more surfactant is needed to create pores in the bilayer. Solubilization of CHOL-EYPC ULL induced by C12NO was studied turbidimetrically. The solubilization curve consists of three parts: saturation of bilayer at low c(C12NO) (liposomes are preserved), followed by solubilization (liposome mixed micelle transition) and post-solubilization. The C12NO concentration needed for the onset of the solubilization raise with the increase of n(CHOL):n(EYPC). The structure of liposomes is still preserved at total calcein release tor all n(CHOL):n(EYPC).
机译:研究了N,N-二甲基-1-十二烷胺N-氧化物(C12NO)与蛋黄磷脂酰胆碱(EYPC)含胆固醇脂质体(CHOL)的相互作用。通过泄漏荧光探针钙黄绿素观察到单层脂质体(ULL)中CHOL-EYPC双层的扰动。在低表面活性剂浓度c(C12NO)下观察到微弱渗漏(双层的最小扰动),随后在中间c(C12NO)处出现严重渗漏(孔隙形成)。在高c(C12NO)(钙素从脂质体完全释放)的情况下,未测量到荧光强度的变化。双层中的CHOL含量越高,则需要更多的表面活性剂才能在双层中形成孔。用比浊法研究了C12NO诱导的CHOL-EYPC ULL的增溶作用。增溶曲线由三部分组成:双层在低c(C12NO)下饱和(脂质体被保留),然后增溶(脂质体混合胶束过渡)和后增溶。溶解开始所需的C12NO浓度随n(CHOL):n(EYPC)的增加而升高。脂质体的结构在全部钙黄绿素释放或全部n(CHOL):n(EYPC)时仍保留。

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