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包埋于热可逆水凝胶中的内部自组装颗粒。

Internally self-assembled particles entrapped in thermoreversible hydrogels.

作者信息

Guillot Samuel, Tomsic Matija, Sagalowicz Laurent, Leser Martin E, Glatter Otto

机构信息

Institute of Chemistry, University of Graz, Heinrichstrasse 28, A-8010 Graz, Austria.

出版信息

J Colloid Interface Sci. 2009 Feb 1;330(1):175-9. doi: 10.1016/j.jcis.2008.10.065. Epub 2008 Oct 30.

Abstract

The present study describes the development of thermogelling emulsions by the entrapment of internally self-assembled emulsion droplets (ISAsomes) within a thermoreversible hydrogel made of kappa-carrageenan. The droplets are emulsified mesophases of cubic or hexagonal order, or emulsified micro-emulsions. Above 60 degrees C, the system was fluid and composed of a mixture of internally nanostructured small droplets and polymer chains dispersed in water. Below 60 degrees C, a physical gel with entrapped droplets was formed. A tuning of the temperature in order to switch between the gel and solution state did not affect the particles in terms of size. The thermoreversible behavior of the loaded polymer network and the effects on the internal structure of cubosomes, hexosomes and emulsified micro-emulsions was investigated by SAXS. We showed that the phase borders may be shifted due to the presence of the kappa-carrageenan network, which alter the internal nanostructure of the droplets. This can induce a transformation from emulsified micro-emulsions to micellar cubosomes. In the hexagonal case, the lattice parameters of the hexosomes are slightly modified.

摘要

本研究描述了通过将内部自组装乳液滴(ISAsomes)包裹在由κ-卡拉胶制成的热可逆水凝胶中来制备热凝胶乳液。这些液滴是立方或六方有序的乳化中间相,或是乳化微乳液。在60摄氏度以上,该体系呈流体状态,由内部具有纳米结构的小液滴和分散在水中的聚合物链的混合物组成。在60摄氏度以下,形成了包裹有液滴的物理凝胶。通过调节温度在凝胶态和溶液态之间切换,不会影响颗粒的大小。利用小角X射线散射(SAXS)研究了负载聚合物网络的热可逆行为以及对立方液晶相、六方液晶相和乳化微乳液内部结构的影响。我们发现,由于κ-卡拉胶网络的存在,相界可能会发生移动,这会改变液滴的内部纳米结构。这可能会导致从乳化微乳液转变为胶束立方液晶相。在六方相的情况下,六方液晶相的晶格参数会略有改变。

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