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十六醇聚醚乳膏的结构与流变学:醇链长度和同系物组成的影响

Structure and rheology of cetomacrogol creams: the influence of alcohol chain length and homologue composition.

作者信息

Eccleston G M

出版信息

J Pharm Pharmacol. 1977 Mar;29(3):157-62. doi: 10.1111/j.2042-7158.1977.tb11274.x.

Abstract

Liquid paraffin-in-water emulsions prepared with cetomacrogol 1000 and alcohols cetostearyl (A), cetyl (B), steryl (C) and myristyl (D) were examined by microscopical, particle size analytical and rheological (continuous shear, small strain creep, and oscillation) techniques at 25 degrees as they aged over 30 days. The particle sizes of the emulsions were similar and did not increase significantly with age. Thus the rheological stabilities were not correlated with particle size distributors, but rather with viscoelastic networks formed in the continuous phases when the non-ionic mixed emulsifiers interacted with water. The rheological properties of emulsions B and D differed from those of emulsion C. Emulsion A, of mixed homologue composition, showed some properties similar to each of the pure alcohol emulsions. Emulsions B and D were semi-solid immediately after preparation whereas emulsion C was so mobile initially that small strain data were not derived. On ageing, the consistencies of B and D changed slightly initially, and then remained essentially constant. In contrast, the consistency of emulsion C increased on ageing, especially over the first few days when there was a change from mobile liquid to semisolid. Emulsion A was a semisolid initially but like emulsion C increased in consistency especially over the first 24 h. Continuous shear data indicated that this emulsion was the most resistant to structure breakdown. Microscopical examination supported the view that the networks formed in emulsion A were the most extensive and that stearyl alcohol networks in C formed comparatively slowly. Although the cetomacrogol/pure alcohol networks were diffuse and sometimes crystallized, they did not rapidly disintegrate on storage as did the ionic surfactant/pure alcohol networks examined previously.

摘要

用十六十八醇、鲸蜡醇、硬脂醇和肉豆蔻醇与聚氧乙烯十六十八醚1000制备的水包液状石蜡乳剂,在25℃下放置30天的老化过程中,通过显微镜、粒度分析和流变学(连续剪切、小应变蠕变和振荡)技术进行了检测。乳剂的粒度相似,且不会随老化而显著增加。因此,流变稳定性与粒度分布无关,而是与非离子混合乳化剂与水相互作用时在连续相中形成的粘弹性网络有关。乳剂B和D的流变特性与乳剂C不同。具有混合同系物组成的乳剂A表现出一些与每种纯醇乳剂相似的特性。乳剂B和D在制备后立即为半固体,而乳剂C最初流动性很强,以至于无法获得小应变数据。老化时,B和D的稠度最初略有变化,然后基本保持不变。相比之下,乳剂C的稠度在老化时增加,尤其是在最初几天,从流动性液体变为半固体时。乳剂A最初是半固体,但与乳剂C一样,稠度增加,尤其是在最初的24小时内。连续剪切数据表明,这种乳剂对结构破坏的抵抗力最强。显微镜检查支持了以下观点:乳剂A中形成的网络最为广泛,而C中的硬脂醇网络形成相对较慢。尽管聚氧乙烯十六十八醚/纯醇网络是分散的,有时会结晶,但它们在储存时不会像先前检测的离子表面活性剂/纯醇网络那样迅速分解。

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