Roy Sangita, Dasgupta Antara, Das Prasanta Kumar
Department of Biological Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700 032, India.
Langmuir. 2007 Nov 6;23(23):11769-76. doi: 10.1021/la701558m. Epub 2007 Oct 6.
The search for low molecular weight hydrogelators (LMWHs) with varying structural motif is getting intense because of its potential application in biomedicines as well as the diversified area of nanobiotechnology. Hydrophobic interaction is one of the most crucial parameters in the design and development of such LMWHs. To this notion, a methodical investigation was carried out to find the influence of varying alkyl chain length of amphiphile on water gelation efficacy, which has been only marginally addressed in the literature to date. We have synthesized a series of low molecular weight L-tryptophan-based gelators, some of which are excellent gelator for plain water, an essential criterion for biological use. The alkyl chain induced hydrophobicity at the molecular level has remarkable influence in modulating water immobilization. Water gelation efficiency was improved more than 100 times on moving from 10 to 18 carbon atoms. The self-aggregation behavior of these thermoreversible hydrogelators investigated through different spectroscopic and microscopic techniques showed that an optimum balance between hydrophilicity and hydrophobicity is indeed essential, which can be largely regulated by varying the alkyl chain length. Thus, the study offers better understanding toward tailoring the properties of gel in plain water and thereby paving the way for potential applications.
由于低分子量水凝胶剂(LMWHs)在生物医学以及纳米生物技术的多个领域具有潜在应用,对具有不同结构基序的LMWHs的研究日益激烈。疏水相互作用是此类LMWHs设计与开发中最关键的参数之一。基于这一理念,我们进行了系统研究,以探寻两亲分子不同烷基链长度对水凝胶化效果的影响,而迄今为止该问题在文献中仅有少量涉及。我们合成了一系列基于L-色氨酸的低分子量凝胶剂,其中一些是纯水的优良凝胶剂,这是生物应用的一个基本标准。烷基链在分子水平上诱导的疏水性对调节水的固定化有显著影响。从10个碳原子增加到18个碳原子时,水凝胶化效率提高了100多倍。通过不同的光谱和显微镜技术对这些热可逆水凝胶剂的自聚集行为进行研究表明,亲水性和疏水性之间的最佳平衡确实至关重要,这可以通过改变烷基链长度在很大程度上进行调节。因此,该研究有助于更好地理解在纯水中定制凝胶性质,从而为潜在应用铺平道路。