Shome Anshupriya, Debnath Sisir, Das Prasanta Kumar
Department of Biological Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, India.
Langmuir. 2008 Apr 15;24(8):4280-8. doi: 10.1021/la704024p. Epub 2008 Mar 7.
The present study describes the rational design and synthesis of amino acid-based amphiphilic hydrogelators, which were systemically fine-tuned at the head group to develop pH-responsive hydrogels. To understand the basic structural requirements of a low molecular weight amphiphilic hydrogelator, 10 analogous amphiphiles based on L-phenylalanine and L-tyrosine with structurally related head group were synthesized. Among them, three with quaternary ammonium substitution at the head group formed transparent hydrogels at room temperature while others were unable to gelate water. To establish correlations between the head group architecture of the gelators and their supramolecular arrangements, a variety of spectroscopic and microscopic techniques were investigated that showed that a balance between hydrophilicity and hydrophobicity is required to achieve hydrogelation. Interestingly, the gelator with tyrosinate in its head group showed remarkable response toward external pH. All hydrogels including the pH-responsive one were used in the controlled and/or pH-triggered release of entrapped (with in hydrogels) vitamin B12 and cytochrome c at different pHs. Since the hydrogels were formed at room temperature without heating, this could be very important during the entrapment of biomolecules such as proteins because of their heat sensitivity. At biological pH (7.4), the release of entrapped biomolecules from all three hydrogels was caused by diffusion through the gel structure, but at endosomal pH (approximately 5.5) and further lower pH, the release rate of biomolecules from the pH-responsive hydrogel with tyrosinate head group (pKa approximately equal to 7.2) increased by 9-10-fold compared to that observed at physiological pH, because of gel dissolution. Retention of the structure and activity of released biomolecule has established the prospect of the hydrogel as an efficient drug delivery vehicle.
本研究描述了基于氨基酸的两亲性水凝胶剂的合理设计与合成,这些水凝胶剂在头部基团进行了系统的微调以开发pH响应性水凝胶。为了了解低分子量两亲性水凝胶剂的基本结构要求,合成了10种基于L-苯丙氨酸和L-酪氨酸且具有结构相关头部基团的类似两亲物。其中,三种在头部基团有季铵取代的在室温下形成透明水凝胶,而其他的则不能使水凝胶化。为了建立凝胶剂的头部基团结构与其超分子排列之间的相关性,研究了各种光谱和显微镜技术,结果表明实现水凝胶化需要亲水性和疏水性之间的平衡。有趣的是,头部基团含有酪氨酸根的凝胶剂对外部pH表现出显著响应。所有水凝胶,包括pH响应性水凝胶,都用于在不同pH下对包裹在水凝胶中的维生素B12和细胞色素c进行可控和/或pH触发释放。由于水凝胶是在室温下无需加热形成的,这在包裹蛋白质等生物分子时可能非常重要,因为它们对热敏感。在生理pH(7.4)下,所有三种水凝胶中包裹的生物分子的释放是通过凝胶结构扩散引起的,但在内体pH(约5.5)及更低pH下,与生理pH下观察到的相比,具有酪氨酸根头部基团(pKa约等于7.2)的pH响应性水凝胶中生物分子的释放速率增加了9至10倍,这是由于凝胶溶解。释放的生物分子的结构和活性的保留确立了水凝胶作为高效药物递送载体的前景。