Deep Eutectic Solvent- and Ionic Liquid-Based Surfactant-Free Microemulsion Stabilized by H-Bonded Clusters: Interfacial Stabilization and Superactivity of Cytochrome-c

IF 4.4 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Langmuir Pub Date : 2026-10-20 Epub Date: 2026-10-06 DOI:10.1021/acs.langmuir.6c03164
Rajwinder Kaur, Muskan Kondal, Ravi Dutt, Raghav Singhal, Jitendra Bahadur, Tejwant Singh Kang
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引用次数: 0

Abstract

The need to develop novel and sustainable media without using conventional surfactants has driven the development of surfactant-free microemulsions (SFMEs). Deep eutectic solvents (DESs) and ionic liquids (ILs) are great alternatives to conventional organic solvents, using which SFMEs can be prepared. Herein, an SFME has been prepared using a DES based on the natural components L-arginine and lactic acid as the polar phase; 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonylimide), a hydrophobic ionic liquid (HIL), as the nonpolar phase; and ethanol as an amphiphile. The SFME has been duly characterized to establish its structural organization at the molecular level by employing various techniques such as conductivity measurements, dynamic light scattering (DLS), small-angle X-ray scattering (SAXS), Fourier-transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. Investigations on the internal structure of the SFME reveal that ethanol does not form an effective barrier layer, instead, it forms hydrogen-bonded (H-bonded) solvent domains interacting mainly with DES nanoclusters, followed by the imidazolium cation at the HIL polar–nonpolar interface. The presence of such nanoinhomogeneity at the solvent interfaces imparts an associative nature to microemulsion droplets, which has never been reported before. The prepared SFME has been employed as a nanoreactor to explore the catalytic activity of cytochrome-c (Cyt-c). Variation in the phase composition of the SFME markedly affects the enzyme activity, wherein the DES-in-HIL phase of the SFME offers an optimal environment for ∼6.5 folds enhancement in enzyme activity as compared to that observed in buffer. The favorable cation-π and H-bonding interactions of arginine and lactic acid at the DES–ethanol interface, along with ethanol clusters, stabilize the structure of Cyt-c. This study provides new insights into the structural and functional aspects of SFMEs, which will encourage the development of new SFME systems for a broad spectrum of biocatalytic applications, along with the utilization of nanoinhomogeneity for constructing hierarchically self-assembled materials.

由H键团簇稳定的深度共析溶剂和离子液体基无表面活性剂微乳液:细胞色素c的界面稳定性和超活性
开发新型和可持续的介质而不使用传统表面活性剂的需求推动了无表面活性剂微乳液(SFMEs)的发展。深共晶溶剂(DESs)和离子液体(ILs)是传统有机溶剂的良好替代品,可用于制备SFMEs。本文以天然成分l -精氨酸和乳酸为极性相的DES制备了SFME;1-乙基-3-甲基咪唑二(三氟甲基磺酰亚胺),疏水离子液体(HIL),作为非极性相;乙醇是两亲性的。利用电导率测量、动态光散射(DLS)、小角x射线散射(SAXS)、傅里叶变换红外(FTIR)光谱和核磁共振(NMR)光谱等多种技术,对SFME进行了表征,并在分子水平上建立了其结构组织。对SFME内部结构的研究表明,乙醇并没有形成有效的阻挡层,而是形成了主要与DES纳米团簇相互作用的氢键(h键)溶剂畴,随后在HIL极性-非极性界面上形成咪唑阳离子。这种纳米不均匀性在溶剂界面的存在赋予微乳液滴一种结合性质,这在以前从未被报道过。制备的SFME作为纳米反应器,研究了细胞色素c (Cyt-c)的催化活性。SFME相组成的变化显著影响酶活性,其中SFME的DES-in-HIL相提供了与缓冲液相比酶活性增强约6.5倍的最佳环境。精氨酸和乳酸在des -乙醇界面上良好的阳离子-π和氢键相互作用,以及乙醇簇,稳定了Cyt-c的结构。这项研究为SFME的结构和功能方面提供了新的见解,这将鼓励开发新的SFME系统,用于广泛的生物催化应用,以及利用纳米不均匀性构建分层自组装材料。
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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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