Progress in nuclear magnetic resonance studies of surfactant systems

Liu, Xingcen; Yu, Qun; Song, Aixin; Dong, Shuli; Hao, Jingcheng

doi:10.1016/j.cocis.2019.10.006

Cited by 11 publications

(11 citation statements)

References 71 publications

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“…The use of 1 H NMR is a well-established method for determination of CMC [ 10 , 27 ]. In this study, the chemical shift of lactate was used to measure changes in the chemical environment due to micelle formation ( Figure 3 ).…”

Section: Resultsmentioning

confidence: 99%

“…Emulsion activity (emulsion activity index; EAI) determines the obtainable interfacial area between oil and water per unit weight of protein or product, and emulsion stabilizing ability (emulsion stability index; ESI) indicates the emulsifying effect over time [ 25 ]. Critical micelle concentration (CMC) indicates the minimum concentration of a product needed for maximum reduction of the surface-tension and can be assessed by different methods based on fluorescence, conductivity, surface-tension, or 1 H nuclear magnetic resonance (NMR) [ 26 , 27 ]. High CMC values imply poor surface-activity, i.e., a high concentration of the given surfactant is needed to reduce the surface-tension [ 10 , 27 ].…”

Section: Introductionmentioning

confidence: 99%

“…Critical micelle concentration (CMC) indicates the minimum concentration of a product needed for maximum reduction of the surface-tension and can be assessed by different methods based on fluorescence, conductivity, surface-tension, or 1 H nuclear magnetic resonance (NMR) [ 26 , 27 ]. High CMC values imply poor surface-activity, i.e., a high concentration of the given surfactant is needed to reduce the surface-tension [ 10 , 27 ]. Measurements of properties related to emulsion capabilities of protein hydrolysates are challenging to standardize.…”

Section: Introductionmentioning

confidence: 99%

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Emulsion and Surface-Active Properties of Fish Solubles Based on Direct Extraction and after Hydrolysis of Atlantic Cod and Atlantic Salmon Backbones

Steinsholm

Oterhals

Underhaug

et al. 2020

Foods

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The focus on natural foods and “clean” labeled products is increasing and encourages development of new biobased ingredients. Fish solubles derived from downstream processing of side stream materials in the fish filleting industries have potential as emulsifiers based on their surface-active and emulsion stabilizing properties. The aim of this study was to evaluate and compare emulsion properties and critical micelle concentration (CMC) of direct protein extracts and protein hydrolysates based on fish backbones, and to identify associations between molecular weight distribution and process yield with the studied physicochemical properties. Protein extracts and enzymatic protein hydrolysates were produced based on two raw materials (cod and salmon backbones), two enzymes with different proteolytic specificity, and varying hydrolysis time. Emulsion activity index (EAI), emulsion stability index (ESI) and CMC were measured and compared with casein as a reference to protein-based emulsifiers. Protein hydrolysis was found to have negative impact on EAI and CMC, likely due to generation of small peptides disrupting the amphiphilic balance. The direct protein extracts had comparable EAI with casein, but the latter had superior ESI values. Protein hydrolysates with acceptable EAI could only be obtained at the expense of product yield. The study emphasizes the complexity of physicochemical properties of protein hydrolysates and discusses the challenges of achieving both good surface-active properties and high product yield.

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Section: Resultsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

Emulsion and Surface-Active Properties of Fish Solubles Based on Direct Extraction and after Hydrolysis of Atlantic Cod and Atlantic Salmon Backbones

Steinsholm

Oterhals

Underhaug

et al. 2020

Foods

View full text Add to dashboard Cite

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“…Isothermal titration calorimetry (ITC) has been considered as the preferred method to characterize the thermodynamics of intermolecular interactions with high sensitivity − and has been applied in many areas such as the interactions between surfactant and small molecule, , biological micromolecule, − or polymer , as well as biomimicking assemblies (e.g., liposomes and micelles). , NMR can provide noninvasively information on microscopic structure, intermolecular interaction, and surfactant aggregation behavior at the molecular level. − The combination of ITC and NMR technology is conducive to a comprehensive understanding of the mechanism of intermolecular interaction from both macro and micro aspects.…”

Section: Introductionmentioning

confidence: 99%

Activation and Inhibition of Isomerization of a Cationic Azobenzene Surfactant in the Large Void Space of Polyglycerol Dendron Micelles

et al. 2023

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Owing to the unique geometric structure of dendritic amphiphiles with voluminous dendrons, their micelles can harbor a large void space, which provides a new research focus and approach for micellar functionalization. In this work, we used the void space to construct a UV responsive micelle system of the mixed dendritic amphiphile (C12-(G3)2) and cationic azobenzene surfactant (C4AzoTAB). The synthesized C12-(G3)2 that possesses double third generation polyglycerol (PG) dendrons and a single alkyl chain is expected to highlight the large void space within the inside of the micelles. Thus, the aims of this work are to achieve the isomerization of C4AzoTAB in situ and to deeply understand the intermolecular interaction in the mixed micelles. The effect of the large void room with a wall decorated with the ether oxygen atoms on the isomerization of C4AzoTAB was studied by isomerization kinetics, conductivity measurements, isothermal titration calorimetry (ITC), and 1H NMR and 2D NOESY spectroscopies. The isomerization behavior of C4AzoTAB in C12-(G3)2 micelles was presented in terms of its kinetic constant, counterionic association, interaction enthalpy, and position and orientation of C4AzoTAB. The results of NMR and conductivity show that the quaternary ammonium group of C4AzoTAB situates on the surface of the mixed micelles with C12-(G3)2 both before and after UV-irradiation, while the position of azobenzene group in C12-(G3)2 micelles depends on its conformation. The C12-(G3)2 micelles can inhibit the UV response of the trans-isomer and activate the thermal relaxation of the cis-isomer, which has a potential application in the field of light-controlled smart nanocarriers.

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“…23 Furthermore, a review has been conducted on the progress made in the characterization of the physicochemical properties of surfactants in solution. 35 The primary objective of this study is to investigate the influence of the benzene ring effect in the headgroup of anionic and cationic surfactants on the transition in the aggregate structure. The hydrophobic carbon chain length is kept uniform at 12 CH 2 units (as depicted in Figure 1).…”

Section: ■ Introductionmentioning

confidence: 99%

Strong Synergistic Molecular Interaction in Catanionic Surfactant Mixtures: Unravelling the Role of the Benzene Ring

Wang,

Xiao,

et al. 2023

Langmuir

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Noncovalent interactions play a crucial role in driving the formation of diverse self-assembled structures in surfactant systems. Surfactants containing a benzene ring structure are an important subset of surfactants. These surfactants exhibit unique colloid and interfacial properties, which give rise to fascinating transformations in the aggregate structures. These transformations are directly influenced by specific noncovalent interactions facilitated by the benzene ring structure including cation−π and π−π interactions. Investigating catanionic surfactant systems that incorporate benzene ring structures provides valuable insights into the distinct noncovalent interactions observed in mixed surfactant systems. Our approach involved studying the enthalpy change ΔH during the titration process, utilizing isothermal titration calorimetry (ITC). Simultaneously, we employed cryogenic transmission electron microscopy (cryo-TEM) to observe the corresponding self-assembly structures. To gain further insight, we delved into the noncovalent interactions of the mixed systems by analyzing the molecular environments variations through chemical shifts of the aggregates using proton magnetic resonance ( 1 H NMR). The intermolecular interaction was also confirmed by the two-dimensional nuclear Overhauser enhancement spectroscopy (2D NOESY). We conducted a systematic study of the effects of NaCl concentrations, molar ratios, and molecular structures of surfactants on aggregate structures. The existence forms of surfactants are closely linked to the shape of the titration curve and the transition of the aggregate structures. When cationic surfactants were titrated into sodium dodecylbenzenesulfonate (SDBS) micelle solutions, the dominant cation−π interaction leads to the direct formation of vesicle structures. Conversely, when the SDBS system is titrated into benzyldimethyldodecylammonium chloride (DDBAC) micelles, a delicate balance of multiple noncovalent interactions, including cation−π, π−π, hydrophobic, and electrostatic forces, results in a range of aggregate structure transformations such as worm-like micelles and vesicular structures.

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Progress in nuclear magnetic resonance studies of surfactant systems

Cited by 11 publications

References 71 publications

Emulsion and Surface-Active Properties of Fish Solubles Based on Direct Extraction and after Hydrolysis of Atlantic Cod and Atlantic Salmon Backbones

Emulsion and Surface-Active Properties of Fish Solubles Based on Direct Extraction and after Hydrolysis of Atlantic Cod and Atlantic Salmon Backbones

Activation and Inhibition of Isomerization of a Cationic Azobenzene Surfactant in the Large Void Space of Polyglycerol Dendron Micelles

Strong Synergistic Molecular Interaction in Catanionic Surfactant Mixtures: Unravelling the Role of the Benzene Ring

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