Lithium Dodecyl Sulfate Research Articles

Association and clouding behaviour of surfactants in aqueous solution of propranolol hydrochloride drug: Understanding of the effects of potassium salts and temperatures

The investigation of the assembly of lithium dodecyl sulfate (LDS) and cloudy creation of triton X-100 (TX-100) in aqueous solution of amphiphilic drug propranolol hydrochloride (PLH) has been carried out by electrical conductivity and cloud point estimation method respectively. The influences of three potassium electrolytes (KCl, K2SO4, and K3PO4) on the micellization of LDS and clouding of TX-100 in presence of PLH drug have been examined. The conductivity experiments were conducted at temperatures between 288.15 and 323.15 K, with a 5 K interval.The introduction of PLH drug promotes the micelle formation of LDS up to 1 mmol kg−1 of drug. The critical micelle concentration (CMC) values of LDS in aqueous solution of PLH were shifted to lower values in aqueous electrolytes media. The cloud point (CP) of TX-100 + PLH system was observed to be increased with the rise in concentrations of PLH in aqueous medium. The reduction in the CP values of TX-100 and PLH mixed system has been attained with the enrichment of the concentrations of electrolytes and at a specific mole fraction of electrolytes, the CP values exhibited the order: CP (KCl (aq.)) > CP (K2SO4 (aq.)) > CP (K3PO4 (aq.)). The Gibbs free energy of assembly (ΔGm0) appeared as negative (spontaneous assembly) whereas ΔGc0 of clouding showed positive magnitudes indicating the nonspontaneous nature of the clouding process. The micellization of LDS demonstrate the endothermic and exothermic nature at lower and higher investigated temperature as revealed from the sign of ΔHm0values.. The positive values of entrpoyΔSm0 exhibit the micellization process to be entropically driven phenomena. The phase separation of TX-100 and PLH mixed system is entropy contributed in aqueous medium while the clouding in the presence of salts is enthalpy contributed evidenced from the negative enthalpy of clouding.

Combined Effects of pH Adjustment and Bentonite Addition Timing on Protein Stability of Sauvignon Blanc Wine

Background and Aims. Bentonite fining is commonly used in white wine production, which can lead to the loss of wine volume and aroma compounds. Many factors influence the efficacy of bentonite fining. The effect of pH adjustment and timing of bentonite addition were studied for their combined effects on Sauvignon Blanc wine protein haze formation and bentonite requirement at microscale and commercial scale. Methods and Results. Three bentonite addition timings were conducted on a juice pH adjustment trial: before fermentation, during fermentation, and after fermentation. The hot and cold test was utilized to determine the bentonite requirement for protein stabilization. Wine proteins were analyzed using a modified Coomassie brilliant blue (CBB) assay, lithium dodecyl sulphate polyacrylamide gel electrophoresis (LDS‐PAGE), and sodium dodecyl sulphate capillary gel electrophoresis (SDS‐CGE). Lower juice pH (2.80 and 3.00) resulted in sluggish fermentation, whereas the presence or absence of bentonite during fermentation showed similar fermentation kinetics at each pH. The presence of bentonite remaining in contact with ferment improved the completion of fermentation for the most sluggish ferment (pH 2.80). Commercial wine made from same batch of juice was adjusted to different pH values, and low‐pH wines had a lower wine protein content and an increasing protein adsorption efficiency of bentonite fining, leading to lower bentonite requirement. Conclusions. Bentonite addition during fermentation was the most efficient in protein removal but fining after fermentation required the least overall bentonite dosage. The different fermentation scales (i.e., microscale versus commercial scale) slightly affected wine protein contents but not molecular weight (MW) profiles. Protein contents and MW profiles in stabilized wines were affected by the original juice pH with more complex patterns from high‐pH juice. Significance of the Study. The findings of this study provide valuable information on optimization of bentonite fining to minimize the dosage so as to reduce the loss of wine volume and quality.

Highly enantioselective hydroxymethylation of unmodified α-substituted aryl ketones in water.

Catalytic asymmetric direct-type aldol reactions of ketones with aldehydes are a perennial puzzle for organic chemists. Notwithstanding the emergence of a myriad of chiral catalysts to address the inherent reversibility of the aldol products, a general method to access acyclic α-chiral ketones from prochiral aryl ketones has remained an unmet synthetic challenge. The approach outlined herein is fundamentally different to that used in conventional catalysis, which typically commences with an α-proton abstraction by a Brønsted base. The use of a chiral 2,2'-bipyridine scandium complex enabled the hydroxymethylation of propiophenone to be run under base-free conditions, which avails effectual suppression of hydrolytic deactivation of the Lewis acid catalyst. Intriguingly, the use of water as a reaction medium had an overriding effect on the progress of the reaction. The sagacious selection of sodium dodecyl sulfate and lithium dodecyl sulfate as surfactants allowed a variety of propiophenone derivatives to react in a highly enantioselective manner.

Lithium‐Ion Batteries Containing Surfactants for the Protection of Graphite Anode against the Passivation Layer Byproducts

AbstractThe electrolyte is an essential component of all electrochemical devices, including lithium‐ion batteries (LIBs). During the initial charging process, a portion of the electrolyte (usually a mixture of organic solvents and lithium salts) decomposes at the anode surface, forming a thin layer of solid electrolyte interface (SEI). This study examines the physicochemical properties of three surfactants: lithium dodecyl sulfate (LiDS), polyoxyethylene ether Forafac 1110D (LiF1110), and lithium perfluoro octanesulfonate Forafac 1185D (LiFOS). Initially, their thermal properties (surface tension and contact angle) are determined. Then, electrochemical tests (cyclic voltammetry, galvanostatic charge‐discharge cycling, and electrochemical impedance spectroscopy) followed by ex‐situ X‐ray photoelectron spectroscopy (XPS) measurements on the graphite anodes in a standard electrolyte ethylene carbonate/propylene carbonate/3 dimethyl carbonate +1 mol L−1 LiPF6 are conducted to compare the surfactants′ action according to their chemical structure, as well as their effect on the interface properties of the formed SEI. The results indicate that surfactants improve electrode interfaces due to their amphiphilic character, preventing the harmful effects of passivation layer salts (LiF, LiOH, Li2O, etc.) that deposit on the graphite interfaces. The three surfactants affect the cycling behavior and performance of the half‐cells differently depending on their ionic or nonionic nature and the polarity or non‐polarity of the salt (e. g., lithium fluoride LiF, lithium oxide Li2O), with LiF1110 demonstrating the best performance.

Multiple Myeloma with Aberrant CD3 Expression in a Red-Lored Amazon Parrot (Amazona autumnalis).

A 20-year-old, female, red-lored Amazon parrot (Amazona autumnalis) was presented for a 2-week history of weakness. On physical examination, the bird was quiet, fluffed, weak, and had a distended coelom. Radiographic and ultrasound imaging revealed coelomic distention, increased pulmonary parenchymal opacity, renomegaly, dilated intestines, and a thickened ventricular wall. The results of a complete blood cell count indicated the patient was anemic (28%) and had intermediate to large lymphocytes with immature chromatin that were suspected to be neoplastic. Immunocytochemistry on peripheral blood determined that the suspected circulating neoplastic cells were cluster of differentiation (CD) 3+ and occasionally expressed multiple myeloma oncogene 1 (MUM1). Abnormalities from a plasma biochemistry panel were moderate hyperphosphatemia (6.8 mg/dL), marked hyperproteinemia (13.6 g/L), analbuminemia (0 g/dL), and marked hyperglobulinemia (13.6 g/dL). Agarose gel plasma protein electrophoresis documented the presence of albumin (1.2 g/dL) and monoclonal bands which, on reduced lithium dodecyl sulfate polyacrylamide gel electrophoresis, resolved as 60-kd and ∼25-kd bands consistent with immunoglobulin Y heavy and light chains. On the basis of these findings, multiple myeloma was diagnosed. Because of a poor prognosis, the bird was euthanized for postmortem examination. Bone marrow cytology from samples collected during the postmortem examination revealed 17.4% plasma cells and 24% large immature cells with occasional plasmacytoid features. Histopathologic findings included aggregates of neoplastic plasma cells in the bone marrow, spleen, kidney, liver, gastrointestinal tract, muscle, ovary, and brain. The neoplastic cells were strongly immunoreactive for MUM1 and cluster of differentiation 3 (CD3), but negative for CD79a, paired box protein 5, and CD20. This confirmed the clinical diagnosis of multiple myeloma. This report describes an avian immunoglobulin Y-secreting multiple myeloma with aberrant CD3 expression and pseudoanalbuminemia. Aberrant CD3 expression by avian multiple myeloma may explain previously published cases of birds with a monoclonal gammopathy and apparent T-cell lymphoma diagnosed by CD3 immunoreactivity.

Concentrated Lithium Dodecyl Sulfate Aqueous Electrolytes: Utilizing Self‐Assembly and Interfacial Adsorption for Aqueous Li‐ion Batteries

AbstractSince aqueous lithium‐ion batteries (LIBs) were first proposed, electrolyte design has been intensively studied. We report a simple anionic surfactant, i. e., a lithium dodecyl sulfate (LiDS)‐based aqueous electrolyte, capable of enhancing the Li ion transport properties in the bulk and protecting the electrode at the interface. The self‐assembly of DS anions into micelles effectively limited anion diffusion, enabling nearly single Li‐ion conduction in the bulk electrolyte. The interfacial adsorption of DS molecules formed a hydrophobic layer at the electrolyte/electrode interface under the electric field of the electric double layer, excluding water molecules from the interface. Consequently, the electrochemical window of the aqueous electrolyte was expanded to 3.0 V. This electrolyte improved the cycle performance and rate capability of the LiFePO4/LiTi2(PO4)3full‐cell compared to a 1.0 mol dm−3Li2SO4/H2O reference electrolyte. These results provide a new twist in the design of liquid electrolytes for aqueous LIBs.

Highly Enforced Rate Capability of a Graphite Anode via Interphase Chemistry Tailoring Based on an Electrolyte Additive.

The rate capability of lithium-ion batteries is highly dependent on the interphase chemistry of graphite anodes. Herein, we demonstrate an anode interphase tailoring based on a novel electrolyte additive, lithium dodecyl sulfate (LiDS), which greatly improves the rate capability and cyclic stability of graphite anodes. Upon application of 1% LiDS in a base electrolyte, the discharge capacity at 2 C is improved from 102 to 240 mAh g-1 and its capacity retention is enhanced from 51% to 94% after 200 cycles at 0.5 C. These excellent performances are attributed to the preferential absorption of LiDS and the as-constructed interphase chemistry that is mainly composed of organic long-chain polyether and inorganic lithium sulfite. The long-chain polyether possesses flexibility endowing the interphase with robustness, while its combination with inorganic lithium sulfite accelerates lithium intercalation/deintercalation kinetics via decreasing the resistance for charge transfer.

Investigation of polymer−surfactant complexes by both micellar solubilization and pre-column derivatization capillary electrophoresis

“Pseudo-polyanions” are formed in some mixtures of nonionic water-soluble polymers and anionic surfactants with ultraviolet (UV) absorption signals, which is verified by capillary electrophoresis (CE) equipped with an UV detector. However, it is still unclear whether two typical mixtures of PEG (polyethylene glycol)−LDS (lithium dodecylsulfate) and PEG−SDS (sodium dodecylsulfate) are pseudo-polyanions or not due to lack of necessary UV absorption. Therefore, with the help of UV probes or UV labeling reagents, micellar solubilization CE and pre-column derivatization CE are implemented to make the mixtures detectable or “visible” by a UV detector. Experimental results show that both PEG–LDS and PEG–SDS complexes are pseudo-polyanions verified by the above strategies. Combined with previous works, most mixtures of nonionic water-soluble polymers and anionic surfactants can form unique pseudo-polyanions by dint of ion bridge no matter whether with or without UV absorption. What’s more, the bridging-to-diffusion ion ratio and the charge-to-size ratio of pseudo-polyanions are dominated by the bridging ions, and the smaller the hydrated ionic radius (H+ < K+ < Na+ < Li+) is, the stronger the polyanion nature is.

Contribution of Different Molecules and Moieties to the Surface Tension in Aqueous Surfactant Solutions. II: Role of the Size and Charge Sign of the Counterions.

Understanding the role of the counterion species in surfactant solutions is a complicated task, made harder by the fact that, experimentally, it is not possible to vary independently bulk and surface quantities. Here, we perform molecular dynamics simulations at constant surface coverage of the liquid/vapor interface of lithium, sodium, potassium, rubidium, and cesium dodecyl sulfate aqueous solutions. We investigate the effect of counterion type and charge sign on the surface tension of the solution, analyzing the contribution of different species and moieties to the lateral pressure profile. The observed trends are qualitatively compatible with the Hofmeister series, with the notable exception of sodium. We point out a possible shortcoming of what is at the moment, in our experience, the most realistic nonpolarizable force field (CHARMM36) that includes the parametrization for the whole series of alkali counterions. In the artificial system where the counterion and surfactant charges are inverted in sign, the counterions become considerably harder. This charge inversion changes considerably the surface tension contributions of the counterions, surfactant headgroups, and water molecules, stressing the key role of the hardness of the counterions in this respect. However, the hydration free energy gain of the counterions, occurring upon charge inversion, is compensated by the concomitant free energy loss of the headgroups and water molecules, leading to a negligible change in the surface tension of the entire system.

Characterization and Specification of a Trivalent Protein-Based Pneumococcal Vaccine Formulation Using an Adjuvant-Free Nanogel Nasal Delivery System.

We previously developed a safe and effective nasal vaccine delivery system using a self-assembled nanosized hydrogel (nanogel) made from a cationic cholesteryl pullulan. Here, we generated three pneumococcal surface protein A (PspA) fusion antigens as a universal pneumococcal nasal vaccine and then encapsulated each PspA into a nanogel and mixed the three resulting monovalent formulations into a trivalent nanogel-PspA formulation. First, to characterize the nanogel-PspA formulations, we used native polyacrylamide gel electrophoresis (PAGE) to determine the average number of PspA molecules encapsulated per nanogel molecule. Second, we adopted two methods-a densitometric method based on lithium dodecyl sulfate (LDS)-PAGE and a biologic method involving sandwich enzyme-linked immunosorbent assay (ELISA)-to determine the PspA content in the nanogel formulations. Third, treatment of nanogel-PspA formulations by adding methyl-β-cyclodextrin released each PspA in its native form, as confirmed through circular dichroism (CD) spectroscopy. However, when nanogel-PspA formulations were heat-treated at 80 °C for 16 h, CD spectroscopy showed that each PspA was released in a denatured form. Fourth, we confirmed that the nanogel-PspA formulations were internalized into nasal mucosa effectively and that each PspA was gradually released from the nanogel in epithelial cells in mice. Fifth, LDS-PAGE densitometry and ELISA both indicated that the amount of trivalent PspA was dramatically decreased in the heat-treated nanogel compared with that before heating. When mice were immunized nasally using the heat-treated formulation, the immunologic activity of each PspA was dramatically reduced compared with that of the untreated formulation; in both cases, the immunologic activity correlated well with the content of each PspA as determined by LDS-PAGE densitometry and ELISA. Finally, we confirmed that the trivalent nanogel-PspA formulation induced equivalent titers of PspA-specific serum IgG and mucosal IgA Abs in immunized mice. These results show that the specification methods we developed effectively characterized our nanogel-based trivalent PspA nasal vaccine formulation.

Physicochemical studies on the micellization of anionic surfactants in the presence of long alkyl chain ionic liquid

The physicochemical properties on micellization of anionic surfactant, sodium dodecyl sulphate (SDS) and lithium dodecyl sulphate (LDS) in the presence of imidazolium-based ionic liquid 1-decyl-3-methylimidazolium tetrafluoroborate [Dmim][BF4] have been studied using surface tension and conductivity techniques. The interfacial and thermodynamic parameters have also been determined. FTIR has studied the aggregation behavior while aggregation number and Stern-Volmer constant is determined by fluorescence measurement. The current results indicate that the addition of [Dmim][BF4] to the anionic surfactant leads to a dramatic decrease in the CMC. The interaction of human serum albumin with micellar solution of SDS and LDS have been examined.

Insights Into the Mechanism of MCT8 Oligomerization.

Mutations in the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) result in MCT8 deficiency, characterized by severe intellectual and motor disability. The MCT8 protein is predicted to have 12 transmembrane domains (TMDs) and is expressed as monomers, homodimers, and homo-oligomers. This study aimed to delineate the mechanism of MCT8 oligomerization. Coimmunoprecipitation studies demonstrated that lithium dodecyl sulfate effectively disrupts MCT8 protein complexes, indicating the involvement of non-covalent interactions. Successive C-terminal truncations of the MCT8 protein altered the oligomerization pattern only if introduced in the N-terminal half of the protein (TMD1-6). The truncation at extracellular loop 1 (E206X) still allowed homodimerization, but completely abrogated homo-oligomerization, whereas both were preserved by the C231X mutant (at TMD2), suggesting that the minimally required oligomerization sites are located proximal of Cys231. However, mutant constructs lacking the intracellular N-terminus or TMD1 and 2 were still capable to form homo-oligomers. Therefore, other domains distal of Cys231 are also likely to be involved in the formation of extensive multidomain interactions. This hypothesis was supported by structural modeling. Despite multiple approaches, MCT8 oligomerization could not be fully abrogated unless a substantial part of the protein was removed, precluding detailed studies into its functional role. Together, our findings suggest that MCT8 oligomerization involves extensive noncovalent interactions between the N-terminal halves of MCT8 proteins. Most mutations identified in patients with MCT8 deficiency have only minor effects on MCT8 oligomerization and, thus, impaired oligomerization does not appear to be an important pathogenic mechanism.

Effective methods for the inactivation of Francisella tularensis.

Francisella tularensis (F. tularensis) is highly pathogenic to humans and must be handled under biosafety level 3 conditions. Samples used for the diagnosis and experimental analysis must be completely inactivated, although methods for the inactivation of F. tularensis are limited. In this study, effective methods for the inactivation of F. tularensis SCHU P9 and five other strains were determined by comparisons of colony-forming units between treated and control samples. The results showed that F. tularensis SCHU P9 was denatured by heat treatment (94°C for 3 min and 56°C for 30 min), filtration with a 0.22 μm filter, and the use of various solutions (i.e. >70% ethanol, methanol, acetone, and 4% paraformaldehyde). F. tularensis SCHU P9 remained viable after treatment with 50% ethanol for 1 min, filtration with a 0.45 μm filter, and treatments with detergents (i.e. 1% lithium dodecyl sulfate buffer, 1% Triton X-100 and 1% Nonidet P-40) at 4°C for 24 h. Additionally, F. tularensis SCHU P9 suspended in fetal bovine serum in plastic tubes was highly resistant to ultraviolet radiation compared to suspensions in water and chemically defined medium. The methods for inactivation of F. tularensis SCHU P9 was applicable to the other five strains of F. tularensis. The data presented in this study could be useful for the establishment of guidelines and standard operating procedures (SOP) to inactivate the contaminated samples in not only F. tularensis but also other bacteria.

Specific Ion Effects of Dodecyl Sulfate Surfactants with Alkali Ions at the Air-Water Interface.

The influence of Li+, Na+ and Cs+ cations on the surface excess and structure of dodecyl sulfate (DS−) anions at the air–water interface was investigated with the vibrational sum-frequency generation (SFG) and surface tensiometry. Particularly, we have addressed the change in amplitude and frequency of the symmetric S-O stretching vibrations as a function of electrolyte and DS− concentration in the presence of Li+, Na+ and Cs+ cations. For the Li+ and Na+ ions, we show that the resonance frequency is shifted noticeably from 1055 cm−1 to 1063 cm−1 as a function of the surfactants’ surfaces excess, which we attribute to the vibrational Stark effect within the static electric field at the air–water interface. For Cs+ ions the resonance frequency is independent of the surfactant concentration with the S-O stretching band centered at 1063 cm−1. This frequency is identical to the frequency at the maximum surface excess when Li+ and Na+ ions are present and points to the ion pair formation between the sulfate headgroup and Cs+ counterions, which reduces the local electric field. In addition, SFG experiments of the O-H stretching bands of interfacial H2O molecules are used in order to calculate the apparent double layer potential and the degree of dissociation between the surfactant head group and the investigated cations. The latter was found to be 12.0%, 10.4% and 7.7% for lithium dodecyl sulfate (LiDS), sodium dodecyl sulfate (SDS) and cesium dodecyl sulfate (CsDS) surfactants, which is in agreement with Collins ‘rule of matching water affinities’.

Effect of Hydrophobic Chains on Solubilization of Hydrocarbon and Fluorocarbon Surfactant Mixtures in Aqueous Solution.

We investigated the solubilization behavior of the hydrocarbon surfactant lithium dodecyl sulfate (LiDS) and the fluorocarbon surfactant lithium 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-1-octanesulfonate (LiFOS) in an aqueous solution to determine the controlled release mechanism of solubilizate. The LiDS system solubilized Sudan III, a hydrocarbon compound, whereas the LiFOS system did not, because of the immiscibility of the hydrocarbon and fluorocarbon compounds. The solubilization ability of the LiDS and LiFOS mixtures gradually decreased with increasing LiFOS bulk composition because the micelles mainly composed of LiDS transformed into micelles mainly composed of LiFOS. Furthermore, Sudan III solubilized in the aqueous LiDS was deposited when an aqueous LiFOS was added. The difference in the solubilization behavior between LiDS and LiFOS enabled the controlled release of the solubilizate.

Formyl Met-Leu-Phe-Stimulated FPR1 Phosphorylation in Plate-Adherent Human Neutrophils: Enhanced Proteolysis but Lack of Inhibition by Platelet-Activating Factor.

N-formyl-Met-Leu-Phe (fMLF) is a model PAMP/DAMP driving human PMN to sites of injury/infection utilizing the GPCR, FPR1. We examined a microtiter plate format for measurement of FPR1 phosphorylation in adherent PMN at high densities and found that a new phosphosensitive FPR1 fragment, 25K-FPR1, accumulates in SDS-PAGE extracts. 25K-FPR1 is fully inhibited by diisopropylfluorophosphate PMN pretreatment but is not physiologic, as its formation failed to be significantly perturbed by ATP depletion, time and temperature of adherence, or adherence mechanism. 25K-FPR1 was minimized by extracting fMLF-exposed PMN in lithium dodecylsulfate at 4°C prior to reduction/alkylation. After exposure of adherent PMN to a 5 log range of PAF before or after fMLF, unlike in suspension PMN, no inhibition of fMLF-induced FPR1 phosphorylation was observed. However, PAF induced the release of 40% of PMN lactate dehydrogenase, implying significant cell lysis. We infer that PAF-induced inhibition of fMLF-dependent FPR1 phosphorylation observed in suspension PMN does not occur in the unlysed adherent PMN. We speculate that although the conditions of the assay may induce PAF-stimulated necrosis, the cell densities on the plates may approach levels observed in inflamed tissues and provide for an explanation of PAF's divergent effects on FPR1 phosphorylation as well as PMN function.

Bioproduction of Citric Acid Exposed to Lithium Dodecyl Sulfate

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Addition of urea and thiourea to electrophoresis sample buffer improves efficiency of protein extraction from TCA/acetone-treated smooth muscle tissues for phos-tag SDS-PAGE.

Phosphorylation analysis by using phos-tag technique has been reported to be suitable for highly sensitive quantification of smooth muscle myosin regulatory light chain (LC20 ) phosphorylation. However, there is another factor that will affect the sensitivity of phosphorylation analysis, that is, protein extraction. Here, we optimized the conditions for total protein extraction out of trichloroacetic acid (TCA)-fixed tissues. Standard SDS sample buffer extracted less LC20 , actin and myosin phosphatase targeting subunit 1 (MYPT1) from TCA/acetone treated ciliary muscle strips. On the other hand, sample buffer containing urea and thiourea in addition to lithium dodecyl sulfate (LDS) or SDS extracted those proteins more efficiently, and thus increased the detection sensitivity up to 4-5fold. Phos-tag SDS-PAGE separated dephosphorylated and phosphorylated LC20 s extracted in LDS/urea/thiourea sample buffer to the same extent as those in standard SDS buffer. We have concluded that LDS (or SDS) /urea/thiourea sample buffer is suitable for highly sensitive phosphorylation analysis in smooth muscle, especially when it is treated with TCA/acetone.

A Routine 'Top-Down' Approach to Analysis of the Human Serum Proteome.

Serum provides a rich source of potential biomarker proteoforms. One of the major obstacles in analysing serum proteomes is detecting lower abundance proteins owing to the presence of hyper-abundant species (e.g., serum albumin and immunoglobulins). Although depletion methods have been used to address this, these can lead to the concomitant removal of non-targeted protein species, and thus raise issues of specificity, reproducibility, and the capacity for meaningful quantitative analyses. Altering the native stoichiometry of the proteome components may thus yield a more complex series of issues than dealing directly with the inherent complexity of the sample. Hence, here we targeted method refinements so as to ensure optimum resolution of serum proteomes via a top down two-dimensional gel electrophoresis (2DE) approach that enables the routine assessment of proteoforms and is fully compatible with subsequent mass spectrometric analyses. Testing included various fractionation and non-fractionation approaches. The data show that resolving 500 µg protein on 17 cm 3–10 non-linear immobilised pH gradient strips in the first dimension followed by second dimension resolution on 7–20% gradient gels with a combination of lithium dodecyl sulfate (LDS) and sodium dodecyl sulfate (SDS) detergents markedly improves the resolution and detection of proteoforms in serum. In addition, well established third dimension electrophoretic separations in combination with deep imaging further contributed to the best available resolution, detection, and thus quantitative top-down analysis of serum proteomes.

Spectroscopic and conductometric studies on the interactions of thionine with anionic and nonionic surfactants

In this study, the interaction of thionine, a cationic dye, with anionic [sodium dodecyl sulphate (SDS), lithium dodecyl sulphate (LiDS), and sodium dodecylbenzene sulphonate (SDBS)], nonionic (Tween 20 and Triton X‐100), and binary mixtures of anionic and nonionic surfactants was studied by conductometric and spectrophotometric measurements. The degree of ionisation, the counterion binding parameters, and the equilibrium constants in the premicellar region were obtained from conductivity data. Binding constants of thionine to anionic, nonionic, and mixtures of anionic and nonionic micelles were determined by spectrophotometric measurements. The binding tendency of thionine to anionic micelles followed the order SDBS &gt; SDS &gt; LiDS. The presence of nonionic surfactants increased significantly the binding affinity of thionine to anionic micelles, and the highest binding constant was calculated in the presence of Tween 20. The results obtained from conductometric studies correlated with those obtained from spectroscopic studies. Data concerning dye–surfactant interaction are important for a fundamental understanding of the performance of single and mixed surfactants and for their industrial application.