Influence Of DMSO Research Articles

Does the ethanolammonium acetate ionic liquid mix homogeneously with molecular solvents?

In order to study micro-structural heterogeneities in the solutions of ionic liquids (ILs), ethanolammonium acetate (EOAA) IL has been synthesized and (1) H NMR spectra of its binary solutions, namely EOAA/DMSO and EOAA/n-butanol, have been measured at 298.15 K. Then the concentration-dependent chemical shifts δ (-CH3 , EOAA), δ (-CH3 , DMSO) and δ (-CH3 , n-butanol) have been correlated separately using the local composition (LC) model. The results indicated that self-association of EOAA played the leading role within EOAA-rich region in mixtures. However with the molecular solvents increasing, the interactions between EOAA and solvents gradually predominated. Moreover the comparisons between DMSO and n-butanol have demonstrated that DMSO could break the network of IL more easily, indicating that the influence of DMSO on the properties of EOAA should be more obvious, which was consistent with experimental results of viscosity and conductivity. Furthermore the maximum difference between the local and the bulk appeared at x(EOAA) ≈ 0.5 for both systems, which reflected remarkable nonideality of mixtures at this concentration. Copyright © 2015 John Wiley & Sons, Ltd.

Preformulation study and influence of DMSO and propylene glycol on the antioxidant action of isocoumarin paepalantine isolated from Paepalanthus bromelioides

Coumarins are phenolic compounds and have various biological properties, including antioxidant activity. The isocoumarin paepalantine, isolated from of Paepalanthus bromelioides Silveira, Eriocaulaceae, exhibits a wide range of biological activities, including antimicrobial, anti-inflammatory, antioxidant and cytotoxic properties. Studies on paepalantine often use dimethylsulfoxide as a solvent. However the dimethylsulfoxide interferes with antimicrobial, cytotoxic and antioxidant assays. Thus, this study aims to evaluate alternative solvents for paepalantine and evaluate their potential to interfere with antioxidant assays (ABTS+, O2−, HOCl). Of the selected solvents, propylene glycol had good solubility and remained stable throughout the study period. The results suggested that there is no interference from propylene glycol in antioxidant assays, while dimethylsulfoxide significantly interfered with the HOCl assay. The antioxidant assays showed that paepalantine demonstrated similar or even better antioxidant activity than Trolox. Thus, propylene glycol may be the solvent of choice for paepalantine, a compound that has significant biological potential.

Physicochemical and biological properties of oxovanadium(IV), cobalt(II) and nickel(II) complexes with oxydiacetate anions.

The potentiometric and conductometric titration methods have been used to characterize the stability of series of VO(IV)-, Co(II)- and Ni(II)-oxydiacetato complexes in DMSO-water solutions containing 0–50 % (v/v) DMSO. The influence of DMSO as a co-solvent on the stability of the complexes as well as the oxydiacetic acid was evaluated. Furthermore, the reactivity of the complexes towards superoxide free radicals was assessed by employing the nitro blue tetrazolium (NBT) assay. The biological properties of the complexes were investigated in relation to their cytoprotective activity against the oxidative damage generated exogenously by using hydrogen peroxide in the Human Dermal Fibroblasts adult (HDFa) cell line as well as to their antimicrobial activity against the bacteria (Bacillus subtilis, Escherichia coli, Enterococcus faecalis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis). The relationship between physicochemical and biological properties of the complexes was discussed.

Influence of DMSO on the inhibition of various cancer cells by water-soluble organotin polyethers

The effect of solvent on the ability to inhibit a group of cell lines was studied employing a series of water-soluble dibutyltin polyethers derived from various hydroxyl-terminated poly(ethylene gl...

Influence of DMSO on Carbon K ultrasoft X-rays induced chromosome aberrations in V79 Chinese hamster cells

Ultrasoft X-rays have been shown to be very efficient in inducing chromosomal aberrations in mammalian cells. The present study was aimed to evaluate the modifying effects of DMSO (a potent scavenger of free radicals) on the frequencies of chromosome aberrations induced by soft X-rays. Confluent held G1 Chinese hamster cells (V79) were irradiated with Carbon K ultrasoft X-rays in the presence and absence of 1 M DMSO and frequencies of chromosome aberrations in the first division cells were determined. DMSO reduced the frequencies of exchange types of aberrations (dicentrics and centric rings) by a factor of 2.1–3.5. The results indicate that free radicals induced by ultrasoft X-rays contribute to a great extent to the induction of chromosome aberrations. The possible implications of these results in interpreting the mechanisms involved in the high efficiency of ultrasoft X-rays in the induction of chromosome aberrations are discussed.

Growth and differentiation of cell hybrids obtained by fusing mouse PCC4aza1 teratocarcinoma cells and mouse spleen cells under different in vitro culture conditions

Cell hybrids obtained by fusing mouse PCC4azal teratocarcinoma cells and spleen cells induced to proliferation and treated with the demethylating agent 5-azacytidine prior to fusion are described. The obtained hybrids demonstrated no expression of T lymphocyte marker genes CD11 and CD45, which indicates possible somatic nucleus reprogramming by factors present in teratocarcinoma cells. Irrespective of culture conditions, cell hybrids demonstrated a relatively stable chromosome number: they lost on average no more than four chromosomes after 30 passages. Culturing in medium containing hypoxanthine, aminopterin, and thymidine (selective conditions) decreased the differentiation capacity of cell hybrids compared to nonselective conditions, which is likely due to the inhibition of their metabolism. For the first time, teratocarcinoma cell hybrid differentiation into cardiomyocytes under the influence of DMSO has been demonstrated in vitro.

Conformation of Nα-Substituted Hydrazino Acetamides in CDCl3, the Precious Help of the Analysis of Δδ between Amidic Hydrogens, and Correlation to the Conformation of Aza-β3-peptides

[structures: see text] We studied the conformation of a series of primary amides in a solution of chloroform. Classical NMR tools such as dilution experiments, influence of DMSO, and 2D-NOESY, together with X-ray diffraction, were combined with an analysis of the difference of the chemical shift Deltadelta between the geminal amidic protons. This study was addressed in order to understand the conformation adopted by hydrazino acetamides 1a and 1b as model compounds for aza-beta3-peptides. In this manner, it was possible to show that the amidic group of these compounds acts as a H-bond donor and interacts with two different H-bond acceptors. We concluded that the hydrazinoturn, a specific bifurcated H-bond system observed in the solid state, is also the preferred conformation of hydrazino acetamides 1a and 1b in solution. Our results show that the short-range interaction with the N(alpha)-nitrogen lone pair not only stabilizes the C8 pseudocycle but could also contribute to the folding process of aza-beta3-peptides. In light of this, it could explain why aza-beta3-peptides develop a different H-bond network in comparison to their isosteric beta3-peptides analogues. Our work is in keeping with the recent interest of hydrazino peptides as an extension of the beta-peptide concept.

Proteomic dissection of dome formation in a mammary cell line: role of tropomyosin-5b and maspin.

In this work we extended the study of genes controlling the formation of specific differentiation structures called "domes" formed by the rat mammary adenocarcinoma cell line LA7 under the influence of DMSO. We have reported previously that an interferon-inducible gene, rat-8, and the beta-subunit of the epithelial sodium channel (ENaC) play a fundamental role in this process. Now, we used a proteomic approach to identify proteins differentially expressed either in DMSO-induced LA7 or in 106A10 cells. Two differentially expressed proteins were investigated. The first, tropomyosin-5b, strongly expressed in DMSO-induced LA7 cells, is needed for dome formation because its synthesis inhibition by the antisense RNA technology abolished domes. The second protein, maspin, strongly expressed in the uninduced 106A10 cell line, inhibits dome formation because 106A10 cells, transfected with rat8 cDNA (the function of which is required for the organization of these structures), acquired the ability to develop domes when cultured in presence of an antimaspin antibody. Dome formation in these cultures are accompanied by ENaC beta-subunit expression in the absence of DMSO. Therefore, dome formation requires the expression of tropomyosin-5b, in addition to the ENaC beta-subunit and the rat8 proteins, and is under the negative control of maspin.

Genetic dissection of dome formation in a mammary cell line: identification of two genes with opposing action.

In this work, we extend the study of the genes controlling the formation of domes in the rat mammary cell line LA7 under the influence of DMSO. The role of the rat8 gene has already been demonstrated. We have now studied two additional genes. The first, called 133, is the rat ortholog of the human epithelial membrane protein 3 (EMP3), a member of the peripheral myelin protein 22 (PMP22)/EMP/lens-specific membrane protein 20 (MP20) gene family that encodes for tetratransmembrane proteins; it is expressed in the LA7 line in the absence of DMSO but not in its presence. The second gene is the beta subunit of the amiloride-sensitive Na(+) channel. Studies with antisense oligonucleotides show that the formation of domes is under the control of all three genes: the expression of rat8 is required for both their formation and their persistence; the expression of the Na(+) channel beta subunit is required for their formation; and the expression of gene 133 blocks the expression of the Na(+) channel genes, thus preventing formation of the domes. The formation of these structures is also accompanied by the expression of alpha(6)beta(1) integrin, followed by that of E-cadherin and cytokeratin 8. It appears, therefore, that dome formation requires the activity of the Na(+) channel and the rat8-encoded protein and is under the negative control of gene 133. DMSO induces dome formation by blocking this control.

Limiting partial molar volumes of electrolytes in dimethyl sulfoxide–water mixtures at 298.15 K

Limiting partial molar volumes of electrolytes in several water-dimethyl sulfoxide mixtures, up to xDMSO= 0.1587, have been determined from density measurements at 298.15 K. A reference electrolyte assumption (TATB) has been used in order to obtain single-ion partial molar volumes of transfer from water to DMSO–water mixtures. The influence of DMSO on ΔtV′0i of alkali metals and halide ions is negligible in the highly water-rich region (up to xDMSO≈ 0.04) except for the I– ion. However, when the DMSO composition is greater than xDMSO≈ 0.04, the variation of ΔtV′0i for alkali metals is the reverse to that of halide ions. The results are discussed on the basis of ion–solvent and solvent–solvent interactions using Conway's model.

Electrode kinetics of the system V(III)/V(II) in aqueous dimethylsulphoxide

The rate constants for the reduction of V(III) and oxidation of V(II) were measured on a mercury electrode in water and water-dimethylsulphoxide mixtures. Their dependance on the concentration of DMSO differs from that in mixtures of water with an organic solvent of lower basicity. This can be attributed to the existence of different solvates of vanadium in solutions and to different values of the rate constant for these solvates on the electrode surface at different coverages with the organic component. The influence of DMSO both in the primary solvation sphere and in the electrode double layer on the electrode reaction rate is discussed.

Differential scanning calorimetry of dimethylsulphoxide-treated human stratum corneum

Differential scanning caloronetry has been employed to investigate the thermal properties of human stratum comeum. The influence of hydration and DMSO concentration on the interstitial lipid lipoprotein and protein peaks has been investigated. Hydration between 10% and 60% water had no discernible effect on these endotherms. The influence of DMSO was most pronounced on the protein peak with a concentration dependence observed for the lipoprotein peak for DMSO > 60%. The T m for the intercellular lipid peak increased linearly as a function of DMSO concentration up to 90%. Neat DMSO abolished the lipid endotherm.

Influence of DMSO on the volumetric behavior of isolated rye protoplasts

Influence of DMSO on the volumetric behavior of isolated rye protoplasts

Effect of hypertonic stress on mammalian cell lines and its relevance to freeze-thaw injury

The effect of subjecting the mammalian cell lines MRC-5 and CHO to hypertonic salt concentrations (0.16 to 2.4 m) and returning them to isotonic conditions was investigated. Parameters for measuring cell size, viability and release of radiochemical markers were used to determine the relative susceptibilities of the two cell lines to hypertonic stress and the relative effects of increasing and decreasing hypertonicity. The aim of this study was to determine how great a role hypertonic stress plays in freeze-thaw damage of mamalian cells. This type of study has been extensively used for erythrocytes but not for nucleated mamamlian cell lines. The findings were that considerable cell shrinkage occurred, with a minimum size at 0.6 m NaCl, but that this caused no cell injury or death. Injury, measured by cation leakage and release of membrane and cytoplasmic labels occurred whilst the cell was swelling after reaching its minimum volume. MRC-5 cells succumbed at relatively low salt concentrations and became denatured. CHO cells withstood far high salt concentrations but were then damaged during dilution back to isotonic conditions. Comparison of the data obtained from hypertonic stress experiments and freeze-thaw experiments showed many similarities for CHO cells and indicated that the cell membrane could withstand high salt concentrations both at constant and changing temperatures but were prone to injury on dilution back to isotonic conditions. MRC-5 cells were shown to be very prone to cold shock and the results indicated that they probably succumb to damage and death during the hypertonic phase of cooling rather than thawing thus explaining their much lower survival from freeze-thaw experiments than CHO cells. The influence of DMSO in delaying cell damage to higher salt concentrations and lessening disruptive swelling during dilution were also demonstrated.

Influence of DMSO on the response of platelets to osmotic stress

Influence of DMSO on the response of platelets to osmotic stress

Influence of DMSO on the Mutagenicity of EMS in Barley

Dry and 18-h soaked Hordeum vulgare seeds were treated with EMS alone and in combination with DMSO for 3 h. Results for the M1 and M2 generations suggested that DMSO was not a good carrier for EMS; a slight decrease in mutation frequency in M2 was obtained with EMS + DMSO treatments. Studies with 3H-EMS indicated inhibition of labeled mutagen uptake in the presence of DMSO The decrease in the mutation frequency in M2 could be due to reduced EMS uptake in both dry and 18-h soaked seeds

The influence of DMSO on the serotonin uptake of human platelets

The influence of DMSO on the serotonin uptake of human platelets

Glucose transport through cellulose acetate membranes: The influence of dimethyl sulfoxide

Abstract The diffusion through cellulose acetate membranes of d -glucose dissolved in water, dimethyl sulfoxide mixed solvents has been measured. A new diffusion cell using polarimetry is described. The mixed solvent system has a maximum viscosity at about 0.35 mol fraction DMSO. The permeability constant decreases with an increase in DMSO content and in solvent viscosity. At the viscosity-maximum composition the permeability constant is seen to decrease steadily in time. Beyond this maximum at higher DMSO concentrations the membrane disintegrates. The inhibitory influence of DMSO on glucose transport probably involves both a viscosity and a membrane-damage effect.

The influence of DMSO on intraperitoneal implantation of tumor cells.

The influence of DMSO on intraperitoneal implantation of tumor cells.