DMSO-water Solutions Research Articles

Sequence-dependent dipeptide solubility in ethanol-water and DMSO-water solutions

Reliable solubility data is crucial for controlling and optimising crystallisation conditions, to provide a cost-effective purification method with the potential for scaling up. This study investigated the effect of amino acid sequence on determining peptides solubility behaviours. Four dipeptides with different sequences and combinations of alanine and glycine were selected to study their temperature dependent (283.15 K to 313.15 K) aqueous solubilities and solubility in the presence of ethanol and DMSO as antisolvent at 298.15 K. Aqueous solubility data of dipeptides presents the following order: glycyl-L-alanine (gly-ala) > L-alanyl-L-alanine (ala-ala) > glycyl glycine (gly-gly) > L-alanyl glycine (ala-gly). This solubility order has been substantiated by solvation free energy calculations using molecular dynamics (MD) simulations, providing insights into the underlying molecular interactions that govern these solubility patterns. The solubility data also demonstrated difference in the temperature dependency that: gly-gly > gly-ala > ala-gly > ala-ala, corresponding to their dissolution enthalpy order. In the presence of antisolvent range from 0 % to 80 % (by mass) concentration, peptide’s solubility was more susceptible to DMSO than ethanol. Accurate prediction of the solubilities validated the effectiveness of non-random two-liquid (NRTL) model for peptide studies.

Nuclear Magnetic Resonance Spectroscopy Investigation on Ultralow Melting Temperature Behavior of Dimethyl Sulfoxide-Water Solutions.

On the basis of the molecular understanding that DMSO has a trigonal pyramidal geometry with one highly polarized sulfinyl group and two hydrophobic methyl groups, we used NMR technology to rationalize why DMSO can act as antifreeze for aqueous solutions. A series of DMSO-water, DMSO-methanol, and acetone-water binary solutions with various molar ratios were tested in specified low temperature conditions. The freezing test results indicated that only DMSO-water solutions with the DMSO-water molar ratio (nDMSO) in a specific range can form apparent ultralow freezing temperature solutions. Among all DMSO-water solutions, the apparent freezing temperature lower than -130 °C was obtained for nDMSO values of 0.25, 0.30, and 0.35, respectively. Multinuclear NMR chemical shifts, 1H diffusion experiment results, and viscosity measurements suggested that molecular rearrangement resulted in the formation of the water-core DMSO-shell aggregation unit in DMSO-water solutions. The weak methyl-methyl London dispersion forces among water-core DMSO-shell aggregation units can explain the apparent ultralow freezing temperatures of these DMSO-water solutions.

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 Three Anionic Gemini Surfactants with Different Chain Lengths on the Optical Properties of a Cationic Polyfluorene

The effects of three sulfonate gemini surfactants with different hydrophobic chain lengths (8, 10, and 12 carbon atoms) on the optical properties of a fluorene-based conjugated cationic polymer poly{[9,9-bis(6'-N,N,N-trimethylammonium)hexyl]-fluorene-phenylene} bromide (PFP) dissolved in DMSO-water solutions (4% v/v) or water were investigated, respectively. When surfactants with PFP dissolved in DMSO-water solutions (4% v/v) are incubated, a decrease in photoluminescence (PL) intensity and a red shift of emission maxima are obtained at low surfactant concentrations. Intriguingly, two different Stern-Volmer constants (KSV1 and KSV2) are obtained and analyzed in detail for the first time. Further increase in the surfactant concentration enhanced PL intensity, and distinct blue shifts of both absorption and emission maxima are observed. Importantly, the turning point between the emission quenching and enhancement is closely related to the hydrophobic chain length: the longer the chain length, the earlier the turning point appears. Simulation studies provide strong evidence to explain these phenomena. Surface tension measurements show more insight on the interactions between PFP and surfactant. On the contrary, no emission quenching is obtained at low surfactant concentrations for PFP dissolved in water.

Amphiphilic O-functionalized calix[4]resocinarenes with tunable structural behavior

Novel amphiphilic calix[4]resorcinarenes oxyethylated at the upper rim and alkylated at the lower rim (CR–CnH2n+1, here n is the number of carbon atoms in the alkyl substituent; n = 2,5,7,8,9,11) were synthesized, and their association behavior in water-organic solvents was explored. Surface properties and the association behavior of CRs were shown to be strongly controlled by their structure and the nature of the co-solvent. Solely CR–C5H11 demonstrates surface activity in the mixed water–DMF and water–DMSO solutions, while no surface activity occurs in the water–THF mixture. The DLS measurements revealed a very low concentration threshold of the aggregation (around 0.01 mM) for the CR series including surface inactive compounds. In water–DMF and water–DMSO solutions the CRs of low hydrophobicity were shown to associate through an open model with the formation of large aggregates of 300–400 nm, while more hydrophobic CRs can associate through a closed model and form rather small micelle-like aggregates of 10 to 20 nm.

Fluorescence Measurements of Aromatic Amino Acids in the Presence of Lipid Membranes

Amphiphilic peptides are capable of finding their way to, and occasionally through, cellular membranes using a mechanism that includes specific amino acid sequences. Physical measurements of amino acid-lipid interactions are of interest for a quantitative description of peptide affinities to biological membranes. In this study, we investigate small peptide-lipid interactions using the fluorescence of the aromatic amino acids tyrosine (Tyr), tryptophan (Trp) and phenylalanine (Phe). Reference spectra in isopropanol-water, ethylene-glycol-water, DMSO-water, and polyethyleneglycol-water solutions are obtain to mimic hydrophobic environments and are used to quantify the interaction of Lys-Tyr-Lys, Trp-Gly, and Gly-Phe with 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2-dioleoyl-sn-glycero-3-phosphoserine (DOPS) lipid membranes. These fluorescence data complement previously reported UV absorption data and have the advantage of eliminating background and scatter from solution. Together with NMR data, these results can be used to more fully characterize lipid-aromatic amino residue interactions.

Effect of water on exenatide acylation in poly(lactide-co-glycolide) microspheres

Peptide or protein degradation often occurs when water flows into the dosage form. The aim of this study was to investigate the effect of water on exenatide acylation in poly(lactide-co-glycolide) (PLGA) microspheres. Exenatide-loaded PLGA microspheres were incubated at different relative humidities (RH) as well as in solutions of different pH for 20 days. The stability of exenatide was monitored using HPLC and HPLC-MS analysis. The alteration of exenatide conformation caused by water was investigated by FT-IR spectroscopy. Exenatide and glycolide were incubated in DMSO-water solutions to verify the effect of exenatide conformation state on the peptide acylation. Exenatide was relatively stable in microspheres at lower RH, and the absorbed water could act as a plasticizer and thus promote the peptide acylation by PLGA. However, when the microspheres were incubated at 100% RH, the excessively absorbed water could cause conformation recovery of exenatide and play an inhibitory effect on acylation. The formation of acylated exenatide incubated in acetate buffer saline of pH 6.0 was more than that of pH 4.5 and 3.0. Stability studies of exenatide in glycolide solutions showed that exenatide in nonnative monomer state was easier to be acylated by eletrophiles than that in aggregation state.

X-Ray Diffraction and Infrared Spectroscopy of N,N- Dimethylformamide and Dimethyl Sulfoxide Solvatomorphs of Betulonic Acid

X-ray diffraction and infrared spectroscopy measurements for the N,N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) solvatomorphs of betulonic acid (BA) were investigated. BA [3-oxolup-20(29)-en-28-oic acid, C(30)H(46)O(3)] exhibits a wide spectrum of biological activities and is considered to be a promising natural agent for the treatment of various cancer diseases. BA as a noncrystalline substance was obtained by oxidation of betulin. Crystal structures and the spectral data allowed analysis of hydrogen bonding (H-bonding), molecular conformation, and crystal packing differences in the solvatomorphs. Crystals of BA solvates were grown from the DMF-acetone (1:10, v/v) and DMSO-water (9:1, v/v) solutions. BA-DMF (1:1) solvate crystallizes in the monoclinic P2(1) space group, Z = 2. The unit cell parameters are as follows: cell lengths a = 13.2458(5) Å, b = 6.6501(2) Å, c = 17.9766(7) Å, and β = 110.513(4)°. BA-DMSO (1:1) solvate crystallizes in the orthorhombic P2(1)2(1)2(1) (Z = 4) space group with the following unit cell parameters: a = 6.6484(4) Å, b = 13.3279(8) Å, and c = 32.6821(19) Å. Conformational analysis of the six-membered rings, cyclopentane ring, and isopropenyl group showed differences in comparison with other betulin derivatives examined earlier. For both solvates, the intermolecular packing arrangement was governed mainly by H-bonds. The shortest H-bonds with D···A distances of 2.604 and 2.657 Å, and almost linear DH···A connection occurred between OH of carboxylic group of BA and oxygen atoms from O=C and O=S groups of DMF and DMSO, respectively.

Formation of luminescent terbium(iii) self-assemblies from pyridyl bis-amidothioureas based ligands in MeOH and in water–DMSO solutions and their use in anion sensing application

The self-assembly between the amidothiourea ligands 1 and 2 and Tb(III) gave rise to the formation of 1:1 and 3:1 (ligand-Tb) supramolecular architectures that were shown to be luminescent in both MeOH and in water-DMSO solutions; preliminary investigations in the latter system also showed that their emission was modulated upon interacting with anions such as acetate and phosphate due to host-guest formation.

Combined study of anion recognition by a carbazole-based neutral tripodal receptor in a competitive environment

Anion recognition studies have been carried out on a series of neutral synthetic receptors in which carbazole-2-carboxamide has been used as building block. Different ligands which include one to three carbazole units in their structure have been prepared. Binding experiments have been performed under competitive conditions in DMSO and DMSO-water solutions. The tripodal receptor offered a better host-guest association due to the synergistic effect of a well arranged set of hydrogen bonds. A selective response towards the biologically important pyrophosphate anion has been achieved. This selectivity is enhanced when studies are carried out with an increasing water content, which gets as high as 20% (v/v) in NMR experiments. The significance of this result lies in the use of a neutral receptor which exclusively interacts with the anionic guest through hydrogen bonding. The influence of multiple equilibria in the studied system has been analysed. Several techniques ((1)H NMR, (31)P NMR, mass spectrometry, diffusion-NMR, ITC, absorption and emission spectroscopy) have been employed to get a better understanding of the different processes taking place in solution for the evaluated receptors.

Polynuclear copper(II) complexes with polydentate nanoligands on the basis of aminoderivatives of the hyperbranched polyesters

Coordinationally active polydentate nanoplatforms on the basis of amino-modified hyperbranched polyesters containing 7 terminal amino fragments are synthesized. Synthetic procedure is developed and polynuclear Cu(II) complexes with polyesteropolyamines are prepared. Their composition and stability of the complex forms in DMSO-water solutions are evaluated. It is found that all the compounds obtained exhibit biological activity with respect to the induced asparagine proteinase of Candida albicans.

Solvent effect on protonation constants of salicylic acid in mixed aqueous organic solutions of DMSO

The first protonation constant of salicylic acid in water–DMSO solutions containing 0–50% (v/v) DMSO has been determined by spectrophotometric and potentiometric methods at 25 °C and an ionic strength of 0.1 M sodium perchlorate. The results indicate that the pK a value of salicylic acid increases with increasing proportion of DMSO in the mixed solvent. The variation of pK a value over the media composition range was explained by a linear solvation energy relationship, and correlations between pK a values and the Kamlet–Taft parameters α (hydrogen bond donor acidity), π* (dipolarity/polarizability), and β (hydrogen bond acceptor basicity), and the dielectric constant were calculated by means of multiple linear regression. The equations obtained can be used to estimate the first protonation constant of salicylic acid in a water–DMSO solvent from the relationship between the pK a values and the Kamlet–Taft parameters of the solvent. Also, the pK a value in aqueous medium was calculated by use of the SPARC online calculator and was compared with the value determined experimentally.

Investigations on the structure of dimethyl sulfoxide and acetone in aqueous solution

Aqueous solutions of dimethyl sulfoxide (DMSO) and acetone have been investigated using neutron diffraction augmented with isotopic substitution and empirical potential structure refinement computer simulations. Each solute has been measured at two concentrations-1:20 and 1:2 solute:water mole ratios. At both concentrations for each solute, the tetrahedral hydrogen bonding network of water is largely unperturbed, though the total water molecule coordination number is reduced in the higher 1:2 concentrations. With higher concentrations of acetone, water tends to segregate into clusters, while in higher concentrations of DMSO the present study reconfirms that the structure of the liquid is dominated by DMSO-water interactions. This result may have implications for the highly nonideal behavior observed in the thermodynamic functions for 1:2 DMSO-water solutions.

Influence of the method of synthesis on the composition and structure of copper(II) complexes with galactaric acid

The influence of the conditions and the method of synthesis on the composition of copper(II) complexes with galactaric acid (H2Gala) has been studied. In aqueous and water-DMSO solutions, 1 : 1 complexes are formed. Depending on the procedure and conditions of the synthesis, CuGala · 4H2O, Cu(HGala)2 · 4H2O, and (CuOH)2Gala · 2H2O compounds have been obtained. The structure of the coordination environment of the metal ion has been identified by IR spectroscopy.

Graft polymerization of vinyl monomers inside macroporous polyacrylamide gel, cryogel, in aqueous and aqueous‐organic media initiated by diperiodatocuprate(III) complexes

AbstractGraft polymerization initiated by diperiodatocuprate(III) complex (Cu(III)) initiator was found to be an effective and convenient method for graft polymerization of vinyl monomers onto macroporous polyacrylamide gels, the so‐called cryogels (pAAm‐cryogels). The effect of time, temperature, monomer and initiator concentration during the graft polymerization in aqueous and aqueous‐organic media was studied. The graft polymerization of water‐soluble monomers as [2‐(methacryloyloxy)ethyl]‐trimethylammonium chloride, 2‐hydroxyethyl methacrylate, N‐isopropylacrylamide, and N,N‐dimethylacrylamide proceeds with higher grafting yield in aqueous medium, as compared with that in aqueous‐organic media. Graft polymerization in aqueous‐organic media such as water–DMSO solutions allows grafting of water‐insoluble monomers such as glycidyl methacrylate and N‐tert‐butylacrylamide with high grafting degrees of 100 and 410%, respectively. It was found that the deposition of initiator on the pore surface of cryogels promoted graft polymerization by facilitating the formation of the redox couple Cu(III)‐acrylamide group. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1952–1963, 2006

An operational pH in aqueous dimethylsulfoxide based upon the acidity dependence of the rate of a simple ionic recombination reaction in the lowest excited singlet state

7-Hydroxy-1-naphthalenesulfonate (2-naphthol-8-sulfonate) monoanion demonstrates proton transfer in the lowest excited singlet state in DMSO–water mixtures as well as in pure water. The dissociation reaction of the directly excited monoanion is strongly solvent-dependent, and independent of solution acidity. The reprotonation of the conjugate base, however, depends predominantly on the acidity of the solution and only on the continuum properties of the solvent. The separability of the dissociation and reprotonation reactions, using steady-state methodology, allows the reprotonation to be treated independent of the dissociation. The linear relationship between the ratio of the relative fluorescence efficiencies of acid and conjugate base, and the hydrogen ion concentration is obtained only if proper Brönsted activity factors are included in the relationship. These factors can be calculated from classical electrostatics and are the fourth powers of the activity coefficients necessary to convert the formal hydrogen ion concentration to hydrogen ion activity. Using this approach, pH was calculated from hydrogen ion concentration in DMSO–water solutions, containing a mole fraction of DMSO up to about 0.4.

Spectrophotometric Study of Luminol in Dimethyl Sulfoxide–Potassium Hydroxide

The spectrophotometric study of luminol (LH2) in dimethyl sulfoxide (DMSO), DMSO-water solutions, and alkaline DMSO and DMSO-water solutions has been done, focusing on the effect of the KOH additon on LH2 absorption and fluorescence properties. The absorption spectra indicate an acid-base equilibrium, and the luminol dianion (L2−) formation at 3 × 10−4 − 2.4 × 10−3M KOH. The decrease of the fluorescence intensity and the variation of the excitation spectra of LH2-DMSO-KOH solutions with KOH concentration have been similarly explained. The acid-base process is reversible. The addition of HCl to the solution with 3.0 × 10−3 M KOH leads to an increase of the fluorescence intensity to its highest value, observed in pure DMSO. The addition of HCl to the LH2-DMSO solution leads to the decrease of the fluorescence intensity as a result of the LH+3 cation formation. In LH2-DMSO-water, the fluorescence band is shifted from 405 nm to 424 nm and increased in the intensity. In the presence of KOH (in LH2-DMSO-water-KOH solution) a new band appears, with the maximum at 485 nm and the band at 405 nm decreased. The changes in fluorescence lifetimes also evidence the different chemical species formed.

Complex formation of O-carboxymethylcalix[4]resorcinolarene with alkaline metal and ammonium ions

Complex formation of 3,5,10,12,17,19,24,26-octa(carboxymethoxy)-1,8,15,22-tetraundecylcalix[4]arene (H8X) with Li+, Na+, K+, and NH4+ ions was studied by 1H NMR spectroscopy and pH-metry in water—DMSO solutions. Binding of one cation occurs during the stepped deprotonation of four carboxymethyl groups in H8X. The K+ ion was found to be bound more efficiently than Li+ and Na+. The further deprotonation to the penta- and hexaanion leads to the coordination with two cations. The most stable binuclear complex is formed with the Li+ ion.

Solvent composition and rheology of starch–DMSO–water solutions

AbstractThe rheology of starch–DMSO–water solutions was studied as a function of water content and temperature. A correlation between flow regime, temperature, and water content was presented so as to characterize amylose conformation change in a novel way. Rheological behavior was characterized using an empirical equation to classify fluids under study as Newtonian, pseudoplastic, or dilatant. The temperature effect was analyzed through the determination of the apparent activation energy and preexponential constant. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1285–1290, 2001

Spectroscopic characterization of titanocene complexes with thionucleobases

The reaction of Cp 2TiCl 2 with thionucleobases affords [Cp 2Ti(L)]Cl 2 complexes, where L=2-thiouracil, 6-thiopurine, 6-thioguanine, 2-thiocytosine, 6-thiopurineribose or 6-thioguanineribose. The ionic character of the chlorides has been determined by conductivity measurements and the coordination patterns of the thionucleobases have been determined by IR and proton NMR spectroscopies. The kinetics of ligand hydrolysis have been pursued to assess the stability of TiL and TiCp bonds in DMSO and DMSO–water solutions.