Biomedical subjects

Olle Söderman

Publications and source records attributed to Olle Söderman.

17 recordsLinked to original sources

PubMed2005

Physicochemical characterization of PEG1500-12-acyloxy-stearate micelles and liquid crystalline phases.

PEG 12-acyloxy-stearates are used as drug delivery carriers that have low cell damage effects. The mechanical and physical properties surrounding these processes and surfactants are still however not known. In this study, the physicochemical micellar properties of PEG 12-acyloxy-stearates were characterized by optical microscopic, nuclear magnetic resonance, and small-angle X-ray scattering techniques. We determined the phase diagrams of the surfactants as a function of surfactant concentration and temperature, the micellar size and shape, and micellar dynamics. We found that each surfactant has a micellar, cubic Im3m, and hexagonal phase. The aggregation number in the discrete cubic phase, as determined by small-angle X-ray scattering, was approximately 150 for each surfactant, and showed no measurable chain-length dependence. The diffusion coefficients of the surfactant showed a discontinuity between the micellar and cubic phases, where the cubic phases gave very low values on the order of 10(-)(16) m(2) s(-)(1): this value indicates a non-bicontinuous cubic structure. In summary, these surfactants behave to a large extent as nonionic poly(ethylene glycol) surfactants with extended PEG headgroups.

Journal Article↗

PubMed2005

Mixtures of mucin and oppositely charged surfactant aggregates with varying charge density. Phase behavior, association, and dynamics.

The nonionic surfactant Tween80 is a commonly used excipient in drug formulations containing an active substance with low aqueous solubility. Model drug vehicles with varying charge density were obtained by mixing Tween80 (PS-80) with the cationic surfactant Tetradecyltrimethylammonium chloride (TTAC), thus forming mixed micelles. The micelles were mixed with the negatively charged polyelectrolyte mucin, which is a component in the protective mucus layer covering epithelial cell linings. Depending on the composition of the mixture, complex-formation could be followed by precipitation. Using X-ray diffraction, it was found that the precipitate contained a lamellar phase with properties sensitive to the proportion of PS-80. Higher amounts of PS-80 were found to oppose phase separation. Further analysis in the one-phase region, or alternatively of the supernatant of two-phase samples, by (1)H NMR, HPLC, and diffusion measurements with PGSE-NMR led to the conclusions that at low proportion of PS-80 aggregates composed of mixed (PS-80 and TTAC) micelles and mucin were formed, whereas increased concentrations of PS-80 favored the dissolution of the precipitate and limited the interactions between mixed micelles and the polymer.

Animals↗

PubMed2005

The water/n-octane/octyl-beta-D-glucoside/1-octanol system: phase diagrams and phase properties.

The partial phase diagram of D2O/n-octyl-beta-D-alkyl-glucoside(C8G1)/n-octane has been determined at T=25 degrees C. The diagram contains a funnel-shaped micellar phase originating from the water corner of the phase diagram D2O/C8G1 with the stem forming a narrow three-phase region, in which the three phases in equilibrium are two microemulsions of similar composition and an excess oil phase. The microemulsions have been characterized with NMR self-diffusion measurements. At high surfactant concentration and no or low n-octane content, branched micelles exist. As the n-octane content is increased, discrete micelles are formed. Upon further addition of n-octane, the phase separation into two microemulsion phases is induced. Possible mechanisms causing the phase separation are discussed. The phase diagram of D2O/(C8G1)/1-octanol has been determined at 25 degrees C. Ten different phase regions were identified. The phases have been characterized with SAXS and deuterium heavy water NMR, and the swelling of the lamellar phase was investigated with SAXS.

Journal Article↗

PubMed2005

Effects of temperature, salt, and deuterium oxide on the self-aggregation of alkylglycosides in dilute solution. 2. n-Tetradecyl-beta-D-maltoside.

The effects of salt, temperature, and deuterium oxide on the self-aggregation of n-tetradecyl-beta-d-maltoside (C(14)G(2)) in dilute solution have been investigated by static light scattering, dynamic light scattering (DLS), small-angle neutron scattering (SANS), tensiometry, and capillary viscometry. SANS data show that the micelles can be described as relatively flexible polymer-like micelles with an elliptical cross section, at least at temperatures between 35 and 50 degrees C. The micelles grow in one dimension with increasing temperature and concentration. DLS and viscometry data suggest that the micelle size reaches a maximum at 60-70 degrees C. Comparison of DLS data in D(2)O and H(2)O shows that the micelles are larger in the former case. The effect of salt on the micelle size was found to follow the Hofmeister series. Thus, at constant salt concentration, the micelle size decreases according to the sequence SO(4)(2)(-) > Cl(-) > NO(3)(-) > I(-) > SCN(-), where I(-) and SCN(-) act as salting-in anions. From tensiometric data, it can be concluded that the temperature effects on micelle morphology do not correlate directly with those on unimer solubility. Rather, the temperature effect on the hydrocarbon chain conformation seems to be decisive for the micelle morphology. At constant temperature, on the other hand, the effect of salt and deuterium isotope is attributable to changes in effective headgroup area, including intermolecular interactions and water of hydration.

Alkylation↗

PubMed2005

Interactions between n-octyl and n-nonyl beta-D-glucosides and alpha- and beta-cyclodextrins as seen by self-diffusion NMR.

In this work (1)H NMR self-diffusion experiments have been performed to determine the self-diffusion coefficients of n-octyl beta-d-glucoside and n-nonyl beta-d-glucoside in alpha-cyclodextrin and beta-cyclodextrin solutions at 25 degrees C. Two questions are addressed. The first concerns the general influence on nonionic surfactant transport properties when cyclodextrins are present in solution. The second question concerns the influence of surfactant-chain length and cyclodextrin cavity volume on the association constant. The self-diffusion coefficients of the alkyl glucosides, in cyclodextrin-containing solutions, depend on the cyclodextrin concentration on account of the formation of complexes. The cyclodextrin diffusion is only mildly influenced, since the complex has similar diffusion coefficients as the free cyclodextrin. There are some obstruction effects at the highest surfactant concentrations which decrease the cyclodextrin diffusion. A set of equations to model the self-diffusion coefficients of the surfactant and cyclodextrin was developed and is presented. On the basis of such equations, properties such as association constants, and micelle and complex diffusion coefficients can be estimated.

Diffusion↗

PubMed2004

Glassy crystalline state and water sorption of alkyl maltosides.

A differential scanning calorimetric and sorption calorimetric study of two alkyl maltosides, C8G2 and C10G2, was performed. In the dry state, C8G2 and C10G2 do not form solid crystals but undergo a glass transition upon temperature change. The glass is partly ordered and has the same lamellar structure as the liquid crystals formed by the two maltosides. To reflect the presence of the glass transition and the structure, the terms "glassy crystals" and "glassy liquid crystals" can be used. A mechanism of the relaxation of the glassy crystals based on the results of small-angle X-ray scattering experiments is proposed. Experiments on water sorption showed that the glassy crystals turn into lyotropic liquid crystals upon sorption of water at constant temperature. This isothermal glass transition can be characterized by water content and change of partial molar enthalpy of mixing of water. A method to calculate the phase diagram liquid crystals-glassy liquid crystals is proposed.

Alkalies↗

PubMed2004

Surfactant diffusion through bicontinuous micellar networks: a case study of the C9G1/C10G1/H2O mixed surfactant system.

Self-diffusion coefficients were obtained by means of NMR diffusometry for differing ratios of n-decyl-beta-D-glucopyranoside (C10G1) and n-nonyl-beta-D-glucopyranoside (C9G1) surfactant mixtures, along dilution lines through the micellar region of the ternary C9G1/C10G1/H2O phase diagram. Networks of bicontinuous micelles have been suggested to exist throughout the micellar regions of the phase diagram. A phase separation into two coexisting liquid solutions is observed in the dilute, C10G1-rich regions of the phase diagram. The fact that the dilution curves follow scaling relations pertaining to surfactant diffusion in a network for mixtures rich in C10G1 indicates that the phase separation is due to differences in the networks in different micellar regions of the phase diagram; networks remain largely intact despite dilution down to the phase separation in the C10G1-rich region, whereas networks with scissions are predicted to exist in the C9G1-rich regions of the micellar phase.

Journal Article↗

PubMed2004

Effects of temperature, salt, and deuterium oxide on the self-aggregation of alkylglycosides in dilute solution. 1. n-nonyl-beta-D-glucoside.

The influence of salt, temperature, and deuterium oxide on the self-aggregation of n-nonyl-beta-D-glucoside (beta-C9G1) in dilute solution has been investigated by static and dynamic light scattering, neutron scattering, and tensiometry. Scattering data show that the micelles can be described as relatively stiff, elongated structures with a circular cross section. With a decrease of temperature, the micelles grow in one dimension, which makes it surprising that the critical micelle concentration (cmc) shows a concomitant increase. On the other hand, substitution of D2O for H2O causes a large increase in micelle size at low temperatures, without any appreciable effect on cmc. With increasing temperature, the deuterium effect on the micelle size diminishes. The effects of salt on the micelle size and cmc were found to follow the Hofmeister series. Thus, at constant salt concentration, the micelle size decreased according to the sequence SO4(2-) > Cl- > Br- > NO3- > I- > SCN-, whereas the effect on cmc displays the opposite trend. Here, I- and SCN are salting-in anions. Similarly, the effects of cations decrease with increasing polarizability in the sequence Li+ > Na+ > K+ > Cs+. At high ionic strength, the systems separate into two micellar phases. The results imply that the size of beta-C9G1 micelles is extremely sensitive to changes in the headgroup size. More specifically, temperature and salt effects on effective headgroup size, including intermolecular interactions and water ofhydration, are suggested to be more decisive for the micelle morphology than the corresponding effects on unimer solubility.

Adsorption↗

PubMed2004

Surfactant/Nonionic polymer interaction. A NMR diffusometry and NMR electrophoretic investigation.

The interaction between the nonionic polymer poly(ethylene oxide) (PEO) of molecular weight 20,000 and surfactants of various types [sodium dodecyl sulfate (SDS), dodecyl trimethylammonium bromide, octyl beta-D-glucoside, and potassium laurate] has been investigated in an aqueous solution at 25 degrees C by 1H NMR pulsed-gradient spin-echo self-diffusion techniques. The SDS/PEO study was further complemented by component-resolved 1H NMR-based studies of the electrophoretic mobility of PEO and the alkyl part of SDS under the same measurement conditions. Through such combined studies, a much more complete picture of the binding and aggregation processes becomes accessible.

Journal Article↗

PubMed2004

NMR diffusometry and the short gradient pulse limit approximation.

In NMR diffusometry, one often uses the short gradient pulse (SGP) limit approximation in the interpretation of data from systems with restricted diffusion. The SGP limit approximation means that the gradient pulse length, delta, is so short that the spins do not diffuse during the pulse duration, but this condition is rarely met. If the length scale of the pores corresponds to the molecular mean square displacement during the gradient pulse, the measured echo intensities become a function of the gradient pulse length. Here, we have studied highly concentrated emulsions to show how the length of the gradient pulse influences NMR diffusion experiments. We have focused on molecules confined to one pore and molecules that can migrate through the porous system. For the former the echo decays give smaller pores than the actual case and for the latter we show large changes in echo decay depending on the gradient pulse length, everything else being equal.

Algorithms↗

PubMed2003

Diffusion in an inhomogeneous system: NMR studies of diffusion in highly concentrated emulsions.

In this study the self-diffusion of different species in highly concentrated water-in-oil emulsions was investigated by means of the NMR diffusometry approach. The emulsions contained 96% aqueous solutions of salt or other additives; heptane was used as the oil phase. The surfactants, used to stabilize the emulsion, were soybean phosphatidylcholine and C(12)EO(4). The water drops were about 1.5 microm in diameter according to diffusion measurements performed on water. Diffusion of tetramethyl ammonium ions and glucose between the emulsion droplets was found to be negligible on the relevant time-scale (<1 s). On the contrary, acetic acid/acetate ions diffused between the droplets and had exchange times which were a function of pH.

Journal Article↗

PubMed2003

Gemini surfactants: new synthetic vectors for gene transfection.

The superior surfactant properties of cationic gemini surfactants are applied to the complex problem of introducing genes into cells. Of almost 250 new compounds tested, of some 20 different structural types, a majority showed very good transfection activity in vitro. The surfactant is shown to bind and compact DNA efficiently, and structural studies and calculations provide a working picture of the "lipoplex" formed. The lipoplex can penetrate the outer membranes of many cell types, to appear in the cytoplasm encapsulated within endosomes. Escape from the endosome--a key step for transfection--may be controlled by changes in the aggregation behavior of the lipoplex as the pH falls. The evidence suggests that DNA may be released from the lipoplex before entry into the nucleus, where the new gene can be expressed with high efficiency.

Genetic Therapy↗

PubMed2003

Experimental determination of pore shape and size using q-space NMR microscopy in the long diffusion-time limit.

The signal obtained with q-space NMR imaging applied to a confined liquid is directly related to the pore shape in the limit where all molecules have sampled the whole pore. We investigate the diffusion of water across a approximately 50 microm thick film formed between planes of glass. The diffusion time t is changed almost three orders of magnitude. For short t, the root-mean-square displacement increases with a rate which is slightly less than for freely diffusing water. At t longer than 0.3 s, the displacement is constant at 24 microm which implies that the water is confined in the measuring direction defined by the applied gradient pulses. Perfectly smooth and aligned planes give rise to sharp diffraction-like features on the echo attenuation curve, i.e., NMR signal vs. the reciprocal space vector q. The experimental data with rather smooth local minima and maxima can be explained in terms of either surface roughness or a misalignment of the planes. We discuss the averaging effect of diffusion along a laterally inhomogeneous film and propose two model-free methods to determine the pore shape from the echo attenuation curve obtained in the long-t limit.

Diffusion Magnetic Resonance Imaging↗

PubMed2003

Predictions of pulsed field gradient NMR echo-decays for molecules diffusing in various restrictive geometries. Simulations of diffusion propagators based on a finite element method.

Pulsed field gradient NMR diffusometry is a promising tool for investigating structures of porous material through determinations of dynamic displacements of molecules in porous systems. A problem with this approach is the lack of closed analytical expressions for echo-decays in anything but idealized pore geometries. We present here an approach based on calculating the appropriate diffusion propagator by means of finite element calculations. The suggested method is quite general, and can be applied to arbitrary porous systems. The protocol for the calculations is outlined and we show results from some different cases: diffusion in confined geometries and in systems that are spatially inhomogeneous with respect to concentration.

Diffusion↗

PubMed2003

Determination of pore space shape and size in porous systems using NMR diffusometry. Beyond the short gradient pulse approximation.

The influence of finite length gradient pulses on NMR diffusion experiments on liquids confined to diffuse between two parallel planes is investigated. It is experimentally verified that the pore size decreases when determined using finite gradient pulses if the results are analyzed within the short gradient pulse approximation. The results are analyzed using the matrix formulation. The observed minima in the echo decay profiles are considerably less sharp than theoretical analysis would indicate and we suggest that this is due to the presence of a distribution of pore sizes in the sample. In addition, effects due to the presence of background gradients are discussed. It is argued that effects due to the finite length gradient pulses are relatively minor and in realistic applications the effects due to inhomogeneities in pore sizes and effects due to background gradients will constitute more serious problems in pore size determinations by means of NMR diffusometry.

Journal Article↗

PubMed2002

Restricted self-diffusion of water in a highly concentrated w/o emulsion studied using modulated gradient spin-echo NMR.

Restricted diffusion of water in a highly concentrated w/o emulsion was studied using pulsed field gradient spin echo techniques. The standard two-pulse version of this technique, suitable for analysis in the time domain, fails to investigate the short time-scale for diffusion inside a single emulsion droplet with radius 0.7 microm. With a pulse-train technique, originally introduced by Callaghan and Stepisnik, shorter time-scales are accessible. The latter approach is analyzed in the frequency domain and yields frequency dependent diffusion coefficients. Predictions for the outcome of the experiment were calculated in the time domain using the Gaussian phase distribution and the pore hopping formalism expressions for the echo attenuation. The results of these calculations were transformed to the frequency domain via a numerical inverse integral transform in order to compare with the experimental results.

Journal Article↗

PubMed2002

Self-diffusion of nonfreezing water in porous carbohydrate polymer systems studied with nuclear magnetic resonance.

Water is an integral part of the structure in biological porous materials such as wood and starch. A problem often encountered in the preparation of samples for, e.g., electron microscopy is that removal of water leads to a decreasing distance between supermolecular structural elements and a distortion of the structure. It is, therefore, of interest to find methods to investigate these materials in the native water-swollen state. We present a method to study water-swollen biological porous structures using NMR to determine the amount and self-diffusion of water within the porous objects. The contribution of bulk water to the NMR signal is eliminated by performing experiments below the bulk freezing temperature. Further decrease of the temperature leads to a gradual freezing of water within the porous objects. The contribution of the freezing water fraction to the migration of water through the porous network is, thus, estimated. The results are rationalized in terms of the ultrastructure of the samples studied, namely, wood pulp fibers and potato starch granules.

Adsorption↗