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An empirical Bayesian solution to the source reconstruction problem in EEG.

Distributed linear solutions of the EEG source localisation problem are used routinely. In contrast to discrete dipole equivalent models, distributed linear solutions do not assume a fixed number of active sources and rest on a discretised fully 3D representation of the electrical activity of the brain. The ensuing inverse problem is underdetermined and constraints or priors are required to ensure the uniqueness of the solution. In a Bayesian framework, the conditional expectation of the source distribution, given the data, is attained by carefully balancing the minimisation of the residuals induced by noise and the improbability of the estimates as determined by their priors. This balance is specified by hyperparameters that control the relative importance of fitting and conforming to various constraints. Here we formulate the conventional "Weighted Minimum Norm" (WMN) solution in terms of hierarchical linear models. An "Expectation-Maximisation" (EM) algorithm is used to obtain a "Restricted Maximum Likelihood" (ReML) estimate of the hyperparameters, before estimating the "Maximum a Posteriori" solution itself. This procedure can be considered a generalisation of previous work that encompasses multiple constraints. Our approach was compared with the "classic" WMN and Maximum Smoothness solutions, using a simplified 2D source model with synthetic noisy data. The ReML solution was assessed with four types of source location priors: no priors, accurate priors, inaccurate priors, and both accurate and inaccurate priors. The ReML approach proved useful as: (1) The regularisation (or influence of the a priori source covariance) increased as the noise level increased. (2) The localisation error (LE) was negligible when accurate location priors were used. (3) When accurate and inaccurate location priors were used simultaneously, the solution was not influenced by the inaccurate priors. The ReML solution was then applied to real somatosensory-evoked responses to illustrate the application in an empirical setting.

Algorithms↗

General solution of cable theory with both ends sealed.

General solution of the cable theory with both ends sealed when injecting an arbitrary current at an arbitrary point of the cable is presented, which is a time-dependent transient solution. The solution is an infinite series, each term of which is the product of a cosine term including a position variable only and an exponential term including a time variable only. The general solution contains almost all solutions reported hitherto as particular cases and the mutual relations among the various solutions of quite different forms are clarified by this general solution. Moreover the shorter the cable becomes, the more rapidly this solution converges, therefore it is useful for an analysis of the short cable in the case where the relative deviation error may grow large. The truncation error can also be estimated as the solution is an infinite series of simple functions.

Animals↗

Schedule induction conditions not only exaggerate intake but also enhance drug solution choice.

In previous research, rats exposed to daily, 3 h sessions of schedule-induced polydipsia (SIP) self-administered high doses of cocaine orally. However, a strong and durable preference for cocaine solution to water requires training in addition to mere oral self-administration exposure. If cocaine is dissolved in a preferred vehicle solution, and the vehicle is subsequently faded to water, then a strong preference for cocaine remains. A similar preference can be instituted for lidocaine solution. Such preferences may develop because the gustatory property of a drug becomes associated with the preferred vehicle and remains to function as a durable conditioned reinforcer after vehicle fading. To determine if drug preference is solely a function of this posited conditioning mechanism, or whether it also depends upon the SIP condition, rats were exposed to daily, 3 h sessions of single-ration feeding, rather than the SIP condition. A preferred vehicle (glucose/saccharin solution) was slowly faded from a 0.19 mg/ml lidocaine solution, which was presented concurrently with a choice for water. Although a preference for lidocaine solution to water could be generated, it occurred for only 5 out of 9 rats, and the preference was relatively unstable. By contrast, in two previous studies using SIP, 26 out of 27 rats maintained a preference for lidocaine solution. Thus, SIP not only exaggerates the amount of drug solution ingested but also contributes to the fixation of the associative drug solution choice.

Animals↗

Solute transport under non-linear sorption and decay.

Contaminant transport in aquifers is usually represented by a solution to the advective-dispersive differential equation. When the contaminant is subject to non-linear degradation or decay, or it is characterized by a chemical constituent that follows a non-linear sorption isotherm, the resulting differential equation is non-linear. Using the method of decomposition, series solutions were obtained for the non-linear equation. The series were used to derive and test "simulant" solutions that aries using the concept of double decomposition. Simulant solutions are closed-form analytic expressions that approximate part of the series These expression are simple, stable, and flexible. They permit an accurate forecasting of contaminant propagation .under non-linearity in laboratory or field investigations at early or prolonged times after the spill. In this article, the practical scenario of an instantaneous spill, and that of a constant concentration boundary condition, is studied for situations of non-linear decay, non-linear Freundlich isotherm, and non-linear Langmuir isotherm. The solutions are verified with limited well-known analytical solutions of the linear reactive and non-reactive equations with excellent agreement, and with limited finite difference solutions. Plumes undergoing non-linear decay experience a profile re-scaling with respect to that of linear decay, the degree of which is controlled by magnitude of the non-linear parameter b. The direction of the scaling (scaling up or scaling down with respect to the linear decay plume) is controlled by the magnitude of C (whether greater or less than 1) in relation to the magnitude of b (whether greater or less than 1). When C>1, values of b<1 produce plumes that experience less decay (i.e., are scaled up) than that of the linear decay, whereas values of b> 1 produce non-linear plumes that experience more decay (i.e., are scaled down) than that of the linear decay. The opposite effect is observed when concentrations are less than 1. In other words, when C<1, values of beta<1 produce non-linear plumes that experience more decay (i.e., are scaled down) than that of the linear decay, whereas values of b>1, produce non-linear plumes that experience less decay (i.e., are scaled up) than that of the linear decay. A plume undergoing non-linear sorption according to a Freundlich isotherm retards the processses of advection and dispersion with respect to a plume with no sorption. Similar to the case of non-linear decay, whether this retardation is more or less pronounced than that of the linear sorption plume depends on whether the values of b and C are greater or less than 1. The solution presented here for the advective dispersive equation subject to a Freundlich sorption isotherm is restricted to concentration greater than 1. When C>1 and b<1, the decrease in mobility in the non-linear plume is not as pronounced as that of a plume modeled by a linear isotherm. Plume shape may be quite sensitive to the values of the non-linear parameters. Plumes with parameter values b<1 (and C> 1) exhibit the well-know lack of symmetry with respect to their center of mass, sharp fronts, and the tailing effects observed at hazardous waste sites. As the magnitude of the non-linear"retardation" can now be observed quantitatively with models presented herein. The models developed also simulate the case of b> 1 (i.e., "unfavorable" sorption), which produce a plume even more retarded than the linear. The shape of a contaminant plume following a non-linear Langmuir isotherm is very sensitive to the magnitude of the non-linear parameter alpha. Approximate solutions for mild non-linearity are presented.

Models, Theoretical↗

Aluminium speciation in forest soil solution--modelling the contribution of low molecular weight organic acids.

The concentrations of Al bound to identified low molecular weight organic acids (LMWOAs), phosphate and humic compounds in soil solutions (O1, O2, E, B1 and B2 horizons) from Fennoscandinavian coniferous forest soils were calculated. Two models were evaluated: WHAM (Winderemere Humic Aqueous Model) and a model treating the natural organic acids as monoprotic. The WHAM model was calibrated to find an average charge balance of unity, and then used for Al speciation. This was achieved considering approximately 80% of the natural fulvic acid to be 'active'. For the monoprotic model, constants obtained from previous fitting of soil solution data were used and the model was calibrated using acid/base titrations. The modelling confirms that the low molecular weight acids are important complex formers, binding on average 11-42% (O), 19-20% (E), and 0-30% (B) of the total Al in solution depending on the model used. The monoprotic model yielded higher concentrations than WHAM. Both models predicted that the major part of Al in solution was organically complexed to humic substances and LMWOAs, which was consistent with analytical values of 'quickly reacting' Al (monomenc inorganic forms; 12-14% of Al(tot) on average in the E and B1 solutions). Both models could predict the magnitude of the analytical values (RMSD = 4-5 microM). On average the WHAM model showed a better fit for the E horizon solutions and the monoprotic model for the upper B horizon. The pH dependence of the low molecular weight fraction of Al was modelled in the pH range 3-5.5 for a 'typical' O1 and E solution assuming no other changes in soil solution composition. The extrapolation showed that the models had a different pH dependence. The concentration of Al bound to LMWOAs in WHAM decreased with higher pH while the opposite was seen for the monoprotic model. Also the influence of the concentration of total Al in solution was modelled. The models showed similar trends but for the 'typical' O1 horizon sample the monoprotic model yielded higher concentrations of Al bound to LMWOAs than WHAM.

Aluminum↗

Forced-choice discrimination of equimolar NaCl and LiCl solutions in rats: effects of ablating the chemosensitive area postrema on acquisition and retention.

The area postrema (AP), a chemosensitive organ located in the fourth ventricle, has been shown to mediate the formation of a lithium-induced conditioned taste avoidance (CTA) in rats. The present experiments examined the role of the AP in the discrimination between two equimolar solutions of sodium chloride (NaCl) and lithium chloride (LiCl). In the first experiment adult male rats were trained to discriminate between equimolar (0.12 M) solutions of NaCl and LiCl in a forced-choice procedure over a 10-day acquisition phase. Subsequently half of the rats (n = 7) received AP lesions (APX) and the other half (n = 7) were given sham lesions (SHAM). In the retention phase all animals were again exposed to the same salt solutions over a 10-day period. Good discrimination (P < 0.001) between the two salt solutions was demonstrated by the end of the acquisition phase and both the APX and SHAM groups exhibited robust retention (P < 0.01) of this discrimination in the second phase. However, when only a LiCl solution was available the APX group ingested significantly more (P < 0.01) than the SHAM rats. No significant group difference emerged when only NaCl was available. In the second experiment rats received ablations of AP or sham lesions and were then trained to discriminate between 0.12 M NaCl and LiCl solutions in a forced-choice procedure over a 10-day period. Both groups exhibited a clear discrimination (P < 0.01) between the two solutions by the end of the acquisition phase. APX rats ingested significantly more LiCl (P < 0.01) than did the SHAM group when this was the only type of fluid available. Again, no such difference was evident when only NaCl was available. These experiments demonstrate that the AP is not necessary for either the acquisition or retention of a discrimination between equimolar solutions of NaCl and LiCl in a forced-choice procedure and that this discrimination is not mediated by a conditioned taste aversion to the LiCl solution.

Animals↗

Experimental infusion phlebitis: importance of titratable acidity on phlebitic potential of infusion solution.

The titratable acidity of infusion solutions has never been taken into account in infusion phlebitis. This study aims to clarify the importance of titratable acidity on the phlebitic potential of infusion solutions. Solutions with different titratable acidity (from 0.16 to 12 mEq/L) were infused into the ear veins of 6 rabbits for 6 h at 10 mL/kg/h, and the veins were later examined histopathologically. Even at pH 4.0, a commercial 10% glucose solution scarcely caused any changes because of its very low titratable acidity (0.16 mEq/L). A 10% glucose solution with its titratable acidity adjusted to 3 mEq/L (pH 4.3) with citrate and NaOH, however, caused phlebitic changes in all 6 rabbits, and adjusting the titratable acidity to 12 mEq/L (pH 4.4) increased the degree of phlebitis. On the other hand, a 10% glucose solution with a pH of 5.4 and a titratable acidity of 6 mEq/L caused slight phlebitic changes in half the rabbits. These results suggest that 1) the titratable acidity of infusion solutions is important to the phlebitic potential when the pH is low, 2) when the pHs are similar, the phlebitic potential of infusion solutions depend on the titratable acidity, and 3) the phlebitic potential of infusion solutions can not be estimated by pH or titratable acidity alone.

Journal Article↗

Short term maintenance of sheep preantral follicles in situ in 0.9% saline and Braun-Collins solution.

The present study has investigated the efficiency of 0.9% saline solution and Braun-Collins solution in the preservation of sheep preantral follicles in situ, at different temperatures and different incubation periods. The ovaries were divided into 19 fragments for each animal. One ovarian fragment was taken randomly and immediately fixed for histology (control-time zero). The other 18 ovarian fragments were randomly distributed in tubes containing 2ml of 0.9% saline solution or Braun-Collins solution at 4, 20 or 39 degrees C for 4, 12 or 24h. A total of 1629, 208 and 63 primordial, primary and secondary follicles were examined, respectively. Histological analysis showed that the storage of ovarian fragments in both solutions at 20 or 39 degrees C significantly reduced the percentage of morphologically normal preantral follicles (MNPF) when compared with the control, except after preservation in 0.9% saline solution at 20 degrees C for 4h. In contrast, the preservation at 4 degrees C, in both solutions, kept the percentage of MNPF similar to control values. In conclusion, this study shows for the first time that sheep preantral follicles can be preserved in situ successfully at 4 degrees C in 0.9% saline solution or Braun-Collins solution for up to 24h.

Journal Article↗

In situ gelling of alginate/pluronic solutions for ophthalmic delivery of pilocarpine.

We prepared a series of alginate and Pluronic-based solutions as the in situ gelling vehicles for ophthalmic delivery of pilocarpine. The rheological properties, in vitro release as well as in vivo pharmacological response of polymer solutions, including alginate, Pluronic solution, and alginate/Pluronic solution, were evaluated. The optimum concentration of alginate solution for the in situ gel-forming delivery systems was 2% (w/w) and that for Pluronic solution was 14% (w/w). The mixture of 0.1% alginate and 14% Pluronic solutions showed a significant increase in gel strength in the physiological condition; this gel mixture was also found to be free flowing at pH 4.0 and 25 degrees C. Both in vitro release and in vivo pharmacological studies indicated that the alginate/Pluronic solution retained pilocarpine better than the alginate or Pluronic solutions alone. The results demonstrated that the alginate/Pluronic mixture can be used as an in situ gelling vehicle to increase ocular bioavailability.

Alginates↗

Turbulence effects on volatilization rates of liquids and solutes.

Volatilization rates of neat liquids (benzene, toluene, fluorobenzene, bromobenzene, ethylbenzene, m-xylene, o-xylene, o-dichlorobenzene, and 1-methylnaphthalene) and of solutes (phenol, m-cresol, benzene, toluene, ethylbenzene, o-xylene, and ethylene dibromide) from dilute water solutions have been measured in the laboratory over a wide range of air speeds and water-stirring rates. The overall transfer coefficients (K(L)) for individual solutes are independent of whether they are in single- or multi-solute solutions. The gas-film transfer coefficients (kG) for solutes in the two-film model, which have hitherto been estimated by extrapolation from reference coefficients, can now be determined directly from the volatilization rates of neat liquids through a new algorithm. The associated liquid-film transfer coefficients (kL) can then be obtained from measured K(L) and kG values and solute Henry law constants (H). This approach provides a novel means for checking the precision of any kL and kG estimation methods for ultimate prediction of K(L). The improved kG estimation enables accurate K(L) predictions for low-volatility (i.e., low-H) solutes where K(L) and kGH are essentially equal. In addition, the prediction of K(L) values for high-volatility (i.e., high-H) solutes, where K(L) approximately equal to kL, is also improved by using appropriate reference kL values.

Algorithms↗

Automatic and subsequent dissolution and precipitation process in inorganic macroionic solutions.

We report an interesting phenomenon in the NaCl-containing aqueous solution of {Mo72Fe30} macroions, where dissolution and precipitation processes of hydrophilic macroions automatically and subsequently occur without changing external conditions or chemical reactions. Our previous work indicates that {Mo72Fe30} macroions tend to slowly self-assemble into single-layer, vesicle-like "blackberries". Such macroions have two solute states in solutions: the entropy-favored general state (homogeneous distribution) and the free-energy favored second solute state (blackberries). With additional salts, the originally stable blackberries become less stable due to their shortened screening length, and they tend to further aggregate and precipitate at much lower concentrations. Therefore, in such a solution, we can observe a subsequent process: crystal solids --> homogeneous single macroion solution --> homogeneous blackberry solution --> precipitates containing noncrystalline solids. In other words, we observed the behaviors of both soluble inorganic ions and colloids in the same solution due to the unique features of the macroions. Static and dynamic laser light scattering, as well as AFM measurements, were used to characterize both the macroionic solutions and the precipitates.

Journal Article↗

Solution properties and sweetness response of selected bulk and intense sweeteners.

Two bulk sweeteners (sucrose and maltitol) and four intense sweeteners (acesulfame K, aspartame, sodium cyclamate, and sodium saccharin) are used in this study. Densities and sound velocity values of the sweeteners in solution are measured at 20 degrees C, and their apparent molar and specific volumes, their isentropic apparent molar and specific compressibilities, as well as their compressibility hydration numbers are calculated and reported. The introduction of solute molecules in water results in a volume change of the solvent as a result of attractive forces exerted by the solute molecules; such forces are in the form of electrostrictive or hydrogen-bonding forces, or charge-dipole attraction. Changes of molar volumes with increasing concentration give an indication of the extent of solute-solute interaction, whereas isentropic compressibilities give a direct measurement of the state of hydration of the solute molecules. The compressibility hydration numbers reported give an indication of the number of water molecules disturbed by the presence of each solute molecule in solution. Isentropic compressibilities seem to be a more sensitive parameter for distinguishing the bulk sweeteners from the artificial sweeteners. The sweetness response of the sweeteners is then explained in terms of their solution behaviors.

Aspartame↗

Effect of storage temperature and pyruvate on kinetics of anthocyanin degradation, vitisin A derivative formation, and color characteristics of model solutions.

The formation of vitisin A, an anthocyanin formed naturally in small quantities in maturing port wines, was studied in model wine solutions at several storage temperatures (10, 15, 20, and 32 degrees C). Vitisin A was formed through the interaction between malvidin 3-glucoside and pyruvic acid, Acylated forms of vitisin A, having the 6-position of the sugar acylated with acetic acid (3-acetylvitisin A) and p-coumaric acid (3-p-coumarylvitisin A), were also formed through the interaction between pyruvic acid and malvidin 3-acetylglucoside and malvidin 3-p-coumarylglucoside, respectively. A maximum degradation of the anthocyanins was obtained at higher temperatures, and it followed a first-order kinetics both with and without pyruvic acid in the solution. Whereas at low temperatures (10 and 15 degrees C) the presence of pyruvic acid accelerated the kinetic reaction, at higher temperatures (20 and 32 degrees C) it decreased it. The activation energy values for the degradation of the three anthocyanins in model solutions without and with pyruvic acid were not significantly different from each other. At low temperatures the highest concentrations of vitisin A compounds were obtained. All solutions showed a decrease in L value, indicating that all solutions became darker. This change increased with increasing temperature. All model solutions increased in the hue angle, indicating that the solutions changed from a bluish-red to an orange-red or even brownish-red color. Samples without pyruvic acid remained lighter and became browner than those with pyruvic acid. A good correlation between the amount of vitisin A in the solution and hue angle was found, indicating that vitisin A may contribute the orange-red of solutions, compared to the browner control.

Acetylation↗

Encapsulation of saline solution by tetrahydrofuran clathrate hydrates and inclusion migration by recrystallization.

Encapsulation of saline solution as an impurity in tetrahydrofuran clathrate hydrates grown in a stoichiometric solution with 3 wt % NaCl and the release of a saline solution during melting along with inclusion migration by hydrate recrystallization during annealing are studied using a directional growth apparatus in combination with a Mach-Zender interferometer. Interferometric observation revealed that the salt concentration increased locally in the solution near the growth interface. The time evolution of salt concentration in the solution was in accordance with the numerical results obtained from the diffusion equation for salt, assuming perfect rejection of salt by the hydrate. However, after the interfacial pattern developed into a serrated pattern (periodical array of trough and crest), the salt concentration in the solution ceased to increase, deviating from the theoretical value. This indicates that the saline solution was encapsulated by the growth hydrate. On the other hand, upon melting of the slowly grown hydrate, the salt concentration near the interface was observed to be locally high at the location of the trough during growth, whereas it was dilute at the location of the growth crest. Furthermore, when the hydrate was annealed under an applied temperature gradient, the inclusions (encapsulated saline solution) in the hydrate migrated toward the bulk solution and were finally expelled by hydrate recrystallization. The migration speed of the inclusions increased with a larger temperature gradient. By melting the sample over a sufficiently long anneal time, the melt was determined to be completely desalinated.

Journal Article↗

Three-dimensional etching profiles and surface speciations (via attenuated total reflection-fourier transform infrared spectroscopy) of silicon nanowires in NH4F-buffered HF solutions: a double passivation model.

A systematic study of the etching behavior, in terms of three-dimensional profiles, of one-dimensional (1-D) silicon nanowires (SiNWs) in NH(4)F-buffered hydrofluoric acid (BHF) solutions of varying concentrations and pH values and the surface speciations of the resulting etched SiNW surfaces, as characterized by attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, is reported. It was found that SiNWs are stable only in relatively narrow pH ranges of the BHF solutions. The results are rationalized in terms of a "double passivation" model. When SiNWs are etched in BHF solutions with pH values of 1-3, the surfaces are passivated with hydrogen (inner layer) giving rise to surface moieties such as Si-H(x) species (x = 1-3); at high HF concentrations, the H-terminated Si surfaces are covered with a hydrogen bonding network of HF and related molecules (oligomers, etc.), providing an outer-layer passivation. When SiNWs are etched in BHF solutions with pH values of 11-14 (by adding a strong base such as NaOH), the surfaces are oxygen-terminated with surface moieties such as Si-(O(-))(x)() species (x = 1-3); at high NH(4)F concentrations, the negatively charged Si surfaces are stabilized by NH(4)(+) ions via ionic bonding, again providing outer-layer passivation. In BHF solutions with pH values of 3-11, the surface speciation, consisting of Si-(OH)(x)(O(-))(y) (x + y = 1-3) species, is unstable and etched away rapidly. The surface speciations of SiNWs etched in various BHF solutions were explored via ATR-FTIR spectroscopy. It was found that, while etching SiNWs with HF-rich BHF solutions with pH < 4 gave rise to Si-H(x)() surface species, no surface Si-H(x) species were observed with SiNWs etched in BHF solutions with pH >/= 4 (HF/NH(4)F </= 1:1). In sharp contrast, etching of two-dimensional (2-D) Si wafers with either HF, NH(4)F, or BHF etchants produces Si-H(x) species on the surface. Finally, while HF is a much more efficient etchant than NH(4)F for 2-D Si surfaces, NH(4)F is found to be as efficient an etchant as HF for SiNWs (this work). We believe that these differences can be attributed to the nanometer size (corresponding to the roughness scale in 2-D wafers) of SiNWs on one hand and the lack of "passivation" by the hydrogen bonding network of HF and related molecules at pH >/= 4 on the other. These two factors, among others, contribute to the rapid hydrolysis of the surface Si-H(x)() species (and the etching of the SiNWs), particularly in BHF solutions with low HF/NH(4)F ratios and high pH values (pH >/= 4).

Journal Article↗

Studies of diffusional release of a dispersed solute from polymeric matrixes by finite element method.

This paper presents systematic analyses by the finite element method of release kinetics of a dispersed solute from various matrixes (i.e. , slab, sphere, cylinder, and convex tablet), with or without boundary-layer resistance, into a finite or an infinite external volume. In the case of sink conditions, the numerical results agree well with the existing analytical solutions. For the problems of solute release into a finite external volume, where the analytical solutions are not available, this work has provided numerical solutions of the differential equations describing the release kinetics, moving boundaries, and concentration profiles. This work has also revealed the dependence of release kinetics on the initial solute loading, the external volume, and the boundary-layer thickness. The method presented here can describe the entire process of diffusional release before and after the dispersed solute has been dissolved without the pseudo steady-state assumption and it is applicable to both small and large ratio of initial solute loading to the solute solubility in the matrix.

Algorithms↗

Salt tolerance of an aqueous solution of a novel amphiphilic polysaccharide derivative.

An aqueous solution of an amphiphilic polysaccharide derivative, hydrophobically (stearyl alkyl group) and hydrophilically (sulfonic-acid salt group) modified hydroxyethylcellulose (HHM-HEC), showed increased viscosity, elasticity, and thixotropic properties in response to the addition of monovalent and divalent salts. Furthermore, the HHM-HEC solution had a transparent appearance at a NaCl concentration of 7 wt %. Since it showed superior salt tolerance to HEC, we focused attention on the two substituents of HHM-HEC and prepared HEC derivatives, namely, hydrophobically modified hydroxyethylcellulose (R-HEC), hydrophilically modified hydroxyethylcellulose (S-HEC), and nonmodified hydroxyethylcellulose (HEC). In addition, we used oscillatory, thixotropic, and fluorometric methods to compare the rheological properties of HHM-HEC with those of other derivatives in the presence of NaCl and ZnCl2, and attempted to elucidate the respective roles of the two substituents of HHM-HEC solution in the salt-tolerance mechanism. As the NaCl concentration in the HHM-HEC solution increased, the values of the elastic modulus G' and the viscous modulus G'' increased, and, moreover, the relative intensities of the first (I1 = 372 nm) and the third (I3 = 383 nm) vibronic bands of the pyrene monomer emission spectrum (the I1/I3 ratio) decreased. These results suggested that the added salt strengthened the three-dimensional network structure of the HHM-HEC polymer by the formation of cross-linkages through the association of hydrophobic substituents. This hydrophobic substituent was therefore essential in allowing HHM-HEC to exhibit a high viscosity in a salt solution. Although the R-HEC solution showed a higher viscosity than did the HHM-HEC solution in the absence of added salts, it became cloudy and lost its viscosity at high NaCl concentrations, apparently because of the shrinkage of its network structure. This signified that the hydrophilic substituent was essential for the sufficient solubility of HHM-HEC to show its rheological properties in a salt-rich solution. We propose to explain how the viscosity of HHM-HEC increases in the presence of salts as follows: Added salts weaken the electrostatic repulsion between the hydrophilic substituents, thereby enhancing the interactions of hydrophobic substituents and consequently increasing the rigidity of the HHM-HEC solution.

Journal Article↗

Effects of depolarizing or non-depolarizing preservation solutions on human endothelial cells during cold hypoxia.

1. Hypothermic storage of whole organs flushed with a preservation solution is common practice in clinical transplantation. This procedure leaves vascular endothelial cells in direct contact with the preservation solution during the length of the cold ischaemic period. 2. Aiming to study the effects of organ preservation on vascular endothelium, we subjected cultures of human umbilical vein endothelial cells to hypoxic and hypothermic storage conditions in vitro for 3 or 16 h. Four preservation solutions with different levels of sodium and potassium were tested. Morphometric analysis and 51Cr leakage index were used to assess monolayer continuity, cell viability and membrane integrity. 3. Hypothermic storage resulted in severe changes in endothelial cell morphology with formation of intercellular gaps that destroyed monolayer continuity after only 3h. Cellular blebbing was a common feature in seriously damaged cells. 4. Morphometric analysis and 51Cr leakage results correlated well. No significant differences between the solutions tested were found after 3h of hypothermic hypoxic storage. After 16h, viability and monolayer continuity were significantly better preserved (Mann-Whitney, P < 0.01) in cells stored in lactobionate-based solutions than in hypertonic citrate solutions. No significant differences were found between endothelial cells stored in extracellular versus intracellular types of solutions for the lactobionate-based solutions. 5. The results of the present experiment showed that after a period of hypothermic hypoxic storage, vascular endothelial cells appeared morphologically deformed and poorly attached in vitro. Lactobionate-based preservation solutions were more effective in preserving viability and continuity. Protection of vascular endothelium under cold hypoxic conditions could be a critical factor in successfully preserving organs for transplantation.

Cell Hypoxia↗