No abstract

Sphingolipids are key lipid regulators of cell viability: ceramide is one of the key molecules in inducing programmed cell death (apoptosis), whereas other sphingolipids, such as ceramide 1-phosphate, are mitogenic. The thermotropic and structural behavior of binary systems of N-hexadecanoyl-D-erythro-ceramide (C(16)-ceramide) or N-hexadecanoyl-D-erythro-ceramide-1-phosphate (C(16)-ceramide-1-phosphate; C(16)-C1P) with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was studied with DSC and deuterium nuclear magnetic resonance ((2)H-NMR). Partial-phase diagrams (up to a mole fraction of sphingolipids X = 0.40) for both mixtures were constructed based on DSC and (2)H-NMR observations. For C(16)-ceramide-containing bilayers DSC heating scans showed already at X(cer) = 0.025 a complex structure of the main-phase transition peak suggestive of lateral-phase separation. The transition width increased significantly upon increasing X(cer), and the upper-phase boundary temperature of the mixture shifted to approximately 65 degrees C at X(cer) = 0.40. The temperature range over which (2)H-NMR spectra of C(16)-ceramide/DPPC-d(62) mixtures displayed coexistence of gel and liquid crystalline domains increased from approximately 10 degrees for X(cer) = 0.1 to approximately 21 degrees for X(cer) = 0.4. For C16-C1P/DPPC mixtures, DSC and (2)H-NMR observations indicated that two-phase coexistence was limited to significantly narrower temperature ranges for corresponding C1P concentrations. To complement these findings, C(16)-ceramide/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and C16-C1P/POPC mixtures were also studied by (2)H-NMR and fluorescence techniques. These observations indicate that DPPC and POPC bilayers are significantly less perturbed by C(16)-C1P than by C(16)-ceramide and that C(16)-C1P is miscible within DPPC bilayers at least up to X(C1P) = 0.30.

PEG-stabilized lipid aggregates are a promising new class of model membranes in biotechnical and pharmaceutical applications. CE techniques, field-flow fractionation, light scattering, quartz crystal microbalance (QCM), and microscopic techniques were used to study aggregates composed of 1-palmitoyl-2-oleyl-sn-glycero-phosphatidylcholine (POPC) and PEG-lipid conjugates. The PEG-lipids, with PEG molar masses of 1000, 2000, and 3000, were 1,2-diacyl-sn-glycero-3-phosphoethanolamine-N-[methoxy-(PEG)] derivatives with either dimyristoyl (DM, 14:0) or distearoyl (DS, 18:0) acyl groups. The 80/20 mol% POPC/PEG-lipid dispersions in HEPES at pH 7.4 were extruded through 100 nm size membranes. Asymmetrical flow field-flow fractionation (AsFlFFF), photon correlation spectroscopy (PCS), and dynamic light scattering (DLS) were used to determine the sizes of POPC and the PEGylated aggregates. All methods demonstrated that the DSPEG-lipid sterically stabilized aggregates were smaller in size than pure POPC vesicles. The zeta potentials of the aggregates were measured and showed an increase from -19 mV for pure POPC to -4 mV for the POPC/DSPEG3000 aggregates. Atomic force microscopy (AFM), electron cryo-microscopy (EM), and multifrequency QCM studies were made to achieve information about the PEGylated coatings on silica. Lipid aggregates with different POPC/DSPEG3000-lipid ratios were applied as capillary coating material, and the 80/20 mol% composition was found to give the most suppressed and stable EOFs. Mixtures of low-molar-mass drugs and FITC-labeled amino acids were separated with the PEGylated aggregates as carriers (EKC) or as coating material (CEC). Detection was made by UV and LIF.

The proton-induced x-ray emission method was used to analyze lead concentrations in enamel and dentine of deciduous teeth of 105 6- and 9-yr-old children living in two Finnish towns. Helsinki, the capital city, was assumed to represent high lead exposure and Kuopio, a country town in the middle of Finland, low or moderate lead exposure. In all but two teeth the enamel contained higher lead concentrations than dentine. The individual enamel-dentine lead concentration ratio was not stable but varied greatly. The median dentine lead concentration for 9-yr-old children in Helsinki and Kuopio was 2.0 ppm and 2.9 ppm, respectively, and for 6-yr-old children was 2.5 ppm and 2.7 ppm, respectively. The enamel lead concentrations found in 9-yr-olds in Helsinki and Kuopio were 4.2 and 4.5 ppm, and in 6-yr-olds were 9.1 and 4.4 ppm, respectively. The results reveal low or moderate lead concentrations. Nevertheless, a twofold and statistically significant (P less than .01) increase was found in the enamel of Helsinki children born in 1974 compared with those born in 1971.

Fusidic acid (FA), a narrow spectrum steroidal antibiotic, is useful for treatment of most skin, conjunctival, and corneal infections and also in infections caused by atypical microbes in the surface of the eye. Liposome electrokinetic capillary chromatography (LEKC) was used to study the interactions between FA and lipid membranes. Liposomes prepared by extrusion were composed of 1-palmitoyl-2-oleyl-sn-glycero-3-phosphocholine (POPC) and 1-palmitoyl-2-oleyl-sn-glysero-3-phosphor-L-serine (POPS), cholesterol, FA, and sphingomyelin (SM) in various molar ratios. 26 different liposome dispersions were studied as dispersed (pseudostationary) phase in LEKC. The hydrophobicities of the liposomes were evaluated by calculating the retention factors of model neutral steroids. The retention factors were calculated using the EOF and the effective electrophoretic mobilities of the analytes and the liposomes. The latter were separately determined by capillary electrophoresis with a polyacrylamide (PAA)-coated capillary. FA-lipid membrane interactions were studied by determining the retention factor of FA. In addition, liposomes prepared from lipids extracted from Escherichia coli bacterium were studied and used as dispersed phase in LEKC for interaction studies between FA and lipid membranes.