The eþ ects of uniaxial drawing on the free volume of poly(chlorotriýuoroethylene) have been investigated using the positron annihilation lifetime technique. Annealing measurements were made both in unstrained and maximum strained conditions of the polymer to understand the inýuence of residual stre
Influence of Ca2+ and ethanol on the aggregation and thermal phase behaviour of l-dihexadecylphosphatidylcholine liposomes
✍ Scribed by Anu Kõiv; Paavo K.J. Kinnunen
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 648 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0009-3084
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✦ Synopsis
The influence of Ca 2+ and ethanol on vesicle aggregation and thermal phase behaviour of the diether lipid 1,2-dihexadecylphosphatidylcholine (DHPC) was studied by light absorbance and DSC. At temperatures below the pretransition the ethanolinjected vesicles of L-DHPC were rapidly aggregated by Ca 2÷. Upon raising the cation concentration a biphasic increase in aggregation saturating at an approximate [Ca2+]/[lipid] ratio of 1.5:1 was observed. Further increase in [Ca 2÷] up to [Ca2+]/[lipid] stoichiometries exceeding 2.5:1 led to the loss of aggregation. Removal of ethanol by dialysis abolished Ca2+-induced aggregation. Ethanol-injected vesicles of the ester-linked L-dipalmitoylphosphatidylcholine (L-DPPC) or the racemic DL-DHPC were not aggregated by Ca 2+ thus indicating the importance of the absence of ester carbonyls as well as the stereochemical configuration of the lipid in determining the mode of interaction of DHPC with Ca 2+. Differential scanning calorimetry of multilamellar liposomes of L-DHPC showed an increase by 8 ° in the pretransition temperature Tp in the presence of 250 mM ethanol. Both with and without ethanol, increasing concentrations of Ca 2+ corresponding to [Ca2+]/[lipid] ratios of 1:1 to 20:1 caused a gradual decrease in Tp and finally the disappearance of the pretransition. Concomitantly a slight elevation in T m occurred. No principal differences were observed in the thermal phase behaviour of the L-isomer and racemic DL-DHPC.
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