Calcium Oxalate Monohydrate Precipitation at Phospholipid Monolayer Phase Boundaries

2004 ◽  
Vol 823 ◽  
Author(s):  
Isa O. Benítez ◽  
Daniel R. Talham

AbstractThe precipitation of calcium oxalate monohydrate (COM) was observed at biphasic phospholipid Langmuir monolayers with the aid of Brewster angle microscopy. COM appears preferentially at phase boundaries of a monolayer of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in a state of liquid expanded/liquid condensed coexistance. However, when the phase boundary is created by two different phospholipids that are phase segregated, such as DPPC and 1,2-dimiristoyl-sn-glycero-3-phosphocholine (DMPC), crystal formation occurs away from the interface. It is suggested that COM growth at phase boundaries is preferred only when there is molecular exchange between the phases.

2003 ◽  
Vol 774 ◽  
Author(s):  
Isa O. Benítez ◽  
Rénal Backov ◽  
Saeed R. Khan ◽  
Daniel R. Talham

AbstractThe precipitation of calcium oxalate monohydrate (COM) at phospholipid monolayers has been observed in-situ by Brewster angle microscopy (BAM). A monolayer of 1,2-dipalmitoylsn-glycero-3-phosphocholine (DPPC) compressed to a LC state over a calcium oxalate subphase shows the growth of COM as very bright spots. The identity of COM was confirmed in a transferred film by scanning electron microscopy. BAM can also be used to determine where COM precipitates when the monolayer has two phases at equilibrium. Monolayers of DPPC and 1,2-dipalmitoyl-sn-glycero-3-[phospho-rac-(1-glycerol)] (DPPG) crystallize COM at phase boundaries. In addition, phase separated binary phospholipid mixtures of DPPC and 1,2-dimiristoyl-sn-glycero-3-phosphocholine (DMPC) have been prepared and monitored by BAM. The crystal growth in this case is confined to domains of DPPC due to its ability to form a liquid condensed phase.


2005 ◽  
Vol 284 (1) ◽  
pp. 44-50 ◽  
Author(s):  
P. Degen ◽  
H. Rehage ◽  
F. -G. Klärner ◽  
J. Polkowska

1997 ◽  
Vol 106 (5) ◽  
pp. 1913-1920 ◽  
Author(s):  
Ellis Teer ◽  
Charles M. Knobler ◽  
Carsten Lautz ◽  
Stefan Wurlitzer ◽  
John Kildae ◽  
...  

Langmuir ◽  
2001 ◽  
Vol 17 (5) ◽  
pp. 1477-1482 ◽  
Author(s):  
J. Miñones, ◽  
C. Carrera ◽  
P. Dynarowicz-Ła̧tka ◽  
J. Miñones ◽  
O. Conde ◽  
...  

1970 ◽  
Vol 46 (1) ◽  
pp. 47-52
Author(s):  
MM Hossain ◽  
T Kato

The effect of head groups on the thermodynamic properties and morphological features of the domains formed in the Langmuir monolayers at 10 oC has been investigated by a film balance and a Brewster angle microscopy (BAM). 2-hydroxyethyl myristate (2-HEM) and n-tetradecanoyl N-ethanolamide (NHEA-14), having the same chain length but different head groups have been taken as amphiphiles. Both the amphiphiles represent a first-order LE-LC phase transition at 10 oC at the air-water interface. The critical surface pressure necessary for this phase transition is 6.0 mN/m for 2-HEM and 1.0 mN/m for NHEA-14. The surface morphologies of the domains are entirely different. The domains of 2-HEM are circular having internal texture, while those of NHEA-14 are dendritic having directional characteristics. The presence of interfacial hydrogen bonding in the latter amphiphile should be responsible for the formation of such characteristic domains in the case of latter amphiphile. Key words: Langmuir monolayers; Phase transition; Brewster angle microscopy; 2-hydroxyethyl myristate; n-tetradecanoyl Nethanolamide. DOI: http://dx.doi.org/10.3329/bjsir.v46i1.8104 Bangladesh J. Sci. Ind. Res. 46(1), 47-52, 2011


2004 ◽  
Vol 37 (13) ◽  
pp. 4872-4881 ◽  
Author(s):  
Yu. K. Godovsky ◽  
G. Brezesinski ◽  
J. Ruiz-Garcia ◽  
H. Möhwald ◽  
T. R. Jensen ◽  
...  

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