Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Dimyristoyl phosphatidyl

Rudolf and Cliff [3.43] described the inclusion of hemoglobin in liposomes (LEH), to produce a stable blood substitute. The liposomes were formed from a solution of soya bean - phosphatidylcholine (soy PC), cholesterol, dimyristoyl-phosphatidyl, DL-glycerol (DMPG), and alpha-tocopherol with a ratio of 10 9 0.9 0.1. The product was dried and... [Pg.223]

Figure 8-10 2H NMR spectra of dimyristoyl phosphatidyl-cholme-d27/water in lamellar phases at 40°C. One chain of the phosphatidylcholine is fully deuterated, containing 27 atoms of 2H. The mole ratios of water to lipid were 5.0 in (A) and 25.0 in (B). The average interfacial areas per alkyl chain as measured hy X-ray diffraction were 0.252 nm2 for (A) and 0.313 nm2 for (B). 2H NMR spectra are presented as "powder patterns" because the lipid molecules are randomly oriented in the magnetic field of the spectrometer as if in a powder. This gives rise to pairs of peaks symmetrically located on both sides of the origin. The separation distances are a measure of the quadrupole splitting of the NMR absorption line caused by the 2H nucleus. The various splittings of the resonances of the 13 -CH2- and one -CH3 groups reflect differences in mobility.109 The peaks have been assigned tentatively as indicated. From Boden, Jones, and Sixl.115 Courtesy of N. Boden. Figure 8-10 2H NMR spectra of dimyristoyl phosphatidyl-cholme-d27/water in lamellar phases at 40°C. One chain of the phosphatidylcholine is fully deuterated, containing 27 atoms of 2H. The mole ratios of water to lipid were 5.0 in (A) and 25.0 in (B). The average interfacial areas per alkyl chain as measured hy X-ray diffraction were 0.252 nm2 for (A) and 0.313 nm2 for (B). 2H NMR spectra are presented as "powder patterns" because the lipid molecules are randomly oriented in the magnetic field of the spectrometer as if in a powder. This gives rise to pairs of peaks symmetrically located on both sides of the origin. The separation distances are a measure of the quadrupole splitting of the NMR absorption line caused by the 2H nucleus. The various splittings of the resonances of the 13 -CH2- and one -CH3 groups reflect differences in mobility.109 The peaks have been assigned tentatively as indicated. From Boden, Jones, and Sixl.115 Courtesy of N. Boden.
We report here the results of a study of the adsorption of the alkaline earth cations to bilayer membranes formed from phosphatidylcholines with saturated chains dipalmitoyl phosphatidyl choline (DPPC) and dimyristoyl phosphatidyl choline (DMPC). Our salient result is that the adsorption of calcium is distinct from the other alkaline earth cations in two respects. First, only calcium adsorbs significantly more strongly to PCs with saturated chains than to phosphatidyl cholines with unsaturated chains, even when all lipids are present in the liquid crystalline state. Second, when the membranes are present in the frozen or gel state, the binding of calcium is significantly enhanced. We used two independent techniques to demonstrate this unique behavior of calcium. [Pg.53]

A variety of weak liquid crystalline media have been used to align carbohydrates. Examples include Pfl phage,147-150 filamentous bacteriophage fd,151 C12E5/ -hexanol,77,152-154 C8E5/ -octanol,155 cetylpyridinium bromide / -hexanol /NaCl,73,156-158 DMPC/DHPC (dimyristoyl-phosphatidyl choline / dihexanoyl-... [Pg.207]

Patel, H Schultz, T.W. and Cronin, M.T.D. (2002) Physico-chemical interpretation and prediction of the dimyristoyl phosphatidyl choline-water partition coefficient. J. Mol. Struct. (Theochem), 593, 9-18. [Pg.1137]

This model system studies the antioxidant potential against the attack of oxygen radicals on biomembranes from aqueous phase [52]. Antioxidant effects of olive phenols depend on their interaction with model membranes [53], e.g., oleuropein interacts with DMPC (dimyristoyl-phosphatidyl-choline) membranes. Oleuropein contains a sugar moiety needed to prevent drug access to lipid membranes [54]. In... [Pg.878]

Dimyristoyl- phosphatidyl-chdline DMPC 1 f" P-0-(CH2fe.N C 0 CH3 0 1 ——C—C13H27 0 II C—C13H27... [Pg.72]

Figure 2.2.6 Crystal structure of dimyristoyl-phosphatidyl-choline (DMPC). (a) Molecular structure. A- and B-forms (b) bilayer crystal sheets, A form.. Figure 2.2.6 Crystal structure of dimyristoyl-phosphatidyl-choline (DMPC). (a) Molecular structure. A- and B-forms (b) bilayer crystal sheets, A form..
Recently, the competitive adsorption dynamics of phospholipid/protein mixed system at the chloroform/water interface was investigated by using the drop volume technique. The three proteins P-Lactoglobulin, P-Casein, and Human Serum Albumin were used in this study. To investigate the influence of the phospholipid structure at concentrations close to the CAC (critic aggregation concentration) the four lipids dipalmitoyl phosphatidyl choline (DPPC), dimyristoyl phosphatidyl choline (DMPC), dimyristoyl phosphatidyl ethanolamine (DMPE)... [Pg.373]

The total lasalocid-membrane binding reaction is a very sensitive fimction of the membrane polar head group composition Incorporation of dimyristoyl phosphati-dic acid (DMPA) or dimyristoyl phosphatidyl ethanolamine (DMPE) into pure DMPC vesicles reduces the total lasalocid fluorescence relative to that observed in pure DMPC vesicles. Fluorescence lifetime experiments indicate the decrease in fluorescence is not due to reduction of the quantum yield of the bound lasalocid but rather to a reduction in the degree of binding. The sensitivity of total ionophore binding to polar head group composition is similar to that observed for the fluorescent spin probe l-anilino-8-naphthalenesulfonate and indicates... [Pg.100]


See other pages where Dimyristoyl phosphatidyl is mentioned: [Pg.342]    [Pg.383]    [Pg.391]    [Pg.408]    [Pg.162]    [Pg.9]    [Pg.45]    [Pg.26]    [Pg.316]    [Pg.252]    [Pg.16]    [Pg.331]   


SEARCH



1,2-Dimyristoyl

Dimyristoyl phosphatidyl ethanolamine

Dimyristoyl-phosphatidyl-choline

© 2024 chempedia.info