Liposomes molecules

Fig. 4.2 Effectof44, 43, 9 and 77 on the photo-oxidative damage of PCioo% liposomes. Molecules added to liposomal solution (8 mM) as solutions in DMSO (33 mM). Control addition of corresponding volume of DMSO only, a 20 mol% compound b 10 mol% compound c 5 mol% compound...

In the case of water-insoluble solutes which do not modify bilayers, such as single-chain alcohol molecules, the solubilization process can be treated within the frame work of a solvent exchange model (40). A liposome molecule (L) has A ax potential sites for alcohol binding. These sites are occupied by water in a buffer solution, and therefore this model is based on the one-to-one exchange of water and solute in the membrane, as follows ... 

Phospholipid molecules form bilayer films or membranes about 5 nm in thickness as illustrated in Fig. XV-10. Vesicles or liposomes are closed bilayer shells in the 100-1000-nm size range formed on sonication of bilayer forming amphiphiles. Vesicles find use as controlled release and delivery vehicles in cosmetic lotions, agrochemicals, and, potentially, drugs. The advances in cryoelec-tron microscopy (see Section VIII-2A) in recent years have aided their characterization [70-72]. Additional light and x-ray scattering measurements reveal bilayer thickness and phase transitions [70, 71]. Differential thermal analysis... 

Experimental investigations of the model system of dye molecules adsorbed onto surfaces of polystyrene spheres have finuly established the sensitivity and surface specificity of the SHG method even for particles of micrometre size [117]. The surface sensitivity of die SHG process has been exploited for probing molecular transport across the bilayer in liposomes [118], for measurement of electrostatic potentials at the surface of small particles [119] and for imaging... 

The main supramolecular self-assembled species involved in analytical chemistry are micelles (direct and reversed), microemulsions (oil/water and water/oil), liposomes, and vesicles, Langmuir-Blodgett films composed of diphilic surfactant molecules or ions. They can form in aqueous, nonaqueous liquid media and on the surface. The other species involved in supramolecular analytical chemistry are molecules-receptors such as calixarenes, cyclodextrins, cyclophanes, cyclopeptides, crown ethers etc. Furthermore, new supramolecular host-guest systems arise due to analytical reaction or process. 

That vesicles and liposomes form at all is a consequence of the amphi-pathic nature of the phospholipid molecule. Ionic interactions between the... 

A large variety of drug delivery systems are described in the literature, such as liposomes (Torchilin, 2006), micro and nanoparticles (Kumar, 2000), polymeric micelles (Torchilin, 2006), nanocrystals (Muller et al., 2011), among others. Microparticles are usually classified as microcapsules or microspheres (Figure 8). Microspheres are matrix spherical microparticles where the drug may be located on the surface or dissolved into the matrix. Microcapsules are characterized as spherical particles more than Ipm containing a core substance (aqueous or lipid), normally lipid, and are used to deliver poor soluble molecules... 

Bilayer rigidity is a parameter which influences biodistribution and biodegradation of liposomes. In vitro a hydrophilic marker molecule (carboxyfluorescein) leaked much faster from the vesicles with bilayers in a fluid state than from bilayers in a gel state (Crommelin and Van Bommel, 1984). An indication of the bilayer rigidity can... 

The fluid lipid film is driven into a state of higher order, especially at low surface pressure [138] S-layer coating of liposomes leads to an ordering effect of the lipid molecules [123]... 

FIG. 18 Schematic drawing of a liposome with entrapped functional molecules, coated with an S-layer lattice, that can be used as immobilization matrix for functional molecules. Alternatively, liposomes can be coated with genetically modified S-layer subunits incorporating functional domains. (Modified from Ref. 59.) (b) Electron micrograph of a freeze-etched preparation of an S-layer-coated liposome (bar, 100 nm). 

When liposomes are formed, they can be made to entrap certain compounds inside themselves, eg, drugs and isolated genes. There is interest in using liposomes to distribute drugs to certain tissues, and if components (eg, antibodies to certain cell surface molecules) could be incorporated into liposomes so that they would be targeted to specific tissues or tumors, the therapeutic impact would be considerable. DNA entrapped inside liposomes appears to be less sensitive to... 

Liposomes — These are synthetic lipid vesicles consisting of one or more phospholipid bilayers they resemble cell membranes and can incorporate various active molecules. Liposomes are spherical, range in size from 0.1 to 500 pm, and are thermodynamically unstable. They are built from hydrated thin lipid films that become fluid and form spontaneously multilameUar vesicles (MLVs). Using soni-cation, freeze-thaw cycles, or mechanical energy (extrusion), MLVs are converted to small unilamellar vesicles (SUVs) with diameters in the range of 15 to 50 nm. ... 

Oleosomes — Also called oil bodies, oleosomes are the natural equivalents of liposomes. They are found in plant seeds or fruits, filled with oils, pigments, and vitamins, and serve as specific organelles to store lipid molecules. A protocol to... 

Solubilization of an active H,K-ATPase is also a prerequisite for reconstitution of the enzyme into liposomes. With these H,K-ATPase proteoliposomes it is then possible to study the transport characteristics of pure H,K-ATPase, without the interference of residual protein contamination that is usually present in native vesicular H,K-ATPase preparations. Rabon et al. [118] first reported the reconstitution of choleate or n-octylglucoside solubilized H,K-ATPase into phosphatidylcholine-cholesterol liposomes. The enzyme was reconstituted asymmetrically into the proteoliposomes with 70% of the pump molecules having the cytoplasmic side extravesicular. In the presence of intravesicular K, the proteoliposomes exhibited an Mg-ATP-dependent H transport, as monitored by acridine orange fluorescence quenching. Moreover, as seen with native H,K-ATPase vesicles, reconstituted H,K-... 

In another study, ATPase reconstituted into liposomes was analyzed by infrared attenuated total reflection spectroscopy and the secondary-structure elements of the molecule were determined from the spectra obtained by Fourier self-deconvolution [42]. Gratifyingly, essentially identical secondary-structure estimates for the ATPase were obtained by this entirely different approach, suggesting quite strongly that these secondary-structure estimates are reasonably accurate. Thus, any future models for the structure of the H -ATPase must take this information into account. 

Concerning the mechanism of action of catechins, studies carried out on S. aureus and E. coli cells by Ikigai et al. [72] reported that their bactericidal effect is primarily involved in the damage of bacterial membranes catechins induce a rapid leakage of small molecules entrapped in the intraliposomal space, determining the aggregation of the liposomes. These actions cause damage in the membrane lipid bilayer and cell death (Table 1). 

Liposomes, which are lipid bilayer vesicles prepared from mixtures of lipids, also provide a useful tool for studying passive permeability of molecules through lipid. This system has, for example, been used to demonstrate the passive nature of the absorption mechanism of monocarboxylic acids [131]. Liposome partitioning of... 

A further partihon system based on the use of liposomes, and commercialized under the name Transil [110, 111], has shown its utiUty as a UpophiUcity measure in PBPK modeling [112]. Fluorescent-labeled liposomes, called fluorosomes, are another means of measuring the rate of penetration of small molecules into membrane bilayers [113, 120]. Similarly, a colorimetric assay amenable to HTS for evaluating membrane interactions and penetrahon has been presented [116]. The platform comprises vesicles of phospholipids and the chromahc Upid-mimehc polydiacetylene. The polymer undergoes visible concentrahon-dependent red-blue transformahons induced through interactions of the vesicles with the studied molecules. 

Liposome-Water Partitioning and the diff 1-2 Approximation in logDyEM-pH Profiles for Monoprotic Molecules... 

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