Encapsulation reversible

Reverse Phase Evaporation Szoka and Papahadjopoulos (1978) developed the so-called reverse phase evaporation method. Vesicles prepared with this technique (REV) show higher encapsulation efficiencies of hydrophilic compounds than unextruded MLV. 

In 2000, the first example of ELP diblock copolymers for reversible stimulus-responsive self-assembly of nanoparticles was reported and their potential use in controlled delivery and release was suggested [87]. Later, these type of diblock copolypeptides were also covalently crossUnked through disulfide bond formation after self-assembly into micellar nanoparticles. In addition, the encapsulation of l-anilinonaphthalene-8-sulfonic acid, a hydrophobic fluorescent dye that fluoresces in hydrophobic enviromnent, was used to investigate the capacity of the micelle for hydrophobic drugs [88]. Fujita et al. replaced the hydrophilic ELP block by a polyaspartic acid chain (D ). They created a set of block copolymers with varying... 

Dynamic light-scattering experiments or the analysis of some physicochemical properties have shown that finite amounts of formamide, A-methylformamide, AA-dimethyl-formamide, ethylene glycol, glycerol, acetonitrile, methanol, and 1,2 propanediol can be entrapped within the micellar core of AOT-reversed micelles [33-36], The encapsulation of formamide and A-methylformamide nanoclusters in AOT-reversed micelles involves a significant breakage of the H-bond network characterizing their structure in the pure state. Moreover, from solvation dynamics measurements it was deduced that the intramicellar formamide is nearly completely immobilized [34,35],... 

The effects of the intramicellar confinement of polar and amphiphilic species in nanoscopic domains dispersed in an apolar solvent on their physicochemical properties (electronic structure, density, dielectric constant, phase diagram, reactivity, etc.) have received considerable attention [51,52]. hi particular, the properties of water confined in reversed micelles have been widely investigated, since it simulates water hydrating enzymes or encapsulated in biological environments [13,23,53-59]. 

The transdermal permation of glyceryl trinitrate encapsulated in AOT-reversed micelles was compared with that of an aqueous solution, and an enhancement in permeation was found as well as the absence of skin irritation [161]. 

Moreover, stable liquid systems made up of nanoparticles coated with a surfactant monolayer and dispersed in an apolar medium could be employed to catalyze reactions involving both apolar substrates (solubilized in the bulk solvent) and polar and amphiphilic substrates (preferentially encapsulated within the reversed micelles or located at the surfactant palisade layer) or could be used as antiwear additives for lubricants. For example, monodisperse nickel boride catalysts were prepared in water/CTAB/hexanol microemulsions and used directly as the catalysts of styrene hydrogenation [215]. 

Water-in-oil microemulsions (w/o-MEs), also known as reverse micelles, provide what appears to be a very unique and well-suited medium for solubilizing proteins, amino acids, and other biological molecules in a nonpolar medium. The medium consists of small aqueous-polar nanodroplets dispersed in an apolar bulk phase by surfactants (Fig. 1). Moreover, the droplet size is on the same order of magnitude as the encapsulated enzyme molecules. Typically, the medium is quite dynamic, with droplets spontaneously coalescing, exchanging materials, and reforming on the order of microseconds. Such small droplets yield a large amount of interfacial area. For many surfactants, the size of the dispersed aqueous nanodroplets is directly proportional to the water-surfactant mole ratio, also known as w. Several reviews have been written which provide more detailed discussion of the physical properties of microemulsions [1-3]. 

REVs Reverse-phase evaporation vesicles LUVs prepared by reverse-phase evaporation method, high encapsulation efficiency 11,12... 

Delivery of physically encapsulated small molecules at targeted sites by dendrimers has been superbly envisioned in a recent report by McGrath and Junge [95]. Second generation Frechet type dendrons linked to a central azo-benzene-derivative (32, Fig. 15) underwent reversible cis/trans isomerization of... 

The miniature fiber optic NO2 sensors based upon dye encapsulation in the silica sol-gel can produce linear and reproducible results87. The nitrogen dioxide sensor based on immobilization of ruthenium complex [Ru(bpy)3]Cl2 demonstrated sensitivity in the hundreds parts per million range with reversibility and rapid response time. 

Similarly to the phospholipid polymers, the MPC polymers show excellent biocompatibility and blood compatibility [43—48]. These properties are based on the bioinert character of the MPC polymers, i.e., inhibition of specific interaction with biomolecules [49, 50]. Recently, the MPC polymers have been applied to various medical and pharmaceutical applications [44-47, 51-55]. The crosslinked MPC polymers provide good hydrogels and they have been used in the manufacture of soft contact lenses. We have applied the MPC polymer hydrogel as a cell-encapsulation matrix due to its excellent cytocompatibility. At the same time, to prepare a spontaneously forming reversible hydrogel, we focused on the reversible covalent bonding formed between phenylboronic acid and polyol in an aqueous system. 

Container molecules are of great interest because their encapsulated guests often exhibit novel and unusual properties, which are not observed in the free or solvated state (8,9). They are used today as probes of isolated molecules and of the intrinsic characteristics of the liquid state, and are capable of enantiose-lective recognition (10), reversible polymerization (11), isolation of reactive species (12-14), and promoting reactions within their interiors (15-18). For a valuable introduction to this area the reader is directed to some excellent review articles (15,19-21). 

The carbonyl complex [Ag(L9)(C0)] (12), also of quite remarkable stability, is obtained by reaction of [Ag(L9)(C2H4)] (11) with CO in hexane. Nevertheless, the CO can be easily removed by increasing the temperature of the solution or by purging with an inert gas. Hence, such a reversible guest encapsulation within a molecular container might find applications for gas separation and storage. Again, one likely reason for the stability of the complexes is the protection offered by the bulky mesityl substituents that surround the ethylene or CO unit. 

McGrath and Junge [36] reported a photoresponsive poly(aryl ether) dendrimer with azobenzene as the dendrimer core. These dendrimers exhibited reversible trans to cis photoisomerization by irradiation at 350 nm. The authors proposed the use of this type of dendrimer as novel photoswitchable transport vectors. This is based on the expected ability of dendrimers to encapsulate or eject small molecules reversibly upon light perturbation. 

The change of capacitance in relation to the temperature is very small and a linear function of the substrate temperature. Unlike the change in metal film capacitors it is completely reversible. The maximum operating temperature of the capacitor chip (more than 200°) is determined by its aluminum gate. For encapsulated systems the bond contacts and the material of the package will determine the upper temperature limit. 

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