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Host encapsulation

As we saw in the previous sections, inclusion compounds have many structural properties which relate them to other systems based on the hierarchy of non-bound interactions, like enzymes or enzyme-substrate complexes. As a matter of fact, most of the so-called artificial enzymes are based on well-known host molecules (e.g. P-cyclodextrin) and are designed to act partly on such bases 108>109). Most of these models, however, take advantage of the inclusion (intra-host encapsulation) phenomena. Construction of proper covalently bound model molecules is a formidable task for the synthetic chemistuo>. Therefore, any kind of advance towards such a goal is welcomed. [Pg.127]

I. van Driessche, S. Hoste, Encapsulations through the sol-gel technique and their applications in functional coatings. In Functional Coatings, Ghosh, S.K., (Ed.) Wiley-VCH, Weinheim, Germany, 2006. [Pg.345]

Figure 13.44. ySCD hosts encapsulate sulfonated porphyrin guests, forming arrays with a host ZnP H2P ratio of 2 2 for 69 and 2 1 1 for 70. [Pg.656]

Dendrimer interior guest-host encapsulation properties for both inorganic and organic guests... [Pg.348]

Hastings CJ, Pluth MD, Biros SM, Bergman RG, Raymond KN (2008) Simultaneously bound guests and chiral recognition a chiral self-assembled supramolecular host encapsulates hydrophobic guests. Tetrahedron 64(36) 8362-8367... [Pg.412]

Parac TN, Scherer M, Raymond KN (2000) Host within a host encapsulation of alkali ion- crown ether complexes into a [Ga4L6] supramolecular cluster. Angew Chem Int Ed 39(7) 1239-1242... [Pg.414]

The HLB system has made it possible to organize a great deal of rather messy information and to plan fairly efficient systematic approaches to the optimiza-tion of emulsion preparation. If pursued too far, however, the system tends to lose itself in complexities [74]. It is not surprising that HLB numbers are not really additive their effective value depends on what particular oil phase is involved and the emulsion depends on volume fraction. Finally, the host of physical characteristics needed to describe an emulsion cannot be encapsulated by a single HLB number (note Ref. 75). [Pg.514]

Another biomedical appHcation of mictocapsules is the encapsulation of Hve mammalian ceUs for transplantation into humans. The purpose of encapsulation is to protect the transplanted ceUs or organisms from rejection by the host. The capsule sheU must prevent entrance of harmful agents into the capsule, aUow free transport of nutrients necessary for ceU functioning into the capsule, and aUow desirable ceUular products to freely escape from the capsule. This type of encapsulation has been carried out with a number of different types of Hve ceUs, but studies with encapsulated pancreatic islets or islets of Langerhans ate most common. The alginate—poly(L-lysine) encapsulation process originally developed in 1981 (54) catalyzed much of the ceU encapsulation work carried out since. A discussion of the obstacles to the appHcation of microencapsulation in islet transplantation reviewed much of the mote recent work done in this area (55). Animal ceU encapsulation has also been researched (56). [Pg.324]

FIGURE 1.25 The virus life cycle. Viruses are mobile bits of genetic iuformatiou encapsulated in a protein coat. The genetic material can be either DNA or RNA. Once this genetic material gains entry to its host cell, it takes over the host machinery for macromolecular synthesis and subverts it to the synthesis of viral-specific nucleic acids and proteins. These virus components are then assembled into mature virus particles that are released from the cell. Often, this parasitic cycle of virus infection leads to cell death and disease. [Pg.31]

Dendritic hosts can be used in aqueous solution to encapsulate water-soluble fluorescent probes. Changes in the photophysical properties of these encapsulated probes are useful to understand the properties of the microenvironment created by the dendritic interior. For example, adamantyl-terminated poly(pro-pylene amine) dendrimers from the first to the fifth generation (36 represents the third generation) can be dissolved in water at pH<7 in the presence of -cyclodextrin because of encapsulation of the hydrophobic adamantyl residue inside the /1-cyclodextrin cavity and the presence of protonated tertiary amine units inside the dendrimer [72]. Under these experimental conditions, 8-anifi-... [Pg.184]


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See also in sourсe #XX -- [ Pg.22 ]




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