Cyclodextrin natural

Harada, A., Li, J., and Kamachi, M. (1993). Synthesis of a tubular polymer from threaded cyclodextrins. Nature (London) 364 516-518. 

Many ionic poly(saccharides), such as heparin, chondroitin sulfates, dextran sulfate, and natural poly(saccharides), such as dextran, dextrin, pullulan, and their charged derivatives have been used as mobile phase additives for the separation of different enantiomers. Figure 10.10 [191,192,205,206]. Dextrins were found to have a wide application range, thought to be due in part to their helical structures. Enantiomer-chiral selector complexes seem to be weaker than for cyclodextrins, and it has not been demonstrated that enantiomer separations obtained by the poly(saccharide) chiral selectors cannot be obtained using cyclodextrins. Natural poly(saccharides) are typically complex mixtures of homologues and isomers, with a composition that can vary for different sources, resulting in differences in enantioselectivity. 

Cyclodextrins Natural Solubihty And Bioavailability Enhancer, Drug Stabihzation, Microparticles, Peptide Dehvery, Permeation Enhancer, Nanoparticles and Nanocapsule Sulindac, Paclitaxel Hydrocortisone... 

Dangles, O. BrouUlard, R. (1992c). Inclusion of natural pigments into cyclodextrins. Natural pigments in competitive spectrophotometric studies of host-guest systems. In Minutes of the Sixth International Symposium on Cyclodextrins (ed. A.R. Hedges), pp. 117-122. Editions de Sante, Paris. 

Calixarenes (from the Latin ca/ x) may be understood as artificial receptor analogues of the natural cyclodextrins (96,97). In its prototypical form they feature a macrocycHc metacyclophane framework bearing protonizable hydroxy groups made from condensation of -substituted phenols with formaldehyde (Fig. 15b). Dependent on the ring size, benzene derivatives are the substrates most commonly included into the calix cavity (98), but other interesting substrates such as C q have also been accommodated (Fig. 8c) (45). 

While the previous receptors are typically used in organic solvents, except for the cyclodextrins, there are special cases of cyclophane receptors supphed with peripheral charges (ammonium units) (107—12) or ionizable groups (carboxylate functions) (113,114) (Fig. 17) to allow substrate recognition, as in nature, in an aqueous medium, profiting from the solvophobic effects of water (115). 

As a final example we consider noncovalent molecular complex formation with the macrocyclic ligand a-cyclodextrin, a natural product consisting of six a-D-glucose units linked 1-4 to form a torus whose cavity is capable of including molecules the size of an aromatic ring. Table 4-3 gives some rate constants for this reaction, where L represents the cyclodextrin and S is the substrate ... 

Figure 10.1 Analysis of racemic 2,5-dimethyl-4-hydroxy-3[2H]-furanone (1) obtained from a strawbeny tea, flavoured with the synthetic racemate of 1 (natural component), using an MDGC procedure (a) dichloromethane extract of the flavoured strawbeny tea, analysed on a Carbowax 20M pre-column (60 m, 0.32 mm i.d., 0.25 p.m film thickness earner gas H2, 1.95 bar 170 °C isothermal) (b) chirospecific analysis of (1) from the sti awbeny tea exti act, ti ansfened foi stereoanalysis by using a pemiethylated /3-cyclodextrin column (47 m X 0.23 mm i.d. canier gas H2, 1.70 bar 110 °C isothemial). Reprinted from Journal of High Resolution Chromatography, 13, A. Mosandl et al., Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , pp. 660-662, 1990, with permission from Wiley-VCH.

The above two models together with Tabushi s cyclodextrin bis(histamine)23) are really elabolate ones, each having a substrate binding cavity, but their catalytic activities are yet far behind of those of natural enzymes. They suggest the difficulties associated with the design of a metal ion center inside of a cavity which activates both substrate and catalytic groups. 

Several model systems related to metalloenzymes such as carboxypeptidase and carbonic anhydrase have been reviewed. Breslow contributed a great deal to this field. He showed how to design precise geometries of bis- or trisimidazole derivatives as in natural enzymes. He was able to synthesize a modified cyclodextrin having both a catalytic metal ion moiety and a substrate binding cavity (26). Murakami prepared a novel macrocyclic bisimidazole compound which has also a substrate binding cavity and imidazole ligands for metal ion complexation. Yet the catalytic activities of these model systems are by no means enzymic. 

The theory and development of a solvent-extraction scheme for polynuclear aromatic hydrocarbons (PAHs) is described. The use of y-cyclodextrin (CDx) as an aqueous phase modifier makes this scheme unique since it allows for the extraction of PAHs from ether to the aqueous phase. Generally, the extraction of PAHS into water is not feasible due to the low solubility of these compounds in aqueous media. Water-soluble cyclodextrins, which act as hosts in the formation of inclusion complexes, promote this type of extraction by partitioning PAHs into the aqueous phase through the formation of complexes. The stereoselective nature of CDx inclusion-complex formation enhances the separation of different sized PAH molecules present in a mixture. For example, perylene is extracted into the aqueous phase from an organic phase anthracene-perylene mixture in the presence of CDx modifier. Extraction results for a variety of PAHs are presented, and the potential of this method for separation of more complex mixtures is discussed. 

Lancrajan, 1. et al.. Carotenoid incorporation into natural membranes from artificial carriers liposomes and P-cyclodextrins, Chem. Phys. Lipids, 112, 1, 2001. 

Szente, L. et al.. Stabilization and solubilization of lipophilic natural colorants with cyclodextrins, J. Inclusion Phen. Mol. Recognition Chem., 32, 91, 1998. 

Thus, despite all the work carried out on starch-iodine, the exact nature of the guest iodine atoms is still not totally resolved. Teitelbaum, Ruby and Marks 156) have examined the compound using Raman and 129I Mossbauer spectroscopy and concluded that the pentaiodide ion 1 was the major chromophore present. However work based on iodine compounds of cyclodextrins 3-134 135) has shown that a variety of polyiodide species is possible, and the starch-iodine inclusion compound could conceivably involve I2 If, I2 I- I2, or I5 species 157). The anhydrous amylose-iodine compound has recently been found to exhibit semiconductor behaviour 158). 

Cyclodextrins have ecologically advantageous properties. Not only are they produced from natural and replenishable sources, they are biodegradable, non-toxic and possess no allergenic potential [32,33]. They are commercially available in bulk quantities at an optional degree of purity and have been used for many years in pharmaceuticals. 

A chiral GC column is able to separate enantiomers of epoxy pheromones in the Type II class, but the applications are very limited as follows a custom-made column packed with a p-cyclodextrin derivative as a liquid phase for the stereochemical identification of natural 3,4- and 6,7-epoxydienes [73, 74] and a commercialized column of an a-cyclodextrin type (Chiraldex A-PH) for the 3,4-epoxydiene [71] (See Table 3). The resolution abilities of chiral HPLC columns have been examined in detail, as shown in Table 7 and Fig. 14 [75,76, 179]. The Chiralpak AD column operated under a normal-phase condition separates well two enantiomers of 9,10-epoxydienes, 6,7-epoxymonoenes and 9,10-epoxymonoenes. Another normal-phase column, the Chiralpak AS column, is suitable for the resolution of the 3,4-epoxydienes. The Chiralcel OJ-R column operated under a reversed-phase condition sufficiently accomplishes enantiomeric separation of the 6,7-epoxydienes and 6,7-epoxymonoenes. 

Recently, NMR spectroscopy has been used to study the effect of substituents in structural PBN (402) and 5,5-dimethylpyrroline A-oxide (DMPO) (403) analogs on their complexing ability with natural (j-cyclodextrin (402, 403). 

Upon threading the oligosilane molecules into the asymmetric y-cyclodextrin cavity to form a pseudorotaxane-type aggregate,335 a bisignate Cotton effect became apparent at about 290 nm, indicating induced PSS helicity. The reason for the bisignate nature of the signal was not clear. 

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