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Cyclodextrins carboxymethyl

Cyclodextrins carboxymethylated at the secondary rim have been evaluated as chemzymes for glycoside hydrolysis. ... [Pg.4]

Terabe, S., Ozaki, H., Otsuka, K., and Ando, T., Electrokinetic chromatography with 2-O-carboxymethyl-P-cyclodextrin as a moving "stationary" phase, /. Ckromatogr., 332, 211, 1985. [Pg.418]

CM-fi-CD Carboxymethyl-beta-cyclodextrin CSP Chiral stationary phase(s)... [Pg.206]

Prbpy, 5-(2-MePr)bpy and 5-(2,2-Mc2Pr)bpy have been prepared and characterized. The mer-and /uc-isomers of each complex have been isolated by use of cation-exchange column chromatography as the steric requirements of the R group increase, the percentage of the /uc-isomer decreases. Enantiomers of [Ru(5-Prbpy)3] + were separated on SP Sephadex C-25. Electro-kinetic chromatography has been used to separate the enantiomers of [Ru(104)3] " anionic carboxymethyl-/ -cyclodextrin was employed as the chiral mobile phase additive. ... [Pg.595]

S Sabbah, GKE Scriba. Separation of dipeptide and tripeptide enantiomers in capillary electrophoresis using carboxymethyl-beta-cyclodextrin and succinyl-beta-cyclodextrin. Influence of the amino acid sequence, nature of the cyclodextrin and pH. Electrophoresis 22 1385-1393, 2001. [Pg.113]

S Sabah, GKE Scriba. pH-Dependent reversal of the chiral recognition of tripeptide enantiomers by carboxymethyl-/3-cyclodextrin. J Chromatogr A 833 261-266, 1999. [Pg.219]

Therefore, the authors have synthesized heptakis(carboxymethyl)-substituted a-cyclodextrin which was combined with hydrophobic ammonium to afford 9 (Figure 13), whereby the number of carboxylate-ammonium ion pairs was regulated to six. This compound was incorporated into BUM and subjected to singlechannel current measurements. The current-voltage plot gave a single straight line to afford a conductance level of 7.7 pS under several different experimental conditions. Then the modified cyclodextrin successfully controlled the ion channel structure and therefore the conductance. [Pg.181]

Many CDs have been successfully used to solubilize insoluble drugs, here are a partial list of CD derivatives reported in the literature fflFCD, SBE-ft-CDs, randomly methylated-P-cyclodextrin (RM-p-CD), 2,3,6-partially methylat flcyclodextrin (PM-ft-CD), glucosyl-ft-CD (G1-P-CD), maltosyl-p-cyclodextrin (G2- -CD), hydroxyethyl-p-cyclodextrin (He-p-CD), diethyl-P-cyclodextrin (DE-p-CD)P-carboxymethyl-Qethyl- -cyclodextrin (CME-p-CD), and (2,6-oG>-methyl)-p-cyclodextrin (DOM-p-CD). [Pg.146]

On-chip chiral separation of enantiomers of adrenaline, noradrenaline, and dopamine was achieved using a mixture of carboxymethyl-p-cyclodextrin (CMCD) and a polyamidoamine dendrimer (Starburst) [120], On-chip chiral separation of enantiomers of homovanillic acid, DOPA, cDOPA, methoxy-tyramine (MT), metanephrine, and normetanephrine was achieved using a mixture of 18-crown-6-ether and carboxymethyl-P-cyclodextrin [120],... [Pg.158]

Zhao, H. and Vance, G. F. (1997). Intercalation of carboxymethyl-p-cyclodextrin into magnesium-aluminium layered double hydroxides. J. Chem. Soc., Dalton Trans., 1961. [Pg.327]

In electrokinetic chromatography (EKC, electroosmosis, electrophoresis) the highly soluble ionic cyclodextrin-derivatives (e.g. carboxymethyl-6-cyclodextrin) are employed (47). A non-charged guest will migrate in the electric field, because it is transported by the charged cyclodextrin host. [Pg.205]

Chankvetadze et al. have demonstrated the potential of flow-counterbalanced capillary electrophoresis (FCCE) in chiral and achiral micropreparative separations [27], Unlimited increase of separation selectivity can be achieved for binary mixtures, such as (+ )-chlorpheniramine with carboxymethyl-(3-cyclodextrin chiral selector, or a- and (3-isomers of a asparatame dipeptide. The carrier of the chiral selector or pseudo-stationary phase, electroosmotic flow (EOF), pressure-driven flow, or hydrodynamic flow can be used as a counterbalancing flow to the electrophoretic mobility of the analyte or vice versa, resulting in dramatic changes of the effective mobilities of the sample mixture components [28], This approach can be used for micropreparative CE, stepwise separations, and fraction collection of multicomponent mixtures [27],... [Pg.285]

A major problem associated with derivatized cyclodextrins is their chemical inhomogeneity due to various degrees of substitution, as has been demonstrated by Linnemayr et al. [457], e.g. for various commercial samples of methylated, (2-hy-droxyjpropylated and carboxymethylated P-cyclodextrins. This has led to the development of single-isomer derivatized CDs by Vigh and co-workers [458-461], e.g. of hepta-6-sulphato-P-CD [459], heptakis(2,3-diacetyl-6-sulphato)-p-CD [458], and hep-takis(2,3-dimethyl-6-sulphato)-p-CD [460, which are now commercialized by Regis Technologies. [Pg.434]

Cserhati, T. Forgacs, E. Charge-transfer chromatographic study of the complex formation of some steroidal drugs with carboxymethyl y-cyclodextrin. Anal. Biochem. 1997, 246 (2), 205-210. [Pg.692]

Adachi, H. Irie, T. Uekama, K. Manako, T. Yano, T. Saita, M. Combination effects of O-carboxymethyl-O-ethyl-P-cyclodextrin and penetration enhancer HPE-101 on transdermal delivery of prostaglandin Ej in hairless mice. Eur. J. Pharm. Sci. 1993, 1, 117-123. [Pg.1323]

Park, S.Y. Park, J.K. Park, J.H. McNeff, C.V. Carr, P.W. Separation of racemic 2,4-dinitrophenyl amino acids on carboxymethyl-beta-cyclodextrin coated zirconia in RPLC. Microchem. J. 2001, 70, 179-185. [Pg.921]

The feasibility of separating the enantiomers of chlopheniramine on a micropreparative scale was also recently shown by applying flow-counterbalanced CE using carboxymethyl (l-cyclodextrin as a chiral selector [200]. All these apphcations were performed at a mg scale or even less and cannot currently compete with the liquid chromatographic methods discussed previously. However, the scope and limitations of the electrophoretic approach still need to be challenged [201]. [Pg.181]

Uekama, K., Horikawa, T., Horiuchi, Y, Hirayama, F. In vitro and in vivo evaluation of delayed-release behaviour of diltiazem from its O-carboxymethyl-O-ediyl-p-cyclodextrin complex. J. Control Release 1993, 25, 99-106. [Pg.837]

Adachi, H., Irie, T., Hirayama, R, Uekama, K. Stabilization of prostaglandin Ej in fatty alcohol propylene glycol ointment by acidic cyclodextrin derivative, O-carboxymethyl- 0-ethyl-(3-cyclodextrin. Chem. Pharm. Bull. 1992, 40, 1586-1591. [Pg.839]

Uekama, K., Adachi, H., Irie, T. et al. Improved transdermal delivery of prostaglandin Ei through hairless mouse skin combined use of carboxymethyl-ethyl-(3-cyclodextrin and penetration enhancers. J. Pharm. Pharmacol. 1992, 44, 119-121. [Pg.839]

Fig. 5 A typical application of capillary electrophoresis for chiral separations of small peptides. Chiral separation of the isomeric dipeptides (A) of Asp-PheOMe and P-Asp-PheOMe and (B) of Asp-PheNH2 and P-Asp-PheNH2. The separation was carried out at pH 3.3 using 15 mg/mL of carboxymethyl-P-cyclodextrin as the chiral selector. (For details of experimental conditions, see Ref. 171.)... Fig. 5 A typical application of capillary electrophoresis for chiral separations of small peptides. Chiral separation of the isomeric dipeptides (A) of Asp-PheOMe and P-Asp-PheOMe and (B) of Asp-PheNH2 and P-Asp-PheNH2. The separation was carried out at pH 3.3 using 15 mg/mL of carboxymethyl-P-cyclodextrin as the chiral selector. (For details of experimental conditions, see Ref. 171.)...
M Fillet, I Bechet, Ph Hubert, J Crommen. Resolution improvement by use of carboxymethyl-P-cyclodextrin as chiral additive for the enantiomeric separation of basic drugs by capillary electrophoresis. J Pharm Biomed Anal 14 1107-1114, 1996. [Pg.384]

Furusaki, E., Ueno, Y., Sakairi, N., Nishi, N., and Tokura, S. 1996. Facile preparation and inclusion ability of chitosan derivative bearing carboxymethyl-beta-cyclodextrin. Carbohydr. Polym. 9, 29-34. [Pg.130]


See other pages where Cyclodextrins carboxymethyl is mentioned: [Pg.64]    [Pg.177]    [Pg.202]    [Pg.203]    [Pg.45]    [Pg.361]    [Pg.364]    [Pg.250]    [Pg.112]    [Pg.92]    [Pg.92]    [Pg.1229]    [Pg.214]    [Pg.582]    [Pg.434]    [Pg.685]    [Pg.279]    [Pg.24]    [Pg.339]    [Pg.828]    [Pg.659]    [Pg.827]   
See also in sourсe #XX -- [ Pg.148 ]




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5- -2-carboxymethyl

Carboxymethyl cyclodextrin

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