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Linear dextrins, complexation

Mild acidic hydrolysis (5mM HCl at 100 C) of cyclohepta-amylose gave an 8% yield of maltoheptaose. The first-order rate constant increased during hydrolysis because the a-(l - 4)-linkages of cyclohepta-amylose and linear dextrins are cleaved at different rates. Various thermodynamic parameters and the dependence of the rate of hydrolysis on pH and on complexation of cyclohepta-amylose with toluene were determined. [Pg.475]

Linear Dextrins. Both linear and cyclic maltodextrins in aqueous solution can form molecular complexes with other small molecules, possibly the most commonly known example being the blue... [Pg.283]

The plot of the reciprocal of k - kf against 1/[L] is linear, with a slope of 1 / [K(kc - kf)] and an intercept of 1 / (kc - kf). Figure 5.36 shows the stabilization of prostacyclin by the derivatives of P-cyclodextrin. However, not all inclusion complexes provide the stabilization of drugs. In many cases, drug degradation is enhanced via inclusion complex formation [e.g., prostaglandin E and E2/p-cyclo-dextrin (P-CD), aspirin/p-CD],... [Pg.335]

The location of the cation in these canal compounds is not clear, but the cation definitely influences the nature of the crystal which is formed. With sodium and lithium iodides, a form II type of complex crystallizes as hexagonal plates. In the sodium iodide-iodine complex, the inclusion compound is not stoichiometric but rather the iodine atoms are packed into the canals in linear rows, with a spacing not related to the spacing of the dextrin molecules. [Pg.251]


See other pages where Linear dextrins, complexation is mentioned: [Pg.682]    [Pg.321]    [Pg.273]    [Pg.288]    [Pg.252]    [Pg.209]    [Pg.107]    [Pg.5]    [Pg.365]    [Pg.141]    [Pg.251]    [Pg.278]    [Pg.696]    [Pg.241]    [Pg.33]    [Pg.331]    [Pg.32]    [Pg.51]    [Pg.54]    [Pg.289]    [Pg.217]   
See also in sourсe #XX -- [ Pg.283 , Pg.285 , Pg.286 , Pg.287 ]




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3- Dextrine

Dextrin

Dextrinated

Dextrinization

Linear complexes

Linear dextrins

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