T. Cserhati et al., INCLUSION COMPLEX-FORMATION OF ANTISENSE NUCLEOTIDES WITH HYDROXYPROPYL-BETA-CYCLODEXTRIN, International journal of pharmaceutics, 141(1-2), 1996, pp. 1-7
The interaction between 26 nucleoside derivatives and hyroxypropyl-bet
a-cyclodextrin (HPBCD) was determined by charge-transfer chromatograph
y. HPBCD interacted with each nucleoside decreasing the lipophilicity
of the guest molecules. Both sterical (specific hydrophobic surface ar
ea) and hydrophobicity parameters of nucleosides influenced the streng
th of interaction. Substituents with longer alkyl chain considerably i
ncreased the strength af interaction whereas the effect of double or t
riple bond in the chain was negligible.