Panosyl-alpha -cyclodextrin was synthesized from alpha -cyclodextrin and pa
nose through the revel-se action of Bacillus acidopullulyticus pullulanase
and purified using high-performance liquid chromatography on ODS and amino
columns. The physicochemical and biological properties and solubilization c
apability of panosyl-alpha -cyclodextrin were compared with those of conven
tional alpha -cyclodextrin and branched alpha -cyclodextrins. The hemolytic
activity of panosyl-alpha -cyclodextrin was lower than those of alpha -cyc
lodextrin and glucosyl-alpha -cyclodextrin. Panosyl-alpha -cyclodextrin was
found to be slightly unstable in an acid solution, with stability similar
to that of maltosyl-alpha -cyclodextrin. The solubilization of panosyl-alph
a -cyclodextrin for drugs slightly soluble or insoluble in water was greate
r than that of alpha -cyclodextrin but the same as that of conventional bra
nched alpha -cyclodextrin. The suppressive effects on the photolysis of mec
obalamine in the presence of alpha -cyclodextrins were in the following ord
er: panosyl-alpha -cyclodextrin > maltosyl-alpha -cyclodextrin > glucosyl-a
lpha -cyclodexatrin > alpha -cyclodextrin.