solubility of cyproterone derivatives in the presence of hydroxypropyl-β-cyclodextrin: experimental and molecular modeling studies

Authors

zahra rezaei

sciences research center, shiraz university of medical sciences, shiraz 71345, iran department of medicinal chemistry, faculty of pharmacy, and pharmaceutical mohammad mehdi zarshenas

department of medicinal chemistry, faculty of pharmacy, and pharmaceutical andia khalili

department of medicinal chemistry, faculty of pharmacy, and pharmaceutical soghra khabnadideh

sciences research center, shiraz university of medical sciences, shiraz 71345, iran department of medicinal chemistry, faculty of pharmacy, and pharmaceutical mohammad reza jafari

abstract

this study presents the influence of hydroxypropyl-β-cyclodextrin (hpbcd) on the aqueous solubility of acyl esters of cyproterone. first, a number of esters of cyproterone were synthesized. then the phase solubility analysis of the compounds in the presence of hpbcd was investigated in phosphate buffer solution at a ph of 7.4. to gain a better understanding of the complexation mechanism, the synthesized compounds were docked inside the hpbcd cavity using the autodock program. the results show that the interaction between the synthesized compounds and hpbcd is of type al and all of the compounds exhibited higher solubility as a result of complexation with hpbcd. the extent of increase in solubility was consistently greater as the ester chain length ascends by 4 carbon atoms. this increase in solubility is in agreement with the results obtained by calculating docking scores.

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Journal title:
iranian journal of pharmaceutical sciences

جلد ۶، شماره ۳، صفحات ۱۸۵-۱۹۰

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