TY - JOUR
T1 - Effect of hydroxypropyl-β-cyclodextrin on the solubility, photostability and in-vitro permeability of alkannin/shikonin enantiomers
AU - Chen, Chau Yang
AU - Chen, Fu An
AU - An-Bang, Wu
AU - Hsu, Hsing Chu
AU - Kang, Jaw Jou
AU - Cheng, Hui Wen
PY - 1996/9/6
Y1 - 1996/9/6
N2 - The influence of hydroxypropyl-β-cyclodextrin (HPCD) on the solubility, photostability, and the in-vitro permeability of alkannin/shikonin enantiomers (A/S) was investigated. Solubility of A/S increased approximately 200 fold at 50% HPCD. The phase-solubility diagram revealed the formation of a 1:1 inclusion complex of A/S-HPCD and a stability constant (k(s)) of 260.5 M-1. Addition of HPCD significantly decreased the photochemical decomposition rate of A/S at pH 9.0. The apparent-first-order photochemical decomposition rate constants of free and complexed A/S were calculated from the Lineweaver-Burk plot to be 0.329 and 0.156 h-1, respectively. The in-vitro permeability study showed that the release of A/S from four test bases followed a Higuchi release model. The presence of HPCD enhanced the A/S release rate by 34 and 54 fold in cream and gel form, respectively, at one-tenth A/S concentration of the control preparation-Shiunko ointment.
AB - The influence of hydroxypropyl-β-cyclodextrin (HPCD) on the solubility, photostability, and the in-vitro permeability of alkannin/shikonin enantiomers (A/S) was investigated. Solubility of A/S increased approximately 200 fold at 50% HPCD. The phase-solubility diagram revealed the formation of a 1:1 inclusion complex of A/S-HPCD and a stability constant (k(s)) of 260.5 M-1. Addition of HPCD significantly decreased the photochemical decomposition rate of A/S at pH 9.0. The apparent-first-order photochemical decomposition rate constants of free and complexed A/S were calculated from the Lineweaver-Burk plot to be 0.329 and 0.156 h-1, respectively. The in-vitro permeability study showed that the release of A/S from four test bases followed a Higuchi release model. The presence of HPCD enhanced the A/S release rate by 34 and 54 fold in cream and gel form, respectively, at one-tenth A/S concentration of the control preparation-Shiunko ointment.
KW - Alkannin/shikonin enantiomers
KW - Hydroxypropyl-β-cyclodextrin
KW - Permeability
KW - Photostability
KW - Solubility
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U2 - 10.1016/0378-5173(96)04634-0
DO - 10.1016/0378-5173(96)04634-0
M3 - Article
AN - SCOPUS:0030572642
SN - 0378-5173
VL - 141
SP - 171
EP - 178
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1-2
ER -