College of Pharmacy, Yeungnam University, Gyongsan 712-749, Korea.
Arch Pharm Res. 2010 Jan;33(1):95-101. doi: 10.1007/s12272-010-2231-9. Epub 2010 Feb 27.
The main purpose of this study was to evaluate the effect of a mixed drug solution containing a surfactant and beta-cyclodextrin (beta-CD) on the solubility and bioavailability of a poorly water soluble drug, flurbiprofen. Solubility, dissolution and in vivo pharmacokinetics of flurbiprofen in the presence of surfactant, beta-CD or mixture of surfactant and beta-CD were investigated. Among the surfactants tested, Tween 80 produced the highest improvement in the aqueous solubility of flurbiprofen. The solubility of flurbiprofen increased linearly as a function of beta-CD, resulting in B8 type that suggested a formation of inclusion complex in a molar ratio of 1:1. The solubility of flurbiprofen increased further when Tween 80 was included in addition to beta-CD, suggesting that a micelle formation in the presence of Tween 80 was the likely reason for additional increase. Furthermore, the data suggested that Tween 80 did not interfere with the inclusion interaction between flurbiprofen and beta-CD. The solubility of flurbiprofen was the highest in the mixed system containing 1.3 mM beta-CD and 0.3% w/v Tween 80, and the maximum solubility of 160 microg/mL was achieved. Consistent with the enhanced solubility, the plasma exposure (both AUC and Cmax) of flurbiprofen when dosed as the mixed system was significantly higher (as much as 2 to 3-fold) than that without surfactant or beta-CD, with surfactant alone, or with beta-CD alone. Therefore, the mixed system consists of surfactant and beta-CD could be used as an effective oral dosage form to improve bioavailability of poorly water soluble drugs such as flurbiprofen.
本研究的主要目的是评价含有表面活性剂和β-环糊精(β-CD)的混合药物溶液对水溶性差的药物氟比洛芬的溶解度和生物利用度的影响。考察了表面活性剂、β-CD 或表面活性剂和β-CD 的混合物存在时氟比洛芬的溶解度、溶出度和体内药代动力学。在所测试的表面活性剂中,吐温 80 可显著提高氟比洛芬的水溶解度。氟比洛芬的溶解度随β-CD 的增加呈线性增加,导致 B8 型,表明形成摩尔比为 1:1 的包合复合物。当除了β-CD 之外还包含吐温 80 时,氟比洛芬的溶解度进一步增加,这表明在吐温 80 的存在下形成胶束是进一步增加的可能原因。此外,数据表明吐温 80 不会干扰氟比洛芬与β-CD 之间的包合相互作用。在含有 1.3mMβ-CD 和 0.3%w/v 吐温 80 的混合体系中,氟比洛芬的溶解度最高,达到 160μg/mL。与溶解度增加一致,当以混合体系给药时,氟比洛芬的血浆暴露量(AUC 和 Cmax)明显高于没有表面活性剂或β-CD、只有表面活性剂或只有β-CD 时,高达 2 至 3 倍。因此,由表面活性剂和β-CD 组成的混合体系可用于改善水溶性差的药物(如氟比洛芬)的生物利用度的有效口服剂型。