Department of Pharmaceutics, Key Laboratory of Smart Drug Delivery, Ministry of Education & PLA, School of Pharmacy, Fudan University, Shanghai, China.
Drug Deliv. 2013;20(1):19-24. doi: 10.3109/10717544.2012.742938.
The purpose of this study was to formulate a reservoir-type transdermal delivery system (TDS) for 2,3,5,6-tetramethylpyrazine (TMP) to enable the delivery of a sufficient dose through human skin to achieve an effective therapeutic plasma concentration. To improve the penetration of TMP in the reservoir-type TDS, several chemical penetration enhancers were investigated using in vitro rat dorsal skin permeation studies. Eucalyptus oil was found to enhance the permeation of TMP to the greatest extent, with the optimal concentration being 5% and the flux being 542.6 ± 49.7 μg/cm(2)/h, which was 4.5-fold greater than control with no enhancer (p < 0.01). The flux of the optimized reservoir-type TDS permeated through the human epidermis was 346.0 ± 27.7 μg/cm(2)/h. Based on the in vitro human skin permeation flux and the pharmacokinetics parameters observed, the clinical surface area of the TDS patch was predicted to be 20 cm(2). The in vivo study conducted in rabbits showed that the TMP TDS patch containing 5% eucalyptus oil had a more favorable pharmacokinetic profile, with a lower C(max) and prolonged T(max) and mean residence time than that observed with the oral administration of TMP. The TMP reservoir-type TDS was shown to be a promising alternative route to oral administration or intravenous infusion of TMP.
本研究旨在制备 2,3,5,6-四甲基吡嗪(TMP)的储库型经皮给药系统(TDS),以便通过人体皮肤递送足够剂量以达到有效的治疗血浆浓度。为了提高 TMP 在储库型 TDS 中的渗透能力,使用体外大鼠背部皮肤渗透研究来研究几种化学渗透增强剂。发现桉树油可最大程度地增强 TMP 的渗透,最佳浓度为 5%,通量为 542.6±49.7μg/cm(2)/h,与无渗透增强剂的对照相比增加了 4.5 倍(p<0.01)。优化的储库型 TDS 透过人体表皮的通量为 346.0±27.7μg/cm(2)/h。基于体外人体皮肤渗透通量和观察到的药代动力学参数,预测 TDS 贴片的临床表面积为 20cm(2)。在兔体内研究中,含有 5%桉树油的 TMP TDS 贴片表现出更有利的药代动力学特征,与 TMP 口服给药相比,C(max)更低,T(max)和平均停留时间延长。TMP 储库型 TDS 是一种有前途的替代口服或静脉输注 TMP 的途径。