Department of Pharmaceutical Technology, Medical University of Gdansk, Gdansk, Poland.
J Pharm Pharmacol. 2013 Oct;65(10):1463-72. doi: 10.1111/jphp.12120. Epub 2013 Aug 6.
The aim was to evaluate ointments for local treatment of anal fissures. Nitroglycerin (NTG) was complexed with β-cyclodextrin (β-CD) to provide prolonged NTG release, with the intention of decreasing systemic drug absorption and thus reducing side effects.
Gels, creams and anhydrous water-emulsifying (AWE) ointment with NTG-CD were compared with preparations containing uncomplexed NTG (diluted with crospovidone, NTG-cP). The in-vitro NTG release and ex-vivo skin absorption were studied.
The prolonged-release ointment with the NTG-CD complex was formulated using AWE base or w/o cream (20% water); release of NTG from a hydrogel was very fast with both the complexed and uncomplexed forms. From the AWE ointment base, 16.4% or 4.5% of the total NTG dose was released after 6 h when NTG-cP or NTG-CD was incorporated, respectively. With the complexed form, NTG absorption to the skin after a 5-h application was 18.1 or 11.1 μg/g from AWE ointment or cream, respectively; absorption of the uncomplexed NTG was higher: 52.3 or 21.9 μg/g from AWE ointment and cream, respectively.
Complexation with β-CD results in prolonged release of NTG from AWE ointment and w/o cream, which was confirmed by the ex-vivo skin absorption results.
评估用于治疗肛裂的局部软膏。将硝酸甘油(NTG)与β-环糊精(β-CD)络合,以提供延长的 NTG 释放,旨在减少系统药物吸收,从而减少副作用。
将含有 NTG-β-CD 的凝胶、乳膏和无水水包油(AWE)软膏与含有未络合的 NTG 的制剂(用交联聚维酮稀释,NTG-cP)进行比较。研究了体外 NTG 释放和离体皮肤吸收。
使用 AWE 基础或无油乳膏(20%水)制备了含有 NTG-CD 复合物的缓释软膏;含有复合物和未复合物的水凝胶中的 NTG 释放非常快。从 AWE 软膏基质中,当分别掺入 NTG-cP 或 NTG-CD 时,6 小时后分别释放了 16.4%或 4.5%的总 NTG 剂量。对于复合形式,在应用 5 小时后,从 AWE 软膏或乳膏中分别吸收 18.1 或 11.1μg/g 的 NTG 到皮肤中;未络合的 NTG 吸收更高:从 AWE 软膏和乳膏中分别吸收 52.3 或 21.9μg/g。
β-CD 的络合导致 AWE 软膏和无油乳膏中 NTG 的释放延长,这通过离体皮肤吸收结果得到证实。