Bhandari Krishna Hari, Newa Madhuri, Yoon Sung Ii, Kim Jung Sun, Jang Ki Young, Kim Jung-Ae, Yoo Bong Kyo, Woo Jong Soo, Lee Jae Hwi, Kim Dae Duk, Choi Hang Gon, Yong Chul Soon
College of Pharmacy, Yeungnam University, Gyongsan, South Korea.
Biol Pharm Bull. 2007 Nov;30(11):2211-6. doi: 10.1248/bpb.30.2211.
The purpose of this study was to evaluate the physicochemical properties, skin permeation and accumulation profiles of model lipophilic ketorolac fatty ester (esters) prodrugs. Ketorolac linoleate (C18:2), oleate (C18:1) and stearate (C18:0) were evaluated for their solubility, capacity factor, enzymatic hydrolysis, chemical stability, and skin permeation and accumulation profiles using the combination of common permeation enhancing techniques such as the use of supersaturated solution of permeants in the enhancer vehicle, lipophilic receptor solution, enhancer pretreatment of skins, removal of stratum corneum and delipidization of skins etc. Esters were highly lipophilic, chemically stable for the duration of observation, enzymatically unstable in hairless mouse skin/liver homogenates and plasma, and impermeable into the receptor solution. Absence of skin permeation, relative enzymatic stability during permeation and chemical stability of these esters could delineate preliminary possibilities for designing safer topical agents without systemic absorption.
本研究的目的是评估模型亲脂性酮咯酸脂肪酸酯前药的物理化学性质、皮肤渗透和蓄积情况。使用常见的渗透增强技术组合,如在增强剂载体中使用渗透剂的过饱和溶液、亲脂性受体溶液、皮肤的增强剂预处理、去除角质层和皮肤脱脂等,对酮咯酸亚油酸酯(C18:2)、油酸酯(C18:1)和硬脂酸酯(C18:0)的溶解度、容量因子、酶促水解、化学稳定性以及皮肤渗透和蓄积情况进行了评估。这些酯具有高度亲脂性,在观察期间化学稳定,在无毛小鼠皮肤/肝脏匀浆和血浆中酶促不稳定,且不能渗透到受体溶液中。这些酯缺乏皮肤渗透、渗透过程中的相对酶稳定性和化学稳定性,这可以为设计无全身吸收的更安全局部用药勾勒出初步可能性。