Bhatia K S, Singh J
Department of Pharmaceutical Sciences, College of Pharmacy, North Dakota State University, Fargo 58105, USA.
Pharm Res. 1998 Dec;15(12):1857-62. doi: 10.1023/a:1011906022903.
The purpose of this study was to investigate the effect of 5% terpenes (i.e., limonene, carvone, thymol, and cineole)/ethanol (EtOH) and iontophoresis on the in vitro permeability of luteinizing hormone releasing hormone (LHRH) through the porcine epidermis and biophysical changes in the stratum comeum (SC) lipids by fourier transform infrared (FT-IR) spectroscopy. Methods. The porcine epidermis was pretreated with enhancer for 2 h. The permeability measurement system included Franz diffusion cells, Ag/AgCl electrodes, and SCEPTOR iontophoretic power source. FT-IR spectroscopy was performed to assess the possible contribution of lipid extraction to the transport enhancement of LHRH.
Terpenes in combination with EtOH significantly (p < 0.05) increased the flux of LHRH in comparison with the control (epidermis which was not enhancer treated). Iontophoresis further enhanced (p < 0.05) the flux of LHRH through terpenes/EtOH treated epidermis in comparison with their passive permeability. Reversibility studies showed that the post-recovery passive flux of LHRH through 5% limonene in EtOH/iontophoresis treated epidermis was significantly (p < 0.05) decreased but did not significantly recover to the baseline flux (i.e., flux through control epidermis). The SC treated with terpenes/ EtOH showed a decrease in peak heights and areas for both asymmetric and symmetric C-H stretching absorbances in comparison to untreated SC. A greater percent decrease in peak heights and areas was obtained by limonene/EtOH. However, treatment of the SC with terpenes/EtOH followed by iontophoresis did not further decrease the percentage of peak height and area over and above terpene/EtOH suggesting that iontophoresis alone does not cause SC lipid extraction.
Terpenes/EtOH increased LHRH permeability by enhancing the extraction of the SC lipids. Iontophoresis synergistically enhanced the permeability of LHRH through terpenes/EtOH treated epidermis. Thus, terpenes can be used as chemical enhancers in combination with iontophoresis to enhance the transdermal delivery of peptides such as LHRH.
本研究旨在探讨5%萜类化合物(即柠檬烯、香芹酮、百里香酚和桉叶油素)/乙醇(EtOH)以及离子导入对促黄体生成素释放激素(LHRH)经猪表皮的体外渗透性以及通过傅里叶变换红外(FT-IR)光谱法观察角质层(SC)脂质的生物物理变化的影响。方法:用增强剂对猪表皮预处理2小时。渗透性测量系统包括弗兰兹扩散池、Ag/AgCl电极和SCEPTOR离子导入电源。采用FT-IR光谱法评估脂质提取对LHRH转运增强的可能作用。
与对照组(未用增强剂处理的表皮)相比,萜类化合物与EtOH联合使用显著(p<0.05)增加了LHRH的通量。与被动渗透性相比,离子导入进一步增强(p<0.05)了LHRH通过萜类化合物/EtOH处理的表皮的通量。可逆性研究表明,LHRH通过乙醇/离子导入处理的表皮中5%柠檬烯后的恢复后被动通量显著(p<0.05)降低,但未显著恢复至基线通量(即通过对照表皮的通量)。与未处理的SC相比,用萜类化合物/EtOH处理的SC在不对称和对称C-H伸缩吸收的峰高和面积方面均有所降低。柠檬烯/EtOH使峰高和面积的降低百分比更大。然而,先用萜类化合物/EtOH处理SC,然后进行离子导入,并未使峰高和面积的百分比进一步降低,超过萜类化合物/EtOH单独处理的情况,这表明单独的离子导入不会导致SC脂质提取。
萜类化合物/EtOH通过增强SC脂质的提取增加了LHRH的渗透性。离子导入协同增强了LHRH通过萜类化合物/EtOH处理的表皮的渗透性。因此,萜类化合物可作为化学增强剂与离子导入联合使用,以增强LHRH等肽类的经皮递送。