College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, Florida, United States of America.
PLoS One. 2013 Dec 12;8(12):e82581. doi: 10.1371/journal.pone.0082581. eCollection 2013.
In the present study, we designed and developed novel lipids that include (Z)-1-(Octadec-9-en-1-yl)-pyrrolidine (Cy5T), 1, 1-Di-((Z)-octadec-9-en-1-yl)pyrrolidin-1-ium iodide (Cy5), (Z)-1-(Octadec-9-en-1-yl)-piperidine (Cy6T), and 1, 1-Di-((Z)-octadec-9-en-1-yl) piperidin-1-ium iodide (Cy6) to enhance the transdermal permeation of some selected drugs. Firstly, we evaluated the transdermal permeation efficacies of these lipids as chemical permeation enhancers in vehicle formulations for melatonin, ß-estradiol, caffeine, α-MSH, and spantide using franz diffusion cells. Among them Cy5 lipid was determined to be the most efficient by increasing the transdermal permeation of melatonin, ß-estradiol, caffeine, α-MSH, and spantide by 1.5 to 3.26-fold more at the epidermal layer and 1.3 to 2.5-fold more at the dermal layer, in comparison to either NMP or OA. Hence we developed a nanoparticle system (cy5 lipid ethanol drug nanoparticles) to evaluate any further improvement in the drug penetration. Cy5 lipid formed uniformly sized nanoparticles ranging from 150-200 nm depending on the type of drug. Further, Cy5 based nanoparticle system significantly (p<0.05) increased the permeation of all the drugs in comparison to the lipid solution and standard permeation enhancers. There were about 1.54 to 22-fold more of drug retained in the dermis for the Cy5 based nanoparticles compared to OA/NMP standard enhancers and 3.87 to 66.67-fold more than lipid solution. In addition, epifluorescent microscopic analysis in rhodamine-PE permeation studies confirmed the superior permeation enhancement of LEDs (detection of fluorescence up to skin depth of 340 μm) more than lipid solution, which revealed fluorescence up to skin depth of only 260 μm. In summary the present findings demonstrate that i) cationic lipid with 5 membered amine heterocyclic ring has higher permeating efficacy than the 6 membered amine hertocyclic ring. ii) The nanoparticle system prepared with Cy5 showed significant (p<0.05) increase in the permeation of the drugs than the control penetration enhancers, oleic acid and NMP.
在本研究中,我们设计并开发了包含(Z)-1-(十八-9-烯-1-基)-吡咯烷(Cy5T)、1,1-二-((Z)-十八-9-烯-1-基)-吡咯啶-1-碘(Cy5)、(Z)-1-(十八-9-烯-1-基)-哌啶(Cy6T)和 1,1-二-((Z)-十八-9-烯-1-基)-哌啶-1-碘(Cy6)的新型脂质,以增强一些选定药物的经皮渗透。首先,我们使用 Franz 扩散池评估了这些脂质作为化学渗透增强剂在载体制剂中对褪黑素、β-雌二醇、咖啡因、α-MSH 和 spantide 的经皮渗透效果。其中 Cy5 脂质被确定为最有效的,它使褪黑素、β-雌二醇、咖啡因、α-MSH 和 spantide 在表皮层的经皮渗透增加了 1.5 至 3.26 倍,在真皮层的经皮渗透增加了 1.3 至 2.5 倍,与 NMP 或 OA 相比。因此,我们开发了一种纳米颗粒系统(Cy5 脂质乙醇药物纳米颗粒),以评估药物渗透的任何进一步改善。Cy5 脂质形成的纳米颗粒大小均匀,范围为 150-200nm,具体取决于药物类型。此外,与脂质溶液和标准渗透增强剂相比,Cy5 基纳米颗粒系统显著(p<0.05)增加了所有药物的渗透。与 OA/NMP 标准增强剂相比,Cy5 基纳米颗粒在真皮中保留的药物约增加了 1.54 至 22 倍,与脂质溶液相比增加了 3.87 至 66.67 倍。此外,在罗丹明-PE 渗透研究中的荧光显微镜分析证实了 LED 的优越渗透增强效果(检测到荧光直至皮肤深度 340μm)优于脂质溶液,脂质溶液仅检测到皮肤深度 260μm 的荧光。总之,本研究结果表明:i)具有 5 元胺杂环的阳离子脂质具有比 6 元胺杂环更高的渗透功效。ii)与对照渗透增强剂油酸和 NMP 相比,用 Cy5 制备的纳米颗粒系统显著(p<0.05)增加了药物的渗透。