Department of Chemical Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Palackeho 1/3, 612 42 Brno, Czech Republic.
Bioorg Med Chem. 2010 Jan 1;18(1):73-9. doi: 10.1016/j.bmc.2009.11.020. Epub 2009 Nov 12.
Skin penetration enhancers are used to allow formulation of transdermal delivery systems for drugs that are otherwise insufficiently skin-permeable. The series of seven esters of substituted 6-aminohexanoic acid as potential transdermal penetration enhancers was formed by multistep synthesis. The synthesis of all newly prepared compounds is presented here. Structure confirmation of all generated compounds was accomplished by (1)H NMR, (13)C NMR, IR and MS spectroscopy. All the prepared compounds were analyzed using RP-HPLC method for the lipophilicity measurement and their lipophilicity (logk) was determined. Hydrophobicities (logP/ClogP) of the studied compounds were also calculated using two commercially available programs and 3D structures of the selected compounds were investigated by means of ab initio/DFT calculations of geometry. All the synthesized esters were tested for their in vitro transdermal penetration enhancer activity. The relationships between the lipophilicity and the chemical structure (SLR) of the studied compounds as well as the relationships between their chemical structure and transdermal penetration activity are mentioned.
皮肤渗透增强剂用于使药物的透皮递送系统制剂化,这些药物否则皮肤渗透性不足。作为潜在的透皮渗透增强剂的取代 6-氨基己酸的七个酯系列是通过多步合成形成的。本文介绍了所有新制备的化合物的合成。通过 (1)H NMR、(13)C NMR、IR 和 MS 光谱对所有生成的化合物进行结构确证。使用反相高效液相色谱法 (RP-HPLC) 对所有制备的化合物进行亲脂性测量,并确定其亲脂性 (logk)。还使用两个商业上可用的程序计算了研究化合物的疏水性 (logP/ClogP),并通过使用从头算/DFT 计算几何结构来研究所选化合物的 3D 结构。所有合成的酯都测试了它们的体外透皮渗透增强活性。提到了研究化合物的亲脂性与其化学结构 (SLR) 之间的关系,以及它们的化学结构与透皮渗透活性之间的关系。