Petrichenko Oksana, Rucins Martins, Vezane Aleksandra, Timofejeva Irena, Sobolev Arkadij, Cekavicus Brigita, Pajuste Karlis, Plotniece Mara, Gosteva Marina, Kozlovska Tatjana, Plotniece Aiva
Latvian Institute of Organic Synthesis, Aizkraukles str. 21, Riga LV-1006, Latvia; Laboratory of Magnetic Soft Matter, Department of Physics, University of Latvia, Zellu str. 8, Riga LV-1002, Latvia.
Latvian Institute of Organic Synthesis, Aizkraukles str. 21, Riga LV-1006, Latvia.
Chem Phys Lipids. 2015 Oct;191:25-37. doi: 10.1016/j.chemphyslip.2015.08.005. Epub 2015 Aug 10.
New amphiphilic pyridine derivatives containing dodecyloxycarbonyl substituents at positions 3 and 5 and cationic moieties at positions 2 and 6 have been designed and synthesised. Compounds of this type can be considered as synthetic lipids. The corresponding 1,4-dihydropyridine (1,4-DHP) derivatives have earlier been proposed as a promising tool for plasmid DNA (pDNA) delivery in vitro. In this work studies of the self-assembling properties of amphiphilic pyridine derivatives leading to the formation of liposomes, determination of particle size, zeta-potential and critical micelle concentration (CMC) with dynamic light scattering (DLS) measurements are described. Furthermore, thermal analysis of pyridine derivatives was performed using thermogravimetry analysis (TGA) and differential thermal analysis (DTA) as well as the ability to deliver the pEGFP-C1 plasmid DNA (that encodes GFP reporter) into the Baby hamster kidney-derived (BHK-21) cell line was used for evaluation of gene delivery properties. We have revealed that the new pyridine derivatives possessed self-assembling properties which were proved by formation of nanoparticles with the average size from 115 to 743nm, the zeta-potentials in the range of 48-79mV and CMC values in the range of 2-67μM. DTA data showed that all processes were endothermic for all compounds. Additionally, we established that among the tested pyridines the representatives with N-methylpyrrolidinium or pyridinium moieties as cationic head-group at the positions 2 and 6 possessed higher pEGFP-C1 transfection activity into the BHK-21 cell line. Nevertheless, the obtained results indicated that correlation of the physicochemical, structural properties and gene delivery activities of the tested compounds were not completely elucidated yet. On the other hand, the synthesised pyridines as possible metabolites of promising delivery systems on the 1,4-DHP core possessed lower pDNA transfection activity than the corresponding 1,4-DHP amphiphiles.
设计并合成了在3和5位含有十二烷氧羰基取代基、在2和6位含有阳离子部分的新型两亲性吡啶衍生物。这类化合物可被视为合成脂质。相应的1,4 - 二氢吡啶(1,4 - DHP)衍生物 earlier 已被提议作为体外递送质粒DNA(pDNA)的一种有前景的工具。在这项工作中,描述了两亲性吡啶衍生物的自组装性质研究,通过动态光散射(DLS)测量来确定脂质体的形成、粒径、zeta电位和临界胶束浓度(CMC)。此外,使用热重分析(TGA)和差示热分析(DTA)对吡啶衍生物进行了热分析,并将pEGFP - C1质粒DNA(编码GFP报告基因)递送至幼仓鼠肾来源(BHK - 21)细胞系的能力用于评估基因递送性质。我们发现,新的吡啶衍生物具有自组装性质,这通过形成平均尺寸为115至743nm的纳米颗粒、zeta电位在48 - 79mV范围内以及CMC值在2 - 67μM范围内得到证明。DTA数据表明所有化合物的所有过程都是吸热的。此外,我们确定在测试的吡啶中,在2和6位以N - 甲基吡咯烷鎓或吡啶鎓部分作为阳离子头基的代表物对BHK - 21细胞系具有更高的pEGFP - C1转染活性。然而,所得结果表明,测试化合物的物理化学、结构性质与基因递送活性之间的相关性尚未完全阐明。另一方面,作为有前景的基于1,4 - DHP核心的递送系统的可能代谢物合成的吡啶,其pDNA转染活性低于相应的1,4 - DHP两亲物。