Mahmoud Gihan, Jedelská Jarmila, Strehlow Boris, Bakowsky Udo
Department of Pharmaceutical Technology and Biopharmaceutics, Marburg University, Ketzerbach 63, 35037 Marburg, Germany; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Helwan University, Ain Helwan, 11795 Cairo, Egypt.
Department of Pharmaceutical Technology and Biopharmaceutics, Marburg University, Ketzerbach 63, 35037 Marburg, Germany.
Eur J Pharm Biopharm. 2015 Sep;95(Pt A):88-98. doi: 10.1016/j.ejpb.2015.04.009. Epub 2015 May 1.
The initial burst release of water-soluble photosensitizers is one of the major problems encountered the development of controlled release formulations. In this study, the freely water soluble chlorin e6 (Ce6) was assembled with cationic lipid 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) to improve its loading efficiency in the liposomal bilayer. Tetraether lipids (TELs) derived from Sulfolobus acidocaldarius were added to DOTAP:Ce6 assembly in a concentration range of 2.5×10(-4)-1.6×10(-3)M to stabilize the membrane rigidity of the liposomes and to provide controlled release system. From the comparative spectroscopic experiments, it has been shown that the assembled DOTAP:Ce6 along with addition of TELs have improved the loading efficiency of Ce6 in TELs-liposomes and obviously modified the release profile of Ce6. The in vitro cell viability of Ce6 in mouse neuro-blastoma (Neuro-2a) and ovarian cell carcinoma (SK-OV-3) confirmed neglected dark cytotoxicity and presented potential photo-induced cytotoxicity with the effect was being more pronounced in Neuro 2a than in SK-OV-3. In-situ IV-injection of chick chorioallantoic membrane (CAM) showed hemorrhage and necrosis 30 min post irradiation at 1.8 mol% TELs (19.9J/cm(2)). Higher TELs of 2.2 and 3.7 mol% in particular demonstrated localized vascular destruction within the irradiated area. Our results suggest that TELs favored slower release rates of Ce6. This, in turn, tetraether lipids can be considered as a versatile class of lipids for photodynamic modality for destruction of cancer cells and tumor vasculature while sparing the quiescent ones.
水溶性光敏剂的初始突释是控释制剂开发过程中遇到的主要问题之一。在本研究中,将水溶性的二氢卟吩e6(Ce6)与阳离子脂质1,2 - 二油酰基-3 - 三甲基铵丙烷(DOTAP)组装,以提高其在脂质体双层中的负载效率。将源自嗜酸热硫化叶菌的四醚脂质(TELs)以2.5×10(-4)-1.6×10(-3)M的浓度范围添加到DOTAP:Ce6组装体中,以稳定脂质体的膜刚性并提供控释系统。通过对比光谱实验表明,组装的DOTAP:Ce6以及添加TELs提高了Ce6在含TELs脂质体中的负载效率,并明显改变了Ce6的释放曲线。Ce6在小鼠神经母细胞瘤(Neuro-2a)和卵巢癌细胞(SK-OV-3)中的体外细胞活力证实其暗毒性可忽略不计,并呈现出潜在的光诱导细胞毒性,且在Neuro 2a中的效果比在SK-OV-3中更明显。在鸡胚绒毛尿囊膜(CAM)上原位静脉注射显示,在1.8 mol% TELs(19.9J/cm(2))照射后30分钟出现出血和坏死。特别是2.2和3.7 mol%的较高TELs浓度在照射区域内表现出局部血管破坏。我们的结果表明TELs有利于Ce6的较慢释放速率。反过来,四醚脂质可被视为一类通用的脂质,用于光动力疗法破坏癌细胞和肿瘤脉管系统,同时使静止细胞免受影响。