Jubeli Emile, Raju Liji, Khalique Nada Abdul, Bk Natalia, Zegel Cory, Chen Agape, Lou Howard H, Øpstad Christer L, Zeeshan Muhammad, Sliwka Hans-Richard, Partali Vassilia, Leopold Philip L, Pungente Michael D
Université Paris-Sud, EA 401, IFR 141, Faculté de pharmacie, Châtenay Malabry, France.
Research Division, Weill Cornell Medical College in Qatar, Doha, Qatar.
Eur J Pharm Biopharm. 2015 Jan;89:280-9. doi: 10.1016/j.ejpb.2014.12.011. Epub 2014 Dec 20.
Cationic lipids are promising non-viral vectors for the cellular delivery of nucleic acids. Important considerations for the development of new delivery vectors are enhanced uptake efficiency, low toxicity and traceability. Traceable gene transfer systems however typically require the inclusion of a labeled excipient, and highly sensitive imaging instrumentation to detect the presence of the label. Recently, we reported the synthesis and characterization of colored, polyene cationic phospholipidoids composed of a rigid, polyenoic acid of predetermined dimension (C20:5 and C30:9) paired with flexible saturated alkyl chains of varying lengths (12:0, 14:0, 16:0, 18:0, 20:0 carbons). Herein, the potential of these cationic phospholipids as siRNA carriers was evaluated through standard liposomal formulations in combination with a neutral helper lipid DOPE. The polyene-based lipids were compared with a standard cationic lipid for siRNA-delivery into luciferase expressing HR5-CL11 cells. Within the series of lipids screened, knockdown results indicated that polyene cationic phospholipids paired with longer saturated alkyl chains are more effective as gene transfer agents, and perform comparably with the commercial lipid EPC. Furthermore, the chromophore associated with the polyene chain allowed tracking of the siRNA delivery using direct observation. The polyene lipoplexes were tracked on both a macroscopic and microscopic level either as a single-component or as a multi-component lipoplex formulation. When combined with a reference EPC, effective knockdown and tracking abilities were combined in a single preparation.
阳离子脂质是用于核酸细胞递送的很有前景的非病毒载体。开发新型递送载体的重要考量因素包括提高摄取效率、降低毒性和可追踪性。然而,可追踪的基因转移系统通常需要包含标记赋形剂以及用于检测标记物存在的高灵敏度成像仪器。最近,我们报道了由预定尺寸的刚性多烯酸(C20:5和C30:9)与不同长度的柔性饱和烷基链(12:0、14:0、16:0、18:0、20:0碳)组成的有色多烯阳离子磷脂类化合物的合成与表征。在此,通过标准脂质体制剂结合中性辅助脂质DOPE评估了这些阳离子磷脂作为siRNA载体的潜力。将基于多烯的脂质与用于将siRNA递送至表达荧光素酶的HR5-CL11细胞的标准阳离子脂质进行了比较。在所筛选的一系列脂质中,敲低结果表明,与较长饱和烷基链配对的多烯阳离子磷脂作为基因转移剂更有效,并且与商业脂质EPC表现相当。此外,与多烯链相关的发色团使得能够通过直接观察追踪siRNA递送。多烯脂质体复合物在宏观和微观层面上均作为单一组分或多组分脂质体复合物制剂进行了追踪。当与参比EPC组合时,在单一制剂中兼具了有效的敲低和追踪能力。