Dimitrov Erik, Toncheva-Moncheva Natalia, Bakardzhiev Pavel, Forys Aleksander, Doumanov Jordan, Mladenova Kirilka, Petrova Svetla, Trzebicka Barbara, Rangelov Stanislav
Institute of Polymers, Bulgarian Academy of Sciences Akad. G. Bonchev St. 103A 1113 Sofia Bulgaria
Centre of Polymer and Carbon Materials, Polish Academy of Sciences M. Curie-Sklodowskiej 34 Zabrze Poland.
Nanoscale Adv. 2022 Aug 9;4(18):3793-3803. doi: 10.1039/d2na00527a. eCollection 2022 Sep 13.
Vesicular spherical nucleic acids are dynamic nucleic acid-based supramolecular structures that are held together non-covalent bonds. They have promising applications as drug and nucleic acid delivery materials, diagnostic and imaging tools and platforms for development of various therapeutic schemes. In this contribution, we report on vesicular spherical nucleic acids, constructed from a non-phospholipid nucleolipid - an original hybrid biomacromolecule, composed of a hydrophobic residue, resembling that of the naturally occurring phospholipids, and a DNA oligonucleotide strand. The nucleolipid was synthesized by coupling of dibenzocyclooctyne-functionalized oligonucleotide and azidated 1,3-dihexadecyloxy-propane-2-ol an azide-alkyne reaction. In aqueous solution it spontaneously self-associated into nanosized supramolecular structures, identified as unilamellar vesicles composed of a self-closed bilayer. Vesicular structures were also formed upon intercalation of the nucleolipid its lipid-mimetic residue in the phospholipid bilayer membrane of liposomes prepared from readily available and FDA-approved lipids (1,2-dipalmitoyl--3-phosphocholine and cholesterol). The vesicular structures are thoroughly investigated by light scattering (dynamic, static, and electrophoretic) and cryogenic TEM and the physical characteristics, in particular, number of strands per particle, grafting density, and conformation of the strands, were compared to those of reference spherical nucleic acids. Finally, the vesicular structures were shown to exhibit cellular internalization with no need of transfection agents and enhanced colloidal and nuclease stability.
囊泡状球形核酸是基于核酸的动态超分子结构,通过非共价键结合在一起。它们作为药物和核酸递送材料、诊断和成像工具以及各种治疗方案开发的平台具有广阔的应用前景。在本论文中,我们报道了由非磷脂核脂质构建的囊泡状球形核酸,核脂质是一种原始的杂合生物大分子,由一个类似于天然磷脂疏水残基的基团和一条DNA寡核苷酸链组成。核脂质是通过将二苯并环辛炔功能化的寡核苷酸与叠氮化的1,3 - 二己基氧基丙烷 - 2 - 醇进行叠氮 - 炔环加成反应合成的。在水溶液中,它自发地自组装成纳米级超分子结构,被鉴定为由自封闭双层组成的单层囊泡。当将核脂质及其类脂残基插入由易于获得且经美国食品药品监督管理局批准的脂质(1,2 - 二棕榈酰 - sn - 3 - 磷酸胆碱和胆固醇)制备的脂质体的磷脂双分子层膜中时,也会形成囊泡结构。通过光散射(动态、静态和电泳)以及低温透射电子显微镜对囊泡结构进行了全面研究,并将其物理特性,特别是每个颗粒的链数、接枝密度和链的构象与参考球形核酸的进行了比较。最后,结果表明囊泡结构无需转染剂即可实现细胞内化,并且具有增强的胶体稳定性和核酸酶稳定性。