Trifaceted Mickey Mouse Amphiphiles for Programmable Self-Assembly, DNA Complexation and Organ-Selective Gene Delivery

被引:8
作者
Carbajo-Gordillo, Ana I. [1 ]
Gonzalez-Cuesta, Manuel [2 ]
Jimenez Blanco, Jose L. [2 ]
Benito, Juan M. [1 ]
Santana-Armas, Maria L. [3 ]
Carmona, Thais [4 ]
Di Giorgio, Christophe [5 ]
Przybylski, Cedric [6 ]
Ortiz Mellet, Carmen [2 ]
Tros de Ilarduya, Conchita [3 ]
Mendicuti, Francisco [4 ]
Garcia Fernandez, Jose M. [1 ]
机构
[1] Univ Seville, CSIC, Inst Chem Res, IIQ, C Amer Vespucio 49, Seville 41092, Spain
[2] Univ Seville, Fac Chem, Dept Organ Chem, C Prof Garcia Gonzalez 1, Seville 41012, Spain
[3] Univ Navarra, Sch Pharm & Nutr, Dept Pharmaceut Technol & Chem, Pamplona 31080, Spain
[4] Univ Alcala, Inst Invest Quim Andres M Del Rio IQAR, Dept Analyt Chem Phys Chem & Chem Engn, Campus Univ,Ctra Madrid Barcelona Km 33-600, Alcala De Henares 28871, Spain
[5] Univ Cote Azur, Inst Chim Nice, UMR 7272, 28 Ave Valrose, F-06108 Nice, France
[6] Sorbonne Univ, CNRS, Inst Parisien Chim Mol, IPCM, Paris, France
关键词
cyclooligosaccharides; macrocycles; molecular nanoparticles; non-viral gene delivery; self-assembling; trehalose; RNA DELIVERY; CYCLODEXTRIN; NANOPARTICLES; CHEMISTRY; CANCER; TRANSFECTION; MOLECULES; DESIGN; VECTOR; CELLS;
D O I
10.1002/chem.202100832
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Instilling segregated cationic and lipophilic domains with an angular disposition in a trehalose-based trifaceted macrocyclic scaffold allows engineering patchy molecular nanoparticles leveraging directional interactions that emulate those controlling self-assembling processes in viral capsids. The resulting trilobular amphiphilic derivatives, featuring a Mickey Mouse architecture, can electrostatically interact with plasmid DNA (pDNA) and further engage in hydrophobic contacts to promote condensation into transfectious nanocomplexes. Notably, the topology and internal structure of the cyclooligosaccharide/pDNA co-assemblies can be molded by fine-tuning the valency and characteristics of the cationic and lipophilic patches, which strongly impacts the transfection efficacy in vitro and in vivo. Outstanding organ selectivities can then be programmed with no need of incorporating a biorecognizable motif in the formulation. The results provide a versatile strategy for the construction of fully synthetic and perfectly monodisperse nonviral gene delivery systems uniquely suited for optimization schemes by making cyclooligosaccharide patchiness the focus.
引用
收藏
页码:9429 / 9438
页数:10
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