Abad Miriam, Martínez-Bueno Alejandro, Mendoza Gracia, Arruebo Manuel, Oriol Luis, Sebastián Víctor, Piñol Milagros
Instituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, 50009 Zaragoza, Spain.
Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Zaragoza, Pedro Cerbuna 12, 50009 Zaragoza, Spain.
Polymers (Basel). 2021 Feb 25;13(5):684. doi: 10.3390/polym13050684.
Hybrid linear-dendritic block copolymers (LDBCs) having dendrons with a precise number of peripheral groups that are able to supramolecular bind functional moieties are challenging materials as versatile polymeric platforms for the preparation of functional polymeric nanocarriers. LDBCs that are based on polyethylene glycol (PEG) as hydrophilic blocks and dendrons derived from bis-MPA having 2,6-diacylaminopyridine (DAP) units have been efficiently synthesized by the click coupling of preformed blocks, as was demonstrated by spectroscopic techniques and mass spectrometry. Self-assembly ability was first checked by nanoprecipitation. A reproducible and fast synthesis of aggregates was accomplished by microfluidics optimizing the total flow rate and phase ratio to achieve spherical micelles and/or vesicles depending on dendron generation and experimental parameters. The morphology and size of the self-assemblies were studied by TEM, Cryogenic Transmission Electron Microscopy (cryo-TEM), and Dynamic Light Scattering (DLS). The cytotoxicity of aggregates synthesized by microfluidics and the influence on apoptosis and cell cycle evaluation was studied on four cell lines. The self-assemblies are not cytotoxic at doses below 0.4 mg mL. Supramolecular functionalization using thymine derivatives was explored for reversibly cross-linking the hydrophobic blocks. The results open new possibilities for their use as drug nanocarriers with a dynamic cross-linking to improve nanocarrier stability but without hindering disassembly to release molecular cargoes.
具有精确数量外围基团的树枝状大分子的杂化线性-树枝状嵌段共聚物(LDBCs)能够超分子结合功能部分,作为制备功能性聚合物纳米载体的多功能聚合物平台,是具有挑战性的材料。基于聚乙二醇(PEG)作为亲水嵌段以及源自具有2,6-二酰氨基吡啶(DAP)单元的双-MPA的树枝状大分子的LDBCs,已通过预制嵌段的点击偶联高效合成,光谱技术和质谱证明了这一点。首先通过纳米沉淀检查自组装能力。通过微流体优化总流速和相比,实现了可重现且快速的聚集体合成,根据树枝状大分子的代数和实验参数获得球形胶束和/或囊泡。通过透射电子显微镜(TEM)、低温透射电子显微镜(cryo-TEM)和动态光散射(DLS)研究了自组装体的形态和尺寸。在四种细胞系上研究了通过微流体合成的聚集体的细胞毒性以及对细胞凋亡和细胞周期评估的影响。在剂量低于0.4 mg/mL时,自组装体无细胞毒性。探索了使用胸腺嘧啶衍生物进行超分子功能化,以可逆地交联疏水嵌段。这些结果为它们作为药物纳米载体的应用开辟了新的可能性,通过动态交联提高纳米载体稳定性,但不妨碍分解以释放分子货物。