Department of Medical Chemistry, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
Department of General Pathology, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland.
J Nanobiotechnology. 2021 Aug 28;19(1):258. doi: 10.1186/s12951-021-00984-4.
The rational chemical design of nanoparticles can be readily controlled and optimized by quantitatively studying protein adsorption at variously charged polymer carriers, determining their fate in biological fluids. We manufactured brain-derived neurotrophic factor (BDNF) -based electrostatic nanocomplexes with a different type of dendrimer core (anionic or cationic), encapsulated or not in polyethylene glycol (PEG), and studied their physicochemical properties and behavior in a biological setting. We investigated whether the electrokinetic charge of dendrimer core influences BDNF loading and desorption from the nanoparticle and serves as a determinant of nanoparticles' behavior in in vitro setting, influencing mitochondrial dysfunction, lipid peroxidation, and general nanoparticles' cellular toxicity.
We found that the electrokinetic charge of the dendrimer core influences nanoparticles in terms of BDNF release profile from their surfaces and their effect on cell viability, mitochondrial membrane potential, cell phenotype, and induction of oxidative stress. The electrostatic interaction of positively charged core of nanoparticles with cell membranes increases their cytotoxicity, as well as serious phenotype alterations compared to negatively charged nanoparticles core in neuron-like differentiated human neuroblastoma cells. Moreover, PEG adsorption at nanoparticles with negatively charged core presents a distinct decrease in metabolic cell activity. On the contrary, charge neutralization due to PEG adsorption on the surface of nanoparticles with positively charged core does not reduce their cytotoxicity, makes them less biocompatible with differentiated cells, and presumably shows non-specific toxicity.
The surface charge transformation after adsorption of protein or polyelectrolyte during nanocarriers formulation has an important role not only in designing nanomaterials with potent neuroprotective and neuroregenerative properties but also in applying them in a cellular environment.
通过定量研究不同带电聚合物载体上的蛋白质吸附情况,可以很好地控制和优化纳米颗粒的合理化学设计,从而确定其在生物流体中的命运。我们制造了基于脑源性神经营养因子(BDNF)的静电纳米复合物,这些复合物具有不同类型的树突状内核(阴离子或阳离子),是否被聚乙二醇(PEG)包裹,并在生物环境中研究了它们的物理化学性质和行为。我们研究了树突状内核的动电电荷是否会影响 BDNF 从纳米颗粒上的加载和解吸,并作为纳米颗粒在体外环境中行为的决定因素,影响线粒体功能障碍、脂质过氧化和一般纳米颗粒的细胞毒性。
我们发现,树突状内核的动电电荷会影响纳米颗粒的 BDNF 从其表面释放的情况,以及它们对细胞活力、线粒体膜电位、细胞表型和诱导氧化应激的影响。与带负电荷的纳米颗粒内核相比,带正电荷的纳米颗粒内核与细胞膜的静电相互作用会增加其细胞毒性,以及严重的表型改变。此外,带负电荷的纳米颗粒内核上吸附 PEG 会明显降低细胞代谢活性。相反,带正电荷的纳米颗粒内核上由于 PEG 吸附导致的电荷中和并不会降低其细胞毒性,使它们与分化细胞的生物相容性降低,可能表现出非特异性毒性。
在纳米载体配方中,蛋白质或聚电解质吸附后表面电荷的转变不仅在设计具有强大神经保护和神经再生特性的纳米材料方面具有重要作用,而且在将其应用于细胞环境方面也具有重要作用。