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Shear Effects on Stability of DNA Complexes in the Presence of Serum

机译:对血清存在下DNA复合物稳定性的剪切效应

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摘要

The behavior of nanocarriers, even though they are well-defined at equilibrium conditions, is unpredictable in living system. Using the complexes formed by plasmid DNA (pDNA) and K-20 (K: lysine), protamine, or polylysine (PLL) as models, we studied the dynamic behavior of gene carriers in the presence of fetal bovine serum (FBS) and under different shear rates, a condition mimicking the internal physical environment of blood vessels. Without shear, all the positively charged complexes bind to the negatively charged proteins in FBS, leading to the formation of large aggregates and even precipitates. The behaviors are quite different under shear. The shear generates two effects: a mechanical force to break down the complex into smaller size particles above a critical shear rate and a stirring effect leading to secondary aggregation of complexes below the critical shear rate. In the studied shear rate from 100 to 3000 s(-1), the mechanical force plays a key role in K-20/pDNA and protamine/pDNA, while the stirring effect is dominant in PLL/pDNA. A model study shows that the interfacial tension, the chain density, and the elasticity of the complexes determine their responsiveness to shear force. This study is helpful to understand the fate of drug/gene carriers under physiological conditions. It also gains insight in designing drug/gene carriers with desirable properties for in vivo applications.
机译:纳米载波的行为,即使它们在均衡条件下定义明确,在生活系统中是不可预测的。使用质粒DNA(PDNA)和K-20(K:赖氨酸),protamine或聚赖氨酸(PLL)形成的复合物作为模型,我们在胎儿牛血清(FBS)存在下基因载体的动态行为不同的剪切速率,一种模仿血管内部物理环境的条件。没有剪切,所有带正电荷的复合物都与FBS中带负电荷的蛋白质结合,导致形成大的聚集体和甚至沉淀物。在剪切下行为完全不同。剪切产生两种效果:将复合物分解成较小尺寸的颗粒以上的临界剪切速率和搅拌效应,导致络合物的二次聚集在临界剪切速率以下。在从100至3000S(-1)的研究中,机械力在K-20 / PDNA和Protamine / PDNA中起关键作用,而搅拌效果在PLL / PDNA中显着。模型研究表明,复合物的界面张力,链密度和弹性决定了对剪切力的反应。本研究有助于了解生理条件下药物/基因载体的命运。它还在体内应用中设计了具有所需性能的药物/基因载体的洞察力。

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