Change in size, morphology and stability of DNA polyplexes with hyperbranched poly(ethyleneimines) containing bulky maltose units
[Display omitted] •Less-toxic DNA polyplexes with maltose-modified poly(ethyleneimine).•Polyplexes with two melting points.•Weak electrostatic, but cooperative H-bonding forces.•Morphology of polyplexes. Polyplexes between Salmon DNA and non-modified hyperbranched poly(ethyleneimines) of varying mol...
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Veröffentlicht in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2016-02, Vol.138, p.78-85 |
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Sprache: | eng |
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•Less-toxic DNA polyplexes with maltose-modified poly(ethyleneimine).•Polyplexes with two melting points.•Weak electrostatic, but cooperative H-bonding forces.•Morphology of polyplexes.
Polyplexes between Salmon DNA and non-modified hyperbranched poly(ethyleneimines) of varying molar mass, i.e., PEI(5k) with 5000g/mol and PEI(25k) with 25,000g/mol, and modified PEI(5k) with maltose units (PEI-Mal) were investigated in dependence on the molar N/P ratio by using dynamic light scattering (DLS), zeta potential measurements, micro differential scanning calorimetry (μ-DSC), scanning-transmission electron microscopy (STEM), and cryo-scanning electron microscopy (cryo-SEM). A reloading of the polyplexes can be observed by adding the unmodified PEI samples of different molar mass. In excess of PEI a morphological transition from core-shell particles (at N/P 8) to loosely packed onion-like polyplexes (at N/P 40) is observed. The shift of the DSC melting peak from 88°C to 76°C indicates a destabilization of the DNA double helix due to the complexation with the unmodified PEI. Experiments with the maltose-modified PEI show a reloading already at a lower N/P ratio. Due to the presence of the sugar units in the periphery of the polycation electrostatic interactions between DNA become weaker, but cooperative H-bonding forces are reinforced. The resulting less-toxic, more compact polyplexes in excess of the PEI-Mal with two melting points and well distributed DNA segments are of special interest for extended gene delivery experiments. |
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ISSN: | 0927-7765 1873-4367 |
DOI: | 10.1016/j.colsurfb.2015.11.061 |