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Table 1 Surface topography and gene delivery. Research papers assessing the effect of different surface topographies on surface-mediated non-viral gene delivery

From: Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems

Biomaterial

Cell type

Transfection system

Change in transfection efficiency

Ref.

Coverslips coated with a lipid film, having 3D-bicontinuous cubic, 2D-inverted hexagonal, or 1D-lamellar nanostructures

HeLa-Luc cell line, stably expressing the luciferase

siRNA directly loaded into the lipid film

Luciferase activity (luminescence/mg protein) was 4 × 105 in the untreated control.

Highest gene silencing efficacy was for 3D-bicontinuous phase (luciferase activity ∼ 1.5. × 105).

In 2D-hexagonal and 1D-lamellar phases, luciferase activity was almost 2.5 × 105.

Bolus delivery (Lipofectamineâ„¢) showed gene silencing efficacy similar to that of 3D-bicontinuous phase.

[145]

Micropatterns with different diameter and aspect ratio

Human MSCs

Cationic polyplexes

Highest transfection efficiency was 20%, for ellipses with aspect ratio 8:1 and surface area 80 μm.

Lowest transfection efficiency was 2%, for circular micropattern with a diameter of 20 μm.

[146]

Nanogrooved and nanopillar surfaces with different width/diameter and height

Normal human lung fibroblasts

Lipofectamineâ„¢ 2000

Highest % of transfection was 50%, in grooves 500 nm in width and 150 nm in height and in nanopillars with a diameter of 500 nm and a width of 150 nm.

In flat surfaces, % transfection was ∼ 30%

[139]

Nanogrooved surfaces with different deep and depth

C2C12 skeletal myoblasts

jetPEI® (Polyplus, US)

Decrease of ∼ 73% in transfection efficiency, on nanogrooved patterns of 400 nm groove width and 400 nm depth, compared to flat surfaces.

Decrease of ∼ 90% on nanogrooved pattern of 800 nm groove width and 500 nm depth, compared to flat surfaces.

[147]

Nanogratins and nanopillar surfaces

Human MSCs

Lipofectamineâ„¢ 2000

Highest % transfection was at 3.3%, for cells on grooves of 250 nm width. In flat surfaces, % transfection was 1.8%

[148]

SiNWs

Jurkat, L1.2 and GPE86

Naked DNA

% of transfection was ∼ 20%, 20% and 5% in GPE86, L1.2 and Jurkat respectively.

% transfection was between 0% and 1%, in flat surfaces for all cell types.

[149]

SiNWs with different heights

Human dental pulp stem cells

Naked DNA

% transfection was ∼ 90% for SiNW with heights of 1.2 and 3.5 μm.

% transfection was less than 10% for SiNW with heights of 0.4 μm and 6.3 μm.

[150]

SiNWs

Mouse embryonic stem cells

Naked DNA

Transfection efficiency lower than 1%.

[151]

Ethanolamine-functionalised SiNWs

HeLa

Naked DNA

Luciferase expression (luminescence/mg protein) was 106 in ethanolamine-functionalised siNWs, compared to 104 in non-functionalised siNWs

[152]

Nanopillars of different diameter

C2C12 skeletal myoblasts

jetPRIME® or Lipofectamine™

For jetPRIME®, luciferase expression (luminescence/mg protein) was ∼ 8 × 103 for pillars with a diameter of 1000 nm, whereas in flat surfaces it was 3 × 103

For Lipofetamine™, luciferase expression was 1 × 103 in nanopillars with a diameter 1000 nm and 5 × 103 in flat surfaces.

[153]