Chemical and morphological characteristics of a biomaterial surface are thought to play an important role in determining cellular differentiation and apoptosis. In this report, we investigate the effect of nanoparticle (NP) assemblies arranged on a flat substrate on cytoskeletal organization, proliferation and metabolic activity on two cell types, Bovine aortic endothelial cells (BAECs) and mouse calvarial preosteoblasts (MC3T3-E1). To vary roughness without altering chemistry, glass substrates were coated with monodispersed silica nanoparticles of 50, 100 and 300 nm in diameter. The impact of surface roughness at the nanoscale on cell morphology was studied by quantifying cell spreading, shape, cytoskeletal F-actin alignment, and recruitment of focal adhesion complexes (FAC) using image analysis. Metabolic activity was followed using a thiazolyl blue tetrazolium bromide assay. In the two cell types tested, surface roughness introduced by nanoparticles had cell type specific effects on cell morphology and metabolism. While BAEC on NP-modified substrates exhibited smaller cell areas and fewer focal adhesion complexes compared to BAEC grown on glass, MC3T3-E1 cells in contrast exhibited larger cell areas on NP-modified surfaces and an increased number of FACs, in comparison to unmodified glass. However, both cell types on 50 nm NP had the highest proliferation rates (comparable to glass control) whereas cells grown on 300 nm NP exhibited inhibited proliferation. Interestingly, for both cell types surface roughness promoted the formation of long, thick F-actin fibers, which aligned with the long axis of each cell. These findings are consistent with our earlier result that osteogenic differentiation of human mesenchymal progenitor cells is enhanced on NP-modified surfaces. Our finding that nanoroughness, as imparted by nanoparticle assemblies, effects cellular processes in a cell specific manner, can have far reaching consequences on the development of “smart” biomaterials especially for directing stem cell differentiation.

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Due to their bioresorbable characteristics biodegradable polyesters are attractive materials for sutures, fracture fixation devices, and drug delivery systems. These polymers degrade primarily through a bulk erosion mechanism. In many instances including drug delivery and fabrication of orthopaedic devices, surface erosion is desired as it confers linearity with respect to degradation and changes in modulus. We hypothesized that surface erosion could be achieved in poly(α,ω-hydroxy acids) by tuning the lipophilicity of the system and hence the water uptake. Toward this end, we used a modular design strategy to manipulate the hydrophilic-lipophilic balance (HLB) of a polymer chain at various stages by judicious choice of building blocks. Using this novel synthetic strategy we have synthesized a library of degradable polyesters derived from poly(lactic acid) (PLA) and poly(lactic-co-glycolic acid) (PLGA) that exhibit surface erosion behavior. Surface erosion was further verified by ultrastructure analysis of degraded polymer pellets and thin films by Scanning Electron Microscopy and tapping mode Atomic Force Microscopy respectively.