- Award ID(s):
- 2100710
- PAR ID:
- 10437462
- Date Published:
- Journal Name:
- Biomedical Sciences Instrumentation
- Volume:
- 58
- Issue:
- 3
- ISSN:
- 1938-1158
- Page Range / eLocation ID:
- 177 to 185
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract We synthesized novel TiO2/ZnO-phosphate (TP/ZP) and polymethyl hydrogen siloxane (PMHS)-based two-layer hydrophobic coatings with potential antimicrobial properties tuned for application on steel substrates. The mathematical method of topological data analysis was applied to surface roughness data. Wetting characterizations showed stable hydrophobic behavior of the two-layer coated samples. Through tribological characterization, we compared the friction behavior of uncoated steel samples and steel samples coated with different coating materials. The coefficient of friction of uncoated base materials (ranging from 0.221 to 0.269) and the two-layer hydrophobic coatings (ranging from 0.234 to 0.273) indicated that the coatings confer hydrophobic properties to the substrates without a notable change in the friction behavior. We observed the correlations between the wetting and friction behaviors and the average roughness of the coated samples. Analysis of the micrographs of the scratched surfaces revealed preliminary information about the durability and abrasion resistance of the coatings.more » « less
-
Abstract This work is concerned with investigating the effect of substrate hydrophobicity and zeta potential on the dynamics and kinetics of the initial stages of bacterial adhesion. For this purpose, bacterial pathogens
Staphylococcus aureus andEscherichia coli O157:H7 were inoculated on the substrates coated with thin thiol layers (i.e., 1-octanethiol, 1-decanethiol, 1-octadecanethiol, 16-mercaptohexadecanoic acid, and 2-aminoethanethiol hydrochloride) with varying hydrophobicity and surface potential. The time-resolved adhesion data revealed a transformation from an exponential dependence to a square root dependence on time upon changing the substrate from hydrophobic or hydrophilic with a negative zeta potential value to hydrophilic with a negative zeta potential for both pathogens. The dewetting of extracellular polymeric substances (EPS) produced byE .coli O157:H7 was more noticeable on hydrophobic substrates, compared to that ofS .aureus , which is attributed to the more amphiphilic nature of staphylococcal EPS. The interplay between the timescale of EPS dewetting and the inverse of the adhesion rate constant modulated the distribution ofE .coli O157:H7 within microcolonies and the resultant microcolonial morphology on hydrophobic substrates. Observed trends in the formation of bacterial monolayers rather than multilayers and microcolonies rather than isolated and evenly spaced bacterial cells could be explained by a colloidal model considering van der Waals and electrostatic double-layer interactions only after introducing the contribution of elastic energy due to adhesion-induced deformations at intercellular and substrate-cell interfaces. The gained knowledge is significant in the context of identifying surfaces with greater risk of bacterial contamination and guiding the development of novel surfaces and coatings with superior bacterial antifouling characteristics. -
Surface morphology, in addition to hydrophobic and electrostatic effects, can alter how proteins interact with solid surfaces. Understanding the heterogeneous dynamics of protein adsorption on surfaces with varying roughness is experimentally challenging. In this work, we use single-molecule fluorescence microscopy to study the adsorption of α-lactalbumin protein on the glass substrate covered with a self-assembled monolayer (SAM) with varying surface concentrations. Two distinct interaction mechanisms are observed: localized adsorption/desorption and continuous-time random walk (CTRW). We investigate the origin of these two populations by simultaneous single-molecule imaging of substrates with both bare glass and SAM-covered regions. SAM-covered areas of substrates are found to promote CTRW, whereas glass surfaces promote localized motion. Contact angle measurements and atomic force microscopy imaging show that increasing SAM concentration results in both increasing hydrophobicity and surface roughness. These properties lead to two opposing effects: increasing hydrophobicity promotes longer protein flights, but increasing surface roughness suppresses protein dynamics resulting in shorter residence times. Our studies suggest that controlling hydrophobicity and roughness, in addition to electrostatics, as independent parameters could provide a means to tune desirable or undesirable protein interactions with surfaces.
-
Polyurethane is a common polymeric coating, providing abrasion resistance, chemical durability, and flexibility to surfaces in the biomedical, marine, and food processing industries with great promise for future materials due to its tunable chemistry. There exists a large body of research focused on modifying polyurethane with additional functionalities, such as antimicrobial, non-fouling, anticorrosive action, or high heat resistance. However, there remains a need for the characterization and surface analysis of fluoro-modified polyurethanes synthesized with commercially available fluorinated polyol. In this work, we have synthesized traditional solvent-borne polyurethane, conventionally found in food processing facilities, boat hulls, and floor coatings, with polyurethane containing 1%, 2%, and 3% perfluoropolyether (PFPE). Polyurethane formation was confirmed by attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy, with the urethane band forming at 1730 cm−1 and the absence of free isocyanate stretching from 2275–2250 cm−1. X-ray photoelectron spectroscopy (XPS) was used to confirm perfluoropolyether polymerization with an increase in the atomic percentage of fluorine. Wettability and hydrophobicity were determined using a dynamic water contact angle with significant differences in advancing the water contact angle with the inclusion of perfluoropolyether blocks (PU–co–1PFPE 131.5° ± 8.0, PU–co–2PFPE 130.9° ± 5.8, and PU–co–3PFPE 128.8° ± 5.2) compared to the control polyurethane (93.6° ± 3.6). The surface orientation of fluorine supported the reduced critical surface tensions of polyurethane modified with PFPE (12.54 mN m−1 for PU–co–3PFPE compared to 17.19 mN m−1 for unmodified polyurethane). This work has demonstrated the tunable chemical qualities of polyurethane by presenting its ability to incorporate fluoropolymer surface characteristics, including low critical surface tension and high hydrophobicity.
-
Abstract The growth of laser-induced nanocarbons, referred to here as laser-induced nanocarbon (LINC) for short, directly on polymeric surfaces is a promising route toward surface engineering of commercial polymers. This paper aims to demonstrate how this new approach can enable achieving varied surface properties based on tuning the nanostructured morphology of the formed graphitic material on commercial polyimide (Kapton) films. We elucidate the effects of tuning laser processing parameters on the achieved nanoscale morphology and the resulting surface hydrophobicity or hydrophilicity. Our results show that by varying lasing power, rastering speed, laser spot size, and line-to-line gap sizes, a wide range of water contact angles are possible, i.e., from below 20 deg to above 110 deg. Combining water contact angle measurements from an optical tensiometer with LINC surface characterization using optical microscopy, electron microscopy, and Raman spectroscopy enables building the process–structur–property relationship. Our findings reveal that both the value of contact angle and the anisotropic wetting behavior of LINC on polyimide are dependent on their hierarchical surface nanostructure which ranges from isotropic nanoporous morphology to fibrous morphology. Results also show that increasing gap sizes lead to an increase in contact angles and thus an increase in the hydrophobicity of the surface. Hence, our work highlight the potential of this approach for manufacturing flexible devices with tailored surfaces.more » « less