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While there has been significant research conducted on bacterial colonization on implant materials, with a focus on developing surface modifications to prevent the formation of bacterial biofilms, the study of Candida albicans biofilms on implantable materials is still in its infancy, despite its growing relevance in implant-associated infections. C. albicans fungal infections represent a significant clinical concern due to their severity and associated high fatality rate. Pathogenic yeasts account for an increasing proportion of implant-associated infections, since Candida spp. readily form biofilms on medical and dental device surfaces. In addition, these biofilms are highly antifungal-resistant, making it crucial to explore alternative solutions for the prevention of Candida implant-associated infections. One promising approach is to modify the surface properties of the implant, such as the wettability and topography of these substrata, to prevent the initial Candida attachment to the surface. This review summarizes recent research on the effects of surface wettability, roughness, and architecture on Candida spp. attachment to implantable materials. The nanofabrication of material surfaces are highlighted as a potential method for the prevention of Candida spp. attachment and biofilm formation on medical implant materials. Understanding the mechanisms by which Candida spp. attach to surfaces will allow such surfaces to be designed such that the incidence and severity of Candida infections in patients can be significantly reduced. Most importantly, this approach could also substantially reduce the need to use antifungals for the prevention and treatment of these infections, thereby playing a crucial role in minimizing the possibility contributing to instances of antimicrobial resistance. In this review we provide a systematic analysis of the role that surface characteristics, such as wettability, roughness, topography and architecture, play on the extent of C. albicans cells attachment that will occur on biomaterial surfaces. We show that exploiting bioinspired surfaces could significantly contribute to the prevention of antimicrobial resistance to antifungal and chemical-based preventive measures. By reducing the attachment and growth of C. albicans cells using surface structure approaches, we can decrease the need for antifungals, which are conventionally used to treat such infections. [Display omitted] [ABSTRACT FROM AUTHOR]

The wings of insects such as cicadas and dragonflies have been found to possess nanostructure arrays that are assembled from fatty acids. These arrays can physically interact with the bacterial cell membranes, leading to the death of the cell. Such mechanobactericidal surfaces are of significant interest, as they can kill bacteria without the need for antibacterial chemicals. Here, we report on the bactericidal effect of two of the main lipid components of the insect wing epicuticle, palmitic (C16) and stearic (C18) fatty acids. Films of these fatty acids were re-crystallised on the surface of highly ordered pyrolytic graphite. It appeared that the presence of two additional CH 2 groups in the alkyl chain resulted in the formation of different surface structures. Scanning electron microscopy and atomic force microscopy showed that the palmitic acid microcrystallites were more asymmetric than those of the stearic acid, where the palmitic acid microcrystallites were observed to be an angular abutment in the scanning electron micrographs. The principal differences between the two types of long-chain saturated fatty acid crystallites were the larger density of peaks in the upper contact plane of the palmitic acid crystallites, as well as their greater proportion of asymmetrical shapes, in comparison to that of the stearic acid film. These two parameters might contribute to higher bactericidal activity on surfaces derived from palmitic acid. Both the palmitic and stearic acid crystallite surfaces displayed activity against Gram-negative, rod-shaped Pseudomonas aeruginosa and Gram-positive, spherical Staphylococcus aureus cells. These microcrystallite interfaces might be a useful tool in the fabrication of effective bactericidal nanocoatings. Statement of Significance Nanostructured cicada and dragonfly wing surfaces have been discovered to be able physically kill bacterial cells. Here, we report on the successful fabrication of bactericidal three-dimensional structures of two main lipid components of the epicuticle of insect wings, palmitic (C16) and stearic (C18) acids. After crystallisation onto highly ordered pyrolytic graphite, both the palmitic and stearic acid films displayed bactericidal activity against both Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus cells. The simplicity of the production of these microcrystallite interfaces suggests that a fabrication technique, based on solution deposition, could be an effective technique for the application of bactericidal nanocoatings. [ABSTRACT FROM AUTHOR]

A combination of eCG (400 IU) and hCG (200 IU) (P.G. 600; Merck Animal Health, Summit, NJ, USA) stimulates puberty in gilts, but variation in the estrual response exists among farms. We hypothesized that some of the variability is a consequence of gilts that have commenced cycling being inadvertently treated. The objective of experiment 1 was to determine the effect of intramuscular (im) P.G. 600 on estrous cycles in sexually mature gilts. Gilts in treatment 1 (n = 16) received P.G. 600 at the onset of daily boar exposure. Gilts in treatments 2 to 5 (n = 16 per treatment) were allowed to express a natural first estrus and were then treated with P.G. 600 during the first estrous cycle as follows: treatment 2 at Day 6, treatment 3 at Day 12, and treatment 4 at Day 18 of the estrous cycle. Treatment 5 gilts received no P.G. 600. The proportion of gilts displaying a normal estrous cycle (18–24 days) was greater (P < 0.05) for treatments 4 (100%) and 5 (100%) compared with treatments 1 (73.3%) and 3 (60%), with treatment 2 having a value (87.5%) that was not different from the other groups. For treatment 3, 33% of gilts displayed an increased interestrus interval that averaged 32.5 days. Concentrations of progesterone remained elevated 20 days after the onset of first estrus in treatment 3 gilts, which supports the concept that P.G. 600 administered at Day 12 of the estrous cycle induced follicular growth, ovulation, and formation of CL that functioned for approximately 15 days, increasing the length of the estrous cycle. It is common for swine producers to have groups of replacement gilts that include both cycling and prepubertal animals, or individuals, the cycling status of which is unknown. The objective of experiment 2 was to evaluate a system using a combination of a progestogen (Matrix; Merck Animal Health) and P.G. 600 to synchronize estrus in replacement gilts. Crossbred gilts, assumed to be a mix of cycling and prepubertal females, were allocated to one of four treatments (n = 12 per treatment): treatment 1, Matrix (15 mg/day) fed for 14 days and im P.G. 600 24 hours after the last feeding of Matrix; treatment 2, Matrix for 7 days and P.G. 600; treatment 3, P.G. 600 only; and treatment 4, im water only. The percentage of gilts in estrus within 7 days after im treatment was the greatest (P < 0.02) and days to estrus the least (P < 0.05) for gilts receiving Matrix for 14 days and P.G. 600 (treatment 1, 91.7% and 5.4 ± 1.9 days; treatment 2, 50% and 9.2 ± 2.0 days; treatment 3, 33% and 13.8 ± 2.1 days; and treatment 4, 50% and 9.1 ± 1.9 days). The results of these experiments suggest that P.G. 600 administered to gilts that have already obtained puberty may cause abnormal estrous cycles and demonstrate to swine producers the need to correctly classify replacement gilts as prepubertal or cycling before administering the product. The use of Matrix and P.G. 600 in combination has potential as an effective strategy for synchronizing estrus in a mix of prepubertal and mature, cycling gilts. [ABSTRACT FROM AUTHOR]

In this review we attempt to clarify the notion of what is meant by the term antibacterial surfaces and categorise the approaches that are commonly used in the design of antibacterial surfaces. Application of surface coatings and the modification of the surface chemistry of substrata are generally considered to be a chemical approach to surface modification (as are surface polymerisation, functionalisation, and derivatisation), whereas, modification of the surface architecture of a substrate can be considered a physical approach. Here, the antifouling and bactericidal effects of antibacterial surfaces are briefly discussed. Finally, several recent efforts to design a new generation of antibacterial surfaces, which are based on mimicking the surface nanotopography of natural surfaces, are considered. [Copyright &y& Elsevier]

Abstract: Despite many synthetic biomaterials having physical properties that are comparable or even superior to those of natural body tissues, they frequently fail due to the adverse physiological reactions they cause within the human body, such as infection and inflammation. The surface modification of biomaterials is an economical and effective method by which biocompatibility and biofunctionality can be achieved while preserving the favorable bulk characteristics of the biomaterial, such as strength and inertness. Amongst the numerous surface modification techniques available, plasma surface modification affords device manufacturers a flexible and environmentally friendly process that enables tailoring of the surface morphology, structure, composition, and properties of the material to a specific need. There are a vast range of possible applications of plasma modification in biomaterial applications, however, the focus of this review paper is on processes that can be used to develop surface morphologies and chemical structures for the prevention of adhesion and proliferation of pathogenic bacteria on the surfaces of in-dwelling medical devices. As such, the fundamental principles of bacterial cell attachment and biofilm formation are also discussed. Functional organic plasma polymerised coatings are also discussed for their potential as biosensitive interfaces, connecting inorganic/metallic electronic devices with their physiological environments. [Copyright &y& Elsevier]

Abstract: Phytochemical investigations of the aqueous extract of Planchonia careya leaves revealed two known flavonol glycosides, kaempferol 3-O-gentiobioside (1) and quercetin 3-O-glucoside (isoquercitrin) (2), and a novel acylated kaempferol tetraglycoside, kaempferol 3-O-[α-rhamnopyranosyl(1→3)-(2-O-p-coumaroyl)]-β-glucopyranoside, 7-O-[α-rhamnopyranosyl-(1→3)-(4-O-p-coumaroyl)]-α-rhamnopyranoside (3). Structural elucidation was achieved using UV, NMR, and mass spectrometry. [Copyright &y& Elsevier]

Abstract: Aim of the study: The leaves of Planchonia careya (F. Muell.) R. Knuth (Lecythidaceae) have been traditionally implemented in the treatment of wounds by the indigenous people of northern Australia, although the compounds responsible for the medicinal properties have not been identified. In this study, antibacterial compounds from the leaf extracts were isolated and characterized, and the biological activity of each compound was assessed. Materials and methods: Compounds were isolated from the leaf extracts using HPLC-piloted activity-guided fractionation. The minimum inhibitory concentrations (MICs) were assessed with plate-hole diffusion assays, and the cytotoxicity was determined with MTT assays using monkey kidney epithelial (MA104) cells. Results: Six known compounds were isolated from the leaf extracts and were identified as 1, (+)-gallocatechin; 2, gallocatechin-(4α→8)-gallocatechin; 3, 9(S)-hydroxy-10E,12Z-octadecadienoic acid (α-dimorphecolic acid); 4, 2α,3β,24-trihydroxyolean-12-en-28-oic acid (hyptatic acid-A); 5, 3β-O-cis-p-coumaroyltormentic acid; and 6, 3β-O-trans-p-coumaroyltormentic acid. Compounds 5 and 6 were weakly selective for vancomycin-resistant Enterococcus (VRE) compared with eukaryotic cells, with an MIC of 59.4μg/mL and a 50% inhibitory concentration (IC50) of 72.0μg/mL for MA104 cells. Conclusions: The isolation of six antibacterial compounds from the leaves of Planchonia careya validates the use of this species as a topical wound-healing remedy. [Copyright &y& Elsevier]

Abstract: Cadmium (II) adsorption onto chemically modified Australian coals has been studied as a function of p[H+] at 25°C. The low rank Collie and Loy Yang coals and the bituminous Norwich Park and Mount Arthur coals were modified with hydrogen peroxide. While both treated bituminous coals showed little affinity for Cd(II) the adsorption properties of the two low rank coals were drastically modified by treatment with hydrogen peroxide. NICA-Donnan model calculations for the treated Collie coal indicated an increase in functionality (ca. 5-fold) which was reflected in the important increase in Cd(II) adsorption obtained from batch adsorption experiments. On the other hand, the modified Loy Yang coal underwent a ca. 6.25 decrease in surface functionality and decomposition of the coal structure itself. These changes were reflected in the DRIFT spectra in bands characteristic of the oxygen-containing functional groups. The Cd(II) adsorption capacity of this modified coal was consequently substantially decreased. The two low rank coals were also treated with ammonia at p[H+] 7.5 and 9.5. This treatment did not, however, induce any substantial change in the adsorption of Cd(II). DRIFT spectra showed that the predominant functional groups present in both Collie and Loy Yang coal remained essentially unchanged after treatment with aqueous ammonia. [Copyright &y& Elsevier]

Microbial contamination of polymer surfaces has become a significant challenge in domestic, industrial, and biomedical applications. Recent progress in our understanding of how topographical features of different length scales can be used to effectively and selectively control the attachment and proliferation of different cell types has provided an alternative strategy for imparting antibacterial activity to these surfaces. Among the well-recognized engineered models of antibacterial surface topographies, self-organized wrinkles have shown particular promise with respect to their antimicrobial characteristics. Here, we critically review the mechanisms by which wrinkles form on the surface of different types of polymer material and how they interact with various biomolecules and cell types. We also discuss the feasibility of using this antimicrobial strategy in real-life biomedical applications. A self-organized wrinkled topography is a potential candidate for the next generation of antibacterial surfaces. A wrinkled topography comprises two characteristic parameters: an amplitude and a wavelength. Wrinkled surfaces containing lubricants, polymer brushes, and fluorinated polymers have antifouling activity via chemical pathways. The scale of the hierarchical wrinkled topology and the stability of air entrapment inhibit microbial attachment by physically limiting the available surface area under static conditions. Wrinkled topographies derived from graphene oxide (GO), reduced GO, or nanosilver show excellent antimicrobial activity due to the intrinsic bactericidal property of these materials. The integration of appropriate materials into wrinkled topographies results in greater control over their interactions with biomolecules and cell lines for biomedical applications. [ABSTRACT FROM AUTHOR]

Abstract: Atomic force microscopy (AFM) is a technique that has long been employed in materials science, but is now increasingly being used in the biological sciences. AFM provides excellent topographical information on prokaryotic and eukaryotic cell surfaces, and the extracellular material produced by the cells. It helps to generate important data on the mechanical properties of cells, such as hardness and elasticity. AFM can also be used to measure the strength of adhesion, attraction, and repulsion forces between cells and surfaces or even between individual molecules. Additionally, by combining AFM with other complementary techniques such as fluorescence microscopy or Raman spectroscopy, the chemistry of given surface structures can be identified. This review aims to provide an update on the AFM techniques currently used in cell biology studies, along with a description of the range of recently developed research methodologies in which AFM plays a key role. [Copyright &y& Elsevier]

Abstract: We discuss the effect of extreme grain refinement in the bulk of commercial purity titanium (CP, Grade-2) on bacterial attachment to the mechano-chemically polished surfaces of the material. The ultrafine crystallinity of the bulk was achieved by severe plastic deformation by means of equal channel angular pressing (ECAP). The chemical composition, wettability, surface topography and roughness of titanium surfaces were characterized using X-ray photoelectron spectroscopy (XPS) and water contact angle (WCA) measurements, as well as atomic force microscopy (AFM) with 3D interactive visualization of the titanium surface morphology. It was found that physico-chemical surface characteristics of the as-received and the ECAP-modified CP titanium did not differ in any significant way, while the surface roughness at the nano-scale did. Optical profilometry performed on large scanning areas of approximately 225 μm × 300 μm showed that there was no significant difference between the roughness parameters R a and R q for surfaces in the two conditions, the overall level of roughness being lower for the ECAP-processed one. By contrast, topographic profile analysis at the nano-scale by AFM did reveal a difference in these parameters. This difference was sensitive to the size of the scanned surface area. A further two surface roughness parameters, skewness (R skw) and kurtosis (R kur), were also used to describe the morphology of titanium surfaces. It was found that the bacterial strains used in this study as adsorbates, viz. Staphylococcus aureus CIP 65.8 and Pseudomonas aeruginosa ATCC 9025, showed preference for surfaces of ECAP-processed titanium. S. aureus cells were found to have a greater propensity for attachment to surfaces of ECAP-modified titanium, while the attachment of P. aeruginosa, while also showing some preference for the ECAP-processed material, was less sensitive to the ECAP processing. [Copyright &y& Elsevier]

Abstract: The attachment behaviour of Staleya guttiformis DSM 11458T on poly(tert-butyl methacrylate) (P(tBMA)) polymeric surfaces has been studied. The electrostatic charge of the S. guttiformis cell surface (measured as zeta potential via microelectrophoresis) was −43.18mV. S. guttiformis cells appeared weakly hydrophilic as the water contact angle measured on lawns of bacterial cells was found to be 55±4.9°. It was found that while attaching on P(tBMA) surfaces, S. guttiformis cells produced extracellular polymeric substances (EPS) as observed from atomic force microscopy (AFM) and scanning electron microscopy (SEM) analysis. The AFM high resolution imaging revealed the nano-topography of the ‘free’ (the EPS that is produced by the bacterial cells, but no longer directly attached to the cells) EPS associated on the cell surface and also found on P(tBMA) surface. The ‘free’ EPS exhibited granular structure with lateral dimensions of 30–50nm and a vertical nano-roughness of 7–10nm. Another type of the EPS secreted by S. guttiformis cells appeared as a hydogel substance, presumably polysaccharide that formed a biopolymer network that facilitated bacterial attachment. [Copyright &y& Elsevier]

• Topography of substrata affects how they interface with plasmas. • Nano- and miscro-scale topography changes how polymers are assembled on surfaces. • Differences in polymer chemistry translate into reduced bactericidal activity. • Substrata nanotopography must be considered when modifying surfaces using plasmas. Plasma processing, e. g., functionalisation and deposition of antibacterial coatings, is often used to enhance surface properties of biomaterials. Plasma is, however, a non-uniform active medium, and the result of processing depends on the nature of both the plasma and the substratum. Here we show that when an antibacterial coating (i. e., polyterpenol) is plasma polymerised onto four types of titanium substrata that differ in their micro- and nano-scale topography (but not the bulk chemistry), the distribution of functional groups, e. g., OH and C O, in the polymer across the surface differs sufficiently, and so does the antibacterial activity of the resulting material system. While the addition of a coating hinders biofilm formation by Staphylococcus aureus and Pseudomonas aeruginosa , the bactericidal effect is significantly stronger in polymers deposited onto surfaces possessing lower degrees of nanoscale roughness, e.g., substrata after mechanical and chemical polishing. The reduced antibacterial efficacy of polymers on substrata with greater surface roughness (e.g. , on mechanically polished or lotus leaf-like surfaces) is attributed to a greater extent of thickness non-uniformity and heterogeneity in the functional group distribution across the surface. These findings suggest that the magnitude and distribution of topographical features of the substratum should be considered when designing plasma-enabled surface modification strategies. [ABSTRACT FROM AUTHOR]