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1.
Langmuir ; 27(24): 15034-47, 2011 Dec 20.
Article in English | MEDLINE | ID: mdl-22053781

ABSTRACT

We describe the synthesis of a series of mono-, di-, and trisaccharide-functionalized alkanethiols as well as the formation of fouling-resistant self-assembled monolayers (SAMs) from these. The SAMs were characterized using ellipsometry, wetting measurements, and infrared reflection-absorption spectroscopy (IRAS). We show that the structure of the carbohydrate moiety affects the packing density and that this also alters the alkane chain organization. Upon increasing the size of the sugar moieties (from mono- to di- and trisaccharides), the structural qualities of the monolayers deteriorated with increasing disorder, and for the trisaccharide, slow reorganization dynamics in response to changes in the environmental polarity were observed. The antifouling properties of these SAMs were investigated through protein adsorption experiments from buffer solutions as well as settlement (attachment) tests using two common marine fouling species, zoospores of the green macroalga Ulva linza and cypris larvae of the barnacle Balanus amphitrite. The SAMs showed overall good resistance to fouling by both the proteins and the tested marine organisms. To improve the packing density of the SAMs with bulky headgroups, we employed mixed SAMs where the saccharide-thiols are diluted with a filler molecule having a small 2-hydroxyethyl headgroup. This method also provides a means by which the steric availability of sugar moieties can be varied, which is of interest for specific interaction studies with surface-bound sugars. The results of the surface dilution study and the low nonspecific adsorption onto the SAMs both indicate the feasibility of this approach.


Subject(s)
Disinfectants/chemical synthesis , Monosaccharides/chemistry , Oligosaccharides/chemistry , Proteins/antagonists & inhibitors , Spores/drug effects , Sulfhydryl Compounds/chemistry , Thoracica/drug effects , Adsorption , Alkanes/chemistry , Animals , Binding Sites , Disinfectants/metabolism , Disinfectants/pharmacology , Protein Binding/drug effects , Proteins/metabolism , Refractometry , Spectrophotometry, Infrared , Spectrum Analysis , Spores/growth & development , Thoracica/physiology , Ulva/drug effects , Ulva/growth & development , Wettability
2.
ACS Appl Mater Interfaces ; 3(10): 3890-901, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21916438

ABSTRACT

Self-assembled monolayers (SAMs) of galactoside-terminated alkanethiols have protein-resistance properties which can be tuned via the degree of methylation [Langmuir 2005, 21, 2971-2980]. Specifically, a partially methylated compound was more resistant to nonspecific protein adsorption than the hydroxylated or fully methylated counterparts. We investigate whether this also holds true for resistance to the attachment and adhesion of a range of marine species, in order to clarify to what extent resistance to protein adsorption correlates with the more complex adhesion of fouling organisms. The partially methylated galactoside-terminated SAM was further compared to a mixed monolayer of ω-substituted methyl- and hydroxyl-terminated alkanethiols with wetting properties and surface ratio of hydroxyl to methyl groups matching that of the galactoside. The settlement (initial attachment) and adhesion strength of four model marine fouling organisms were investigated, representing both micro- and macrofoulers; two bacteria (Cobetia marina and Marinobacter hydrocarbonoclasticus), barnacle cypris larvae (Balanus amphitrite), and algal zoospores (Ulva linza). The minimum in protein adsorption onto the partially methylated galactoside surface was partly reproduced in the marine fouling assays, providing some support for a relationship between protein resistance and adhesion of marine fouling organisms. The mixed alkanethiol SAM, which was matched in wettability to the partially methylated galactoside SAM, consistently showed higher settlement (initial attachment) of test organisms than the galactoside, implying that both wettability and surface chemistry are insufficient to explain differences in fouling resistance. We suggest that differences in the structure of interfacial water may explain the variation in adhesion to these SAMs.


Subject(s)
Aquatic Organisms/physiology , Biofouling/prevention & control , Galactosides/chemistry , Sulfhydryl Compounds/chemistry , Adsorption , Animals , Aquatic Organisms/drug effects , Bacterial Adhesion/drug effects , Cell Adhesion/drug effects , Galactosides/pharmacology , Halomonadaceae/drug effects , Halomonadaceae/physiology , Sulfhydryl Compounds/pharmacology , Surface Properties , Thoracica/drug effects , Thoracica/physiology , Ulva/drug effects , Ulva/physiology
3.
Biofouling ; 25(6): 481-93, 2009.
Article in English | MEDLINE | ID: mdl-19373571

ABSTRACT

Fouling-release coatings were prepared from blends of a fluorinated/siloxane copolymer with a poly(dimethyl siloxane) (PDMS) matrix in order to couple the low modulus character of PDMS with the low surface tension typical for fluorinated polymers. The content of the surface-active copolymer was varied in the blend over a broad range (0.15-10 wt % with respect to PDMS). X-ray photoelectron spectroscopy depth profiling analyses were performed on the coatings to establish the distribution of specific chemical constituents throughout the coatings, and proved enrichment in fluorine of the outermost layers of the coating surface. Addition of the fluorinated/siloxane copolymer to the PDMS matrix resulted in a concentration-dependent decrease in settlement of barnacle, Balanus amphitrite, cyprids. The release of young plants of Ulva, a soft fouling species, and young barnacles showed that adhesion strength on the fluorinated/siloxane copolymer was significantly lower than the siloxane control. However, differences in adhesion strength were not directly correlated with the concentration of copolymer in the blends.


Subject(s)
Fluorine , Polymers , Siloxanes , Thoracica/drug effects , Ulva/drug effects , Adhesiveness , Animals , Dimethylpolysiloxanes/chemical synthesis , Dimethylpolysiloxanes/chemistry , Dimethylpolysiloxanes/pharmacology , Fluorine/chemistry , Fluorine/pharmacology , Polymers/chemical synthesis , Polymers/chemistry , Polymers/pharmacology , Siloxanes/chemistry , Siloxanes/pharmacology , Surface Properties , Thoracica/physiology , Ulva/physiology
4.
Biomacromolecules ; 9(10): 2775-83, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18759475

ABSTRACT

This work describes the fabrication, characterization, and biological evaluation of a thin protein-resistant poly(ethylene glycol) (PEG)-based hydrogel coating for antifouling applications. The coating was fabricated by free-radical polymerization on silanized glass and silicon and on polystyrene-covered silicon and gold. The physicochemical properties of the coating were characterized by infrared spectroscopy, ellipsometry, and contact angle measurements. In particular, the chemical stability of the coating in artificial seawater was evaluated over a six-month period. These measurements indicated that the degradation process was slow under the test conditions chosen, with the coating thickness and composition changing only marginally over the period. The settlement behavior of a broad and diverse group of marine and freshwater fouling organisms was evaluated. The tested organisms were barnacle larvae (Balanus amphitrite), algal zoospores (Ulva linza), diatoms (Navicula perminuta), and three bacteria species (Cobetia marina, Marinobacter hydrocarbonoclasticus, and Pseudomonas fluorescens). The biological results showed that the hydrogel coating exhibited excellent antifouling properties with respect to settlement and removal.


Subject(s)
Hydrogels/chemistry , Materials Testing/methods , Polyethylene Glycols/chemistry , Animals , Bacteria/metabolism , Chemistry, Physical/methods , Eukaryota/metabolism , Free Radicals , Fresh Water , Glass , Marine Biology , Spectrophotometry, Infrared/methods , Surface Properties , Thoracica/metabolism , Ultraviolet Rays , Water Microbiology
5.
Biofouling ; 24(6): 471-81, 2008.
Article in English | MEDLINE | ID: mdl-18726746

ABSTRACT

A computer-controlled force gauge designed to measure the adhesive strength of barnacles on test substrata is described. The instrument was evaluated with adult barnacles grown in situ on Silastic T2(R)-coated microscope slides and epoxy replicas adhered to the same substratum with synthetic adhesive. The force per unit area required to detach the barnacles (critical removal stress) using the new automated system was comparable to that obtained with ASTM D5618 (1994) (0.19 and 0.28 MPa compared with 0.18 and 0.27 MPa for two batches of barnacles). The automated method showed a faster rate of force development compared with the manual spring force gauge used for ASTM D5618 (1994). The new instrument was as accurate and precise at determining surface area as manual delineation used with ASTM D5618 (1994). The method provided significant advantages such as higher throughput speed, the ability to test smaller barnacles (which took less time to grow) and to control the force application angle and speed. The variability in measurements was lower than previously reported, suggesting an improved ability to compare the results obtained by different researchers.


Subject(s)
Automation/instrumentation , Automation/methods , Thoracica/growth & development , Adhesiveness , Animals , Body Size , Equipment Design , Models, Biological , Stress, Mechanical
6.
Biofouling ; 24(4): 291-302, 2008.
Article in English | MEDLINE | ID: mdl-18568667

ABSTRACT

This article reports on the preparation and partial characterisation of silicone-based coatings filled with low levels of either synthetic multiwall carbon nanotubes (MWCNTs) or natural sepiolite (NS). The antifouling and fouling-release properties of these coatings were explored through laboratory assays involving representative soft-fouling (Ulva) and hard-fouling (Balanus) organisms. The bulk mechanical properties of the coatings appeared unchanged by the addition of low amounts of filler, in contrast to the surface properties, which were modified on exposure to water. The release of Ulva sporelings (young plants) was improved by the addition of low amounts of both NS and MWCNTs. The most profound effect recorded was the significant reduction of adhesion strength of adult barnacles growing on a silicone elastomer containing a small amount (0.05%) of MWCNTs. All the data indicate that independent of the bulk properties, the surface properties affect settlement, and more particularly, the fouling-release behaviour, of the filled materials.


Subject(s)
Magnesium Silicates/chemistry , Nanotubes, Carbon/chemistry , Silicones/chemistry , Adhesiveness , Animals , Behavior, Animal , Biofilms , Materials Testing , Spores , Thoracica/physiology , Ulva/physiology
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