Differential MS2 Interaction with Food Contact Surfaces Determined by Atomic Force Microscopy and Virus Recovery.

Enteric viruses are recognized as major etiologies of U.S. foodborne infections. These viruses are easily transmitted via food contact surfaces. Understanding virus interactions with surfaces may facilitate the development of improved means for their removal, thus reducing transmission. Using MS2 coliphage as a virus surrogate, the strength of virus adhesion to common food processing and preparation surfaces of polyvinyl chloride (PVC) and glass was assessed by atomic force microscopy (AFM) and virus recovery assays. The interaction forces of MS2 with various surfaces were measured from adhesion peaks in force-distance curves registered using a spherical bead probe preconjugated with MS2 particles. MS2 in phosphate-buffered saline (PBS) demonstrated approximately 5 times less adhesion force to glass (0.54 nN) than to PVC (2.87 nN) (P < 0.0001). This was consistent with the virus recovery data, which showed 1.4-fold fewer virus PFU recovered from PVC than from glass after identical inoculations and 24 h of cold storage. The difference in adhesion was ascribed to both intrinsic chemical characteristics and the substrate surface porosity (smooth glass versus porous PVC). Incorporating a surfactant micellar solution of sodium dodecyl sulfate (SDS) into the PBS reduced the adhesion force for PVC (∼0 nN) and consistently increased virus recovery by 19%. With direct and indirect evidence of virus adhesion, this study illustrated a two-way assessment of virus adhesion for the initial evaluation of potential means to mitigate virus adhesion to food contact surfaces.IMPORTANCE The spread of foodborne viruses is likely associated with their adhesive nature. Virus attachment on food contact surfaces has been evaluated by quantitating virus recoveries from inoculated surfaces. This study aimed to evaluate the microenvironment in which nanometer-sized viruses interact with food contact surfaces and to compare the virus adhesion differences using AFM. The virus surrogate MS2 demonstrated less adhesion force to glass than to PVC via AFM, with the force-contributing factors including the intrinsic nature and the topography of the contact surfaces. This adhesion finding is consistent with the virus recoveries, which were determined indirectly. Greater numbers of viruses were recovered from glass than from PVC, after application at the same levels. The stronger MS2 adhesion onto PVC could be interrupted by incorporating a surfactant during the interaction between the virus and the contact surface. This study increases our understanding of the virus adhesion microenvironment and indicates ways to mitigate virus adhesion onto contact surfaces.

Calculation of the surface potential and surface charge density by measurement of the three-phase contact angle.

The silica/silicon wafer is widely used in the semiconductor industry in the manufacture of electronic devices, so it is essential to understand its physical chemistry and determine the surface potential at the silica wafer/water interface. However, it is difficult to measure the surface potential of a silica/silicon wafer directly due to its high electric resistance. In the present study, the three-phase contact angle (TPCA) on silica is measured as a function of the pH. The surface potential and surface charge density at the silica/water surface are calculated by a model based on the Young-Lippmann equation in conjunction with the Gouy-Chapman model for the electric double layer. In measurements of the TPCA on silica, two distinct regions were identified with a boundary at pH 9.5-showing a dominance of the surface ionization of silanol groups below pH 9.5 and a dominance of the dissolution of silica into the aqueous solution above pH 9.5. Since the surface chemistry changes above pH 9.5, the model is applied to solutions below pH 9.5 (ionization dominant) for the calculation of the surface potential and surface charge density at the silica/aqueous interface. In order to evaluate the model, a galvanic mica cell was made of a mica sheet and the surface potential was measured directly at the mica/water interface. The model results are also validated by experimental data from the literature, as well as the results obtained by the potentiometric titration method and the electro-kinetic measurements.

Structural transitions in two-dimensional hard-sphere systems.

We spread randomly noncharged steel particles (diameter, 1.59 mm) on a silicon wafer to form a two-dimensional hard-sphere system. The particle structure versus the particle coverage was monitored. We observed the particle structural transition from liquidlike to triangular-lattice crystal-like with increasing particle coverage by analyzing the particle structure factor. The particle coverage at which the structural transition occurs was quantified by the curves of S(max) (A) and G6 (A); S(max) is the amplitude of the first peak of the structure factor (depicting the particle positional order), and G6 is the bond orientation order parameter. We also conducted a Monte Carlo simulation study. The Monte Carlo simulation results show good agreement with the experimental results at low particle area fractions. However, at high area fractions, the experimentally observed particle structure is less organized than that generated by simulations.

Texture and stability of emulsions and suspensions: role of oscillatory structural forces.

The stability of macro-dispersions, such as emulsions and particle suspensions, is characterized in different ways-creaming or sedimentation, flocculation of drops/particles, coalescence between drops or phase separation. Several novel experimental techniques have been developed in our laboratory to examine both the texture and stability of emulsions and suspensions. These methods include direct image analysis to extract the emulsion radial distribution function and to determine the effective inter-droplet interaction, and the Kossel diffraction technique, which is used to obtain the structural factors. The film thinning interferometric technique employing our capillary force balance is used to study the role of the surfactant micelles/colloidal particle-layering phenomenon and the in-layer structure formation. Monte Carlo simulations and a theoretical model based on the Ornstein-Zernike equation of statistical mechanics are used to discern the effects of the micelle/particle structuring and layering phenomenon in confined films between two droplets/particles. These experiments and theoretical calculations are used to gain a fundamental understanding of the role of long-range oscillatory (repulsion/attraction) structural interactions on the stability of both mono- and polydispersed systems. During the past 10 years, our research group has worked on several problems of interest to industry in which structural forces in emulsions and suspensions appear to play an important role. This paper is an overview of some of these relevant examples.

Foaming in simulated radioactive waste.

Radioactive waste treatment process usually involves concentration of radionuclides before waste can be immobilized by storing it in stable solid form. Foaming is observed at various stages of waste processing like SRAT (sludge receipt and adjustment tank) and melter operations. This kind of foaming greatly limits the process efficiency. The foam encountered can be characterized as a three-phase foam that incorporates finely divided solids (colloidal particles). The solid particles stabilize foaminess in two ways: by adsorption of biphilic particles at the surfaces of foam lamella and by layering of particles trapped inside the foam lamella. During bubble generation and rise, solid particles organize themselves into a layered structure due to confinement inside the foam lamella, and this structure provides a barrier against the coalescence of the bubbles, thereby causing foaming. Our novel capillary force balance apparatus was used to examine the particle-particle interactions, which affect particle layer formation in the foam lamella. Moreover, foaminess shows a maximum with increasing solid particle concentration. To explain the maximum in foaminess, a study was carried out on the simulated sludge, a non-radioactive simulant of the radioactive waste sludge at SRS, to identify the parameters that affect the foaming in a system characterized by the absence of surface-active agents. This three-phase foam does not show any foam stability unlike surfactant-stabilized foam. The parameters investigated were solid particle concentration, heating flux, and electrolyte concentration. The maximum in foaminess was found to be a net result of two countereffects that arise due to particle-particle interactions: structural stabilization and depletion destabilization. It was found that higher electrolyte concentration causes a reduction in foaminess and leads to a smaller bubble size. Higher heating fluxes lead to greater foaminess due to an increased rate of foam lamella generation in the sludge system.

Entropically driven ordering in a binary colloidal suspension near a planar wall.

The local ordering of a binary hard-sphere mixture with a size ratio 1:10 near a planar wall is investigated by means of integral equation theory. We find that when the bulk volume fraction of the smaller particles is greater than 15%, the larger particles (at a bulk volume fraction of 1% and higher) become highly localized on the wall surface, forming a quasi-two-dimensional surface-localized monolayer. Our results are discussed and compared against computer simulation data with an effective one-component Hamiltonian that is based on sphere-sphere and sphere-wall depletion potentials.

Density-functional theory for an electrolyte confined by thin charged walls.

Results are reported for the primitive model of an electrolyte and for the solvent primitive model of an electrolyte for the case where these fluids are confined by two charged walls. When the walls are thin, the confined electrolyte inside the walls is affected by the charge on both the inside and the outside of the walls. In the case of the primitive model (PM), this system has been studied previously using a singlet integral equation. Our density-functional (DF) study is more general because the fluids inside and outside the walls are constrained to have the same chemical potential and because solvent effects are considered, albeit at a crude level. The singlet integral equation does not consider the chemical potential constraint explicitly. We find that for the low density PM, the DF and integral equation approaches yield, except for a very narrow pore, very similar results. When solvent molecules are considered, the profiles become oscillatory. The co-ion density profiles are particularily interesting because the repulsive electrostatic potential and the effect of the increased pressure in "pushing" the co-ions against the wall compete.

Analysis of cell-to-bubble attachment in sparged bioreactors in the presence of cell-protecting additives.

To investigate the mechanisms of cell protection provided by medium additives against animal cell injury in sparged bioreactors, we have analyzed the effect of various additives on the cell-to-bubble attachment process using CHO cells in suspension. Cell-to-bubble attachment was examined using three experimental techniques: (1) cell-bubble induction time analysis (cell-to-bubble attachment times); (2) forming thin liquid films and observing the movement and location of cells in the thin films; and (3) foam flotation experiments. The induction times we measured for the various additives are as follows: no additive (50 to 500 ms), polyvinyl pyrrolidone (PVP: 20 to 500 ms), polyethylene glycol (PEG: 200 to 1000 ms), 3% serum (500 to 1000 ms), polyvinyl alcohol (PVA: 2 to 10 s), Pluronic F68 (5 to 20 s), and Methocel (20 to 60 s). In the thin film formation experiments, cells in medium with either F68, PVA, or Methocel quickly flowed out of draining thin liquid films and entered the plateau border. When using media with no additive or with serum, the flow of cells out of the thin liquid film and film drainage were slower than for media containing Pluronic F68. PVA, or Methocel. With PVP and PEG, the thin film drainage was much slower and cells remained trapped in the film. For the foam flotation experiments, a separation factor (ratio of cell concentration in the foam catch to that in the bubble column) was determined for the various additives. In the order of increasing separation factors (i.e., increasing cell attachment to bubbles), the additives are as follows: Methocel, PVA, Pluronic F68, 3% serum, serum-free medium with no additives, PEG, and PVP. Based on the results of these three different cell-to-bubble attachment experiments, we have classified the cell-protecting additives into three groups: (1) Pluronic F68, PVA, and Methocel (reduced cell-to-bubble attachment); (2) PEG and PVP (high or increased cell-to-bubble attachment); and (3) FBS (reduced cell attachment butslower drainage films compared with F68, PVA, and Methocel with some cell entrapment in those films). These phenomena are discussed in relation to the interfacial properties of the media reported in a companion Study (this issue). (c) 1995 John Wiley & Sons Inc.

Interfacial properties of cell culture media with cell-protecting additives.

In an effort to identify key rheological properties that contribute to cell protection against shear damage, we have measured surface shear and dilatationai viscosities, dynamic surface tension, foaminess, and foam stability for media containing cell-protecting additives. In a companion article,(18) we found that cell-to-bubble attachment was decreased in media containing Methocel, Pluronic F68, or polyvinyl alcohol (PVA). In medium containing polyethylene glycol (PEG) or potyvinyl-pyrrolidone (PVP), attachment was increased. PEG, PVP, serum (FBS), and serum albumin (BSA) increased the surface viscosity of the air/medium surface (thus, producing a more rigid interface), whereas F68 and PVA lowered it greatly. Foaming experiments showed that Methocel, PEG, PVA, and F68 decreased the foam half-life while FBS, BSA, and PVP were foam stabilizers. Interestingly, the foam stability of CHO cell suspensions decreased significantly for cell concentrations higher than ca. 2 x 10(6) cells/mL. Nonviable CHO cells reduced foam stability further. Dynamic surface tension values of the media tested were found significantly differentfrom their static surface tension values. The interfacial properties measured and the results presented in the companion study suggest that the additives that lower dynamic surface tension the most (Methocel, F68, and PVA) correlate well with reduced cell-to-bubble attachment, and thus, cell protection. Reduced dynamic surface tension with these additives implies faster surfactant adsorption, mobile interfaces, lower surface viscosity, and foam destabilization. Because PEG and PVP resulted in increased cell-to-bubble attachment and had different interfacial properties, a different mechanism (compared with Methocel, PVP, and F68) is apparently responsible for their protective effect. Finally, cell protection offered by FBS and BSA is attributed to the foam stabilization properties provided by these additives. (c) 1995 John Wiley & Sons Inc.

Hemoglobin multiple emulsion as an oxygen delivery system.

Multiple emulsion technology provides a mechanism for the encapsulation and in vivo delivery of drugs, proteins, and other materials which would otherwise be degraded, cleared rapidly, or toxic to the host. These feasibility studies were performed to evaluate a prototype Hb multiple emulsion as a stable oxygen delivery system. A concentrated solution of hemoglobin (Hb) was encapsulated in the form of a Hb-in-oil-in-water (Hb/O/W) multiple emulsion. Studies using mineral oil demonstrated that Hb multiple emulsions have several important characteristics that are compatible with utility as a blood substitute. These include: satisfactory rheological properties and good hydrodynamic stability compared to whole blood, high encapsulation concentration of Hb and high encapsulation efficiency with little met-hemoglobin generation, and satisfactory oxygen affinity and cooperativity compared to whole blood. Isovolemic exchange transfusions of Hb/O/W multiple emulsion can support life in rats whose hematocrit has been reduced to levels (5% or lower) that are incompatible with survival, and induces no acute toxicity. These results are consistent with the utility of Hb/O/W as an oxygen-carrying red blood cell substitute or organ perfusion media.

A mathematical model for Rn sampling by activated C adsorption.

This paper describes a diffusion/adsorption model that has been developed for the transport of Rn in an activated carbon porous bed. It is useful in studying the carbon canister Rn sampling technique used for monitoring Rn levels in air. The model calculates the amount of Rn adsorbed by the canister for various situations. The predictions of the response of the canister to both constant, as well as a periodic varying concentration of Rn in the surroundings, compares very well with experimental data. Based on this model, it is possible to simulate on a computer the response of the canister for an arbitrarily varying surrounding Rn level. Such computer simulations are effective tools in the design of a more accurate carbon canister monitor.