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Biomedical subjects

R P Buck

Publications and source records attributed to R P Buck.

9 recordsLinked to original sources

Impedances of thin and layered systems: cells with even or odd numbers of interfaces.

Impedance data, e.g., system responses, from perturbing small amplitude applied sinusoid signals of near DC to high kilohertz frequencies, give chemical information. Analysis of frequency-dependent imaginary and real impedance proceeds from equivalent analog circuit elements to chemical and physical significance determined from many model systems. Already, it is possible to interpret bulk transport processes, surface kinetic effects, diffusion phenomena, and dependencies on the type of contacts: symmetric ion contact, symmetric metal contact or asymmetric metal-ion interfaces, and cell design; even (battery or sensor) and odd numbered (constrained junction or immiscible liquid) interfaces in a system. These analyses cover the chemical origins, locations and meanings of the lumped resistances, capacitances and transmission lines that are introduced by engineers in their strict analog interpretations of the impedance data. Examples cover simple ohmic, simple diffusive behavior, complex behavior with surface interfacial kinetics or surface resistances, and with finite (nonblocking) or infinite (blocking) DC impedance. High and low frequency responses may show so-called constant phase element character that suggests fractal behavior. Low frequency data occasionally appear in the second quadrant of impedance plane plots. These results are caused by negative capacitances and resistances. In this paper, chemical interpretations of analog circuit elements are mainly based on theory and observations of thin cells of electrolytes and solid and liquid films (membranes) that are ionic or mixed ionic/electronic conductors. The information should carry over into thickened, gelled, and tissue electrolyte phases and serve as a basis for medically-oriented, perhaps diagnostic impedance measurement applications already pioneered by Herman Schwan.

Electric Conductivity

Mediated, anaerobic voltammetry of sulfite oxidase.

The anaerobic voltammetry of the Mo/Fe enzyme, sulfite oxidase (SO), is described for the mediators cytochrome c, [Ru(NH3)6]3+/2+, TMPD+/0, and [Co(bpy)3]3+/2+. Theory derived for steady-state voltammetric catalysis correctly predicts the observed concentration and scan-rate dependencies of the catalytic waves. The instances for which existing ECcat theories may be applied to two catalytic reactions coupled to an interfacial charge transfer are considered. The biomolecular rate constant for the reaction of [Co(bpy)3]3+ with reduced SO is calculated and determined to be approximately 5 X 10(4) L.mol-1.s-1. The appearance of catalytic prepeaks at low sulfite concentrations is noted and the shape of corresponding i/t curves from chronoamperometry is examined. The analytical implications of the novel time dependence of the catalytic current under these conditions are discussed.

Anaerobiosis

Surgical intervention to reestablish adequate intermaxillary space before fixed or removable prosthodontics.

Supraeruption of the right maxillary molars and concomitant drop of the alveolar ridge resulted in loss of intermaxillary space. With the patient under local anesthesia and intravenous sedation, a posterior segmental osteotomy was performed, on an outpatient basis, to reposition this segment superiorly into the maxillary sinus. Stabilization was accomplished with a prefabricated acrylic splint. The patient quickly resumed her daily routine with normal postoperative healing and satisfactory intermaxillary space.

Adult

Digital simulation of associated and nonassociated liquid membrane electrochemical properties.

The method and results of a digital simulation of electrochemical properties for associated and nonassociated liquid ion-exchange membranes are presented. It is assumed that the membranes is ideally permselective, sites are completely trapped, electroneutrality holds everywhere in the membrane, and the bathing solutions contain no more than two counterions, of which one is completely dissociated in the membrane. Electrochemical properties are simulated for the single counterion case and in the interference region. Concentration profiles, potentiometric responses, transient potential responses to activity steps, and current-voltage curves are given and the effects of ion-pairing and species mobilities are studied. It is found that ion-pairing increases the potentiometric selectivity toward the complexing ion over the noncomplexing ion. Transient responses to an ion activity step are shown to depend in a complex way on the ion-pair formation constant and the various mobilities. Current-voltage curves are simulated for varying degrees of ion-pairing and qualitative agreement is found with previous theoretical treatments, as well as quantitative agreement in those cases where closed-form expressions are known.

Computers

Solid ion-exchange electrode selective for calcium ion.

A calcium-selective electrode with solid ion exchanger was prepared from a solution of the calcium salt of a dialkylphosphoric acid in collodion. The electrode responds rapidly and reproducibly to activity of calcium ion and demonstrates a selective response for calcium ion in the presence of alkaline earth and alkali metal cations.

Calcium