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S J Prince

Publications and source records attributed to S J Prince.

At least 19 recordsLinked to original sources

The precision of single neuron responses in cortical area V1 during stereoscopic depth judgments.

The performance of single neurons in cortical area V1 of alert macaque monkeys was compared against the animals' psychophysical performance during a binocular disparity discrimination task. Performance was assessed with stimuli that consisted of a patch of dynamic random dots, whose disparity varied from trial to trial, surrounded by an annulus of similar dots at a fixed disparity. On each trial, the animals indicated whether the depth of the central patch was in front of or behind the annulus. For each disparity of the center patch, neural performance was assessed by calculating the probability that the response of the neuron was greater or less than the response when the center disparity was the same as that of the annulus. Initially the animals performed the task simultaneously with the neural recording. However, the range of disparities used, which was appropriate for the neuronal recording, may have affected performance, because the thresholds were substantially lower (2.6x) when the psychophysical measurements were repeated later. Average neuronal thresholds were approximately 4x poorer than these behavioral thresholds, although the best neurons were marginally better than the animals' behavior. Thus, the well known precision of relative depth judgments can be supported with signals from a small number of V1 neurons. Interference with the relative depth information in the stimulus profoundly affected behavioral thresholds, which were approximately 10x poorer when the surround was absent or contained binocularly uncorrelated dots. In this case, single V1 neurons consistently outperform the observer: presumably here, psychophysical thresholds are limited by other factors (such as uncertainty about vergence eye position).

Animals↗

Weighted directional energy model of human stereo correspondence.

Previous work [Prince, S. J. D, & Eagle, R. A. (1999). Size-disparity correlation in human binocular depth perception. Proceedings of the Royal Society: Biological Sciences, 266, 1361-1365] has demonstrated that disparity sign discrimination performance in isolated bandpass patterns is supported at disparities much larger than a phase disparity model might predict. One possibility is that this extended performance relies on a separate second-order system [Hess, R. F., & Wilcox, L. M. (1994). Linear and non-linear filtering in stereopsis. Vision Research, 34, 2431-2438]. Here, a 'weighted directional energy' model is developed which explains a large body of crossed versus uncrossed disparity discrimination data with a single mechanism. This model assumes a population of binocular complex cells at every image point with a range of position disparity shifts. These cells sample a local energy function which is weighted so that energy at large disparities is relatively attenuated. Disparity sign is determined by summing and comparing energy at crossed and uncrossed disparities in the presence of noise. The model qualitatively predicts matching data for one-dimensional Gabor stimuli. This scheme also predicts DMax in Gabor stimuli and filtered noise. Moreover, a range of 'non-linear' phenomena, in which disparity is perceived from contrast envelope information alone, can be explained. The weighted directional energy model presents a biologically plausible, parsimonious explanation of matching behaviour in bandpass stimuli for both 'first-order' and 'second-order' stimuli which obviates the need for multiple mechanisms in stereo correspondence.

Depth Perception↗

Stereo correspondence in one-dimensional Gabor stimuli.

Previous data [Prince, S.J.D., & Eagle, R.A., (1999). Size-disparity correlation in human binocular depth perception. Proceedings of the Royal Society of London B, 266, 1361-1365] have demonstrated that the upper disparity limit for stereopsis (DMax) is considerably smaller in filtered noise stereograms than in isolated Gabor patches of the same spatial frequency. This discrepancy is not currently understood. Here, the solution of the correspondence problem for bandpass stereograms was further examined. On each trial observers were presented with two one-dimensional Gabor stimuli containing disparities of equal magnitude but opposite sign. Subjects were required to indicate which interval contained the crossed disparity stimulus. It was found that matching behaviour changed as a function of Gabor envelope size. As a function of disparity magnitude, performance cycled between mostly correct and mostly incorrect at large envelope sizes but was always correct at small envelope sizes. At intermediate envelope sizes performance was cyclical at small disparities but always correct at large disparities. The critical envelope size at which performance changed from mostly correct to mostly incorrect at 270 degrees phase disparity was used as a measure of the matching performance as other parameters of the Gabor were varied. Both absolute and relative contrast were shown to influence the perceived sign of matches. Critical envelope size was also found to decrease as a function of spatial frequency, but more slowly than a phase-based limit would predict. These data cannot be predicted by current models of stereopsis, and can be used to constrain future models.

Contrast Sensitivity↗

Size-disparity correlation in human binocular depth perception.

To use the small horizontal disparities between images projected to the eyes for the recovery of three-dimensional information, our visual system must first identify which feature in one eye's image corresponds with which in the other. The earliest level of disparity processing in primates (V1) contains cells that are spatial-frequency tuned. If such cells have a disparity range that covers only a single period of their mean tuning frequency, there will always be exactly one potential match within this range. Here, this 'size-disparity' hypothesis was tested by measuring the contrast sensitivity of stereopsis as a function of disparity for single bandpass-filtered items. It was found that thresholds were low and relatively constant up to disparities an order of magnitude larger than is predicted by this constraint. Furthermore, peak sensitivity was relatively independent of spatial frequency. A control experiment showed that binocular correlation of the carrier is necessary for this task. In a third experiment, the maximum disparity that supports threshold performance was compared for an isolated bandpass item and bandpass-filtered noise. This limit was found to be five times larger for the isolated stimuli. In summary, these findings show that the initial stage of disparity detection is not limited by the size-disparity constraint. For stimuli with multiple false targets, however, processes subsequent to this stage reduce the disparity range over which the correspondence problem can be solved.

Depth Perception↗

Analysis of benzalkonium chloride and its homologs: HPLC versus HPCE.

Benzalkonium chloride (BAK) is a mixture of alkylbenzyldimethylammonium chloride homologs with n-C,2H25, n-C,4H29, and n-C16H33 comprising a major portion of the alkyl groups present. An analytical method for BAK must differentiate and quantitate the homologs in the BAK mixture. Reversed-phase high performance liquid chromatography (HPLC) separates compounds based on their affinity for a nonpolar column, which is a direct correlation to the compounds' polarity. High performance capillary electrophoresis (HPCE), however, separates compounds in an electric field according to their charge and size. The BAK homologs are suitable for separation by either of these methods because their polarity and sizes differ significantly. The HPLC method employed a mobile phase of 60% acetonitrile and 40% 0.1 M sodium acetate buffer pH 5 pumped at 1.0 ml min(-1), a 4.6 x 250 mm cyano column with 5 microm packing, and UV detection at 254 nm. The HPCE method utilized a run buffer of 30% acetonitrile and 70% 0.05 M sodium phosphate pH 3.06, a 50 microm x 20 cm open silica capillary, 7.5 kV electric field and UV detection at 214 nm. Both HPLC and HPCE demonstrated good linearity in the range of 0.025 to 0.8 mg ml(-1) with r2 values of approximately 0.99. The HPLC method produced good separation of the homolog peaks with a total analysis time of 25 min. HPCE run time was less than 5 min and demonstrated good separation of the three homologs. The HPLC method, however, was superior to HPCE in the areas of sensitivity and precision. The HPLC has been extensively used in the routine quantitation and qualitation of benzalkonium chloride concentrations in various products; however, long analysis times make this method inefficient. The HPCE method produced comparable results to the HPLC method but with much shorter analysis times. An HPCE analysis method, as presented here, may prove to be a much more useful and efficient method for the analysis of benzalkonium chloride and its homologs.

Benzalkonium Compounds↗

Sensitivity to disparity corrugations in peripheral vision.

Disparity discrimination thresholds are known to increase with both retinal eccentricity and distance from the horopter. However, little is known about how the detectability of cyclopean gratings varies with retinal position. Thresholds for disparity corrugations were measured as a function of corrugation frequency for different visual eccentricities. Subjects viewed annular displays of random dot stereograms, and judged in which of two intervals a circumferential disparity modulation was present. For any given eccentricity, visual sensitivity to disparity corrugations was bandpass. As eccentricity increased from 3.5 to 21.0 degrees, peak-to-trough thresholds were found to increase, the optimal corrugation frequency for detection decreased, and the upper cutoff corrugation frequency also decreased. The M-Scaling functions of Rovamo and Virsu were used to replot the data in terms of cycles per unit cortical distance. Peak detection frequency was constant at 0.8 cycles per mm of cortex after this rescaling, demonstrating that acuity for disparity modulations is approximately M-scaled beyond the fovea.

Depth Perception↗

Contrast masking reveals spatial-frequency channels in stereopsis.

Yang and Blake (1991 Vision Research 31 1177-1189) investigated depth detection in stereograms containing spatially narrow-band signal and noise energies. The resulting masking functions led them to conclude that stereo vision was subserved by only two channels peaking at 3 and 5 cycles deg-1. Glennerster and Parker (1997 Vision Research 37 2143-2152) re-analysed these data, taking into account the relative attenuation of low- and high-frequency noise masks as a consequence of the modulation transfer function (MTF) of the early visual system. They transformed the data using an estimated MTF and found that peak masking was always at the signal frequency across a 2.8 octave range. Here we determine the MTF of the early visual system for individual subjects by measuring contrast thresholds in a 2AFC orientation-discrimination task (horizontal vs vertical) using band-limited stimuli presented in a 7 deg x 7 deg window at 4 deg eccentricity. The filtered stimuli had a bandwidth of 1.5 octaves in frequency and 15 degrees in orientation at half-height. In the subsequent stereo experiment, the same (vertical) filters were used to generate both signal and noise bands. The noise was binocularly uncorrelated and scaled by each subject's MTF. Subjects performed a 2AFC depth-discrimination task (crossed vs uncrossed disparity) to determine threshold signal contrast as a function of signal and mask frequency. The resulting functions showed that peak masking was at the signal frequency over the three octave range tested (0.4-3.2 cycles deg-1). Comparison with simple luminance-masking data from experiments with similar stimuli shows that bandwidths for stereo masking are considerably larger. These data suggest that there are multiple bandpass channels feeding into stereopsis but that their characteristics differ from luminance channels in pattern vision.

Depth Perception↗

Variations in immunoglobulins and IgA subclasses of human uterine cervical secretions around the time of ovulation.

The quantity and subclass distribution of IgA produced by the human uterine cervix may have a significant impact on the defence against sexually transmitted diseases as well as the regulation of fertility. Cervical mucus was obtained from 15 normal ovulating women around the time of ovulation. The total amounts of secreted IgA (including IgA1 and IgA2), IgG, and IgM were determined by ELISA. IgA was detected at high levels in all samples of cervical mucus. When ovulation was ascertained by daily urinary luteinizing hormone testing, IgA production was maximal 2-3 days before ovulation. Equal proportions of IgA1 and IgA2 were detected in cervical mucus, and 80% of the IgA occurred in the polymeric forms. The increased levels of IgA, the ratios of IgA1 to IgA2, and the predominance of polymeric IgA indicate that much of the IgA in human uterine cervical fluid originates from local production.

Adult↗

Stability of cefpirome sulfate in the presence of commonly used intensive care drugs during simulated Y-site injection.

The stability of cefpirome sulfate during simulated Y-site injection with drugs commonly used in the intensive care unit was studied. Cefpirome sulfate was constituted and diluted to 50 mg/mL with 0.9% sodium chloride injection, 0.45% sodium chloride injection, 5% dextrose injection, and lactated Ringer's injection. Each cefpirome sulfate solution was mixed 1:1 (simulating Y-site injection) with amikacin 5.0 mg/mL (as the sulfate salt), amphotericin B 0.1 mg/mL, cefazolin 10 mg/mL (as the sodium salt), clindamycin 12.0 mg/mL (as the phosphate ester), dexamethasone phosphate 4.0 mg/mL (as the sodium salt), dopamine hydrochloride 0.8 mg/mL, epinephrine 0.1 mg/mL (as the hydrochloride salt), fluconazole 2.0 mg/mL, gentamicin 1.0 mg/mL (as the sulfate salt), and vancomycin 5.0 mg/mL (as the hydrochloride salt). All the drug combinations were prepared in triplicate and maintained at 23 degrees C. The combinations were observed visually at intervals up to eight hours, pH was measured, and samples were tested for drug concentration by high-performance liquid chromatography. Cefpirome was stable in the presence of each of the secondary drugs throughout the study period. All the secondary drugs except amphotericin B were stable in the presence of cefpirome. There were no visual phenomena indicating incompatibility. Changes in pH were minimal. Cefpirome 50 mg/mL (as the sulfate salt) in four different diluents was stable in the presence of each of 10 commonly used intensive care drugs for at least eight hours during simulated Y-site administration. Amphotericin B 0.1 mg/mL was not stable in the presence of cefpirome sulfate.

Amphotericin B↗

Stability of ramipril in water, apple juice, and applesauce.

The stability of ramipril in water, in apple juice, and in applesauce was studied. The contents of a single capsule each of ramipril 1.25, 2.5, and 5 mg were mixed in glass beakers with 120 mL of deionized and filtered water, apple juice, or applesauce. Each mixture was apportioned into 10 120-mL amber polyethylene terephthalate (PET) containers. Five of the containers in each set were stored at 23 degrees C, and samples were taken at 0, 1, 2, 6, 12, and 24 hours. The other five containers were stored at 3 degrees C, and samples were taken at 4, 8, 12, 24, and 48 hours. The samples were analyzed for ramipril concentration by stability-indicating high-performance liquid chromatography (HPLC). The quantity of drug remaining in the PET container after "administration" was determined by mixing the contents of single 5-mg ramipril capsules with 60 mL of apple juice, pouring the mixture into a waste receptacle, rinsing the PET container three separate times with 10 mL of water, and analyzing the pooled fluid from these rinses for ramipril concentration by HPLC. Under no condition did the percentage of ramipril remaining drop below 90%. No peaks for degradation products appeared in the chromatograms. The mean +/- S.D. quantity of ramipril remaining in the PET containers after draining was 0.3 +/- 0.3% for the apple juice. Ramipril from 1.25-, 2.5-, and 5-mg capsules mixed in water, in apple juice, and in applesauce was stable for 24 hours at 23 degrees C and for 48 hours at 3 degrees C.

Angiotensin-Converting Enzyme Inhibitors↗

Human immune responses to influenza virus vaccines administered by systemic or mucosal routes.

Healthy adult volunteers were immunized by parenteral or oral routes with trivalent inactivated influenza vaccine (A/Chile/1/83 (H1N1), A/Mississippi/1/85 (H3N2), and B/Ann Arbor/1/86), or intranasally with live attenuated, cold-adapted influenza type A/Texas/1/85 (H1N1) reassortant virus. In all volunteers, cells spontaneously secreting IgA, IgG or IgM antibodies specific to influenza virus were detected in peripheral blood on days 6-13 after immunization, and specific IgA, IgG and IgM antibodies to influenza vaccine were measured in sera and external secretions (saliva and nasal lavage). Following systemic immunization, a raise in specific antibodies of all isotypes was observed in sera beginning on day 13. Although small variations in IgA and IgM antibodies in saliva and nasal lavages were detected, antigen-specific IgG significantly increased between days 13 and 27. Intranasal administration of attenuated virus induced IgA and IgG antibodies in serum as well as in secretions. Serum antibodies were not substantially influenced by oral immunization, only a small increase in all isotypes was observed in volunteers' sera 21 days after ingestion of vaccine. However, in secretions, antigen-specific IgA and IgG responses were detected one week after immunization and reached a peak response on day 20. These studies show that different routes of immunization can be effective for the induction of specific antibodies, and support the concept of the common mucosal immune system in humans by demonstrating that the oral or intranasal administration of antigen-induced specific antibodies of IgA isotype in external secretions, preceded by the transient appearance in peripheral blood of specific antibody-producing cells.

Administration, Intranasal↗

Intraperitoneal immunization of human subjects with tetanus toxoid induces specific antibody-secreting cells in the peritoneal cavity and in the circulation, but fails to elicit a secretory IgA response.

Five patients on continuous ambulatory peritoneal dialysis (CAPD) were immunized intraperitoneally with tetanus toxoid (TT) through an indwelling catheter. Four control patients on CAPD received the same dose of TT intramuscularly. Before immunization, virtually no anti-TT antibody-secreting cells (AbSC) were detected by the enzyme-linked immunospot (ELISPOT) assay in peripheral blood or peritoneal fluid from patients of either group. One to 2 weeks after immunization, high frequencies of TT-specific AbSC were detected in the circulation and peritoneal cavity. More than 80% of those cells were of the IgG isotype, with IgA accounting for most of the remainder. Patients receiving TT by the i.p. route showed significantly higher frequencies of specific IgG and IgA AbSC in the peritoneal cavity than patients immunized intramuscularly. Frequencies of AbSC in peripheral blood did not significantly differ between the two groups. Immunization with TT by both routes resulted in a significant increase of IgG anti-TT antibodies in serum, saliva and peritoneal fluid. A significant IgA antibody response was seen only in serum and peritoneal effluents. Therefore, i.p. immunization of human subjects with TT elicited both a localized response in the peritoneal cavity as well as a systemic response in serum, but did not induce a salivary IgA response.

Adult↗

Stability of octreotide acetate in polypropylene syringes.

The stability of octreotide acetate in polypropylene syringes was studied. Polypropylene syringes were aseptically filled with 1 mL of octreotide acetate 0.2 mg/mL and stored at 3 or 23 degrees C under light protection or light exposure. Three syringes were prepared for each condition and each sampling time. Unopened 5-mL glass vials of the drug served as controls. Samples were removed immediately and at 8, 15, 22, and 29 days and analyzed by high-performance liquid chromatography. At 3 degrees C, octreotide stored in light-protected syringes maintained more than 90% of its initial concentration for up to 29 days. However, at 22 days the concentration in the syringes stored at that temperature and exposed to light was less than 90% when the standard deviation is considered. At 23 degrees C, the drug was stable for only up to 15 days (light protection) and 22 days (light exposure) when the standard deviation is considered. Octreotide acetate in polypropylene syringes was stable for up to 29 days when stored at 3 degrees C and protected from light and for up to 22 days when stored at 23 degrees C and exposed to light.

Chemistry, Pharmaceutical↗