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J Buettner

Publications and source records attributed to J Buettner.

7 recordsLinked to original sources
PubMed2000

Chromatographic resolution of tryptophan enantiomers with L-Leu-L-Leu-L-Leu peptide effects of mobile phase composition and chromatographic support.

Tryptophan enantiomers have been separated by zwitterion pair chromatography using L-leucine-L-leucine-L-leucine peptide as the zwitterion pairing agent. The peptide ligand is adsorbed onto an octadecylsilane support with excess ligand present in bulk solution. This article examines the roles of the hydrophobic matrix and the mobile phase components on tryptophan enantiomer binding and resolution. Capacity factors and enantioselectivites are given for both hydrophobic and hydrophilic matrices using mobile phases containing Leu-Leu-Leu peptide and/or salt. A decrease in selectivity upon the addition of mobile phase salt suggests that quadrupolar ion-pairing contributes to chiral recognition. Results indicate that binding is significantly reduced and separation is not achieved when Leu-Leu-Leu is coupled onto cross-linked or polymerized hydrophilic resins as well as onto macroporous polystyrene resin. However, resin-immobilized Leu-Leu-Asp-Leu-Leu-Leu, Leu-Leu-Glu-Leu-Leu-Leu, and Leu-Leu-Leu-Glu-Leu-Leu peptides, with ion-pairing sites designed to mimic the Leu-Leu-Leu-saturated C18 support, also do not resolve tryptophan enantiomers. This suggests the Leu-Leu-Leu structure is critical for enantiomer resolution. Because D- and L-tryptophan are separated in the absence of bulk Leu-Leu-Leu, chiral discrimination is believed to occur at the surface of the octadecylsilane support.

Chromatography, High Pressure Liquid↗
PubMed1995

How accurately can videokeratographic systems measure surface elevation?

INTRODUCTION: Surface topography, as opposed to dioptric topography, defines the corneal surface in simple terms without assumptions. Accordingly, it is important to know how well surface topography can be measured with current videokeratometric machines. PURPOSE: The purpose of this paper is to quantify the accuracy with which the TMS-1 Corneal Modeling System can measure the surface topography of calibrated spherical, elliptical, and bicurve surfaces. METHODS: The Computed Anatomy TMS-1 videokeratometer was used to measure three spherical, three elliptical, and two bicurve surfaces with known characteristics. Surface characteristics were either back-calculated from the dioptric files or directly obtained from the TMS-1 elevation file for each of 6400 points (256 points in each of 25 rings). The accuracy with which each method determined the true surface was quantified by calculating the root mean squared error (RMSE) of the 6400 measured surface elevations from the known surface elevation at each sampling point. RESULTS: (1) For spherical and elliptical surfaces, back-calculation of surface elevation from the dioptric file can be made with RMSE of 5 mu or less. (2) For spheres but not elliptical surfaces the TMS-1 elevation file defines the surface with RMSE 5 mu or less. (3) The surface area measured by placido-based videokeratometers varies with surface curvature. (4) RMSE in measured surface elevation increase as the distance from the videokeratometric axis increases. (5) For bicurves, the dioptric maps are smoothed by the TMS-1 over abrupt transitions and for large transitions never recover. Additionally, our back-calculation methods further smooth abrupt transitions, making the RMSE of the bicurve surface that is back-calculated from the dioptric file larger than the RMSE of the surface generated from the TMS-1 elevation file. CONCLUSIONS: Surface elevations can be back-calculated from dioptric files with RMSE of 5 microns or less for spheres and elliptical surfaces as long as there are no areas of abrupt transition. If areas of abrupt transition exist, the TMS-1 elevation file provides more accurate surface profile data.

Cornea↗
PubMed1990

Contribution of the nucleus of the optic tract to optokinetic nystagmus and optokinetic afternystagmus in the monkey: clinical implications.

1. The role of the pretectal NOT and the DTN in producing horizontal OKN and OKAN were studied using electrical stimulation and lesions. Positive stimulation sites lay in NOT, DTN, and in a fiber bundle in the pulvinar that is presumably a cortical input to NOT. 2. When the region of NOT was electrically stimulated in darkness, horizontal nystagmus was evoked with ipsilateral slow phases. Eye velocity rose slowly to a steady-state level and was followed by afternystagmus at the end of stimulation. The time constant of rise of stimulus-induced nystagmus was similar to the slow rise of slow-phase eye velocity during OKN. The saturation velocity of the induced nystagmus and the falling time constant of the stimulus afternystagmus were the same as those of OKAN. This suggests that electrical stimulation of NOT and DTN had elicited the slow component of OKN, i.e., that component produced by the velocity storage mechanism in the vestibular system. 3. Consistent with this postulate, activity induced by NOT stimulation could enhance, prolong, or block the slow component of OKN and OKAN depending on whether slow phases were to the same or opposite side. Stimulus-induced activity also interacted with vestibular nystagmus as would OKN and OKAN. 4. Unilateral lesions of NOT and DTN caused a loss of OKAN and the slow rise in OKN to the ipsilateral side. Steady-state velocities of OKN were reduced. The initial jump of OKN slow-phase velocity was the same or somewhat less after lesions but was not lost. 5. Partial lesions of a fiber bundle in the lateral pulvinar caused a transient change in OKN and OKAN, consistent with the idea that it carries activity for the slow component from the cortex to NOT. A lesion of the MRF, just rostral to the superior colliculus, caused a transient loss of the rapid component of OKN. This region appears to carry activity responsible for the initial jump in slow-phase velocity at the onset of stimulation. 6. We conclude that: (a) NOT and probably DTN lie in the indirect pathway that produces the slow component of horizontal OKN and OKAN to the ipsilateral side in the rhesus monkey. This pathway activates the velocity storage mechanism in the vestibular nuclei. (b) At the level of NOT, the pathway responsible for the slow component of OKN and OKAN is anatomically distinct from the pathway responsible for rapid changes in eye velocity at the onset of OKN.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1989

Computing high order wave aberration coefficients from variations of best focus for small artificial pupils.

Van den Brink (1962) measured the variation of best focus of vertical bar targets through a 1.4 mm aperture across the pupil of the eye. He expressed his results in contour maps of isodioptric lines across the pupil. The relative focus of a portion of the pupil is a function of the curvature of the wave front within the aperture. The curvature, in turn, is proportional to the second derivative of the wave aberration polynomial. Thus it is possible to make estimates of some of the coefficients of the wave aberration polynomial from Van den Brink's focusing data. This has been done for two states of accommodation. The results indicate that the wave aberration polynomial of the measured eye contains some significant terms of a power higher than hitherto measured.

Accommodation, Ocular↗
PubMedDate not supplied

Serum levels of mepivacaine-HCl during continuous axillary brachial plexus block.

In order to find out whether repeated doses of plain mepivacaine are appropriate for long-lasting microvascular surgery, a catheter-induced axillary plexus block was performed in 17 patients by using 400 mg of mepivacaine-HC1 every two hours. All patients underwent replantation surgery of one or more amputated fingers. Duration of operation varied from 8 to 24 hours. In all cases, there was adequate analgesia and muscle relaxation for the surgical procedure. Serum levels of mepivacaine were determined before, and 15 and 60 minute after the initial injection. With each following injection of mepivacaine, blood samples were taken at the same time schedule. Within the first eight hours, after four 400 mg doses of mepivacaine were given, all serum levels remained below the level of 5 to 6 micrograms/ml, which is said to be the lower level for mild cerebral toxic reactions in venous blood (blood/plasma distribution 0.92 +/- 0.04). After this time, when more than 1600 mg of mepivacaine had been administered, two patients exceeded the level of 6 micrograms/ml. The highest serum concentration observed in any of the patients was 7.0 micrograms/ml. This was 15 minutes after the 12th injection of 400 mg of mepivacaine and an overall dosage of 4800 mg. None of the patients showed evident signs of central nervous system or cardiovascular toxicity.

Adult↗
PubMedDate not supplied

Postdural puncture headache: comparison of 25-gauge Whitacre and Quincke needles.

BACKGROUND AND OBJECTIVES: To evaluate the influence of the shape of the needle tip on postdural puncture headache (PDPH) independent of the needle diameter, a 25-gauge Whitacre and a 25-gauge Quincke needle were compared. METHODS: In a prospective, randomized, double-blind fashion, the study was carried out on 400 patients who received spinal anesthesia for operations of the lower extremities. The 25-gauge Whitacre needle (group 1) and the 25-gauge Quincke needle (group 2) were randomly assigned to the patients, 200 in each group. Patients were interviewed postoperatively on days 1, 3, 5, and 7 using a standardized questionnaire. Only postural headache was defined as PDPH. The intensity of both postural and nonpostural headache were quantified using a 4-point rating scale and a visual analog pain scale (VAS). Statistical analysis was performed with parametric and nonparametric tests when appropriate, p < or = 0.05 was considered as significant. RESULTS: There were no differences in age and sex distribution between the two groups. Significantly more patients in group 2 (8.5%) complained of PDPH than in group 1 (3%, p < or = 0.02). Duration of PDPH ranged from 1-3 days (median: 1) in group 1, and from 1-9 days (median: 3) in group 2. This difference closely approached significance (p = 0.058). The mean maximal intensity of PDPH was comparable in both groups. Severe PDPH occurred only in two patients of group 2. One of them required a blood patch. With respect to the nonpostural headache, no significant differences were seen. CONCLUSIONS: The use of a conical tipped Whitacre needle results in significantly less PDPH compared to a standard Quincke spinal needle of the same size.

Adult↗