28 results match your criteria: "1 University Station Stop[Affiliation]"

Enhancement of transepidermal skin clearing agent delivery using a 980 nm diode laser.

Lasers Surg Med

October 2005

The University of Texas at Austin, Biomedical Engineering Laser Laboratory, ENS 639, 1 University Station Stop C0800, Austin, Texas 78712, USA.

Background And Objectives: Patient compliant optical skin clearing requires non-invasive topical delivery of clearing agents such as glycerol. This requires reducing the skin barrier function by disrupting stratum corneum integrity, which was achieved using a 980 nm diode laser with artificial absorption substrates on the skin surface. Reduction of light scattering has the potential to improve many current and novel diagnostic and therapeutic applications of lasers in medicine.

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Objectives: This study utilized pharmacokinetics/pharmacodynamics to compare beta-lactam regimens for the empirical and definitive treatment of gram-negative pulmonary infections in the ICU.

Methods: Susceptibility data were extracted from the 2002 Intensive Care Unit Surveillance System (ISS) and pharmacokinetic parameters were obtained from published human studies. Monte Carlo simulation was used to model the free percent time above the MIC (free %T > MIC) for 18 beta-lactam regimens against all gram-negative isolates, Enterobacteriaceae, Pseudomonas aeruginosa and Acinetobacter baumannii.

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Competitive intermolecular pericyclic reactions of free and complexed cyclopentyne.

J Org Chem

December 2003

Department of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station Stop A5300, Austin, Texas 78712, USA.

Intermolecular competition for cyclopentyne by different alkenes supports the hypothesis that organolithium-promoted decomposition of precursors to cyclopentyne affords one or more lithium-ion-complexed species. Competition reactions with mixtures of 2,3-dihydropyran do not clearly differentiate between complexed and unencumbered (free) forms of cyclopentyne, but those involving spirodiene 2 and cyclohexene do. Remarkably, the cycloaddition reactions of free cyclopentyne are not diffusion-controlled despite its high reactivity.

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