Beyond the absorption-limited nonlinear phase shift with microring resonators

We show that the nonlinear phase shift produced by a ring resonator constructed from a given nonlinear optical material can be greater than the phase shift produced by a single pass through an infinite length of the same material when linear and nonlinear absorption are taken into consideration. The figure of merit (defined by the phase shift times the throughput) also improves for the ring resonator over that of the native nonlinear absorbing material. We finally show that these benefits of using the ring resonator as a nonlinear phase-shifting element can enhance the switching characteristics of a Mach-Zehnder interferometer.     

Conversion of unpolarized light to polarized light with greater than 50% efficiency by photorefractive two-beam coupling

All known polarizers operate through a separation of orthogonal electric field components, one of which is subsequently discarded. As a result, 50% of the unpolarized incident light is wasted in the process of conversion to polarized light. We demonstrate a new method by which we use the optical power in the ordinarily discarded component as the pump to amplify the retained component through photorefractive two-beam coupling to achieve greater than 50% throughput.     

High-performance liquid chromatographic assay with ultraviolet detection for the determination of etoperidone and two active metabolites, 5-(1-hydroxyethyl) etoperidone and 1-(3-chlorophenyl)piperazine, in plasma

A selective and sensitive high-performance liquid chromatographic assay with ultraviolet detection for the determination of the antidepressant drug etoperidone and two active metabolites in plasma is described. The drug, metabolites and internal standard are isolated from plasma using a two-step liquid-liquid extraction procedure. The resulting sample is chromatographed on a C18 column (10 cm x 2.1 mm I.D.) with ultraviolet detection at 254 nm. Standard curves are linear for each compound over the concentration range 2-1000 ng/ml. The accuracy and precision of the assay, expressed as the percentage deviation of measured values from the true value and the relative standard deviation (inter-run), are less than or equal to 10% at all concentrations except the minimum quantification limit. Using an automated injector and computerized data acquisition, eighty samples can be routinely processed in one day. The assay has been successfully used for the analysis of plasma samples from pharmacokinetic studies in mice, rats, dogs and humans.