726 research outputs found

    Rapid characterization of the ultraviolet induced fiber Bragg grating complex coupling coefficient as a function of irradiance and exposure time

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    We report the application of optical frequency domain reflectometry and a discrete-layer-peeling inverse scattering algorithm to the spatial characterization of the UV induced complex coupling coefficient during fiber Bragg grating growth. The fiber grating is rapidly characterized using this technique to give irradiance dependent growth as a function of exposure time, thereby providing the complete characterization of the coupling coefficient in the form of a "growth surface," which is related to the fiber's photosensitivity. We compare measurements of fiber Bragg grating growth in SMF-28 when exposed to continuous wave 244 nm irradiation from 0 to 90 W cm(-2) for exposure times up to 3230 s with a selection of other fibers including high germanium concentration fiber and erbium doped fiber. (c) 2007 Optical Society of America

    Efficient large-scale multiplexing of fiber Bragg grating and fiber Fabry-Perot sensors for structural health monitoring applications

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    Fiber Bragg gratings have been demonstrated as a versatile sensor for structural health monitoring. We present an efficient and cost effective multiplexing method for fiber Bragg grating and fiber Fabry-Perot sensors based on a broadband mode-locked fiber laser source and interferometric interrogation. The broadband, pulsed laser source permits time and wavelength division multiplexing to be employed to achieve very high sensor counts. Interferometric interrogation also permits high strain resolutions over large frequency ranges to be achieved. The proposed system has the capability to interrogate several hundred fiber Bragg gratings or fiber Fabry-Perot sensors on a single fiber, whilst achieving sub-microstrain resolution over bandwidths greater than 100 kHz. Strain resolutions of 30n epsilon/Hz(1/2) and 2 n epsilon/Hz(1/2) are demonstrated with the fiber Bragg grating and fiber Fabry-Perot sensor respectively. The fiber Fabry-Perot sensor provides an increase in the strain resolution over the fiber Bragg grating sensor of greater than a factor of 10. The fiber Bragg gratings are low reflectivity and could be fabricated during the fiber draw process providing a cost effective method for array fabrication. This system would find applications in several health monitoring applications where large sensor counts are necessary, in particular acoustic emission

    The Need for Translational Research on Drug-drug Interactions

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    Efficient fiber Bragg grating and fiber Fabry-Pe'rot sensor multiplexing scheme using a broadband pulsed mode-locked laser

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    A pulsed broadband mode-locked laser (MLL) combined with interferometric interrogation is shown to yield an efficient means of multiplexing a large number of fiber Bragg grating (FBG) or fiber Fabry-Perot (FFP) strain sensors with high performance. System configurations utilizing time division multiplexing (TDM) permit high resolution, accuracy, and bandwidth strain measurements along with high sensor densities. Strain resolutions of 23-60 n epsilon/Hz(1/2) at frequencies up to 800 Hz (expandable to 139 kHz) and a differential strain-measurement accuracy of +/- 1 mu epsilon are demonstrated. Interrogation of a low-finesse FFP sensor is also demonstrated, from which a strain resolution of 2 n epsilon/Hz(1/2) and strain-measurement accuracy of +/- 31 n epsilon are achieved. The system has the capability of interrogating well in excess of 50 sensors per fiber depending on crosstalk requirements. A discussion on sensor spacing, bandwidth, dynamic range, and measurement accuracy is also given

    The Unfinished Business of US Drug Safety Regulation

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    Posted with permission from FDLI ; Food and Drug Law Journal Various proposals have been advanced in response to recent problems with the safety of Food and Drug Administration (FDA)-approved drugs. Many call for incremental change, such as new safety oversight bodies or minor expansions of FDA's existing powers. "Fixing" FDA may not fix the problem, without related reform of the broader legal framework in which FDA operates. Key reform challenges include promoting clinical compliance with important safety warnings while preserving needed flexibility for physicians to adapt drug use to the individual patient; developing a clearer distinction between pre- and postapproval safety regulation; and devising mechanisms for funding investments in safety improvements. Until these fundamental problems are addressed, the United States will face ongoing problems with drug safety and patients will be denied the full measure of safety and therapeutic benefit that today's technologies could support. This article proposes a new direction to address these problems in the context of an insurance-based framework for promoting drug safety

    Polarization properties of interferometrically interrogated fiber Bragg grating and tandem-interferometer strain sensors

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    Lead sensitivity in low-coherence interferometric fiber-optic sensors is a well-known problem. It can lead to a severe degradation in the sensor resolution and accuracy through its effect on the fringe visibility and interferometric phase. These sensitivities have been attributed to birefringence in the various components. In the current work, an analysis of the polarization properties of fiber Bragg grating and tandem-interferometer strain sensors, using Stokes calculus and the Poincare sphere, is presented. The responses of these sensors as a function of the birefringence properties of the various components under different illuminating conditions are derived. The predicted responses demonstrate very good agreement with experimentally measured responses. These models provide a clear insight into the evolution of the polarization states through the sensor networks. Methods to overcome the lead sensitivity are discussed and demonstrated, which yield a differential strain measurement accuracy of 18 n epsilon - rms for a fiber Bragg grating sensor

    The Engineering Academy : increasing access to engineering

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    The Engineering Academy (EA) is an integrated programme between the University of Strathclyde, partner colleges and industry to widen access to undergraduate degrees in engineering. A partnership model was developed where students successfully complete an enhanced HNC at a partner college before transferring to second year of their chosen undergraduate degree within the Faculty of Engineering. EA entry requirements are lower than direct entry applications. Additional contextual information based on postcode; the Scottish Index of Multiple Deprivation; schools with low progression to university; or time in care, is used in selection. The programme also aligns with and accepts adult learner applicants from the Scottish Wider Access Programme. Three enhanced HNC pathways: Chemical Engineering, Electronic and Electrical Engineering and General Engineering require bespoke student transition activities tailored to the engineering discipline. The presentation will follow the evolution of the EA programme model from its inception to current day. This will include changes in the programme management; the establishment of curriculum and subject working groups to review, refine and share teaching practice; and development of transition activities. The results of these show a successful transition model into undergraduate engineering degrees for students from a range of backgrounds

    Is personalized medicine achievable in obstetrics?

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    Personalized medicine seeks to identify the right dose of the right drug for the right patient at the right time. Typically, individualization of therapy is based on the pharmacogenomic makeup of the individual and environmental factors that alter drug disposition and response. In addition to these factors, during pregnancy, a woman's body undergoes many changes that can impact the therapeutic efficacy of medications. Yet, there is minimal research regarding personalized medicine in obstetrics. Adoption of pharmacogenetic testing into the obstetrical care is dependent on evidence of analytical validity, clinical validity, and clinical utility. Here, we briefly present information regarding the potential utility of personalized medicine for treating the obstetric patient for pain with narcotics, hypertension, and preterm labor, and discuss the impediments of bringing personalized medicine to the obstetrical clinic

    Ultra-high-sensitivity two-dimensional bend sensor

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    A multicore fibre Fabry-Perot-based strain sensor interrogated with tandem interferometry for bend measurement is described. Curvature in two dimensions is obtained by measuring the difference in strain between three co-located low finesse Fabry-Perot interferometers formed in each core of the fibre by pairs of Bragg gratings. This sensor provides a responsivity enhancement of up to 30 times that of a previously reported fibre Bragg grating based sensor. Strain resolutions of 0.6 n epsilon/Hz(1/2) above 1 Hz are demonstrated, which corresponds to a curvature resolution of similar to 0.012 km(-1)/Hz(1/2)

    Differential quantification of CYP2D6 gene copy number by four different quantitative real-time PCR assays

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    Copy number variations (CNVs) in the CYP2D6 gene contribute to interindividual variation in drug metabolism. As the most common duplicated allele in Asian populations is the nonfunctional CYP2D6*36 allele, the goal of this study was to identify CNV assays that can differentiate between multiple copies of the CYP2D6*36 allele and multiple copies of other CYP2D6 alleles. We determined CYP2D6 gene copy numbers in 32 individuals with known CYP2D6 CNVs from the Coriell Japanese-Chinese panel using four quantitative real-time PCR assays. These assays target different regions of the CYP2D6 gene: 5'-flanking region, intron 2, intron 6, and exon 9 (Ex9). The specific target site of the Ex9 assay was verified by sequencing the PCR amplicon. Three of the CYP2D6 CNV assays (5'-flanking region, intron 2, and intron 6) estimated CYP2D6 copy numbers that were concordant for all 32 individuals. However, the Ex9 assay was concordant in only 10 of 32 samples. The 10 concordant samples did not contain any CYP2D6*36 alleles and the 22 discordant samples contained at least one CYP2D6*36 allele. In addition, the Ex9 assay accurately quantified all of the non-CYP2D6*36 alleles in all samples. Ex9 amplicon sequencing indicated that it targets a region of CYP2D6 exon 9 that undergoes partial gene-conversion in the CYP2D6*36 allele. In conclusion, CYP2D6 Ex9 CNV assay can be used to determine the copy number of non-CYP2D6*36 alleles. Selective amplification of non-CYP2D6*36 sequence by the Ex9 assay should be useful in determining the number of functional copies of CYP2D6 in Asian populations
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