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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 29 (1907), S. 1747-1750 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
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    Boston, Mass., etc. : Periodicals Archive Online (PAO)
    The North American Review. 103:1 (1866:July) 89 
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 181 (1958), S. 1337-1338 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Table l. DEOXYRIBONUCLEIO ACID CONTENT IN Vicia faba ROOTS No. of cells per 1 cm. tip Deoxyribonucleic acid (/ugm.) per 1 cm. tip determined as phosphorus sugar bases Deoxyribonucleic acid per cell (gin. x 10"11) determined as phosphorus sugar bases Control 3 days at 5 ° C. 3 days at 0 ° ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 165 (1950), S. 408-408 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A rapid method which has proved very efficient is as follows. (1) Fix root tips, anthers, etc., for 12-24 hr. in Navashin's fluid ; (2) place root tips on a clean slide, previously coated with a thin smear of Mayer's albumen, in a drop of macerating fluid (1 part HC1/1 part alcohol 95 per cent); ...
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0428
    Keywords: Glucose sensor ; enzyme electrode ; biosensor ; glucose oxidase ; ferrocene ; diabetes mellitus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Miniature, amperometric glucose sensors were constructed for implantation in the subcutaneous tissue of normal and insulin-dependent diabetic subjects. To minimise dependence on fluctuating tissue oxygen tension, we employed the technology of mediated electron transfer, with 1,1′-dimethylferrocene acting as the redox shuttle between immobilized glucose oxidase and a platinum base electrode. In 6 normal subjects, the subcutaneous sensor responses mirrored the simultaneously-measured changes in blood glucose concentration after a 75 g oral glucose load and after intravenous injection of 0.15 U/kg short-acting insulin, though increases and decreases in the sensor output were slower than the glycaemic changes. The mean peak delay in sensor response after the oral glucose was 40 min (range 0–45 min) and the delay in the hypoglycaemic nadir was 4 min (range 0–15 min). In 5 insulin-dependent diabetic subjects, spontaneous and induced hypoglycaemia was detectable by the implanted sensor. In addition, marked and frequent oscillations in the sensor current occurred in several normal and diabetic individuals as the blood glucose fell below about 1.9 mmol/l. These oscillations were present in a diabetic subject who had lost adrenergic warning symptoms to hypoglycaemia. Continuous metabolic monitoring in diabetes, particularly the detection of hypoglycaemia, may be possible with implanted sensors based on this technology.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Acta diabetologica 30 (1993), S. 143-148 
    ISSN: 1432-5233
    Keywords: Biosensor ; Enzyme electrode ; Glucose sensor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Glucose sensors based on immobilized glucose oxidase and hydrogen peroxide detection at a platinum base electrode were constructed and studied before, during and after implantation into the subcutaneous tissue of 11 non-diabetic subjects. A 75-g oral glucose load was given to elevate the blood glucose concentration. Seven of 14 sensors responded to the oral glucose administration with an increase in current and the output of the remainder was unchanged by the glucose load. Apparent subcutaneous glucose levels calculated from the pre-implantation calibration were a mean 58% of the plasma glucose values at baseline. A two-point in vivo calibration using paired current and glucose readings at baseline and at the maximum glucose and current after glucose ingestion showed a significantly reduced sensitivity in vivo compared with pre-implantation values (mean±SEM 52±21.5 vs 369±127 pA/mmol−1 per litre,P=0.003). Recalibration of the subcutaneous glucose concentrations using the in vivo calibration sensitivity and extrapolated background current (I o) gave values similar to those in plasma. The sensitivity of five sensors recalibrated in vitro after explantation was also reduced compared with pre-implantation levels and not significantly different from the in vivo characteristics. Responding and nonresponding sensors did not differ with respect to preimplantationI o, sensitivity or response time. However, provisional examination of some explanted sensors by scanning electron microscopy showed coating by cellular and other amorphous material in the non-functioning electrodes. We conclude that the sensitivity of glucose sensors of this design is markedly reduced, sometimes to zero, on implantation in the subcutaneous tissue of humans. Though several factors may contribute to this effect, a likely explanation is coating of or interaction with the sensor by components of the biological matrix.
    Type of Medium: Electronic Resource
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