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  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Twenty female Sprague-Dawley rats (Charles River Laboratories, Wilmington, Mass.), weighing 126–154 g at the time of partial hepatectomy, were used. They were housed in individual cages in air-conditioned quarters and were fed Purina chow and water ad libitum. The animals were divided equally ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Psychophysiology 13 (1976), S. 0 
    ISSN: 1469-8986
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine , Psychology
    Notes: The response of hyperkinetic (HK) boys to light flashes of four different intensities were measured with averaged visual evoked potential (AVEP). Latency, amplitude and stability data, including the slope of the regression of these measures with flash intensity, were obtained in initial and replicate samples of HK and control subjects. Repeated tests were done in attending and inattending conditions in a drug-free condition, and 1 hr. 1 week, and 5 weeks after treatment with dextroamphetamine.The data failed to support the hypotheses that HK children show small response to weak stimuli and normal to increased response to strong stimuli or “hyperaugmentation.” that they show increased response to weak stimuli or “reduction” when they are treated with dextroamphetamine, and that behavioral responsiveness In this drug is related to the degree of augmentation. The data also failed to support the hypothesis that detection of AVEP abnormalities in HK subjects is enhanced by testing in an attending condition. However, a few replicated findings were obtained which suggest that some AVEP factors other than the augmentation reduction measure may be related to both the degree of initial hyperactivity and the degree of decrease of hyperactivity with dextroamphetamine.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 21 (1965), S. 6-7 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Résumé La phagocytose intrautérine est un phénomène physiologique et non spécifique qui se produit par la présence de divers corps étrangers y-compris les spermatozoïdes.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 20 (1964), S. 694-696 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Résumé Des études autoradiographiques avec la thymidine tritiée ont mis en évidence l'augmentation de la synthèse de l'acide déribonucléïque et la prolifération cellulaire de la thyroïde et de la pituitaire pendant l'hypertrophie compensatoire rénale. Les sections de la glande thyroïde de rats néphrectomisés unilatéralement montraient une plus grande activité des follicules columnaires et perte de colloïde.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 228 (1970), S. 1097-1099 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] During menstruation, when necrotic endometrial tissue releases its store of activator into the plasminogen rich environment of intrauterine blood, intense fibrinolysis (and fibrinogeriolysis) is predictable. The role and magnitude of fibrinolytic activity in the uterus between menses, however, are ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 7 (1973), S. 193-200 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The rate of diffusion of pyrimethamine, a pyrimidine-based antimalarial drug, from silicone rubber is compared to the diffusion of this drug from a flexible epoxy. Specific amounts of drug were mixed into the epoxy resin prior to the addition of an aliphatic diamine curing agent in the reparation of the epoxy-drug capsules and into the silicone rubber prior to vulcanization with stannous octoate in the preparation of silicone drug capsules. These capsules, in the form of discs, were separately immersed in water which was replenished at regular time intervals. The amount of drug released was determined spectrophotometrically (λ max = 275 mμ). Silicone rubber discs with 20 mg of drug incorporated/disc showed a much higher initial release rate than epoxy discs with an equivalent amount of drug incorporated. The rate of drug release is shown to be a nonlinear function of the amount of drug initially incorporated. The amine functional groups on pyrimethamine, and the possibility of its participation in the curing of the epoxy is noted. In silicone rubber, such interaction is not expected. The addition of a silica filler to the epoxy drug mixture is associated with greater uniformity in the observed drug release rates of capsules made from the same batch of polymer drug mixture. The Shore A durometer hardness of these drug capsules are 30 and 70 for silicone rubber and epoxy, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 12 (1978), S. 249-254 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The daily in vitro release of hydrocortisone from composite polymer capsules is reported here for over 120 days. Increase in vinyl acetate comonomer content of the ethylene-vinyl acetate copolymer matrix brought about an increase in the diffusion rate. Variation in the initial drug content of the capsules from 40 mg to 20 mg affects the daily drug release less significantly than the variation in copolymer ratio. The correlation between vinyl acetate comonomer content and the percent crystallinity of the copolymer matrix is suggested as one of the possible major factors in controlling diffusion rate from this drug-polymer system. The diffusion constant (D) calculated was 0.212 × 10-10 cm2/sec when the copolymer carrier has 30% vinyl acetate content and 0.430 × 10-11 cm2/sec when the copolymer carrier has 20% vinyl acetate content for capsules with 20 mg initial drug content, and 0.118 × 10-11 cm2/sec and 0.226 × 10-11 cm2/sec, respectively, for capsules with 40 mg initial drug content.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 10 (1976), S. 743-758 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The derivation and experimental verification of a unified mathematical model for the estimation of drug release rate from drug-polymer composite tablets are presented. Cylindrical coordinates are utilized in the solution of the diffusion equation for a three-dimensional system. The model is applicable to tablets that range from the shape of a flat disk (radius 〉 thickness) to that of a cylindrical rod (radius 〈 thickness). The general solution for the fraction of drug released at a time t is \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{M\left(t \right)}}{{M\left(\infty \right)}} = 1 - \frac{8}{{l^2 a^2 }}\sum\limits_{m = 1}^{10} {\exp \left({ - D\alpha _m ^2 t} \right)\left({\alpha _m ^{ - 2} } \right)\sum\limits_{n = 1}^{10} {\exp \left({ - D\beta ^2 _n t} \right)} \left({\beta _n ^{ - 2} } \right)} $$\end{document} This approach to a three-dimensiona system, utilizing cylindrical coordinates, presents a comprehensive method for the estimation of drug release rates from sustained release tablets with drug distributed homogeneously throughout a polymer matrix. The calculated and experimental drug diffusion rate of pyrimethamine from pyrimethamine-silicone rubber composite tablets that range in shape from that of a disk to a cylinder, and of hydrocortisone from EVA, poly-caprolactone, and PVA terpolymer, are compared.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 7 (1973), S. 71-78 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Quantitative investigation of the rate of diffusion (in vitro) of chloroquine diphosphate, an antimalarial drug, from silicone rubber (Silastic) discs is reported here. The viscosity of the polymer is reduced to facilitate the formation of a more homogeneous drug-polymer mixture from which the discs are made. The average quantity of drug released daily from these vulcanized silicone rubber discs is measured as a function of the amount of drug initially incorporated in the polymeric mass. Discs with 9 and 36 mg of chloroquine diphosphate incorporated continue to release drug in microgram quantities for a period of over four months. The presence of low viscosity silicone fluid (20 centistokes) in the discs was found to cause no significant alteration in the drug release rate. The effect of agitation of the fluid in which the discs are immersed is also investigated. Results from samples prepared from different batches of polymer showed comparable results, indicating the rather homogeneous nature of the polymer-drug system. All samples showed high release rates during the first few days followed by much lower and more or less constant drug release on subsequent days over a period of months.Concentrations of the drug in the eluant is determined spectrophotometrically by utilizing the 220- and 343-mμ peaks of chloroquine diphosphate as well as spectrofluorometrically by measuring the percent fluorescence at 405 mμ (360-mμ excitation).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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