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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 5 (1988), S. 488-494 
    ISSN: 1573-904X
    Keywords: swelling ; dissolution ; matrix ; tablet ; cimetidine · HC1 ; sodium diclofenac ; diprophylline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The swelling and dissolution behavior of pharmaceutical systems containing a drug and a polymer can be analyzed by a mathematical model which predicts the drug released and the gel layer thickness as a function of time. It is possible to approximate the values of several of the physicochemical parameters of this model in order to obtain an order-of-magnitude analysis of the tablet dissolution process. Selected experimental results of tablet dissolution and drug release are analyzed and conclusions are made about the importance of the drug and polymer content and solubility in the release behavior.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 36 (1997), S. 125-130 
    ISSN: 0021-9304
    Keywords: poly(vinyl alcohol) ; controlled drug delivery ; swelling controlled-release systems ; hydrogels ; crystallinity ; dissolution ; metronidazole ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Novel semicrystalline, poly(vinyl alcohol) (PVA)-based phase erosion systems were developed. The rate of drug release from these systems is controlled by the rate of crystal dissolution. PVA devices loaded with metronidazole were exposed to temperatures ranging from 90 to 120 C for times of 10-90 min to obtain samples with different degrees of crystallinity. Degrees of crystallinity were measured by differential scanning calorimetry and attenuated total reflectance Fourier transform infrared spectroscopy. In vitro release of metronidazole from such systems into deionized water at 37°C was monitored. The influence of parameters such as polymer molecular weight, annealing time and temperature, and surface pretreatment on the crystal dissolution, and hence the drug release rate, were investigated. Measurements of water-front movements were carried out to study the effect of parameters such as drug solubility on the release rate. The drug release rate was found to be dependent on the crystallization conditions of the samples. Surface pretreatment was found to reduce the burst effect observed during the release. © 1997 John Wiley & Sons, Inc. J Biomed Mater Res, 36, 125-130, 1997.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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