Relevant bibliographies by topics / ETOPHYLLINE

Academic literature on the topic 'ETOPHYLLINE'

Author: Grafiati
Published: 21 September 2023

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Journal articles on the topic "ETOPHYLLINE"

1

TANAKA, Rumiko, Masayuki HARAMURA, Akito TANAKA, and Noriaki HIRAYAMA. "Structure of Etophylline." Analytical Sciences: X-ray Structure Analysis Online 21 (2005): x165—x166. http://dx.doi.org/10.2116/analscix.21.x165.

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Haberbosch, W., A. Gnasso, W. Ziegler, and J. Augustin. "The effect of etophylline clofibrate on HDL subfractions." Atherosclerosis 55, no. 1 (April 1985): 71–80. http://dx.doi.org/10.1016/0021-9150(85)90167-4.

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3

Tavipatana, Wattanaporn, and James W. Ayres. "Etophylline and theophylline pharmacokinetics when administered concomitantly in rabbits." International Journal of Pharmaceutics 30, no. 2-3 (June 1986): 143–50. http://dx.doi.org/10.1016/0378-5173(86)90074-8.

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4

Coutts-Lendon, Carrie, and Jack L. Koenig. "Investigation of the Aqueous Dissolution of Semicrystalline Poly(Ethylene Oxide) Using Infrared Chemical Imaging: The Effects of Molecular Weight and Crystallinity." Applied Spectroscopy 59, no. 8 (August 2005): 976–85. http://dx.doi.org/10.1366/0003702054615232.

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Fourier transform infrared (FT-IR) imaging was used to successfully explore several factors influencing the dissolution of poly(ethylene oxide). The effect of the degree of crystallinity on the rate of dissolution of mid-range molecular weight PEO was negligible over the temperature ranges studied. The influence of molecular weight on polymer dissolution was found to be much greater than the changes in morphology. An examination of the polymer and solvent images and absorbance profiles, compared with the results of the bulk polymer/solvent boundary movement, confirmed this relationship. An investigation of the bulk polymer/solvent boundary using a crystalline-sensitive polymer band showed the crystalline to amorphous phase change occurred over a short distance. Moreover, solvent diffusion ahead of the bulk polymer/solvent front was minimal, most likely a result of the required phase change, which in turn regulated the degree of solvent ingress. Modeling of the dissolution was performed using the Peppas (power law) model. Physical parameters of the dissolution process were obtained from fitting the release profiles to the power law (fraction released = k × tn, where k is the dissolution rate constant and n is the release exponent). Results indicated the model worked well to describe dissolution at all molecular weights. By varying the number of data points input to the model and then comparing the generated graphs, it becomes clear that not only does the dissolution slow down over the course of the experiment, but an increase in molecular weight enhances this effect. The effect of different types of drug on the rate of polymer dissolution was also studied. The dissolution of neat polymer was compared to the dissolution of polymer containing 10% (by weight) of theophylline, etophylline, or testosterone. The general trend of all the dissolution curves was the same, with the addition of etophylline and testosterone tracing almost the same route in terms of movement of the bulk polymer/solvent front.
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Chauhan, B. L., B. S. Doshi, and R. D. Kulkarni. "Diurnal variation in the pharmacokinetics of intravenous theophylline and etophylline in healthy subjects." European Journal of Clinical Pharmacology 30, no. 5 (1986): 635–36. http://dx.doi.org/10.1007/bf00542428.

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6

Nandwani, Yash S., Santosh V. Gandhi, and Shreeyash R. Tapale. "DEVELOPMENT AND VALIDATION OF FIRST ORDER DERIVATIVE SPECTROPHOTOMETRIC METHOD FOR SIMULTANEOUS ESTIMATION OF TERBUTALINE AND ETOPHYLLINE." International Journal of Advances in Pharmacy and Biotechnology 03, no. 01 (March 15, 2017): 1–7. http://dx.doi.org/10.38111/ijapb.20170301001.

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7

Fo¨ger, B., M. Lechleitner, K. P. Pfeiffer, A. Ritsch, G. Tro¨binger, T. Hopferwieser, and J. R. Patsch. "Treatment of primary mixed hyperlipidemia with etophylline clofibrate: effects on lipoprotein composition, lipoprotein-modifying enzymes and postprandial lipoprotein metabolism." Atherosclerosis 109, no. 1-2 (September 1994): 128. http://dx.doi.org/10.1016/0021-9150(94)93522-x.

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8

Khan, Mohammad Azaz, Senthil Selvi, and P. Perumal. "Formulation development and evaluation of sustained release matrix tablets of Theophylline and Etophylline and study of polymers effect on dissolution rate." Asian Journal of Pharmacy and Pharmacology 5, no. 1 (December 2018): 101–10. http://dx.doi.org/10.31024/ajpp.2019.5.1.15.

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9

Föger, Bernhard, Gabriele Tröbinger, Andreas Ritsch, Monika Lechleitner, Thomas Hopferwieser, Hans-Jürgen Menzel, Gerd Utermann, Karl P. Pfeiffer, and Josef R. Patsch. "Treatment of primary mixed hyperlipidemia with etophylline clofibrate: effects on lipoprotein-modifying enzymes, postprandial lipoprotein metabolism, and lipoprotein distribution and composition." Atherosclerosis 117, no. 2 (October 1995): 253–61. http://dx.doi.org/10.1016/0021-9150(95)05580-p.

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10

Kajal, Ramender Kumar, Priyanka Meena, and Sudhir G. Warkar. "Development and characterization of pH-responsive CMTKG/PAM/PEG hydrogel for oral administration of etophylline." Colloid and Polymer Science, August 7, 2023. http://dx.doi.org/10.1007/s00396-023-05152-8.

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Books on the topic "ETOPHYLLINE"

1

Saini, Amandeep Kaur. Interpenetrating Polymer Networks in Drug Delivery System: Development & Characterization of Poly Vinyl Alcohal/Acrylic Acid IPN for carrying Etophylline. VDM Verlag Dr. Müller, 2011.

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