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Molecular Enzymology and Drug Targets

  • Journal h-index: 5
  • Journal CiteScore: 0.46
  • Journal Impact Factor: 0.45
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
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lbrahim A. lsarr

Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 1 1451, Kingdom of Saudi Arabia, Saudi Arabia

Publications
  • Perspective   
    Modulatinn intestinal uptake of Atenolol
    Author(s): lbrahim A. lsarr

    Drug permeation across membranes or targeting to specific tissues. Having a considerable ability to improve the permeability of drugs through lipoid membranes, niosomes have been utilized as carriers to enhance atenolol absorption from the gastrointestinal tract. Two methods have been adopted to prepare niosomes, the proniosome-derived method and the conventional film hydration method. The products from the two methods were compared in terms of their morphology, vesicle size, drug encapsulation efficiency, in vitro drug release and enhancement effect on drug permeation across the intestinal membrane using an averted sac technique. Proniosome-derived niosomes were smoother and exhibited a smaller (5 pm) vesicle size compared to those prepared by conventional methods (1 2 pm). High encapsulation efficiencies of 98.6% and 93.4% were achieved by methods A and B, respectively. In vitro dru.. View More»

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