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Autor(en): 
  • Ajit Kulkarni
  • Manish Bhatia
  • Design of Regioselective Bilayer Floating Tablets of Propranolol Hydrochloride and Lovastatin for Biphasic Release Profile 
     

    (Buch)
    Dieser Artikel gilt, aufgrund seiner Grösse, beim Versand als 2 Artikel!


    Übersicht

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    Lieferstatus:   i.d.R. innert 5-10 Tagen versandfertig
    Veröffentlichung:  Januar 2015  
    Genre:  Naturwissensch., Medizin, Technik 
     
    Bilayer / biphasic / Design / floating / hydrochloride / Lovastatin / Profile / propranolol
    ISBN:  9783656855552 
    EAN-Code: 
    9783656855552 
    Verlag:  Grin Verlag 
    Einband:  Kartoniert  
    Sprache:  English  
    Dimensionen:  H 210 mm / B 148 mm / D 3 mm 
    Gewicht:  56 gr 
    Seiten:  28 
    Bewertung: Titel bewerten / Meinung schreiben
    Inhalt:
    Research Paper (postgraduate) from the year 2014 in the subject Pharmacology, grade: 2, , language: English, abstract: The purpose of the study was to design bilayer floating tablets of Propranolol hydrochloride and Lovastatin to give immediate release of Lovastatin and controlled release of Propranolol hydrochloride. Bilayer floating tablets comprised of two layers, immediate release layer and controlled release layer. Direct compression method was employed for formulation of the bilayer tablets. Short term accelerated stability studies were carried out on the prepared tablets. All the formulations floated for more than 12h. More than 90% Lovastatin was released within 30 min. from the formulations. HPMC K4M and Xanthan gum retarded the release of Propranolol hydrochloride from the controlled release layer for 12h. After stability studies, apparent degradation of both the drugs were found but the drug content was found to be within the range. Diffusion exponent (n) was determined for all the formulations (0.53-7). Based on coefficient of correlation(R), the release of Propranolol hydrochloride was found to follow mixed release pattern of Hixson-Crowell, Korsmeyer-Peppas and matrix, except formulation F6 and F9, which followed zero order release pattern. Statistical analysis revealed that there was no significant difference in in vitro release pattern of the drugs before and after stability studies.

      



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