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PUBMED FOR HANDHELDS

Journal Abstract Search


218 related items for PubMed ID: 11699832

  • 1. Influence of dissolution medium agitation on release profiles of sustained-release tablets.
    Paulo, Sousa Lobo JM.
    Drug Dev Ind Pharm; 2001 Sep; 27(8):811-7. PubMed ID: 11699832
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  • 2. Divisability of diltiazem matrix sustained-release tablets.
    Costa P, Sousa Lobo JM.
    Pharm Dev Technol; 2001 Aug; 6(3):343-51. PubMed ID: 11485176
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  • 5. Drug release kinetic analysis and prediction of release data via polymer molecular weight in sustained release diltiazem matrices.
    Adibkia K, Ghanbarzadeh S, Mohammadi G, Khiavi HZ, Sabzevari A, Barzegar-Jalali M.
    Drug Res (Stuttg); 2014 Mar; 64(3):118-23. PubMed ID: 23986307
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  • 6. Assessment of xanthan gum based sustained release matrix tablets containing highly water-soluble propranolol HCl.
    Ali A, Iqbal M, Akhtar N, Khan HM, Ullah A, Uddin M, Khan MT.
    Acta Pol Pharm; 2013 Mar; 70(2):283-9. PubMed ID: 23614284
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  • 7. In-vitro and in-vivo characteristics of a modified-release double-pulse formulation for a water soluble drug.
    Avramoff A, Domb AJ.
    Int J Clin Pharmacol Ther; 2010 Apr; 48(4):250-8. PubMed ID: 20353746
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  • 10. Mechanistic Approach to Understanding the Influence of USP Apparatus I and II on Dissolution Kinetics of Tablets with Different Operating Release Mechanisms.
    Lu Z, Fassihi R.
    AAPS PharmSciTech; 2017 Feb; 18(2):462-472. PubMed ID: 27106916
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  • 11. Preparation and in vitro evaluation of a novel combined multiparticulate delayed-onset sustained-release formulation of diltiazem hydrochloride.
    Chen S, Zhu J, Cheng J.
    Pharmazie; 2007 Dec; 62(12):907-13. PubMed ID: 18214341
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  • 12. Design of floating bilayer tablets of diltiazem hydrochloride and lovastatin.
    Kulkarni AS, Bhatia MS.
    PDA J Pharm Sci Technol; 2008 Dec; 62(5):344-52. PubMed ID: 19055230
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  • 17. Novel use of similarity factors f2 and Sd for the development of diltiazem HCl modified-release tablets using a 3(2) factorial design.
    Gohel MC, Panchal MK.
    Drug Dev Ind Pharm; 2002 Jan; 28(1):77-87. PubMed ID: 11858527
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  • 18. In vitro release studies of furosemide reference tablets: influence of agitation rate, USP apparatus, and dissolution media.
    Medina-López R, Guillén-Moedano S, Hurtado M.
    ADMET DMPK; 2020 Jan; 8(4):411-423. PubMed ID: 35300193
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  • 19. Development and validation of dissolution tests for fexofenadine hydrochloride capsules and coated tablets.
    Breier AR, Paim CS, Steppe M, Schapoval EE.
    J Pharm Pharm Sci; 2005 Aug 11; 8(2):289-98. PubMed ID: 16124939
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