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PUBMED FOR HANDHELDS

Journal Abstract Search


183 related items for PubMed ID: 24526655

  • 1. Application of QbD principles for the evaluation of empty hard capsules as an input parameter in formulation development and manufacturing.
    Stegemann S, Connolly P, Matthews W, Barnett R, Aylott M, Schrooten K, Cadé D, Taylor A, Bresciani M.
    AAPS PharmSciTech; 2014 Jun; 15(3):542-9. PubMed ID: 24526655
    [Abstract] [Full Text] [Related]

  • 2. Excipient variability and its impact on dosage form functionality.
    Dave VS, Saoji SD, Raut NA, Haware RV.
    J Pharm Sci; 2015 Mar; 104(3):906-15. PubMed ID: 25561249
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  • 3. Challenges and opportunities in the encapsulation of liquid and semi-solid formulations into capsules for oral administration.
    Cole ET, Cadé D, Benameur H.
    Adv Drug Deliv Rev; 2008 Mar 17; 60(6):747-56. PubMed ID: 18096270
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  • 4. Investigations into the use of pregelatinised starch to develop powder-filled hard capsules.
    Gohil UC, Podczeck F, Turnbull N.
    Int J Pharm; 2004 Nov 05; 285(1-2):51-63. PubMed ID: 15488679
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  • 5. Bio-relevant dissolution testing of hard capsules prepared from different shell materials using the dynamic open flow through test apparatus.
    Garbacz G, Cadé D, Benameur H, Weitschies W.
    Eur J Pharm Sci; 2014 Jun 16; 57():264-72. PubMed ID: 24021609
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  • 9. Effect of fill weight, capsule shell, and sinker design on the dissolution behavior of capsule formulations of a weak acid drug candidate BMS-309403.
    Wu Y, Zhao F, Paborji M.
    Pharm Dev Technol; 2003 Jun 16; 8(4):379-83. PubMed ID: 14601962
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  • 10. Performance qualification of a new hypromellose capsule: part I. Comparative evaluation of physical, mechanical and processability quality attributes of Vcaps Plus, Quali-V and gelatin capsules.
    Sherry Ku M, Li W, Dulin W, Donahue F, Cade D, Benameur H, Hutchison K.
    Int J Pharm; 2010 Feb 15; 386(1-2):30-41. PubMed ID: 19900518
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  • 11. Integrated Application of Quality-by-Design Principles to Drug Product Development: A Case Study of Brivanib Alaninate Film-Coated Tablets.
    Badawy SI, Narang AS, LaMarche KR, Subramanian GA, Varia SA, Lin J, Stevens T, Shah PA.
    J Pharm Sci; 2016 Jan 15; 105(1):168-81. PubMed ID: 26852852
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  • 12. Pharmaceutical quality by design: product and process development, understanding, and control.
    Yu LX.
    Pharm Res; 2008 Apr 15; 25(4):781-91. PubMed ID: 18185986
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  • 13. Quality by design approach for formulation development: a case study of dispersible tablets.
    Charoo NA, Shamsher AA, Zidan AS, Rahman Z.
    Int J Pharm; 2012 Feb 28; 423(2):167-78. PubMed ID: 22209997
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  • 14. The influence of polymorphism on the manufacturability and in vitro dissolution of sulindac-containing hard gelatin capsules.
    Guadalupe Sánchez-González E, Yépez-Mulia L, Jesús Hernández-Abad V, Jung Cook H.
    Pharm Dev Technol; 2015 May 28; 20(3):306-13. PubMed ID: 24417644
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  • 16. Modified conventional hard gelatin capsules as fast disintegrating dosage form in the oral cavity.
    Ciper M, Bodmeier R.
    Eur J Pharm Biopharm; 2006 Feb 28; 62(2):178-84. PubMed ID: 16260126
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  • 19. Quality by design approach for optimizing the formulation and physical properties of extemporaneously prepared orodispersible films.
    Visser JC, Dohmen WM, Hinrichs WL, Breitkreutz J, Frijlink HW, Woerdenbag HJ.
    Int J Pharm; 2015 May 15; 485(1-2):70-6. PubMed ID: 25746737
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  • 20. [A review on liquid-filled hard gelatin capsules].
    Ma JH, Yang M, Zeng M, Chen XM, Lan J.
    Zhongguo Zhong Yao Za Zhi; 2008 Mar 15; 33(5):602-5. PubMed ID: 18536390
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