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Volumn 2, Issue 1, 2010, Pages 155-161

Optimization of formulation parameters on famotidine nanosuspension using factorial design and the desirability function

Author keywords

Factorial design; Famotidine; Nanosuspension; Optimization; Quality by design

Indexed keywords

FAMOTIDINE; POLOXAMER;

EID: 77953377683     PISSN: None     EISSN: 09744304     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (8)
  • 1
    • 33846852628 scopus 로고    scopus 로고
    • Quality by design: Understanding the formulation variables of a cyclosporine a self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function
    • Zidan A.S, Sammourb O.A, Hammad M.A, Megrab N.A, Habib M.J. and Khana M.A, Quality by design: Understanding the formulation variables of a cyclosporine a self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function. Int. J.Pharm., 2007, 332, 55-63.
    • (2007) Int. J.Pharm , vol.332 , pp. 55-63
    • Zidan, A.S.1    Sammourb, O.A.2    Hammad, M.A.3    Megrab, N.A.4    Habib, M.J.5    Khana, M.A.6
  • 2
    • 67650122795 scopus 로고    scopus 로고
    • Quality by design: Optimization of a liquid filled ph-responsive macroparticles using draper-lin composite design
    • Rafati H, Talebpour Z, Adlnasab L. and Ebrahimi S.N, Quality by design: optimization of a liquid filled ph-responsive macroparticles using draper-lin composite design, J. Pharma. Sci., 2009, 1-11.
    • (2009) J. Pharma. Sci , pp. 1-11
    • Rafati, H.1    Talebpour, Z.2    Adlnasab, L.3    Ebrahimi, S.N.4
  • 3
    • 0025098743 scopus 로고
    • Improvement of the in vitro dissolution characteristics of famotidine by inclusion in β-cyclodextrin
    • Hassan M.A, Suleiman M.S. and Najib N.M, Improvement of the in vitro dissolution characteristics of famotidine by inclusion in β-cyclodextrin, Int. J. Pharm., 1990, 58, 19-24.
    • (1990) Int. J. Pharm , vol.58 , pp. 19-24
    • Hassan, M.A.1    Suleiman, M.S.2    Najib, N.M.3
  • 4
    • 48149089157 scopus 로고    scopus 로고
    • Enhancement of famotidine dissolution rate through liquisolid tablets formulation: In vitro and in vivo evaluation
    • Rania H.F. and Mohammed A.K, Enhancement of famotidine dissolution rate through liquisolid tablets formulation: In vitro and in vivo evaluation, Eur. J. Pharm. Biopharm., 2008, 69, 993-1003.
    • (2008) Eur. J. Pharm. Biopharm , vol.69 , pp. 993-1003
    • Rania, H.F.1    Mohammed, A.K.2
  • 5
    • 0035845740 scopus 로고    scopus 로고
    • Emulsions containing partially water-miscible solvents for the preparation of drug nanosuspensions
    • Trotta M, Gallarete M, Pattarino F. and Morel S, Emulsions containing partially water-miscible solvents for the preparation of drug nanosuspensions, J. Control. Rel., 2001, 76, 119-128.
    • (2001) J. Control. Rel , vol.76 , pp. 119-128
    • Trotta, M.1    Gallarete, M.2    Pattarino, F.3    Morel, S.4
  • 6
    • 0028824401 scopus 로고
    • Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats
    • Liversidge G.G. and Conzentino P, Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats, Int. J. Pharma., 1995, 125, 309-313.
    • (1995) Int. J. Pharma , vol.125 , pp. 309-313
    • Liversidge, G.G.1    Conzentino, P.2
  • 7
    • 11144228000 scopus 로고    scopus 로고
    • Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles
    • Bilati U, Allemann E. and Doelker E, Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles, Eur. J. Pharm. BioPharm., 2005, 24, 67-75.
    • (2005) Eur. J. Pharm. BioPharm , vol.24 , pp. 67-75
    • Bilati, U.1    Allemann, E.2    Doelker, E.3
  • 8
    • 33749454734 scopus 로고    scopus 로고
    • Optimization of self-microemulsifying drug delivery systems (smedds) using a d-optimal design and the desirability function
    • Holm R, Jensen I.H.M. and Sonnergaard J, Optimization of self-microemulsifying drug delivery systems (smedds) using a d-optimal design and the desirability function, Drug Dev. Ind. Pharm., 2006, 32,1025-1032.
    • (2006) Drug Dev. Ind. Pharm , vol.32 , pp. 1025-1032
    • Holm, R.1    Jensen, I.H.M.2    Sonnergaard, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.