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Volumn 1, Issue 3, 2009, Pages 431-437

Preparation and in vitro characterization of valsartan solid dispersions using skimmed milk powder as carrier

Author keywords

Dissolution; Skimmed milk powder; Solid dispersion; Solubility; Valsartan

Indexed keywords

POLYMER; VALSARTAN;

EID: 77953452865     PISSN: None     EISSN: 09744304     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (33)

References (23)
  • 1
    • 0037074108 scopus 로고    scopus 로고
    • The mechanisms of drug release from solid dispersions in water-soluble polymers
    • . Craig DQM . The mechanisms of drug release from solid dispersions in water-soluble polymers. Int J Pharm . 2002 ; 231 : 131 - 144 .
    • (2002) Int J Pharm , vol.231 , pp. 131-144
    • Craig, D.Q.M.1
  • 2
    • 0022650603 scopus 로고
    • The current status of solid dispersions
    • . Ford JL . The current status of solid dispersions. Pharm Acta Helv .1986 ; 61 : 69 - 88
    • (1986) Pharm Acta Helv , vol.61 , pp. 69-88
    • Ford, J.L.1
  • 3
    • 0000837071 scopus 로고    scopus 로고
    • New preparation method of solid dispersion by twin screw extruder
    • . Nakamichi K , Yasuura H , Kukui H , et al . New preparation method of solid dispersion by twin screw extruder. Pharm Technol Jpn .1996 ; 12 : 715 - 729 .
    • (1996) Pharm Technol Jpn , vol.12 , pp. 715-729
    • Nakamichi, K.1    Yasuura, H.2    Kukui, H.3
  • 5
    • 77953452318 scopus 로고    scopus 로고
    • The Biopharmaceutics Classification System (BCS) Guidance, accessed 12.01.08
    • The Biopharmaceutics Classification System (BCS) Guidance, Office of Pharmaceutical Science, http://www.fda.gov/cder/OPS/BCS-guidance.htm (accessed 12.01.08)
    • Office of Pharmaceutical Science
  • 7
    • 0347249950 scopus 로고    scopus 로고
    • Solubilization of nimesulide; use of co-solvents
    • Seedher N, Kaur J. Solubilization of nimesulide; use of co-solvents. IJPS, 2003:65(1); 58-61.
    • (2003) IJPS , vol.65 , Issue.1 , pp. 58-61
    • Seedher, N.1    Kaur, J.2
  • 8
    • 21644468027 scopus 로고    scopus 로고
    • Insulin nanoparticles: A novel formulation approach for poorly water soluble Zn-Insulin
    • Mersiko-Liversidge E, MGurk SL, Liversidge GG. Insulin nanoparticles: a novel formulation approach for poorly water soluble Zn-Insulin. Pharm Res.,2004: 21(9): 1545-1553.
    • (2004) Pharm Res , vol.21 , Issue.9 , pp. 1545-1553
    • Mersiko-Liversidge, E.1    MGurk, S.L.2    Liversidge, G.G.3
  • 9
    • 33845942743 scopus 로고
    • Solubility enhancement in supercritical fluids
    • Benjamin C-Y.Lu, Dingan Zang, Wei Sheng, Solubility enhancement in supercritical fluids. Pure & Appl.Chem.,1990:62(12);2277-2285.
    • (1990) Pure & Appl.Chem , vol.62 , Issue.12 , pp. 2277-2285
    • Lu, B.C.-Y.1    Zang, D.2    Wei, S.3
  • 10
    • 0032885450 scopus 로고    scopus 로고
    • Abu T.M.Serajuddin. Solid dispersion of poorly soluble drugs-Early promises, subsequent problems, and recent breakthroughs, J. Pharm Sci.,2000:88(10); 1058-1066.
    • Abu T.M.Serajuddin. Solid dispersion of poorly soluble drugs-Early promises, subsequent problems, and recent breakthroughs, J. Pharm Sci.,2000:88(10); 1058-1066.
  • 11
    • 77953388876 scopus 로고    scopus 로고
    • nd ed. WVG, Stuttgart, 1998.
    • nd ed. WVG, Stuttgart, 1998.
  • 12
    • 77953369324 scopus 로고    scopus 로고
    • nd ed. WVG, Stuttgart, 1998
    • nd ed. WVG, Stuttgart, 1998
  • 14
    • 0033735518 scopus 로고    scopus 로고
    • Chowdary K.P.R., Srinivasa Rao.S. Investigation of dissolution enhancement of Itraconazole in Superdisintegrants. Drug Development and Industrial Pharmacy. 2000; 26: 1217-1220.
    • Chowdary K.P.R., Srinivasa Rao.S. Investigation of dissolution enhancement of Itraconazole in Superdisintegrants. Drug Development and Industrial Pharmacy. 2000; 26: 1217-1220.
  • 16
    • 77953455566 scopus 로고    scopus 로고
    • accessed on 23.12.08
    • www.cder.com/valsartan (accessed on 23.12.08)
  • 17
    • 21844461846 scopus 로고    scopus 로고
    • Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of Nifedipine
    • Hecq J, Deleers M, Fanara D, Vranckx H, Amighi K. Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of Nifedipine. International Journal of Pharmaceutics. 2005; 299: 167-177.
    • (2005) International Journal of Pharmaceutics , vol.299 , pp. 167-177
    • Hecq, J.1    Deleers, M.2    Fanara, D.3    Vranckx, H.4    Amighi, K.5
  • 18
    • 0037965572 scopus 로고    scopus 로고
    • Processing of Nimesulide-PEG 400-PEG-PVP solid dispersions: Preparation, Characterization and In-vitro dissolution
    • Gohel M.C, Patel L.D. Processing of Nimesulide-PEG 400-PEG-PVP solid dispersions: Preparation, Characterization and In-vitro dissolution. Drug Development and Industrial Pharmacy. 2003; 29: 299-310.
    • (2003) Drug Development and Industrial Pharmacy , vol.29 , pp. 299-310
    • Gohel, M.C.1    Patel, L.D.2
  • 19
    • 36749010777 scopus 로고    scopus 로고
    • Sunil K.B, Michael A.R, Soumyajit M, Rao.Y. Formulation and evaluation of rapidly disintegrating Fenoverine tablets: Effect of superdisintegrant. Drug development and industrial pharmacy.2007; 33:1225-1232.
    • Sunil K.B, Michael A.R, Soumyajit M, Rao.Y. Formulation and evaluation of rapidly disintegrating Fenoverine tablets: Effect of superdisintegrant. Drug development and industrial pharmacy.2007; 33:1225-1232.
  • 21
    • 31344449575 scopus 로고    scopus 로고
    • Development and evaluation of an in vitro method for prediction of human drug absorption 1. Assessment of artificial membrane composition
    • Giovanna C, Francesca M, Marzia C, Sandra F, Paola M. Development and evaluation of an in vitro method for prediction of human drug absorption 1. Assessment of artificial membrane composition. European journal of pharmaceutical sciences. 2006; 27: 346-353.
    • (2006) European journal of pharmaceutical sciences , vol.27 , pp. 346-353
    • Giovanna, C.1    Francesca, M.2    Marzia, C.3    Sandra, F.4    Paola, M.5
  • 22
    • 0036689113 scopus 로고    scopus 로고
    • Characterization and quantitation of Clarithromycin polymorphs by powder X-Ray diffractometry and solid state NMR spectroscopy
    • Yuichi T, Atsutoshi I, Hiiroko S, Toshio O, Keiji Y. Characterization and quantitation of Clarithromycin polymorphs by powder X-Ray diffractometry and solid state NMR spectroscopy. Chem Pharm Bull .2002; 50:1128-1130.
    • (2002) Chem Pharm Bull , vol.50 , pp. 1128-1130
    • Yuichi, T.1    Atsutoshi, I.2    Hiiroko, S.3    Toshio, O.4    Keiji, Y.5
  • 23
    • 77953389837 scopus 로고    scopus 로고
    • Process optimization and characterization of Poloxamer solid dispersions of a poorly water soluble drug
    • Tejal J.S, Avani F.A, Jolly R.P, Rajesh H.P. Process optimization and characterization of Poloxamer solid dispersions of a poorly water soluble drug. Pharm Sci Tech. 2007; 89: E1-E7.
    • (2007) Pharm Sci Tech , vol.89
    • Tejal, J.S.1    Avani, F.A.2    Jolly, R.P.3    Rajesh, H.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.