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Volumn 34, Issue 2, 2010, Pages 77-87

Studies on formulation development of a poorly water-soluble drug through solid dispersion technique

Author keywords

Aceclofenac; BCS class II; Dissolution enhancement; Poorly water soluble drug; Solid dispersion; Water soluble carriers

Indexed keywords

ACECLOFENAC; BETA CYCLODEXTRIN; DRUG CARRIER; MACROGOL 6000;

EID: 77956259504     PISSN: 01254685     EISSN: 19054637     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (13)
  • 2
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    • Preparation and characterization of etoricoxibpolyethylene glycol 4000 plus polyvinylpyrrolidone K30 solid dispersions
    • B. N. Suhagia, H. M. Patel, S. A. Shah, I. Rathod, and V. K. Parmar. Preparation and characterization of etoricoxibpolyethylene glycol 4000 plus polyvinylpyrrolidone K30 solid dispersions, Acta Pharm. 56: 285-298 (2006).
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    • Suhagia, B.N.1    Patel, H.M.2    Shah, S.A.3    Rathod, I.4    Parmar, V.K.5
  • 3
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    • Solid dispersions of poorly water soluble drugs: Early promises, susbsequent problems and recent breakthroughs
    • A. T. M. Serajuddin. Solid dispersions of poorly water soluble drugs: early promises, susbsequent problems and recent breakthroughs, J. Pharm. Sci. 88: 1058-1086 (1999).
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    • Serajuddin, A.T.M.1
  • 4
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    • Improved dissolution of a poorly water-soluble drugs from solid dispersion in polyethylene glycol:Polysorbate 80 mixtures
    • A. T. M. Serajuddin, P. C. Sheen, and Augustine M. A. Improved dissolution of a poorly water-soluble drugs from solid dispersion in polyethylene glycol:polysorbate 80 mixtures, J. Pharm. Sci. 79: 463-464 (1990).
    • (1990) J. Pharm. Sci , vol.79 , pp. 463-464
    • Serajuddin, A.T.M.1    Sheen, P.C.2    Augustine, M.A.3
  • 5
    • 0029586490 scopus 로고
    • Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques
    • G. V. Betageri, and K. R. Makarla. Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques, Int. J. Pharm. 126: 155-160 (1995).
    • (1995) Int. J. Pharm , vol.126 , pp. 155-160
    • Betageri, G.V.1    Makarla, K.R.2
  • 6
    • 0033735234 scopus 로고    scopus 로고
    • Effect of water soluble carriers on dissolution characteristics of nifedipine solid dispersions
    • S. Chutimaworapan, G. C. Ritthidej, E. Yonemochi, T. K. Oguchi, and T. Yamamoto. Effect of water soluble carriers on dissolution characteristics of nifedipine solid dispersions, Drug Dev. Ind. Pharm. 26: 1141-1150 (2000).
    • (2000) Drug Dev. Ind. Pharm , vol.26 , pp. 1141-1150
    • Chutimaworapan, S.1    Ritthidej, G.C.2    Yonemochi, E.3    Oguchi, T.K.4    Yamamoto, T.5
  • 7
    • 0026783391 scopus 로고
    • Characterization of solid dispersions of piroxicam/poly (ethylene glycol) 4000
    • M. Fernandez, I. C. Rodriguez, M. V. Margarit, and A. Cerezo. Characterization of solid dispersions of piroxicam/poly (ethylene glycol) 4000, Int. J. Pharm. 84: 197-202 (1992).
    • (1992) Int. J. Pharm , vol.84 , pp. 197-202
    • Fernandez, M.1    Rodriguez, I.C.2    Margarit, M.V.3    Cerezo, A.4
  • 8
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    • United States Pharmacopoeia, 27, NF 18, The USP Convention, Rockville
    • United States Pharmacopoeia, 27, NF 18, The USP Convention, Rockville 1995, pp. 2303-2304.
    • (1995) , pp. 2303-2304
  • 9
    • 77953845524 scopus 로고    scopus 로고
    • Analysis of dissolution data
    • In: J. B. Dressman, and H. Lennernas, Marcel Dekker, New York
    • R. Christoher, and N. Eleftheria. Analysis of dissolution data. In: J. B. Dressman, and H. Lennernas (eds), Oral Drug Absortion: Prediction and Assessment, Marcel Dekker, New York, 2000, pp. 241-242.
    • (2000) Oral Drug Absortion: Prediction and Assessment , pp. 241-242
    • Christoher, R.1    Eleftheria, N.2
  • 10
    • 84923690893 scopus 로고
    • Guidance for Industry: Immediate Release Solid Oral Dosage Forms - Scale-up and Post-Approval Changes: Chemistry, Manufacturing and Controls
    • FDA Center for Drug Evaluation and Research, FDA, Rockville, MD, November
    • [] FDA Center for Drug Evaluation and Research. Guidance for Industry: Immediate Release Solid Oral Dosage Forms - Scale-up and Post-Approval Changes: Chemistry, Manufacturing and Controls, In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation (SUPAC-IR), FDA, Rockville, MD, November 1995.
    • (1995) Vitro Dissolution Testing and In Vivo Bioequivalence Documentation (SUPAC-IR)
  • 11
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    • Improving drug solubility for oral delivery using solid dispersions
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    • (2000) Eur. J. Pharm. Biopharm , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 12
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    • The mechanism of solid dispersions in water soluble polymers
    • D. Q. M. Craig. The mechanism of solid dispersions in water soluble polymers, Int. J. Pharm. 231: 131-144 (2002).
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    • Craig, D.Q.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.