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Volumn 20, Issue 2, 2010, Pages 143-148

Comparison of different in vitro tests to assess oral lipid-based formulations using a poorly soluble acidic drug

Author keywords

Biorelevant media; Dispersion; Lipolysis; Oral drug absorption; Self microemulsifying drug delivery systems (sMEDDS)

Indexed keywords

DRUG CARRIER; INDOMETACIN; LIPID; MALEIC ANHYDRIDE; PANCREATIN; PEPSIN A; PHOSPHATIDYLCHOLINE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM HYDROXIDE; TAUROCHOLIC ACID;

EID: 77950619099     PISSN: 17732247     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1773-2247(10)50019-4     Document Type: Article
Times cited : (11)

References (31)
  • 1
    • 29244485443 scopus 로고    scopus 로고
    • A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption
    • Hong J.Y., Kim J.K., Song Y.K., Park J.S., Kim C.K. - A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption. - J. Contr. Release, 110, 332-338, 2006.
    • (2006) J. Contr. Release , vol.110 , pp. 332-338
    • Hong, J.Y.1    Kim, J.K.2    Song, Y.K.3    Park, J.S.4    Kim, C.K.5
  • 2
    • 39149092022 scopus 로고    scopus 로고
    • Enhancing intestinal drug solubilisation using lipid-based delivery systems
    • Porter C., Pouton C.W., Cuine J.F., Charman W.N. - Enhancing intestinal drug solubilisation using lipid-based delivery systems. - Adv. Drug Del. Rev., 60, 673-691, 2008.
    • (2008) Adv. Drug Del. Rev. , vol.60 , pp. 673-691
    • Porter, C.1    Pouton, C.W.2    Cuine, J.F.3    Charman, W.N.4
  • 3
    • 39149113817 scopus 로고    scopus 로고
    • Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies
    • Pouton C.W. - Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies. - Adv. Drug Del. Rev., 60, 625-637, 2008.
    • (2008) Adv. Drug Del. Rev. , vol.60 , pp. 625-637
    • Pouton, C.W.1
  • 4
    • 1242337285 scopus 로고    scopus 로고
    • Solubilizing excipients in oral and injectable formulations
    • Strickley R.G. - Solubilizing excipients in oral and injectable formulations. - Pharm. Res., 21, 201-230, 2004.
    • (2004) Pharm. Res. , vol.21 , pp. 201-230
    • Strickley, R.G.1
  • 5
  • 6
    • 0033805858 scopus 로고    scopus 로고
    • Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying, and self-microemulsifying drug delivery systems
    • Pouton C.W. - Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying, and self-microemulsifying drug delivery systems. - Eur. J. Pharm. Sci., 11 (2), S93-S98, 2000.
    • (2000) Eur. J. Pharm. Sci. , vol.11 , Issue.2
    • Pouton, C.W.1
  • 7
    • 33751014029 scopus 로고    scopus 로고
    • Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
    • Pouton C.W. - Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. - Eur. J. Pharm. Sci., 29, 278-287, 2006.
    • (2006) Eur. J. Pharm. Sci. , vol.29 , pp. 278-287
    • Pouton, C.W.1
  • 8
    • 38749146264 scopus 로고    scopus 로고
    • Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers
    • Woo J.S., Song Y.K., Hong J.Y., Lim S., Kim C.K. - Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers. - Eur. J. Pharm. Sci., 33, 159-165, 2007.
    • (2007) Eur. J. Pharm. Sci. , vol.33 , pp. 159-165
    • Woo, J.S.1    Song, Y.K.2    Hong, J.Y.3    Lim, S.4    Kim, C.K.5
  • 9
    • 70349238697 scopus 로고    scopus 로고
    • Design of lipid-based formulations for oral administration of poorly water-soluble drugs: Precipitation of drug after dispersion of formulations in aqueous solution
    • Mohsin K., Long M.A., Pouton C.W. - Design of lipid-based formulations for oral administration of poorly water-soluble drugs: precipitation of drug after dispersion of formulations in aqueous solution. - J. Pharm. Sci., 98 (10), 3582-3595, 2008.
    • (2008) J. Pharm. Sci. , vol.98 , Issue.10 , pp. 3582-3595
    • Mohsin, K.1    Long, M.A.2    Pouton, C.W.3
  • 10
    • 37849030987 scopus 로고    scopus 로고
    • Self-microemulsifying drug delivery system (SMEDDS) of vinpocetine: Formulation development and in vivo assessment
    • Chen Y., Xianggen G.L., Chen Z., Hang J., Qin B., Chen S., Wang R. - Self-microemulsifying drug delivery system (SMEDDS) of vinpocetine: formulation development and in vivo assessment. - Biol. Pharm. Bull., 31 (1), 118-125, 2008.
    • (2008) Biol. Pharm. Bull. , vol.31 , Issue.1 , pp. 118-125
    • Chen, Y.1    Xianggen, G.L.2    Chen, Z.3    Hang, J.4    Qin, B.5    Chen, S.6    Wang, R.7
  • 11
    • 41349096647 scopus 로고    scopus 로고
    • Preparation and evaluation of self-microemulsifying drug delivery system of oridonin
    • Zhang P., Liu Y., Feng N., Xu J. - Preparation and evaluation of self-microemulsifying drug delivery system of oridonin. - Int. J. Pharm., 355, 269-276, 2008.
    • (2008) Int. J. Pharm. , vol.355 , pp. 269-276
    • Zhang, P.1    Liu, Y.2    Feng, N.3    Xu, J.4
  • 12
    • 0034836387 scopus 로고    scopus 로고
    • A dynamic in vitro lipolysis model. I. Controlling the rate of lipolysis by continuous addition of calcium
    • Zangenberg N.H., Müllertz A., Kristensen H.G., Hovgaard L. - A dynamic in vitro lipolysis model. I. Controlling the rate of lipolysis by continuous addition of calcium. - Eur. J. Pharm. Sci., 14, 237-244, 2001.
    • (2001) Eur. J. Pharm. Sci. , Issue.14 , pp. 237-244
    • Zangenberg, N.H.1    Müllertz, A.2    Kristensen, H.G.3    Hovgaard, L.4
  • 14
    • 39149091886 scopus 로고    scopus 로고
    • Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic self-emulsifying formulations to dog
    • Cuiné J.F., McEvoy C.L., Charman W.N., Pouton C.W., Edwards G.A., Benameur H., Porter C.J. - Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic self-emulsifying formulations to dog. - J. Pharm. Sci., 97 (2), 995-1012, 2007.
    • (2007) J. Pharm. Sci. , vol.97 , Issue.2 , pp. 995-1012
    • Cuiné, J.F.1    McEvoy, C.L.2    Charman, W.N.3    Pouton, C.W.4    Edwards, G.A.5    Benameur, H.6    Porter, C.J.7
  • 17
    • 21544447265 scopus 로고    scopus 로고
    • Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds
    • Vertzoni M., Dressman J., Butler J., Hempenstall J., Reppas C. - Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds. - Eur. J. Pharm. Biopharm., 60, 413-417, 2005.
    • (2005) Eur. J. Pharm. Biopharm. , vol.60 , pp. 413-417
    • Vertzoni, M.1    Dressman, J.2    Butler, J.3    Hempenstall, J.4    Reppas, C.5
  • 18
    • 77950604011 scopus 로고    scopus 로고
    • Indomethacin
    • nd ed., Churchill Livingstone, Edinburgh, London
    • nd ed., Churchill Livingstone, Edinburgh, London, 1998, pp. 141-143.
    • (1998) Therapeutic Drugs , pp. 141-143
    • Dollery, C.1
  • 19
    • 77950596697 scopus 로고
    • Wissenschaftliche Tabellen, 7. Auflage - Documenta Geigy, Basel
    • Geigy J.R. - Pharma AG - Wissenschaftliche Tabellen, 7. Auflage - Documenta Geigy, Basel, 1973.
    • (1973) Pharma AG
    • Geigy, J.R.1
  • 22
    • 0031750861 scopus 로고    scopus 로고
    • Evaluation of various dissolution media for predicting in vivo performance of Class I and II drugs
    • Galia E., Nicolaides E., Hörter D., Löbenberg R., Reppas C., Dressman J.B. - Evaluation of various dissolution media for predicting in vivo performance of Class I and II drugs. - Pharm. Res., 15(5), 698-705, 1998.
    • (1998) Pharm. Res. , vol.15 , Issue.5 , pp. 698-705
    • Galia, E.1    Nicolaides, E.2    Hörter, D.3    Löbenberg, R.4    Reppas, C.5    Dressman, J.B.6
  • 23
    • 1842684453 scopus 로고    scopus 로고
    • Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
    • DOI 10.1016/j.biopha.2004.02.001, PII S0753332204000319
    • Gursoy R.N., Benita S. - Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. - Biomed. & Pharmacoth., 58, 173-182, 2004. (Pubitemid 38479922)
    • (2004) Biomedicine and Pharmacotherapy , vol.58 , Issue.3 , pp. 173-182
    • Gursoy, R.N.1    Benita, S.2
  • 24
    • 60749084743 scopus 로고    scopus 로고
    • A systematic dilution study of self-microemulsifying drug delivery systems in artificial intestinal fluid using dynamic laser light backscattering
    • Ditner C., Bravo R., Imanidis G., Kuentz M. - A systematic dilution study of self-microemulsifying drug delivery systems in artificial intestinal fluid using dynamic laser light backscattering. - Drug Dev. Ind. Pharm., 35, 199-208, 2009.
    • (2009) Drug Dev. Ind. Pharm. , vol.35 , pp. 199-208
    • Ditner, C.1    Bravo, R.2    Imanidis, G.3    Kuentz, M.4
  • 25
    • 0034601204 scopus 로고    scopus 로고
    • Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
    • Gershanik T., Benita S. - Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. - Eur. J. Pharm. Biopharm., 50, 179-188, 2000.
    • (2000) Eur. J. Pharm. Biopharm. , vol.50 , pp. 179-188
    • Gershanik, T.1    Benita, S.2
  • 26
    • 0030614844 scopus 로고    scopus 로고
    • Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH
    • Charman W.N., Porter C., Mithani S., Dressman J.B. - Physicochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH. - J. Pharm. Sci., 86 (3), 269-282, 1996.
    • (1996) J. Pharm. Sci. , vol.86 , Issue.3 , pp. 269-282
    • Charman, W.N.1    Porter, C.2    Mithani, S.3    Dressman, J.B.4
  • 27
    • 0036195307 scopus 로고    scopus 로고
    • Forecasting the oral absorption behavior of poorly soluble weak bases using solubility and dissolution studies in biorelevant media
    • Kostewicz E.S., Brauns U., Becker R., Dressman J.B. - Forecasting the oral absorption behavior of poorly soluble weak bases using solubility and dissolution studies in biorelevant media. - Pharm. Res., 19, 345-349, 2001.
    • (2001) Pharm. Res. , vol.19 , pp. 345-349
    • Kostewicz, E.S.1    Brauns, U.2    Becker, R.3    Dressman, J.B.4
  • 29
    • 1242337282 scopus 로고    scopus 로고
    • The "high solubility" definition of the Current FDA Guidance on Biopharmaceutical Classification System may be too strict for acidic drugs
    • Yazdanian M., Briggs K., Jankovsky C., Hawi A. - The "high solubility" definition of the Current FDA Guidance on Biopharmaceutical Classification System may be too strict for acidic drugs. - Pharm. Res., 21 (2), 293-299, 2004.
    • (2004) Pharm. Res. , vol.21 , Issue.2 , pp. 293-299
    • Yazdanian, M.1    Briggs, K.2    Jankovsky, C.3    Hawi, A.4
  • 30
    • 57149095631 scopus 로고    scopus 로고
    • Drug absorption modeling as a tool to define strategy in clinical formulations development
    • Kuentz M. - Drug absorption modeling as a tool to define strategy in clinical formulations development. - AAPS J., 10 (3), 473-479, 2008.
    • (2008) AAPS J. , vol.10 , Issue.3 , pp. 473-479
    • Kuentz, M.1
  • 31
    • 0033992180 scopus 로고    scopus 로고
    • Enhanced absorption of Indomethacin after oral or rectal administration of a self-emulsifying system containing Indomethacin in rats
    • Kim J.Y., Ku Y.S. - Enhanced absorption of Indomethacin after oral or rectal administration of a self-emulsifying system containing Indomethacin in rats. - Int. J. Pharm., 194, 81-89, 2000.
    • (2000) Int. J. Pharm. , vol.194 , pp. 81-89
    • Kim, J.Y.1    Ku, Y.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.