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Volumn 104, Issue 9, 2015, Pages 2941-2947

Head-To-Head Comparison of Different Solubility-Enabling Formulations of Etoposide and Their Consequent Solubility-Permeability Interplay

Author keywords

BCS; intestinal permeability; oral drug absorption; solubility enabling formulations; solubility permeability interplay

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; DODECYL SULFATE SODIUM; ETOPOSIDE; MACROGOL 400; 2-HYDROXYPROPYL-BETA-CYCLODEXTRIN; ARTIFICIAL MEMBRANE; BETA CYCLODEXTRIN DERIVATIVE; CYCLODEXTRIN; MACROGOL DERIVATIVE; SURFACTANT;

EID: 84939269694     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.24496     Document Type: Article
Times cited : (69)

References (35)
  • 2
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski CA, Lombardo F, Dominy BW, Feeney PJ,. 2001. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 46 (1-3): 3-26.
    • (2001) Adv Drug Deliv Rev , vol.46 , Issue.13 , pp. 3-26
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 3
    • 84878660708 scopus 로고    scopus 로고
    • Provisional classification and in silico study of biopharmaceutical system based on caco-2 cell permeability and dose number
    • Pham-The H, Garrigues T, Bermejo M, González-Álvarez I, Monteagudo MC, Cabrera-Pérez MÁ,. 2013. Provisional classification and in silico study of biopharmaceutical system based on caco-2 cell permeability and dose number. Mol Pharm 10 (6): 2445-2461.
    • (2013) Mol Pharm , vol.10 , Issue.6 , pp. 2445-2461
    • Pham-The, H.1    Garrigues, T.2    Bermejo, M.3    González-Álvarez, I.4    Monteagudo, M.C.5    Má, C.-P.6
  • 4
    • 80054697161 scopus 로고    scopus 로고
    • Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications
    • Kawabata Y, Wada K, Nakatani M, Yamada S, Onoue S,. 2011. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications. Int J Pharm 420 (1): 1-10.
    • (2011) Int J Pharm , vol.420 , Issue.1 , pp. 1-10
    • Kawabata, Y.1    Wada, K.2    Nakatani, M.3    Yamada, S.4    Onoue, S.5
  • 5
    • 51249095402 scopus 로고    scopus 로고
    • Use of the biopharmaceutical classification system in early drug development
    • Ku MS,. 2008. Use of the biopharmaceutical classification system in early drug development. AAPS J 10 (1): 208-212.
    • (2008) AAPS J , vol.10 , Issue.1 , pp. 208-212
    • Ku, M.S.1
  • 6
    • 14744272833 scopus 로고    scopus 로고
    • The use of biopharmaceutic classification of drugs in drug discovery and development: Current status and future extension
    • Lennernäs H, Abrahamsson B,. 2005. The use of biopharmaceutic classification of drugs in drug discovery and development: Current status and future extension. J Pharm Pharmacol 57 (3): 273-285.
    • (2005) J Pharm Pharmacol , vol.57 , Issue.3 , pp. 273-285
    • Lennernäs, H.1    Abrahamsson, B.2
  • 7
    • 84908073820 scopus 로고    scopus 로고
    • Provisional in-silico biopharmaceutics classification (BCS) to guide oral drug product development
    • Wolk O, Agbaria R, Dahan A,. 2014. Provisional in-silico biopharmaceutics classification (BCS) to guide oral drug product development. Drug Design Dev Ther 2014 (8): 1563-1575.
    • (2014) Drug Design Dev Ther , vol.2014 , Issue.8 , pp. 1563-1575
    • Wolk, O.1    Agbaria, R.2    Dahan, A.3
  • 9
    • 84931824661 scopus 로고    scopus 로고
    • Self-nano-emulsifying drug delivery systems: An update of the biopharmaceutical aspects
    • (in Press)
    • Cherniakov I, Domb A, Hoffman A,. 2015. Self-nano-emulsifying drug delivery systems: An update of the biopharmaceutical aspects. Expert Opin Drug Deliv (in Press).
    • (2015) Expert Opin Drug Deliv
    • Cherniakov, I.1    Domb, A.2    Hoffman, A.3
  • 10
    • 67349130543 scopus 로고    scopus 로고
    • Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs
    • Miller JM, Dahan A, Gupta D, Varghese S, Amidon GL,. 2009. Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs. J Control Release 137 (1): 31-37.
    • (2009) J Control Release , vol.137 , Issue.1 , pp. 31-37
    • Miller, J.M.1    Dahan, A.2    Gupta, D.3    Varghese, S.4    Amidon, G.L.5
  • 11
    • 34547914142 scopus 로고    scopus 로고
    • Solubilization of poorly soluble compounds using 2-pyrrolidone
    • Jain P, Yalkowsky SH,. 2007. Solubilization of poorly soluble compounds using 2-pyrrolidone. Int J Pharm 342 (1-2): 1-5.
    • (2007) Int J Pharm , vol.342 , Issue.12 , pp. 1-5
    • Jain, P.1    Yalkowsky, S.H.2
  • 13
    • 79953685905 scopus 로고    scopus 로고
    • Nanonization strategies for poorly water-soluble drugs
    • Chen H, Khemtong C, Yang X, Chang X, Gao J,. 2011. Nanonization strategies for poorly water-soluble drugs. Drug Discov Today 16 (7-8): 354-360.
    • (2011) Drug Discov Today , vol.16 , Issue.78 , pp. 354-360
    • Chen, H.1    Khemtong, C.2    Yang, X.3    Chang, X.4    Gao, J.5
  • 14
    • 34548134519 scopus 로고    scopus 로고
    • Cyclodextrins as pharmaceutical solubilizers
    • Brewster ME, Loftsson T,. 2007. Cyclodextrins as pharmaceutical solubilizers. Adv Drug Del Revi 59 (7): 645-666.
    • (2007) Adv Drug del Revi , vol.59 , Issue.7 , pp. 645-666
    • Brewster, M.E.1    Loftsson, T.2
  • 15
    • 84857506982 scopus 로고    scopus 로고
    • Assessing the performance of amorphous solid dispersions
    • Newman A, Knipp G, Zografi G,. 2012. Assessing the performance of amorphous solid dispersions. J Pharm Sci 101 (4): 1355-1377.
    • (2012) J Pharm Sci , vol.101 , Issue.4 , pp. 1355-1377
    • Newman, A.1    Knipp, G.2    Zografi, G.3
  • 16
    • 84858039015 scopus 로고    scopus 로고
    • The solubility-permeability interplay and its implications in formulation design and development for poorly soluble drugs
    • Dahan A, Miller J,. 2012. The solubility-permeability interplay and its implications in formulation design and development for poorly soluble drugs. AAPS J 14 (2): 244-251.
    • (2012) AAPS J , vol.14 , Issue.2 , pp. 244-251
    • Dahan, A.1    Miller, J.2
  • 17
    • 72949123710 scopus 로고    scopus 로고
    • Prediction of solubility and permeability class membership: Provisional BCS classification of the world's top oral drugs
    • Dahan A, Miller J, Amidon G,. 2009. Prediction of solubility and permeability class membership: Provisional BCS classification of the world's top oral drugs. AAPS J 11 (4): 740-746.
    • (2009) AAPS J , vol.11 , Issue.4 , pp. 740-746
    • Dahan, A.1    Miller, J.2    Amidon, G.3
  • 18
    • 0028948839 scopus 로고
    • A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
    • Amidon GL, Lennernäs H, Shah VP, Crison JR,. 1995. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 12 (3): 413-420.
    • (1995) Pharm Res , vol.12 , Issue.3 , pp. 413-420
    • Amidon, G.L.1    Lennernäs, H.2    Shah, V.P.3    Crison, J.R.4
  • 19
    • 84862025527 scopus 로고    scopus 로고
    • The fraction dose absorbed, in humans, and high jejunal human permeability relationship
    • Dahan A, Lennernäs H, Amidon GL,. 2012. The fraction dose absorbed, in humans, and high jejunal human permeability relationship. Mol Pharm 9 (6): 1847-1851.
    • (2012) Mol Pharm , vol.9 , Issue.6 , pp. 1847-1851
    • Dahan, A.1    Lennernäs, H.2    Amidon, G.L.3
  • 20
    • 0343527392 scopus 로고    scopus 로고
    • Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
    • Lobenberg R, Amidon GL,. 2000. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur J Pharm Biopharm 50 (1): 3-12.
    • (2000) Eur J Pharm Biopharm , vol.50 , Issue.1 , pp. 3-12
    • Lobenberg, R.1    Amidon, G.L.2
  • 21
    • 84889097231 scopus 로고    scopus 로고
    • The interaction of nifedipine with selected cyclodextrins and the subsequent solubility-permeability trade-off
    • Beig A, Miller JM, Dahan A,. 2013. The interaction of nifedipine with selected cyclodextrins and the subsequent solubility-permeability trade-off. Eur J Pharm Biopharm 85 (3, Part B): 1293-1299.
    • (2013) Eur J Pharm Biopharm , vol.85 , Issue.3 PART B , pp. 1293-1299
    • Beig, A.1    Miller, J.M.2    Dahan, A.3
  • 22
    • 84885081422 scopus 로고    scopus 로고
    • Biopharmaceutical classification of poorly soluble drugs with respect to "enabling formulations"
    • Buckley ST, Frank KJ, Fricker G, Brandl M,. 2013. Biopharmaceutical classification of poorly soluble drugs with respect to "enabling formulations". Eur J Pharm Sci 50 (1): 8-16.
    • (2013) Eur J Pharm Sci , vol.50 , Issue.1 , pp. 8-16
    • Buckley, S.T.1    Frank, K.J.2    Fricker, G.3    Brandl, M.4
  • 23
    • 79959877984 scopus 로고    scopus 로고
    • In-vitro permeability of poorly water soluble drugs in the phospholipid vesicle-based permeation assay: The influence of nonionic surfactants
    • Fischer SM, Flaten GE, Hagesæther E, Fricker G, Brandl M,. 2011. In-vitro permeability of poorly water soluble drugs in the phospholipid vesicle-based permeation assay: The influence of nonionic surfactants. J Pharm Pharmacol 63 (8): 1022-1030.
    • (2011) J Pharm Pharmacol , vol.63 , Issue.8 , pp. 1022-1030
    • Fischer, S.M.1    Flaten, G.E.2    Hagesæther, E.3    Fricker, G.4    Brandl, M.5
  • 24
    • 84861593280 scopus 로고    scopus 로고
    • Accounting for the solubility-permeability interplay in oral formulation development for poor water solubility drugs: The effect of PEG-400 on carbamazepine absorption
    • Beig A, Miller JM, Dahan A,. 2012. Accounting for the solubility-permeability interplay in oral formulation development for poor water solubility drugs: The effect of PEG-400 on carbamazepine absorption. Eur J Pharm Biopharm 81: 386-391.
    • (2012) Eur J Pharm Biopharm , vol.81 , pp. 386-391
    • Beig, A.1    Miller, J.M.2    Dahan, A.3
  • 25
    • 84877077844 scopus 로고    scopus 로고
    • The twofold advantage of the amorphous form as an oral drug delivery practice for lipophilic compounds: Increased apparent solubility and drug flux through the intestinal membrane
    • Dahan A, Beig A, Ioffe-Dahan V, Agbaria R, Miller J,. 2013. The twofold advantage of the amorphous form as an oral drug delivery practice for lipophilic compounds: Increased apparent solubility and drug flux through the intestinal membrane. AAPS J 15 (2): 347-353.
    • (2013) AAPS J , vol.15 , Issue.2 , pp. 347-353
    • Dahan, A.1    Beig, A.2    Ioffe-Dahan, V.3    Agbaria, R.4    Miller, J.5
  • 26
    • 84866732706 scopus 로고    scopus 로고
    • Amorphous solid dispersion enhances permeation of poorly soluble ABT-102: True supersaturation vs. Apparent solubility enhancement
    • Frank KJ, Rosenblatt KM, Westedt U, Hölig P, Rosenberg J, Mägerlein M, Fricker G, Brandl M,. 2012. Amorphous solid dispersion enhances permeation of poorly soluble ABT-102: True supersaturation vs. apparent solubility enhancement. Int J Pharm 437 (1-2): 288-293.
    • (2012) Int J Pharm , vol.437 , Issue.12 , pp. 288-293
    • Frank, K.J.1    Rosenblatt, K.M.2    Westedt, U.3    Hölig, P.4    Rosenberg, J.5    Mägerlein, M.6    Fricker, G.7    Brandl, M.8
  • 27
    • 84901261550 scopus 로고    scopus 로고
    • What is the mechanism behind increased permeation rate of a poorly soluble drug from aqueous dispersions of an amorphous solid dispersion?
    • Frank KJ, Westedt U, Rosenblatt KM, Hölig P, Rosenberg J, Mägerlein M, Fricker G, Brandl M,. 2014. What is the mechanism behind increased permeation rate of a poorly soluble drug from aqueous dispersions of an amorphous solid dispersion? J Pharm Sci 103 (6): 1779-1786.
    • (2014) J Pharm Sci , vol.103 , Issue.6 , pp. 1779-1786
    • Frank, K.J.1    Westedt, U.2    Rosenblatt, K.M.3    Hölig, P.4    Rosenberg, J.5    Mägerlein, M.6    Fricker, G.7    Brandl, M.8
  • 28
    • 84863301279 scopus 로고    scopus 로고
    • A win-win solution in oral delivery of lipophilic drugs: Supersaturation via amorphous solid dispersions increases apparent solubility without sacrifice of intestinal membrane permeability
    • Miller JM, Beig A, Carr RA, Spence JK, Dahan A,. 2012. A win-win solution in oral delivery of lipophilic drugs: Supersaturation via amorphous solid dispersions increases apparent solubility without sacrifice of intestinal membrane permeability. Mol Pharm 9 (7): 2009-2016.
    • (2012) Mol Pharm , vol.9 , Issue.7 , pp. 2009-2016
    • Miller, J.M.1    Beig, A.2    Carr, R.A.3    Spence, J.K.4    Dahan, A.5
  • 29
    • 84901210403 scopus 로고    scopus 로고
    • The complexity of intestinal permeability: Assigning the correct BCS classification through careful data interpretation
    • Zur M, Hanson AS, Dahan A,. 2014. The complexity of intestinal permeability: Assigning the correct BCS classification through careful data interpretation. Eur J Pharm Sci 61 (0): 11-17.
    • (2014) Eur J Pharm Sci , vol.61 , pp. 11-17
    • Zur, M.1    Hanson, A.S.2    Dahan, A.3
  • 31
    • 0014876437 scopus 로고
    • Binding specificity between small organic solutes in aqueous solution: Classification of some solutes into two groups according to binding tendencies
    • Higuchi T, Kristiansen H,. 1970. Binding specificity between small organic solutes in aqueous solution: Classification of some solutes into two groups according to binding tendencies. J Pharm Sci 59 (11): 1601-1608.
    • (1970) J Pharm Sci , vol.59 , Issue.11 , pp. 1601-1608
    • Higuchi, T.1    Kristiansen, H.2
  • 32
    • 38549101558 scopus 로고    scopus 로고
    • The oral absorption of phospholipid prodrugs: In vivo and in vitro mechanistic investigation of trafficking of a lecithin-valproic acid conjugate following oral administration
    • Dahan A, Duvdevani R, Shapiro I, Elmann A, Finkelstein E, Hoffman A,. 2008. The oral absorption of phospholipid prodrugs: In vivo and in vitro mechanistic investigation of trafficking of a lecithin-valproic acid conjugate following oral administration. J Control Release 126 (1): 1-9.
    • (2008) J Control Release , vol.126 , Issue.1 , pp. 1-9
    • Dahan, A.1    Duvdevani, R.2    Shapiro, I.3    Elmann, A.4    Finkelstein, E.5    Hoffman, A.6
  • 33
    • 84899843284 scopus 로고    scopus 로고
    • The low/high BCS permeability class boundary: Physicochemical comparison of metoprolol and labetalol
    • Zur M, Gasparini M, Wolk O, Amidon GL, Dahan A,. 2014. The low/high BCS permeability class boundary: Physicochemical comparison of metoprolol and labetalol. Mol Pharm 11 (5): 1707-1714.
    • (2014) Mol Pharm , vol.11 , Issue.5 , pp. 1707-1714
    • Zur, M.1    Gasparini, M.2    Wolk, O.3    Amidon, G.L.4    Dahan, A.5
  • 34
    • 84880483077 scopus 로고    scopus 로고
    • Oral delivery of lipophilic drugs: The tradeoff between solubility increase and permeability decrease when using cyclodextrin-based formulations
    • Beig A, Agbaria R, Dahan A,. 2013. Oral delivery of lipophilic drugs: The tradeoff between solubility increase and permeability decrease when using cyclodextrin-based formulations. PLoS One 8 (7): e68237.
    • (2013) PLoS One , vol.8 , Issue.7 , pp. e68237
    • Beig, A.1    Agbaria, R.2    Dahan, A.3
  • 35
    • 84860702965 scopus 로고    scopus 로고
    • Predicting the solubility-permeability interplay when using cyclodextrins in solubility-enabling formulations: Model validation
    • Miller JM, Dahan A,. 2012. Predicting the solubility-permeability interplay when using cyclodextrins in solubility-enabling formulations: Model validation. Int J Pharm 430 (1-2): 388-391.
    • (2012) Int J Pharm , vol.430 , Issue.12 , pp. 388-391
    • Miller, J.M.1    Dahan, A.2


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