메뉴 건너뛰기




Volumn , Issue , 2007, Pages 107-123

In vitro-in vivo correlation

Author keywords

[No Author keywords available]

Indexed keywords


EID: 80052859175     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (7)

References (26)
  • 1
    • 0021810434 scopus 로고
    • In vitro-in vivo correlation of dissolution, a time scaling problem? Transformation of in vitro results to the in vivo situation, using theophylline as a practical example
    • Brockmeier D, Dengier HJ, Voegele D. In vitro-in vivo correlation of dissolution, a time scaling problem? Transformation of in vitro results to the in vivo situation, using theophylline as a practical example. Eur J Clin Pharmacol 1985; 28(3): 291-300.
    • (1985) Eur J Clin Pharmacol , vol.28 , Issue.3 , pp. 291-300
    • Brockmeier, D.1    Dengier, H.J.2    Voegele, D.3
  • 2
    • 0023236625 scopus 로고
    • Evaluation of in vivo drug release by numerical deconvolution using oral solution data as the weighting function
    • Chan KK, Langenbucher F, Gibaldi M. Evaluation of in vivo drug release by numerical deconvolution using oral solution data as the weighting function. J Pharm Sci 1987; 76(6):446-450.
    • (1987) J Pharm Sci , vol.76 , Issue.6 , pp. 446-450
    • Chan, K.K.1    Langenbucher, F.2    Gibaldi, M.3
  • 4
    • 84870555790 scopus 로고
    • < 1088 > 23rd ed. Rockville: U.S. Pharmacopeial Convention
    • The United States Pharmacopeia. In vitro and in vivo evaluation of dosage forms. < 1088 > 23rd ed. Rockville: U.S. Pharmacopeial Convention, 1995:1924-1929.
    • (1995) In vitro and in vivo evaluation of dosage forms , pp. 1924-1929
  • 5
    • 85122646852 scopus 로고    scopus 로고
    • Regulatory considerations for oral extended release dosage forms and in vitro (dissolution)/in vivo (bioavailability) correlations
    • Sahajwalla CH, ed. Regulatory paradigms for clinical pharmacology and biopharmaceutics. New York: Marcel Dekker, Inc
    • Uppoor RS, Marroum PJ. Regulatory considerations for oral extended release dosage forms and in vitro (dissolution)/in vivo (bioavailability) correlations. In: Sahajwalla CH, ed. New Drug Development. Regulatory paradigms for clinical pharmacology and biopharmaceutics. New York: Marcel Dekker, Inc., 2004:417-448.
    • (2004) New Drug Development , pp. 417-448
    • Uppoor, R.S.1    Marroum, P.J.2
  • 6
    • 0041886129 scopus 로고    scopus 로고
    • Vitro dissolution testing and in vivo bioequivalence documentation. US Department of Health and Human Services, Food and Drug Administration. Sep
    • Center for Drug Evaluation and Research (CDER). SUPAC-MR: modified release solid dosage forms. Scale-up and postapproval changes: chemistry, manufacturing, and controls; In Vitro dissolution testing and in vivo bioequivalence documentation. US Department of Health and Human Services, Food and Drug Administration. Sep 1997.
    • (1997) SUPAC-MR: Modified release solid dosage forms. Scale-up and postapproval changes: Chemistry, manufacturing, and controls
  • 7
    • 0030658987 scopus 로고    scopus 로고
    • Level A in vivo-in vitro correlation: Nonlinear models and statistical methodology
    • Dunne A, O'Hare T, Devane J. Level A in vivo-in vitro correlation: nonlinear models and statistical methodology. J Pharm Sci 1997; 86(11):1245-1249.
    • (1997) J Pharm Sci , vol.86 , Issue.11 , pp. 1245-1249
    • Dunne, A.1    O'Hare, T.2    Devane, J.3
  • 8
    • 0034434385 scopus 로고    scopus 로고
    • Application of an in vitro-in vivo correlation (IVIVC) in setting formulation release specifications
    • Modi NB, Lam, A, Lindemulder E, Wang B, Gupta SK. Application of an in vitro-in vivo correlation (IVIVC) in setting formulation release specifications. Biopharm Drug Dispos 2000; 21(8):321-326.
    • (2000) Biopharm Drug Dispos , vol.21 , Issue.8 , pp. 321-326
    • Modi, N.B.1    Lam, A.2    Lindemulder, E.3    Wang, B.4    Gupta, S.K.5
  • 9
    • 0034981697 scopus 로고    scopus 로고
    • A semiparametric deconvolution model to establish in vivo-in vitro correlation applied to OROS® oxybutynin
    • Pitsiu M, Sathyan G, Gupta S, Verotta S. A semiparametric deconvolution model to establish in vivo-in vitro correlation applied to OROS® oxybutynin. J Pharm Sci 2001; 90(6):702-712.
    • (2001) J Pharm Sci , vol.90 , Issue.6 , pp. 702-712
    • Pitsiu, M.1    Sathyan, G.2    Gupta, S.3    Verotta, S.4
  • 11
    • 0036139704 scopus 로고    scopus 로고
    • Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: I. Principles and some general algorithms
    • Langenbucher F. Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: I. Principles and some general algorithms. Eur J Pharm Biopharm 2002; 53(1):1-7.
    • (2002) Eur J Pharm Biopharm , vol.53 , Issue.1 , pp. 1-7
    • Langenbucher, F.1
  • 12
    • 0242288840 scopus 로고    scopus 로고
    • Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: III. Convolution and deconvolution
    • Langenbucher F. Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: III. Convolution and deconvolution. Eur J Pharm Biopharm 2003; 56(3):429-437.
    • (2003) Eur J Pharm Biopharm , vol.56 , Issue.3 , pp. 429-437
    • Langenbucher, F.1
  • 13
    • 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, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995; 2(3):413-420.
    • (1995) Pharm Res , vol.2 , Issue.3 , pp. 413-420
    • Amidon, G.L.1    Lennernas, H.2    Shah, V.P.3    Crison, J.R.4
  • 14
    • 0022352260 scopus 로고
    • In vitro and in vivo deconvolution assessment of drug release kinetics from oxprenolol Oros preparations
    • Langenbucher F, Mysicka J. In vitro and in vivo deconvolution assessment of drug release kinetics from oxprenolol Oros preparations. Br J Clin Pharmac 1985; 19(suppl 2):151S-162S.
    • (1985) Br J Clin Pharmac , vol.19 , pp. 151S-162S
    • Langenbucher, F.1    Mysicka, J.2
  • 15
    • 0028966473 scopus 로고
    • In vitro and in vivo evaluation of a once-daily controlled-release pseudoephedrine product
    • Hwang SS, Gorsline J, Louie J, Dye D, Guinta D, Hamel L. In vitro and in vivo evaluation of a once-daily controlled-release pseudoephedrine product. J Clin Pharmacol 1995; 35(3):259-267.
    • (1995) J Clin Pharmacol , vol.35 , Issue.3 , pp. 259-267
    • Hwang, S.S.1    Gorsline, J.2    Louie, J.3    Dye, D.4    Guinta, D.5    Hamel, L.6
  • 16
    • 0037432153 scopus 로고    scopus 로고
    • Local drug delivery via coronary stent with programmable release pharmacokinetics
    • Finkelstein A, McClean D, Kar S, et al. Local drug delivery via coronary stent with programmable release pharmacokinetics. Circulation 2003; 107(5):777-784.
    • (2003) Circulation , vol.107 , Issue.5 , pp. 777-784
    • Finkelstein, A.1    McClean, D.2    Kar, S.3
  • 17
    • 0030935847 scopus 로고    scopus 로고
    • Sustained local delivery of dexamethasone by a novel intravascular eluting stent to prevent restenosis in the porcine coronary injury model
    • Lincoff AM, Furst JG, Ellis SG, Tuch RJ, Topol EJ. Sustained local delivery of dexamethasone by a novel intravascular eluting stent to prevent restenosis in the porcine coronary injury model. J Am Coll Cardiol 1997; 29(4):808-816.
    • (1997) J Am Coll Cardiol , vol.29 , Issue.4 , pp. 808-816
    • Lincoff, A.M.1    Furst, J.G.2    Ellis, S.G.3    Tuch, R.J.4    Topol, E.J.5
  • 18
    • 0035838322 scopus 로고    scopus 로고
    • An in vivo/in vitro comparison with a leuprolide osmotic implant for the treatment of prostrate cancer
    • Wright JC, Leonard ST, Stevenson CL, et al. An in vivo/in vitro comparison with a leuprolide osmotic implant for the treatment of prostrate cancer. J Contr Rel 2001; 75(1-2):1-10.
    • (2001) J Contr Rel , vol.75 , Issue.1-2 , pp. 1-10
    • Wright, J.C.1    Leonard, S.T.2    Stevenson, C.L.3
  • 19
    • 0026521395 scopus 로고
    • System functionality and physicochemical model of fentanyl transdermal system
    • Gupta SK, Southam M, Gale R, Hwang SS. System functionality and physicochemical model of fentanyl transdermal system. J Pain Symptom Manag 1992; 7(suppl 3): S17-S26.
    • (1992) J Pain Symptom Manag , vol.7 , pp. S17-S26
    • Gupta, S.K.1    Southam, M.2    Gale, R.3    Hwang, S.S.4
  • 20
    • 0003621598 scopus 로고
    • Pharmacokinetic and pharmacodynamic modeling of transdermal products
    • Shah VP, Maiback HI, eds. New York: Plenum Press
    • Gupta SK, Bashaw ED, Hwang SS. Pharmacokinetic and pharmacodynamic modeling of transdermal products. In: Shah VP, Maiback HI, eds. Topical Drug Bioavailability, and Penetration. New York: Plenum Press, 1993:311-332.
    • (1993) Topical Drug Bioavailability, and Penetration , pp. 311-332
    • Gupta, S.K.1    Bashaw, E.D.2    Hwang, S.S.3
  • 21
    • 0038700505 scopus 로고    scopus 로고
    • Convolution method to predict drug concentration profiles of 2,3,5,6-tetramethylpyrazine following transdermal application
    • Qi X, Liu R, Sun D, Ackermann C, Hou H. Convolution method to predict drug concentration profiles of 2,3,5,6-tetramethylpyrazine following transdermal application. Int J Pharm 2003; 259(1-2):39-45.
    • (2003) Int J Pharm , vol.259 , Issue.1-2 , pp. 39-45
    • Qi, X.1    Liu, R.2    Sun, D.3    Ackermann, C.4    Hou, H.5
  • 22
    • 8444233183 scopus 로고    scopus 로고
    • Clinical pharmacokinetic and pharmacodynamic evaluation of transdermal drug delivery systems of salbutamol sulfate
    • Murthy SN, Hiremath SR. Clinical pharmacokinetic and pharmacodynamic evaluation of transdermal drug delivery systems of salbutamol sulfate. Int J Pharm 2004; 287(1-2):47-53.
    • (2004) Int J Pharm , vol.287 , Issue.1-2 , pp. 47-53
    • Murthy, S.N.1    Hiremath, S.R.2
  • 23
    • 0032484042 scopus 로고    scopus 로고
    • A simple in vitro model to study the release kinetics of liposome encapsulated material
    • Peschka R, Dennehy C, Szoka FC. A simple in vitro model to study the release kinetics of liposome encapsulated material. J Control Release 1998; 56(1-3):41-51.
    • (1998) J Control Release , vol.56 , Issue.1-3 , pp. 41-51
    • Peschka, R.1    Dennehy, C.2    Szoka, F.C.3
  • 24
    • 0037028044 scopus 로고    scopus 로고
    • Development of an in vitro drug release assay that accurately predicts in vivo drug retention for liposomal-based drug delivery systems
    • Shabbits JA, Chiu GNC, Mayer LD. Development of an in vitro drug release assay that accurately predicts in vivo drug retention for liposomal-based drug delivery systems. J Control Release 2002; 84(3):161-170.
    • (2002) J Control Release , vol.84 , Issue.3 , pp. 161-170
    • Shabbits, J.A.1    Chiu, G.N.C.2    Mayer, L.D.3
  • 25
    • 0014982603 scopus 로고
    • Drug-absorption analysis for pharmacological data I: Method and confirmation exemplified for the mydriatic drug tropicamide
    • Smolen VF, Schoenwald RD. Drug-absorption analysis for pharmacological data I: method and confirmation exemplified for the mydriatic drug tropicamide. J Pharm Sci 1971; 60(1):96-103.
    • (1971) J Pharm Sci , vol.60 , Issue.1 , pp. 96-103
    • Smolen, V.F.1    Schoenwald, R.D.2
  • 26
    • 0017596548 scopus 로고
    • Predictive conversion of in vivo drug dissolution data into in vivo drug response versus time profiles exemplified for plasma levels of warfarin
    • Smolen VF, Erb RJ. Predictive conversion of in vivo drug dissolution data into in vivo drug response versus time profiles exemplified for plasma levels of warfarin. J Pharm Sci 1977; 66(3):297-304.
    • (1977) J Pharm Sci , vol.66 , Issue.3 , pp. 297-304
    • Smolen, V.F.1    Erb, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.