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Volumn 75, Issue 2, 2013, Pages 312-318

In vitro-in vivo correlations: General principles and methodologies, regulatory aspects and applications (Part 2)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; CURVE FITTING; DOSIMETRY; DRUG ABSORPTION; DRUG BLOOD LEVEL; DRUG ELIMINATION; DRUG RELEASE; DRUG SOLUBILITY; INTRAVENOUS ADMINISTRATION; LAPLACE TRANSFORMATION; LOO RIEGELMAN METHOD; MASS BALANCE METHOD; MATHEMATICAL ANALYSIS; MATHEMATICAL MODEL; MEASUREMENT ERROR; ORAL DRUG ADMINISTRATION; PLASMA CONCENTRATION-TIME CURVE; REGRESSION ANALYSIS; STOCHASTIC MODEL; WAGNER NELSON METHOD;

EID: 84876587731     PISSN: 0031711X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (55)
  • 1
    • 70449212108 scopus 로고
    • Correlation of in vivo with in vitro disintegration times of enteric coated tablets
    • Sep
    • Wagner JG, VeldkampW, Long S. Correlation of in vivo with in vitro disintegration times of enteric coated tablets. J Am Pharm Assoc Am Pharm Assoc (Baltim). 1958 Sep;47(9):681-5.
    • (1958) J Am Pharm Assoc Am Pharm Assoc (Baltim) , vol.47 , Issue.9 , pp. 681-685
    • Wagner, J.G.1    Veldkampw Long, S.2
  • 2
    • 0017211682 scopus 로고
    • Theoretical and computational basis for drug bioavailability determinations using pharmacological data. I. General considerations and procedures
    • Smolen VF. Theoretical and computational basis for drug bioavailability determinations using pharmacological data. I. General considerations and procedures. J Pharmacokinet Biopharm. 1976 Aug;4(4):337-53. (Pubitemid 8122216)
    • (1976) Journal of Pharmacokinetics and Biopharmaceutics , vol.4 , Issue.4 , pp. 337-353
    • Smolen, V.F.1
  • 3
    • 0002915214 scopus 로고
    • United States Pharmacopeial Convention. Pharmacopeial Forum Stimuli Article
    • United States Pharmacopeial Convention. Pharmacopeial Forum Stimuli Article. In Vitro/In Vivo Correlation for Extended Release Oral Dosage Forms. 1988. 4160-4161.
    • (1988) Vitro/In Vivo Correlation for Extended Release Oral Dosage Forms , pp. 4160-4161
  • 4
    • 84870555790 scopus 로고
    • United States Pharmacopeial Convention. USP 23 <1088>
    • United States Pharmacopeial Convention. USP 23 <1088>. In Vitro and In Vivo Evaluation of Dosage Forms. 1995. 1924-1929.
    • (1995) Vitro and in Vivo Evaluation of Dosage Forms , pp. 1924-1929
  • 5
    • 0003701605 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for Industry Available from
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for Industry. Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations. 1997. Available from: http://www.fda.gov/downloads/Drugs/ GuidanceComplianceRegulatoryInformation/Guidances/UCM070239.pdf
    • (1997) Extended Release Oral Dosage Forms: Development, Evaluation, and Application of in Vitro/in Vivo Correlations
  • 7
    • 0003428585 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER) Available from
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms. 1997. Available from: http://www.fda.gov/downloads/ Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM070237.pdf
    • (1997) Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms
  • 8
    • 84923690893 scopus 로고    scopus 로고
    • Guidance for Industry. SUPAC-IR: Immediate release solid oral dosage forms. scale-up and postapproval changes: Chemistry, manufacturing, and controls
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER) Available from
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for Industry. SUPAC-IR: Immediate Release Solid Oral Dosage Forms. Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls, In Vitro Dissolution Testing, and In Vivo Bioequivalence Documentation. 1995. Available from: http://www.fda.gov/downloads/Drugs/ GuidanceComplianceRegulatoryInformation/Guidances/UCM070636.pdf
    • (1995) Vitro Dissolution Testing, and in Vivo Bioequivalence Documentation
  • 10
    • 84923690893 scopus 로고    scopus 로고
    • Guidance for industry. SUPAC-MR: Modified release solid oral dosage forms. Scale-up and postapproval changes: Chemistry, manufacturing, and controls
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER) Available from
    • U.S. Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for Industry. SUPAC-MR: Modified Release Solid Oral Dosage Forms. Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation. 1997. Available from: http://www.fda.gov/downloads/Drugs/ GuidanceComplianceRegulatoryInformation/Guidances/UCM070640.pdf
    • (1997) Vitro Dissolution Testing and in Vivo Bioequivalence Documentation
  • 12
    • 84876577959 scopus 로고    scopus 로고
    • Committee for medicinal products for human use (CHMP)
    • European Medicines Agency (EMA) CPMP/EWP/QWP/1401/98 Rev Available from
    • European Medicines Agency (EMA). Committee for Medicinal Products for Human Use (CHMP). Guideline on the Investigation of Bioequivalence. 2010. CPMP/EWP/QWP/1401/98 Rev. 1. Available from: http://www.ema.europa.eu/docs/en- GB/document-library/Scientific-guideline/2010/01/WC500070039.pdf
    • (2010) Guideline on the Investigation of Bioequivalence , pp. 1
  • 14
    • 84876553898 scopus 로고    scopus 로고
    • United States Pharmacopeial Convention. USP 34 <1088>
    • United States Pharmacopeial Convention. USP 34 <1088>. In Vitro and In Vivo Evaluation of Dosage Forms. 2011. 612-617.
    • (2011) Vitro and in Vivo Evaluation of Dosage Forms , pp. 612-617
  • 15
    • 77954073585 scopus 로고    scopus 로고
    • Use of in Vitro-In Vivo Correlation (IVIVC) to facilitate the development of polymer-based controlled release injectable formulation
    • Jun
    • Mitra A, Wu Y. Use of In Vitro-In Vivo Correlation (IVIVC) to facilitate the development of polymer-based controlled release injectable formulation. Recent Pat Drug Deliv Formul. 2010 Jun;4(2):94-104.
    • (2010) Recent Pat Drug Deliv Formul , vol.4 , Issue.2 , pp. 94-104
    • Mitra, A.1    Wu, Y.2
  • 16
    • 45249109321 scopus 로고    scopus 로고
    • In vitro and in vivo considerations associated with parenteral sustained release products: A review based upon information presented and points expressed at the 2007 Controlled Release Society Annual Meeting
    • Jul.14
    • Martinez M, Rathbone M, Burgess D, Huynh M. In vitro and in vivo considerations associated with parenteral sustained release products: a review based upon information presented and points expressed at the 2007 Controlled Release Society Annual Meeting. J Control Release. 2008 Jul 14;129(2):79-87.
    • (2008) J Control Release , vol.12 , Issue.2 , pp. 79-87
    • Martinez, M.1    Rathbone, M.2    Burgess, D.3    Huynh, M.4
  • 17
    • 63549141348 scopus 로고    scopus 로고
    • Assuring quality and performance of sustained and controlled release parenterals: EUFEPS workshop report
    • Mar
    • Burgess DJ, Crommelin DJ, Hussain AS, Chen ML. Assuring quality and performance of sustained and controlled release parenterals: EUFEPS workshop report. AAPS PharmSci. 2004 Mar 22;6(1):E11.
    • (2004) AAPS PharmSci. , vol.22 , Issue.61
    • Burgess, D.J.1    Crommelin, D.J.2    Hussain, A.S.3    Chen, M.L.4
  • 18
    • 52449096784 scopus 로고    scopus 로고
    • Assuring quality and performance of sustained and controlled release parenterals: Workshop report
    • Burgess DJ, Hussain AS, Ingallinera TS, Chen ML. Assuring quality and performance of sustained and controlled release parenterals: workshop report. AAPS PharmSci. 2002;4(2):E7.
    • (2002) AAPS PharmSci. , vol.4 , Issue.2
    • Burgess, D.J.1    Hussain, A.S.2    Ingallinera, T.S.3    Chen, M.L.4
  • 19
    • 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
    • DOI 10.1007/BF00543326
    • Brockmeier D, Dengler 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. (Pubitemid 15085155)
    • (1985) European Journal of Clinical Pharmacology , vol.28 , Issue.3 , pp. 291-300
    • Brockmeier, D.1    Dengler, H.J.2    Voegele, D.3
  • 22
    • 0001319970 scopus 로고
    • Per cent absorbed time plots derived from blood level and/or urinary excretion data
    • Jun
    • Wagner JG, Nelson E. Per cent absorbed time plots derived from blood level and/or urinary excretion data. J Pharm Sci. 1963 Jun;52:610-1.
    • (1963) J Pharm Sci. , vol.52 , pp. 610-611
    • Wagner, J.G.1    Nelson, E.2
  • 23
    • 0014297946 scopus 로고
    • New method for calculating the intrinsic absorption rate of drugs
    • Jun
    • Loo JC, Riegelman S. New method for calculating the intrinsic absorption rate of drugs. J Pharm Sci. 1968 Jun;57(6):918-28.
    • (1968) J Pharm Sci. , vol.57 , Issue.6 , pp. 918-928
    • Loo, J.C.1    Riegelman, S.2
  • 24
    • 0000463679 scopus 로고
    • Correlation of in vitro drug release with in vivo response kinetics
    • Langenbucher F, Moeller H. Correlation of in vitro drug release with in vivo response kinetics. Pharm Ind. 1983;45(6):623-28.
    • (1983) Pharm Ind. , vol.45 , Issue.6 , pp. 623-628
    • Langenbucher, F.1    Moeller, H.2
  • 25
    • 0242288840 scopus 로고    scopus 로고
    • Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: III. Convolution and deconvolution
    • DOI 10.1016/S0939-6411(03)00140-1
    • Langenbucher F. Handling of computational in vitro/in vivo correlation problems by Microsoft Excel: III. Convolution and deconvolution. Eur J Pharm Biopharm. 2003 Nov;56(3):429-37. (Pubitemid 37346517)
    • (2003) European Journal of Pharmaceutics and Biopharmaceutics , vol.56 , Issue.3 , pp. 429-437
    • Langenbucher, F.1
  • 26
    • 0017807805 scopus 로고
    • Mathematical basis of point area deconvolution method for determining in vivo input functions
    • Vaughan DP, Dennis M. Mathematical basis of point-area deconvolution method for determining in vivo input functions. J Pharm Sci. 1978 May;67(5):663-5. (Pubitemid 8364971)
    • (1978) Journal of Pharmaceutical Sciences , vol.67 , Issue.5 , pp. 663-665
    • Vaughan, D.P.1    Dennis, M.2
  • 27
    • 0018840933 scopus 로고
    • New compartment- and model-independent method for rapid calculation of drug absorption rates
    • Chiou WL. New compartment- and model-independent method for rapid calculation of drug absorption rates. J Pharm Sci. 1980 Jan; 69(1):57-62. (Pubitemid 10136821)
    • (1980) Journal of Pharmaceutical Sciences , vol.69 , Issue.1 , pp. 57-62
    • Chiou, W.L.1
  • 28
    • 0015874073 scopus 로고
    • Pitfalls in digital computation of the impulse response of vascular beds from indicator-dilution curves
    • Apr
    • Gamel J, Rousseau WF, Katholi CR, Mesel E. Pitfalls in digital computation of the impulse response of vascular beds from indicator-dilution curves. Circ Res. 1973 Apr;32(4):516-23.
    • (1973) Circ Res. , vol.32 , Issue.4 , pp. 516-523
    • Gamel, J.1    Rousseau, W.F.2    Katholi, C.R.3    Mesel, E.4
  • 29
    • 0018190102 scopus 로고
    • Numerical deconvolution by least squares: Use of prescribed input functions
    • Cutler DJ. Numerical deconvolution by least squares: use of prescribed input functions. J Pharmacokinet Biopharm. 1978 Jun; 6(3):227-41. (Pubitemid 8379262)
    • (1978) Journal of Pharmacokinetics and Biopharmaceutics , vol.6 , Issue.3 , pp. 227-241
    • Cutler, D.J.1
  • 30
    • 0017823608 scopus 로고
    • Numerical deconvolution by least squares: Use of polynomials to represent the input function
    • Cutler DJ. Numerical deconvolution by least squares: use of polynomials to represent the input function. J Pharmacokinet Biopharm. 1978 Jun;6(3):243-63. (Pubitemid 8379263)
    • (1978) Journal of Pharmacokinetics and Biopharmaceutics , vol.6 , Issue.3 , pp. 243-263
    • Cutler, D.J.1
  • 31
    • 0019277294 scopus 로고
    • An algorithm and computer program for deconvolution in linear pharmacokinetics
    • DOI 10.1007/BF01059546
    • Veng-Pedersen P. An algorithm and computer program for deconvolution in linear pharmacokinetics. J Pharmacokinet Biopharm. 1980 Oct;8(5):463-81. (Pubitemid 11136585)
    • (1980) Journal of Pharmacokinetics and Biopharmaceutics , vol.8 , Issue.5 , pp. 463-481
    • Veng-Pedersen, P.1
  • 32
    • 0022344635 scopus 로고
    • A polyexponential deconvolution method. Evaluation of the 'gastrointestinal bioavailability' and mean in vivo dissolution time of some ibuprofen dosage forms
    • DOI 10.1007/BF01065657
    • Gillespie WR, Veng-Pedersen P. A polyexponential deconvolution method. Evaluation of the "gastrointestinal bioavailability" and mean in vivo dissolution time of some ibuprofen dosage forms. J Pharmacokinet Biopharm. 1985 Jun;13(3):289-307. (Pubitemid 16194626)
    • (1985) Journal of Pharmacokinetics and Biopharmaceutics , vol.13 , Issue.3 , pp. 289-307
    • Gillespie, W.R.1    Veng-Pedersen, P.2
  • 33
    • 0035844740 scopus 로고    scopus 로고
    • Noncompartmentally-based pharmacokinetic modeling
    • DOI 10.1016/S0169-409X(01)00119-3, PII S0169409X01001193
    • Veng-Pedersen P. Noncompartmentally-based pharmacokinetic modeling. Adv Drug Deliv Rev. 2001 Jun 11;48(2-3):265-300. (Pubitemid 32434407)
    • (2001) Advanced Drug Delivery Reviews , vol.48 , Issue.2-3 , pp. 265-300
    • Veng-Pedersen, P.1
  • 34
    • 0027718065 scopus 로고
    • Two constrained deconvolution methods using spline functions
    • Verotta D. Two constrained deconvolution methods using spline functions. J Pharmacokinet Biopharm. 1993 Oct;21(5):609-36. (Pubitemid 24037113)
    • (1993) Journal of Pharmacokinetics and Biopharmaceutics , vol.21 , Issue.5 , pp. 609-636
    • Verotta, D.1
  • 35
    • 0027691238 scopus 로고
    • Estimation and model selection in constrained deconvolution
    • Verotta D. Estimation and model selection in constrained deconvolution. Ann Biomed Eng. 1993 Nov-Dec;21(6):605-20. (Pubitemid 24026379)
    • (1993) Annals of Biomedical Engineering , vol.21 , Issue.6 , pp. 605-620
    • Verotta, D.1
  • 36
    • 0017388072 scopus 로고
    • A new numerical calculation method for deconvolution in linear compartment analysis of pharmacokinetics
    • Kiwada H, Morita K, Hayashi M, Awazu S, Hanano M. A new numerical calculation method for deconvolution in linear compartment analysis of pharmacokinetics. Chem Pharm Bull (Tokyo). 1977 Jun;25(6):1312-8. (Pubitemid 8127160)
    • (1977) Chemical and Pharmaceutical Bulletin , vol.25 , Issue.6 , pp. 1312-1318
    • Kiwada, H.1    Morita, K.2    Hayashi, M.3
  • 37
    • 0029554724 scopus 로고
    • A nonparametric subject-specific population method for deconvolution: I. Description, internal validation, and real data examples
    • DOI 10.1007/BF02353463
    • Fattinger KE, Verotta D. A nonparametric subject-specific population method for deconvolution: I. Description, internal validation, and real data examples. J Pharmacokinet Biopharm. 1995 Dec; 23(6):581-610. (Pubitemid 26155335)
    • (1995) Journal of Pharmacokinetics and Biopharmaceutics , vol.23 , Issue.6 , pp. 581-610
    • Fattinger, K.E.1    Verotta, D.2
  • 38
    • 0029556136 scopus 로고
    • A nonparametric subject-specific population method for deconvolution: II. External validation
    • DOI 10.1007/BF02353464
    • Fattinger KE, Verotta D. A nonparametric subject-specific population method for deconvolution: II. External validation. J Pharmacokinet Biopharm. 1995 Dec;23(6):611-34. (Pubitemid 26155336)
    • (1995) Journal of Pharmacokinetics and Biopharmaceutics , vol.23 , Issue.6 , pp. 611-634
    • Fattinger, K.E.1    Verotta, D.2
  • 39
    • 0030810301 scopus 로고    scopus 로고
    • In vitro-in vivo relationships for oral extended-release drug products
    • Mauger DT, Chinchilli VM. In vitro-in vivo relationships for oral extended-release drug products. J Biopharm Stat. 1997 Nov;7(4): 565-78. (Pubitemid 27502174)
    • (1997) Journal of Biopharmaceutical Statistics , vol.7 , Issue.4 , pp. 565-578
    • Mauger, D.T.1    Chinchilli, V.M.2
  • 40
    • 0030658987 scopus 로고    scopus 로고
    • Level A in vivo-in vitro correlation: Nonlinear models and statistical methodology
    • DOI 10.1021/js970155d
    • Dunne A, O'Hara T, Devane J. Level A in vivo-in vitro correlation: nonlinear models and statistical methodology. J Pharm Sci. 1997 Nov;86(11):1245-9. (Pubitemid 27486095)
    • (1997) Journal of Pharmaceutical Sciences , vol.86 , Issue.11 , pp. 1245-1249
    • Dunne, A.1    O'Hara, T.2    Devane, J.3
  • 41
    • 0033618483 scopus 로고    scopus 로고
    • A new approach to modelling the relationship between in vitro and in vivo drug dissolution/absorption
    • Jul 30 discussion 77
    • Dunne A, O'Hara T, Devane J. A new approach to modelling the relationship between in vitro and in vivo drug dissolution/absorption. Stat Med. 1999 Jul 30;18(14):1865-76; discussion 77.
    • (1999) Stat Med. , vol.18 , Issue.14 , pp. 1865-1876
    • Dunne, A.1    O'hara, T.2    Devane, J.3
  • 43
    • 0030806512 scopus 로고    scopus 로고
    • Convolution-based approaches for in vivo-in vitro correlation modeling
    • Gillespie WR. Convolution-based approaches for in vivo-in vitro correlation modeling. Adv Exp Med Biol. 1997;423:53-65. (Pubitemid 27347192)
    • (1997) Advances in Experimental Medicine and Biology , vol.423 , pp. 53-65
    • Gillespie, W.R.1
  • 44
    • 0020400710 scopus 로고
    • Numerical convolution/deconvolution as a tool for correlating in vitro with in vivo drug availability
    • Langenbucher F. Numerical convolution/deconvolution as a tool for correlating in vitro with in vivo drug availability. Pharm Ind. 1982;44(11):1166-72. (Pubitemid 13137274)
    • (1982) Pharmazeutische Industrie , vol.44 , Issue.11 , pp. 1166-1172
    • Langenbucher, F.1
  • 45
    • 19944416570 scopus 로고    scopus 로고
    • Deconvolution based approach for level A in vivo/in vitro correlation modelling: Statistical considerations
    • DOI 10.1081/CRP-200054957
    • Dunne A, Gaynor C, Davis J. Deconvolution based approach for level A in vivo-in vitro correlation modelling: statistical considerations. Clin Res Regul Aff. 2005;22(1):1-14. (Pubitemid 40756840)
    • (2005) Clinical Research and Regulatory Affairs , vol.22 , Issue.1 , pp. 1-14
    • Dunne, A.1    Gaynor, C.2    Davis, J.3
  • 46
    • 52449110507 scopus 로고    scopus 로고
    • A comparison of the prediction accuracy of two IVIVC modelling techniques
    • Aug
    • Gaynor C, Dunne A, Davis J. A comparison of the prediction accuracy of two IVIVC modelling techniques. J Pharm Sci. 2008 Aug; 97(8):3422-32.
    • (2008) J Pharm Sci. , vol.97 , Issue.8 , pp. 3422-3432
    • Gaynor, C.1    Dunne, A.2    Davis, J.3
  • 47
    • 0031908782 scopus 로고    scopus 로고
    • CODE: A deconvolution program implementing a regularization method of deconvolution constrained to non-negative values. Description and pilot evaluation
    • DOI 10.1002/(SICI)1099-081X(19 9801)19:1<39::AID-BDD7 3>3.0.CO;2-M
    • Hovorka R, Chappell MJ, Godfrey KR, Madden FN, Rouse MK, Soons PA. CODE: a deconvolution program implementing a regularization method of deconvolution constrained to non-negative values. Description and pilot evaluation. Biopharm Drug Dispos. 1998 Jan; 19(1):39-53. (Pubitemid 28064490)
    • (1998) Biopharmaceutics and Drug Disposition , vol.19 , Issue.1 , pp. 39-53
    • Hovorka, R.1    Chappell, M.J.2    Godfrey, K.R.3    Madden, F.N.4    Rouse, M.K.5    Soons, P.A.6
  • 48
    • 0032960016 scopus 로고    scopus 로고
    • Artificial neural networks applied to the in vitro-in vivo correlation of an extended-release formulation: Initial trials and experience
    • DOI 10.1021/js970148p
    • Dowell JA, Hussain A, Devane J, Young D. Artificial neural networks applied to the in vitro-in vivo correlation of an extended-release formulation: initial trials and experience. J Pharm Sci. 1999 Jan; 88(1):154-60. (Pubitemid 29037384)
    • (1999) Journal of Pharmaceutical Sciences , vol.88 , Issue.1 , pp. 154-160
    • Dowell, J.A.1    Hussain, A.2    Devane, J.3    Young, D.4
  • 49
    • 33847193134 scopus 로고    scopus 로고
    • An investigation into the usefulness of generalized regression neural network analysis in the development of level A in vitro-in vivo correlation
    • Mar
    • Parojcic J, Ibric S, Djuric Z, Jovanovic M, Corrigan OI. An investigation into the usefulness of generalized regression neural network analysis in the development of level A in vitro-in vivo correlation. Eur J Pharm Sci. 2007 Mar;30(3-4):264-72.
    • (2007) Eur J Pharm Sci. , vol.30 , Issue.3-4 , pp. 264-272
    • Parojcic, J.1    Ibric, S.2    Djuric, Z.3    Jovanovic, M.4    Corrigan, O.I.5
  • 50
    • 84863219203 scopus 로고    scopus 로고
    • Computer-based evolutionary search for a nonlinear conversion function for establishing In Vitro-In Vivo Correlation (IVIVC) of Oral Drug Formulations
    • Jun 25
    • Yamashita F, Fujita A, Zhang X, Sasa Y, Mihara K, Hashida M. Computer-based Evolutionary Search for a Nonlinear Conversion Function for Establishing In Vitro-In Vivo Correlation (IVIVC) of Oral Drug Formulations. Drug Metab Pharmacokinet. 2012 Jun 25;27(3):280-5.
    • (2012) Drug Metab Pharmacokinet , vol.27 , Issue.3 , pp. 280-285
    • Yamashita, F.1    Fujita, A.2    Zhang, X.3    Sasa, Y.4    Mihara, K.5    Hashida, M.6
  • 51
    • 68249162210 scopus 로고    scopus 로고
    • Prediction of modified release pharmacokinetics and pharmacodynamics from in vitro, immediate release, and intravenous data
    • Jun
    • Lukacova V, Woltosz WS, Bolger MB. Prediction of modified release pharmacokinetics and pharmacodynamics from in vitro, immediate release, and intravenous data. Aaps J. 2009 Jun;11(2):323-34.
    • (2009) Aaps J. , vol.11 , Issue.2 , pp. 323-334
    • Lukacova, V.1    Woltosz, W.S.2    Bolger, M.B.3
  • 52
    • 79953296456 scopus 로고    scopus 로고
    • Simulation of human intravenous and oral pharmacokinetics of 21 diverse compounds using physiologically based pharmacokinetic modeling
    • May
    • Jones HM, Gardner IB, Collard WT, Stanley PJ, Oxley P, Hosea NA, et al. Simulation of human intravenous and oral pharmacokinetics of 21 diverse compounds using physiologically based pharmacokinetic modelling. Clin Pharmacokinet. 2011 May;50(5):331-47.
    • (2011) Clin Pharmacokinet , vol.50 , Issue.5 , pp. 331-347
    • Jones, H.M.1    Gardner, I.B.2    Collard, W.T.3    Stanley, P.J.4    Oxley, P.5    Hosea, N.A.6
  • 53
    • 84862771517 scopus 로고    scopus 로고
    • A technique to estimate in vivo dissolution profiles without data from a solution
    • Sep
    • Cook JA. A technique to estimate in vivo dissolution profiles without data from a solution. Aaps J. 2012 Sep;14(3):433-6.
    • (2012) Aaps J. , vol.14 , Issue.3 , pp. 433-436
    • Cook, J.A.1
  • 54
    • 80054738759 scopus 로고    scopus 로고
    • Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part 1: Oral solutions
    • Dec
    • Thelen K, Coboeken K, Willmann S, Burghaus R, Dressman JB, Lippert J. Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part 1: oral solutions. J Pharm Sci. 2011 Dec;100(12):5324-45.
    • (2011) J Pharm Sci. , vol.100 , Issue.12 , pp. 5324-5345
    • Thelen, K.1    Coboeken, K.2    Willmann, S.3    Burghaus, R.4    Dressman, J.B.5    Lippert, J.6
  • 55
    • 84855870739 scopus 로고    scopus 로고
    • Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part II: Extension to describe performance of solid dosage forms
    • Mar
    • Thelen K, Coboeken K, Willmann S, Dressman JB, Lippert J. Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part II: extension to describe performance of solid dosage forms. J Pharm Sci. 2012 Mar;101(3):1267-80.
    • (2012) J Pharm Sci. , vol.101 , Issue.3 , pp. 1267-1280
    • Thelen, K.1    Coboeken, K.2    Willmann, S.3    Dressman, J.B.4    Lippert, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.