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Volumn 99, Issue 6, 2010, Pages 2544-2556

Biowaiver monographs for immediate release solid oral dosage forms: Furosemide

Author keywords

Absorption; Bioequivalence; Biopharmaceutics classification system (BCS); Furosemide; Permeability; Regulatory science; Solubility

Indexed keywords

APHAR; BEXAL; CINFA; DIURAPID; DIUSEMIDE; EXCIPIENT; FUROBETA; FUROGAMMA; FUROMIN; FUROSAL; FUROSEMIDE; JUFURIX; ROSEFUR; UNCLASSIFIED DRUG;

EID: 77951629023     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.22030     Document Type: Note
Times cited : (123)

References (101)
  • 1
    • 3843072170 scopus 로고    scopus 로고
    • Biowaiver monographs for immediate release solid oral dosage forms based on Biopharmaceutics Classification System (BCS) literature data: Verapamil hydrochloride, propranolol hydrochloride, and atenolol
    • DOI 10.1002/jps.20131
    • Vogelpoel H, Welink J, Amidon GL, Junginger HE, Midha KK, Möller H, Olling M, Shah VP, Barends DM. 2004. Biowaiver monographs for immediate release solid oral dosage forms based on Biopharmaceutics Classification System (BCS). Literature data: Verapamil Hydrochloride, Propranolol Hydrochloride, and Atenolol. J Pharm Sci 93:1945-1956. (Pubitemid 39045477)
    • (2004) Journal of Pharmaceutical Sciences , vol.93 , Issue.8 , pp. 1945-1956
    • Vogelpoel, H.1    Welink, J.2    Amidon, G.L.3    Junginger, H.E.4    Midha, K.K.5    Moller, H.6    Olling, M.7    Shah, V.P.8    Barends, D.M.9
  • 6
    • 23844542010 scopus 로고    scopus 로고
    • Biowaiver monographs for immediate release solid oral dosage forms based on biopharmaceutics classification system (BCS) literature data: Chloroquine phosphate, chloroquine sulfate, and chloroquine hydrochloride
    • Verbeeck RK, Junginger HE, Midha KK, Shah VP, Barends DM. 2005. Biowaiver monographs for immediate release solid oral dosage forms based on biopharmaceutics classification system (BCS) literature data: Chloroquine phosphate, chloroquine sulfate, and chloroquine hydrochloride. J Pharm Sci 94:1389-1395.
    • (2005) J Pharm Sci , vol.94 , pp. 1389-1395
    • Verbeeck, R.K.1    Junginger, H.E.2    Midha, K.K.3    Shah, V.P.4    Barends, D.M.5
  • 20
    • 70349328788 scopus 로고    scopus 로고
    • Sweetman S, editor. Electronic version Pharmaceutical Press, Thomson/MICROMEDEX, London, UK/Greenwood Village, Colorado
    • Sweetman S, editor. 2009. Martindale: The complete drug reference. Electronic version. Pharmaceutical Press, Thomson/MICROMEDEX, London, UK/Greenwood Village, Colorado.
    • (2009) Martindale: The Complete Drug Reference
  • 21
    • 0037472364 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersion of furosemide with TPGS
    • DOI 10.1016/S0378-5173(02)00586-0, PII S0378517302005860
    • Shin S-C, Kim J. 2003. Physicochemical characterization of solid dispersion of furosemide with TPGS. Int J Pharm 251:79-84. (Pubitemid 36071462)
    • (2003) International Journal of Pharmaceutics , vol.251 , Issue.1-2 , pp. 79-84
    • Shin, S.-C.1    Kim, J.2
  • 22
    • 0017090220 scopus 로고
    • Some aspects of the photochemical degradation of frusemide
    • Rowbotham PC, Stanford JB, Sugden JK. 1976. Some aspects of the photochemical degradation of frusemide. Pharm Acta Helv 51:304-307.
    • (1976) Pharm Acta Helv , vol.51 , pp. 304-307
    • Rowbotham, P.C.1    Stanford, J.B.2    Sugden, J.K.3
  • 23
    • 36048929111 scopus 로고    scopus 로고
    • Effect of pH on the solubility and release of furosemide from polyamidoamine (PAMAM) dendrimer complexes
    • DOI 10.1016/j.ijpharm.2007.05.039, PII S0378517307004693
    • Devarakonda B, Otto DP, Judefeind A, Hill RA, de Villiers M. 2007. Effect of pH on the solubility and release of furosemide from polyamidoamine (PAMAM) dendrimer complexes. Int J Pharm 345:142-153. (Pubitemid 350087542)
    • (2007) International Journal of Pharmaceutics , vol.345 , Issue.1-2 , pp. 142-153
    • Devarakonda, B.1    Otto, D.P.2    Judefeind, A.3    Hill, R.A.4    De Villiers, M.M.5
  • 26
    • 40549099693 scopus 로고    scopus 로고
    • Technical Report Series, No.937, 40th Report, Annex 7 of WHO Expert committee on specifications for pharmaceutical preparations accessed May 18, 2009
    • WHO. 2006. Multisource (generic) pharmaceutical products: Guidelines on registration requirements to establish interchangeability. Technical Report Series, No.937, 40th Report, Annex 7 of WHO Expert committee on specifications for pharmaceutical preparations. http://whqlibdoc.who.int/trs/WHO-TRS-937-eng. pdf. (accessed May 18, 2009).
    • (2006) Multisource (Generic) Pharmaceutical Products: Guidelines on Registration Requirements to Establish Interchangeability
  • 29
    • 67649932264 scopus 로고    scopus 로고
    • CPMP/EWP/QWP/1401/98 Rev.1. (accessed May 18, 2009)
    • EMEA. 2008. Draft Guideline on the Investigation of Bioequivalence. CPMP/EWP/QWP/1401/98 Rev.1. (accessed May 18, 2009). http://www.emea.europa.eu/ pdfs/human/qwp/140198enrev1.pdf.
    • (2008) Draft Guideline on the Investigation of Bioequivalence
  • 30
    • 85031332283 scopus 로고    scopus 로고
    • The United States Pharmacopeial Convention, Inc. USP;1; 32 - NF 27. Rockville MD 2085
    • The United States Pharmacopeial Convention, Inc. 2009. USP;1; 32 - NF 27. The United States Pharmacopeia - The National Formulary, Rockville MD 2085.
    • (2009) The United States Pharmacopeia - The National Formulary
  • 31
    • 0025261002 scopus 로고
    • Physicochemical characterization of furosemide modifications
    • Matsuda Y, Tatsumi E. 1990. Physicochemical characterization of furosemide modifications. Int J Pharm 60:11-26.
    • (1990) Int J Pharm , vol.60 , pp. 11-26
    • Matsuda, Y.1    Tatsumi, E.2
  • 33
    • 20344391910 scopus 로고    scopus 로고
    • Trends in solubility of polymorphs
    • Pudipeddi M, Serajuddin TM. 2005. Trends in solubility of polymorphs. J Pharm Sci 94:929-939.
    • (2005) J Pharm Sci , vol.94 , pp. 929-939
    • Pudipeddi, M.1    Serajuddin, T.M.2
  • 34
    • 33749075557 scopus 로고    scopus 로고
    • Molecular dynamics of solid furosemide (4-chloro-2-furfurylamino-5- sulfamoyl-benzoic acid) studied by NMR and DFT methods
    • DOI 10.1016/j.cplett.2006.08.080, PII S0009261406012413
    • Latosinska JN, Latosinska M, Medycki W, Osuchowicz J. 2006. Molecular dynamics of solid furosemide (4-chloro-2- furfurylamino-5-sulfamoyl-benzoic acid) studied by NMR and DFT methods. Chem Phy Lett 430:127-132. (Pubitemid 44465854)
    • (2006) Chemical Physics Letters , vol.430 , Issue.1-3 , pp. 127-132
    • Latosinska, J.N.1    Latosinska, M.2    Medycki, W.3    Osuchowicz, J.4
  • 35
    • 0033557581 scopus 로고    scopus 로고
    • Hydrophobicity of ionizable compounds. a theoretical study and measurements of diuretic octanol-water partition coefficients by countercurrent chromatography
    • Berthod A. 1999. Hydrophobicity of ionizable compounds. A theoretical study and measurements of diuretic octanol-water partition coefficients by countercurrent chromatography. Anal Chem 71:879-888.
    • (1999) Anal Chem , vol.71 , pp. 879-888
    • Berthod, A.1
  • 36
    • 1242292997 scopus 로고    scopus 로고
    • Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant
    • DOI 10.1016/j.chroma.2003.10.097
    • Ruiz-Angel MJ, Carda-Broch SC, García-Alvarez-coque MC, Berthod A. 2004. Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant. J Chromatogr A 1030:279-288. (Pubitemid 38221340)
    • (2004) Journal of Chromatography a , vol.1030 , Issue.1-2 , pp. 279-288
    • Ruiz-Angel, M.J.1    Carda-Broch, S.2    Garcia-Alvarez-Coque, M.C.3    Berthod, A.4
  • 38
    • 33749252978 scopus 로고    scopus 로고
    • 16th list, March accessed May 8, 2009
    • WHO.WHOmodel list of essential medicines. 16th list, March 2009. http://www.who.int/selection-medicines/committees/expert/17/WEB-unedited-16th- LIST.pdf. (accessed May 8, 2009).
    • (2009) WHOmodel List of Essential Medicines
  • 40
    • 85031339094 scopus 로고    scopus 로고
    • The Danish Medicines Agency accessed May 8, 2009
    • The Danish Medicines Agency. http://www.dkma.dk. (accessed May 8, 2009).
  • 41
    • 85031341952 scopus 로고    scopus 로고
    • accessed May 15, 2009
    • National Agency for Medicines. http://www.nam.fi. (accessed May 15, 2009).
  • 42
    • 85031335046 scopus 로고    scopus 로고
    • accessed May 15, 2009
    • VIDAL. Fiches médicaments. http://www.vidal.fr. (accessed May 15, 2009).
    • Fiches Médicaments
  • 43
    • 85031345359 scopus 로고    scopus 로고
    • accessed May 8, 2009
    • College ter Beoordeling van Geneesmiddelen-Medicines Evaluation Board. http://www.cbg-meb.nl. (accessed May 8, 2009).
  • 44
    • 85031337086 scopus 로고    scopus 로고
    • NorwegianMedicinesAgency accessed May 15, 2009
    • NorwegianMedicinesAgency. http://www.legemiddelverket.no. (accessed May 15, 2009).
  • 45
    • 85031339210 scopus 로고    scopus 로고
    • accessed May 15
    • Agencia Española de Medicamentos y Productos Sanitarios. http://www.agemed.es. (accessed May 15, 2009).
    • (2009)
  • 46
    • 85031339176 scopus 로고    scopus 로고
    • accessed May 15, 2009
    • Läkemedelsverket. http://www.lakemedelsverket.se. (accessed May 15, 2009).
  • 47
    • 85031343366 scopus 로고    scopus 로고
    • Datapharm Communications Ltd. accessed May 15, 2009
    • Datapharm Communications Ltd. http://www.medicines.org. uk. (accessed May 15, 2009).
  • 48
    • 85031339293 scopus 로고    scopus 로고
    • accessed May 15, 2009
    • DailyMed. http://www.dailymed.nlm.nih.gov. (accessed May 15, 2009).
  • 49
    • 0025238474 scopus 로고
    • Furosemide (frusemide). A pharmacokinetic/pharmacodynamic review (Part I)
    • Ponto LL, Schoenwald RD. 1990. Furosemide (frusemide). A pharmacokinetic/pharmacodynamic review (Part I). Clin Pharmacokinet 18:381-408.
    • (1990) Clin Pharmacokinet , vol.18 , pp. 381-408
    • Ponto, L.L.1    Schoenwald, R.D.2
  • 50
    • 0025367715 scopus 로고
    • Furosemide (frusemide). A pharmacokinetic/pharmacodynamic review (Part II)
    • Ponto LL, Schoenwald RD. 1990. Furosemide (frusemide). A pharmacokinetic/pharmacodynamic review (Part II). Clin Pharmacokinet 18:460-471.
    • (1990) Clin Pharmacokinet , vol.18 , pp. 460-471
    • Ponto, L.L.1    Schoenwald, R.D.2
  • 51
    • 0021236365 scopus 로고
    • Pharmacokinetics of furosemide in man after intravenous and oral administration. Application of moment analysis
    • Hammarlund MM, Paalzow LK, Odlind B. 1984. Pharmacokinetics of furosemide in man after intravenous and oral administration: Application of moment analysis. Eur J Clin Pharmacol 26:197-207. (Pubitemid 14130430)
    • (1984) European Journal of Clinical Pharmacology , vol.26 , Issue.2 , pp. 197-207
    • Hammarlund, M.M.1    Paalzow, L.K.2    Odlind, B.3
  • 53
    • 0021714621 scopus 로고
    • Implications of intraindividual variability in bioavailability studies of furosemide
    • DOI 10.1007/BF00556898
    • Grahnén A, Hammarlund M, Lundqvist T. 1984. Implications of intraindividual variability in bioavailability studies of furosemide. Eur J Clin Pharmacol 27:595-602. (Pubitemid 15176768)
    • (1984) European Journal of Clinical Pharmacology , vol.27 , Issue.5 , pp. 595-602
    • Grahnen, A.1    Hammarlund, M.2    Lundqvist, T.3
  • 54
    • 0018642661 scopus 로고
    • Gastrointestinal sites of furosemide absorption in rats
    • Chungi VS, Dittert LW, Smith RB. 1979. Gastrointestinal sites of furosemide absorption in rats. Int J Pharm 4:27-38.
    • (1979) Int J Pharm , vol.4 , pp. 27-38
    • Chungi, V.S.1    Dittert, L.W.2    Smith, R.B.3
  • 56
    • 0023874321 scopus 로고
    • Comparative bioavailability of furosemide from solution and 40 mg tablets with different dissolution characteristics following oral administration in normal men
    • Waller ES, Crismon M, Smith R, Bauga M, Doluisio J. 1988. Comparative bioavailability of furosemide from solution and 40mg tablets with different dissolution characteristics following oral administration in normal men. Biopharm Drug Dis 9:211-218. (Pubitemid 18079352)
    • (1988) Biopharmaceutics and Drug Disposition , vol.9 , Issue.2 , pp. 211-218
    • Waller, E.S.1    Crismon, M.L.2    Smith, R.V.3    Bauza, M.T.4    Doluisio, J.T.5
  • 59
    • 0018322365 scopus 로고
    • Clinical pharmacokinetics of frusemide
    • Cutler RE, Blair AD. 1979. Clinical pharmacokinetics of frusemide. Clin Pharmacokinet 4:279-296.
    • (1979) Clin Pharmacokinet , vol.4 , pp. 279-296
    • Cutler, R.E.1    Blair, A.D.2
  • 60
    • 0022632573 scopus 로고
    • Reduced bioavailability and effect of furosemide given with food
    • DOI 10.1007/BF00615967
    • Beermann B, Midskov C. 1986. Reduced bioavailability and effect of furosemide given with foof. Eur J Clin Pharmacol 29:725-727. (Pubitemid 16155749)
    • (1986) European Journal of Clinical Pharmacology , vol.29 , Issue.6 , pp. 725-727
    • Beermann, B.1    Midskov, C.2
  • 62
    • 0018948662 scopus 로고
    • Absorption and disposition of furosemide in healthy volunteers, measured with a metabolite- Specific assay
    • Smith DE, Lin ET, Benet LZ. 1980. Absorption and disposition of furosemide in healthy volunteers, measured with a metabolite- specific assay. Drug Metab Dis 8:337-342.
    • (1980) Drug Metab Dis , vol.8 , pp. 337-342
    • Smith, D.E.1    Lin, E.T.2    Benet, L.Z.3
  • 63
    • 0019952632 scopus 로고
    • Disposition and absolute bioavailability of furosemide in healthy males
    • DOI 10.1002/jps.2600711006
    • Waller E, Hamilton SF, Massarella JW, Sharanevych MA, Smith RV, Yakatan GJ, Doluisio JT. 1982. Disposition and absolute bioavailability of furosemide in healthy males. J Pharm Sci 71:1105-1108. (Pubitemid 12032671)
    • (1982) Journal of Pharmaceutical Sciences , vol.71 , Issue.10 , pp. 1105-1108
    • Waller, E.S.1    Hamilton, S.F.2    Massarella, J.W.3
  • 64
    • 0344383697 scopus 로고
    • Human effective permeability data for furosemide, hydrochlothiazide, ketoprofen and naproxen to be used in the proposed biopharmaceutical classification for IR products
    • Lennernas H, Knutson L, Knutson T, Lesko L, Salmonson T, Amidon GL. 1995. Human effective permeability data for furosemide, hydrochlothiazide, ketoprofen and naproxen to be used in the proposed biopharmaceutical classification for IR products. Pharm Res 12:S-396.
    • (1995) Pharm Res , vol.12
    • Lennernas, H.1    Knutson, L.2    Knutson, T.3    Lesko, L.4    Salmonson, T.5    Amidon, G.L.6
  • 66
    • 31344451056 scopus 로고    scopus 로고
    • Development and evaluation of an in vitro method for prediction of human drug absorption: II. Demonstration of the method suitability
    • DOI 10.1016/j.ejps.2005.11.005, PII S0928098705003350
    • Corti G, Maestrelli F, Cirri M, Zerrouk N, Mura P. 2006. Development and evaluation of an in vitro method for prediction of human drug absorption II. Demonstration on the method suitability. Eur J Pharm Sci 27:354-362. (Pubitemid 43143261)
    • (2006) European Journal of Pharmaceutical Sciences , vol.27 , Issue.4 , pp. 354-362
    • Corti, G.1    Maestrelli, F.2    Cirri, M.3    Zerrouk, N.4    Mura, P.5
  • 67
    • 33646478910 scopus 로고    scopus 로고
    • Prediction of the permeability of drugs through study on quantitative structure-permeability relationship
    • Jung SJ, Choi SO, Um SY, Il Kim JI, Choo HYP, Cho SYi, Chung SY. 2006. Prediction of the permeability of drugs through study on quantitative structure-permeability relationship. J Pharm Biom Anal 41:469-475.
    • (2006) J Pharm Biom Anal , vol.41 , pp. 469-475
    • Jung, S.J.1    Choi, S.O.2    Um, S.Y.3    Kim Il, J.I.4    Choo, H.Y.P.5    Syi, C.6    Chung, S.Y.7
  • 68
    • 0033014877 scopus 로고    scopus 로고
    • Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat Jejunum
    • Flanagan SD, Benet LZ. 1999. Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat Jejunum. Pharm Res 16:221-224.
    • (1999) Pharm Res , vol.16 , pp. 221-224
    • Flanagan, S.D.1    Benet, L.Z.2
  • 69
    • 0030792730 scopus 로고    scopus 로고
    • Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in the Caco-2 cell culture model
    • DOI 10.1023/A:1012111008617
    • Pade V, Stavchansky S. 1997. Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in Caco-2 cell culture model. Pharm Res 14:1210-1215. (Pubitemid 27432545)
    • (1997) Pharmaceutical Research , vol.14 , Issue.9 , pp. 1210-1215
    • Pade, V.1    Stavchansky, S.2
  • 70
    • 0035157333 scopus 로고    scopus 로고
    • Effect of common excipients on Caco-2 transport of low-permeability drugs
    • Rege BD, Yu LX, Hussain AS, Polli JE. 2001. Effect of common excipients on Caco-2 transport of low-permeability drugs. J Pharm Sci 90:1776-1786.
    • (2001) J Pharm Sci , vol.90 , pp. 1776-1786
    • Rege, B.D.1    Yu, L.X.2    Hussain, A.S.3    Polli, J.E.4
  • 71
    • 0033973754 scopus 로고    scopus 로고
    • Caco-2 versus Caco-2/HT29- MTX co-cultured cell lines: Permeabilities via diffusion, inside- and outside directed carrier-mediated transport
    • Hilgendorf C, Spahn-Langguth H, Regardh CG, Lipka E, Amidon GL, Langguth P. 2000. Caco-2 versus Caco-2/HT29- MTX co-cultured cell lines: Permeabilities via diffusion, inside- and outside directed carrier-mediated transport. J Pharm Sci 89:63-75.
    • (2000) J Pharm Sci , vol.89 , pp. 63-75
    • Hilgendorf, C.1    Spahn-Langguth, H.2    Regardh, C.G.3    Lipka, E.4    Amidon, G.L.5    Langguth, P.6
  • 72
    • 0032480901 scopus 로고    scopus 로고
    • Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. a multivariate data analysis approach
    • DOI 10.1021/jm9810102
    • Winiwarter S, Bonham NM, Ax F, Hallberg A, Lennernäs H, Karlén A. 1998. Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach. J Med Chem 41:4939-4949. (Pubitemid 28555452)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.25 , pp. 4939-4949
    • Winiwarter, S.1    Bonham, N.M.2    Ax, F.3    Hallberg, A.4    Lennernas, H.5    Karlen, A.6
  • 73
    • 33344459216 scopus 로고    scopus 로고
    • Influence of vitamin e TPGS poly(ethylene glycol) chain length on apical efflux transporters in Caco-2 cell monolayers
    • DOI 10.1016/j.jconrel.2005.11.005, PII S0168365905006474
    • Collnot EM, Baldes C, Wempe MF, Hyatt J, Navarro L, Edgar KJ, Friedrich Schaeffer U, Lehr CM. 2006. Influence of vitamin ETPGS poly(ethylene glycol) chain length on apical efflux transporters in Caco-2 cell monolayers. J Control Release 111:35-40. (Pubitemid 43289992)
    • (2006) Journal of Controlled Release , vol.111 , Issue.1-2 , pp. 35-40
    • Collnot, E.-M.1    Baldes, C.2    Wempe, M.F.3    Hyatt, J.4    Navarro, L.5    Edgar, K.J.6    Schaefer, U.F.7    Lehr, C.-M.8
  • 76
    • 0019274525 scopus 로고
    • Bioequivalence studies with furosemide
    • HabermannW, Rudolph F. 1980. Bioequivalence studies with furosemide. N Z Med J 92:476.
    • (1980) N Z Med J , vol.92 , pp. 476
    • Habermann, W.1    Rudolph, F.2
  • 77
    • 0021243165 scopus 로고
    • Comparative bioavailability of two furosemide formulations in humans
    • Martin BK, Uihlein M, Ings RM, Stevens LA, McEwen J. 1984. Comparative bioavailability of two furosemide formulations in humans. J Pharm Sci 73:437-441. (Pubitemid 14134313)
    • (1984) Journal of Pharmaceutical Sciences , vol.73 , Issue.4 , pp. 437-441
    • Martin, B.K.1    Uihlein, M.2    Ings, R.M.J.3
  • 83
    • 85031337430 scopus 로고    scopus 로고
    • BioINequivalence: Concept and Definition
    • accessed October 25, 2009
    • Yu LX. 2004. BioINequivalence: Concept and Definition. ACPS Meeting, October 19-20. http://www.fda.gov/ohrms/dockets/ac/04/slides/2004-4078 S2-07-YU.ppt. (accessed October 25, 2009).
    • (2004) ACPS Meeting, October 19-20
    • Yu, L.X.1
  • 85
    • 0018214750 scopus 로고
    • The effect of four tablet binders on the bioavailability of frusemide from 40MG tablets
    • Rubinstein MH, Rughani JM. 1978. The effect of four tablet binders on the bioavailability of frusemide from 40MG tablets. Drug Dev Ind Pharm 4:541-553. (Pubitemid 9123621)
    • (1978) Drug Development and Industrial Pharmacy , vol.4 , Issue.6 , pp. 541-553
    • Rubinstein, M.H.1    Rughani, J.M.2
  • 86
    • 0019986952 scopus 로고
    • The pharmaceutical and biological availability of commercial preparations of furosemide
    • Stüber W, Mutschler E, Steinbach D. 1982. The pharmaceutical and biological availability of commercial preparations of furosemide. Arzneimittelforschung Drug Res 32:693-697. (Pubitemid 12092988)
    • (1982) Arzneimittel-Forschung/Drug Research , vol.32 , Issue.6 , pp. 693-697
    • Stuber, W.1    Mutschler, E.2    Steinbach, D.3
  • 87
    • 0019949690 scopus 로고
    • Dissolution medium - A critical parameter to identify bioavailability problems of furosemide tablets
    • Prasad VK, Rapaka RS, Knight PW, Cabana BE. 1982. Dissolution medium - A critical parameter to identify bioavailability problems of furosemide tablets. Int J Pharm 11:81-90.
    • (1982) Int J Pharm , vol.11 , pp. 81-90
    • Prasad, V.K.1    Rapaka, R.S.2    Knight, P.W.3    Cabana, B.E.4
  • 88
    • 0021281479 scopus 로고
    • An in-vivo - In-vitro correlation for the bioavailability of frusemide tablets
    • Kingsford M, Eggers NJ, Soteros G. 1984. An in vivo-in vitro correlation for the bioavailability of frusemide tablets. J Pharm Pharmacol 36:536-538. (Pubitemid 14096775)
    • (1984) Journal of Pharmacy and Pharmacology , vol.36 , Issue.8 , pp. 536-538
    • Kingsford, M.1    Eggers, N.J.2    Soteros, G.3
  • 89
    • 0031704891 scopus 로고    scopus 로고
    • Assessment of pharmaceutical quality of furosemide tablets from multinational markets
    • Qureshi SA, McGilveray IJ. 1998. Assessment of pharmaceutical quality of furosemide tablets from multinational markets. Drug Dev Ind Pharm 24:995-1005.
    • (1998) Drug Dev Ind Pharm , vol.24 , pp. 995-1005
    • Qureshi, S.A.1    McGilveray, I.J.2
  • 91
    • 0024547591 scopus 로고
    • Furosemide pharmacokinetics and pharmacodynamics in health and disease - An update
    • DOI 10.1007/BF01059086
    • Hammarlund-Idemaes M, Benet LZ. 1989. Furosemide pharmacokinetics and pharmacodynamics in health and disease - An update. J Biopharmacokinet Biopharm 17:1-46. (Pubitemid 19111988)
    • (1989) Journal of Pharmacokinetics and Biopharmaceutics , vol.17 , Issue.1 , pp. 1-46
    • Hammarlund-Udenaes, M.1    Benet, L.Z.2
  • 92
    • 0035286778 scopus 로고    scopus 로고
    • Caco-2 monolayers in experimental and theoretical predictions of drug transport
    • DOI 10.1016/S0169-409X(00)00128-9, PII S0169409X00001289
    • Artursson P, Palm K, Luthaman K. 2001. Caco-2 monolayers in experimental and theoretical predictions of drug transport. Adv Drug Del Rev 46:27-43. (Pubitemid 33653412)
    • (2000) Advanced Drug Delivery Reviews , vol.46 , Issue.1-3 , pp. 27-43
    • Artursson, P.1    Palm, K.2    Luthman, K.3
  • 93
    • 0348107338 scopus 로고    scopus 로고
    • Quantitative Biopharmaceutics Classification System: The Central Role of Dose/Solubility Ratio
    • DOI 10.1023/B:PHAM.0000008037.57884.11
    • Rinaki E, Valsami G, Macheras P. 2003. Quantitative biopharmaceutics classification system: The central role of dose/ solubility ratio. Pharm Res 20:1917-1925. (Pubitemid 38005521)
    • (2003) Pharmaceutical Research , vol.20 , Issue.12 , pp. 1917-1925
    • Rinaki, E.1    Valsami, G.2    Macheras, P.3
  • 94
    • 0031780682 scopus 로고    scopus 로고
    • Correlation between oral drug absorption in humans, and apparent drug permeability in TC-7 cells, a human epithelial intestinal cell line: Comparison with the parental Caco-2 cell line
    • DOI 10.1023/A:1011919003030
    • Gres M-C, Julian B, Bourre M, Meunier V, Roques C, Berger M, Boulenc X, Berger Y, Fabre G. 1998. Correlation between oral drug absorption in humans and apparent drug permeability in TC-7 cells, a human epithelial intestinal cell line: Comparison with the parental Caco-2 cell line. Pharm Res 15:726-733. (Pubitemid 28275649)
    • (1998) Pharmaceutical Research , vol.15 , Issue.5 , pp. 726-733
    • Gres, M.-C.1    Julian, B.2    Bourrie, M.3    Meunier, V.4    Roques, C.5    Berger, M.6    Boulenc, X.7    Berger, Y.8    Fabre, G.9
  • 95
    • 3843097202 scopus 로고    scopus 로고
    • Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system
    • DOI 10.1016/j.ejpb.2004.03.001, PII S0939641104000438
    • Lindenberg M, Kopp S, Dressman JB. 2004. Classification of orally administered drugs on the World Health Organization model list of essential medicines according to the biopharmaceutics classification system. Eur J Pham Biopharm 58:265-278. (Pubitemid 39037234)
    • (2004) European Journal of Pharmaceutics and Biopharmaceutics , vol.58 , Issue.2 , pp. 265-278
    • Lindenberg, M.1    Kopp, S.2    Dressman, J.B.3
  • 96
    • 17644380257 scopus 로고    scopus 로고
    • Predicting drug disposition via application of BCS: Transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system
    • Wu C-Y, Benet LZ. 2005. Predicting drug disposition via application of BCS: Transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res 22:11-23.
    • (2005) Pharm Res , vol.22 , pp. 11-23
    • Wu, C.-Y.1    Benet, L.Z.2
  • 97
    • 0038300714 scopus 로고    scopus 로고
    • Therapeutic and toxic blood concentrations of more than 800 drugs and other xenobiotics
    • Schulz M, Schmoldt A. 2003. Therapeutic and toxic blood concentrations of more than 800 drugs and other xenobiotics. Pharmazie 58:447-474. (Pubitemid 36869876)
    • (2003) Pharmazie , vol.58 , Issue.7 , pp. 447-474
    • Schulz, M.1    Schmoldt, A.2
  • 98
    • 85031344379 scopus 로고    scopus 로고
    • Code of Federal Regulations. Title 21, Part 320 accessed May 18, 2009
    • FDA. Code of Federal Regulations. Title 21, Part 320: Bioavailability and Bioequivalence requirements. Section 320.33. 2003. http://www.accessdata.fda. gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=320.33. (accessed May 18, 2009).
    • (2003) Bioavailability and Bioequivalence Requirements. Section 320.33.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.