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Volumn , Issue , 2010, Pages 245-256

Dissolution Testing: In Vitro Characterizatio of Oral Controlled Release Dosage Forms

Author keywords

Dissolution testing in vitro characterization of oral controlled release dosage forms; Dissolution testing, integral part of pharmaceutical development and batch quality assurance for product safety and efficacy; Dissolution, vital part of pharmaceutical development for controlled release formulation

Indexed keywords


EID: 84885536012     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9780470640487.ch15     Document Type: Chapter
Times cited : (4)

References (54)
  • 1
    • 84885544150 scopus 로고    scopus 로고
    • Guidance for Industry
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, September .
    • Guidance for Industry. SUPAC-MR: Modified Release Solid Oral Dosage Forms, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, September 1997.
    • (1997) SUPAC-MR: Modified Release Solid Oral Dosage Forms
  • 2
    • 0006176150 scopus 로고    scopus 로고
    • Guidance for Industry
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, September .
    • Guidance for Industry. Extended Release Oral Dosage Forms: Development, Evaluation and Application of In- Vitro/In-Vivo correlations, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, September 1997.
    • (1997) Extended Release Oral Dosage Forms: Development, Evaluation and Application of In- Vitro/In-Vivo correlations
  • 3
    • 0034212876 scopus 로고    scopus 로고
    • Swellable matrices for controlled drug delivery: gel-layer behavior, mechanisms and optimal performance
    • Colombo P, Bettini R, Santi P, Peppas NA. Swellable matrices for controlled drug delivery: gel-layer behavior, mechanisms and optimal performance. Pharm. Sci. Technol. Today 2000; 3(6):198-204.
    • (2000) Pharm. Sci. Technol. Today , vol.3 , Issue.6 , pp. 198-204
    • Colombo, P.1    Bettini, R.2    Santi, P.3    Peppas, N.A.4
  • 4
    • 51449120732 scopus 로고    scopus 로고
    • Effect of drug solubility on polymer hydration and drug dissolution from polyethylene oxide (PEO) matrix tablets
    • Li H, Hardy RJ, Gu X. Effect of drug solubility on polymer hydration and drug dissolution from polyethylene oxide (PEO) matrix tablets. AAPS PharmSciTech 2008;9(2): 437-443.
    • (2008) AAPS Pharm Sci Tech , vol.9 , Issue.2 , pp. 437-443
    • Li, H.1    Hardy, R.J.2    Gu, X.3
  • 5
    • 0032899524 scopus 로고    scopus 로고
    • Properties of sustained-release tablets prepared by hot-melt extrusion
    • Zhang F, McGinity JW. Properties of sustained-release tablets prepared by hot-melt extrusion. Pharm. Dev. Technol. 1999; 4(2):241-250.
    • (1999) Pharm. Dev. Technol. , vol.4 , Issue.2 , pp. 241-250
    • Zhang, F.1    McGinity, J.W.2
  • 6
    • 0027428857 scopus 로고
    • Prediction of drug release from hydroxypropyl methylcellulose (HPMC) matrices: effect of polymer concentration
    • Shah N, Zhang GH. Prediction of drug release from hydroxypropyl methylcellulose (HPMC) matrices: effect of polymer concentration. Pharm. Res. 1993;10(12):1693-1695.
    • (1993) Pharm. Res. , vol.10 , Issue.12 , pp. 1693-1695
    • Shah, N.1    Zhang, G.H.2
  • 7
    • 0027249440 scopus 로고
    • Zero-order drug release from hydrocolloid matrices
    • Mockeland JE, Lippold BC. Zero-order drug release from hydrocolloid matrices. J. Pharm. Sci. 1993;10(7):1066-1070.
    • (1993) J. Pharm. Sci. , vol.10 , Issue.7 , pp. 1066-1070
    • Mockeland, J.E.1    Lippold, B.C.2
  • 8
    • 0031913402 scopus 로고    scopus 로고
    • Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms
    • Dressman JB, Amidon G, Reppas C, Shah VP. Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms. Pharm. Res. 1998;15(1):11-22.
    • (1998) Pharm. Res. , vol.15 , Issue.1 , pp. 11-22
    • Dressman, J.B.1    Amidon, G.2    Reppas, C.3    Shah, V.P.4
  • 9
    • 0028948839 scopus 로고
    • A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
    • Amiden GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 1995;12(3):413-420.
    • (1995) Pharm. Res. , vol.12 , Issue.3 , pp. 413-420
    • Amiden, G.L.1    Lennernas, H.2    Shah, V.P.3    Crison, J.R.4
  • 10
    • 78149235691 scopus 로고    scopus 로고
    • Guidance for Industry
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, August .
    • Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, August 1997.
    • (1997) Dissolution Testing of Immediate Release Solid Oral Dosage Forms
  • 12
    • 33746101876 scopus 로고    scopus 로고
    • Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-a technical note
    • Jamzad S, Fassihi R. Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-a technical note. AAPS PharmSciTech 2006;7(2):E1-E6.
    • (2006) AAPS Pharm Sci Tech , vol.7 , Issue.2
    • Jamzad, S.1    Fassihi, R.2
  • 13
    • 0037006928 scopus 로고    scopus 로고
    • Dissolution testing of a poorly soluble compound using the flow-through cell apparatus
    • Battchar SN Wesley JA Fioritto A, Martin PJ Babu SR. Dissolution testing of a poorly soluble compound using the flow-through cell apparatus. Int. J. Pharm. 2002; 236:135-143.
    • (2002) Int. J. Pharm. , vol.236 , pp. 135-143
    • Battchar, S.N.1    Wesley, J.A.2    Fioritto, A.3    Martin, P.J.4    Babu, S.R.5
  • 14
    • 41549083263 scopus 로고    scopus 로고
    • Development of a discriminating in vitro dissolution method for a poorly soluble NO-donating selective cyclooxygenase-2 inhibitor
    • Papp R, Luk P, Mullett WM Kwong E, Debnath S, Thibert R. Development of a discriminating in vitro dissolution method for a poorly soluble NO-donating selective cyclooxygenase-2 inhibitor. J. Pharm. Biomed. Anal. 2008;47:16-22.
    • (2008) J. Pharm. Biomed. Anal. , vol.47 , pp. 16-22
    • Papp, R.1    Luk, P.2    Mullett, W.M.3    Kwong, E.4    Debnath, S.5    Thibert, R.6
  • 15
    • 0036913259 scopus 로고    scopus 로고
    • Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs
    • Rasenack N, Muller BW. Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs. Pharm. Res. 2002;19(12):1894-1900.
    • (2002) Pharm. Res. , vol.19 , Issue.12 , pp. 1894-1900
    • Rasenack, N.1    Muller, B.W.2
  • 16
    • 0037074121 scopus 로고    scopus 로고
    • The impact of low levels of amorphous material (<5%) on the blending characteristics of a direct compression formulation
    • Machin L, Sartnurak S, Thomas I, Moore S. The impact of low levels of amorphous material (<5%) on the blending characteristics of a direct compression formulation. Int. J. Pharm. 2002;231:213-226.
    • (2002) Int. J. Pharm. , vol.231 , pp. 213-226
    • Machin, L.1    Sartnurak, S.2    Thomas, I.3    Moore, S.4
  • 17
    • 0032531665 scopus 로고    scopus 로고
    • Determination of surface properties and flow characteristics of salbutamol sulphate, before and after micronisation
    • Feeley JC, York P, Sumby BS, Dicks H. Determination of surface properties and flow characteristics of salbutamol sulphate, before and after micronisation. Int. J. Pharm. 1998; 172:89-96.
    • (1998) Int. J. Pharm. , vol.172 , pp. 89-96
    • Feeley, J.C.1    York, P.2    Sumby, B.S.3    Dicks, H.4
  • 18
    • 0035937590 scopus 로고    scopus 로고
    • Nanoparticulate systems for improved drug delivery
    • Kaqashima Y. Nanoparticulate systems for improved drug delivery. Adv. Drug Deliv. Rev. 2001;47(1):1-2.
    • (2001) Adv. Drug Deliv. Rev. , vol.47 , Issue.1 , pp. 1-2
    • Kaqashima, Y.1
  • 19
    • 43949120725 scopus 로고    scopus 로고
    • Development and validation of dissolution test for lopinavir, a poorly water-soluble drug, in soft gel capsules, based on in vivo data
    • Donato EM, Martins LA, Froehlich PE, Bergold AM. Development and validation of dissolution test for lopinavir, a poorly water-soluble drug, in soft gel capsules, based on in vivo data. J. Pharm. Biomed. Anal. 2008;47:547-552.
    • (2008) J. Pharm. Biomed. Anal. , vol.47 , pp. 547-552
    • Donato, E.M.1    Martins, L.A.2    Froehlich, P.E.3    Bergold, A.M.4
  • 20
    • 84962050781 scopus 로고    scopus 로고
    • New and extended applications for USP drug release apparatus 3
    • Dissolution Technologies, February
    • Borst I, Ugwu S, Beckett AH.New and extended applications for USP drug release apparatus 3, Dissolution Technologies, February 1997, pp. 11-18.
    • (1997) , pp. 11-18
    • Borst, I.1    Ugwu, S.2    Beckett, A.H.3
  • 21
    • 43249100112 scopus 로고    scopus 로고
    • Dissolution test for site-specific release ionized pellets in USP apparatus (reciprocating cylinder): optimization using response surface methodology
    • Joshi A, Pund S, Nivsarkar M, Vasu K, Shishoo C. Dissolution test for site-specific release ionized pellets in USP apparatus (reciprocating cylinder): optimization using response surface methodology. Eur. J. Pharm. Biopharm. 2008;69: 769-775.
    • (2008) Eur. J. Pharm. Biopharm. , vol.69 , pp. 769-775
    • Joshi, A.1    Pund, S.2    Nivsarkar, M.3    Vasu, K.4    Shishoo, C.5
  • 22
    • 0030906756 scopus 로고    scopus 로고
    • USP dissolution apparatus 3 (reciprocating cylinder) for screening of guar-based colonic delivery formulations
    • Wong D, Larrabee S, Clifford K, Tremblay J, Friend DR. USP dissolution apparatus 3 (reciprocating cylinder) for screening of guar-based colonic delivery formulations. J. Control. Release 1997;47:173-179.
    • (1997) J. Control. Release , vol.47 , pp. 173-179
    • Wong, D.1    Larrabee, S.2    Clifford, K.3    Tremblay, J.4    Friend, D.R.5
  • 23
    • 23144459633 scopus 로고    scopus 로고
    • vitro evaluation of dissolution behavior for a colon-specific drug delivery system (CODES™) in multi-pH media using United States pharmacopoeia apparatus II and III
    • article 33
    • Li J, Yang L, Ferguson SM, Hudson TJ, Watanabe S, Katsuma M, Fix JA. In vitro evaluation of dissolution behavior for a colon-specific drug delivery system (CODES™) in multi-pH media using United States pharmacopoeia apparatus II and III. AAPS PharmSciTech 2002;3(4): article 33.
    • (2002) AAPS Pharm Sci Tech , vol.3 , Issue.4
    • Li, J.1    Yang, L.2    Ferguson, S.M.3    Hudson, T.J.4    Watanabe, S.5    Katsuma, M.6    Fix, J.A.7
  • 24
    • 23144440784 scopus 로고    scopus 로고
    • Comparison of the dissolution of metaxalone tablets (Skelaxin) using USP apparatus 2 and 3
    • article 6
    • Cacace J, Reilly EE, Amann A. Comparison of the dissolution of metaxalone tablets (Skelaxin) using USP apparatus 2 and 3. AAPS PharmSciTech 2004;5(1): article 6.
    • (2004) AAPS Pharm Sci Tech , vol.5 , Issue.1
    • Cacace, J.1    Reilly, E.E.2    Amann, A.3
  • 25
    • 15044361803 scopus 로고    scopus 로고
    • Release characteristic of dimenhydrinate from an eroding and swelling matrix: selection of appropriate dissolution apparatus
    • Missaghi S, Fassihi R. Release characteristic of dimenhydrinate from an eroding and swelling matrix: selection of appropriate dissolution apparatus. Int. J. Pharm. 2005;293:35-42.
    • (2005) Int. J. Pharm. , vol.293 , pp. 35-42
    • Missaghi, S.1    Fassihi, R.2
  • 26
    • 0037413414 scopus 로고    scopus 로고
    • Assessment of oral availability enhancing approaches of SB-using flow through cell dissolution testing as one of the screens
    • Perng CY, Kearney AS, Palepu NR, Smith BR, Azzarano LM. Assessment of oral availability enhancing approaches of SB-using flow through cell dissolution testing as one of the screens. Int. J. Pharm. 2003;250:147-156.
    • (2003) Int. J. Pharm. , vol.250 , pp. 147-156
    • Perng, C.Y.1    Kearney, A.S.2    Palepu, N.R.3    Smith, B.R.4    Azzarano, L.M.5
  • 27
    • 48749094715 scopus 로고    scopus 로고
    • In-vitro-in-vivo correlation of wet milled tablet of poorly soluble cilostazol
    • Jinno J, et al. In-vitro-in-vivo correlation of wet milled tablet of poorly soluble cilostazol. J. Control. Release 2008;130(1): 29-37.
    • (2008) J. Control. Release , vol.130 , Issue.1 , pp. 29-37
    • Jinno, J.1
  • 28
    • 0034713283 scopus 로고    scopus 로고
    • Predicting of dissolution though hydrodynamics: salicylic acid tablets in flowthrough cell dissolution
    • Cammarn SR, Sakr A. Predicting of dissolution though hydrodynamics: salicylic acid tablets in flowthrough cell dissolution. Int. J. Pharm. 2000;201:199-209.
    • (2000) Int. J. Pharm. , vol.201 , pp. 199-209
    • Cammarn, S.R.1    Sakr, A.2
  • 29
    • 34247516835 scopus 로고    scopus 로고
    • Permeability assessment for solid oral drug formulations based on Caco-2 monolayer in combination with a flow through dissolution cell
    • Motz SA, Schaefer UF, Balbach S, Eichinger T, Lehr C-M. Permeability assessment for solid oral drug formulations based on Caco-2 monolayer in combination with a flow through dissolution cell. Eur. J. Pharm. Biopharm. 2007;66:286-295.
    • (2007) Eur. J. Pharm. Biopharm. , vol.66 , pp. 286-295
    • Motz, S.A.1    Schaefer, U.F.2    Balbach, S.3    Eichinger, T.4    Lehr, C.-M.5
  • 30
    • 84962086952 scopus 로고    scopus 로고
    • The effects of buffer molarity, agitation rate, and mesh size on verapamil release from modified-release mini-tablets using USP apparatus 3
    • Dissolution Technologies, May
    • Khamanga SMM, Walker RB. The effects of buffer molarity, agitation rate, and mesh size on verapamil release from modified- release mini-tablets using USP apparatus 3, Dissolution Technologies, May 2007, pp. 19-23.
    • (2007) , pp. 19-23
    • Khamanga, S.M.M.1    Walker, R.B.2
  • 31
    • 39149118920 scopus 로고    scopus 로고
    • Velocity distribution and shear rate variability resulting from changes in the impeller location in the USP dissolution testing apparatus II
    • Bai G, Armenante PM. Velocity distribution and shear rate variability resulting from changes in the impeller location in the USP dissolution testing apparatus II. Pharm. Res. 2008; 25(2):320-336.
    • (2008) Pharm. Res. , vol.25 , Issue.2 , pp. 320-336
    • Bai, G.1    Armenante, P.M.2
  • 32
    • 0037413390 scopus 로고    scopus 로고
    • Measurement of agitation force in dissolution test and mechanical destructive force in disintegration test
    • Kamba M, Seta Y, Takeda N, Hamaura T, Kusai A, Nakane H, Nishimura K. Measurement of agitation force in dissolution test and mechanical destructive force in disintegration test. Int. J. Pharm. 2003;250:99-109.
    • (2003) Int. J. Pharm. , vol.250 , pp. 99-109
    • Kamba, M.1    Seta, Y.2    Takeda, N.3    Hamaura, T.4    Kusai, A.5    Nakane, H.6    Nishimura, K.7
  • 33
    • 0017128216 scopus 로고
    • Effects of various hydrodynamic conditions on dissolution rate determinations
    • Underwood FL, Cadwallader DE. Effects of various hydrodynamic conditions on dissolution rate determinations. J. Pharm. Sci. 1976;65:697-700.
    • (1976) J. Pharm. Sci. , vol.65 , pp. 697-700
    • Underwood, F.L.1    Cadwallader, D.E.2
  • 34
    • 84974601997 scopus 로고    scopus 로고
    • Evaluation of dissolution hydrodynamics in the USP, Peak™ and flat-bottom vessels using different solubility drugs
    • Mirza T, Joshi Y, Liu Q, Vivilecchia R. Evaluation of dissolution hydrodynamics in the USP, Peak™ and flat-bottom vessels using different solubility drugs. Dissolution Technologies 2005, 11-16.
    • (2005) Dissolution Technologies , pp. 11-16
    • Mirza, T.1    Joshi, Y.2    Liu, Q.3    Vivilecchia, R.4
  • 35
    • 84962062605 scopus 로고    scopus 로고
    • Comparative evaluation of mixing dynamics in USP apparatus 2 using standard USP vessels and Peak™ vessels
    • May
    • Collins CC, Nair RR. Comparative evaluation of mixing dynamics in USP apparatus 2 using standard USP vessels and Peak™ vessels, Dissolution Technologies, May 1998, pp. 17-21.
    • (1998) Dissolution Technologies , pp. 17-21
    • Collins, C.C.1    Nair, R.R.2
  • 36
    • 0029046476 scopus 로고
    • USP dissolution apparatus 3 (reciprocating cylinder): instrument parameter effects on drug release from sustained release formulations
    • Rohrs BR, Bruch-Clark DL Witt MJ, Stelzer DJ. USP dissolution apparatus 3 (reciprocating cylinder): instrument parameter effects on drug release from sustained release formulations. J. Pharm. Sci. 1995;84:922-926.
    • (1995) J. Pharm. Sci. , vol.84 , pp. 922-926
    • Rohrs, B.R.1    Bruch-Clark, D.L.2    Witt, M.J.3    Stelzer, D.J.4
  • 37
    • 33750151347 scopus 로고    scopus 로고
    • Solubilization and dissolution of insoluble weak acid, ketoprofen: effects of pH combined with surfactant
    • Sheng JJ, Kasim NA, Chandrasekharan R, Amidon GL. Solubilization and dissolution of insoluble weak acid, ketoprofen: effects of pH combined with surfactant. Eur. J. Pharm. Sci. 2006;29:306-314.
    • (2006) Eur. J. Pharm. Sci. , vol.29 , pp. 306-314
    • Sheng, J.J.1    Kasim, N.A.2    Chandrasekharan, R.3    Amidon, G.L.4
  • 38
    • 0024232705 scopus 로고
    • Reaction plane approach for estimating the effects of buffers on the dissolution rate of acidic drugs
    • McNamara DP, Amidon GL. Reaction plane approach for estimating the effects of buffers on the dissolution rate of acidic drugs. J. Pharm. Sci. 1988;77:511-517.
    • (1988) J. Pharm. Sci. , vol.77 , pp. 511-517
    • McNamara, D.P.1    Amidon, G.L.2
  • 39
    • 1642457354 scopus 로고    scopus 로고
    • Effect of sodium lauryl sulfate in dissolution media on dissolution of hard gelatin capsule shells
    • Zhao F, Malayev V, Rao V, Hussain M. Effect of sodium lauryl sulfate in dissolution media on dissolution of hard gelatin capsule shells. Pharm. Res. 2004;21:144-148.
    • (2004) Pharm. Res. , vol.21 , pp. 144-148
    • Zhao, F.1    Malayev, V.2    Rao, V.3    Hussain, M.4
  • 42
    • 0024784657 scopus 로고
    • Influence of he buffering capacity of the medium on the dissolution of he drug excipient mixtures
    • Ramtoola Z, Corrigan OI. Influence of he buffering capacity of the medium on the dissolution of he drug excipient mixtures. Drug Dev. Ind. Pharm. 1989;15:2359-2374.
    • (1989) Drug Dev. Ind. Pharm. , vol.15 , pp. 2359-2374
    • Ramtoola, Z.1    Corrigan, O.I.2
  • 43
    • 0142042438 scopus 로고    scopus 로고
    • Use of a physiological bicarbonate buffer system for dissolution characterization of ionizable drugs
    • McNamara DP, Whitney KM, Goss SL. Use of a physiological bicarbonate buffer system for dissolution characterization of ionizable drugs. Pharm. Res. 2003;20:1641-1646.
    • (2003) Pharm. Res. , vol.20 , pp. 1641-1646
    • McNamara, D.P.1    Whitney, K.M.2    Goss, S.L.3
  • 44
    • 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, Horter D, Lobenberg R, Reppas C, Dressman JB. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm. Res. 1998;15:698-705.
    • (1998) Pharm. Res. , vol.15 , pp. 698-705
    • Galia, E.1    Nicolaides, E.2    Horter, D.3    Lobenberg, R.4    Reppas, C.5    Dressman, J.B.6
  • 45
    • 0034080127 scopus 로고    scopus 로고
    • Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide
    • Lobenberg R, Kramer J, Shah VP, Amidon GL, Dressman JB. Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide. Pharm. Res. 2000; 17(4):439-444.
    • (2000) Pharm. Res. , vol.17 , Issue.4 , pp. 439-444
    • Lobenberg, R.1    Kramer, J.2    Shah, V.P.3    Amidon, G.L.4    Dressman, J.B.5
  • 46
    • 0033452575 scopus 로고    scopus 로고
    • Forecasting in vivo performance of four low solubility drugs from their in vitro dissolution data.
    • Nicolaides E, Galia E, Efthymiopoulos C, Dressman JB, Reppas C. Forecasting in vivo performance of four low solubility drugs from their in vitro dissolution data. Pharm. Res. 1999; 16(12):1876-1882.
    • (1999) Pharm. Res. , vol.16 , Issue.12 , pp. 1876-1882
    • Nicolaides, E.1    Galia, E.2    Efthymiopoulos, C.3    Dressman, J.B.4    Reppas, C.5
  • 47
    • 0033805179 scopus 로고    scopus 로고
    • In vitro-in vivo corrections for lipophilic, poorly water-soluble drugs
    • Dressman JB, Reppas C. In vitro-in vivo corrections for lipophilic, poorly water-soluble drugs. Eur. J. Pharm. Sci. 2000;11(2):S73-S80.
    • (2000) Eur. J. Pharm. Sci. , vol.11 , Issue.2
    • Dressman, J.B.1    Reppas, C.2
  • 48
    • 0034948871 scopus 로고    scopus 로고
    • Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration
    • Nicolaides E, Symillides M, Dressman JB, Reppas C. Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration. Pharm. Res. 2001;18:380-388.
    • (2001) Pharm. Res. , vol.18 , pp. 380-388
    • Nicolaides, E.1    Symillides, M.2    Dressman, J.B.3    Reppas, C.4
  • 49
    • 44749087279 scopus 로고    scopus 로고
    • Dissolution media simulating conditions in the proximal human gastrointestinal tract: an update
    • Jantratid E, Janssen N, Reppas C, Dressman JB. Dissolution media simulating conditions in the proximal human gastrointestinal tract: an update. Pharm. Res. 2008;25(7):1663-1676.
    • (2008) Pharm. Res. , vol.25 , Issue.7 , pp. 1663-1676
    • Jantratid, E.1    Janssen, N.2    Reppas, C.3    Dressman, J.B.4
  • 51
    • 84962053078 scopus 로고    scopus 로고
    • In-situ dissolution testing using different UV fiber optic probes and instruments, Dissolution Technologies
    • November
    • Lu X, Lozano R, Shah P. In-situ dissolution testing using different UV fiber optic probes and instruments, Dissolution Technologies. November 2003 6-15.
    • (2003) , pp. 6-15
    • Lu, X.1    Lozano, R.2    Shah, P.3
  • 54
    • 84885489917 scopus 로고    scopus 로고
    • U.S. Pharmacopoeia 31, Rockville, MD.
    • U.S. Pharmacopoeia 31, Rockville, MD.


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