-
1
-
-
84885544150
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
-
11
-
-
34249701272
-
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. Waiver for In Vivo Bioavailability and Bioequivalence Studies for Immediate Release Solid Oral Dosage Form Based on a Biopharmaceutics Classification System, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville, MD, August 2000.
-
(2000)
Waiver for In Vivo Bioavailability and Bioequivalence Studies for Immediate Release Solid Oral Dosage Form Based on a Biopharmaceutics Classification System
-
-
-
12
-
-
33746101876
-
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
-
14
-
-
41549083263
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
41
-
-
0022394657
-
Dissolution of carboxylic acids III: effect of polyionizable buffers
-
Aunins JG, Southard MZ, Meyers RA, Himmelstein KJ, Stella VJ. Dissolution of carboxylic acids III: effect of polyionizable buffers. J. Pharm. Sci. 1985;74:1305-1316.
-
(1985)
J. Pharm. Sci.
, vol.74
, pp. 1305-1316
-
-
Aunins, J.G.1
Southard, M.Z.2
Meyers, R.A.3
Himmelstein, K.J.4
Stella, V.J.5
-
42
-
-
0024784657
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
50
-
-
43249127225
-
Using biorelevant dissolution to obtain IVIVC of solid dosage forms containing a poorlysoluble model compound
-
Lue BM, Nielsen FS, Magnussen T, Schou HM, Krisensen K, Jacobsen LO, Mullertz A. Using biorelevant dissolution to obtain IVIVC of solid dosage forms containing a poorlysoluble model compound. Eur. Pharm. Biopharm. 2008; 69:648-657.
-
(2008)
Eur. Pharm. Biopharm.
, vol.69
, pp. 648-657
-
-
Lue, B.M.1
Nielsen, F.S.2
Magnussen, T.3
Schou, H.M.4
Krisensen, K.5
Jacobsen, L.O.6
Mullertz, A.7
-
51
-
-
84962053078
-
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
-
52
-
-
84962119086
-
Analytical performance of a fiber optic probes dissolution system
-
November
-
Bynum K,Roinestad K, KassisA, Procreva J,Gehriein L, Cheng F, Palermo P.Analytical performance of a fiber optic probes dissolution system, Dissolution Technologies, November 2001, pp. 13-22.
-
(2001)
Dissolution Technologies
, pp. 13-22
-
-
Bynum, K.1
Roinestad, K.2
Kassis, A.3
Procreva, J.4
Gehriein, L.5
Cheng, F.6
Palermo, P.7
-
53
-
-
77954678690
-
Technical evaluation of a fiber-optic probe dissolution system
-
Liu L,Fitzgerald G, Embry M, Cantu R, Pack B.Technical evaluation of a fiber-optic probe dissolution system, Dissolution Technologies, 2008, pp. 10-20.
-
(2008)
Dissolution Technologies
, pp. 10-20
-
-
Liu, L.1
Fitzgerald, G.2
Embry, M.3
Cantu, R.4
Pack, B.5
-
54
-
-
84885489917
-
-
U.S. Pharmacopoeia 31, Rockville, MD.
-
U.S. Pharmacopoeia 31, Rockville, MD.
-
-
-
|