SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Martin Kuentz, Analytical technologies for real-time drug dissolution and precipitation testing on a small scale, Journal of Pharmacy and Pharmacology, 2014, 66, 10
  2. 2
    Andreas Niederquell, Martin Kuentz, Biorelevant dissolution of poorly soluble weak acids studied by UV imaging reveals ranges of fractal-like kinetics, International Journal of Pharmaceutics, 2014, 463, 1, 38

    CrossRef

  3. 3
    José Raúl Medina, Dulce Karina Salazar, Marcela Hurtado, Alma Rosa Cortés, Adriana Miriam Domínguez-Ramírez, Comparative in vitro dissolution study of carbamazepine immediate-release products using the USP paddles method and the flow-through cell system, Saudi Pharmaceutical Journal, 2014, 22, 2, 141

    CrossRef

  4. 4
    C. Labay, J.M. Canal, A. Navarro, C. Canal, Corona plasma modification of polyamide 66 for the design of textile delivery systems for cosmetic therapy, Applied Surface Science, 2014, 316, 251

    CrossRef

  5. 5
    Noraini Ahmad, Roland Ramsch, Meritxell Llinàs, Conxita Solans, Rauzah Hashim, Hairul Anuar Tajuddin, Influence of nonionic branched-chain alkyl glycosides on a model nano-emulsion for drug delivery systems, Colloids and Surfaces B: Biointerfaces, 2014, 115, 267

    CrossRef

  6. 6
    Frans Franek, Per Holm, Frank Larsen, Bente Steffansen, Interaction between fed gastric media (Ensure Plus®) and different hypromellose based caffeine controlled release tablets: Comparison and mechanistic study of caffeine release in fed and fasted media versus water using the USP dissolution apparatus 3, International Journal of Pharmaceutics, 2014, 461, 1-2, 419

    CrossRef

  7. 7
    Nikhil Biswas, Arijit Guha, Ranjan Kumar Sahoo, Ketousetuo Kuotsu, Pulse release of doxazosin from hydroxyethylcellulose compression coated tablet: Mechanistic and in vivo study, International Journal of Biological Macromolecules, 2014,

    CrossRef

  8. 8
    Simon J. Holder, Glen Woodward, Beulah McKenzie, Nico A. J. M. Sommerdijk, Semi-crystalline block copolymer bicontinuous nanospheres for thermoresponsive controlled release, RSC Advances, 2014, 4, 50, 26354

    CrossRef

  9. 9
    J. D. Gomez-Mantilla, U. F. Schaefer, V. G. Casabo, T. Lehr, C. M. Lehr, Statistical Comparison of Dissolution Profiles to Predict the Bioequivalence of Extended Release Formulations, The AAPS Journal, 2014, 16, 4, 791

    CrossRef

  10. 10
    Stefan Scheler, The polymer free volume as a controlling factor for drug release from poly(lactide-co-glycolide) microspheres, Journal of Applied Polymer Science, 2014, 131, 1
  11. 11
    Marguerite J. Kutyła, Michael W. Boehm, Jason R. Stokes, P. Nicholas Shaw, Nigel M. Davies, Ross P. McGeary, Jonathan Tuke, Benjamin P. Ross, Cyclodextrin-Crosslinked Poly(Acrylic Acid): Adhesion and Controlled Release of Diflunisal and Fluconazole from Solid Dosage Forms, AAPS PharmSciTech, 2013, 14, 1, 301

    CrossRef

  12. 12
    Firat Yerlikaya, Aysegul Ozgen, Imran Vural, Olgun Guven, Ergun Karaagaoglu, Mansoor A. Khan, Yilmaz Capan, Development and Evaluation of Paclitaxel Nanoparticles Using a Quality-by-Design Approach, Journal of Pharmaceutical Sciences, 2013, 102, 10
  13. 13
    Yusuke Hattori, Yoshimasa Haruna, Makoto Otsuka, Dissolution process analysis using model-free Noyes–Whitney integral equation, Colloids and Surfaces B: Biointerfaces, 2013, 102, 227

    CrossRef

  14. 14
    Mohamed Fatnassi, Corine Tourné-Péteilh, Pradial Peralta, Thomas Cacciaguerra, Philippe Dieudonné, Jean-Marie Devoisselle, Bruno Alonso, Encapsulation of complementary model drugs in spray-dried nanostructured materials, Journal of Sol-Gel Science and Technology, 2013, 68, 2, 307

    CrossRef

  15. 15
    José-David Gómez-Mantilla, Vicente Germán Casabó, Ulrich F. Schaefer, Claus-Michael Lehr, Permutation Test (PT) and Tolerated Difference Test (TDT): Two new, robust and powerful nonparametric tests for statistical comparison of dissolution profiles, International Journal of Pharmaceutics, 2013, 441, 1-2, 458

    CrossRef

  16. 16
    M.S. Sokar, A.S. Hanafy, A.H. El-Kamel, S.S. El-Gamal, Pulsatile core-in-cup valsartan tablet formulations: In vitro evaluation, Asian Journal of Pharmaceutical Sciences, 2013, 8, 4, 234

    CrossRef

  17. 17
    David C. Bock, Kenneth J. Takeuchi, Amy C. Marschilok, Esther S. Takeuchi, Silver vanadium oxide and silver vanadium phosphorous oxide dissolution kinetics: a mechanistic study with possible impact on future ICD battery lifetimes, Dalton Transactions, 2013, 42, 38, 13981

    CrossRef

  18. 18
    João M. Tiago, Luís Padrela, Miguel A. Rodrigues, Henrique A. Matos, António J. Almeida, Edmundo Gomes de Azevedo, Single-Step Co-Crystallization and Lipid Dispersion by Supercritical Enhanced Atomization, Crystal Growth & Design, 2013, 13, 11, 4940

    CrossRef

  19. 19
    Binfeng Xia, Tycho Heimbach, Tsu-han Lin, Shoufeng Li, Hefei Zhang, Jennifer Sheng, Handan He, Utility of Physiologically Based Modeling and Preclinical In Vitro/In Vivo Data to Mitigate Positive Food Effect in a BCS Class 2 Compound, AAPS PharmSciTech, 2013, 14, 3, 1255

    CrossRef

  20. 20
    Martin Bergstrand, Erik Söderlind, Ulf G Eriksson, Werner Weitschies, Mats O Karlsson, A Semi-mechanistic Modeling Strategy to Link In Vitro and In Vivo Drug Release for Modified Release Formulations, Pharmaceutical Research, 2012, 29, 3, 695

    CrossRef

  21. 21
    Kirstin Thelen, Katrin Coboeken, Stefan Willmann, Jennifer B. Dressman, Jörg Lippert, 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, Journal of Pharmaceutical Sciences, 2012, 101, 3
  22. 22
    E. D'Aurizio, P. Sozio, L. S. Cerasa, M. Vacca, L. Brunetti, G. Orlando, A. Chiavaroli, R. J. Kok, W. E. Hennink, A. Di Stefano, Biodegradable Microspheres Loaded with an Anti-Parkinson Prodrug: Anin VivoPharmacokinetic Study, Molecular Pharmaceutics, 2011, 8, 6, 2408

    CrossRef

  23. 23
    Zongming Gao, Mathematical modeling of variables involved in dissolution testing, Journal of Pharmaceutical Sciences, 2011, 100, 11
  24. 24
    Jakub Cupera, Petr Lansky, Random effects in drug dissolution, European Journal of Pharmaceutical Sciences, 2010, 41, 3-4, 430

    CrossRef

  25. 25
    Yi Tsong, Pradeep M. Sathe, Vinod P. Shah, Encyclopedia of Biopharmaceutical Statistics, 2010,

    CrossRef

  26. 26
    A.K. Sahu, S.D. Bhat, S. Pitchumani, P. Sridhar, V. Vimalan, C. George, N. Chandrakumar, A.K. Shukla, Novel organic–inorganic composite polymer-electrolyte membranes for DMFCs, Journal of Membrane Science, 2009, 345, 1-2, 305

    CrossRef

  27. 27
    Rafael Villalobos, Armando Domínguez, Adriana Ganem, Ana Maria Vidales, Salomón Cordero, One-dimensional drug release from finite Menger sponges: In silico simulation, Chaos, Solitons & Fractals, 2009, 42, 5, 2875

    CrossRef

  28. 28
    Qiongyu Guo, Pamela T. Knight, Patrick T. Mather, Tailored drug release from biodegradable stent coatings based on hybrid polyurethanes, Journal of Controlled Release, 2009, 137, 3, 224

    CrossRef

  29. 29
    Anikó Szepes, Zsolt Makai, Christoph Blümer, Karsten Mäder, Péter Kása, Piroska Szabó-Révész, Characterization and drug delivery behaviour of starch-based hydrogels prepared via isostatic ultrahigh pressure, Carbohydrate Polymers, 2008, 72, 4, 571

    CrossRef

  30. 30
    Luciana A. Corá, Paulo R. Fonseca, Madileine F. Américo, Ricardo B. Oliveira, Oswaldo Baffa, José Ricardo A. Miranda, Influence of compression forces on tablets disintegration by AC Biosusceptometry, European Journal of Pharmaceutics and Biopharmaceutics, 2008, 69, 1, 372

    CrossRef

  31. 31
    Van Eerdenbrugh Bernard, Vercruysse Sofie, Martens Johan A, Vermant Jan, Froyen Ludo, Van Humbeeck Jan, Van den Mooter Guy, Augustijns Patrick, Microcrystalline cellulose, a useful alternative for sucrose as a matrix former during freeze-drying of drug nanosuspensions – A case study with itraconazole, European Journal of Pharmaceutics and Biopharmaceutics, 2008, 70, 2, 590

    CrossRef

  32. 32
    Sébastien Casault, Gary W. Slater, Systematic characterization of drug release profiles from finite-sized hydrogels, Physica A: Statistical Mechanics and its Applications, 2008, 387, 22, 5387

    CrossRef

  33. 33
    Anikó Szepes, Joachim Ulrich, Zsuzsanna Farkas, József Kovács, Piroska Szabó-Révész, Freeze-casting technique in the development of solid drug delivery systems, Chemical Engineering and Processing: Process Intensification, 2007, 46, 3, 230

    CrossRef

  34. 34
    Aristides Dokoumetzidis, Lida Kalantzi, Nikoletta Fotaki, Predictive models for oral drug absorption: from in silico methods to integrated dynamical models, Expert Opinion on Drug Metabolism & Toxicology, 2007, 3, 4, 491

    CrossRef

  35. 35
    Aristides Dokoumetzidis, Panos Macheras, A century of dissolution research: From Noyes and Whitney to the Biopharmaceutics Classification System, International Journal of Pharmaceutics, 2006, 321, 1-2, 1

    CrossRef

  36. 36
    Davis Yohanes Arifin, Lai Yeng Lee, Chi-Hwa Wang, Mathematical modeling and simulation of drug release from microspheres: Implications to drug delivery systems, Advanced Drug Delivery Reviews, 2006, 58, 12-13, 1274

    CrossRef

  37. 37
    Thomas Schreiner, Ulrich F. Schaefer, Helmut Loth, Immediate drug release from solid oral dosage forms, Journal of Pharmaceutical Sciences, 2005, 94, 1
  38. 38
    Undina Zeo, Elena Tarabukina, Tatiana Budtova, Kinetics of shear-induced gel deswelling/solvent release, Journal of Controlled Release, 2005, 108, 1, 73

    CrossRef

  39. 39
    Aristides Dokoumetzidis, Kosmas Kosmidis, Panos Argyrakis, Panos Macheras, Modeling and Monte Carlo Simulations in Oral Drug Absorption, Basic & Clinical Pharmacology & Toxicology, 2005, 96, 3
  40. 40
    Stefan Horkovics-Kovats, Characterization of an Active Pharmaceutical Ingredient by Its Dissolution Properties: Amoxicillin Trihydrate as a Model Drug, Chemotherapy, 2004, 50, 5, 234

    CrossRef

  41. 41
    Gesine Schliecker, Carsten Schmidt, Stefan Fuchs, Andreas Ehinger, Jürgen Sandow, Thomas Kissel, In vitro and in vivo correlation of buserelin release from biodegradable implants using statistical moment analysis, Journal of Controlled Release, 2004, 94, 1, 25

    CrossRef

  42. 42
    Letı́cia S Koester, George G Ortega, Paulo Mayorga, Valquiria L Bassani, Mathematical evaluation of in vitro release profiles of hydroxypropylmethylcellulose matrix tablets containing carbamazepine associated to β-cyclodextrin, European Journal of Pharmaceutics and Biopharmaceutics, 2004, 58, 1, 177

    CrossRef

  43. 43
    Stéphane Gibaud, Najim Jabir Al Awwadi, Camille Ducki, Alain Astier, Poly(ε-caprolactone) and Eudragit® microparticles containing fludrocortisone acetate, International Journal of Pharmaceutics, 2004, 269, 2, 491

    CrossRef

  44. 44
    Q. Wang, P.R. Ellis, S.B. Ross-Murphy, Dissolution kinetics of guar gum powders. I. Methods for commercial polydisperse samples, Carbohydrate Polymers, 2002, 49, 2, 131

    CrossRef

  45. 45
    E Adams, D Coomans, J Smeyers-Verbeke, D.L Massart, Non-linear mixed effects models for the evaluation of dissolution profiles, International Journal of Pharmaceutics, 2002, 240, 1-2, 37

    CrossRef

  46. 46
    Shein-Chung Chow, Jun Shao, ON THE ASSESSMENT OF SIMILARITY FOR DISSOLUTION PROFILES OF TWO DRUG PRODUCTS, Journal of Biopharmaceutical Statistics, 2002, 12, 3, 311

    CrossRef

  47. 47
    P. Costa, An alternative method to the evaluation of similarity factor in dissolution testing, International Journal of Pharmaceutics, 2001, 220, 1-2, 77

    CrossRef

  48. 48
    Paulo Costa, José Manuel Sousa Lobo, Modeling and comparison of dissolution profiles, European Journal of Pharmaceutical Sciences, 2001, 13, 2, 123

    CrossRef

  49. 49
    P. Cerezo, C. Viseras Iborra, A. Lopez-Galindo, F. Ferrari, C. Caramella, Use of water uptake and capillary suction time measures for evaluation of the anti-diarrhoeic properties of fibrous clays, Applied Clay Science, 2001, 20, 1-2, 81

    CrossRef

  50. 50
    E. Bulgarelli, F. Forni, M.T. Bernabei, Effect of matrix composition and process conditions on casein–gelatin beads floating properties, International Journal of Pharmaceutics, 2000, 198, 2, 157

    CrossRef

  51. 51
    Sayeh F. Ahrabi, Sverre A. Sande, Tor Waaler, Christina Graffner, Influence of neutron activation factors on the physico–chemical properties of suppositories and their excipients, European Journal of Pharmaceutical Sciences, 1999, 8, 3, 193

    CrossRef

  52. 52
    T Waaler, S.A Sande, B.W Müller, G Schüller Lisether, Influence of neutron irradiation on Eudragit® coated tablets: validation of neutron activation II, European Journal of Pharmaceutical Sciences, 1999, 7, 4, 287

    CrossRef

  53. 53
    T Waaler, S.A Sande, B.W Müller, G Schüller Lisether, Influence of the coating thickness and type of oral delivery system (tablets, pellets) on the stability towards degradation by neutron irradiation, European Journal of Pharmaceutical Sciences, 1999, 7, 4, 295

    CrossRef

  54. 54
    Georgia Valsami, Aristides Dokoumetzidis, Panos Macheras, Modeling of supersaturated dissolution data, International Journal of Pharmaceutics, 1999, 181, 2, 153

    CrossRef

  55. 55
    Thomas O'Hara, Adrian Dunne, Jackie Butler, John Devane, A review of methods used to compare dissolution profile data, Pharmaceutical Science & Technology Today, 1998, 1, 5, 214

    CrossRef

  56. 56
    O. V. Nikiforova, A. P. Arzamastsev, A. A. Kruchenkov, Comparative analysis of the pharmaceutical accessibility of omeprazole in capsules from various manufacturers, Pharmaceutical Chemistry Journal, 1998, 32, 12, 625

    CrossRef

  57. 57
    Anurag Sood, Ramesh Panchagnula, Drug release evaluation of diltiazem CR preparations1NIPER communication no. 14.1, International Journal of Pharmaceutics, 1998, 175, 1, 95

    CrossRef

  58. 58
    Daniel O. Opota, Hélène Maillols, Joseph Joachim, Régine Acquier, Henri Delonca, Tamba-Vemba, Effect of temperature on the dissolution of theophylline tablets containing three different molecular weights of hydroxypropylcellulose as binder, Pharmaceutica Acta Helvetiae, 1997, 72, 2, 87

    CrossRef

  59. 59
    Shein-Chung Chow, Y.c.Ki Fanny, Statistical comparison between dissolution profiles of drug products, Journal of Biopharmaceutical Statistics, 1997, 7, 2, 241

    CrossRef

  60. 60
    T. Waaler, S.A. Sande, B.W. Müller, G.Schüller Lisether, The influence of thermal neutron irradiation on the in vitro characteristics of ASA oral dosage forms validation of neutron activation, European Journal of Pharmaceutics and Biopharmaceutics, 1997, 43, 2, 159

    CrossRef

  61. 61
    Raluca-Ioana Stefan, Hassan Y. Aboul-Enein, Disopyramide-Selective Membrane Electrode∗, Analytical Letters, 1996, 29, 13, 2333

    CrossRef

  62. 62
    M.A. Vandelli, G. Salvioli, A. Mucci, R. Panini, L. Malmusi, F. Forni, 2-Hydroxypropyl-β-cyclodextrin complexation with ursodeoxycholic acid, International Journal of Pharmaceutics, 1995, 118, 1, 77

    CrossRef

  63. 63
    Tone Østberg, Christina Graffner, Calcium alginate matrices for oral multiple unit administration: III. Influence of calcium concentration, amount of drug added and alginate characteristics on drug release, International Journal of Pharmaceutics, 1994, 111, 3, 271

    CrossRef

  64. 64
    H.P. Jones, R. Clements, D.J. Hearn, M.J. Gamlen, Development and application of a pharmacokinetic simulation program for oral controlled release dosage forms — DIPS, International Journal of Pharmaceutics, 1994, 104, 3, 253

    CrossRef

  65. 65
    Andrei A. Bunaciu, Mariana S. Ionescu, Raluca I. Stefan, Iuditha Ioan, Hassan Y. Aboul-Enein, Mianserin Ion-Selective Membrane Electrode and its Pharmaceutical Applications, Analytical Letters, 1994, 27, 9, 1647

    CrossRef

  66. 66
    H. Lindner, P. Kleinebudde, Use of Powdered Cellulose for the Production of Pellets by Extrusion/Spheronization, Journal of Pharmacy and Pharmacology, 1994, 46, 1
  67. 67
    P. Kleinebudde, Application of low substituted hydroxypropylcellulose (L-HPC) in the production of pellets using extrusion/spheronization, International Journal of Pharmaceutics, 1993, 96, 1-3, 119

    CrossRef

  68. 68
    K. S. Murthy, Isaac Ghebre-Sellassie, Current perspectives on the dissolution stability of solid oral dosage forms, Journal of Pharmaceutical Sciences, 1993, 82, 2
  69. 69
    Valentina Iannuccelli, Flavio Fomi, Maria Angela Vandelli, Maria Teresa Bernabei, Effect of the loading method on the drug release from crosslinked carboxymethylcellulose beads, Journal of Controlled Release, 1993, 23, 1, 13

    CrossRef

  70. 70
    J.L. Johnson, J. Holinej, M.D. Williams, Influence of ionic strength on matrix integrity and drug release from hydroxypropyl cellulose compacts, International Journal of Pharmaceutics, 1993, 90, 2, 151

    CrossRef

  71. 71
    P. Arnaud, C. Elkoubi, C. Renaux, A. Le Hir, Computerized linearization test for tablet dissolution kinetics, International Journal of Pharmaceutics, 1992, 80, 1-3, 129

    CrossRef

  72. 72
    Gopi K. Vudathala, James A. Rogers, Dissolution of fludrocortisone from phospholipid coprecipitates, Journal of Pharmaceutical Sciences, 1992, 81, 3
  73. 73
    J. T. Carstensen, Miriam Franchini, Keith Ertel, Statistical approaches to stability protocol design, Journal of Pharmaceutical Sciences, 1992, 81, 3
  74. 74
    Marcio Labastie, Reynaldo Nacco, Jean Cumps, Tablet dissolution parameters: A statistical evaluation, Journal of Pharmaceutical and Biomedical Analysis, 1992, 10, 10-12, 1105

    CrossRef

  75. 75
    P. BOTTENBERG, R. CLEYMAET, C. MUYNCK, J. P. REMON, D. COOMANS, Y. MICHOTTE, D. SLOP, Development and Testing of Bioadhesive, Fluoride-containing Slow-release Tablets for Oral Use, Journal of Pharmacy and Pharmacology, 1991, 43, 7
  76. 76
    Chetan Lathia, John Wood, Pharmaceutical Dissolution Testing, 1991,

    CrossRef

  77. 77
    Flavio Forni, Gilberto Coppi, Maria Angela Vandelli, Maria Teresa Bernabei, An interpretation of the diffusion-type mechanism of drug release from microcapsules, International Journal of Pharmaceutics, 1990, 60, 2, 83

    CrossRef

  78. 78
    Sverre A. Sande, Jan Karlsen, Curve fitting of dissolution data by personal computer, International Journal of Pharmaceutics, 1989, 55, 2-3, 193

    CrossRef

  79. 79
    Nidal F. Farraj, Stanley S. Davis, Graham D. Parr, Howard N.E. Stevens, Studies on the simultaneous dissolution and degradation of progabide powders, International Journal of Pharmaceutics, 1989, 52, 1, 19

    CrossRef

  80. 80
    Shan-Yang Lin, Juei-Chyi Yang, Bioavailability studies of theophylline ethylcellulose microcapsules prepared by using ethylene-vinyl acetate copolymer as a coacervation-inducing agent, Journal of Pharmaceutical Sciences, 1987, 76, 3
  81. 81
    P. Macheras, C. Reppas, Dissolution and in vitro permeation behaviours of dicumarol nitrofurantoin and sulfamethizole in the presence of protein, International Journal of Pharmaceutics, 1987, 37, 1-2, 103

    CrossRef

  82. 82
    Paolo Colombo, Ubaldo Conte, Carla Caramella, Aldo La Manna, Mario Geddo, Disintegrating force as a new formulation parameter, Journal of Pharmaceutical Sciences, 1984, 73, 5
  83. 83
    J.R. Leary, N. Randall, S.D. Ross, The use of finite differences in the study of some chemical reactions, International Journal of Pharmaceutics, 1983, 15, 1, 1

    CrossRef

  84. 84
    Adnan El-Yazigi, Disintegration-dissolution analysis of percent dissolved-time data, Journal of Pharmaceutical Sciences, 1981, 70, 5
  85. 85
    Fritz Nimmerfall, Joachim Rosenthaler, Dependence of area under the curve on proquazone particle size and in vitro dissolution rate, Journal of Pharmaceutical Sciences, 1980, 69, 5
  86. 86
    J. T. Carstensen, Rohit Kothari, V. K. Prasad, Jane Sheridan, Time and temperature dependence of disintegration and correlation between dissolution and disintegration rate constants, Journal of Pharmaceutical Sciences, 1980, 69, 3
  87. 87
    Mamoru Sugiura, Masayuki Kurobe, Sumihiro Tamura, Shinichi Ikeda, Kinetics of digestive enzyme stability in solid state I: Application of weibull distribution function to solid-state enzyme inactivation, Journal of Pharmaceutical Sciences, 1979, 68, 11
  88. 88
    K. G. Nelson, L. Y. Wang, Determination of time course of tablet disintegration II: Method using continuous functions, Journal of Pharmaceutical Sciences, 1978, 67, 1
  89. 89
    J. A. GOLDSMITH, N. RANDALL, S. D. ROSS, On methods of expressing dissolution rate data, Journal of Pharmacy and Pharmacology, 1978, 30, 1
  90. 90
    J. T. Carstensen, J. L. Wright, Kenneth Blessel, Jane Sheridan, USP dissolution III: Semilogarithmic dissolution patterns of tablets in rotating-basket assemblies, Journal of Pharmaceutical Sciences, 1978, 67, 7
  91. 91
    K. G. Nelson, L. Y. Wang, Determination of time course of tablet disintegration I: Numerical method, Journal of Pharmaceutical Sciences, 1977, 66, 12
  92. 92
    C. Voellmy, P. Speiser, M. Soliva, Microencapsulation of phenobarbital by spray polycondensation, Journal of Pharmaceutical Sciences, 1977, 66, 5
  93. 93
    Kwon Ho Kim, Charles I. Jarowski, Surface tension lowering and dissolution rate of hydrocortisone from solid solutions of selected n-acyl esters of cholesterol, Journal of Pharmaceutical Sciences, 1977, 66, 11
  94. 94
    C. Cakiryildiz, P. J. Mehta, W. Rahmen, D. Schoenleber, Dissolution studies with a multichannel continuous-flow apparatus, Journal of Pharmaceutical Sciences, 1975, 64, 10
  95. 95
    Ashok C. Shah, Allen K. Herd, Pharmaceutical sciences—1972: Literature review of pharmaceutics I, Journal of Pharmaceutical Sciences, 1973, 62, 7
  96. 96
    A.K. Tiwary, Bharti Sapra, Subheet Jain, Dissolution, Pharmaceutical Sciences Encyclopedia,