Zusammenfassung
Tabletten werden durch Verpressen eines konstanten Volumens von Substanzteilchen hergestellt. Die Teilchen bestehen aus einem oder mehreren Wirkstoffen mit oder ohne Zusatz von Füll-, Binde-, Spreng-, Gleit- und/oder Schmiermitteln sowie von Substanzen, die das Verhalten der Tabletten im Verdauungstrakt bestimmen.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
Wiegel S ( 1996) Systematik der Entwicklung direktverpreßter Tabletten. Dissertation Universität Heidelberg
Ahlneck C, Zografi G (1990) The molecular basis of moisture effects on the physical and chemical stability of drugs in the solid state. Int J Pharm 62: 87–95
Antequera MVV, Munoz-Ruiz A, Perales MCM, Ballesteros MRJ-C (1994) Effect of the addition of three disintegrants on the tabletability of calcium-phosphate based materials. Eur J Pharm Biopharm 40: 344–347
Armstrong NA, Palvrey L (1989) The effect of machine speed on the consolidation of four directly compressible tablet diluents. J Pharm Pharmacol 41:149–151
Association American Pharmaceutical, Britain, The Pharmaceutical Society of Great (1986) Handbook of Pharmaceutical Excipients. The Pharmaceutical Press, London
Bangudu AB, Pilpel N (1985) Effects of composition moisture and stearic acid on the plasto-elasticity and tableting of paracetamol-microcristalline cellulose mixtures. J Pharm Pharmacol 37: 289–293
Bauer-Brandl A (1993) Hochleistungsrundlaufpressen. Pharm Ind 55: 404
Bermann J, Planchard JA (1995) Blend uniformity and unit dosage sampling. Drug Dev Ind Phar 21: 1257–1283
Bertoni M, Ferrari F, Bonferoni MC, Rossi S, Caramella C (1995) Functionality tests for tablet disintegrants. the case of sodium carboxymethylcelluloses. Pharm Technol: 17–24
Bogs U, Lenhardt E ( 1971 ) Zur Kenntnis thermischer Vorgänge beim Tablettenpressen. Pharm Ind 33: 850–854
Bolhuis GK, Arends-Scholte AW, Stuut GJ, de Vries JA (1994) disintegration efficiency of sodium starch glycolates prepared from native starches. Eur J Pharm Biopharm 40: 317–320
Bolhuis GK, de Jong SW, Lerk CF (1987) The effect of magnesium stearate admixing in different types of laboratory and industrial mixers on tablet crushing strength. Drug Dev Ind Pharm 13:1547–1567
Bolhuis GK, Reichman G, Lerk CF, van Kamp HV, Zuurman K (1985) Evaluation of Anhydrous a-Lactose a New Excipient in Direct Compression. Drug Dev Ind Pharm 11: 1657–1681
Bolhuis GK, Smallenbroek AJ, Lerk CF (1981) Interaction of tablet disintegrants and magnesium stearate duringmixing i: effect on tablet disintegration. J Pharm Sci 70: 1328–1330
Bolhuis GK, van Kamp HV, Lerk CF, Sessink FGM (1982) On the mechanism of action of modern disintegrants. Acta Pharm Technol 28:111–114
Bose M, Sakr A, Warner A (1993) Effect of lubricants on the characteristics of triamteren /hydrochlorothiazide directly compressed tablets. Pharm Ind 55: 519–522
Bossert J, Stamm A (1980) Effect of mixing on the lubrication of crystalline lactose by magnesium stearate. Drug Dev Ind Pharm 6: 573–589
Botzolakis JE, Augsburger LL (1988) Disintegrating agents in hard gelatine capsules, part II: swelling efficiency. Drug Dev Ind Pharm 14: 1235–1248
Callahan JC, Cleary GW, Elefant M, Kaplan G, Kensler T, Nash RA (1982) Equilibrium moisture content of pharmaceutical excipients. Drug Dev Ind Pharm 8: 355–369
Caramella C, Colombo P, Conte U, La Manna A (1987) Tablet disintegration update: the dynamic approach. Drug Dev Ind Pharm 13: 2111–2145
Caramella C, Ferrari F, Bonferoni MC, Ronchi M (1990) Disintegrants in solid dosage forms. Drug Dev Ind Pharm 16: 2561–2577
Carstensen JT, Chan PL Relation between Particle Size and Repose Angles of PowdersPowder Technol 15:129–131 (1976)
Carstensen JT, Erteil C (1990) Physical and chemical properties of calcium phosphates for solid state pharmaceutical formulations. Drug Dev Ind Pharm 16: 1121–1133
Carstensen JT, Geoffroy JM, Dellamonica C (1990) Compression characteristics of binary mixtures. Powder Technol 62:119–124
Carstensen JT, Rhodes CT (1984) Optimization of preblending in random mixing. Drug Dev Ind Pharm 10:1017–1024
Casahoursat L, Lemagnen G, Larrouture D (1989) Dependence of compression phase on elasticity of the material. Drug Dev Ind Pharm 15: 2213–2226
Castillo-Rubio S, Villafuerte-Robles L (1995) Compactability of binary mixtures of pharmaceutical powders. Eur J Pharm Biopharm 41: 309–314
Celik M, Marshall K (1989) Use of a compaction simulator system in tabletting research. Drug Dev Ind Pharm 15: 759–800
Celik M, Okutgen E (1995) Compaction data bank (1) batch-to-batch plant-to-plant and manufacture-to-manufacture consistency of microcrystalline cellulose and dicalcium phosphate. Proc 1st World Meeting APGI/APV Budapest 9-11 May: 163–164
Chang R-K, Badawy S, Hussain MA, Buehler JDA (1995) Comparison of free-flowing segregating and non-free-flowing cohesive mixing systems in assessing the performance of a modified v-shaped solids mixer. Drug Dev Ind Pharm 21: 361–368
Chowhan ZT (1993) Excipients and their functionality in drug product development. Pharm Technol 9: 72–82
Danjo K, Erteil C, Carstensen JT (1989) Effect of compaction speed and die diameter on athy-heckel and hardness parameters of compressed tablets. Drug Dev Ind Pharm 15:1–10
Dawoodbhai S, Rhodes CT (1989) The effect of moisture on powder flow and on compaction and physical stability. Drug Dev Ind Pharm 15:1577–1600
de Haan P, Kroon C, Sam AP (1990) Decomposition and stabilization of the tablet excipient calcium hydrogenphosphat dihydrate. Drug Dev Ind Pharm 16: 2031–2055
de Villiers MM, van der Watt JG (1989) Interactive mixing between agglomerated drug particles and coarse carrier particles. Drug Dev Ind Pharm 15: 2055–2061
Djuric M, Jovanovic M, Djuric Z (1986) Effect of dioctylsodiumsulphosuccinat (DSS) on tablet disintegration. Pharmazie 41: 816–817
Doelker E, Mordier D, Iten H, Humbert-Droz P (1987) Comparative Tableting Properties of Sixteen Microcrystalline Celluloses. Drug Dev Ind Pharm 13:1847–1875
Doldán C, Souto C, Martínez-Pacheco R, Gómez-Amoza JL, Concheiro A (1995) Dicalcium Phosphate Dihydrate and Anhydrous Dicalcium Phosphate for Direct Compression: A Comparative Study. Int J Pharm 124: 69–74
Egermann H (1982) Definition and Conversion of the Mean Particle Diameter Referring to Mixing Homogeneity. Powder Technol 31: 231–232
Egermann H (1991) Mischen von Feststoffen. Hagers Handbuch der Pharmazeutischen Praxis. Springer, Berlin Heidelberg New York Tokyo
Egermann H (1979) Studien zum Mischverhalten kohäsiver Pulver. Pharm Ind 41: 285–289
Eriksson M, Alderborn G (1995) The effect of particle fragmentation and deformation on the interparticulate bond formation process during powder compaction. Pharm Res 12: 1031–1039
Faroongsarng D, Peck GE (1994) Surface morphology study of solid pow-ders evaluated by particle size distributi-on and nitrogen adsorption. Drug Dev Ind Pharm 20: 2353–2367
Fassihi AR, Falamarzian M, Parker MS (1980) The influence of the rate of production of tablets at constant pressure upon their physical properties. Drug Dev Ind Pharm 6: 441–450
Fassihi AR, Kanfer I (1986) Effect of compressibility and powder flow properties on tablet weight variation. Drug Dev Ind Pharm 12:1947–1966
Fell JT, Newton JM (1970) Prediction of the tensile strength of tablets. J Pharm Pharmacol 22:247–248
Fiedler HP (1989) Lexikon der Hilfsstoffe für Pharmazie Kosmetik und angrenzende Gebiete. Editio Cantor, Aulendorf
Filbry (1986) Homogenität des Druckes in Tabletten verschiedener Wölbung und ihr Einfluß auf errechnete und gemessene Parameter der Verdichtung verschiedener Substanzen. Dissertation Institut für Pharmazeutische Chemie, Abt Pharmazeutische Technologie Hamburg
Fisher DG, Rowe RC (1976) The adhesion of film coatings to tablet surfaces-instrumentation and preliminary evaluation. J Pharm Pharmac 28: 886–889
Führer C, Bayraktar-Alpmen G, Schmidt M (1977) Untersuchungen von Kraft-Weg-Diagrammen bei der Tablettierung von Pulvermischungen. Acta Pharm Technol 23: 215–224
Gabaude CM, Guillot M, Gautier J-C (1999) Effects of true density compacted mass compression speed and punch deformation on the mean yield pressure. Journal of Pharmaceutical Sciences 88: 22–28
Garr JSM, Rubinstein MH (1991) An investigation into the capping of paracetamol at increasing speeds of compression. Int J Pharm 72:117–122
Garr JSM, Rubinstein MH (1991) Compaction properties of a cellulose-lactose direct compression excipient. Pharm Technol Int 15(7): 24–27
Garr JSM, Rubinstein MH (1992) Consolidation and compaction characteristics of a three-component particulate system. Int J Pharm 82: 71–77
Glombitza BW, Schmidt PC (1995) Surface acidity of solid pharmaceutical excipients-ii effect of the surface acidity on the decomposition rate of acetylsalicylic acid. Eur J Pharm Biopharm 41: 114–119
Gordon MS, Chowhan ZT (1990) The effect of aging on disintegrant efficiency in direct compression tablets with varied solubility and hygroscopicity in terms of dissolution. Drug Dev Ind Pharm 16: 437–447
Graf E, Ghanem AH, Mahmoud H (1982) Studies on the direct compression of pharmaceuticals. Part 8: role of liquid penetration and humudity on tablet formulations. Pharm Ind 44: 200–203
Graf E, Sakr A, Gaftiteanu E (1979) Studies on the direct compression of pharmaceuticals. 3. Ephedrine tablets, a) Effect of excipients and compression pressure on the characteristics of directly compressed ephedrine-HCl tablets. Pharm Ind 41: 884–886
Hauer B, Remmele T, Sucker H (1993) Gezieltes Entwickeln und Optimieren von Kapselformulierungen mit einer instrumentierten Dosierröhrchen-Kapselfüllmaschine; 2. Mitteilung: Grundlagen der Optimierungsstrategie. Pharm Ind 55: 780–786
Hedge RP, Rheingold JL, Welch S, Rhodes CT (1985) Studies of powder flow using a recording powder flowmeter and measurement of the dynamic angle of repose. J Pharm Sci 74: 11–15
Heng PWS, Wan LSC, Ang TSH (1990) Role of surfactant on drug release from tablets, drug dev ind pharm 16: 951–962
Hoblitzell JR, Rhodes CT (1990) Instrumented tablet press studies on the effect of some formulation and processing variables on the compaction process. Drug Dev Ind Pharm 16: 469–507
Hoblitzell JR, Rhodes CT (1986) Preliminary investigations on the parity of tablet compression data obtained from different instrumented tablet presses. Drug Dev Ind Pharm 12: 507–525
Holman LE (1991) The Compressibility of Pharmaceutical Particulate Systems An Illustration of Percolation. Int J Pharm 71: 81–94
Holman LE, Leuenberger H (1990) The effect of varying the composition of binary powder mixtures and compacts on their properties: A percolation phenomenon. Powder Technol 60: 249–258
Hölzer AW, Sjögren J (1981) Evaluation of some lubricants by the comparison of friction coefficients and tablet properties. Acta Pharm Suec 18:139–148
Huber GMW, Becker R, Müller RH (1994) Zusammenhang zwischen Fließeigenschaften und Oberfläche pulverförmiger Rezepturen. Pharm Ind 56: 389–392
Hwang R, Peck GR (2001) A systematic evaluation of the compression of tablets characteristics of microcristalline cellulose. Pharmaceutical Technology (3): 112–132
Hwang R, Peck GR (2001) A systematic evaluation of the compression of tablets lactose microcristalline cellulose and dibasic calcium phosphate. Pharmaceutical Technology (3): 55–81
Ibrahim H, Sallam E, Takieddin M, Shamat MA (1988) Dissolution characteristics of interactive powder mixtures part one: Effect of solubility and partcle size of excipients. Drug Dev Ind Phar 14:1249–1276
Illkka J, Paronen P (1993) Prediction of the compression behaviour of powder mixtures by the Heckel equation. Int J Pharm 94: 181–187
Imbert C, Tchoreloff BL, Couarraze G (1997) Indices of tableting performance and application of percolation theory to powder compaction. European Journal of Pharmaceutics and Biopharmaceutics 44: 273–282
Kikuta J, Kitamori N (1994) Effect of mixing time on the lubricating properties of magnesium stearate and the final characteristics of the compressed tablets. Drug Dev Ind Pharm 20(3): 343–356
Jarosz PJL, Parrott E (1984) Effect of lubricants on tensile strengths of tablets. Drug Dev Ind Pharm 10: 259–274
Jetzer WE (1986) Compaction characteristics of binary mixtures. Int J Pharm 31: 201–207
Johansson ME, Nicklasson M (1986) Investigation of the film formation of magnesium stearate by applying a flow-through dissolution technique. J Pharm Sci 38: 51–54
Johnson MCR (1972) Particle Size Distribution of the Active Ingerdient for Solid Dosage Forms of Low Dosage. Pharm Acta Helv 47: 546–559
Jones TM (1978) Prefomulation studies to predict the compaction properties of materials used in tablets and capsules. Acta Pharm Technol 6:141–159
Jovanovic M, Samardzic Z, Djuric Z, Mihailovic D, Milanovic V, Srentic M, Rudez B (1987) An evaluation of the sodium laurylsulphate as tablet adjuvant. Pharmazie 42: 741–742
Jvaid KA (1983) Disintegration and dissolution parameters of compressed tablets prepared by direct compression-wet granulation process and compression of granulation of both sections. Drug Dev Ind Pharm 9: 1061–1072
Kahn KA, Rhodes CT (1972) Effect of compaction pressure on the dissolution efficiency of some direct compression systems. Pharm Acta Helv 47: 594–607
Karehill PG, Nyström C (1990) Studies on direct compression of tablets xxii investigation of strength increase upon ageing and bonding mechanisms for some plastically deforming materials. Int J Pharm 64: 27–34
Khan KA, Musikabhumma P, Rubinstein MH (1983) The effect of mixing time of magnesium stearate on the tableting properties of dried microcristalline cellulose. Pharm Acta Helv 58:109–111
Khan KA, Rhodes CT (1975) Disintegration properties of calcium phosphat dibasic dihydrate tablets. J Pharm Sci 64: 166–168
Kikuta J, Kitamori N (1985) Frictional properties of tablet lubricants. Drug Dev Ind Pharm 11:845–854
Koch H (1990) Bewertung der Presseigenschaften pharmazeutischer Wirk-und Hilfsstoffe anhand von Presskraft-Zeit-Kurven. Institut für Pharmazeutische Technologie der Philipps-Universtität Marburg/Lahn
Krycer I, Pope DG, Hersey JA (1982) An evaluation of the techniques employed to investigate powder compaction behaviour. Int J Pharm 12:113–134
Kuentz M, Leuenberger H (2000) A new theoretical approach to tablet strength of a binary mixture consisting of a well and a poorly compactable substance. European Journal of Pharmaceutics and Biopharmaceutics 49: 151–159
Lahdenpää E, Niskanen M, Yliruusi J (1997) Crushing strength disintegration time and weight variation of tablets compressed from three Avicel-PH grades and their mixtures. European Journal of Pharmaceutics and Biopharmaceutics 43 S315–322
Laich T, Hundt T, Kissel T (1995) Experimentelle Untersuchungen zur Reibungsarbeit beim Tablettieren mit Hilfe der axialen Matrizenwandkraftmessung. Pharm Ind 57: 686–693
Langenbucher F (1972) Statistical analysis of the USP XVIII content uniformity sampling plan for tablets. Pharm Acta Helv 47: 142–152
Lerk CF, Bolhuis GK (1977) Interaction of lubricants and colloidal silicea during mixing with excipientsii its effect on wettability and dissolution velocity. Pharm Acta Helv 52: 39–44
Lerk CF, Bolhuis GK, Smallenbroek AJ, Zuurman K (1982) Interaction of tablet disintegrants and magnesium stearate during mixingii effect on dissolution rate. Pharm Acta Helv 57: 282–286
Lerk CF, Bolhuis GK, Smedema SS (1977) Interaction of lubricants and colloidal silicea during mixing with excipientsi its effect on tableting. Pharm Acta Helv 52: 33–39
Leuenberger H, Bonny JD, Lerk CF, Vromans H (1989) Relation between crushing strength and internal specific surface of lactose compacts. Int J Pharm 52: 91–100
Leuenberger H, Rohera BD (1986) Fundamentals of powder compression. I. The compactability and compressibility of pharmaceutical powders. Pharm Res 3:12–22
Leuenberger H, Rohera BD (1986) Fundamentals of powder compression. II. The compression of binary powder mixtures. Pharm Res 3: 65–74
Levy G, Gumtow RH (1963) Effect of certain tablet formulation factors on dissolution rate of the active ingredient III. J Pharm Sci 52: 1139–1144
Lieberman HA, Lachman L (1980) Pharmaceutical Dosage Forms. Tablets 1. Marcel Dekker, New York, Basel
Liebner E (1990) Über die Rückdehnung von Tabletten aus Cellulosen-Strukturrelevante physikalische Eigenschaften während Lagerung bei verschiedenen relativen Feuchten. Dissertation Institut für Pharmazeutische Chemie, Abt. für Pharmazeutische Technologie, Hamburg
Lindberg N-O, Hansson E, Holmquist B (1987) The granulation of a tablet formulation in a high-speed mixer diosna p25 influence on intragranular porosity and liquid saturation. Drug Dev Ind Pharm 13:1069–1079
Lindberg N-O, Holmquist B (1987) Optimizing the friability of a tablet formulation. Drug Dev Ind Pharm 13:1063–1067
Lindberg N-O, Holmquist C, Jönsson B (1985) Optimization of disintegration time and crushing strength of a tablet formulation. Drug Dev Ind Pharm 11: 931–943
Lindberg N-O, Jönsson C (1983) Granulation of lactose in a recording high-speed mixer diosna P25. Drug Dev Ind Pharm 9: 959–970
List PH, Muazzam UA (1981) Quellung-die treibende Kraft beim Tablettenzerfall. 4. Mitteilung. Pharm Ind 43: 480–484
Lordi N, Shiromani P (1985) Compressibility of salts. Drug Dev Ind Pharm 11:13–30
Lowenthal W (1973) Mechanism of action of tablet disintegrants. Pharm Acta Helv 48: 589–609
Malamataris S, Goidas P, Dimitriou A (1991) Moisture sorption and tensile strength of some tableted direct compression excipients. Int J Pharm 68: 51–60
Miseta M, Pintye-Hódi K, Szabó-Révész P, Szalay L, Sághi P (1993) Investigation of new commercial sodium starch glycolate products. Pharm Ind 55: 515–518
Mitrevej A, Augsburger L (1980) Adhesion of tablets in a rotary tablet press instrumentation and preliminary study of variables affecting adhesion. Drug Dev Ind Pharm 6: 331–377
Mitrevej KT, Augsburger LL (1982) Adhesion of tablets in a rotary tablet press iieffects of blending time running time and lubrication concentration. Drug Dev Ind Pharm 8: 237–282
Mollan MJ Jr, Celik M (1996) The effects of lubrication on the compaction and postcompaction properties of directly compressible maltodextrins. International Journal of Pharmaceutics 144: 1–9
Mufrod Parrot EL (1990) Effect of pressure on disintegration of tablets and dissolution of ephedrine sulfate. Drug Dev Ind Pharm 16: 1081–1090
Munos-Ruiz A, Villar TP, Munoz NM, Perales MCM, Jimenez-Castellanos MR (1994) Analysis of the physical characterization and the tabletability of calcium phosphate-based materials. Int J Pharm 110: 37–45
Munoz-Ruiz A, Antequera MV, del Perales MCM Ballesteros MRJ-C (1994) Tabletting Properties of New Granular Microcristalline Celluloses. Eur J Pharm Biopharm 40: 36–40
Muñoz-Ruiz A, Perales MCM, Antequera MW, Villar TP, Munoz-Munoz N, Jiménez-Castellanos MR (1993) Rheology and compression characteristics of lactose based direct compression excipients. Int J Pharm 95: 201–207
Nadkarni PD, Kildsig DO, Kramer P, Banker GS (1975) Effect of surface roughness and coating solvent on film adhesion to tablets. J Pharm Sci 64:1554–1557
Newton JM, Alderborn G, Nyström C, Stanley P (1993) The compressive to tensile strength ratio of pharmceutical compacts. Int J Pharm 93:249–251
Newton JM, Bader F (1981) The prediction of the bulk densities of powder mixtures and its relationsship to the filling of hard gelatine capsules. J Pharm Pharmacol 33: 621–626
Newton JM, Cook DT, Hollebon CE (1977) The strength of tablets of mixed components. J Pharm Pharmacol 29: 247–249
Nokhodchi A, Rubinstein MH, Larhrib H, Guyot JC (1995) The effect of moisture content on the energies involved in the compaction of ibuprofen. Int J Pharm 120: 13–20
Nürnberg E, Hopp A (1981) Flüssigkristalle und berührungslose Temperaturmessung — ihre Anwendung in der Tablettierung. Deutsche Apotheker Zeitung 121:1133–1142
Nyström C, Mazur J, Sjögren J (1982) Studies on direct compression of tablets. II. The influence of the particle size of a dry binder on the mechanical strength of tablets. Int J Pharm 10: 209–218
Otsuka M, Gao J, Matsuda Y (1993) Effects of mixer and mixing time on the pharmaceutical properties of theophylline tablets containing various kinds of lactose as diluents. Drug Dev Ind Pharm 19: 333–348
Paronen P (1986) Heckel plot as indicators of elastic properties of pharmaceuticals. Drug Dev Ind Pharm 12:1903–1912
Paronen P, Juslin M (1983) Compressional characteristics of four starches. J Pharm Pharmacol 35: 627–635
Patel NK, Patel IJ, Cutie AJ, Wadke DA, Monkhouse DC, Reier GE (1988) The effect of selected direct compression excipients on the stability of aspirin as a model hydrolyzable drug. Drug Dev Ind Pharm 14: 77–98
Patel NK, Patel IJ, Cutie AJ, Wadke DA, Monkhouse DC, Reier GE (1988) The effect of selected direct compression excipients on the stability of aspirin as a model hydrolyzable drug.Drug Dev Ind Pharm 14: 77–98
Patel NK, Upadhyay AH, Bergum JS, Reier GE (1994) An evaluation of microcristalline cellulose and lactose excipients using an instrumented single station tablet press. Int J Pharm: 203–210
Perales MCM, Munoz-Ruiz A, Antequera MW, Munoz NM, Jiminez-Castellanos MR (1994) Analysis comparative of methods to evaluate consolidation mechanisms in plastic and viscoelastic materials used as direct compression excipients. Drug Dev Ind Pharm 20: 327–342
Perales MCM, Munoz-Ruiz A, Antequera MW, Ballesteros MRJ-C (1994) Study of the compaction mechanisms of lactose-based direct compression excipients using indentation hardness and Heckel plots. J Pharm Pharmacol 46:177–181
Pesonen T, Paronen P (1990) The effect of particle and powder properties on the mechanical properties of directly compressed cellulose tablets. Drug Dev Ind Pharm 16: 31–54
Pesonen T, Paronen P, Ketolainen J (1989) Disintegrant properties of agglomerated cellulose powder. Int J Pharm 57:139–147
Pintye-Hódi K, Gyurkó E, Szabó-Révész P, Miseta M (1991) Gemeinsamer Einfluss von Hilfsstoffen und Presskraft auf die Parameter von Tabletten mit gut verpressbaren Wirkstoffen. Pharm Ind 53: 591–594
Podczeck F, Miah Y (1996) The influence of particle size and shape on the angle of internal friction and the flow factor of unlubricated and lubricated powders. International Journal of Pharmaceutics 144:187–194
Podczeck F, Wenzel U (1989) Untersuchungen zur Direkttablettierung von Arzneistoffen. Pharm Ind 51: 524–527
Ponchel G, Duchene D (1990) Evaluation of Formalin-Casein as a Tablet Disintegrant. Drug Dev Ind Pharm 16: 613–628
Proost JH, Bolhuis GK, Lerk CF (1983) The effect of the swelling capacity of disintegrants on the in-vitro and in-vivo availability of diazepam tablets containing magnesium stearate as a lubricant. Int J Pharm 13: 287–296
Rees JE, Rue PJ (1978) Time-dependent deformation of some direct compression excipients. J Pharm Pharmac 30: 601–607
Reisen P (1987) Untersuchungen zur Wirkung von Schmiermitteln bei der Tablettierung auf Exzenter-und Rundläufertablettenpressen am Beispiel verschiedener Magnesiumstearate. Pharmazeutisches Institut der Christian-Albrechts-Universität
Riepma KA, Lerk CF, de Boer AH, Bolhuis GK, Kussendrager KD (1990) Consolidation and compaction of powder mixtures i binary mixtures of same particle size fractions of different types of crystalline lactose. Int J Pharm 66: 47–52
Riepma KA, Veenstra J, de Boer AH, Bolhuis GK, Zuurman K, Lerk CF, Vromans H (1991) Consolidation and compaction of powder mixtures: II. Binary mixtures of different particle size fractions of a-lactose monohydrate. Int J Pharm 76: 9–15
Riepma KA, Vromans H, Lerk CFA (1993) Coherent matrix model for the consolidation and compaction of an excipient with magnesium stearate. Int J Pharm 97: 195–203
Riepma KA, Zuurman K, Bolhuis GK, de Boer AH, Lerk CF (1992) Consolidation and compaction of powder mixtures: III. Binary mixtures of different particle size fractions of different types of crystalline lactose. Int J Pharm 85:121–128
Ringard J (1988) Calculation of Disintegrant Critical Concentration in Order to Optimize Tablets Disintegration. Drug Dev Ind Pharm 14: 2321–2339
Ritter M, Dürrenberger Sucker H (1978) Messmethode zur Quantifizierung des Klebens von Tabletten. Pharm Ind 40:1181–1183
Roberts RJ, Rowe RC (1999) Relationships between the modulus of elasticity and tensile strength for pharmaceutical drugs and excipients. J Pharm Pharmacol 51: 975–977
Roberts RJ, Rowe RC (1985) The effect of punch velocity on the compaction of a variety of materials. J Pharm Pharmacol 37: 377–384
Roberts RJ, Rowe RC (1986) The effect of the relationship between punch velocity and particle size on the compaction behaviour of materials with varying deformation mechanisms. J Pharm Pharmacol 38: 567–571
Roberts RJ, Rowe RC (1987) The Young’s modulus of pharmaceutical materials. Int J Pharm 37: 15–18
Rowe RC (1978) The measurement of the adhesion of film coatings to tablet surfaces: the effect of tablet porosity surface roughness and film thickness. J Pharm Pharmac 30: 343–346
Rubensdörfer C (1993) Einsatz und Charakterisierung von Ludipress als Direkttablettierhilfsmittel. Dissertation Fakultät für Chemie und Pharmazie der Eberhard-Karls-Universität Tübingen
Rue PJ, Rees JE (1978) Limitations of the Heckel relation for predicting powder compaction mechanisms. J Pharm Pharmac 30: 642
Sakr AM, Kassem AA, Farrag NA (1975) Carboxy Methyl-Starch: A New Tablet Disintegrant. Pharm Ind 37: 283–287
Sangekar SA, Sarli M, Sheth PR (1972) Effect of Moisture on Physical Characteristics of Tablets Prepared from Direct Compression Excipients. J Pharm Sci 61: 939–944
Schmidt PC, Ebel S, Koch H, Profitlich T, Tenter U (1988) Presskraft-und Weg-Zeit-Charakteristik von Rundlauftablettenpressen. 4. Mitteilung: Quantitative Auswertung von Presskraft-Zeit-Kurven. Pharm Ind 50: 1409–1412
Schmidt PC, Steffens K-J, Knebel G (1983) Vereinfachung der Registrierung physikalischer Parameter bei der Tablettierung. 3. Mitteilung: Quantitative Erfassung des „Klebens“ von Pressmassen. Pharm Ind 45: 800–805
Schmidt PC, Tenter U (1988) Presskraft-und Weg-Zeit-Charakteristik von Rundlauftablettenpressen. 3. Mitteilung: Vergleich verschiedener Pressmaterialien. Pharm Ind 50:376–381
Schmidt PC, Leitritz M (1997) Compression force/time-profiles of microcrystalline cellulose dicalcium phosphate dihydrate and their binary mixtures-a critical consideration of experimental parameters. European Journal of Pharmaceutics and Biopharmaceutics 44: 303–313
Schlack H (2001) Vergleich der Kompressionseigenschaften an Rundläufer-und Exzenterpressen, Dissertation Universität Freiburg
Schwabe L, Schuppan D, Rietbrock N, Frömming K-H (1981) Einfluss von Tabletten-Füllstoffen auf die In-vitro-Freisetzung und die relative Bioverfügbarkeit von Nitrofurantoin. Pharm Ind 43:1134–1138
Schwartz JB, Martin ET, Dehner EJ (1975) Intragranular starch: comparison of starch usp and modified cornstarch. J Pharm Sci 64: 328–332
Sheik-Salem M, Alkaysi H, Fell JT (1988) The tensile strength of tablets of binary mixtures lubricated with magnesium stearate. Drug Dev Ind Pharm 14: 895–903
Stamm A, Mathis C (1976) Verpressbarkeit von festen Hilfsstoffen für Direkttablettierung. Acta Pharm Technol Suppl. 1: 7–16
Staniforth JN (1993) The Design and use of Tableting Excipients. Drug Dev Ind Pharm 19: 2273–2308
Stanley P (2001) Mechanical strength testing of compacted powders. International Journal of Pharmaceutics 227: 27–38
Steffens K-J, Müller BW, List PH (1982) Tribologische Gesetzmäßigkeiten und Erkenntnisse in der Tablettentechnologie. 7. Mitteilung. Pharm Ind 44: 826–830
Sucker H, Fuchs P, Speiser P (1991) Pharmazeutische Technologie. Thieme, Stuttgart New York
Szabo-Révész P, Petö K, Pintye-Hódi K (1986) Untersuchung der Verwendbarkeit von mikrokristallinen Cellulosen bei der Herstellung von Phenobarbital-Tabletten. 2. Mitteilung: Einfluss von Avicel PH 101 sowie von Avicel PH 101 und Maisstärke auf die Parameter von Tabletten. Pharm Ind 48: 289–291
Thwaites PM (1992) The effect of mixing time and mixing intensity on the compression properties of tablettose. Drug Dev Ind Pharm 18: 2001–2010
Thwaites PM, Mashadi AB, Moore WD (1991) An investigation of the effect of high speed mixing on the mechanical and physical properties of direct compression lactose. Drug Dev Ind Pharm 17: 503–517
Udeala OK, Aly SAS (1989) Linear relationship between tablet properties in systems compressed under fixed compression force. Drug Dev Ind Pharm 15:133–145
Van der Voort Maarschalk K, Bolhuis GK (1999) Improving Properties of Materials for Direct Compaction. Pharmaceutical Technology (5): 34
van der Watt JG, de Villiers MM (1997) The effect of V-mixer scale-up on the mixing of magnesium stearate with direct compression microcrystalline cellulose. European Journal of Pharmaceutics and Biopharmaceutics 43: 91–94
van Kamp HV, Bolhuis GK, de Boer AH, Lerk CF, Lie-A-Huen L (1986) The role of water uptake on tablet disintegration. Pharm Acta Helv 61: 22–29
Van Veen B, van der Voort Maarschalk K, Bolhuis GK (2000) Tensile strength of tablets containing two materials with a different compaction behaviour. International Journal of Pharmaceutics 203: 71–79
Varthalis S, Pilpel N (1977) The action of colloidal silicon dioxide as a glidant for lactose paracetamol Oxytetracycline and their mixtures. J Pharm Pharmacol 29: 37–40
Velasco M.V, Munoz-Ruiz A, Monedero MC, Jimenez-Castellanos MR (1995) Study of flowability of powders effect of the addition of lubricants. Drug Dev Ind Pharm 21: 2385–2391
Vezin WR, Pang HM, Khan KA, Malkowska S (1983) The effect of precompression in a rotary machine on tablet strength. Drug Dev Ind Pharm 9:1465–1474
Vromans H, de Boer AH, Bolhuis GK, Lerk CF, Kussendrager KD (1986) Studies on tableting properties of lactose: The effect of initial particle size on binding properties and dehydration characteristics of α-lactose monohydrate. Drug Dev Ind Pharm 12:1715–1730
Wade A, Weller PJ (1994) Handbook of Pharmaceutical Excipients. The Pharmaceutical Press, London
Walz M (1988) Haftung und Kleben von Tablettenmassen an Presswerkzeugen, Dissertation, Institut für Pharmazeutische Technologie und Biopharmazie der Ruprecht-Karls-Universität Heidelberg
Wan LS, Heng PWS (1986) Action of Surfactant on Disintegration and Dissolution of Tablets containing Microcrystalline cellulose. Pharm Acta Helv 61:157–163
Wang L-H, Chowhan ZT (1990) Drug-excipient interaction resulting from powder mixing v role of sodium lauryl sulfate. Int J Pharm 60: 61–78
Warring MJ, Sen H, Forrester JW, Salmon JR (1986) Instrumented and computer interfaced single punch tablet press for the rapid evaluation of compression and lubrication behavior. Drug Dev Ind Pharm 12:1847–1868
Weinekötter R (1995) Mischzeiten in Feststoffmischern-Gestaltung von Chargenmischprozessen. Schüttgut 1:125–128
Wells JI 1988 Pharmaceutical preformulation-the physicochemical properties of drug substances. Ellis Horwood, Chichester
Westerberg M, Nyström C (1991) Physicochemical aspects of drug release. XII. The effect of some carrier particle properties and lubricant admixture on drug dissolution from tableted ordered mixtures. Int J Pharm 69: 129–141
Whiteman M, Yarwood RJ (1990) Variations in lactose NF from different sources and their influence on tablet properties. Drug Dev Ind Pharm 16:1815–1827 5-190. Williams RO, McGinity JW (1988) The use of tableting properties to study the compaction properties of powders. Drug Dev Ind Pharm 14: 1823–1844
Zhang Y, Johnson KC (1997) Effect of drug particle size on content uniformity of lowdose solid dosage forms. International Journal of Pharmaceutics 154: 179–183
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2003 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Sticker, H. (2003). Entwicklung von Tabletten (Direktverpressung). In: Arzneiformen-Entwicklung. Springer-Lehrbuch. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-18982-1_5
Download citation
DOI: https://doi.org/10.1007/978-3-642-18982-1_5
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-62393-6
Online ISBN: 978-3-642-18982-1
eBook Packages: Springer Book Archive