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Tu Van Duong & Guy Van den Mooter. (2016) The role of the carrier in the formulation of pharmaceutical solid dispersions. Part I: crystalline and semi-crystalline carriers. Expert Opinion on Drug Delivery 13:11, pages 1583-1594.
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Kerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, Peter Hölig, Jörg Rosenberg, Markus Mägerlein, Gert Fricker & Martin Brandl. (2012) The amorphous solid dispersion of the poorly soluble ABT-102 forms nano/microparticulate structures in aqueous medium: impact on solubility. International Journal of Nanomedicine 7, pages 5757-5768.
Read now
Read now
Rutesh H. Dave, Ashwinkumar D. Patel, Edward Donahue & Hardikkumar H. Patel. (2012) To evaluate the effect of addition of an anionic surfactant on solid dispersion using model drug indomethacin. Drug Development and Industrial Pharmacy 38:8, pages 930-939.
Read now
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Christina M. Hentzschel, Albrecht Sakmann & Claudia S. Leopold. (2011) Suitability of various excipients as carrier and coating materials for liquisolid compacts. Drug Development and Industrial Pharmacy 37:10, pages 1200-1207.
Read now
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Ali Nokhodchi, Christina M Hentzschel & Claudia S Leopold. (2011) Drug release from liquisolid systems: speed it up, slow it down. Expert Opinion on Drug Delivery 8:2, pages 191-205.
Read now
Read now
Madhuri Newa, Krishna H. Bhandari, Jung-Ae Kim, Bong-Kyu Yoo, Han-Gon Choi, Chul-Soon Yong, Jong-Soo Woo & Won-Seok Lyoo. (2008) Preparation and Evaluation of Fast Dissolving Ibuprofen-Polyethylene Glycol 6000 Solid Dispersions. Drug Delivery 15:6, pages 355-364.
Read now
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Madhuri Newa, Krishna Hari Bhandari, Dong Xun Lee, Jung Hoon Sung, Jung Ae Kim, Bong Kyu Yoo, Jong Soo Woo, Han Gon Choi & Chul Soon Yong. (2008) Enhanced Dissolution of Ibuprofen Using Solid Dispersion with Polyethylene Glycol 20000. Drug Development and Industrial Pharmacy 34:10, pages 1013-1021.
Read now
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M. Valleri, P. Mura, F. Maestrelli, M. Cirri & R. Ballerini. (2004) Development and Evaluation of Glyburide Fast Dissolving Tablets Using Solid Dispersion Technique. Drug Development and Industrial Pharmacy 30:5, pages 525-534.
Read now
Read now
M. Cirri, P. Mura, A. M. Rabasco, J. M. Ginés, J. R. Moyano & M. L. Gònzalez‐Rodrìguez. (2004) Characterization of Ibuproxam Binary and Ternary Dispersions with Hydrophilic Carriers. Drug Development and Industrial Pharmacy 30:1, pages 65-74.
Read now
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A. Forster, J. Hempenstall, I. Tucker & T. Rades. (2001) The Potential of Small-Scale Fusion Experiments and the Gordon-Taylor Equation to Predict the Suitability of Drug/Polymer Blends for Melt Extrusion. Drug Development and Industrial Pharmacy 27:6, pages 549-560.
Read now
Read now
P. Dangprasirt & S. Pongwai. (1998) Development of Diclofenac Sodium Controlled Release Solid Dispersion Powders and Capsules by Freeze Drying Technique Using Ethylcellulose and Chitosan as Carriers. Drug Development and Industrial Pharmacy 24:10, pages 947-953.
Read now
Read now
D. H. Doshi, W. R. Ravis & G. V. Betageri. (1997) Carbamazepine and Polyethylene Glycol Solid Dispersions: Preparation, in Vitro Dissolution, and Characterization. Drug Development and Industrial Pharmacy 23:12, pages 1167-1176.
Read now
Read now
D. Q. M. Craig. (1990) Polyethyelene Glycols and Drug Release. Drug Development and Industrial Pharmacy 16:17, pages 2501-2526.
Read now
Read now
J. Akbuĝa, A. Gürsoy & E. Kendi. (1988) The Preparation and Stability of Fast Release Furosemide – PVP Solid Dispersion. Drug Development and Industrial Pharmacy 14:10, pages 1439-1464.
Read now
Read now
Z. Ramtoola & O. I. Corrigan. (1987) Dissolution Characteristics of Benzoic Acid and Salicylic Acid Mixtures in Reactive Media. Drug Development and Industrial Pharmacy 13:9-11, pages 1703-1720.
Read now
Read now
Owen I. Corrigan. (1986) Retardation of Polymeric Carrier Dissolution by Dispersed Drugs: Factors Influencing the Dissolution of Solid Dispersions Containing Polyethlene Glycols. Drug Development and Industrial Pharmacy 12:11-13, pages 1777-1793.
Read now
Read now
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Crossref
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Camila G. Jange, Carl R. Wassgren & Kingsly Ambrose. (2023) The Significance of Tablet Internal Structure on Disintegration and Dissolution of Immediate-Release Formulas: A Review. Powders 2:1, pages 99-123.
Crossref
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Dr Zakir Hussain, Dr Mukkamalla Suresh, B. Hemalata & Shaik Shireen. (2022) Articulation Expansion including Artificial Insemination Estimation of Dextromethorphan Tablet by Solid Dispersion Recipe for Solubility Enhancement. International Journal of Pharmaceutical Sciences Review and Research, pages 53-59.
Crossref
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Clara E. Correa-Soto, Yi Gao, Anura S. Indulkar, Geoff G.Z. Zhang & Lynne S. Taylor. (2022) Role of surfactants in improving release from higher drug loading amorphous solid dispersions. International Journal of Pharmaceutics 625, pages 122120.
Crossref
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Anura S. Indulkar, Xiaochun Lou, Geoff G. Z. Zhang & Lynne S. Taylor. (2022) Role of Surfactants on Release Performance of Amorphous Solid Dispersions of Ritonavir and Copovidone. Pharmaceutical Research 39:2, pages 381-397.
Crossref
Crossref
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Crossref
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Christi A. Wilkins, Lissinda H. du Plessis & Joe M. Viljoen. (2021) Investigating In Vitro and Ex Vivo Properties of Artemether/Lumefantrine Double-Fixed Dose Combination Lipid Matrix Tablets Prepared by Hot Fusion. Pharmaceutics 13:7, pages 922.
Crossref
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Sugandha Saboo, Dana E. Moseson, Umesh S. Kestur & Lynne S. Taylor. (2020) Patterns of drug release as a function of drug loading from amorphous solid dispersions: A comparison of five different polymers.. European Journal of Pharmaceutical Sciences 155, pages 105514.
Crossref
Crossref
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Crossref
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Crossref
Crossref
Sugandha Saboo, Umesh S. Kestur, Daniel P. Flaherty & Lynne S. Taylor. (2020) Congruent Release of Drug and Polymer from Amorphous Solid Dispersions: Insights into the Role of Drug-Polymer Hydrogen Bonding, Surface Crystallization, and Glass Transition. Molecular Pharmaceutics 17:4, pages 1261-1275.
Crossref
Crossref
Alfonso Toro-Córdova, Beatriz Sanz & Gerardo F. Goya. (2020) A Concise Review of Nanomaterials for Drug Delivery and Release. Current Nanoscience 16:3, pages 399-412.
Crossref
Crossref
Yi Rang Han, Yingshan Ma & Ping I. Lee. (2019) Impact of phase separation morphology on release mechanism of amorphous solid dispersions. European Journal of Pharmaceutical Sciences 136, pages 104955.
Crossref
Crossref
Na Li & Lynne S. Taylor. (2019) Microstructure Formation for Improved Dissolution Performance of Lopinavir Amorphous Solid Dispersions. Molecular Pharmaceutics 16:4, pages 1751-1765.
Crossref
Crossref
Anura S. Indulkar, Xiaochun Lou, Geoff G. Z. Zhang & Lynne S. Taylor. (2019) Insights into the Dissolution Mechanism of Ritonavir–Copovidone Amorphous Solid Dispersions: Importance of Congruent Release for Enhanced Performance. Molecular Pharmaceutics 16:3, pages 1327-1339.
Crossref
Crossref
Sugandha Saboo, Naila A. Mugheirbi, Dmitry Y. Zemlyanov, Umesh S. Kestur & Lynne S. Taylor. (2019) Congruent release of drug and polymer: A “sweet spot” in the dissolution of amorphous solid dispersions. Journal of Controlled Release 298, pages 68-82.
Crossref
Crossref
Luke Schenck, Amanda K.P. Mann, Zhen Liu, Mikolaj Milewski, Siwei Zhang, Jie Ren, Kristel Dewitt, Andre Hermans & Aaron Cote. (2019) Building a better particle: Leveraging physicochemical understanding of amorphous solid dispersions and a hierarchical particle approach for improved delivery at high drug loadings. International Journal of Pharmaceutics 559, pages 147-155.
Crossref
Crossref
Laura I. Mosquera-Giraldo, Na Li, Venecia R. Wilson, Brittany L.B. Nichols, Kevin J. Edgar & Lynne S. Taylor. (2018) Influence of Polymer and Drug Loading on the Release Profile and Membrane Transport of Telaprevir. Molecular Pharmaceutics 15:4, pages 1700-1713.
Crossref
Crossref
Ludmila A.G. Pinho, Stephania G.B. Lima, Lorena F.B. Malaquias, Felipe de Q. Pires, Lívia L. Sá-Barreto, Lucio Cardozo-Filho, Tais Gratieri, Guilherme M. Gelfuso & Marcilio Cunha-Filho. (2018) Improvements of theobromine pharmaceutical properties using solid dispersions prepared with newfound technologies. Chemical Engineering Research and Design 132, pages 1193-1201.
Crossref
Crossref
Hitesh S. Purohit & Lynne S. Taylor. (2017) Phase Behavior of Ritonavir Amorphous Solid Dispersions during Hydration and Dissolution. Pharmaceutical Research 34:12, pages 2842-2861.
Crossref
Crossref
Smruti P. Chaudhari & Rohit P. Dugar. (2017) Application of surfactants in solid dispersion technology for improving solubility of poorly water soluble drugs. Journal of Drug Delivery Science and Technology 41, pages 68-77.
Crossref
Crossref
Tian Xie, Wei Gao & Lynne S. Taylor. (2017) Impact of Eudragit EPO and hydroxypropyl methylcellulose on drug release rate, supersaturation, precipitation outcome and redissolution rate of indomethacin amorphous solid dispersions. International Journal of Pharmaceutics 531:1, pages 313-323.
Crossref
Crossref
Anura S. Indulkar, Jan E. Waters, Huaping Mo, Yi Gao, Shweta A. Raina, Geoff G.Z. Zhang & Lynne S. Taylor. (2017) Origin of Nanodroplet Formation Upon Dissolution of an Amorphous Solid Dispersion: A Mechanistic Isotope Scrambling Study. Journal of Pharmaceutical Sciences 106:8, pages 1998-2008.
Crossref
Crossref
Roberta Censi, Maria Rosa Gigliobianco, Alessandra Dubbini, Ladjan Malaj & Piera Di Martino. (2015) New Nanometric Solid Dispersions of Glibenclamide in Neusilin® UFL2. AAPS PharmSciTech 17:5, pages 1204-1212.
Crossref
Crossref
Lynne S. Taylor & Geoff G.Z. Zhang. (2016) Physical chemistry of supersaturated solutions and implications for oral absorption. Advanced Drug Delivery Reviews 101, pages 122-142.
Crossref
Crossref
Paul Harmon, Kendra Galipeau, Wei Xu, Chad Brown & W. Peter Wuelfing. (2016) Mechanism of Dissolution-Induced Nanoparticle Formation from a Copovidone-Based Amorphous Solid Dispersion. Molecular Pharmaceutics 13:5, pages 1467-1481.
Crossref
Crossref
Tian Xie & Lynne S. Taylor. (2016) Improved Release of Celecoxib from High Drug Loading Amorphous Solid Dispersions Formulated with Polyacrylic Acid and Cellulose Derivatives. Molecular Pharmaceutics 13:3, pages 873-884.
Crossref
Crossref
Duy Hieu Truong, Tuan Hiep Tran, Thiruganesh Ramasamy, Ju Yeon Choi, Han-Gon Choi, Chul Soon Yong & Jong Oh Kim. (2015) Preparation and characterization of solid dispersion using a novel amphiphilic copolymer to enhance dissolution and oral bioavailability of sorafenib. Powder Technology 283, pages 260-265.
Crossref
Crossref
Kenjirou Higashi, Hiroki Hayashi, Keiji Yamamoto & Kunikazu Moribe. (2015) The effect of drug and EUDRAGIT® S 100 miscibility in solid dispersions on the drug and polymer dissolution rate. International Journal of Pharmaceutics 494:1, pages 9-16.
Crossref
Crossref
Grace A. Ilevbare, Wei Xu, Christopher T. John, James D. Ormes, Jesse L. Kuiper, Allen C. Templeton & Annette Bak. 2010. Pharmaceutical Sciences Encyclopedia. Pharmaceutical Sciences Encyclopedia
1
41
.
Grace Ilevbare, Patrick Marsac & Amitava Mitra. 2015. Discovering and Developing Molecules with Optimal Drug-Like Properties. Discovering and Developing Molecules with Optimal Drug-Like Properties
287
343
.
Sheng Qi, William J McAuley, Ziyi Yang & Pratchaya Tipduangta. (2014) Physical stabilization of low-molecular-weight amorphous drugs in the solid state: a material science approach. Therapeutic Delivery 5:7, pages 817-841.
Crossref
Crossref
David R. Ely, R. Edwin Garc?a & Markus Thommes. (2014) Ostwald?Freundlich diffusion-limited dissolution kinetics of nanoparticles. Powder Technology 257, pages 120-123.
Crossref
Crossref
Krishna Sanka, Sravanthi Poienti, Abdul Bari Mohd & Prakash V. Diwan. (2014) Improved oral delivery of clonazepam through liquisolid powder compact formulations: In-vitro and ex-vivo characterization. Powder Technology 256, pages 336-344.
Crossref
Crossref
Maria Fátima Pina, Min Zhao, João F. Pinto, João J. Sousa & Duncan Q.M. Craig. (2014) The Influence of Drug Physical State on the Dissolution Enhancement of Solid Dispersions Prepared Via Hot-Melt Extrusion: A Case Study Using Olanzapine. Journal of Pharmaceutical Sciences 103:4, pages 1214-1223.
Crossref
Crossref
Waleed Faisal, Therese Ruane-O’Hora, Caitriona M. O’Driscoll & Brendan T. Griffin. (2013) A novel lipid-based solid dispersion for enhancing oral bioavailability of Lycopene – In vivo evaluation using a pig model. International Journal of Pharmaceutics 453:2, pages 307-314.
Crossref
Crossref
Amrit Paudel, Zelalem Ayenew Worku, Joke Meeus, Sandra Guns & Guy Van den Mooter. (2013) Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations. International Journal of Pharmaceutics 453:1, pages 253-284.
Crossref
Crossref
Taher Boukhris, Malika Lahiani-Skiba, Damien Martin & Mohamed Skiba. (2012) Pre-formulation of an oral cyclosporine free of surfactant. Journal of Inclusion Phenomena and Macrocyclic Chemistry 75:3-4, pages 323-332.
Crossref
Crossref
Zhongjiang Jia, Duk Soon Choi & Hitesh Chokshi. (2013) Determination of Drug-Polymer Binding Constants by Affinity Capillary Electrophoresis for Aryl Propionic Acid Derivatives and Related Compounds. Journal of Pharmaceutical Sciences 102:3, pages 960-966.
Crossref
Crossref
Venkateskumar Krishnamoorthy, Suchandrasen & Verma Priya Ranjan Prasad. (2012) Physicochemical characterization and in vitro dissolution behavior of olanzapine-mannitol solid dispersions. Brazilian Journal of Pharmaceutical Sciences 48:2, pages 243-255.
Crossref
Crossref
Jin Li, Pan Liu, Jian-Ping Liu, Wen-Li Zhang, Ji-Kun Yang & Yong-Qing Fan. (2012) Novel Tanshinone II A ternary solid dispersion pellets prepared by a single-step technique: In vitro and in vivo evaluation. European Journal of Pharmaceutics and Biopharmaceutics 80:2, pages 426-432.
Crossref
Crossref
Laxmikant Ramvallabh Zawar & Sanjay Baburao Bari. (2012) Preparation, Characterization and in Vivo Evaluation of Antihyperglycemic Activity of Microwave Generated Repaglinide Solid Dispersion. Chemical and Pharmaceutical Bulletin 60:4, pages 482-487.
Crossref
Crossref
C.M. Hentzschel, M. Alnaief, I. Smirnova, A. Sakmann & C.S. Leopold. (2012) Enhancement of griseofulvin release from liquisolid compacts. European Journal of Pharmaceutics and Biopharmaceutics 80:1, pages 130-135.
Crossref
Crossref
Sheraz Khan, Hannah Batchelor, Peter Hanson, Yvonne Perrie & Afzal R. Mohammed. (2011) Physicochemical characterisation, drug polymer dissolution and in vitro evaluation of phenacetin and phenylbutazone solid dispersions with polyethylene glycol 8000. Journal of Pharmaceutical Sciences 100:10, pages 4281-4294.
Crossref
Crossref
Jun-Hyung Park, Myung-Kwan Chun, Hoon Cho & Hoo-Kyun Choi. (2011) Solid Dispersion as a Strategy to Improve Drug Bioavailability. KSBB Journal 26:4, pages 283-292.
Crossref
Crossref
David E. Alonzo, Yi Gao, Deliang Zhou, Huaping Mo, Geoff G.Z. Zhang & Lynne S. Taylor. (2011) Dissolution and Precipitation Behavior of Amorphous Solid Dispersions. Journal of Pharmaceutical Sciences 100:8, pages 3316-3331.
Crossref
Crossref
Vibha Puri, Ajay K. Dantuluri & Arvind K. Bansal. (2011) Investigation of Atypical Dissolution Behavior of an Encapsulated Amorphous Solid Dispersion. Journal of Pharmaceutical Sciences 100:6, pages 2460-2468.
Crossref
Crossref
Yuebin GE. (2010) An Investigation into the Mechanisms of Rapid Release of Standard Extract from <i>Ginkgo biloba</i> leaf in Polyethylene Glycol 6000 Solid Dispersions. YAKUGAKU ZASSHI 130:3, pages 425-430.
Crossref
Crossref
Dionysios Douroumis, Nikolaos Bouropoulos & Alfred Fahr. (2007) Physicochemical characterization of solid dispersions of three antiepileptic drugs prepared by solvent evaporation method. Journal of Pharmacy and Pharmacology 59:5, pages 645-653.
Crossref
Crossref
Angus Forster, John Hempenstall & Thomas Rades. (2001) Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with hydrophilic amorphous polymers. Journal of Pharmacy and Pharmacology 53:3, pages 303-315.
Crossref
Crossref
Mohammad Barzegar-Jalali, Hadi Valizadeh, Mohammad-Reza Siahi Shadbad, Khosro Adibkia, Ghobad Mohammadi, Amin Farahani, Zeynab Arash & Ali Nokhodchi. (2010) Cogrinding as an approach to enhance dissolution rate of a poorly water-soluble drug (gliclazide). Powder Technology 197:3, pages 150-158.
Crossref
Crossref
I.U. Khan, N.M. Ranjha & H.Q. Mehmood. (2010) Development of ethylcellulose-polyethylene glycol and ethylcellulose-polyvinyl pyrrolidone blend oral microspheres of ibuprofen. Journal of Drug Delivery Science and Technology 20:6, pages 439-444.
Crossref
Crossref
Tapan Kumar GIRI & Biswanath SA. (2009) Statistical Evaluation of Influence of Polymers Concentration on Disintegration Time and Diazepam Release from Quick Disintegrating Rapid Release Tablet. YAKUGAKU ZASSHI 129:9, pages 1069-1075.
Crossref
Crossref
Michael Tobyn, Jonathan Brown, Andrew B Dennis, Michael Fakes, Qi gao, John Gamble, Yaroslav Z Khimyak, Gary Mcgeorge, Chhaya Patel, Wayne Sinclair, Peter Timmins & Shawn Yin. (2009) Amorphous Drug-PVP Dispersions: Application of Theoretical, Thermal and Spectroscopic Analytical Techniques to the Study of a Molecule With Intermolecular Bonds in Both the Crystalline and Pure Amorphous State. Journal of Pharmaceutical Sciences 98:9, pages 3456-3468.
Crossref
Crossref
Sandrien Janssens, Michael Anné, Patrick Rombaut & Guy Van den Mooter. (2009) Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions. European Journal of Pharmaceutical Sciences 37:3-4, pages 241-248.
Crossref
Crossref
Jessica Albers, Rainer Alles, Karin Matth?e, Klaus Knop, Julia Schulze Nahrup & Peter Kleinebudde. (2009) Mechanism of drug release from polymethacrylate-based extrudates and milled strands prepared by hot-melt extrusion. European Journal of Pharmaceutics and Biopharmaceutics 71:2, pages 387-394.
Crossref
Crossref
Madhuri Newa, Krishna Hari Bhandari, Dong Hoon Oh, Young Ran Kim, Joon Ho Sung, Jong Oh Kim, Jong Soo Woo, Han Gon Choi & Chul Soon Yong. (2008) Enhanced dissolution of ibuprofen using solid dispersion with poloxamer 407. Archives of Pharmacal Research 31:11, pages 1497-1507.
Crossref
Crossref
Angela Mary Barrett, Fariba Dehghani & Neil R. Foster. (2007) Increasing the Dissolution Rate of Itraconazole Processed by Gas Antisolvent Techniques using Polyethylene Glycol as a Carrier. Pharmaceutical Research 25:6, pages 1274-1289.
Crossref
Crossref
Smiti KUMARGarima CHAWLAArvind K. BANSAL. (2008) Role of Additives like Polymers and Surfactants in the Crystallization of Mebendazole. YAKUGAKU ZASSHI 128:2, pages 281-289.
Crossref
Crossref
Madhuri Newa, Krishna Hari Bhandari, Jong Oh Kim, Jong Seob Im, Jung Ae Kim, Bong Kyu Yoo, Jong Soo Woo, Han Gon Choi & Chul Soon Yong. (2008) Enhancement of Solubility, Dissolution and Bioavailability of Ibuprofen in Solid Dispersion Systems. Chemical and Pharmaceutical Bulletin 56:4, pages 569-574.
Crossref
Crossref
Madhuri Newa, Krishna Hari Bhandari, Dong Xun Li, Jong Oh Kim, Dong Sung Yoo, Jung-Ae Kim, Bong-Kyu Yoo, Jong-Soo Woo, Han-Gon Choi & Chul-Soon Yong. (2008) Preparation and Evaluation of Immediate Release Ibuprofen Solid Dispersions Using Polyethylene Glycol 4000. Biological and Pharmaceutical Bulletin 31:5, pages 939-945.
Crossref
Crossref
Sau Lawrence Lee, Andre S. Raw & Lawrence Yu. 2008. Biopharmaceutics Applications in Drug Development. Biopharmaceutics Applications in Drug Development
47
74
.
Shyam Sunder Bansal, Aditya Mohan Kaushal & Arvind Kumar Bansal. (2007) Molecular and Thermodynamic Aspects of Solubility Advantage from Solid Dispersions. Molecular Pharmaceutics 4:5, pages 794-802.
Crossref
Crossref
Carina Dahlberg, Anna Fureby, Michael Schuleit, Sergey V. Dvinskikh & Istv?n Fur?. (2007) Polymer mobilization and drug release during tablet swelling. A 1H NMR and NMR microimaging study. Journal of Controlled Release 122:2, pages 199-205.
Crossref
Crossref
Evangelos Karavas, Emmanuel Georgarakis, Michael P. Sigalas, Konstantinos Avgoustakis & Dimitrios Bikiaris. (2007) Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug–polymer interactions. European Journal of Pharmaceutics and Biopharmaceutics 66:3, pages 334-347.
Crossref
Crossref
Evangelos Karavas, Georgios Ktistis, Aristotelis Xenakis & Emmanouel Georgarakis. (2006) Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone. European Journal of Pharmaceutics and Biopharmaceutics 63:2, pages 103-114.
Crossref
Crossref
Solmaz Esnaashari, Yousef Javadzadeh, Hannah K. Batchelor & Barbara R. Conway. (2005) The use of microviscometry to study polymer dissolution from solid dispersion drug delivery systems. International Journal of Pharmaceutics 292:1-2, pages 227-230.
Crossref
Crossref
D.J. van Drooge, W.L.J. Hinrichs & H.W. Frijlink. (2004) Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions. Journal of Controlled Release 97:3, pages 441-452.
Crossref
Crossref
Mayumi Asada, Hirokazu Takahashi, Hirokazu Okamoto, Hideo Tanino & Kazumi Danjo. (2004) Theophylline particle design using chitosan by the spray drying. International Journal of Pharmaceutics 270:1-2, pages 167-174.
Crossref
Crossref
Richer Chen, Maya Tagawa, Noboru Hoshi, Toshihiro Ogura, Hirokazu Okamoto & Kazumi Danjo. (2004) Improved Dissolution of an Insoluble Drug Using a 4-Fluid Nozzle Spray-Drying Technique. CHEMICAL & PHARMACEUTICAL BULLETIN 52:9, pages 1066-1070.
Crossref
Crossref
S Verheyen, N Blaton, R Kinget & G Van den Mooter. (2002) Mechanism of increased dissolution of diazepam and temazepam from polyethylene glycol 6000 solid dispersions. International Journal of Pharmaceutics 249:1-2, pages 45-58.
Crossref
Crossref
Owen I Corrigan & Abina M Crean. (2002) Comparative physicochemical properties of hydrocortisone?PVP composites prepared using supercritical carbon dioxide by the GAS anti-solvent recrystallization process, by coprecipitation and by spray drying. International Journal of Pharmaceutics 245:1-2, pages 75-82.
Crossref
Crossref
Karen M. O'Connor & Owen I. Corrigan. (2002) Effect of a basic organic excipient on the dissolution of diclofenac salts. Journal of Pharmaceutical Sciences 91:10, pages 2271-2281.
Crossref
Crossref
Duncan Q.M Craig. (2002) The mechanisms of drug release from solid dispersions in water-soluble polymers. International Journal of Pharmaceutics 231:2, pages 131-144.
Crossref
Crossref
Zerrouk Naima, Toscani Siro, Gines-Dorado Juan-Manuel, Chemtob Chantal, Ceólin René & Dugué Jerome. (2001) Interactions between carbamazepine and polyethylene glycol (PEG) 6000: characterisations of the physical, solid dispersed and eutectic mixtures. European Journal of Pharmaceutical Sciences 12:4, pages 395-404.
Crossref
Crossref
Narong Sarisuta, Somboon Jateleela & Tudsong Tourtip. (2000) Dissolution Kinetics of Three‐Component Compressed Solid Mixtures with Largely Different Solubilities: Flaking Spheres. Journal of Pharmaceutical Sciences 89:9, pages 1196-1211.
Crossref
Crossref
S Hülsmann, T Backensfeld, S Keitel & R Bodmeier. (2000) Melt extrusion – an alternative method for enhancing the dissolution rate of 17β-estradiol hemihydrate. European Journal of Pharmaceutics and Biopharmaceutics 49:3, pages 237-242.
Crossref
Crossref
Margareta Emås & Håkan Nyqvist. (2000) Methods of studying aging and stabilization of spray-congealed solid dispersions with carnauba wax. 1. Microcalorimetric investigation. International Journal of Pharmaceutics 197:1-2, pages 117-127.
Crossref
Crossref
Abu T.M. Serajuddin. (1999) Solid dispersion of poorly water‐soluble drugs: Early promises, subsequent problems, and recent breakthroughs. Journal of Pharmaceutical Sciences 88:10, pages 1058-1066.
Crossref
Crossref
G.R. Lloyd, D.Q.M. Craig & A. Smith. (1997) An investigation into the production of paracetamol solid dispersions in PEG 4000 using hot stage differential interference contrast microscopy. International Journal of Pharmaceutics 158:1, pages 39-46.
Crossref
Crossref
Marie Wulff & Maggie Ald?n. (1995) Phase equilibria in drug-polymer-surfactant systems. Thermochimica Acta 256:1, pages 151-165.
Crossref
Crossref
Eva Sj?kvist Saers & Duncan Q.M. Craig. (1992) An investigation into the mechanisms of dissolution of alkyl p-aminobenzoates from polyethylene glycol solid dispersions. International Journal of Pharmaceutics 83:1-3, pages 211-219.
Crossref
Crossref
Eva Sj?kvist, Christer Nystr?m, Maggie Ald?n & Ninus Caram-Lelham. (1992) Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions. International Journal of Pharmaceutics 79:1-3, pages 123-133.
Crossref
Crossref
D.Q.M. Craig & J.M. Newton. (1992) The dissolution of nortriptyline HCl from polyethylene glycol solid dispersions. International Journal of Pharmaceutics 78:1-3, pages 175-182.
Crossref
Crossref
Umesh Banakar. 1991. Pharmaceutical Dissolution Testing. Pharmaceutical Dissolution Testing
133
187
.
Umesh Banakar. 1991. Pharmaceutical Dissolution Testing. Pharmaceutical Dissolution Testing
19
51
.
Abu T.M. Serajuddin, Daniel Mufson, David F. Bernstein, Pai-Chang Sheen & Matthew A. Augustine. (1988) Effect of Vehicle Amphiphilicity on the Dissolution and Bioavailability of a Poorly Water-Soluble Drug from Solid Dispersions. Journal of Pharmaceutical Sciences 77:5, pages 414-417.
Crossref
Crossref