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Panagiotis Barmpalexis, Kyriakos Kachrimanis & Emanouil Georgarakis. (2014) Physicochemical characterization of nimodipine–polyethylene glycol solid dispersion systems. Drug Development and Industrial Pharmacy 40:7, pages 886-895.
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Parijat Kanaujia, Wai Kiong Ng & Reginald B. H. Tan. (2014) Solid self-emulsifying drug delivery system (S-SEDDS) for improved dissolution rate of fenofibrate. Journal of Microencapsulation 31:3, pages 293-298.
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Ahmed A. Aboelwafa & Rania H. Fahmy. (2012) A pilot human pharmacokinetic study and influence of formulation factors on orodispersible tablet incorporating meloxicam solid dispersion using factorial design. Pharmaceutical Development and Technology 17:1, pages 1-14.
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Parinda Srinarong, Hans de Waard, Henderik W Frijlink & Wouter LJ Hinrichs. (2011) Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations. Expert Opinion on Drug Delivery 8:9, pages 1121-1140.
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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.
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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.
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N. S. Barakat. (2006) Etodolac-Liquid-Filled Dispersion into Hard Gelatin Capsules: An Approach to Improve Dissolution and Stability of Etodolac Formulation. Drug Development and Industrial Pharmacy 32:7, pages 865-876.
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Manish K. Gupta, Robin H. Bogner, David Goldman & Yin-Chao Tseng. (2002) Mechanism for Further Enhancement in Drug Dissolution from Solid-Dispersion Granules upon Storage. Pharmaceutical Development and Technology 7:1, pages 103-112.
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S. Chutimaworapan, G. C. Ritthidej, E. Yonemochi, T. Oguchi & K. Yamamoto. (2000) Effect of Water-Soluble Carriers on Dissolution Characteristics of Nifedipine Solid Dispersions. Drug Development and Industrial Pharmacy 26:11, pages 1141-1150.
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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
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S. K. Dordunoo, J. L Ford & M. H. Rubinstein. (1991) Preformulation Studies on Solid Dispersions Containing Triamterene or Temazepam in Polyethylene Glycols or Gelucire 44/14 for Liquid Filling of Hard Gelatin Capsules. Drug Development and Industrial Pharmacy 17:12, pages 1685-1713.
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179
216
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Ashok Neelkanth MahajanNaazneen SurtiPriyal PatelAshwini PatelDimal ShahVandana Patel. (2020) Melt Dispersion Adsorbed onto Porous Carriers: An Effective Method to Enhance the Dissolution and Flow Properties of Raloxifene Hydrochloride. ASSAY and Drug Development Technologies 18:6, pages 282-294.
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Doaa Ahmed El-Setouhy, Emad B. Basalious & Nevine Shawky Abdelmalak. (2017) Effect of Different Meltable Binders on the Disintegration and Dissolution Behavior of Zolmitriptan Oromucosal Fast Melt Tablets. Journal of Pharmacy and Nutrition Sciences 7:1, pages 13-23.
Crossref
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Soraya Hengsawas Surasarang & Robert O. WilliamsIIIIII. 2016. Formulating Poorly Water Soluble Drugs. Formulating Poorly Water Soluble Drugs
215
256
.
Muqdad Alhijjaj, Jacob Bouman, Nikolaus Wellner, Peter Belton & Sheng Qi. (2015) Creating Drug Solubilization Compartments via Phase Separation in Multicomponent Buccal Patches Prepared by Direct Hot Melt Extrusion–Injection Molding. Molecular Pharmaceutics 12:12, pages 4349-4362.
Crossref
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Shanshan Li, Lili Wang, Jian Jiang, Peixiao Tang, Qing Wang, Di Wu & Hui Li. (2015) Investigations of bisacodyl with modified β-cyclodextrins: Characterization, molecular modeling, and effect of PEG. Carbohydrate Polymers 134, pages 82-91.
Crossref
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Thiago Caon, Jadel Muller Kratz, Gislaine Kuminek, Melina Heller, Ricardo Augusto Konig, Gustavo Amadeu Micke, Letícia Scherer Koester & Cláudia Maria Oliveira Simões. (2015) Oral saquinavir mesylate solid dispersions: In vitro dissolution, Caco-2 cell model permeability and in vivo absorption studies. Powder Technology 269, pages 200-206.
Crossref
Crossref
Hamdy Abdelkader, Ossama Y Abdallah, Hesham Salem, Adam W G Alani & Raid G Alany. (2014) Eutectic, monotectic and immiscibility systems of nimesulide with water-soluble carriers: phase equilibria, solid-state characterisation and in-vivo/pharmacodynamic evaluation. Journal of Pharmacy and Pharmacology 66:10, pages 1439-1450.
Crossref
Crossref
Kayleen T. Campbell, Duncan Q. M. Craig & Tony McNally. (2014) Modification of ibuprofen drug release from poly(ethylene glycol) layered silicate nanocomposites prepared by hot-melt extrusion. Journal of Applied Polymer Science 131:10, pages n/a-n/a.
Crossref
Crossref
Nikoletta Fotaki, Chiau Ming Long, Kin Tang & Hitesh Chokshi. 2014. Amorphous Solid Dispersions. Amorphous Solid Dispersions
487
514
.
Ziyaur Rahman, Akhtar Siddiqui & Mansoor A. Khan. (2013) Characterization of a Nonribosomal Peptide Antibiotic Solid Dispersion Formulation by Process Analytical Technologies Sensors. Journal of Pharmaceutical Sciences 102:12, pages 4337-4346.
Crossref
Crossref
Ziyaur Rahman & Mansoor A. Khan. (2013) Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic. International Journal of Pharmaceutics 456:2, pages 572-582.
Crossref
Crossref
Qing Zhu, Scott J. Toth, Garth J. Simpson, Hsin-Yun Hsu, Lynne S. Taylor & Michael T. Harris. (2013) Crystallization and Dissolution Behavior of Naproxen/Polyethylene Glycol Solid Dispersions. The Journal of Physical Chemistry B 117:5, pages 1494-1500.
Crossref
Crossref
Sharipah Razali & Tin Wui Wong. (2013) Design of superdisintegrant- and effervescent agent-less dispersible fast-release melt pellets. Powder Technology 235, pages 289-298.
Crossref
Crossref
Roya Yadollahi, Krasimir Vasilev, Clive A. Prestidge & Spomenka Simovic. (2013) Polymeric Nanosuspensions for Enhanced Dissolution of Water Insoluble Drugs. Journal of Nanomaterials 2013, pages 1-10.
Crossref
Crossref
Hywel D. Williams, Natalie L. Trevaskis, Susan A. Charman, Ravi M. Shanker, William N. Charman, Colin W. Pouton & Christopher J. H. Porter. (2013) Strategies to Address Low Drug Solubility in Discovery and Development. Pharmacological Reviews 65:1, pages 315-499.
Crossref
Crossref
Ankita V. Shah & Abu T. M. Serajuddin. (2012) Development of Solid Self-Emulsifying Drug Delivery System (SEDDS) I: Use of Poloxamer 188 as Both Solidifying and Emulsifying Agent for Lipids. Pharmaceutical Research 29:10, pages 2817-2832.
Crossref
Crossref
Qing Zhu, Michael T. Harris & Lynne S. Taylor. (2012) Modification of Crystallization Behavior in Drug/Polyethylene Glycol Solid Dispersions. Molecular Pharmaceutics 9:3, pages 546-553.
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
Feng Zhang & James C. DiNunzio. 2012. Formulating Poorly Water Soluble Drugs. Formulating Poorly Water Soluble Drugs
171
208
.
Hind Al-Zein, Khalil Sakeer & Fars K. Alanazi. (2011) Designing an extended release waxy matrix tablet containing nicardipine–hydroxy propyl β cyclodextrin complex. Saudi Pharmaceutical Journal 19:4, pages 245-253.
Crossref
Crossref
Phuong Ha-Lien Tran, Thao Truong-Dinh Tran, Jun Bom Park & Beom-Jin Lee. (2011) Controlled Release Systems Containing Solid Dispersions: Strategies and Mechanisms. Pharmaceutical Research 28:10, pages 2353-2378.
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
Wanchai Sutananta, Duncan Q M Craig & J Michael Newton. (1995) An Evaluation of the Mechanisms of Drug Release from Glyceride Bases. Journal of Pharmacy and Pharmacology 47:3, pages 182-187.
Crossref
Crossref
Jun-Heok Kang, Yi-Dong Yan, Hyun-Chan Kim, Sung-Neung Lee, Chul-Soon Yong & Han-Gon Choi. (2010) Enhanced Dissolution of Coenzyme Q10 using Solid Dispersions Prepared by Low Temperature Melting Method. Journal of Pharmaceutical Investigation 40:5, pages 277-283.
Crossref
Crossref
Qing Zhu, Lynne S. Taylor & Michael T. Harris. (2010) Evaluation of the Microstructure of Semicrystalline Solid Dispersions. Molecular Pharmaceutics 7:4, pages 1291-1300.
Crossref
Crossref
Heike Bley, Bernd Fussnegger & Roland Bodmeier. (2010) Characterization and stability of solid dispersions based on PEG/polymer blends. International Journal of Pharmaceutics 390:2, pages 165-173.
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
Sunil Kumar Jain, Meenakshi Shukla & Vivek Shrivastava. (2010) Development and in Vitro Evaluation of Ibuprofen Mouth Dissolving Tablets Using Solid Dispersion Technique. CHEMICAL & PHARMACEUTICAL BULLETIN 58:8, pages 1037-1042.
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
Riikka Laitinen, Eero Suihko, Kaisa Toukola, Mikko Björkqvist, Joakim Riikonen, Vesa Pekka Lehto, Kristiina Järvinen & Jarkko Ketolainen. (2009) Intraorally fast-dissolving particles of a poorly soluble drug: Preparation and in vitro characterization. European Journal of Pharmaceutics and Biopharmaceutics 71:2, pages 271-281.
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
Sandrien Janssens, Samgar Denivelle, Patrick Rombaut & Guy Van den Mooter. (2008) Influence of polyethylene glycol chain length on compatibility and release characteristics of ternary solid dispersions of itraconazole in polyethylene glycol/hydroxypropylmethylcellulose 2910 E5 blends. European Journal of Pharmaceutical Sciences 35:3, pages 203-210.
Crossref
Crossref
Patrick J. Marsac, Daniel P. Romary, Sheri L. Shamblin, Jared A. Baird & Lynne S. Taylor. (2008) Spontaneous Crystallinity Loss of Drugs in the Disordered Regions of Poly(Ethylene Oxide) in the Presence of Water. Journal of Pharmaceutical Sciences 97:8, pages 3182-3194.
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
Sandrien Janssens, Hector Novoa de Armas, Clive J. Roberts & Guy Van den Mooter. (2008) Characterization of Ternary Solid Dispersions of Itraconazole, PEG 6000, and HPMC 2910 E5. Journal of Pharmaceutical Sciences 97:6, pages 2110-2120.
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
Hamdy Abdelkader, Ossama Y Abdallah & Hesham S Salem. (2007) Comparison of the effect of tromethamine and polyvinylpyrrolidone on dissolution properties and analgesic effect of nimesulide. AAPS PharmSciTech 8:3, pages E110-E117.
Crossref
Crossref
Sudha R. Vippagunta, Zeren Wang, Stefanie Hornung & Steven L. Krill. (2007) Factors Affecting the Formation of Eutectic Solid Dispersions and Their Dissolution Behavior. Journal of Pharmaceutical Sciences 96:2, pages 294-304.
Crossref
Crossref
Sengodan Gurusamy VIJAYA KUMAR & Dina Nath MISHRA. (2006) Preparation, Characterization and <i>In vitro </i>Dissolution Studies of Solid Dispersion of Meloxicam with PEG 6000<sup>1)</sup>. YAKUGAKU ZASSHI 126:8, pages 657-664.
Crossref
Crossref
Sabiruddin Mirza, Jyrki Heinämäki, Inna Miroshnyk, Jukka Rantanen, Leena Christiansen, Milja Karjalainen & Jouko Yliruusi. (2006) Understanding processing-induced phase transformations in erythromycin–PEG 6000 solid dispersions. Journal of Pharmaceutical Sciences 95:8, pages 1723-1732.
Crossref
Crossref
Siriporn Okonogi & Satit Puttipipatkhachorn. (2006) Dissolution improvement of high drug-loaded solid dispersion. AAPS PharmSciTech 7:2, pages E148-E153.
Crossref
Crossref
Nobuyuki Tanaka, Keiji Imai, Kazuto Okimoto, Satoshi Ueda, Yuji Tokunaga, Rinta Ibuki, Kazutaka Higaki & Toshikiro Kimura. (2006) Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nilvadipine (II): In vivo evaluation. Journal of Controlled Release 112:1, pages 51-56.
Crossref
Crossref
Denny Mahlin, Johan Unga, Annika Ridell, Göran Frenning & Sven Engström. (2005) Influence of polymer molecular weight on the solid-state structure of PEG/monoolein mixtures. Polymer 46:26, pages 12210-12217.
Crossref
Crossref
Adamo Fini, José R. Moyano, Juan M. Ginés, José I. Perez-Martinez & Antonio M. Rabasco. (2005) Diclofenac salts, II. Solid dispersions in PEG6000 and Gelucire 50/13. European Journal of Pharmaceutics and Biopharmaceutics 60:1, pages 99-111.
Crossref
Crossref
Nora Anne Urbanetz & Bernhard Christian Lippold. (2005) Solid dispersions of nimodipine and polyethylene glycol 2000: dissolution properties and physico-chemical characterisation. European Journal of Pharmaceutics and Biopharmaceutics 59:1, pages 107-118.
Crossref
Crossref
Sambhaji Pisal, Rana Zainnuddin, Pradeep Nalawade, Kakasaheb Mahadik & Shivajirao Kadam. (2004) Drug release properties of polyethylene-glycol-treated ciprofloxacin-Indion 234 complexes. AAPS PharmSciTech 5:4, pages 101-106.
Crossref
Crossref
Beatrice Perissutti, Fulvio Rubessa, Mariarosa Moneghini & Dario Voinovich. (2003) Formulation design of carbamazepine fast-release tablets prepared by melt granulation technique. International Journal of Pharmaceutics 256:1-2, pages 53-63.
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
A Fini, L Rodriguez, C Cavallari, B Albertini & N Passerini. (2002) Ultrasound-compacted and spray-congealed indomethacin/polyethyleneglycol systems. International Journal of Pharmaceutics 247:1-2, pages 11-22.
Crossref
Crossref
Sudha R. Vippagunta, Karin A. Maul, Siva Tallavajhala & David J.W. Grant. (2002) Solid-state characterization of nifedipine solid dispersions. International Journal of Pharmaceutics 236:1-2, pages 111-123.
Crossref
Crossref
Beatrice Perissutti, John Michael Newton, Fridrun Podczeck & Fulvio Rubessa. (2002) Preparation of extruded carbamazepine and PEG 4000 as a potential rapid release dosage form. European Journal of Pharmaceutics and Biopharmaceutics 53:1, pages 125-132.
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
Devalina Law, Steven L. Krill, Eric A. Schmitt, James J. Fort, Yihong Qiu, Weili Wang & William R. Porter. (2001) Physicochemical considerations in the preparation of amorphous ritonavir–poly(ethylene glycol) 8000 solid dispersions. Journal of Pharmaceutical Sciences 90:8, pages 1015-1025.
Crossref
Crossref
M. Moneghini, I. Kikic, D. Voinovich, B. Perissutti & J. Filipović-Grčić. (2001) Processing of carbamazepine–PEG 4000 solid dispersions with supercritical carbon dioxide: preparation, characterisation, and in vitro dissolution. International Journal of Pharmaceutics 222:1, pages 129-138.
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
Jens Carstensen. 2000. Advanced Pharmaceutical Solids. Advanced Pharmaceutical Solids
169
189
.
G.R Lloyd, D.Q.M Craig & A Smith. (1999) A calorimetric investigation into the interaction between paracetamol and polyethlene glycol 4000 in physical mixes and solid dispersions. European Journal of Pharmaceutics and Biopharmaceutics 48:1, pages 59-65.
Crossref
Crossref
M.J Arias, J.R Moyano & J.M Ginés. (1998) Study by DSC and HSM of the oxazepam–PEG 6000 and oxazepam–D-mannitol systems: Application to the preparation of solid dispersions. Thermochimica Acta 321:1-2, pages 33-41.
Crossref
Crossref
Hind El-Zein, Lillian Riad & Ahmed Abd El-Bary. (1998) Enhancement of carbamazepine dissolution: in vitro and in vivo evaluation. International Journal of Pharmaceutics 168:2, pages 209-220.
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
N Delahaye, R Duclos & J.M Saiter. (1997) Characterization of PEG6000 phase transitions. International Journal of Pharmaceutics 157:1, pages 27-34.
Crossref
Crossref
S Okonogi, T Oguchi, E Yonemochi, S Puttipipatkhachorn & K Yamamoto. (1997) Improved dissolution of ofloxacin via solid dispersion. International Journal of Pharmaceutics 156:2, pages 175-180.
Crossref
Crossref
G.R. Lloyd, D.Q.M. Craig & A. Smith. (1997) An Investigation into the Melting Behavior of Binary Mixes and Solid Dispersions of Paracetamol and PEG 4000. Journal of Pharmaceutical Sciences 86:9, pages 991-996.
Crossref
Crossref
Roberto Frontini & Jobst B. Mielck. (1997) Interactions between bendroflumethiazide and water soluble polymers. I. Solubility of bendroflumethiazide in water from solid dispersions and formation of associates under climatic stress. European Journal of Pharmaceutics and Biopharmaceutics 43:2, pages 185-191.
Crossref
Crossref
M. Kuhnert-Brandstätter & U. J. Griesser. (1995) Ungewöhnliche Phasendiagramme der Polyethylenglykole 6000 und 4000 mit Harnstoff. Journal of Thermal Analysis 45:3, pages 559-572.
Crossref
Crossref
Ching-Wei Lin & Thau-Ming Cham. (1995) Compression behavior and tensile strength of heat-treated polyethylene glycols. International Journal of Pharmaceutics 118:2, pages 169-179.
Crossref
Crossref
Duncan Q.M. Craig. (1995) A review of thermal methods used for the analysis of the crystal form, solution thermodynamics and glass transition behaviour of polyethylene glycols. Thermochimica Acta 248, pages 189-203.
Crossref
Crossref
Sohair El-Shanawany. (1993) Sustained release of nitrofurantoin from inert wax matrixes. Journal of Controlled Release 26:1, pages 11-19.
Crossref
Crossref
D. Q. M. Craig, R. M. Hill & J. M. Newton. (1993) Characterization of the structure of drug dispersions in polyethylene glycols using low-frequency dielectric spectroscopy. Journal of Materials Science 28:7, pages 1978-1982.
Crossref
Crossref
D.Q.M. Craig & J.M. Newton. (1991) Characterisation of polyethylene glycol solid dispersions using differential scanning calorimetry and solution calorimetry. International Journal of Pharmaceutics 76:1-2, pages 17-24.
Crossref
Crossref