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Peter York
Peter York
Verified email at bradford.ac.uk
Title
Cited by
Cited by
Year
Pharmaceutics: The science of dosage form design
ME Aulton
(No Title), 2002
30272002
Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates
N Blagden, M de Matas, PT Gavan, P York
Advanced drug delivery reviews 59 (7), 617-630, 2007
18372007
Solubility parameters as predictors of miscibility in solid dispersions
DJ Greenhalgh, AC Williams, P Timmins, P York
Journal of pharmaceutical sciences 88 (11), 1182-1190, 1999
7761999
Crystallization processes in pharmaceutical technology and drug delivery design
BY Shekunov, P York
Journal of crystal growth 211 (1-4), 122-136, 2000
5852000
Process control and scale-up of pharmaceutical wet granulation processes: a review
A Faure, P York, RC Rowe
European journal of pharmaceutics and biopharmaceutics 52 (3), 269-277, 2001
4692001
The use of solubility parameters in pharmaceutical dosage form design
BC Hancock, P York, RC Rowe
International journal of pharmaceutics 148 (1), 1-21, 1997
3991997
Strategies for particle design using supercritical fluid technologies
P York
Pharmaceutical science & technology today 2 (11), 430-440, 1999
3701999
Hydrocortisone nanosuspensions for ophthalmic delivery: a comparative study between microfluidic nanoprecipitation and wet milling
HSM Ali, P York, AMA Ali, N Blagden
Journal of controlled release 149 (2), 175-181, 2011
3162011
Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors
HSM Ali, P York, N Blagden
International journal of pharmaceutics 375 (1-2), 107-113, 2009
2992009
Solid-state properties of powders in the formulation and processing of solid dosage forms
P York
International Journal of Pharmaceutics 14 (1), 1-28, 1983
2841983
Cocrystalization and simultaneous agglomeration using hot melt extrusion
RS Dhumal, AL Kelly, P York, PD Coates, A Paradkar
Pharmaceutical research 27, 2725-2733, 2010
2632010
Determination of surface properties and flow characteristics of salbutamol sulphate, before and after micronisation
JC Feeley, P York, BS Sumby, H Dicks
International journal of pharmaceutics 172 (1-2), 89-96, 1998
2441998
Phase behavioral effects on particle formation processes using supercritical fluids
S Palakodaty, P York
Pharmaceutical research 16, 976-985, 1999
2341999
Crystal engineering and particle design for the powder compaction process
P York
Drug development and industrial pharmacy 18 (6-7), 677-721, 1992
2081992
Preparation of amorphous cefuroxime axetil nanoparticles by sonoprecipitation for enhancement of bioavailability
RS Dhumal, SV Biradar, S Yamamura, AR Paradkar, P York
European Journal of Pharmaceutics and Biopharmaceutics 70 (1), 109-115, 2008
1902008
Optimisation of the predictive ability of artificial neural network (ANN) models: a comparison of three ANN programs and four classes of training algorithm
AP Plumb, RC Rowe, P York, M Brown
European Journal of Pharmaceutical Sciences 25 (4-5), 395-405, 2005
1882005
Moisture induced polymorphic transition of mannitol and its morphological transformation
T Yoshinari, RT Forbes, P York, Y Kawashima
International journal of pharmaceutics 247 (1-2), 69-77, 2002
1862002
Method and apparatus for the formation of particles
M Hanna, P York
US Patent 6,063,138, 2000
1852000
Analysis of the surface energy of pharmaceutical powders by inverse gas chromatography
IM Grimsey, JC Feeley, P York
Journal of pharmaceutical sciences 91 (2), 571-583, 2002
1742002
Particle formation by mixing with supercritical antisolvent at high Reynolds numbers
BY Shekunov, J Baldyga, P York
Chemical Engineering Science 56 (7), 2421-2433, 2001
1632001
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