Srinivas Palakodaty
University of Bradford
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Featured researches published by Srinivas Palakodaty.
Pharmaceutical Research | 1999
Srinivas Palakodaty; Peter York
The application of supercritical fluid (SF) processing in pharmaceutical research is increasing particularly in the field of particle formation for drug delivery systems. The SF processes have benefits over the existing particle formation methods in terms of improved control, flexibility and operational ease. This review highlights the fundamental concepts of fluid phase behaviour and their influence on the various processes involving particle formation with supercritical fluids. Several phase behaviour systems are discussed to provide an insight into the factors influencing the process paths and their effects on the characteristics of the particles.
Pharmaceutical Research | 1998
Srinivas Palakodaty; Peter York; John Pritchard
AbstractPurpose. The objective of the work was to study the factors influencing the crystallisation of α-lactose monohydrate from aqueous solution using the Solution Enhanced Dispersion by Supercritical Fluids (SEDS) technique. Methods. An aqueous solution of α-lactose monohydrate is dispersed with a homogeneous mixture of carbon dioxide-ethanol/methanol using a co-axial nozzle. Crystallised lactose particles were analysed for water content by Karl-Fisher analysis, anomeric composition by Differential Scanning Calorimetry (DSC) and characterised for crystallinity by powder X-ray diffraction and morphology by scanning electron microscopy. Results. Water content in the lactose recrystallised with ethanol was higher compared to the product obtained with methanol as cosolvent. Rate of crystallisation could be altered by varying the CO2 flow thereby modifying the water content in the lactose. At low flow rates of CO2, the crystallisation occurred in a cosolvent rich antisolvent phase causing rapid crystallisation whereas high flow rates of CO2 favoured a much slower crystallisation mechanism in the water rich phase. As a consequence, the morphology changed from thin long bands to large agglomerated chunks with mean particle size between 5 and 31 microns. Conclusions. The SEDS process is an efficient method for forming micron sized particles of water-soluble compounds with controlled physico-chemical properties.
International Journal of Pharmaceutics | 2004
Helena Schiavone; Srinivas Palakodaty; Andrew Clark; Peter York; Stelios T Tzannis
Journal of Pharmaceutical Sciences | 2005
Jennifer M. Lobo; Helena Schiavone; Srinivas Palakodaty; Peter York; Andrew Clark; Stelios T. Tzannis
Archive | 2005
Sarma P. Duddu; Srinivas Palakodaty; David Lechuga-Ballesteros; Danforth P. Miller; Alan R. Kugler; Christopher Frantz; Trixie Tan; Richard Malcolmson; Keith Washco; Theresa D. Sweeney; Thomas E. Tarara; Sarvajna Kumar Dwivedi
Archive | 2005
Sarma P. Duddu; Srinivas Palakodaty; David Lechuga-Ballesteros; Danforth P. Miller; Alan R. Kugler; Christopher Frantz; Trixie Tan; Richard Malcolmson; Keith Washco; Theresa D. Sweeney; Thomas E. Tarara; Sarvajna Kumar Dwivedi
Archive | 2005
Srinivas Palakodaty; Jiang Zhang; Andreas Kordikowski; Linda Sharon Daintree; Sarma P. Duddu; Alan R. Kugler; Herm Snyder; David Lechuga-Ballesteros; Nagesh Palepu
Archive | 2005
Jennifer Anne Green; Linda Sharon Daintree; Andreas Kordikowski; Sarma Duddu; Jiang Zhang; Srinivas Palakodaty; Maurine Tong
Archive | 2002
Peter York; Srinivas Palakodaty; Andreas Kordikowski; Raymond Sloan
Archive | 2005
Srinivas Palakodaty; Andreas Kordikowski; Linda Sharon Daintree; Sarma P. Duddu; Alan R. Kugler; Jiang Zhang; Herman Snyder; David Lechuga; Nagesh Palepu