Adrian L. Kelly

Bio: Adrian L. Kelly is an academic researcher from University of Bradford. The author has contributed to research in topics: Plastics extrusion & Extrusion. The author has an hindex of 21, co-authored 88 publications receiving 1488 citations.

Cocrystalization and Simultaneous Agglomeration Using Hot Melt Extrusion

Abstract: To explore hot melt extrusion (HME) as a scalable, solvent-free, continuous technology to design cocrystals in agglomerated form. Cocrystal agglomerates of ibuprofen and nicotinamide in 1:1 ratio were produced using HME at different barrel temperature profiles, screw speeds, and screw configurations. Product was characterized for crystallinity by XRPD and DSC, while the morphology was determined by SEM. Dissolution rate and tabletting properties were compared with ibuprofen. Process parameters significantly affected the extent of cocrystallization which improved with temperature, applied shear and residence time. Processing above eutectic point was required for cocrystallization to occur, and it improved with mixing intensity by changing screw configuration. Product was in the form of spherical agglomerates, which showed directly compressible nature with enhanced dissolution rate compared to ibuprofen. This marks an important advantage over the conventional techniques, as it negates the need for further size modification steps. A single-step, scalable, solvent-free, continuous cocrystallization and agglomeration technology was developed using HME, offering flexibility for tailoring the cocrystal purity. HME being an established technology readily addresses the regulatory demand of quality by design (QbD) and process analytical technology (PAT), offering high potential for pharmaceuticals.

Pluronic F127 thermosensitive injectable smart hydrogels for controlled drug delivery system development.

Abstract: Understanding structure-property relationships is critical for the development of new drug delivery systems. This study investigates the properties of Pluronic smart hydrogel formulations for future use as injectable controlled drug carriers. The smart hydrogels promise to enhance patient compliance, decrease side effects and reduce dose and frequency. Pharmaceutically, these systems are attractive due to their unique sol-gel phase transition in the body, biocompatibility, safety and injectability as solutions before transforming into gel matrices at body temperature. We quantify the structural changes of F127 systems under controlled temperature after flow, as experienced during real bodily injection. Empirical formulae combining the coupled thermal and shear dependency are produced to aid future application of these systems. Induced structural transitions measured in-situ by small angle x-ray and neutron scattering reveal mixed oriented structures that can be exploited to tailor the drug release profile.

The effect of screw geometry on melt temperature profile in single screw extrusion

Abstract: Experimental observations of melt temperature profiles and melting performance of extruder screws are reported. A novel temperature sensor consisting of a grid of thermocouple junctions was used to take multiple temperature readings in real time across melt flow in a single screw extruder. Melt pressure in the die and power consumption were also monitored. Three extruder screws at a range of screw speeds were examined for a commercial grade of low density polyethylene. Results showed melt temperature fields at low throughputs to be relatively independent of screw geometry with a flat-shaped temperature profile dominated by conduction. At high throughputs, melting performance and measured temperature fields were highly dependent upon screw geometry. A barrier-flighted screw with Maddock mixer achieved significantly better melting than single flighted screws. Low temperature “shoulder” regions were observed in the temperature profiles of single-flighted screws at high throughput, due to late melting of the solid bed. Stability of the melt flow was also dependent upon screw geometry and the barrier-flighted screw achieving flow with lower variation in melt pressure and temperature. Dimensionless numbers were used to analyze the relative importance of conduction, convection, and viscous shear to the state of the melt at a range of extrusion conditions. Polym. Eng. Sci. 46:1706–1714, 2006. © 2006 Society of Plastics Engineers

A comparative study of the effect of spray drying and hot-melt extrusion on the properties of amorphous solid dispersions containing felodipine.

Abstract: Objectives To compare the properties of solid dispersions of felodipine for oral bioavailability enhancement using two different polymers, polyvinylpyrrolidone (PVP) and hydroxypropyl methylcellulose acetate succinate (HPMCAS), by hot-melt extrusion (HME) and spray drying. Methods Felodipine solid dispersions were prepared by HME and spray drying techniques. PVP and HPMCAS were used as polymer matrices at different drug : polymer ratios (1 : 1, 1 : 2 and 1 : 3). Detailed characterization was performed using differential scanning calorimetry, powder X-ray diffractometry, scanning electron microscopy and in-vitro dissolution testing. Dissolution profiles were evaluated in the presence of sodium dodecyl sulphate. Stability of different solid dispersions was studied under accelerated conditions (40°C/75% RH) over 8 weeks. Key findings Spray-dried formulations were found to release felodipine faster than melt extruded formulations for both polymer matrices. Solid dispersions containing HMPCAS exhibited higher drug release rates and better wettability than those produced with a PVP matrix. No significant differences in stability were observed except with HPMCAS at a 1 : 1 ratio, where crystallization was detected in spray-dried formulations. Conclusions Solid dispersions of felodipine produced by spray drying exhibited more rapid drug release than corresponding melt extruded formulations, although in some cases improved stability was observed for melt extruded formulations.

Microinjection molding of thermoplastic polymers: a review

Abstract: Microinjection molding (µIM) appears to be one of the most efficient processes for the large-scale production of thermoplastic polymer microparts. The microinjection molding process is not just a scaling down of the conventional injection process; it requires a rethinking of each part of the process. This review proposes a comparative description of each step of the microinjection molding process (µIM) with conventional injection molding (IM). Micromolding machines have been developed since the 1990s and a comparison between the existing ones is made. The techniques used for the realization of mold inserts are presented, such as lithography process (LIGA), laser micromachining and micro electrical discharge machining (µEDM). Regarding the molding step, the variotherm equipment used for the temperature variation is presented and the problems to solve for each molding phase are listed. Throughout this review, the differences existing between µIM and conventional molding are highlighted.