Adhesion of Pharmaceutical Powders on Tools During Compaction


Book Description

A common concern in pharmaceutical tablet manufacturing is the propensity for powder to adhere to and accumulate on the tooling components, also known as sticking. This is a problem that needs to be addressed in the development stage because it becomes excessively disruptive and expensive to deal with during technology transfer and scale-up of manufacturing. The current work focused on the development, evaluation and understanding of objective risk assessment with an emphasis on techniques that: (a) are material sparing and (b) provide mechanistic insight to the problem as well as the determination of conditions that are required for consistent and unambiguous results. Prior work in the literature on this problem clearly indicates that the fundamentals and the mechanisms are not well understood. Our results include the evaluation of (a) a removable punch tip coupled with SEM imaging analysis and (b) an adhesion punch. The first technique is objective and material sparing, but time consuming and destructive (the punch cannot continue to be used after microscopy imaging). Also, the sensitivity of the adhered materials to interactions with the electron beam and the SEM environment need to be considered. For materials that are reasonably stable in the SEM environment, it provides rich insight into fundamental mechanisms. The adhesion punch is a quasi-online and nondestructive technique. Our experimental and computational work shows that it is difficult to obtain objective results for the ranking of materials. Finally, a detailed examination of the effect of surface preparation on the experimental results for sticking was conducted using a laser reflection-based technique developed in our lab. Based on the SEM imaging, we understand now that there is (a) a non-uniform sticking distribution across the punch face reflecting the non-uniformity of compaction and separation of punch from the tablet, (b) that sticking is a non-monotonic phenomenon at the local scale with deposition and removal of the material at the same time, and (c) that fragmentation and local defects may lead to cracks that promote detachment during unloading. Computational modeling of the adhesion punch led to an understanding of the non-uniform stress state leading to a non-uniform unloading which concerns the normalization of the force over an unknown area that is last in contact. DEM also showed that there is no unique relationship between powder/wall adhesion and the force required to separate the upper punch and the compact. While we addressed the weaknesses of the design, our work showed that there are ambiguities in the adhesion punch design that makes it difficult to use it for detailed work on sticking. The consistent surface preparation technique that was developed highlighted important phenomena that had not been explored before in the context of pharmaceutical engineering such as the rapid aging of the punch surface due to the interaction of the atmosphere. Our results point to the importance of the evolution of the punch surface due to continuous interaction with environment and the formulation components that may lead to sticking, and to the need to understand such interaction so that appropriate tests can be designed to provide objective information outside the production environment.




Pharmaceutical Powder Compaction Technology


Book Description

Compaction of powder constituents-both active ingredient and excipients-is examined to ensure consistent and reproducible disintegration and dispersion profiles. Revised to reflect modern pharmaceutical compacting techniques, this second edition of Pharmaceutical Powder Compaction Technology guides pharmaceutical engineers, formulation scientists,




Particle-particle Adhesion In Pharmaceutical Powder Handling


Book Description

This monograph describes the physical principles of adhesion between particles and surfaces. These principles are applied to pharmaceutical processes involved in the manufacture of solid dosage forms such as powders, granules, tablets and dry powder inhalations. To help in the understanding of these systems, physical properties of solid surfaces, and an introduction to the theory of friction is given. Techniques for measuring particle adhesion and fracture mechanical properties of powders are introduced, as far as these are relevant to the processes discussed. The philosophy of the book deviates from that of standard pharmaceutical textbooks, in that it focuses primarily on physical principles involved in the manufacture of dosage forms rather than describing these processes purely by observation.




Investigation of Compaction Behavior of Pharmaceutical Powders


Book Description

Pharmaceutical product development has evolved from conventional empirical approach towards the more systematic and science based approach over the past decades. However, the process of tableting and compaction behavior of pharmaceutical powders is still ambiguous and not well understood. In the present study, a comprehensive attempt has been made to understand this complex and dynamic process of compaction of disordered pharmaceutical powders using percolation phenomenon. Commonly used pharmaceutical powder materials, spheres and their binary mixtures of different particle sizes, crystal structure and deformation behavior were compressed at varying compression loads at different relative densities. Mechanical strength of tablets, namely radial tensile strength, compressive strength and elastic modulus, were evaluated and studied according to the classical models of powder compaction and percolation phenomenon. It was found that percolation phenomenon has a significant effect on the compaction of powder materials and can be used to characterize deformation and bonding behavior of powder materials. A model developed on the fundamentals of percolation theory was found to predict the compactibility of disordered powder materials and their binary mixtures with higher accuracy compared to the established classical compaction models. Moreover, it was found that the developed model can predict the dilution capacity of excipients and can be used as a material-sparing tool in the initial formulation development of tablet dosage forms. It was also found that percolation theory can help to understand mechanics of tablet formation more clearly by establishing a relationship between compressibility and compactibility phenomena of powder materials. Further, a closer look at tableting process reveals that process of tableting closely mimics 3-dimensional correlated diffusive percolation phenomenon with a universal critical exponent value of q = 2 and percolation thresholds, Ï1c = 0.634 (z = 12) and 0.366 (z = 6) depending on the type of material used. Similar results were also observed in the case of powders compacted using an industrial scale rotary tablet press thus confirming that tableting of pharmaceutical powders is far from an equilibrium process depending upon the variability of time and space. Thus it can be concluded that comprehensive application of percolation theory can serve as a single effective tool in the study of compaction behavior of pharmaceutical powders and can be effectively used in the current quality by design (QbD) practice to establish robust design space for the formulation development of tablet dosage forms.




Pharmaceutical Powder ComPattion Technology


Book Description

This unique reference examines the modern pharmaceutical compacting techniques used to form tablets out of powders-describing the physical structure of pharmaceutical compacts, the bonding phenomena that occur during powder compaction, and the compression mechanisms of pharmaceutical particles.




Development of Predictive Tools for the Characterisation of Milling Behaviour of Pharmaceutical Powders / Entwicklung Von Methoden Zur Vorhersage Der Zerkleinerungseigenschaften Pharmazeutischer Pulver


Book Description

This work examines the main influence factors on the breakage behaviour of pharmaceutical substances and other organic crystals. Particle surface characterisation is done via Atomic Force Microscopy, thus examining the transport properties of the powders. The breakage behaviour is characterised by single particle impact experiments. Mechanical properties are determined by indentation. The results show a clear correlation between the breakage behaviour -- expressed by the breakage probability and the breakage function -- and the hardness and fracture toughness of the material. This allows an estimate about the breakage behaviour of a substance from indentation experiments with far less material consumption than in conventional milling experiments.




Thermo-mechanical Behavior of Pharmaceutical Powders During Compaction Processes


Book Description

Dry granulation / roller compaction is an enlargement process by agglomeration of the primary powders without adding any solvent. This operation makes it possible to homogenize the properties of pharmaceutical formulations and improve the flow properties necessary for the manufacture of tablets using rotary presses. In this process, temperature variations in the product are rarely considered. However, recent studies have shown that for pharmaceutical powders, such variations can lead to changes in mechanical and physico-chemical properties. In this thesis, a new method based on in-line measurements of powders temperature compacted by a roller press is developed using an infrared camera. Temperature distributions on the surface of the compact were determined using infrared radiation emitted by the compact after leaving the gap. These distributions showed a correlation with the microstructural properties of the compact, confirming the potential of this procedure in monitoring product quality. To understand the potential sources of the heating of pharmaceutical products in dry granulation, a heat balance model was established in anticipation of the numerical simulation of the thermomechanical coupling of the process by finite element method. As the thermal properties of the compact depend on the relative density, the thermal conductivity and the specific heat were characterized for two model pharmaceutical excipients. In addition, the impact of dry granulation on the rearrangement and densification of granules in die compression is studied using a mathematical model (Cooper-Eaton) which allowed to a better understanding of the contribution of dry granulation to tableting process.




Formulation Tools for Pharmaceutical Development


Book Description

A range of new and innovative tools used for preformulation and formulation of medicines help optimize pharmaceutical development projects. Such tools also assist with the performance evaluation of the pharmaceutical process, allowing any potential gaps to be identified. These tools can be applied in both basic research and industrial environment. Formulation tools for pharmaceutical development considers these key research and industrial tools. Nine chapters by leading contributors cover: Artificial neural networks technology to model, understand, and optimize drug formulations; ME_expert 2.0: a heuristic decision support system for microemulsions formulation development; Expert system for the development and formulation of push-pull osmotic pump tablets containing poorly water-soluble drugs; SeDeM Diagram: an expert system for preformulation, characterization and optimization of tables obtained by direct compression; New SeDeM-ODT expert system: an expert system for formulation of orodispersible tablets obtained by direct compression; and 3D-cellular automata in computer-aided design of pharmaceutical formulations: mathematical concept and F-CAD software. Coverage of artificial intelligence tools, new expert systems, understanding of pharmaceutical processes, robust development of medicines, and new ways to develop medicines Development of drugs and medicines using mathematical tools Compilation of expert system developed around the world







Evaluation and Study on the Adhesion of Powder Onto Punch Faces During Tablet Compaction


Book Description

Sticking during tablet compaction is an issue that is commonly experienced during tablet manufacturing operations. The term 'Sticking' refers to a phenomenon that results in the adherence of materials onto the punch faces and die wall even after the tooling has left contact with the tablet. The occurrence of sticking during large scale tablet manufacture can produce defective tablets, halt manufacturing operations, and can be very costly. Currently, the mechanisms by which this phenomenon occurs is not clearly understood. However, numerous factors dealing with powder characteristics and instrumentation parameters are reported in literature to affect sticking. Therefore, sticking is a complex multifaceted phenomenon in which multiple factors can simultaneously contribute to the issue. The aim of the work conducted in this thesis is to study the process of sticking. Ibuprofen was chosen as a model compound in this work as it is widely known to cause this issue. In addition, evaluation of the sticking propensity of Acetylsalicylic Acid (ASA) and of a confidential compound is also presented. A customized punch with a removable punch tip was used to quantify the mass of adhered material on the punch tip during tablet compaction. The effect of particle size on sticking with ibuprofen was evaluated. Formulations containing 30% ibuprofen (AS-IS) and 30% micronized ibuprofen with 0.5% magnesium stearate and 69.5% microcrystalline cellulose were tested. Results with micronized ibuprofen showed a marked increase in sticking compared to non-micronized ibuprofen. Significant triboelectric charging was observed with micronized ibuprofen. Analysis of the adhered material on the punch tip by SEM reveals the presence of both heavily deformed particles and minimally deformed fragments that are on the size order of well below 50Îơm. Triboelectric charging was also demonstrated to occur upon compaction with ASA. Results suggest that that particle size, static charging and fragmentation may play important roles in the mechanism of sticking in ibuprofen formulations. Furthermore, it is observed that sticking in ibuprofen can be influenced by cleaning of punch faces by solvents and by capping defects in tablets.