Publications by authors named "Natalie MacLean"

This paper presents a system of hybrid models that combine both mechanistic and data-driven approaches to predict physical powder blend properties from their raw component properties. Mechanistic, probabilistic models were developed to predict the particle size and shape, represented by aspect ratio, distributions of pharmaceutical blends using those of the raw components. Additionally, the accuracy of existing mixture rules for predicting the blend's true density and bulk density was assessed.

View Article and Find Full Text PDF

In this study, a compartmental disintegration and dissolution model is proposed for the prediction and evaluation of the dissolution performance of directly compressed tablets. This dissolution model uses three compartments (Bound, Disintegrated, and Dissolved) to describe the state of each particle of active pharmaceutical ingredient. The disintegration of the tablet is captured by three fitting parameters.

View Article and Find Full Text PDF
Article Synopsis
  • Stability studies check if drugs remain safe and effective during storage, focusing on changes in dissolution performance that could affect bioavailability.
  • Three griseofulvin formulations using microcrystalline cellulose with different excipients were tested under various temperature and humidity conditions for their physical properties.
  • Results showed that increased humidity negatively impacted the dissolution rate for all samples, with specific formulations experiencing premature swelling or dissolution issues during storage.
View Article and Find Full Text PDF

With advancements in the pharmaceutical industry pushing more towards tailored medicines, novel approaches to tablet manufacture are in high demand. One of the main drivers towards micro-scale batch production is the ability to fine-tune drug release. This study demonstrates the use of rapid tooling injection moulding (RTIM) for tablet manufacture.

View Article and Find Full Text PDF
Article Synopsis
  • Stability studies are crucial for drug development, focusing on both chemical and physical stability to ensure drug performance is not compromised during storage.
  • In the study, 16 tablet formulations were tested under various humidity and temperature conditions to analyze changes in properties like breaking force, porosity, and disintegration time after 2 and 4 weeks.
  • Results indicated that tablets subjected to high humidity showed increased porosity and reduced strength, especially with hygroscopic fillers like microcrystalline cellulose, while high temperatures primarily affected wettability.
View Article and Find Full Text PDF

The disintegration process of pharmaceutical tablets is a crucial step in the oral delivery of a drug. Tablet disintegration does not only refer to the break up of the interparticle bonds, but also relates to the liquid absorption and swelling behaviour of the tablet. This study demonstrates the use of the sessile drop method coupled with image processing and models to analyse the surface liquid absorption and swelling kinetics of four filler combinations (microcrystalline cellulose (MCC)/mannitol, MCC/lactose, MCC/dibasic calcium phosphate anhydrous (DCPA) and DCPA/lactose) with croscarmellose sodium as a disintegrant.

View Article and Find Full Text PDF
Article Synopsis
  • The study explores the complexities in tablet design and manufacturing, focusing on how the properties of raw materials and their interactions affect drug disintegration and dissolution.
  • Researchers tested 16 immediate-release placebo formulations, each containing two fillers, a disintegrant, and a lubricant, using various combinations of popular fillers like microcrystalline cellulose (MCC) and mannitol.
  • The findings revealed different disintegration mechanisms based on the fillers used, with implications that slight changes in product formulation can significantly alter tablet performance, highlighting the need for careful formulation and manufacturing processes.
View Article and Find Full Text PDF

Objective: To evaluate the clinical outcomes of intracavernosal injection (ICI) use in an undifferentiated group of men with erectile dysfunction at various stages after radical prostatectomy.

Methods: Retrospective charts, mailed questionnaires, and a telephone survey of patients after radical prostatectomy prescribed ICI by a single urologist from January 2006 to January 2008. The patient demographics and prostate cancer profiles, current ICI use patterns, adverse outcome, and clinical efficacy were collected.

View Article and Find Full Text PDF

The thorough characterization of transgenic mouse models of human central nervous system diseases is a necessary step in realizing the full benefit of using animal models to investigate disease processes and potential therapeutics. Because of the labor- and resource-intensive nature of high-resolution imaging, detailed investigation of possible structural or biochemical alterations in brain sections has typically focused on specific regions of interest as determined by the researcher a priori. For example, Parkinson's disease researchers often focus imaging on regions of the brain expected to exhibit pathology such as the substantia nigra and striatum.

View Article and Find Full Text PDF