Despite the fact that the pharmaceutical industry has produced tablets for more than a hundred years, the development of a new formulation and the choice of manufacturing processes and excipients is often based on trial-and-error approach. This trail and error approach poses several challenges during tableting ( e.g. low tensile strength, excessive friability, and strain rate sensitivity
Based on characterization of a wide range of fillers and APIs, thirty divergent blends were composed...
In early development, pharmaceutical formulation scientists are often faced with challenges of devel...
The composition of pharmaceutical formulations at developmental stage is often subjected to trials a...
To develop a model to non-destructively estimate particle size changes in powder compacts using tera...
The design and manufacture of tablets is a challenging process due to the complex interrelationships...
In oral solid-dosage manufacturing through direct compression, lubrication is used to enhance powder...
peer-reviewedThe ability to predict formulation behaviour at production scale during formulation des...
AbstractTablets make up approximately one third of all drug dosage forms which makes tablet manufact...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2009.Includes...
peer-reviewedIn this work, the transfer of oral solid dosage forms, currently manufactured via wet g...
Direct compaction tabletting, a widely used secondary downstream processing operation, has recently ...
With the ever-increasing need for development speed, the ability to complete a thorough characteriza...
The general objective of this work was to understand the role of compression speed and powder co-pro...
Oral solid dosage (OSD) forms are the most common formulations for marketed pharmaceuticals, while t...
This work is a collection of problems all focused on mechanical strength of pharmaceutical tablets. ...
Based on characterization of a wide range of fillers and APIs, thirty divergent blends were composed...
In early development, pharmaceutical formulation scientists are often faced with challenges of devel...
The composition of pharmaceutical formulations at developmental stage is often subjected to trials a...
To develop a model to non-destructively estimate particle size changes in powder compacts using tera...
The design and manufacture of tablets is a challenging process due to the complex interrelationships...
In oral solid-dosage manufacturing through direct compression, lubrication is used to enhance powder...
peer-reviewedThe ability to predict formulation behaviour at production scale during formulation des...
AbstractTablets make up approximately one third of all drug dosage forms which makes tablet manufact...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2009.Includes...
peer-reviewedIn this work, the transfer of oral solid dosage forms, currently manufactured via wet g...
Direct compaction tabletting, a widely used secondary downstream processing operation, has recently ...
With the ever-increasing need for development speed, the ability to complete a thorough characteriza...
The general objective of this work was to understand the role of compression speed and powder co-pro...
Oral solid dosage (OSD) forms are the most common formulations for marketed pharmaceuticals, while t...
This work is a collection of problems all focused on mechanical strength of pharmaceutical tablets. ...
Based on characterization of a wide range of fillers and APIs, thirty divergent blends were composed...
In early development, pharmaceutical formulation scientists are often faced with challenges of devel...
The composition of pharmaceutical formulations at developmental stage is often subjected to trials a...