A Nanostructured Drug Delivery Approach (ID:1)
Published:
31 August 2017
A lipid based oral formulation has been prepared by loading glyceryl monostearate (GMS) into a porous solid 244P silica. The formulation is hypothesised to be well redispersed in the gastrointenstinal trace to ensure improved release of the model drug, lovastatin. To test the redispersability of this formulation, particle size measurements were performed using the Malvern mastersizer.
Data and resources
Other resources collected by the researchers may be available subject to researcher approval. Please contact Mr Andrew Robinson.
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Period covered by the dataset
| Start date: |
01 Jan 2012
|
| End date: |
31 Dec 2015
|
Access rights
Access to the collection may be subject to licence and privacy conditions. Requests for access can be made through the listed contact. All rights reserved.
Data citation
Prestidge, C 2017, A Nanostructured Drug Delivery Approach (ID:1), University of South Australia, viewed 21 November 2024, retrieved from <https://researchoutputs.unisa.edu.au/11541.1/a1da6a3eb1de44ddaaafcea344c17548>.