Data

A Nanostructured Drug Delivery Approach (ID:1)

Adelaide University
Prestidge, Clive
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.25954/s28c-vx95&rft.title=A Nanostructured Drug Delivery Approach (ID:1)&rft.identifier=10.25954/s28c-vx95&rft.publisher=University of South Australia&rft.description=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.&rft.creator=Prestidge, Clive &rft.edition=1&rft_rights= https://creativecommons.org/licenses/by/4.0/&rft_subject=Pharmaceutical sciences&rft_subject=drug release&rft_subject=gastrointestinal&rft_subject=GMS&rft_subject=Health&rft_subject=lipid&rft_subject=particle size&rft_subject=redispersibility&rft_subject=silica&rft.type=dataset&rft.language=English Access the data
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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.

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Subjects
GMS | Health | Pharmaceutical sciences | drug release | gastrointestinal | lipid | particle size | redispersibility | silica |

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Identifiers
ACN 633 798 857