Data

A Nanostructured Drug Delivery Approach (ID:1)

University of South Australia
Prof Clive Prestidge (Principal investigator)
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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=https://researchoutputs.unisa.edu.au/11541.1/a1da6a3eb1de44ddaaafcea344c17548&rft.title=A Nanostructured Drug Delivery Approach (ID:1)&rft.identifier=http://research.unisa.edu.au/dataset/217663&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=Prof Clive Prestidge&rft.date=2023&rft_subject=Human Pharmaceutical Products not elsewhere classified&rft_subject=MANUFACTURING&rft_subject=HUMAN PHARMACEUTICAL PRODUCTS&rft_subject=111500&rft_subject=lipid&rft_subject=GMS&rft_subject=silica&rft_subject=drug release&rft_subject=gastrointestinal&rft_subject=redispersibility&rft_subject=particle size&rft.type=dataset&rft.language=English Access the data
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Contact Information

Andrew.Robinson@unisa.edu.au

Brief 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.
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The following instruments/equipment were used to generate or capture the data:
local : DSET_INST_DATA_CAPTURE
Malvern Mastersizer 2000

Data time period: 2012 to 31 12 2015

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Subjects
111500 | GMS | Human Pharmaceutical Products | Human Pharmaceutical Products Not Elsewhere Classified | Manufacturing | drug release | gastrointestinal | lipid | particle size | redispersibility | silica |

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