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We hope you have enjoyed this limited-length demo
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1. Drug discovery and development- Dr. Wayne Carter
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2. Chemical synthesis
- Dr. Wayne Carter
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3. In silico selection- Dr. Wayne Carter
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4. In vitro drug screening
- Dr. Wayne Carter
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5. Drug refinement
- Dr. Wayne Carter
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6. In vivo drug screening
- Dr. Wayne Carter
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7. Drug pharmacokinetics
- Dr. Wayne Carter
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8. Drug safety- Dr. Wayne Carter
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9. Clinical trials
- Dr. Wayne Carter
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10. Intellectual property and patents
- Dr. Wayne Carter
Printable Handouts
Navigable Slide Index
Topics Covered
- Hit and lead
- High throughput screening
- Lead optimisation
- Cycle of drug testing
- Drug optimisation and refinement
Links
Series:
Categories:
Talk Citation
Carter, W. (2026, July 30). Drug refinement [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved August 9, 2026, from https://doi.org/10.69645/VLJI4600.Export Citation (RIS)
Publication History
- Published on July 30, 2026
Financial Disclosures
- There are no commercial/financial matters to disclose.
A selection of talks on Pharmaceutical Sciences
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Dr. Wayne Carter.
Welcome to this lecture
entitled drug refinement.
Hit and lead.
0:08
The detection of a molecule
active against the target
macromolecule in a screening
assay is termed a hit.
A hit compound will likely
though require further
modification and optimisation
in order for it to be
suitably efficacious.
A lead compound is one that
has undergone some
level of optimisation,
and therefore
displays promise for
further pre-clinical development
as a possible drug candidate.
0:42
High-throughput
screening Part 1.
A hit compound may be detected
using high-throughput
screening (HTS).
This involves the assessment of
libraries of chemicals,
that is the ligands,
to identify activity against a
molecular target or targets.
It can be undertaken without
any prior knowledge of
the drug binding site,
and/or after prior
in silico screening
in an attempt to reduce the
number of screened compounds.
1:14
High throughput
screening Part 2.
The high throughput
screening needs to be rapid,
but also importantly
cost-effective
in order to be able to assess
the large number of chemicals
that may be present in
a chemical library.
This can be more than
a million chemicals.
It can utilise microtiter
plates such as shown
in the image here to perform
individualised reactions.
Subsequent tests, though,
are needed to ensure that
the hit is validated
to counter the risk
of false positives.
Lead optimisation.