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- Nonlinear mixed effect modeling – a bed time story
- Export control in a digital world – is synthetic data the future for clinical studies?
- Neural ODEs vs ODEs – what’s the difference?
- ScienceJournalJourney3 – the translation problem in drug development
- ScienceJournalJourney2 – The one surprising use of Fexofenadine (Telfast)
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Author Archives: janice goh
Nobel prize-winning neural nets and pharmacometrics
As a (mostly) computational scientist, I was excited to see both the Nobel prizes in physics and chemistry being awarded for computational work last week. In particular, the Physics price on Artificial neural networks, a fundamental building block in many … Continue reading
How can pharmacometrics benefit clinical practice and vice versa?
Last weekend, I had the privilege of speaking about my work in pharmacogenomics at the Singapore Pharmacy Congress. It was a good time of getting to meet old friends and network with the new generation of pharmacists. Just as how … Continue reading
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Tagged bioinformatics, education, health, pharmacist, Pharmacokinetics, pharmacometrics, pharmacy, research, singapore pharmacometrics
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A quick visual check for saturated clearance
In many animal studies, a wide range of doses are often used. At high doses, it is possible to have way more drug than its clearance pathway can handle, resulting in less drug than expected being eliminated. This is called … Continue reading
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Tagged data science, Pharmacokinetics, pharmacology, pharmacometrics, singapore pharmacometrics
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Direct vs Indirect effect models
When you take a drug, the drug needs time to be absorbed after, it needs to reach the effect site and then cause a biological process to happen before an effect occurs. All these processes take time. Some of them … Continue reading
How to build a PK-PD model?
Hello fellow coffee and cat lovers, as with the first caffeine simulator, I will be going through how to run PK-PD simulations too. Link to coffee simulator 2: https://lnkd.in/dAiS3igB We have previously covered how to run PK simulations which you … Continue reading
Why do pharmacokinetic-pharmacodynamic (PK-PD) modeling?
It takes 2 hands to clap. Previously, in my first coffee simulator, https://janicegoh.shinyapps.io/CoffeeSimulator/ we used a simple threshold to determine caffeine efficacy and toxicity. However, this efficacy alone does not tell us exactly how alert we will be with a … Continue reading
Artificial sweetener choices – to absorb or not to absorb?
Artificial sweeteners are in the news again regarding potential new health risks. In particular, xylitol (a common artificial sugar) has been called into question as a prothrombotic (causing an increased risk of blood clots and thus stroke and heart attacks) … Continue reading
A sticky situation
Researchers, if your compound It’s not your next big hit. It could be an aggregator instead. These are some general pointers for flagging out false positives when screening for new hits (B. Shiochet PMID: 16793529). As PK scientists, this is also … Continue reading
How do I know two drugs can be safely taken together? – understanding drug-drug interactions
In my previous life as a pharmacist, many patients used to ask if it was safe to take two medications they were prescribed together. Unless otherwise stated e.g. explicit instructions were given to take the medications at least 2 hours … Continue reading
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Tagged Pharmacodynamics, Pharmacokinetics, pharmacology, singapore pharmacometrics
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What are enteric-coated tablets, and how does enteric coating affect PK?
Most tablets and capsules taken by mouth enter the stomach and dissolve there, before entering the small intestine for absorption. On the other hand, enteric-coated tablets are designed with a special coating to allow the medication to pass through the … Continue reading