Our paper @ Adv Drug Del Rev

Our new article on the challenges associated with market translation of nanotechnology-related products has been accepted by Advanced Drug Delivery Reviews.

The international team of experts has done a great job in providing their expertise. Thanks to you Margareth Marques (USP), Choo Qiuyi (HSA), Mukul Ashtikar (Fraunhofer IME), Thais Correa Rocha (ANVISA) and Susanne Bremer-Hoffmann (EC-JRC).

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Research in Spotlight


For the first time I was doing a science slam hosted by Goethe University in Frankfurt. Amazing evening and we all had a lot of fun


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#SavingThePlanet?

Everyone wants to have access to medicines! For many years, we know that an aging population together with the quality of life we got used to leads to higher consumption of pharmaceuticals. But there’s also a rising concern that pharmaceutical drugs pollute our planet. Environmental scientists do not hesitate to say how disappointed they are with the pharmaceutical industry. Many comments indicate a total lack of understanding of the way our healthcare system works. Once a medicine has passed the clinical trials and market approval has been granted by a national authority, a company has no freedom at all to “just change the recipe”. Along this line, nanotechnology has been described to have a strong negative impact on different ecosystems.
So how are we saving our planet? Our latest research paper written by Fabian Jung was just accepted by Environmental Research. It uses release testing, a method commonly applied by the pharmaceutical industry in development, to select drug formulations that are likely to succeed during clinical trials. We are combining this technique with computer-based simulations (ISERA model) and a lifecycle assessment to pre-select the excipients used in production. Because we are stopping the use of non-sustainable excipients very early in drug development, we still have all the freedom we need to make medicines more sustainable. Additionally, we present the application of nanomaterials to reduce environmental pollution. To do so, we combine smart technologies to identify drug formulations that are effective and safe in patients without posing a risk to the environment. Once the paper is online we will share the link on our website.


#ScienceSavesThePlant #EnjoyReading #WackerResearchLab #ExplainMyResearch

Illustration of drug product development using ISERA and LCA.
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Advances in Interdisciplinary Pharmaceutical Research

The AAPS student chapter of the National University of Singapore organizes a symposium together with Monash University putting interdisciplinary research in the spotlight. The event takes place on the 23rd of September. What would be more inspiring than bright young minds presenting their vision of the future? Please watch out for the latest announcements of NUS Pharmacy.

#AAPS-NUS #NUSPharmacy #NUSFacultyOfScience

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Simulate SubQ

Our latest research article on drug release testing of a long-acting depot formulation was just accepted by the International Journal of Pharmaceutics. This is great work by the young first author Ge Fiona Gao. One year ago she won a Best Abstract Award of the AAPS Annual Meeting, now she has done a tremendous job showing the influences of the physiological environment on formulations that remain at the injection site for several weeks.
The release assay elucidated the influence of proteins on microparticle release and how they affect discrimination between different batches of drug products. Even without affecting solubility, proteins stabilize particles and may affect the performance in the subcutaneous tissue. A mechanistic model helped us to understand the influences of such parameters and formulation characteristics on pharmacokinetics. Why does it matter? Without understanding what are the major drivers of drug release there will always be a high risk of failure when testing new long-acting therapeutics for chronic diseases.

#SaferMedicines #EnjoyReading #ExplainMyResearch

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The PBNB model: Unlock your PK data

Today, our manuscript on the Physiologically-based Nanocarrier Biopharmaceutics (PBNB) Model was finally accepted for publication by the European Journal of Pharmaceutics and Biopharmaceutics. I explained the purpose of this model in my talk during the Explain-My-Research Virtual Conference in May 2020 and will go more into detail during a Live Webinar organized by Malvern Panalytical in July. Rather than providing a ‘convenient fit’ only, the model is designed to link the pharmacokinetics of nanocarriers to a physiologically-based distribution. Interesting parameters you may obtain with this model are, for example, the targeting capability and the mean residence time of the nanocarrier in the blood plasma. A lowered plasma concentration often indicates that more drug has been released from the carrier and is not available for targeting any more. The PBNB model recognizes such changes and calculates how much carrier-bounded drug is accumulated before this release happens. Expressed as a fraction of the total dose, this is the targeting capability (Ftarget) . The mean residence time of the carrier (MRTc) in the blood plasma indicates how much time the delivery system had for this accumulation process and is a marker for targeting accuracy.

Some of the simulations our PBNB model is capable of are provided on the servers of our collaborator isee systems.

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Guest judge @ SPDS

I was very happy to act as a guest judge for the Society for Pharmaceutical Dissolution Science. For the last 10 years, my group has been passionate about developing novel release assays and it was good to have a conference putting this important part of drug product development in the spotlight. Students from all over India submitted their work on drug release testing. Congratulations to the finalists.

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Save the Environment

It is really difficult to publish translational manuscripts these days, but this is a prime example of a good collaboration between pharmaceutical and environmental sciences. As pharmaceutical scientists, we sometimes have to use a certain material to facilitate drug therapy. But if we have a choice and more than one coating or one polymer actually works, why not choose the one which is best for the environment? This study helps you sort that out.

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Predicting Nanomedicines

A wide variety of models have been established to predict the performance of nanomedicines for the peroral route of administration, but only a handful for injectables. Liposomal temoporfin has been evaluated in a phase I clinical trial. This investigation was focused on the prediction of the performance of liposomes in humans using preclinical in vitro and in vivo data. Congratulations to our young researcher Laura Jablonka who is responsible for this great accomplishment. Also, it is a prime example for international collaborations by involving researchers from Germany and Singapore…

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Our research@CRS Indian chapter

I am pleased to be an invited speaker at the CRS conference in Mumbai in February 2020. I will talk about our work on in vitro-in vivo correlation for nanodelivery systems. For more information check out the conference brochure.

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Our research @ USP workshop


I will speak at the USP workshop in Rockville about our efforts to develop drug release methods for drug products comprising nanomaterials. You can register here for the event.

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Editorial board @ JPP

Today, I was informed that I will join the Editorial Board of the Journal of Pharmacy and Pharmacology of the Royal Pharmaceutical Society. Thanks to David Jones and all the editors for this honor…

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