Formulation of Nanosuspensions of Challenging Drugs Using Amphiphilic Janus-Dendrimers as Stabilizing Agents
Sami Nummelin – Senior Researcher, BioHybrid Materials, Aalto University; Mauri Kostiainen – Full Professor, BioHybrid Materials, Aalto University; Vera Moura – Director, Basinnov Life Sciences; Ana Fortuna – Researcher and Full Assistant Professor, CIBIT - Coimbra Institute for Biomedical Imaging and Translational Research and Faculty of Pharmacy, University of Coimbra; Luís Bimbo – Assistant Professor, Center for Neuroscience and Cell Biology - Centre for Innovative Biomedicine and Biotechnology and Faculty of Pharmacy, University of Coimbra
PhD Student University of Coimbra Leiria, Leiria, Portugal
Introduction: Poor solubility and instability continue to limit the bioavailability of many drugs [1]. Nanosuspensions offer a way to address these challenges, but their performance relies heavily on the choice of stabiliser [2]. Conventional agents often struggle to maintain long‑term stability across different drug types [2]. Amphiphilic Janus dendrimers (JDs) provide tunable architectures and have already shown superior stabilisation in drug suspensions [3]. This project develops JD‑based nanosuspensions for ceftazidime, ampicillin and glucagon to establish structure–activity relationships and improve formulation stability.
Learning Objectives:
Understand how Janus dendrimer structural features influence nanosuspension stabilisation.
Learn how formulation strategies vary for weak acids, weak bases and peptides using JD stabilisers.
Identify how JD architecture affects dissolution, stability and in vivo pharmacokinetic behaviour.