| Literature DB >> 28532676 |
Katrin Göke1, Thomas Lorenz2, Alexandros Repanas3, Frederic Schneider4, Denise Steiner5, Knut Baumann6, Heike Bunjes7, Andreas Dietzel8, Jan H Finke9, Birgit Glasmacher10, Arno Kwade11.
Abstract
Low aqueous solubility of active pharmaceutical ingredients presents a serious challenge in the development process of new drug products. This article provides an overview on some of the current approaches for the formulation of poorly water-soluble drugs with a special focus on strategies pursued at the Center of Pharmaceutical Engineering of the TU Braunschweig. These comprise formulation in lipid-based colloidal drug delivery systems and experimental as well as computational approaches towards the efficient identification of the most suitable carrier systems. For less lipophilic substances the preparation of drug nanoparticles by milling and precipitation is investigated for instance by means of microsystem-based manufacturing techniques and with special regard to the preparation of individualized dosage forms. Another option to overcome issues with poor drug solubility is the incorporation into nanospun fibers.Entities:
Keywords: Colloidal lipid carriers; Computational carrier selection; Drug delivery systems; Drug nanosuspensions; Electrospinning; Microfluidics; Orodispersible films; Solubility
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Year: 2017 PMID: 28532676 DOI: 10.1016/j.ejpb.2017.05.008
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571