This submission belongs to the session a. Advances in the solid state field of the event The 2nd Electronic Conference on Pharmaceutical Sciences
Published date
24 Apr, 2012
Citation
Daniel Bar-Shalom, Jukka Rantanen, Thomas Rades, Anette Müllertz, Johan Boetker, Kaisa Naelapää, SOLUPLUS® FOR MODIFYING THE RELEASE OF HIGHLY WATER SOLUBLE APIs, in Proceedings of The 2nd Electronic Conference on Pharmaceutical Sciences, 1 May–31 May 2012, MDPI: Basel, Switzerland, doi: 10.3390/ecps2012-00824
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SOLUPLUS® FOR MODIFYING THE RELEASE OF HIGHLY WATER SOLUBLE APIs
Kaisa Naelapää 1
Johan Boetker 1
Anette Müllertz 1
Thomas Rades 1
Jukka Rantanen 1
Daniel Bar-Shalom 1
1. Department of Pharmacy, School of Pharmaceutical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark
Abstract
Well established techniques for increasing the solubility of poorly water soluble APIs are available. However, formulating highly water soluble APIs into dosage forms exhibiting modified release profile is gaining interest. In this work a new application for Soluplus®, a graft copolymer, is launched. A novel approach where Soluplus® is used as a dissolution modifying agent for highly water soluble APIs is introduced. Acetaminophen (APAP) and guaifenesin (GF) were used as model water soluble APIs. 95:5 and 90:10 ratios of respective API and Soluplus® were either physically mixed (PM) together or melted together on a hot plate. Melts were investigated using DSC and XRPD and compacts were submitted to dissolution studies. In case of APAP:Soluplus® a single melting event with an onset similar to pure APAP was determined by DSC. The XRPD diffractogram of molten material exhibited an amorphous halo, however further processing caused the material to crystallize. The compacts made of ground molten materials had a similar release profile and showed a slower release compared to compacts prepared from PMs. When GF:Soluplus® melts were submitted to DSC a single melting event occurred. The onset of this event did not match with the melting event of pure GF. The XRPD diffractogram of the molten samples revealed that a new polymorphic form of GF had crystallized. GF:Soluplus® compacts made of molten material revealed faster release of GF compared to compacts made of PMs of GF:Soluplus®. Using Soluplus® as a dissolution modifying agent enables tailoring of the release of the API. In this work the release of two highly water soluble APIs was modified by two different methods. Furthermore, presence of a new polymorphic form of GF was identified.
Keywords
solid dispersion
Soluplus®
polymorphism
water soluble APIs
modified release
Characteristics and drug release of drug-loaded microparticles prepared with different solvents using electrospraying
Characterization of powder properties using a powder rheometer