Literature DB >> 21953470

Supersaturating drug delivery systems: fast is not necessarily good enough.

Patrick Augustijns1, Marcus E Brewster.   

Abstract

An emerging technology subtype that has been adopted by formulators to address low-solubility issues is the supersaturating drug delivery system; this system is based on the "spring" and "parachute" design elements, which have been applied to lipid-based formulations, S(M)EDDS, solid dispersions, nano-based systems, and many others. This broad formulation approach attempts to delicately balance the need of creating intraluminal drug concentrations in excess of its thermodynamic solubility while at the same time providing for sufficient solution stability to allow for useful drug absorption. The conundrum created is that the higher the extent of supersaturation, the lower the physical stability of the metastable solution based on an increased tendency for a solubilized drug to precipitate. Traditional dissolution testing is a touchstone of formulation development based on the need for useful dissolution rates and drug availability. Dissolution testing is likewise important in the development and characterization of enabling and supersaturating drug delivery systems; however, their execution and interpretation are distinct from that associated with conventional dosage forms. The nature of the dissolution assay (sink versus nonsink, apparatus type, and rate and extent of supersaturation) can impact the ability to efficiently use the dissolution data in the configuration of these enabling formulations.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21953470     DOI: 10.1002/jps.22750

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  15 in total

Review 1.  Haste Makes Waste: The Interplay Between Dissolution and Precipitation of Supersaturating Formulations.

Authors:  Dajun D Sun; Ping I Lee
Journal:  AAPS J       Date:  2015-09-03       Impact factor: 4.009

2.  Impact of Solubilizing Additives on Supersaturation and Membrane Transport of Drugs.

Authors:  Shweta A Raina; Geoff G Z Zhang; David E Alonzo; Jianwei Wu; Donghua Zhu; Nathaniel D Catron; Yi Gao; Lynne S Taylor
Journal:  Pharm Res       Date:  2015-05-28       Impact factor: 4.200

3.  Biorelevant in vitro performance testing of orally administered dosage forms-workshop report.

Authors:  Christos Reppas; Horst-Dieter Friedel; Amy R Barker; Lucinda F Buhse; Todd L Cecil; Susanne Keitel; Johannes Kraemer; J Michael Morris; Vinod P Shah; Mary P Stickelmeyer; Chikako Yomota; Cynthia K Brown
Journal:  Pharm Res       Date:  2014-03-19       Impact factor: 4.200

Review 4.  Current Status of Supersaturable Self-Emulsifying Drug Delivery Systems.

Authors:  Heejun Park; Eun-Sol Ha; Min-Soo Kim
Journal:  Pharmaceutics       Date:  2020-04-16       Impact factor: 6.321

5.  Hypromellose acetate succinate based amorphous solid dispersions via hot melt extrusion: Effect of drug physicochemical properties.

Authors:  Sandeep Sarabu; Venkata Raman Kallakunta; Suresh Bandari; Amol Batra; Vivian Bi; Thomas Durig; Feng Zhang; Michael A Repka
Journal:  Carbohydr Polym       Date:  2020-01-10       Impact factor: 9.381

Review 6.  The Precipitation Behavior of Poorly Water-Soluble Drugs with an Emphasis on the Digestion of Lipid Based Formulations.

Authors:  Jamal Khan; Thomas Rades; Ben Boyd
Journal:  Pharm Res       Date:  2015-11-23       Impact factor: 4.200

7.  Influence of Copolymer Composition on In Vitro and In Vivo Performance of Celecoxib-PVP/VA Amorphous Solid Dispersions.

Authors:  Matthias Manne Knopp; Julia Hoang Nguyen; Huiling Mu; Peter Langguth; Thomas Rades; René Holm
Journal:  AAPS J       Date:  2016-01-14       Impact factor: 4.009

8.  The amorphous solid dispersion of the poorly soluble ABT-102 forms nano/microparticulate structures in aqueous medium: impact on solubility.

Authors:  Kerstin J Frank; Ulrich Westedt; Karin M Rosenblatt; Peter Hölig; Jörg Rosenberg; Markus Mägerlein; Gert Fricker; Martin Brandl
Journal:  Int J Nanomedicine       Date:  2012-11-12

9.  Improved oral bioavailability of poorly water-soluble indirubin by a supersaturatable self-microemulsifying drug delivery system.

Authors:  Zhi-Qiang Chen; Ying Liu; Ji-Hui Zhao; Lan Wang; Nian-Ping Feng
Journal:  Int J Nanomedicine       Date:  2012-02-23

10.  Automated PET-RAFT Polymerization Towards Pharmaceutical Amorphous Solid Dispersion Development.

Authors:  Rahul Upadhya; Ashish Punia; Mythili J Kanagala; Lina Liu; Matthew Lamm; Timothy A Rhodes; Adam J Gormley
Journal:  ACS Appl Polym Mater       Date:  2021-02-15
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