Structural and Dynamic Properties of Amorphous Solid Dispersions: The Role of Solid‐State Nuclear Magnetic Resonance Spectroscopy and Relaxometry

Amrit Paudel, Marco Geppi, Guy Van den Mooter

Research output: Contribution to journalArticlepeer-review

Abstract

Amorphous solid dispersions (ASDs) are one of the frontier strategies to improve solubility and dissolution rate of poorly soluble drugs and hence tackling the growing challenges in oral bioavailability. Pharmaceutical performance, physicochemical stability, and downstream processability of ASD largely rely on the physical structure of the product. This necessitates in‐depth characterization of ASD microstructure. Solid‐state nuclear magnetic resonance (SS‐NMR) techniques bear the ultimate analytical capabilities to provide the molecular level information on the dynamics and phase compositions of amorphous dispersions. SS‐NMR spectroscopy/relaxometry, as a single and nondestructive technique, can reveal diverse and critical structural information of complex ASD formulations that are barely amenable from any other existing technique. The purpose of the current article is to review the recent most important studies on various sophisticated and information‐rich one‐dimensional and two‐dimensional SS‐NMR spectroscopy/relaxometry for the analysis of molecular mobility, miscibility, drug–carrier interactions, crystallinity, and crystallization in ASD. Some specific examples on microstructural elucidations of challenging ASD using multidimensional and multinuclear SS‐NMR are presented. Additionally, some relevant examples on the utility of solution‐NMR and NMR‐imaging techniques for the investigation of the dissolution behavior of ASD are gathered.
Original languageEnglish
JournalJournal of Pharmaceutical Sciences
Publication statusPublished - 8 Apr 2014

Fingerprint

Dive into the research topics of 'Structural and Dynamic Properties of Amorphous Solid Dispersions: The Role of Solid‐State Nuclear Magnetic Resonance Spectroscopy and Relaxometry'. Together they form a unique fingerprint.

Cite this