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Micro- and macrostructural characterization of polyvinylpirrolidone rotary-spun fibers. | LitMetric

AI Article Synopsis

  • High-speed rotary spinning is an effective technique for creating fibrous materials used in drug delivery systems and conventional dosage forms.
  • Polyvinylpyrrolidone (PVP) and its copolymer with vinyl acetate were processed into micro- and nanofibers to study how different concentrations and solvent ratios impact fiber production.
  • Advanced techniques like scanning electron microscopy and positron annihilation lifetime spectroscopy were used to analyze the fibers' structure and properties, leading to the identification of optimal conditions for enhancing their mechanical attributes.

Article Abstract

The application of high-speed rotary spinning can offer a useful mean for either preparation of fibrous intermediate for conventional dosage forms or drug delivery systems. Polyvinylpyrrolidone (PVP) and poly(vinylpyrrolidone-vinylacetate) (PVP VA) micro- and nanofibers of different polymer concentrations and solvent ratios were prepared with a high-speed rotary spinning technique. In order to study the influence of parameters that enable successful fiber production from polymeric viscous solutions, a complex micro- and macrostructural screening method was implemented. The obtained fiber mats were subjected to detailed morphological analysis using scanning electron microscope (SEM), and rheological measurements while the microstructural changes of fiber samples, based on the free volume changes, was analyzed by positron annihilation lifetime spectroscopy (PALS) and compared with their mechanical characteristics. The plasticizing effect of water tracked by ortho-positronium lifetime changes in relation to the mechanical properties of fibers. A concentration range of polyvinylpyrrolidone solutions was defined for the preparation of fibers of optimum fiber morphology and mechanical properties. The method enabled fiber formulation of advantageous functionality-related properties for further formulation of solid dosage forms.

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Source
http://dx.doi.org/10.3109/03639045.2015.1013967DOI Listing

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