Structure formation and coarsening kinetics of phase-separated spin-coated ethylcellulose/hydroxypropylcellulose filmsShow others and affiliations
2022 (English)In: Soft Matter, ISSN 1744-683X, E-ISSN 1744-6848, Vol. 18, no 16, p. 3206-3217Article in journal (Refereed) Published
Abstract [en]
Porous phase-separated ethylcellulose/hydroxypropylcellulose (EC/HPC) films are used to control drug transport from pharmaceutical pellets. The drug transport rate is determined by the structure of the porous films that are formed as water-soluble HPC leaches out. However, a detailed understanding of the evolution of the phase-separated structure in the films is lacking. In this work, we have investigated EC/HPC films produced by spin-coating, mimicking the industrial fluidized bed spraying. The aim was to investigate film structure evolution and coarsening kinetics during solvent evaporation. The structure evolution was characterized using confocal laser scanning microscopy and image analysis. The effect of the EC:HPC ratio (15 to 85 wt% HPC) on the structure evolution was determined. Bicontinuous structures were found for 30 to 40 wt% HPC. The growth of the characteristic length scale followed a power law, L(t) ∼ t(n), with n ∼ 1 for bicontinuous structures, and n ∼ 0.45-0.75 for discontinuous structures. The characteristic length scale after kinetic trapping ranged between 3.0 and 6.0 μm for bicontinuous and between 0.6 and 1.6 μm for discontinuous structures. Two main coarsening mechanisms could be identified: interfacial tension-driven hydrodynamic growth for bicontinuous structures and diffusion-driven coalescence for discontinuous structures. The 2D in-plane interface curvature analysis showed that the mean curvature decreased as a function of time for bicontinuous structures, confirming that interfacial tension is driving the growth. The findings of this work provide a good understanding of the mechanisms responsible for morphology development and open for further tailoring of thin EC/HPC film structures for controlled drug release. © 2022 The Royal Society of Chemistry
Place, publisher, year, edition, pages
Royal Society of Chemistry , 2022. Vol. 18, no 16, p. 3206-3217
Keywords [en]
Coarsening, Controlled drug delivery, Fluidized beds, Kinetics, Ostwald ripening, Bicontinuous structures, Characteristic length, Coarsening kinetics, Ethylcellulose, Film structure, Formation kinetics, Hydroxypro-pylcellulose, Length scale, Structure evolution, Structure formations, Separation, cellulose, hydroxypropylcellulose, solvent, water, chemistry, porosity, Solvents
National Category
Medical Materials
Identifiers
URN: urn:nbn:se:ri:diva-59252DOI: 10.1039/d2sm00113fScopus ID: 2-s2.0-85128483936OAI: oai:DiVA.org:ri-59252DiVA, id: diva2:1660258
Note
Funding details: 2019-01295; Funding details: Stiftelsen för Strategisk Forskning, SSF, FID16-0013; Funding details: Vetenskapsrådet, VR, 2018-03986; Funding text 1: The Swedish Foundation for Strategic Research (SSF grant FID16-0013), the Swedish Research Council (VR grant 2018-03986), and the Swedish Research Council for Sustainable Development (grant 2019-01295) are gratefully acknowledged for the funding. AstraZeneca is acknowledged for the financial support and materials. Philip Townsend, RISE/Chalmers, is acknowledged for his contribution to the 2D-curvature estimation.
2022-05-232022-05-232023-05-26Bibliographically approved