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The effect of plasticizers on the erosion and mechanical properties of polymeric films

Producción científica: Articlerevisión exhaustiva

25 Citas (Scopus)

Resumen

Cellulose acetate phthalate and Pluronic F-127 combined together (70:30 wt:wt) create a rigid, surface-eroding association polymer. To impart flexibility into the polymer system and allow for a drug delivery film that can contour to varying wound shapes, plasticizers were added. Triethyl citrate or tributyl citrate was combined with cellulose acetate phthalate and Pluronic F-127 at 0, 10, or 20 wt%. Mechanical analysis was performed on the films as they were prepared and following a 2-h incubation in phosphate-buffered saline. Tensile tests showed that higher plasticizer content increased the % elongation but decreased the elastic modulus and ultimate tensile strength. The effect triethyl citrate had on the % elongation was twice as much than that of tributyl citrate. After incubation, % elongation, elastic modulus, and ultimate tensile strength all increased because plasticizer leached out of the films. Microcomputed tomography and scanning electron microscopy were performed on the samples both before and after incubation to determine how erosion and leaching of plasticizer affected the interior and exterior structure of the films. Porosity increased as plasticizer content increased; however, plasticizer content did not have a significant effect on the rate of erosion. The mechanical properties of cellulose acetate phthalate-Pluronic films can be adjusted by the type and amount of plasticizer added to the system and therefore can be tailored for different drug delivery applications.

Idioma originalEnglish
Páginas (desde-hasta)779-789
Número de páginas11
PublicaciónJournal of Biomaterials Applications
Volumen28
N.º5
DOI
EstadoPublished - ene 2014

Nota bibliográfica

Funding Information:
This research was supported in part by the NIH (DE019645 and AR060964) and NSF (EPS-0814194 and EEC-0851716). CR was supported by NSF IGERT (DGE-0653710).

Financiación

This research was supported in part by the NIH (DE019645 and AR060964) and NSF (EPS-0814194 and EEC-0851716). CR was supported by NSF IGERT (DGE-0653710).

FinanciadoresNúmero del financiador
National Science Foundation (NSF)EEC-0851716, EPS-0814194, DGE-0653710
National Institutes of Health (NIH)DE019645
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR060964

    ASJC Scopus subject areas

    • Biomaterials
    • Biomedical Engineering

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