Critical material attributes (CMAs) of strip films loaded with poorly water-soluble drug nanoparticles: I. Impact of plasticizer on film properties and dissolution

Document Type

Article

Publication Date

9-20-2016

Abstract

Recent studies have demonstrated polymer films to be a promising platform for delivery of poorly water-soluble drug particles. However, the impact of critical material attributes, for example plasticizer, on the properties of and drug release from such films has yet to be investigated. In response, this study focuses on the impact of plasticizer and plasticizer concentration on properties and dissolution rate of polymer films loaded with poorly water-soluble drug nanoparticles. Glycerin, triacetin, and polyethylene glycol were selected as film plasticizers. Griseofulvin was used as a model Biopharmaceutics Classification System class II drug and hydroxypropyl methylcellulose was used as a film-forming polymer. Griseofulvin nanoparticles were prepared via wet stirred media milling in aqueous suspension. A depression in film glass transition temperature was observed with increasing plasticizer concentration, along with a decrease in film tensile strength and an increase in film elongation, as is typical of plasticizers. However, the type and amount of plasticizer necessary to produce strong yet flexible films had no significant impact on the dissolution rate of the films, suggesting that film mechanical properties can be effectively manipulated with minimal impact on drug release. Griseofulvin nanoparticles were successfully recovered upon redispersion in water regardless of plasticizer or content, even after up to 6 months' storage at 40 °C and 75% relative humidity, which contributed to similar consistency in dissolution rate after 6 months' storage for all films. Good content uniformity (< 4% R.S.D. for very small film sample size) was also maintained across all film formulations.

Identifier

84978881219 (Scopus)

Publication Title

European Journal of Pharmaceutical Sciences

External Full Text Location

https://doi.org/10.1016/j.ejps.2016.07.005

e-ISSN

18790720

ISSN

09280987

PubMed ID

27402100

First Page

146

Last Page

155

Volume

92

Grant

NIH-U01

Fund Ref

National Science Foundation

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