Volume 135, Issue 14 46068
Article

Biodegradable polymeric injectable implants for long-term delivery of contraceptive drugs

Ohan S. Manoukian

Ohan S. Manoukian

Department of Orthopaedic Surgery, University of Connecticut Health, Farmington, Connecticut

Department of Biomedical Engineering, University of Connecticut, Storrs, Connecticut

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Michael R. Arul

Michael R. Arul

Department of Orthopaedic Surgery, University of Connecticut Health, Farmington, Connecticut

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Naseem Sardashti

Naseem Sardashti

Department of Biomedical Engineering, University of Connecticut, Storrs, Connecticut

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Teagan Stedman

Teagan Stedman

Department of Orthopaedic Surgery, University of Connecticut Health, Farmington, Connecticut

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Roshan James

Roshan James

Department of Orthopaedic Surgery, University of Connecticut Health, Farmington, Connecticut

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Swetha Rudraiah

Swetha Rudraiah

Department of Pharmaceutical Sciences, School of Pharmacy, University of Saint Joseph, Hartford, Connecticut, 06103

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Sangamesh G. Kumbar

Corresponding Author

Sangamesh G. Kumbar

Department of Orthopaedic Surgery, University of Connecticut Health, Farmington, Connecticut

Department of Biomedical Engineering, University of Connecticut, Storrs, Connecticut

Department of Materials Science and Engineering, University of Connecticut, Storrs, Connecticut

Correspondence to: S.G. Kumbar (E-mail: [email protected])Search for more papers by this author
First published: 29 November 2017
Citations: 80

ABSTRACT

Development of injectable, long-lasting, contraceptive drug delivery formulations, and implants are highly desired to avoid unplanned pregnancies while improving patient compliance and reducing adverse side effects and treatment costs. The present study reports on the fabrication and characterization of two levonorgestrel (LNG) microsphere injectable formulations. Poly(ɛ-caprolactone) (PCL) with 12.5% and 24% (w/w) LNG were fabricated into microspheres, measuring 300 ± 125 µm, via the oil-in-water (o/w) emulsion solvent evaporation technique. Formulations showed sustained drug release up to 120 days. FTIR, XRD, DSC, and TGA confirmed the absence of LNG chemical interaction with PCL as well as its molecular level distribution. The in vitro release of LNG was calculated to be Fickian diffusion controlled and properly characterized. The inclusion of multiple elevated release temperatures allowed for the application of the Arrhenius model to calculate drug release constants and representative sampling intervals, demonstrating the use of elevated temperatures for accelerated-time drug release studies. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46068.

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