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Research ArticleOpen Access

PABA Release from Chitosan-PCL with Induced Electric Current

Volume 7 - Issue 3

Jennifer M Miller and Roche C de Guzman*

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    • Department of Engineering, Hofstra University, USA

    *Corresponding author: Roche C de Guzman,133 Hofstra University, 203 Weed Hall, Hempstead, NY 11549, USA

Received: July 24, 2018;   Published: July 31, 2018

DOI: 10.26717/BJSTR.2018.07.001512

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Controlled drug delivery systems such as the stimulation-based biomaterial scaffolds for sequestration and release of drugs offer safety and regulated therapeutic approach. In this study, the drug: para-aminobenzoic acid (PABA) was absorbed into a crosslinked chitosan and poly(caprolactone) (PCL) hydrogel and its release kinetics quantified under different conditions. It was experimentally-observed that the higher the pH (or the more basic the pH), the slower the PABA saturation release trended over time. At the acidic environment of pH 4, PABA was released the fastest, and enhanced by the degradation of chitosan-PCL gel. When a constant electric current of 0.6 mA as applied, PABA release was induced at pH 10. However, at pH 7, PABA was stably-bound to the chitosan-PCL matrix, with or without the external current. The selective sequestration of PABA at basic pH and its stimulated release via electric current application can be further explored for clinical translatability.

Keywords: Drug Delivery; Chitosan; PCL; Biomaterial Scaffolds; PABA; Electrical Stimulation; Electrostatic Interaction

Abbreviations: DDS: Drug Delivery Systems; PCL: Poly(Caprolactone); PABA: Para-Aminobenzoic Acid; DCC: N,N’-Dicyclohexylcarbodiimide; DBTDL: Dibutyltin Dilaurate; DMACA: 4-(Diethylamino)Cinnamaldehyde; MOPS: 4-Morpholinepropanesulfonic Acid

Abstract | Introduction | Materials and Methods | Results | Discussion | Conclusion | Acknowledgement | References |