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Original Research Article | OPEN ACCESS

Development of fast-release piroxicam/polyethylene glycol capsules by solid dispersion and curing using full factorial design

Benchawan Chamsai, Wipada Samprasit

Department of Pharmaceutical Technology, College of Pharmacy, Rangsit University, PathumThani, 12000, Thailand;

For correspondence:-  Wipada Samprasit   Email: swipada@hotmail.com

Accepted: 18 May 2018        Published: 30 June 2018

Citation: Chamsai B, Samprasit W. Development of fast-release piroxicam/polyethylene glycol capsules by solid dispersion and curing using full factorial design. Trop J Pharm Res 2018; 17(6):781-790 doi: 10.4314/tjpr.v17i6.1

© 2018 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop fast-release piroxicam (PRX) capsules by solid dispersion with polyethylene glycol (PEG) using melting and curing in a heated coating pan.
Methods: A full factorial design was conducted to investigate the main and interaction effects of molecular weight (4000 - 8000 Da) and amount (10 - 30 mg PEG to 10 mg PRX) on the dissolution rate of PRX. Temperature (50 - 70 °C) and duration of the curing process (15 - 45 min) were also systematically selected by factorial design.
Results: The molecular weight and amount of PEG significantly impacted on the dissolution rate of PRX (p = 0.04 and 0.01, respectively), while temperature and duration of the curing process were not significant effects (p = 0.10 and 0.17, respectively). Based on the results, a fast dissolution rate and burst release of PRX was obtained from capsules formulated by PRX/PEG 8000 (1:3 weight ratio) as a solid dispersion compared to the physical mixture and free drug. Furthermore, this capsule was in the acceptance range for the labeled amount, weight variation and disintegration time.
Conclusion: PRX/PEG melted solid dispersion capsule may be a suitable immediate release drug delivery system with improved dissolution rate and increased drug absorption.

Keywords: Capsules, Solid dispersion, Piroxicam, Polyethylene glycol, Fast release, Full factorial design

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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