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A novel electrostatic dry powder coating process for pharmaceutical dosage forms: immediate release coatings for
Mingxi Qiao1, Liqiang Zhang, Yingliang Ma
1Department of Chemical and Biochemical Engineering, University of Western Ontario, Ontario, London, Ont, Canada.
A novel electrostatic dry powder coating process was developed for pharmaceutical tablets using a pan coater. This method enhances particle deposition and film formation, offering a viable alternative to traditional liquid coating methods.
Area of Science:
- Pharmaceutical Technology
- Materials Science
Background:
- Traditional pharmaceutical coating methods often involve aqueous or solvent-based systems.
- These methods can be limited by drying times, environmental concerns, and potential drug degradation.
Purpose of the Study:
- To develop and evaluate a novel electrostatic dry powder coating process for pharmaceutical solid dosage forms.
- To assess the feasibility of applying immediate-release coating compositions using this new technique.
Main Methods:
- An electrostatic dry powder coating process was established in a pan coater system.
- Tablet cores were treated with a liquid plasticizer to enhance conductivity and lower the glass transition temperature of the coating polymer.
- Charged coating particles (Opadry® AMB and Eudragit® EPO) were electrostatically sprayed onto tablet cores.
- Coating film formation was achieved through curing at acceptable processing temperatures.
Main Results:
- The electrostatic dry powder coating process successfully applied two immediate-release coating compositions.
- Tablet core conductivity was significantly increased, and particle deposition was enhanced.
- Scanning Electron Microscopy (SEM) confirmed the formation of a coalesced coating film.
- The resulting coated tablets exhibited smooth surfaces, uniform coatings, and comparable release profiles to uncoated cores.
Conclusions:
- The developed electrostatic dry powder coating technique is a viable alternative to conventional aqueous or solvent-based coating processes.
- This novel method offers potential advantages in efficiency and formulation flexibility for pharmaceutical solid dosage forms.
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