High efficiency dry coating of non-subcoated pellets for sustained drug release formulations using amino methacrylate copolymers

Abstract

Dry coating utilizing a fluidized bed was evaluated in order to produce films with sustained drug release using amino methacrylate copolymers as film former. In contrast to other dry coating procedures using amino methacrylate copolymers, the described method enables an appropriate polymer adhesion by the selection of a plasticizer additive mixture in combination with the use of a three-way nozzle for simultaneous application. Well spreading fatty acid esters were found to increase the coating efficiency from 73% to approximately 86%, when they were used in conjunction with the plasticizer. Pellets were used as drug cores without previous treatment. After a curing step at 55 °C, the pellets exhibited a prolongation of the drug release over a period of about 6 h. Mainly the three parameters, coating level, composition of the polymers in the coating mixture, and the type of plasticizer, were found to exert distinct influence on the dissolution profile. Despite the differences in the coating procedure, the dissolution profiles of the coated pellets as well as the influencing parameters were similar to those known from conventional coating techniques.

Keywords:

• Coating efficiency
• contact angle
• dry powder coating
• film formation
• isopropyl stearate
• thermomechanical analysis

Acknowledgements

The authors would like to thank the companies Evonik Industries Pharma Polymers, Jungbunzlauer Ladenburg, and Temmler Ireland for the kind support with materials.

Disclosure statement

The authors report no conflicts of interest.