International Journal of Pharmaceutical Investigation, 2016, 6, 1, 39-46.
DOI: 10.4103/2230-973X.176474
Published: February 2016
Type: Original Article
Authors:
Neha Sureshrao Raut
Department of Quality Assurance, Shrimati Kishoritai Bhoyar College of Pharmacy, Nagpur, Maharashtra, India.
Swapnil Jamaiwar
Department of Quality Assurance, Shrimati Kishoritai Bhoyar College of Pharmacy, Nagpur, Maharashtra, India.
Milind Janrao Umekar
Department of Quality Assurance, Shrimati Kishoritai Bhoyar College of Pharmacy, Nagpur, Maharashtra, India.
Nandkishor Ramdas Kotagale
Department of Quality Assurance, Shrimati Kishoritai Bhoyar College of Pharmacy, Nagpur, Maharashtra, India.
ABSTRACT
Introduction: This study focused on the potential effects of compression forces experienced during lactose (InhaLac 70, 120, and 230) storage and transport on the flowability and aerosol performance in dry powder inhaler formulation. Materials and Methods: Lactose was subjected to typical compression forces 4, 10, and 20 N/cm2. Powder flowability and particle size distribution analysis of un-compressed and compressed lactose was evaluated by Carr’s index, Hausner’s ratio, the angle of repose and by laser diffraction method. Aerosol performance of un-compressed and compressed lactose was assessed in dispersion studies using glass twin-stage-liquid-impenger at flow rate 40-80 L/min. Results: At compression forces, the flowability of compressed lactose was observed same or slightly improved. Furthermore, compression of lactose caused a decrease in in vitro aerosol dispersion performance. Conclusion: The present study illustrates that, as carrier size increases, a concurrent decrease in drug aerosolization performance was observed. Thus, the compression of the lactose fines onto the surfaces of the larger lactose particles due to compression pressures was hypothesized to be the cause of these observed performance variations. The simulations of storage and transport in an industrial scale can induce significant variations in formulation performance, and it could be a source of batch-to-batch variations.
Keywords: Aerosolisation, compression pressure, Dry powder inhalation, Lactose, Particle size .