Dry Powder Inhalers II: Enhancing bioavailability through product design
Instructor:
Claudio Cerati
Product ID: 702013
- Duration: 85 Min
Why Should You Attend:
Drug action when delivered through a dry powder inhaler device is closely related to both physical considerations and chemical interactions between the interface, between well defined inhaled particles and the respiratory tract surface . Many patented products developed in this area takes into account the spherical shape and also hollow characteristics of carrier particles.
No attempts have been made till now to combine a carrier with usual aerodynamic diameter and develop active spherical particles that can be adhered to the carrier with and adhesion force similar to those obtained with a traditional powder mix. Impact on bioavailability is in close relationship with both carrier and active particle design and formulation.
In this webinar we will analyze the interaction of new product design and both usual impactor equipments and drug delivery devices.
Areas Covered in the Seminar:
- API particle size and shape.
- How to control those parameters.
- Formulating spherical particles.
- Optimizing formulations to achieve reproducibility.
- Strategies to enhance drug bioavailability.
- Device and product impact on bioavailability.
- Understanding in vitro testing and relating to in vivo results.
Who Will Benefit:
This webinar will provide a valuable point of view for those professionals working in the field of Dry Powder Inhalers and inhalator drug delivery systems. Professionals who will benefit include
- R&D Professionals
- R&D Technical people
- New Product Project Developers
- Pharma Production Professionals
- Consultants
Claudio Cerati , is an independant consultant in the pharmaceutical industry was Director of Research and Development Department at Tecnoquimicas SA in the city of Cali, Colombia and in Pharmaceutical companies in Argentina (Phoenix Laboratories ). During the last twenty five years , he was directly involved in R&D, Quality Control and Manufacturing areas in national and multinational companies in latin américa ( Argentina and Brazil) with the direct responsibility of developing and scaling up pharmaceutical processes.
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