Biologic Comparison of Inhaled Insulin Formulations: ExuberaTM and Novel Spray-Dried Engineered Particles of Dextran-10

Inhaled peptides and proteins have promise for respiratory and systemic disease treatment. Engineered spray-dried powder formulations have been shown to stabilize peptides and proteins and optimize aerosol properties for pulmonary delivery. The current study was undertaken to investigate the in vitro and in vivo inhalation performance of a model spray-dried powder of insulin and dextran 10 in comparison to Exubera™. Dextrans are a class of glucans that are generally recognized as safe with optimum glass transition temperatures well suited for spray drying. A 70% insulin particle loading was prepared by formulating with 30% (w/v) dextran 10. Physical characterization revealed a “raisin like” particle. Both formulations were generated to produce a similar bimodal particle size distribution of less than 3.5 μm MMAD. Four female Beagle dogs were exposed to each powder in a crossover design. Similar presented and inhaled doses were achieved with each powder. Euglycemia was achieved in each dog prior and subsequent to dosing and blood samples were drawn out to 245 min post-exposure. Pharmacokinetic analyses of post-dose insulin levels were similar for both powders. Respective dextran 10-insulin and Exubera exposures were similar producing near identical area under the curve (AUC), 7,728 ± 1,516 and 6,237 ± 2,621; concentration maximums (Cmax), 126 and 121 (μU/mL), and concentration–time maximums, 20 and 14 min, respectively. These results suggest that dextran-10 and other dextrans may provide a novel path for formulating peptides and proteins for pulmonary delivery.

[1]  W. Hinrichs,et al.  Unraveling protein stabilization mechanisms: vitrification and water replacement in a glass transition temperature controlled system. , 2013, Biochimica et biophysica acta.

[2]  A. Hickey Back to the future: inhaled drug products. , 2013, Journal of pharmaceutical sciences.

[3]  M. Grant,et al.  Peptide therapeutics: it's all in the delivery. , 2012, Therapeutic delivery.

[4]  J. Foidart,et al.  Nebulized anti-IL-13 monoclonal antibody Fab' fragment reduces allergen-induced asthma. , 2012, American journal of respiratory cell and molecular biology.

[5]  J. Weers,et al.  Development of an inhaled dry-powder formulation of tobramycin using PulmoSphere™ technology. , 2011, Journal of aerosol medicine and pulmonary drug delivery.

[6]  Dan E. Dobry,et al.  Formulation Development and In Vivo Evaluation of a New Dry Powder Formulation of Albuterol Sulphate in Beagle Dogs , 2010, Pharmaceutical Research.

[7]  E. B. Getz,et al.  Inhaled vs subcutaneous effects of a dual IL‐4/IL‐13 antagonist in a monkey model of asthma , 2010, Allergy.

[8]  T. Buffington,et al.  Clinical Veterinary Advisor: Dogs and Cats , 2006 .

[9]  D. Edgerton,et al.  Inhalation of Human Insulin Is Associated with Improved Insulin Action Compared with Subcutaneous Injection and Endogenous Secretion in Dogs , 2006, Journal of Pharmacology and Experimental Therapeutics.

[10]  D. Edgerton,et al.  Inhalation of insulin (Exubera) is associated with augmented disposal of portally infused glucose in dogs. , 2005, Diabetes.

[11]  D. Edgerton,et al.  Inhalation of insulin in dogs: assessment of insulin levels and comparison to subcutaneous injection. , 2004, Diabetes.

[12]  M. Dolovich,et al.  Pulmonary drug delivery. Part I: physiological factors affecting therapeutic effectiveness of aerosolized medications. , 2003, British journal of clinical pharmacology.

[13]  P. Davidson,et al.  Effect of dextran molecular weight on protein stabilization during freeze-drying and storage. , 2001, Cryo letters.

[14]  M. Pikal,et al.  The Stability of Insulin in Crystalline and Amorphous Solids: Observation of Greater Stability for the Amorphous Form , 1997, Pharmaceutical Research.

[15]  H. Chan,et al.  Pulmonary Delivery of Peptides and Proteins , 2011 .

[16]  J. Patton,et al.  The lungs as a portal of entry for systemic drug delivery. , 2004, Proceedings of the American Thoracic Society.