Formulation, stability and pharmacokinetics of sugar-based salmon calcitonin-loaded nanoporous/nanoparticulate microparticles (NPMPs) for inhalation

• Published in: International journal of pharmaceutics Vol. 483; no. 1-2; pp. 6 - 18
• Main Authors: Amaro, Maria Inês, Tewes, Frederic, Gobbo, Oliviero, Tajber, Lidia, Corrigan, Owen I., Ehrhardt, Carsten, Healy, Anne Marie
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 10-04-2015; Elsevier
• Subjects: Administration, Inhalation; Calcitonin - administration & dosage; Calcitonin - chemistry; Calcitonin - pharmacokinetics; Carbohydrates - chemistry; Chemistry, Pharmaceutical; Drug Stability; Dry Powder Inhalers; Inhalation; Life Sciences; Microbiology and Parasitology; Nanoparticles - chemistry; Non-reducing sugars; Particle Size; Pharmaceutical sciences; Pharmacokinetics; Porosity; Salmon calcitonin; Stability; Surface Properties; Non-reducing sugars; Stability; Pharmacokinetics; Salmon calcitonin; Inhalation
• ISSN: 0378-5173; 1873-3476
• DOI: 10.1016/j.ijpharm.2015.02.003

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A challenge exists to produce dry powder inhaler (DPI) formulations with appropriate formulation stability, biological activity and suitable physicochemical and aerosolisation characteristics that provide a viable alternative to parenteral formulations. The present study aimed to produce sugar-based nanoporous/nanoparticulate microparticles (NPMPs) loaded with a therapeutic peptide – salmon calcitonin (sCT). The physicochemical properties of the powders and their suitability for pulmonary delivery of sCT were determined. Production of powders composed of sCT loaded into raffinose or trehalose with or without hydroxypropyl-β-cyclodextrin was carried out using a laboratory scale spray dryer. Spray dried microparticles were spherical, porous and of small geometric size (≤2μm). Aerodynamic assessment showed that the fine particle fraction (FPF) less than 5μm ranged from 45 to 86%, depending on the formulation. The mass median aerodynamic diameter (MMAD) varied between 1.9 and 4.7μm. Compared to unprocessed sCT, sCT:raffinose composite systems presented a bioactivity of approximately 100% and sCT:trehalose composite systems between 70–90% after spray drying. Storage stability studies demonstrated composite systems with raffinose to be more stable than those containing trehalose. These sugar-based salmon calcitonin-loaded NPMPs retain reasonable sCT bioactivity and have micromeritic and physicochemical properties which indicate their suitability for pulmonary delivery. Formulations presented a similar pharmacokinetic profile to sCT solution. Hence the advantage of a dry powder formulation is its non-invasive delivery route and ease of administration of the sCT.