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Updated: May 1, 2026

Disposable Dosators for Pulmonary Insufflation of Therapeutic Agents to Small Animals
Published on: March 30, 2017
Capreomycin inhalable powders prepared with an innovative spray-drying technique
Aurélie Schoubben1, Stefano Giovagnoli1, Maria Cristina Tiralti1
1Dipartimento di Scienze Farmaceutiche, Università degli Studi di Perugia, Via del Liceo 1, Perugia 06123, Italy.
This study developed inhalable capreomycin sulfate powders using novel nano spray-drying technology. Optimized conditions yielded powders with excellent aerodynamic properties for inhalation therapy.
Area of Science:
- Pharmaceutical Technology
- Drug Delivery Systems
- Materials Science
Background:
- Inhalable drug delivery offers targeted treatment for respiratory diseases.
- Developing stable and respirable drug powders is crucial for effective inhalation therapy.
- Capreomycin is an important antibiotic for treating multidrug-resistant tuberculosis.
Purpose of the Study:
- To produce inhalable capreomycin sulfate powders using a novel spray-drying technology.
- To optimize the spray-drying process for desirable powder characteristics like size, morphology, flowability, and aerodynamic properties.
- To evaluate the potential of nano spray-drying for producing respirable capreomycin sulfate formulations.
Main Methods:
- A 2(3) factorial design was employed to identify optimal spray-drying parameters.
- Powders were characterized for particle size (mean volume diameter, dv), span, yield, morphology, flowability, and aerodynamic properties.
- Mathematical models were used to assess process predictivity.
- Optimization was performed using bacitracin as a model drug, followed by capreomycin sulfate processing.
Main Results:
- Optimal conditions for spray-drying were determined, achieving high desirability based on small particle size and high yield.
- Mathematical models demonstrated good predictivity (biases < 20%).
- Initial processing of capreomycin sulfate yielded inhalable powder (yield 82%, dv 3.83 μm, span 1.04). Further optimization improved characteristics (yield ~71%, dv 3.25 μm, span 0.95).
- Formulated capreomycin sulfate powders achieved high emitted dose (87%) and respirable fraction (~27%).
Conclusions:
- Novel nano spray-drying technology can successfully produce inhalable capreomycin sulfate powders.
- Optimized process parameters are critical for achieving desired aerodynamic properties for inhalation.
- The developed capreomycin sulfate powders demonstrate significant potential for effective pulmonary drug delivery in tuberculosis treatment.
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