4.7 Article

Co-Delivery of a High Dose of Amphotericin B and Itraconazole by Means of a Dry Powder Inhaler Formulation for the Treatment of Severe Fungal Pulmonary Infections

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PHARMACEUTICS
卷 15, 期 11, 页码 -

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MDPI
DOI: 10.3390/pharmaceutics15112601

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amphotericin B; itraconazole; dry powder inhaler; lung deposition; infection; aspergillosis

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In recent decades, the increasing incidence and prevalence of pulmonary fungal infections has become a global health problem due to the lack of specific antifungal therapies for pulmonary administration. This study developed microparticles and dry powder inhalers to improve the pharmacological effect of antifungal drugs, providing new options for pulmonary treatment.
Over the past few decades, there has been a considerable rise in the incidence and prevalence of pulmonary fungal infections, creating a global health problem due to a lack of antifungal therapies specifically designed for pulmonary administration. Amphotericin B (AmB) and itraconazole (ITR) are two antifungal drugs with different mechanisms of action that have been widely employed in antimycotic therapy. In this work, microparticles containing a high dose of AmB and ITR (20, 30, and 40% total antifungal drug loading) were engineered for use in dry powder inhalers (DPIs) with an aim to improve the pharmacological effect, thereby enhancing the existing off-label choices for pulmonary administration. A Design of Experiment (DoE) approach was employed to prepare DPI formulations consisting of AmB-ITR encapsulated within gamma-cyclodextrin (gamma-CD) alongside functional excipients, such as mannitol and leucine. In vitro deposition indicated a favourable lung deposition pattern characterised by an upper ITR distribution (mass median aerodynamic diameter (MMAD) similar to 6 mu m) along with a lower AmB deposition (MMAD similar to 3 mu m). This offers significant advantages for treating fungal infections, not only in the lung parenchyma but also in the upper respiratory tract, considering that Aspergillus spp. can cause upper and lower airway disorders. The in vitro deposition profile of ITR and larger MMAD was related to the higher unencapsulated crystalline fraction of the drug, which may be altered using a higher concentration of gamma-CD.

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