Inhalable Microparticles Embedding Biocompatible Magnetic Iron-Doped Hydroxyapatite Nanoparticles

Author:

Quarta Eride1ORCID,Chiappi Michele2,Adamiano Alessio3ORCID,Tampieri Anna3,Wang Weijie2,Tetley Teresa D.2,Buttini Francesca14ORCID,Sonvico Fabio14ORCID,Catalucci Daniele5ORCID,Colombo Paolo6,Iafisco Michele3ORCID,Degli Esposti Lorenzo3ORCID

Affiliation:

1. Department of Food and Drug, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy

2. National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London SW7 0AZ, UK

3. Institute of Science, Technology and Sustainability for Ceramic Materials (ISSMC), National Research Council (CNR), Via Granarolo 64, 48018 Faenza, Italy

4. Interdepartmental Center for Innovation in Health Products, Biopharmanet_TEC, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy

5. Institute of Genetic and Biomedical Research (IRGB), National Research Council (CNR), UOS Milan and IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy

6. PlumeStars srl, Parco Area Delle Scienze, 27/A, 43125 Parma, Italy

Abstract

Recently, there has been increasing interest in developing biocompatible inhalable nanoparticle formulations, as they have enormous potential for treating and diagnosing lung disease. In this respect, here, we have studied superparamagnetic iron-doped calcium phosphate (in the form of hydroxyapatite) nanoparticles (FeCaP NPs) which were previously proved to be excellent materials for magnetic resonance imaging, drug delivery and hyperthermia-related applications. We have established that FeCaP NPs are not cytotoxic towards human lung alveolar epithelial type 1 (AT1) cells even at high doses, thus proving their safety for inhalation administration. Then, D-mannitol spray-dried microparticles embedding FeCaP NPs have been formulated, obtaining respirable dry powders. These microparticles were designed to achieve the best aerodynamic particle size distribution which is a critical condition for successful inhalation and deposition. The nanoparticle-in-microparticle approach resulted in the protection of FeCaP NPs, allowing their release upon microparticle dissolution, with dimensions and surface charge close to the original values. This work demonstrates the use of spray drying to provide an inhalable dry powder platform for the lung delivery of safe FeCaP NPs for magnetically driven applications.

Funder

European Union’s Horizon 2020

Publisher

MDPI AG

Subject

Biomedical Engineering,Biomaterials

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