4.5 Article

Mesoporous zirconia nanoparticles as drug delivery systems: Drug loading, stability and release

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ELSEVIER
DOI: 10.1016/j.jddst.2020.102189

Keywords

Zirconia nanoparticles; Drug delivery systems; Mesoporous material; Drug stability; Drug loading

Funding

  1. Universit`a Ca' Foscari, Ministero dell'Universit`a e della Ricerca and Brenta srl

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Mesoporous zirconia nanoparticles (MZNs) have been found to be a promising drug delivery system with high loading and release efficiencies for a wide range of active pharmaceutical ingredients (API). The study demonstrated that MZNs efficiently loaded and released most of the investigated API, maintaining high inertness towards various functional groups even during long-term loading.
Drug delivery systems have been a milestone in medical research in the last twenty years, still representing a key aspect of innovation and evolution in pharmacokinetics and pharmacodynamics. Among several proposed solutions, inorganic mesoporous materials could be a promising vehicle. Their specific chemical-physical properties make them ideal candidates for the adsorption and loading of active pharmaceutical ingredients (API). Recently, mesoporous zirconia nanoparticles (MZNs) have been described as a novel drug delivery system due to their high surface area and biocompatibility. In this work, we investigated the loading and release efficiencies of a wide range of API on MZNs characterized by suitable pore volume and versatility, focusing on the integrity of the released drugs investigated through solution NMR and E SI-MS techniques. In order to explore the potentialities of MZNs for biomedical applications, we selected ibuprofen, N-acetyl-L-cysteine, vancomycin, gentamicin, nitrofurantoin, and indomethacin as benchmark API characterized by a wide range of polarity, molecular weight and presence of different functional groups. MZNs showed to efficiently load and release most of the API investigated. Long time loadings were also investigated observing that, after more than three months, no side reaction occurred on the released drugs except for intrinsically more labile API like NTF and NAC. MZNs ensured high inertness towards a wide range of functional groups such as aliphatic and aromatic amides, acetals of sugar residues as well as several chiral moieties bearing tertiary stereocenters.

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