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Development of Triazole-based Dry Powder Formulations for Inhalation

Authors :
Amighi, Karim
Wauthoz, Nathalie
Langer, Ingrid
Fontaine, Véronique
Van Antwerpen, Pierre
Vanderbist, Francis
Flament, Marie-Pierre
Schoubben, Aurélie
Merlos, Romain
Amighi, Karim
Wauthoz, Nathalie
Langer, Ingrid
Fontaine, Véronique
Van Antwerpen, Pierre
Vanderbist, Francis
Flament, Marie-Pierre
Schoubben, Aurélie
Merlos, Romain
Publication Year :
2019

Abstract

Among the different pulmonary fungal infections, aspergillosis, and in particular invasive pulmonary aspergillosis (IPA), are becoming the most worrying diseases in immunocompromised patients. This is due to their high incidence and mortality. Indeed, invasive aspergillosis manifests as invasive pulmonary disease accounting for 50/60% of all cases, with a mortality of 50-90% in severely immunocompromised patients. Triazoles act by inhibiting 14-α demethylase, a fungal cytochrome P450 enzyme implicated in the synthesis of ergosterol, an essential constituent of fungal cell walls. Moreover, they interact with the same cytochrome present in large quantities in the human liver, inducing possible drug-drug interactions in IPA patients. Consequently, interactions resulting from inhibitors, inductors, or substrates of cytochromes can modify the plasmatic concentrations of triazoles or other drugs administered concomitantly. To overcome these important issues, pulmonary delivery of triazoles could be an interesting alternative to conventional routes.The aim of this work was to develop triazole-based dry powders for inhalation able to be deposited adequately in the lungs, with a release of drug and a lung retention that can optimize its pharmacological action. This work focused on two active pharmaceutical ingredients (API): itraconazole (ITZ), for which improved solubility was needed, and voriconazole (VCZ), for which slow release was required.Concerning ITZ, solid dispersions for inhalation (SDIs) comprising ITZ and mannitol were previously developed in our laboratory. The selected SDI showed interesting results in terms of improved dissolution and lung retention in vivo in mice during a pharmacokinetic study. Therefore, this SDI was tested in a murine preclinical model of IPA and showed promising results in terms of prophylaxis efficacy. One aim of this work was to continue the pharmaceutical development of this promising SDI by making a scaling-up study. These methods we<br />Doctorat en Sciences biomédicales et pharmaceutiques (Pharmacie)<br />info:eu-repo/semantics/nonPublished

Details

Database :
OAIster
Notes :
4 full-text file(s): application/pdf | application/pdf | application/pdf | application/vnd.openxmlformats-officedocument.wordprocessingml.document, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1110018063
Document Type :
Electronic Resource