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dc.contributor.authorAlbariqi, Ahmed H.en_AU
dc.contributor.authorKe, Wei-Renen_AU
dc.contributor.authorKhanal, Dipeshen_AU
dc.contributor.authorKalfas, Stefanieen_AU
dc.contributor.authorTang, Patriciaen_AU
dc.contributor.authorBritton, Warwick Jen_AU
dc.contributor.authorDrago, Johnen_AU
dc.contributor.authorChan, Hak-Kimen_AU
dc.date.accessioned2022-04-28T02:44:59Z
dc.date.available2022-04-28T02:44:59Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/2123/28304
dc.description.abstractBackground: Ivermectin has received worldwide attention as a potential COVID-19 treatment after showing antiviral activity against SARS-CoV-2 in vitro. However, the pharmacokinetic limitations associated with oral administration have been postulated as limiting factors to its bioavailability and efficacy. These limitations can be overcome by targeted delivery to the lungs. In this study, inhalable dry powders of ivermectin and lactose crystals were prepared and characterized for the potential treatment of COVID-19. Methods: Ivermectin was co-spray dried with lactose monohydrate crystals and conditioned by storage at two different relative humidity points (43% and 58% RH) for a week. The in vitro dispersion performance of the stored powders was examined using a medium-high resistance Osmohaler connecting to a next-generation impactor at 60_L/min flow rate. The solid-state characteristics including particle size distribution and morphology, crystallinity, and moisture sorption profiles of raw and spray-dried ivermectin samples were assessed by laser diffraction, scanning electron microscopy, Raman spectroscopy, X-ray powder diffraction, thermogravimetric analysis, differential scanning calorimetry, and dynamic vapor sorption. Results: All the freshly spray-dried formulation (T0) and the conditioned samples could achieve the anticipated therapeutic dose with fine particle dose of 300__g, FPFrecovered of 70%, and FPFemitted of 83%. In addition, the formulations showed a similar volume median diameter of 4.3__m and span of 1.9. The spray-dried formulations were stable even after conditioning and exposing to different RH points as ivermectin remained amorphous with predominantly crystalline lactose. Conclusion: An inhalable and stable dry powder of ivermectin and lactose crystals was successfully formulated. This powder inhaler ivermectin candidate therapy appears to be able to deliver doses that could be safe and effective to treat the SARS-COV-2 infection. Further development of this therapy is warranted.en_AU
dc.language.isoenen_AU
dc.subjectCOVID-19en_AUI
dc.subjectCoronavirusen_AUI
dc.titlePreparation and Characterization of Inhalable Ivermectin Powders as a Potential COVID-19 Therapyen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1089/jamp.2021.0059


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