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Aerosolized liposomal Amphotericin B: A potential prophylaxis of invasive pulmonary aspergillosis in immunocompromised patients

dc.contributor.authorHarutai Kamalapornen_US
dc.contributor.authorKitty Leungen_US
dc.contributor.authorMark Nagelen_US
dc.contributor.authorSaranya Kittanakomen_US
dc.contributor.authorBattista Calvierien_US
dc.contributor.authorReinhart A F Reithmeieren_US
dc.contributor.authorAllan L. Coatesen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherHospital for Sick Children University of Torontoen_US
dc.contributor.otherTrudell Medical Internationalen_US
dc.contributor.otherUniversity of Torontoen_US
dc.contributor.otherUniversity of Toronto Faculty of Medicineen_US
dc.date.accessioned2018-11-09T03:02:05Z
dc.date.available2018-11-09T03:02:05Z
dc.date.issued2014-01-01en_US
dc.description.abstractBackground Aerosolized liposomal Amphotericin B may reduce the incidence of invasive pulmonary Aspergillosis in adults with chemotherapy-induced prolonged neutropenia with less nephrotoxicity. The breath-actuated AeroEclipse® BAN nebulizer is very efficient and minimizes environmental drug contamination since no aerosol is produced, unless the patient is inspiring through the device. Our aim is to develop an appropriate delivery system suitable for children that does not disrupt the liposomes due to the shear forces in nebulization. Methods This is an in vitro experimental study in vitro. Six ml of 4 mg/ml liposomal Amphotericin B solution (AmBisome®; Astellas Pharma Inc., Markham, Ontario, CA) was nebulized with the breath-actuated nebulizer (AeroEclipse®; Trudell Medical International, Canada) and captured by the glass liquid impinger. Sodium dodecyl sulfate was used as detergent to disrupt the liposomes in control samples. Gel filtration, electron microscopy, and high performance liquid chromatography (HPLC) were used to compare the size and shape of the liposomes, and amount of the drug before and after nebulization. The aerosol particle size was obtained by the laser diffraction. Results After nebulization, 97.5% of amphotericin B was captured by the liquid impinger and detected by HPLC. Gel filtration and electron microscopy demonstrated that the drug remained in its liposomal configuration after nebulization. The mass median diameter (MMD) was 3.7 μm and 66% of aerosol particles were less than 5 μm in diameter. Conclusions We demonstrated that liposomal Amphotericin B can be nebulized successfully without disrupting the liposomes and minimize drug loss by using the breath-actuated nebulizer. © 2013 Wiley Periodicals, Inc.en_US
dc.identifier.citationPediatric Pulmonology. Vol.49, No.6 (2014), 574-580en_US
dc.identifier.doi10.1002/ppul.22856en_US
dc.identifier.issn10990496en_US
dc.identifier.issn87556863en_US
dc.identifier.other2-s2.0-84900010976en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/34777
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84900010976&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAerosolized liposomal Amphotericin B: A potential prophylaxis of invasive pulmonary aspergillosis in immunocompromised patientsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84900010976&origin=inwarden_US

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