Oral particle uptake and organ targeting drives the activity of amphotericin B nanoparticles
Serrano, Dolores R. and Lalatsa, Aikaterini and Dea-Ayuela, M. Auxiliadora and Bilbao-Ramos, Pablo E. and Garrett, Natalie L. and Moger, Julian and Guarro, Josep and Capilla, Javier and Ballesteros, M. Paloma and Schätzlein, Andreas G. and Bolás, Francisco and Torrado, Juan J. and Uchegbu, Ijeoma F. (2015) Oral particle uptake and organ targeting drives the activity of amphotericin B nanoparticles. Molecular Pharmaceutics, 12 (2). pp. 420-431. ISSN 1543-8384 (https://doi.org/10.1021/mp500527x)
Preview |
Text.
Filename: Serrano_etal_MP2015_Oral_particle_uptake_organ_targeting_drives_activity_amphotericin_B_nanoparticles.pdf
Accepted Author Manuscript Download (1MB)| Preview |
Abstract
There are very few drug delivery systems that target key organs via the oral route, as oral delivery advances normally address gastrointestinal drug dissolution, permeation, and stability. Here we introduce a nanomedicine in which nanoparticles, while also protecting the drug from gastric degradation, are taken up by the gastrointestinal epithelia and transported to the lung, liver, and spleen, thus selectively enhancing drug bioavailability in these target organs and diminishing kidney exposure (relevant to nephrotoxic drugs). Our work demonstrates, for the first time, that oral particle uptake and translocation to specific organs may be used to achieve a beneficial therapeutic response. We have illustrated this using amphotericin B, a nephrotoxic drug encapsulated within N-palmitoyl-N-methyl-N,N-dimethyl-N,N,N-trimethyl-6-O-glycol chitosan (GCPQ) nanoparticles, and have evidenced our approach in three separate disease states (visceral leishmaniasis, candidiasis, and aspergillosis) using industry standard models of the disease in small animals. The oral bioavailability of AmB-GCPQ nanoparticles is 24%. In all disease models, AmB-GCPQ nanoparticles show comparable efficacy to parenteral liposomal AmB (AmBisome). Our work thus paves the way for others to use nanoparticles to achieve a specific targeted delivery of drug to key organs via the oral route. This is especially important for drugs with a narrow therapeutic index.
ORCID iDs
Serrano, Dolores R., Lalatsa, Aikaterini ORCID: https://orcid.org/0000-0003-4791-7468, Dea-Ayuela, M. Auxiliadora, Bilbao-Ramos, Pablo E., Garrett, Natalie L., Moger, Julian, Guarro, Josep, Capilla, Javier, Ballesteros, M. Paloma, Schätzlein, Andreas G., Bolás, Francisco, Torrado, Juan J. and Uchegbu, Ijeoma F.;-
-
Item type: Article ID code: 80815 Dates: DateEvent2 February 2015PublishedNotes: Publisher Copyright: © 2015 American Chemical Society. Subjects: Medicine > Pharmacy and materia medica Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 19 May 2022 09:53 Last modified: 11 Nov 2024 13:29 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/80815