Triamcinolone acetonide can be detected in cerebrospinal fluid after intratympanic injection.


Journal

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 08 04 2021
revised: 30 10 2021
accepted: 28 11 2021
pubmed: 6 12 2021
medline: 22 3 2022
entrez: 5 12 2021
Statut: ppublish

Résumé

Intratympanically applied treatments are of increasing interest to the otologic community to treat sudden sensorineural hearing loss or vestibular disorders but also to deliver gene therapy agents, or biologics to the inner ear. Further diversion from the middle ear and perilymph to blood circulation and cerebrospinal fluid via the cochlear aqueduct are one of the limiting factors and so far not understood well enough. In this study, intratympanically applied triamcinolone acetonide was determined in cerebrospinal fluid. Additionally, perilymph was sampled through the round window membrane as well as at the lateral semicircular canal to determine drug levels. Of the twenty-one included patients, triamcinolone acetonide was quantifiable in cerebrospinal fluid in 43% at very low levels (range 0 ng/ml-6.2 ng/ml) which did not correlate with perilymph levels. Drug levels at the two different perilymph sampling sites were within a range of 13.5 ng/ml to 1180.0 ng/ml. Results suggest an equal distribution of triamcinolone acetonide to semicircular canals, which might support the use of triamcinolone acetonide as a treatment option for vestibular pathologies such as Menièrés disease. On the other hand, the distribution to cerebrospinal fluid might be limiting current approaches in gene therapy where a central distribution is unwanted.

Identifiants

pubmed: 34864199
pii: S0939-6411(21)00340-4
doi: 10.1016/j.ejpb.2021.11.009
pii:
doi:

Substances chimiques

Glucocorticoids 0
Triamcinolone Acetonide F446C597KA

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

52-58

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Valerie Dahm (V)

Medical University of Vienna, Vienna, Austria, Department of Otorhinolaryngology, Head and Neck Surgery, Austria. Electronic address: valerie.dahm@meduniwien.ac.at.

Matthias Millesi (M)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria. Electronic address: matthias.millesi@meduniwien.ac.at.

Julia C Gausterer (JC)

Department of Pharmaceutical Technology and Biopharmaceutics, University of Vienna, Vienna, Austria. Electronic address: julia.clara.gausterer@univie.ac.at.

Alice B Auinger (AB)

Medical University of Vienna, Vienna, Austria, Department of Otorhinolaryngology, Head and Neck Surgery, Austria. Electronic address: alice.auinger@meduniwien.ac.at.

Franz Gabor (F)

Department of Pharmaceutical Technology and Biopharmaceutics, University of Vienna, Vienna, Austria. Electronic address: franz.gabor@univie.ac.at.

Gottfried Reznicek (G)

Department of Pharmacognosy, University of Vienna, Vienna, Austria. Electronic address: gottfried.reznicek@univie.ac.at.

Dominik Riss (D)

Medical University of Vienna, Vienna, Austria, Department of Otorhinolaryngology, Head and Neck Surgery, Austria. Electronic address: dominik.riss@meduniwien.ac.at.

Ursula Schwarz-Nemec (U)

Medical University of Vienna, Vienna, Austria, Department of Radiology, Division of Neuroradiology and Musculoskeletal Radiology, Austria. Electronic address: ursula.schwarz-nemec@meduniwien.ac.at.

Christian Matula (C)

Department of Neurosurgery, Medical University of Vienna, Vienna, Austria. Electronic address: christian.matula@meduniwien.ac.at.

Christoph Arnoldner (C)

Medical University of Vienna, Vienna, Austria, Department of Otorhinolaryngology, Head and Neck Surgery, Austria. Electronic address: christoph.arnoldner@meduniwien.ac.at.

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Classifications MeSH