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A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery
Hearing loss is the most common sensory deficit worldwide with no approved therapeutics for treatment. Local neurotrophin delivery into the cochlea has shown great potential in protecting and repairing the sensory cells important for hearing. However, delivery of these factors into the inner ear at...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549113/ https://www.ncbi.nlm.nih.gov/pubmed/33072529 http://dx.doi.org/10.1016/j.mex.2020.101078 |
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author | Lam, Patrick Gunewardene, Niliksha Ma, Yutian Caruso, Frank Nguyen, Trung Flynn, Brianna Wise, Andrew K. Richardson, Rachael T. |
author_facet | Lam, Patrick Gunewardene, Niliksha Ma, Yutian Caruso, Frank Nguyen, Trung Flynn, Brianna Wise, Andrew K. Richardson, Rachael T. |
author_sort | Lam, Patrick |
collection | PubMed |
description | Hearing loss is the most common sensory deficit worldwide with no approved therapeutics for treatment. Local neurotrophin delivery into the cochlea has shown great potential in protecting and repairing the sensory cells important for hearing. However, delivery of these factors into the inner ear at therapeutic levels over a sustained period of time has remained a challenge restricting clinical translation. We have developed a method to test the pharmacokinetics of neurotrophin released from porous silica particles called ‘supraparticles’ that can provide sustained release of neurotrophins to the inner ear. • This report describes a radiolabeling method to examine neurotrophin retention and distribution in the cochlea. The neurotrophin was labeled with a radioactive tracer (iodine 125: (125)I) and delivered into the cochlea via the supraparticle system. • Gamma counts reveal drug levels and clearance in the intact cochlea, as well as accumulation in off-target organs (safety test). Autoradiography analyses using film and emulsion permit quantification and visualization of drug distribution at the cellular level. The method has a detection limit of 0.8 pg of radiolabeled neurotrophin-3 in cochlear sections exposed to film. • The tracer (125)I with a half-life of 59.4 days can be used to label other drugs/substances with a tyrosine residue and therefore be broadly applicable for long-term pharmacokinetic studies in other systems. |
format | Online Article Text |
id | pubmed-7549113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75491132020-10-16 A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery Lam, Patrick Gunewardene, Niliksha Ma, Yutian Caruso, Frank Nguyen, Trung Flynn, Brianna Wise, Andrew K. Richardson, Rachael T. MethodsX Method Article Hearing loss is the most common sensory deficit worldwide with no approved therapeutics for treatment. Local neurotrophin delivery into the cochlea has shown great potential in protecting and repairing the sensory cells important for hearing. However, delivery of these factors into the inner ear at therapeutic levels over a sustained period of time has remained a challenge restricting clinical translation. We have developed a method to test the pharmacokinetics of neurotrophin released from porous silica particles called ‘supraparticles’ that can provide sustained release of neurotrophins to the inner ear. • This report describes a radiolabeling method to examine neurotrophin retention and distribution in the cochlea. The neurotrophin was labeled with a radioactive tracer (iodine 125: (125)I) and delivered into the cochlea via the supraparticle system. • Gamma counts reveal drug levels and clearance in the intact cochlea, as well as accumulation in off-target organs (safety test). Autoradiography analyses using film and emulsion permit quantification and visualization of drug distribution at the cellular level. The method has a detection limit of 0.8 pg of radiolabeled neurotrophin-3 in cochlear sections exposed to film. • The tracer (125)I with a half-life of 59.4 days can be used to label other drugs/substances with a tyrosine residue and therefore be broadly applicable for long-term pharmacokinetic studies in other systems. Elsevier 2020-09-24 /pmc/articles/PMC7549113/ /pubmed/33072529 http://dx.doi.org/10.1016/j.mex.2020.101078 Text en © 2020 The Author(s). Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Method Article Lam, Patrick Gunewardene, Niliksha Ma, Yutian Caruso, Frank Nguyen, Trung Flynn, Brianna Wise, Andrew K. Richardson, Rachael T. A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title | A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title_full | A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title_fullStr | A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title_full_unstemmed | A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title_short | A radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
title_sort | radiolabeled drug tracing method to study neurotrophin-3 retention and distribution in the cochlea after nano-based local delivery |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549113/ https://www.ncbi.nlm.nih.gov/pubmed/33072529 http://dx.doi.org/10.1016/j.mex.2020.101078 |
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