Cargando…

Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237

Human papilloma virus (HPV) is the main culprit in cervical cancers. Although the HPV vaccine is now available, the slow and gradual process for HPV cancers to form means little will change, even for vaccinated individuals. This warrants the development of new therapeutic strategies in both the newl...

Descripción completa

Detalles Bibliográficos
Autores principales: Tayyar, Yaman, Shiels, Ryan, Bulmer, Andrew C., Lam, Alfred K., Clarke, Daniel, Idris, Adi, McMillan, Nigel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880999/
https://www.ncbi.nlm.nih.gov/pubmed/31774882
http://dx.doi.org/10.1371/journal.pone.0225774
_version_ 1783473854373429248
author Tayyar, Yaman
Shiels, Ryan
Bulmer, Andrew C.
Lam, Alfred K.
Clarke, Daniel
Idris, Adi
McMillan, Nigel A.
author_facet Tayyar, Yaman
Shiels, Ryan
Bulmer, Andrew C.
Lam, Alfred K.
Clarke, Daniel
Idris, Adi
McMillan, Nigel A.
author_sort Tayyar, Yaman
collection PubMed
description Human papilloma virus (HPV) is the main culprit in cervical cancers. Although the HPV vaccine is now available, the slow and gradual process for HPV cancers to form means little will change, even for vaccinated individuals. This warrants the development of new therapeutic strategies in both the newly diagnosed and recurrent patients. We have previously shown that Alisertib (MLN8237), an Aurora A kinase inhibitor, potently and selectively kills HPV-positive cervical cancer cells. However, Alisertib is known for its unfavorable side effects when administered systemically. A targeted delivery approach is therefore warranted. The topical delivery of drugs to the cervix for the treatment of cervical cancer is an underexplored area of research that has the potential to significantly improve therapeutic outcome. Here, we design a novel topical drug delivery system for localized delivery in the vaginal tract using intravaginal silicone rings loaded with Alisertib. We assessed the suitability of the drug for the application and delivery method and develop a high-performance liquid chromatography method, then show that the vaginal rings were effective at releasing Alisertib over an extended period of time. Furthermore, we showed that Alisertib-loaded vaginal rings did not induce overt inflammation in the mouse vaginal tract. Our work has major translational implications for the future development of vaginal ring devices for the topical treatment of cervical cancer.
format Online
Article
Text
id pubmed-6880999
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-68809992019-12-08 Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237 Tayyar, Yaman Shiels, Ryan Bulmer, Andrew C. Lam, Alfred K. Clarke, Daniel Idris, Adi McMillan, Nigel A. PLoS One Research Article Human papilloma virus (HPV) is the main culprit in cervical cancers. Although the HPV vaccine is now available, the slow and gradual process for HPV cancers to form means little will change, even for vaccinated individuals. This warrants the development of new therapeutic strategies in both the newly diagnosed and recurrent patients. We have previously shown that Alisertib (MLN8237), an Aurora A kinase inhibitor, potently and selectively kills HPV-positive cervical cancer cells. However, Alisertib is known for its unfavorable side effects when administered systemically. A targeted delivery approach is therefore warranted. The topical delivery of drugs to the cervix for the treatment of cervical cancer is an underexplored area of research that has the potential to significantly improve therapeutic outcome. Here, we design a novel topical drug delivery system for localized delivery in the vaginal tract using intravaginal silicone rings loaded with Alisertib. We assessed the suitability of the drug for the application and delivery method and develop a high-performance liquid chromatography method, then show that the vaginal rings were effective at releasing Alisertib over an extended period of time. Furthermore, we showed that Alisertib-loaded vaginal rings did not induce overt inflammation in the mouse vaginal tract. Our work has major translational implications for the future development of vaginal ring devices for the topical treatment of cervical cancer. Public Library of Science 2019-11-27 /pmc/articles/PMC6880999/ /pubmed/31774882 http://dx.doi.org/10.1371/journal.pone.0225774 Text en © 2019 Tayyar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tayyar, Yaman
Shiels, Ryan
Bulmer, Andrew C.
Lam, Alfred K.
Clarke, Daniel
Idris, Adi
McMillan, Nigel A.
Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title_full Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title_fullStr Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title_full_unstemmed Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title_short Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237
title_sort development of an intravaginal ring for the topical delivery of aurora kinase a inhibitor, mln8237
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880999/
https://www.ncbi.nlm.nih.gov/pubmed/31774882
http://dx.doi.org/10.1371/journal.pone.0225774
work_keys_str_mv AT tayyaryaman developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT shielsryan developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT bulmerandrewc developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT lamalfredk developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT clarkedaniel developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT idrisadi developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237
AT mcmillannigela developmentofanintravaginalringforthetopicaldeliveryofaurorakinaseainhibitormln8237