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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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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 |
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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 |
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