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Modulated release from implantable ocular silicone oil tamponade drug reservoirs
Complicated cases of retinal detachment can be treated with silicone oil tamponades. There is the potential for silicone oil tamponades to have adjunctive drug releasing behaviour within the eye, however the lipophilic nature of silicone oil limits the number of drugs that are suitable, and drug rel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873246/ https://www.ncbi.nlm.nih.gov/pubmed/29610546 http://dx.doi.org/10.1002/pola.28973 |
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author | Cauldbeck, Helen Le Hellaye, Maude McDonald, Tom O. Long, Mark Williams, Rachel L. Rannard, Steve P. Kearns, Victoria R. |
author_facet | Cauldbeck, Helen Le Hellaye, Maude McDonald, Tom O. Long, Mark Williams, Rachel L. Rannard, Steve P. Kearns, Victoria R. |
author_sort | Cauldbeck, Helen |
collection | PubMed |
description | Complicated cases of retinal detachment can be treated with silicone oil tamponades. There is the potential for silicone oil tamponades to have adjunctive drug releasing behaviour within the eye, however the lipophilic nature of silicone oil limits the number of drugs that are suitable, and drug release from the hydrophobic reservoir is uncontrolled. Here, a radiometric technique was developed to accurately measure drug solubility in silicone oil and measure release into culture media. All‐trans retinoic acid (atRA), a lipophilic drug known to act as an anti‐proliferative within the eye, was used throughout this work. Chain‐end modification of polydimethylsiloxane with atRA produced a polydimethylsiloxane retinoate (PDMS‐atRA), which was used as an additive to silicone oil to modify the solvent environment within the silicone oil and the distribution coefficient. Blends of PDMS‐atRA and silicone oil containing different concentrations of free atRA were produced. The presence of PDMS‐atRA in silicone oil had a positive effect on atRA solubility and the longevity of release in vitro. The drug release period was independent of atRA starting concentration and dependent on the PDMS‐atRA concentration in the blend. A clinically relevant release period of atRA over 7 weeks from a silicone oil blend with PDMS‐atRA was observed. © 2018 The Authors. Journal of Polymer Science Part A: Polymer Chemistry Published by Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 938–946 |
format | Online Article Text |
id | pubmed-5873246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58732462018-03-31 Modulated release from implantable ocular silicone oil tamponade drug reservoirs Cauldbeck, Helen Le Hellaye, Maude McDonald, Tom O. Long, Mark Williams, Rachel L. Rannard, Steve P. Kearns, Victoria R. J Polym Sci A Polym Chem Articles Complicated cases of retinal detachment can be treated with silicone oil tamponades. There is the potential for silicone oil tamponades to have adjunctive drug releasing behaviour within the eye, however the lipophilic nature of silicone oil limits the number of drugs that are suitable, and drug release from the hydrophobic reservoir is uncontrolled. Here, a radiometric technique was developed to accurately measure drug solubility in silicone oil and measure release into culture media. All‐trans retinoic acid (atRA), a lipophilic drug known to act as an anti‐proliferative within the eye, was used throughout this work. Chain‐end modification of polydimethylsiloxane with atRA produced a polydimethylsiloxane retinoate (PDMS‐atRA), which was used as an additive to silicone oil to modify the solvent environment within the silicone oil and the distribution coefficient. Blends of PDMS‐atRA and silicone oil containing different concentrations of free atRA were produced. The presence of PDMS‐atRA in silicone oil had a positive effect on atRA solubility and the longevity of release in vitro. The drug release period was independent of atRA starting concentration and dependent on the PDMS‐atRA concentration in the blend. A clinically relevant release period of atRA over 7 weeks from a silicone oil blend with PDMS‐atRA was observed. © 2018 The Authors. Journal of Polymer Science Part A: Polymer Chemistry Published by Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 938–946 John Wiley and Sons Inc. 2018-02-09 2018-04-15 /pmc/articles/PMC5873246/ /pubmed/29610546 http://dx.doi.org/10.1002/pola.28973 Text en © 2018 The Authors. Journal of Polymer Science Part A: Polymer Chemistry Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Cauldbeck, Helen Le Hellaye, Maude McDonald, Tom O. Long, Mark Williams, Rachel L. Rannard, Steve P. Kearns, Victoria R. Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title | Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title_full | Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title_fullStr | Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title_full_unstemmed | Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title_short | Modulated release from implantable ocular silicone oil tamponade drug reservoirs |
title_sort | modulated release from implantable ocular silicone oil tamponade drug reservoirs |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873246/ https://www.ncbi.nlm.nih.gov/pubmed/29610546 http://dx.doi.org/10.1002/pola.28973 |
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