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Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination
The local administration of analgesic combinations by means of degradable polymeric drug delivery systems is an alternative for the management of postoperative pain. We formulated a Tramadol–Dexketoprofen combination (TDC) loaded in poly(vinyl alcohol) (PVA) film. Films were prepared by the solvent...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105240/ https://www.ncbi.nlm.nih.gov/pubmed/33961138 http://dx.doi.org/10.1007/s10856-021-06529-3 |
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author | Flores-Arriaga, Juan Carlos Chavarría-Bolaños, Daniel Pozos-Guillén, Amaury de Jesús Escobar-Barrios, Vladimir Alonso Cerda-Cristerna, Bernardino Isaac |
author_facet | Flores-Arriaga, Juan Carlos Chavarría-Bolaños, Daniel Pozos-Guillén, Amaury de Jesús Escobar-Barrios, Vladimir Alonso Cerda-Cristerna, Bernardino Isaac |
author_sort | Flores-Arriaga, Juan Carlos |
collection | PubMed |
description | The local administration of analgesic combinations by means of degradable polymeric drug delivery systems is an alternative for the management of postoperative pain. We formulated a Tramadol–Dexketoprofen combination (TDC) loaded in poly(vinyl alcohol) (PVA) film. Films were prepared by the solvent casting method using three different molecular weights of PVA and crosslinking those films with citric acid, with the objective of controlling the drug release rate, which was evaluated by UV–vis spectrometry. Non-crosslinked PVA films were also evaluated in the experiments. Differential scanning calorimetry (DSC) analysis of samples corroborated the crosslinking of PVA by the citric acid. Blank and loaded PVA films were tested in vitro for its impact on blood coagulation prothrombin time (PT) and partial thromboplastin time (PTT). The swelling capacity was also evaluated. Crosslinked PVA films of higher-molecular weight showed a prolonged release rate compared with that of the lower-molecular-weight films tested. Non-crosslinked PVA films released 11–14% of TDC. Crosslinked PVA films released 80% of the TDC loaded (p < 0.05). This suggests that crosslinking films can modify the drug release rate. The blank and loaded PVA films induced PT and PTT in the normal range. The results showed that the polymeric films evaluated here have the appropriate properties to allow films to be placed directly on surgical wounds and have the capacity for controlled drug release to promote local analgesia for the control of postoperative pain. [Image: see text] |
format | Online Article Text |
id | pubmed-8105240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-81052402021-06-03 Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination Flores-Arriaga, Juan Carlos Chavarría-Bolaños, Daniel Pozos-Guillén, Amaury de Jesús Escobar-Barrios, Vladimir Alonso Cerda-Cristerna, Bernardino Isaac J Mater Sci Mater Med Delivery Systems The local administration of analgesic combinations by means of degradable polymeric drug delivery systems is an alternative for the management of postoperative pain. We formulated a Tramadol–Dexketoprofen combination (TDC) loaded in poly(vinyl alcohol) (PVA) film. Films were prepared by the solvent casting method using three different molecular weights of PVA and crosslinking those films with citric acid, with the objective of controlling the drug release rate, which was evaluated by UV–vis spectrometry. Non-crosslinked PVA films were also evaluated in the experiments. Differential scanning calorimetry (DSC) analysis of samples corroborated the crosslinking of PVA by the citric acid. Blank and loaded PVA films were tested in vitro for its impact on blood coagulation prothrombin time (PT) and partial thromboplastin time (PTT). The swelling capacity was also evaluated. Crosslinked PVA films of higher-molecular weight showed a prolonged release rate compared with that of the lower-molecular-weight films tested. Non-crosslinked PVA films released 11–14% of TDC. Crosslinked PVA films released 80% of the TDC loaded (p < 0.05). This suggests that crosslinking films can modify the drug release rate. The blank and loaded PVA films induced PT and PTT in the normal range. The results showed that the polymeric films evaluated here have the appropriate properties to allow films to be placed directly on surgical wounds and have the capacity for controlled drug release to promote local analgesia for the control of postoperative pain. [Image: see text] Springer US 2021-05-07 2021 /pmc/articles/PMC8105240/ /pubmed/33961138 http://dx.doi.org/10.1007/s10856-021-06529-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Delivery Systems Flores-Arriaga, Juan Carlos Chavarría-Bolaños, Daniel Pozos-Guillén, Amaury de Jesús Escobar-Barrios, Vladimir Alonso Cerda-Cristerna, Bernardino Isaac Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title | Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title_full | Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title_fullStr | Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title_full_unstemmed | Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title_short | Synthesis of a PVA drug delivery system for controlled release of a Tramadol–Dexketoprofen combination |
title_sort | synthesis of a pva drug delivery system for controlled release of a tramadol–dexketoprofen combination |
topic | Delivery Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105240/ https://www.ncbi.nlm.nih.gov/pubmed/33961138 http://dx.doi.org/10.1007/s10856-021-06529-3 |
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