Cargando…
Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol
The development of oral dissolving film (ODF) of atenolol is an attempt to enhance convenience and compliance for geriatric patients suffering from hypertension. Film former is the most essential component in ODF that determines the physical characteristic and drug release. In this study, three diff...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537485/ https://www.ncbi.nlm.nih.gov/pubmed/34684021 http://dx.doi.org/10.3390/pharmaceutics13101727 |
_version_ | 1784588262716735488 |
---|---|
author | Rani, Karina Citra Parfati, Nani Aryani, Ni Luh Dewi Winantari, Agnes Nuniek Fitriani, Endang Wahyu Pradana, Aditya Trias Nawatila, Roisah Putranti, Astridani Rizky Irine, Florencia Angelica, Florentia Yohanes, Cintya Avanti, Christina |
author_facet | Rani, Karina Citra Parfati, Nani Aryani, Ni Luh Dewi Winantari, Agnes Nuniek Fitriani, Endang Wahyu Pradana, Aditya Trias Nawatila, Roisah Putranti, Astridani Rizky Irine, Florencia Angelica, Florentia Yohanes, Cintya Avanti, Christina |
author_sort | Rani, Karina Citra |
collection | PubMed |
description | The development of oral dissolving film (ODF) of atenolol is an attempt to enhance convenience and compliance for geriatric patients suffering from hypertension. Film former is the most essential component in ODF that determines the physical characteristic and drug release. In this study, three different types of film former including HPMC E5 4% (w/v), 5% (w/v), CMC-Na 3% (w/v), 4% (w/v), and Na-alginate 2.5% (w/v), 3% (w/v) were optimized in Formula 1 (F1) to Formula 6 (F6), respectively. A solvent casting method was employed to develop ODF of atenolol. The films formed by HPMC E5 produced a smooth and flexible surface, whereas CMC-Na and Na-alginate produced gritty textured films. Satisfactory results were obtained from several physical parameters such as film thickness, folding endurance, swelling index, and disintegration time. The homogeneity, drug content, and dissolution properties of ODF with HPMC exhibited better characteristics than the other formulas. Formula 1 exhibited the highest drug release compared to the other ODFs. The molecular docking results showed that there was a hydrogen bonding between atenolol and film formers which was also supported by the FTIR spectrum. The findings of this study suggest that HPMC E5 is the most favorable film former for ODF of atenolol. |
format | Online Article Text |
id | pubmed-8537485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85374852021-10-24 Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol Rani, Karina Citra Parfati, Nani Aryani, Ni Luh Dewi Winantari, Agnes Nuniek Fitriani, Endang Wahyu Pradana, Aditya Trias Nawatila, Roisah Putranti, Astridani Rizky Irine, Florencia Angelica, Florentia Yohanes, Cintya Avanti, Christina Pharmaceutics Article The development of oral dissolving film (ODF) of atenolol is an attempt to enhance convenience and compliance for geriatric patients suffering from hypertension. Film former is the most essential component in ODF that determines the physical characteristic and drug release. In this study, three different types of film former including HPMC E5 4% (w/v), 5% (w/v), CMC-Na 3% (w/v), 4% (w/v), and Na-alginate 2.5% (w/v), 3% (w/v) were optimized in Formula 1 (F1) to Formula 6 (F6), respectively. A solvent casting method was employed to develop ODF of atenolol. The films formed by HPMC E5 produced a smooth and flexible surface, whereas CMC-Na and Na-alginate produced gritty textured films. Satisfactory results were obtained from several physical parameters such as film thickness, folding endurance, swelling index, and disintegration time. The homogeneity, drug content, and dissolution properties of ODF with HPMC exhibited better characteristics than the other formulas. Formula 1 exhibited the highest drug release compared to the other ODFs. The molecular docking results showed that there was a hydrogen bonding between atenolol and film formers which was also supported by the FTIR spectrum. The findings of this study suggest that HPMC E5 is the most favorable film former for ODF of atenolol. MDPI 2021-10-19 /pmc/articles/PMC8537485/ /pubmed/34684021 http://dx.doi.org/10.3390/pharmaceutics13101727 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rani, Karina Citra Parfati, Nani Aryani, Ni Luh Dewi Winantari, Agnes Nuniek Fitriani, Endang Wahyu Pradana, Aditya Trias Nawatila, Roisah Putranti, Astridani Rizky Irine, Florencia Angelica, Florentia Yohanes, Cintya Avanti, Christina Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title | Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title_full | Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title_fullStr | Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title_full_unstemmed | Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title_short | Development, Evaluation, and Molecular Docking of Oral Dissolving Film of Atenolol |
title_sort | development, evaluation, and molecular docking of oral dissolving film of atenolol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537485/ https://www.ncbi.nlm.nih.gov/pubmed/34684021 http://dx.doi.org/10.3390/pharmaceutics13101727 |
work_keys_str_mv | AT ranikarinacitra developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT parfatinani developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT aryaniniluhdewi developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT winantariagnesnuniek developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT fitrianiendangwahyu developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT pradanaadityatrias developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT nawatilaroisah developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT putrantiastridanirizky developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT irineflorencia developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT angelicaflorentia developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT yohanescintya developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol AT avantichristina developmentevaluationandmoleculardockingoforaldissolvingfilmofatenolol |