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Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method
OBJECTIVE(S): Folic acid is an essential vitamin, labile to hydrolysis in the acidic environment of the stomach with low water solubility and bioavailability. In order to solve these problems, enteric oral folic acid-loaded microfibers with a pH-sensitive polymer by electrospinning method were prepa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148407/ https://www.ncbi.nlm.nih.gov/pubmed/35656189 http://dx.doi.org/10.22038/IJBMS.2022.61563.13625 |
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author | Akhgari, Abbas Iraji, Pariya Rahiman, Niloufar Hasanzade Farouji, Akram Abbaspour, Mohammadreza |
author_facet | Akhgari, Abbas Iraji, Pariya Rahiman, Niloufar Hasanzade Farouji, Akram Abbaspour, Mohammadreza |
author_sort | Akhgari, Abbas |
collection | PubMed |
description | OBJECTIVE(S): Folic acid is an essential vitamin, labile to hydrolysis in the acidic environment of the stomach with low water solubility and bioavailability. In order to solve these problems, enteric oral folic acid-loaded microfibers with a pH-sensitive polymer by electrospinning method were prepared. MATERIALS AND METHODS: Electrospinning was performed at different folic acid ratios and voltages. Fibers were evaluated in terms of mechanical strength, acidic resistance, and drug release. Additionally, DSC (Differential Scanning Calorimetry), FTIR (Fourier-transform infrared spectroscopy), and XRD (X-ray diffraction) analyses were performed on the optimal formulation. RESULTS: Drug ratio and voltage had a considerable effect on fibers’ entrapment efficiency, acid resistance, and mechanical strength. Based on the obtained results, the optimum formulation containing 1.25% of the drug/polymer was prepared at 18 kV. The entrapment efficiency of the optimal sample was above 90% with an acid resistance of higher than 70%. The tensile test confirmed the high mechanical properties of the optimum microfiber. DSC and XRD tests indicated that folic acid was converted to an amorphous form in the fiber structure and the FTIR test confirmed the formation of a chemical bond between the drug and the polymer. The release of the drug from the optimal fiber was about 90% in 60 min. CONCLUSION: In conclusion, the optimal formulation of folic acid with proper mechanical properties can be used as a candidate dosage form for further bioavailability investigations. |
format | Online Article Text |
id | pubmed-9148407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-91484072022-06-01 Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method Akhgari, Abbas Iraji, Pariya Rahiman, Niloufar Hasanzade Farouji, Akram Abbaspour, Mohammadreza Iran J Basic Med Sci Original Article OBJECTIVE(S): Folic acid is an essential vitamin, labile to hydrolysis in the acidic environment of the stomach with low water solubility and bioavailability. In order to solve these problems, enteric oral folic acid-loaded microfibers with a pH-sensitive polymer by electrospinning method were prepared. MATERIALS AND METHODS: Electrospinning was performed at different folic acid ratios and voltages. Fibers were evaluated in terms of mechanical strength, acidic resistance, and drug release. Additionally, DSC (Differential Scanning Calorimetry), FTIR (Fourier-transform infrared spectroscopy), and XRD (X-ray diffraction) analyses were performed on the optimal formulation. RESULTS: Drug ratio and voltage had a considerable effect on fibers’ entrapment efficiency, acid resistance, and mechanical strength. Based on the obtained results, the optimum formulation containing 1.25% of the drug/polymer was prepared at 18 kV. The entrapment efficiency of the optimal sample was above 90% with an acid resistance of higher than 70%. The tensile test confirmed the high mechanical properties of the optimum microfiber. DSC and XRD tests indicated that folic acid was converted to an amorphous form in the fiber structure and the FTIR test confirmed the formation of a chemical bond between the drug and the polymer. The release of the drug from the optimal fiber was about 90% in 60 min. CONCLUSION: In conclusion, the optimal formulation of folic acid with proper mechanical properties can be used as a candidate dosage form for further bioavailability investigations. Mashhad University of Medical Sciences 2022-03 /pmc/articles/PMC9148407/ /pubmed/35656189 http://dx.doi.org/10.22038/IJBMS.2022.61563.13625 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Akhgari, Abbas Iraji, Pariya Rahiman, Niloufar Hasanzade Farouji, Akram Abbaspour, Mohammadreza Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title | Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title_full | Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title_fullStr | Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title_full_unstemmed | Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title_short | Preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
title_sort | preparation of stable enteric folic acid-loaded microfiber using the electrospinning method |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148407/ https://www.ncbi.nlm.nih.gov/pubmed/35656189 http://dx.doi.org/10.22038/IJBMS.2022.61563.13625 |
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