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Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid
In this study, tranexamic acid (TA) was used as a model compound to study the charge effect on the physicochemical properties of poly(lactic-co-glycolic acid) (PLGA) microparticles (MPs). Charged PLGA MPs were elaborated by the incorporation of a quaternary ammonium, cetyltrimethylammonium bromide (...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240418/ https://www.ncbi.nlm.nih.gov/pubmed/32260323 http://dx.doi.org/10.3390/polym12040808 |
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author | Huang, Ming-Hsi Huang, Shun-Ying Chen, Yi-Xuan Chen, Cheng-You Lin, Yung-Sheng |
author_facet | Huang, Ming-Hsi Huang, Shun-Ying Chen, Yi-Xuan Chen, Cheng-You Lin, Yung-Sheng |
author_sort | Huang, Ming-Hsi |
collection | PubMed |
description | In this study, tranexamic acid (TA) was used as a model compound to study the charge effect on the physicochemical properties of poly(lactic-co-glycolic acid) (PLGA) microparticles (MPs). Charged PLGA MPs were elaborated by the incorporation of a quaternary ammonium, cetyltrimethylammonium bromide (CTAB), during the double emulsion solvent evaporation process. Three TA-CTAB-carrying modes of PLGA MPs were designed in the CTAB-free (TA-MP), adsorption (TA-CTAB(AD)), or encapsulation (TA-CTAB(EN)) form. The obtained MPs were characterized by morphology and TA-MP affinity. The experiment revealed that the three prepared MPs were spherical and smooth, with pores on their surfaces. TA-CTAB(AD) had a relatively narrow size distribution, compared with that of TA-MP and TA-CTAB(EN). The particle sizes of TA-MP, TA-CTAB(EN), TA-CTAB(AD) were measured as 59 ± 17, 54 ± 20, and 19 ± 8 μm, respectively. The zeta potential of the three MPs was found to be in the order: TA-CTAB(AD) > TA-CTAB(EN) > TA-MP. Differential scanning calorimetry (DSC) indicated that the manufacturing process had no influence on the glass transition temperature of the MPs, which was close to 48 °C. Thermogravimetric analysis illustrated that the presence of CTAB slightly changed the thermal stability of PLGA MPs. In vitro release showed that TA-CTAB(AD) exhibited faster TA release than TA-MP and TA-CTAB(EN) in a basic environment (pH of 13), probably because of electrostatic attraction. At pH = 1, the release of TA from TA-CTAB(EN) was faster than those from TA-MP and TA-CTAB(AD), probably because of electrostatic repulsion. However, the effect of electrostatic interaction was not significant at pH = 7.4. |
format | Online Article Text |
id | pubmed-7240418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72404182020-06-02 Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid Huang, Ming-Hsi Huang, Shun-Ying Chen, Yi-Xuan Chen, Cheng-You Lin, Yung-Sheng Polymers (Basel) Article In this study, tranexamic acid (TA) was used as a model compound to study the charge effect on the physicochemical properties of poly(lactic-co-glycolic acid) (PLGA) microparticles (MPs). Charged PLGA MPs were elaborated by the incorporation of a quaternary ammonium, cetyltrimethylammonium bromide (CTAB), during the double emulsion solvent evaporation process. Three TA-CTAB-carrying modes of PLGA MPs were designed in the CTAB-free (TA-MP), adsorption (TA-CTAB(AD)), or encapsulation (TA-CTAB(EN)) form. The obtained MPs were characterized by morphology and TA-MP affinity. The experiment revealed that the three prepared MPs were spherical and smooth, with pores on their surfaces. TA-CTAB(AD) had a relatively narrow size distribution, compared with that of TA-MP and TA-CTAB(EN). The particle sizes of TA-MP, TA-CTAB(EN), TA-CTAB(AD) were measured as 59 ± 17, 54 ± 20, and 19 ± 8 μm, respectively. The zeta potential of the three MPs was found to be in the order: TA-CTAB(AD) > TA-CTAB(EN) > TA-MP. Differential scanning calorimetry (DSC) indicated that the manufacturing process had no influence on the glass transition temperature of the MPs, which was close to 48 °C. Thermogravimetric analysis illustrated that the presence of CTAB slightly changed the thermal stability of PLGA MPs. In vitro release showed that TA-CTAB(AD) exhibited faster TA release than TA-MP and TA-CTAB(EN) in a basic environment (pH of 13), probably because of electrostatic attraction. At pH = 1, the release of TA from TA-CTAB(EN) was faster than those from TA-MP and TA-CTAB(AD), probably because of electrostatic repulsion. However, the effect of electrostatic interaction was not significant at pH = 7.4. MDPI 2020-04-04 /pmc/articles/PMC7240418/ /pubmed/32260323 http://dx.doi.org/10.3390/polym12040808 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huang, Ming-Hsi Huang, Shun-Ying Chen, Yi-Xuan Chen, Cheng-You Lin, Yung-Sheng Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title | Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title_full | Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title_fullStr | Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title_full_unstemmed | Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title_short | Elaboration of Charged Poly(Lactic-co-Glycolic Acid) Microparticles for Effective Release of Tranexamic Acid |
title_sort | elaboration of charged poly(lactic-co-glycolic acid) microparticles for effective release of tranexamic acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240418/ https://www.ncbi.nlm.nih.gov/pubmed/32260323 http://dx.doi.org/10.3390/polym12040808 |
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