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Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery
A multi-(amino acid) copolymer (MAC) based on ω-aminocaproic acid, γ-aminobutyric acid, L-alanine, L-lysine, L-glutamate, and hydroxyproline was synthetized, and MAC microspheres encapsulating bovine serum albumin (BSA) were prepared by a double-emulsion solvent extraction method. The experimental r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019614/ https://www.ncbi.nlm.nih.gov/pubmed/24855351 http://dx.doi.org/10.2147/IJN.S57048 |
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author | Chen, Xingtao Lv, Guoyu Zhang, Jue Tang, Songchao Yan, Yonggang Wu, Zhaoying Su, Jiacan Wei, Jie |
author_facet | Chen, Xingtao Lv, Guoyu Zhang, Jue Tang, Songchao Yan, Yonggang Wu, Zhaoying Su, Jiacan Wei, Jie |
author_sort | Chen, Xingtao |
collection | PubMed |
description | A multi-(amino acid) copolymer (MAC) based on ω-aminocaproic acid, γ-aminobutyric acid, L-alanine, L-lysine, L-glutamate, and hydroxyproline was synthetized, and MAC microspheres encapsulating bovine serum albumin (BSA) were prepared by a double-emulsion solvent extraction method. The experimental results show that various preparation parameters including surfactant ratio of Tween 80 to Span 80, surfactant concentration, benzyl alcohol in the external water phase, and polymer concentration had obvious effects on the particle size, morphology, and encapsulation efficiency of the BSA-loaded microspheres. The sizes of BSA-loaded microspheres ranged from 60.2 μm to 79.7 μm, showing different degrees of porous structure. The encapsulation efficiency of BSA-loaded microspheres also ranged from 38.8% to 50.8%. BSA release from microspheres showed the classic biphasic profile, which was governed by diffusion and polymer erosion. The initial burst release of BSA from microspheres at the first week followed by constant slow release for the next 7 weeks were observed. BSA-loaded microspheres could degrade gradually in phosphate buffered saline buffer with pH value maintained at around 7.1 during 8 weeks incubation, suggesting that microsphere degradation did not cause a dramatic pH drop in phosphate buffered saline buffer because no acidic degradation products were released from the microspheres. Therefore, the MAC microspheres might have great potential as carriers for protein delivery. |
format | Online Article Text |
id | pubmed-4019614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40196142014-05-22 Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery Chen, Xingtao Lv, Guoyu Zhang, Jue Tang, Songchao Yan, Yonggang Wu, Zhaoying Su, Jiacan Wei, Jie Int J Nanomedicine Original Research A multi-(amino acid) copolymer (MAC) based on ω-aminocaproic acid, γ-aminobutyric acid, L-alanine, L-lysine, L-glutamate, and hydroxyproline was synthetized, and MAC microspheres encapsulating bovine serum albumin (BSA) were prepared by a double-emulsion solvent extraction method. The experimental results show that various preparation parameters including surfactant ratio of Tween 80 to Span 80, surfactant concentration, benzyl alcohol in the external water phase, and polymer concentration had obvious effects on the particle size, morphology, and encapsulation efficiency of the BSA-loaded microspheres. The sizes of BSA-loaded microspheres ranged from 60.2 μm to 79.7 μm, showing different degrees of porous structure. The encapsulation efficiency of BSA-loaded microspheres also ranged from 38.8% to 50.8%. BSA release from microspheres showed the classic biphasic profile, which was governed by diffusion and polymer erosion. The initial burst release of BSA from microspheres at the first week followed by constant slow release for the next 7 weeks were observed. BSA-loaded microspheres could degrade gradually in phosphate buffered saline buffer with pH value maintained at around 7.1 during 8 weeks incubation, suggesting that microsphere degradation did not cause a dramatic pH drop in phosphate buffered saline buffer because no acidic degradation products were released from the microspheres. Therefore, the MAC microspheres might have great potential as carriers for protein delivery. Dove Medical Press 2014-05-07 /pmc/articles/PMC4019614/ /pubmed/24855351 http://dx.doi.org/10.2147/IJN.S57048 Text en © 2014 Chen et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Xingtao Lv, Guoyu Zhang, Jue Tang, Songchao Yan, Yonggang Wu, Zhaoying Su, Jiacan Wei, Jie Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title | Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title_full | Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title_fullStr | Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title_full_unstemmed | Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title_short | Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
title_sort | preparation and properties of bsa-loaded microspheres based on multi-(amino acid) copolymer for protein delivery |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019614/ https://www.ncbi.nlm.nih.gov/pubmed/24855351 http://dx.doi.org/10.2147/IJN.S57048 |
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