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Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes
BACKGROUND: Particle-based drug delivery systems (DDSs) have a demonstrated value for drug discovery and development. However, some problems remain to be solved, such as limited stimuli, visual-monitoring. AIM: To develop an intelligent multicolor DDSs with both near-infrared (NIR) controlled releas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367737/ https://www.ncbi.nlm.nih.gov/pubmed/32764929 http://dx.doi.org/10.2147/IJN.S249009 |
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author | Sun, Xiaoyan Liu, Lingzi Zou, Hui Yao, Caixia Yan, Zhengyu Ye, Baofen |
author_facet | Sun, Xiaoyan Liu, Lingzi Zou, Hui Yao, Caixia Yan, Zhengyu Ye, Baofen |
author_sort | Sun, Xiaoyan |
collection | PubMed |
description | BACKGROUND: Particle-based drug delivery systems (DDSs) have a demonstrated value for drug discovery and development. However, some problems remain to be solved, such as limited stimuli, visual-monitoring. AIM: To develop an intelligent multicolor DDSs with both near-infrared (NIR) controlled release and macroscopic color changes. MATERIALS AND METHODS: Microparticles comprising GO/pNIPAM/PEGDA composite hydrogel inverse opal scaffolds, with dextran and calcium alginate hydrogel were synthesized using SCCBs as the template. The morphology of microparticle was observed under scanning electron microscopy, and FITC-dextran-derived green fluorescence images were determined using a confocal laser scanning microscope. During the drug release, FITC-dextran-derived green fluorescence images were captured using fluorescent inverted microscope. The relationship between the power of NIR and the drug release rate was obtained using the change in optical density (OD) values. Finally, the amount of drug released could be estimated quantitatively used the structural color or the reflection peak position. RESULTS: A fixed concentration 8% (v/v) of PEGDA and 4mg/mL of GO was chosen as the optimal concentration based on the balance between appropriate volume shrinkage and structure color. The FITC-dextran was uniformly encapsulated in the particles by using 0.2 wt% sodium alginate. The microcarriers shrank because of the photothermal response and the intrinsic fluorescence intensity of FITC-dextran in the microparticles gradually decreased at the same time, indicating drug release. With an increasing duration of NIR irradiation, the microparticles gradually shrank, the reflection peak shifted toward blue and the structural color changed from red to orange, yellow, green, cyan, and blue successively. The drug release quantity can be predicted by the structural color of microparticles. CONCLUSION: The multicolor microparticles have great potential in drug delivery systems because of its vivid reporting color, excellent photothermal effect, and the good stimuli responsivity. |
format | Online Article Text |
id | pubmed-7367737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-73677372020-08-05 Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes Sun, Xiaoyan Liu, Lingzi Zou, Hui Yao, Caixia Yan, Zhengyu Ye, Baofen Int J Nanomedicine Original Research BACKGROUND: Particle-based drug delivery systems (DDSs) have a demonstrated value for drug discovery and development. However, some problems remain to be solved, such as limited stimuli, visual-monitoring. AIM: To develop an intelligent multicolor DDSs with both near-infrared (NIR) controlled release and macroscopic color changes. MATERIALS AND METHODS: Microparticles comprising GO/pNIPAM/PEGDA composite hydrogel inverse opal scaffolds, with dextran and calcium alginate hydrogel were synthesized using SCCBs as the template. The morphology of microparticle was observed under scanning electron microscopy, and FITC-dextran-derived green fluorescence images were determined using a confocal laser scanning microscope. During the drug release, FITC-dextran-derived green fluorescence images were captured using fluorescent inverted microscope. The relationship between the power of NIR and the drug release rate was obtained using the change in optical density (OD) values. Finally, the amount of drug released could be estimated quantitatively used the structural color or the reflection peak position. RESULTS: A fixed concentration 8% (v/v) of PEGDA and 4mg/mL of GO was chosen as the optimal concentration based on the balance between appropriate volume shrinkage and structure color. The FITC-dextran was uniformly encapsulated in the particles by using 0.2 wt% sodium alginate. The microcarriers shrank because of the photothermal response and the intrinsic fluorescence intensity of FITC-dextran in the microparticles gradually decreased at the same time, indicating drug release. With an increasing duration of NIR irradiation, the microparticles gradually shrank, the reflection peak shifted toward blue and the structural color changed from red to orange, yellow, green, cyan, and blue successively. The drug release quantity can be predicted by the structural color of microparticles. CONCLUSION: The multicolor microparticles have great potential in drug delivery systems because of its vivid reporting color, excellent photothermal effect, and the good stimuli responsivity. Dove 2020-07-12 /pmc/articles/PMC7367737/ /pubmed/32764929 http://dx.doi.org/10.2147/IJN.S249009 Text en © 2020 Sun et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Sun, Xiaoyan Liu, Lingzi Zou, Hui Yao, Caixia Yan, Zhengyu Ye, Baofen Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title | Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title_full | Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title_fullStr | Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title_full_unstemmed | Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title_short | Intelligent Drug Delivery Microparticles with Visual Stimuli-Responsive Structural Color Changes |
title_sort | intelligent drug delivery microparticles with visual stimuli-responsive structural color changes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367737/ https://www.ncbi.nlm.nih.gov/pubmed/32764929 http://dx.doi.org/10.2147/IJN.S249009 |
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