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Aza-BODIPY based polymeric nanoparticles for cancer cell imaging

Near infrared (NIR) fluorescent dyes that are widely used for cancer imaging usually suffer from their hydrophobicity. To overcome this problem, a water-suspendable and biodegradable NIR-light-activating aza-BODIPY (AZB-NO(2)) encapsulated in polymeric nanoparticles was prepared as a new class of de...

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Autores principales: Chansaenpak, Kantapat, Tanjindaprateep, Similan, Chaicharoenaudomrung, Nipha, Weeranantanapan, Oratai, Noisa, Parinya, Kamkaew, Anyanee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090774/
https://www.ncbi.nlm.nih.gov/pubmed/35558043
http://dx.doi.org/10.1039/c8ra08145j
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author Chansaenpak, Kantapat
Tanjindaprateep, Similan
Chaicharoenaudomrung, Nipha
Weeranantanapan, Oratai
Noisa, Parinya
Kamkaew, Anyanee
author_facet Chansaenpak, Kantapat
Tanjindaprateep, Similan
Chaicharoenaudomrung, Nipha
Weeranantanapan, Oratai
Noisa, Parinya
Kamkaew, Anyanee
author_sort Chansaenpak, Kantapat
collection PubMed
description Near infrared (NIR) fluorescent dyes that are widely used for cancer imaging usually suffer from their hydrophobicity. To overcome this problem, a water-suspendable and biodegradable NIR-light-activating aza-BODIPY (AZB-NO(2)) encapsulated in polymeric nanoparticles was prepared as a new class of deep-tissue imaging agent. AZB-NO(2) possesses an intense, broad NIR absorption band (600–800 nm) with a remarkably high fluorescent quantum yield. After being encapsulated with a biodegradable polycaprolactone (PCL) and a Kolliphor P188 surfactant by emulsification-solvent evaporation method, the AZB-NO(2) formed a spherical shape as observed in scanning electron micrographs (SEM) with a hydrodynamic average size of 201 nm (average PDI = 0.185). The results from transmission electron micrographs (TEM) and energy dispersive X-ray spectroscopy (EDS) elemental mapping indicated that the AZB-NO(2) homogeneously distributed in the polymeric shell. UV-visible-NIR and fluorescence spectra of the obtained nanoparticles, AZB-NO(2)@PCL, revealed that the nanoparticles prepared by using 0.8 mg dye loading exhibited the highest fluorescence quantum yield. These nanoparticles were then applied for fluorescence imaging in human glioblastoma cell line (U-251). After the cells were exposed to AZB-NO(2)@PCL, the materials appeared to be localized inside U-251 cells within 3 h and the fluorescence signal enhanced along with the increased incubation times. Moreover, 3D cell culture was used in this study to mimic in vivo tumor environments. The AZB-NO(2)@PCL exhibited bright fluorescence from U-251 cells inside 3D Ca-alginate scaffolds after 24 h incubation. Our study successfully demonstrated that the encapsulation of hydrophobic aza-BODIPY dye could enhance the water-suspendability of the dye yielding biocompatible nanoparticles efficiently used in cancer cell imaging applications.
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spelling pubmed-90907742022-05-11 Aza-BODIPY based polymeric nanoparticles for cancer cell imaging Chansaenpak, Kantapat Tanjindaprateep, Similan Chaicharoenaudomrung, Nipha Weeranantanapan, Oratai Noisa, Parinya Kamkaew, Anyanee RSC Adv Chemistry Near infrared (NIR) fluorescent dyes that are widely used for cancer imaging usually suffer from their hydrophobicity. To overcome this problem, a water-suspendable and biodegradable NIR-light-activating aza-BODIPY (AZB-NO(2)) encapsulated in polymeric nanoparticles was prepared as a new class of deep-tissue imaging agent. AZB-NO(2) possesses an intense, broad NIR absorption band (600–800 nm) with a remarkably high fluorescent quantum yield. After being encapsulated with a biodegradable polycaprolactone (PCL) and a Kolliphor P188 surfactant by emulsification-solvent evaporation method, the AZB-NO(2) formed a spherical shape as observed in scanning electron micrographs (SEM) with a hydrodynamic average size of 201 nm (average PDI = 0.185). The results from transmission electron micrographs (TEM) and energy dispersive X-ray spectroscopy (EDS) elemental mapping indicated that the AZB-NO(2) homogeneously distributed in the polymeric shell. UV-visible-NIR and fluorescence spectra of the obtained nanoparticles, AZB-NO(2)@PCL, revealed that the nanoparticles prepared by using 0.8 mg dye loading exhibited the highest fluorescence quantum yield. These nanoparticles were then applied for fluorescence imaging in human glioblastoma cell line (U-251). After the cells were exposed to AZB-NO(2)@PCL, the materials appeared to be localized inside U-251 cells within 3 h and the fluorescence signal enhanced along with the increased incubation times. Moreover, 3D cell culture was used in this study to mimic in vivo tumor environments. The AZB-NO(2)@PCL exhibited bright fluorescence from U-251 cells inside 3D Ca-alginate scaffolds after 24 h incubation. Our study successfully demonstrated that the encapsulation of hydrophobic aza-BODIPY dye could enhance the water-suspendability of the dye yielding biocompatible nanoparticles efficiently used in cancer cell imaging applications. The Royal Society of Chemistry 2018-11-23 /pmc/articles/PMC9090774/ /pubmed/35558043 http://dx.doi.org/10.1039/c8ra08145j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Chansaenpak, Kantapat
Tanjindaprateep, Similan
Chaicharoenaudomrung, Nipha
Weeranantanapan, Oratai
Noisa, Parinya
Kamkaew, Anyanee
Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title_full Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title_fullStr Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title_full_unstemmed Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title_short Aza-BODIPY based polymeric nanoparticles for cancer cell imaging
title_sort aza-bodipy based polymeric nanoparticles for cancer cell imaging
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090774/
https://www.ncbi.nlm.nih.gov/pubmed/35558043
http://dx.doi.org/10.1039/c8ra08145j
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