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Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads

We present a single-step, room-temperature synthesis of fluorescent organosilica nanobeads (FOS NBs). The FOS NBs were synthesized under aqueous conditions using (3-aminopropyl)triethoxysilane (APTES) as the silicon source in the presence of l-ascorbic acid (L-AA). In the APTES/L-AA/water ternary ph...

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Autores principales: Baipaywad, Phornsawat, Hong, Seong Vin, Kim, Jong Bae, Hwang, Jangsun, Choi, Jonghoon, Park, Hansoo, Paik, Taejong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901841/
https://www.ncbi.nlm.nih.gov/pubmed/35254532
http://dx.doi.org/10.1186/s40580-022-00303-z
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author Baipaywad, Phornsawat
Hong, Seong Vin
Kim, Jong Bae
Hwang, Jangsun
Choi, Jonghoon
Park, Hansoo
Paik, Taejong
author_facet Baipaywad, Phornsawat
Hong, Seong Vin
Kim, Jong Bae
Hwang, Jangsun
Choi, Jonghoon
Park, Hansoo
Paik, Taejong
author_sort Baipaywad, Phornsawat
collection PubMed
description We present a single-step, room-temperature synthesis of fluorescent organosilica nanobeads (FOS NBs). The FOS NBs were synthesized under aqueous conditions using (3-aminopropyl)triethoxysilane (APTES) as the silicon source in the presence of l-ascorbic acid (L-AA). In the APTES/L-AA/water ternary phase, the hydrolysis and condensation reaction of APTES occurred under acidic conditions to form spherical FOS NBs with an average diameter of 426.8 nm. FOS NBs exhibit excellent colloidal stability in aqueous media. The formation of FOS NBs was complete within a 10 min reaction time, which indicates potential for large-scale mass-production synthesis of luminescent colloidal NBs. The FOS NBs exhibited blue photoluminescence (PL) under UV excitation in the absence of an additional high temperature calcination process or with the incorporation of any fluorophores. This phenomenon is attributed to the presence of carbon-containing defects, which act as luminescent centers formed by the reaction between amino groups in the APTES and l-ascorbic acid reductant. Finally, the results of a cytotoxicity test and cellular uptake experiments revealed that the FOS NBs showed potential as optical contrast agents for bioimaging. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40580-022-00303-z.
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spelling pubmed-89018412022-03-15 Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads Baipaywad, Phornsawat Hong, Seong Vin Kim, Jong Bae Hwang, Jangsun Choi, Jonghoon Park, Hansoo Paik, Taejong Nano Converg Full Paper We present a single-step, room-temperature synthesis of fluorescent organosilica nanobeads (FOS NBs). The FOS NBs were synthesized under aqueous conditions using (3-aminopropyl)triethoxysilane (APTES) as the silicon source in the presence of l-ascorbic acid (L-AA). In the APTES/L-AA/water ternary phase, the hydrolysis and condensation reaction of APTES occurred under acidic conditions to form spherical FOS NBs with an average diameter of 426.8 nm. FOS NBs exhibit excellent colloidal stability in aqueous media. The formation of FOS NBs was complete within a 10 min reaction time, which indicates potential for large-scale mass-production synthesis of luminescent colloidal NBs. The FOS NBs exhibited blue photoluminescence (PL) under UV excitation in the absence of an additional high temperature calcination process or with the incorporation of any fluorophores. This phenomenon is attributed to the presence of carbon-containing defects, which act as luminescent centers formed by the reaction between amino groups in the APTES and l-ascorbic acid reductant. Finally, the results of a cytotoxicity test and cellular uptake experiments revealed that the FOS NBs showed potential as optical contrast agents for bioimaging. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40580-022-00303-z. Springer Nature Singapore 2022-03-07 /pmc/articles/PMC8901841/ /pubmed/35254532 http://dx.doi.org/10.1186/s40580-022-00303-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Full Paper
Baipaywad, Phornsawat
Hong, Seong Vin
Kim, Jong Bae
Hwang, Jangsun
Choi, Jonghoon
Park, Hansoo
Paik, Taejong
Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title_full Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title_fullStr Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title_full_unstemmed Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title_short Single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
title_sort single-step acid-catalyzed synthesis of luminescent colloidal organosilica nanobeads
topic Full Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901841/
https://www.ncbi.nlm.nih.gov/pubmed/35254532
http://dx.doi.org/10.1186/s40580-022-00303-z
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