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3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons
BACKGROUND: The desktop vat polymerization process or stereolithography printing is an ideal approach to develop multifunctional nanocomposites wherein a conventional solid dosage form is used as a reservoir for compliant administration of drug-loaded nanocarriers. METHODS: In this study, a nanocomp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762875/ https://www.ncbi.nlm.nih.gov/pubmed/35038049 http://dx.doi.org/10.1186/s41205-022-00130-2 |
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author | Sharma, Peeyush Kumar Choudhury, Dinesh Yadav, Vivek Murty, U. S. N. Banerjee, Subham |
author_facet | Sharma, Peeyush Kumar Choudhury, Dinesh Yadav, Vivek Murty, U. S. N. Banerjee, Subham |
author_sort | Sharma, Peeyush Kumar |
collection | PubMed |
description | BACKGROUND: The desktop vat polymerization process or stereolithography printing is an ideal approach to develop multifunctional nanocomposites wherein a conventional solid dosage form is used as a reservoir for compliant administration of drug-loaded nanocarriers. METHODS: In this study, a nanocomposite drug delivery system, that is, hydrogel nanoparticles of an approved nutraceutical, berberine entrapped within vat photopolymerized monoliths, was developed for drug delivery applications. For the fabrication of the nanocomposite drug delivery systems/pills, a biocompatible vat photopolymerized resin was selected as an optimum matrix capable of efficiently delivering berberine from stereolithography mediated 3D printed nanocomposite pill. RESULTS: The obtained data reflected the efficient formation of berberine-loaded hydrogel nanoparticles with a mean particle diameter of 95.05 ± 4.50 nm but low loading. Stereolithography-assisted fabrication of monoliths was achieved with high fidelity (in agreement with computer-aided design), and photo-crosslinking was ascertained through Fourier-transform infrared spectroscopy. The hydrogel nanoparticles were entrapped within the pills during the stereolithography process, as evidenced by electron microscopy. The nanocomposite pills showed a higher swelling in an acidic environment and consequently faster berberine release of 50.39 ± 3.44% after 4 h. The overall results suggested maximal release within the gastrointestinal transit duration and excretion of the exhausted pills. CONCLUSIONS: We intended to demonstrate the feasibility of making 3D printed nanocomposite pills achieved through the desktop vat polymerization process for drug delivery applications. |
format | Online Article Text |
id | pubmed-8762875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-87628752022-01-18 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons Sharma, Peeyush Kumar Choudhury, Dinesh Yadav, Vivek Murty, U. S. N. Banerjee, Subham 3D Print Med Research BACKGROUND: The desktop vat polymerization process or stereolithography printing is an ideal approach to develop multifunctional nanocomposites wherein a conventional solid dosage form is used as a reservoir for compliant administration of drug-loaded nanocarriers. METHODS: In this study, a nanocomposite drug delivery system, that is, hydrogel nanoparticles of an approved nutraceutical, berberine entrapped within vat photopolymerized monoliths, was developed for drug delivery applications. For the fabrication of the nanocomposite drug delivery systems/pills, a biocompatible vat photopolymerized resin was selected as an optimum matrix capable of efficiently delivering berberine from stereolithography mediated 3D printed nanocomposite pill. RESULTS: The obtained data reflected the efficient formation of berberine-loaded hydrogel nanoparticles with a mean particle diameter of 95.05 ± 4.50 nm but low loading. Stereolithography-assisted fabrication of monoliths was achieved with high fidelity (in agreement with computer-aided design), and photo-crosslinking was ascertained through Fourier-transform infrared spectroscopy. The hydrogel nanoparticles were entrapped within the pills during the stereolithography process, as evidenced by electron microscopy. The nanocomposite pills showed a higher swelling in an acidic environment and consequently faster berberine release of 50.39 ± 3.44% after 4 h. The overall results suggested maximal release within the gastrointestinal transit duration and excretion of the exhausted pills. CONCLUSIONS: We intended to demonstrate the feasibility of making 3D printed nanocomposite pills achieved through the desktop vat polymerization process for drug delivery applications. Springer International Publishing 2022-01-17 /pmc/articles/PMC8762875/ /pubmed/35038049 http://dx.doi.org/10.1186/s41205-022-00130-2 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sharma, Peeyush Kumar Choudhury, Dinesh Yadav, Vivek Murty, U. S. N. Banerjee, Subham 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title | 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title_full | 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title_fullStr | 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title_full_unstemmed | 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title_short | 3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
title_sort | 3d printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762875/ https://www.ncbi.nlm.nih.gov/pubmed/35038049 http://dx.doi.org/10.1186/s41205-022-00130-2 |
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