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Novel Drug Carrier: 5-Fluorouracil Formulation in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof of Concept
[Image: see text] The ever-growing demand for novel, cheaper, and more effective drugs has put nanomedicine and targeted drug delivery to the forefront of scientific innovation. Owing to its porous three-dimensional (3D)-nanostructure and properties, the biogenic calcite from wasted blue crab shells...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552355/ https://www.ncbi.nlm.nih.gov/pubmed/34722978 http://dx.doi.org/10.1021/acsomega.1c03285 |
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author | Lazar, Geza Nekvapil, Fran Hirian, Razvan Glamuzina, Branko Tamas, Tudor Barbu-Tudoran, Lucian Pinzaru, Simona Cinta |
author_facet | Lazar, Geza Nekvapil, Fran Hirian, Razvan Glamuzina, Branko Tamas, Tudor Barbu-Tudoran, Lucian Pinzaru, Simona Cinta |
author_sort | Lazar, Geza |
collection | PubMed |
description | [Image: see text] The ever-growing demand for novel, cheaper, and more effective drugs has put nanomedicine and targeted drug delivery to the forefront of scientific innovation. Owing to its porous three-dimensional (3D)-nanostructure and properties, the biogenic calcite from wasted blue crab shells is employed in the present work as a new drug carrier for 5-fluorouracil (5-FU), a drug widely used in cancer therapy. The drug solution has been loaded in the porous nanoarchitecture of the powdered biogenic material and further pelleted in tablets with a 5-FU concentration of 1.748 mg/g. Their structural and morphological properties were characterized using Raman, X-ray diffraction, and scanning electron microscopy. Confocal micro-Raman spectra of tablet surface showed a typical signal of biogenic carbonate with preserved carotenoids and carotenoproteins found in the native waste shell, while the drug Raman signal was absent, indicating its adsorption in the intricate nanoporous biogenic carrier. The slow release of the drug from the newly formulated tablet was investigated by tracking the surface-enhanced Raman scattering (SERS) signal of the tablet solution in a series of time-dependent experiments. The SERS signal quantification is achieved using the well-known SERS spectral fingerprint of 5-fluorouracil aqueous solution adsorbed on Ag nanoparticles. The proof of concept is demonstrated by quantifying the slow release of the drug through the characteristic SERS band intensity of 5-FU in a time course of 26 h. This proof of concept boosted further investigations concerning the released drug identity in simulated solutions that mimic the pH of the upper- and lower gastrointestinal tract, as well as the multiple possibilities to control porosity and composition during powdering and treatment of biogenic material, to achieve the most convenient formulation for relevant biomedical drug delivery. Nonetheless, the present results showed great promise for innovative reusing waste biogenic 3D-nanomaterials of aquatic origin as advantageous drug carriers for slow release purposes, in line with the concept of blue bioeconomy. |
format | Online Article Text |
id | pubmed-8552355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85523552021-10-29 Novel Drug Carrier: 5-Fluorouracil Formulation in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof of Concept Lazar, Geza Nekvapil, Fran Hirian, Razvan Glamuzina, Branko Tamas, Tudor Barbu-Tudoran, Lucian Pinzaru, Simona Cinta ACS Omega [Image: see text] The ever-growing demand for novel, cheaper, and more effective drugs has put nanomedicine and targeted drug delivery to the forefront of scientific innovation. Owing to its porous three-dimensional (3D)-nanostructure and properties, the biogenic calcite from wasted blue crab shells is employed in the present work as a new drug carrier for 5-fluorouracil (5-FU), a drug widely used in cancer therapy. The drug solution has been loaded in the porous nanoarchitecture of the powdered biogenic material and further pelleted in tablets with a 5-FU concentration of 1.748 mg/g. Their structural and morphological properties were characterized using Raman, X-ray diffraction, and scanning electron microscopy. Confocal micro-Raman spectra of tablet surface showed a typical signal of biogenic carbonate with preserved carotenoids and carotenoproteins found in the native waste shell, while the drug Raman signal was absent, indicating its adsorption in the intricate nanoporous biogenic carrier. The slow release of the drug from the newly formulated tablet was investigated by tracking the surface-enhanced Raman scattering (SERS) signal of the tablet solution in a series of time-dependent experiments. The SERS signal quantification is achieved using the well-known SERS spectral fingerprint of 5-fluorouracil aqueous solution adsorbed on Ag nanoparticles. The proof of concept is demonstrated by quantifying the slow release of the drug through the characteristic SERS band intensity of 5-FU in a time course of 26 h. This proof of concept boosted further investigations concerning the released drug identity in simulated solutions that mimic the pH of the upper- and lower gastrointestinal tract, as well as the multiple possibilities to control porosity and composition during powdering and treatment of biogenic material, to achieve the most convenient formulation for relevant biomedical drug delivery. Nonetheless, the present results showed great promise for innovative reusing waste biogenic 3D-nanomaterials of aquatic origin as advantageous drug carriers for slow release purposes, in line with the concept of blue bioeconomy. American Chemical Society 2021-10-11 /pmc/articles/PMC8552355/ /pubmed/34722978 http://dx.doi.org/10.1021/acsomega.1c03285 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lazar, Geza Nekvapil, Fran Hirian, Razvan Glamuzina, Branko Tamas, Tudor Barbu-Tudoran, Lucian Pinzaru, Simona Cinta Novel Drug Carrier: 5-Fluorouracil Formulation in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof of Concept |
title | Novel Drug Carrier: 5-Fluorouracil Formulation
in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof
of Concept |
title_full | Novel Drug Carrier: 5-Fluorouracil Formulation
in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof
of Concept |
title_fullStr | Novel Drug Carrier: 5-Fluorouracil Formulation
in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof
of Concept |
title_full_unstemmed | Novel Drug Carrier: 5-Fluorouracil Formulation
in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof
of Concept |
title_short | Novel Drug Carrier: 5-Fluorouracil Formulation
in Nanoporous Biogenic Mg-calcite from Blue Crab Shells—Proof
of Concept |
title_sort | novel drug carrier: 5-fluorouracil formulation
in nanoporous biogenic mg-calcite from blue crab shells—proof
of concept |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552355/ https://www.ncbi.nlm.nih.gov/pubmed/34722978 http://dx.doi.org/10.1021/acsomega.1c03285 |
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