Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release
Herein, poly (<i>N</i>-(4-aminophenyl) methacrylamide))-carbon nano-onions (PAPMA-CNOs = f-CNOs) and anilinated-poly (ether ether ketone) (AN-PEEK) have synthesized, and AN-PEEK/f-CNOs composite thin films were primed via layer-by-layer (LbL) self-assembly for stimuli-responsive drug rel...
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doaj-08f862590aa04aa682ff3b37a4dd09df2020-12-14T00:00:32ZengMDPI AGPharmaceutics1999-49232020-12-01121208120810.3390/pharmaceutics12121208Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug ReleaseNarsimha Mamidi0Ramiro Manuel Velasco Delgadillo1Aldo Gonzáles Ortiz2Enrique V. Barrera3Department of Chemistry and Nanotechnology, School of Engineering and Sciences, Tecnologico de Monterrey, Ave. Eugenio Garza Sada 2501, Monterrey NL-64849, MexicoDepartment of Chemistry and Nanotechnology, School of Engineering and Sciences, Tecnologico de Monterrey, Ave. Eugenio Garza Sada 2501, Monterrey NL-64849, MexicoDepartment of Chemistry and Nanotechnology, School of Engineering and Sciences, Tecnologico de Monterrey, Ave. Eugenio Garza Sada 2501, Monterrey NL-64849, MexicoDepartment of Materials Science and Nanoengineering, Rice University, Houston, TX 77005, USAHerein, poly (<i>N</i>-(4-aminophenyl) methacrylamide))-carbon nano-onions (PAPMA-CNOs = f-CNOs) and anilinated-poly (ether ether ketone) (AN-PEEK) have synthesized, and AN-PEEK/f-CNOs composite thin films were primed via layer-by-layer (LbL) self-assembly for stimuli-responsive drug release. The obtained thin films exhibited pH-responsive drug release in a controlled manner; pH 4.5 = 99.2% and pH 6.5 = 59.3% of doxorubicin (DOX) release was observed over 15 days. Supramolecular π-π stacking interactions between f-CNOs and DOX played a critical role in controlling drug release from thin films. Cell viability was studied with human osteoblast cells and augmented viability was perceived. Moreover, the thin films presented 891.4 ± 8.2 MPa of the tensile strength (<inline-formula><math display="inline"><semantics><mrow><msub><mi>σ</mi><mrow><mi>u</mi><mi>l</mi><mi>t</mi></mrow></msub></mrow></semantics></math></inline-formula>), 43.2 ± 1.1 GPa of Young’s modulus (E), and 164.5 ± 1.7 Jg<sup>−1</sup> of toughness (K). Quantitative scrutiny revealed that the well-ordered aligned nanofibers provide critical interphase, and this could be responsible for augmented tensile properties. Nonetheless, a pH-responsive and mechanically robust biocompatible thin-film system may show potential applications in the biomedical field.https://www.mdpi.com/1999-4923/12/12/1208nanocomposite thin filmslayer-by-layer assemblystrengthYoung’s modulustoughnesspH-responsive drug release |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Narsimha Mamidi Ramiro Manuel Velasco Delgadillo Aldo Gonzáles Ortiz Enrique V. Barrera |
spellingShingle |
Narsimha Mamidi Ramiro Manuel Velasco Delgadillo Aldo Gonzáles Ortiz Enrique V. Barrera Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release Pharmaceutics nanocomposite thin films layer-by-layer assembly strength Young’s modulus toughness pH-responsive drug release |
author_facet |
Narsimha Mamidi Ramiro Manuel Velasco Delgadillo Aldo Gonzáles Ortiz Enrique V. Barrera |
author_sort |
Narsimha Mamidi |
title |
Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release |
title_short |
Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release |
title_full |
Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release |
title_fullStr |
Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release |
title_full_unstemmed |
Carbon Nano-Onions Reinforced Multilayered Thin Film System for Stimuli-Responsive Drug Release |
title_sort |
carbon nano-onions reinforced multilayered thin film system for stimuli-responsive drug release |
publisher |
MDPI AG |
series |
Pharmaceutics |
issn |
1999-4923 |
publishDate |
2020-12-01 |
description |
Herein, poly (<i>N</i>-(4-aminophenyl) methacrylamide))-carbon nano-onions (PAPMA-CNOs = f-CNOs) and anilinated-poly (ether ether ketone) (AN-PEEK) have synthesized, and AN-PEEK/f-CNOs composite thin films were primed via layer-by-layer (LbL) self-assembly for stimuli-responsive drug release. The obtained thin films exhibited pH-responsive drug release in a controlled manner; pH 4.5 = 99.2% and pH 6.5 = 59.3% of doxorubicin (DOX) release was observed over 15 days. Supramolecular π-π stacking interactions between f-CNOs and DOX played a critical role in controlling drug release from thin films. Cell viability was studied with human osteoblast cells and augmented viability was perceived. Moreover, the thin films presented 891.4 ± 8.2 MPa of the tensile strength (<inline-formula><math display="inline"><semantics><mrow><msub><mi>σ</mi><mrow><mi>u</mi><mi>l</mi><mi>t</mi></mrow></msub></mrow></semantics></math></inline-formula>), 43.2 ± 1.1 GPa of Young’s modulus (E), and 164.5 ± 1.7 Jg<sup>−1</sup> of toughness (K). Quantitative scrutiny revealed that the well-ordered aligned nanofibers provide critical interphase, and this could be responsible for augmented tensile properties. Nonetheless, a pH-responsive and mechanically robust biocompatible thin-film system may show potential applications in the biomedical field. |
topic |
nanocomposite thin films layer-by-layer assembly strength Young’s modulus toughness pH-responsive drug release |
url |
https://www.mdpi.com/1999-4923/12/12/1208 |
work_keys_str_mv |
AT narsimhamamidi carbonnanoonionsreinforcedmultilayeredthinfilmsystemforstimuliresponsivedrugrelease AT ramiromanuelvelascodelgadillo carbonnanoonionsreinforcedmultilayeredthinfilmsystemforstimuliresponsivedrugrelease AT aldogonzalesortiz carbonnanoonionsreinforcedmultilayeredthinfilmsystemforstimuliresponsivedrugrelease AT enriquevbarrera carbonnanoonionsreinforcedmultilayeredthinfilmsystemforstimuliresponsivedrugrelease |
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