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Ionic Liquid Green Assembly-Mediated Migration of Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug Delivery System
[Image: see text] Biocompatible surface-active ionic liquid (SAIL) was used first to study the deintercalation process of a well-known natural compound piperine (PIP) as an anticancer drug, obtained from PIP–calf thymus DNA (ctDNA) complex under controlled experimental conditions. In this study, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921251/ https://www.ncbi.nlm.nih.gov/pubmed/31867492 http://dx.doi.org/10.1021/acsomega.9b02246 |
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author | Maurya, Neha Parray, Zahoor Ahmad Maurya, Jitendra Kumar Islam, Asimul Patel, Rajan |
author_facet | Maurya, Neha Parray, Zahoor Ahmad Maurya, Jitendra Kumar Islam, Asimul Patel, Rajan |
author_sort | Maurya, Neha |
collection | PubMed |
description | [Image: see text] Biocompatible surface-active ionic liquid (SAIL) was used first to study the deintercalation process of a well-known natural compound piperine (PIP) as an anticancer drug, obtained from PIP–calf thymus DNA (ctDNA) complex under controlled experimental conditions. In this study, we have been exploring the interaction of PIP in SAIL (1-butyl-3-methylimidazolium octyl sulfate ionic liquid ([C(4)mim][C(8)OSO(3)])), ctDNA, and deintercalation of PIP from the PIP–ctDNA complex through SAIL micelle using various spectroscopic techniques. Absorption, emission, and lifetime decay measurements provide strong evidence of the relocation of PIP molecules from ctDNA to SAIL micelle. Fluorescence quenching and steady-state fluorescence anisotropy were employed to examine the exact location of PIP in different media. Moreover, the surface tension technique was also employed to confirm the release of PIP molecules from the PIP–ctDNA complex in the presence of SAIL. Circular dichroism analysis suggested that SAIL micelle does not perturb the ctDNA structure, which supported the fact that SAIL micelle can be used as a safe vehicle for PIP. Overall, the study highlighted a novel strategy for deintercalation of drug using SAIL because the release of the drug can be controlled over a period by varying the concentration and composition of the SAIL. |
format | Online Article Text |
id | pubmed-6921251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69212512019-12-20 Ionic Liquid Green Assembly-Mediated Migration of Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug Delivery System Maurya, Neha Parray, Zahoor Ahmad Maurya, Jitendra Kumar Islam, Asimul Patel, Rajan ACS Omega [Image: see text] Biocompatible surface-active ionic liquid (SAIL) was used first to study the deintercalation process of a well-known natural compound piperine (PIP) as an anticancer drug, obtained from PIP–calf thymus DNA (ctDNA) complex under controlled experimental conditions. In this study, we have been exploring the interaction of PIP in SAIL (1-butyl-3-methylimidazolium octyl sulfate ionic liquid ([C(4)mim][C(8)OSO(3)])), ctDNA, and deintercalation of PIP from the PIP–ctDNA complex through SAIL micelle using various spectroscopic techniques. Absorption, emission, and lifetime decay measurements provide strong evidence of the relocation of PIP molecules from ctDNA to SAIL micelle. Fluorescence quenching and steady-state fluorescence anisotropy were employed to examine the exact location of PIP in different media. Moreover, the surface tension technique was also employed to confirm the release of PIP molecules from the PIP–ctDNA complex in the presence of SAIL. Circular dichroism analysis suggested that SAIL micelle does not perturb the ctDNA structure, which supported the fact that SAIL micelle can be used as a safe vehicle for PIP. Overall, the study highlighted a novel strategy for deintercalation of drug using SAIL because the release of the drug can be controlled over a period by varying the concentration and composition of the SAIL. American Chemical Society 2019-12-05 /pmc/articles/PMC6921251/ /pubmed/31867492 http://dx.doi.org/10.1021/acsomega.9b02246 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Maurya, Neha Parray, Zahoor Ahmad Maurya, Jitendra Kumar Islam, Asimul Patel, Rajan Ionic Liquid Green Assembly-Mediated Migration of Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug Delivery System |
title | Ionic Liquid Green Assembly-Mediated Migration of
Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug
Delivery System |
title_full | Ionic Liquid Green Assembly-Mediated Migration of
Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug
Delivery System |
title_fullStr | Ionic Liquid Green Assembly-Mediated Migration of
Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug
Delivery System |
title_full_unstemmed | Ionic Liquid Green Assembly-Mediated Migration of
Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug
Delivery System |
title_short | Ionic Liquid Green Assembly-Mediated Migration of
Piperine from Calf-Thymus DNA: A New Possibility of the Tunable Drug
Delivery System |
title_sort | ionic liquid green assembly-mediated migration of
piperine from calf-thymus dna: a new possibility of the tunable drug
delivery system |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921251/ https://www.ncbi.nlm.nih.gov/pubmed/31867492 http://dx.doi.org/10.1021/acsomega.9b02246 |
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