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Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study

Lithium carbonate is considered an effective drug against mania and acts as a mood stabilizer. It is found that it enhances antidepressants targeting depression, consequently it is prone to have risk factors that leads to adverse effects. The study is devised in confronting depression under nanoscal...

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Autores principales: Margret, A. Anita, Dhayabaran, V. Violet, Kumar, A. Ganesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700908/
https://www.ncbi.nlm.nih.gov/pubmed/29116617
http://dx.doi.org/10.1007/s40204-017-0076-8
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author Margret, A. Anita
Dhayabaran, V. Violet
Kumar, A. Ganesh
author_facet Margret, A. Anita
Dhayabaran, V. Violet
Kumar, A. Ganesh
author_sort Margret, A. Anita
collection PubMed
description Lithium carbonate is considered an effective drug against mania and acts as a mood stabilizer. It is found that it enhances antidepressants targeting depression, consequently it is prone to have risk factors that leads to adverse effects. The study is devised in confronting depression under nanoscale by preparing nanocomposites which is a matrix of biopolymer chitosan that encapsulates lithium carbonate by ionic gelation method. This facilitates the drug delivery in a regulated manner targeting the therapeutic action with a limited dosage that lessens the side effects in the course of treatment. The drug polymer interaction was validated by XRD studies, whereas the morphology and size characterization by SEM and zetasizer. The average particle size was determined as 193 ± 0.18 nm with a positive zeta potential of 37.9 mV. The in vitro drug release patterns of nanocomposites were comparatively assayed with the standard lithium carbonate which rendered a controlled release in its profile. The in vivo investigation by animal despair studies bestowed a significant difference in the duration of immobility during force swimming and tail suspension tests. These results were substantiated with histopathological examinations of cerebral cortex region which showed mild cellular edema, degenerative changes and lymphocytic infiltration when compared with the control groups. Consequently, the efficacy of nanocomposites encased with lithium carbonate fortifies targeted drug delivery and restrains adverse effects by endorsing it as a lead compound in brain drug developmental research.
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spelling pubmed-57009082017-12-04 Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study Margret, A. Anita Dhayabaran, V. Violet Kumar, A. Ganesh Prog Biomater Original Research Lithium carbonate is considered an effective drug against mania and acts as a mood stabilizer. It is found that it enhances antidepressants targeting depression, consequently it is prone to have risk factors that leads to adverse effects. The study is devised in confronting depression under nanoscale by preparing nanocomposites which is a matrix of biopolymer chitosan that encapsulates lithium carbonate by ionic gelation method. This facilitates the drug delivery in a regulated manner targeting the therapeutic action with a limited dosage that lessens the side effects in the course of treatment. The drug polymer interaction was validated by XRD studies, whereas the morphology and size characterization by SEM and zetasizer. The average particle size was determined as 193 ± 0.18 nm with a positive zeta potential of 37.9 mV. The in vitro drug release patterns of nanocomposites were comparatively assayed with the standard lithium carbonate which rendered a controlled release in its profile. The in vivo investigation by animal despair studies bestowed a significant difference in the duration of immobility during force swimming and tail suspension tests. These results were substantiated with histopathological examinations of cerebral cortex region which showed mild cellular edema, degenerative changes and lymphocytic infiltration when compared with the control groups. Consequently, the efficacy of nanocomposites encased with lithium carbonate fortifies targeted drug delivery and restrains adverse effects by endorsing it as a lead compound in brain drug developmental research. Springer Berlin Heidelberg 2017-11-07 /pmc/articles/PMC5700908/ /pubmed/29116617 http://dx.doi.org/10.1007/s40204-017-0076-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Margret, A. Anita
Dhayabaran, V. Violet
Kumar, A. Ganesh
Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title_full Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title_fullStr Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title_full_unstemmed Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title_short Nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
title_sort nanoparticulated polymeric composites enfolding lithium carbonate as brain drug in persuading depression: an in vivo study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700908/
https://www.ncbi.nlm.nih.gov/pubmed/29116617
http://dx.doi.org/10.1007/s40204-017-0076-8
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