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Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement
The production of layered double hydroxide(LDH) nanocomposite as an alternative drug delivery system against various ailments is on the increase. Their toxicity potential is usually dose and time dependent with particle sizes, shapes and surface charge playing some role both in the in vitro and in v...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149231/ https://www.ncbi.nlm.nih.gov/pubmed/25177361 http://dx.doi.org/10.1186/s13065-014-0047-2 |
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author | Kura, Aminu Umar Hussein, Mohd Zobir Fakurazi, Sharida Arulselvan, Palanisamy |
author_facet | Kura, Aminu Umar Hussein, Mohd Zobir Fakurazi, Sharida Arulselvan, Palanisamy |
author_sort | Kura, Aminu Umar |
collection | PubMed |
description | The production of layered double hydroxide(LDH) nanocomposite as an alternative drug delivery system against various ailments is on the increase. Their toxicity potential is usually dose and time dependent with particle sizes, shapes and surface charge playing some role both in the in vitro and in vivo studies. The reticular endothelial system of especially the liver and spleen were shown to sequestrate most of these nanocomposite, especially those with sizes greater than 50 nm. The intracellular drug delivery by these particles is mainly via endocytotic pathways aided by the surface charges in most cases. However, structural modification of these nanocomposite via coating using different types of material may lower the toxicity where present. More importantly, the coating may serve as targeting ligand hence, directing drug distribution and leading to proper drug delivery to specific area of need; it equally decreases the unwanted nanocomposite accumulation in especially the liver and spleen. These nanocomposite have the advantage of wider bio-distribution irrespective of route of administration, excellent targeted delivery potential with ease of synthetic modification including coating. |
format | Online Article Text |
id | pubmed-4149231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-41492312014-08-30 Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement Kura, Aminu Umar Hussein, Mohd Zobir Fakurazi, Sharida Arulselvan, Palanisamy Chem Cent J Review The production of layered double hydroxide(LDH) nanocomposite as an alternative drug delivery system against various ailments is on the increase. Their toxicity potential is usually dose and time dependent with particle sizes, shapes and surface charge playing some role both in the in vitro and in vivo studies. The reticular endothelial system of especially the liver and spleen were shown to sequestrate most of these nanocomposite, especially those with sizes greater than 50 nm. The intracellular drug delivery by these particles is mainly via endocytotic pathways aided by the surface charges in most cases. However, structural modification of these nanocomposite via coating using different types of material may lower the toxicity where present. More importantly, the coating may serve as targeting ligand hence, directing drug distribution and leading to proper drug delivery to specific area of need; it equally decreases the unwanted nanocomposite accumulation in especially the liver and spleen. These nanocomposite have the advantage of wider bio-distribution irrespective of route of administration, excellent targeted delivery potential with ease of synthetic modification including coating. Springer International Publishing 2014-08-10 /pmc/articles/PMC4149231/ /pubmed/25177361 http://dx.doi.org/10.1186/s13065-014-0047-2 Text en © Kura et al. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Kura, Aminu Umar Hussein, Mohd Zobir Fakurazi, Sharida Arulselvan, Palanisamy Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title | Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title_full | Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title_fullStr | Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title_full_unstemmed | Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title_short | Layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
title_sort | layered double hydroxide nanocomposite for drug delivery systems; bio-distribution, toxicity and drug activity enhancement |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149231/ https://www.ncbi.nlm.nih.gov/pubmed/25177361 http://dx.doi.org/10.1186/s13065-014-0047-2 |
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