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Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid

BACKGROUND: We characterize a novel nanocomposite that acts as an efficient anticancer agent. METHODS: This nanocomposite consists of zinc layered hydroxide intercalated with protocatechuate (an anionic form of protocatechuic acid), that has been synthesized using a direct method with zinc oxide and...

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Autores principales: Barahuie, Farahnaz, Hussein, Mohd Zobir, Abd Gani, Shafinaz, Fakurazi, Sharida, Zainal, Zulkarnain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079826/
https://www.ncbi.nlm.nih.gov/pubmed/25061291
http://dx.doi.org/10.2147/IJN.S59541
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author Barahuie, Farahnaz
Hussein, Mohd Zobir
Abd Gani, Shafinaz
Fakurazi, Sharida
Zainal, Zulkarnain
author_facet Barahuie, Farahnaz
Hussein, Mohd Zobir
Abd Gani, Shafinaz
Fakurazi, Sharida
Zainal, Zulkarnain
author_sort Barahuie, Farahnaz
collection PubMed
description BACKGROUND: We characterize a novel nanocomposite that acts as an efficient anticancer agent. METHODS: This nanocomposite consists of zinc layered hydroxide intercalated with protocatechuate (an anionic form of protocatechuic acid), that has been synthesized using a direct method with zinc oxide and protocatechuic acid as precursors. RESULTS: The resulting protocatechuic acid nanocomposite (PAN) showed a basal spacing of 12.7 Å, indicating that protocatechuate was intercalated in a monolayer arrangement, with an angle of 54° from the Z-axis between the interlayers of the zinc layered hydroxide, and an estimated drug loading of about 35.7%. PAN exhibited the properties of a mesoporous type material, with greatly enhanced thermal stability of protocatechuate as compared to its free counterpart. The presence of protocatechuate in the interlayers of the zinc layered hydroxide was further supported by Fourier transform infrared spectroscopy. Protocatechuate was released from PAN in a slow and sustained manner. This mechanism of release was well represented by a pseudo-second order kinetics model. PAN has shown increased cytotoxicity compared to the free form of protocatechuic acid in all cancer cell lines tested. Tumor growth suppression was extensive, particularly in HepG2 and HT29 cell lines. CONCLUSION: PAN is suitable for use as a controlled release formulation, and our in vitro evidence indicates that PAN is an effective anticancer agent. PAN may have potential as a chemotherapeutic drug for human cancer.
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spelling pubmed-40798262014-07-24 Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid Barahuie, Farahnaz Hussein, Mohd Zobir Abd Gani, Shafinaz Fakurazi, Sharida Zainal, Zulkarnain Int J Nanomedicine Original Research BACKGROUND: We characterize a novel nanocomposite that acts as an efficient anticancer agent. METHODS: This nanocomposite consists of zinc layered hydroxide intercalated with protocatechuate (an anionic form of protocatechuic acid), that has been synthesized using a direct method with zinc oxide and protocatechuic acid as precursors. RESULTS: The resulting protocatechuic acid nanocomposite (PAN) showed a basal spacing of 12.7 Å, indicating that protocatechuate was intercalated in a monolayer arrangement, with an angle of 54° from the Z-axis between the interlayers of the zinc layered hydroxide, and an estimated drug loading of about 35.7%. PAN exhibited the properties of a mesoporous type material, with greatly enhanced thermal stability of protocatechuate as compared to its free counterpart. The presence of protocatechuate in the interlayers of the zinc layered hydroxide was further supported by Fourier transform infrared spectroscopy. Protocatechuate was released from PAN in a slow and sustained manner. This mechanism of release was well represented by a pseudo-second order kinetics model. PAN has shown increased cytotoxicity compared to the free form of protocatechuic acid in all cancer cell lines tested. Tumor growth suppression was extensive, particularly in HepG2 and HT29 cell lines. CONCLUSION: PAN is suitable for use as a controlled release formulation, and our in vitro evidence indicates that PAN is an effective anticancer agent. PAN may have potential as a chemotherapeutic drug for human cancer. Dove Medical Press 2014-06-26 /pmc/articles/PMC4079826/ /pubmed/25061291 http://dx.doi.org/10.2147/IJN.S59541 Text en © 2014 Barahuie et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Barahuie, Farahnaz
Hussein, Mohd Zobir
Abd Gani, Shafinaz
Fakurazi, Sharida
Zainal, Zulkarnain
Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title_full Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title_fullStr Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title_full_unstemmed Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title_short Anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
title_sort anticancer nanodelivery system with controlled release property based on protocatechuate–zinc layered hydroxide nanohybrid
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079826/
https://www.ncbi.nlm.nih.gov/pubmed/25061291
http://dx.doi.org/10.2147/IJN.S59541
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