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Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin
The approach of drug delivery systems emphasizes the use of nanoparticles as a vehicle, offering the optional property of delivering drugs as a single dose rather than in multiple doses. The current study aims to improve antioxidant and drug release properties of curcumin loaded gum Arabic-sodium al...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249151/ https://www.ncbi.nlm.nih.gov/pubmed/32397633 http://dx.doi.org/10.3390/molecules25092244 |
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author | Hassani, Abdelkader Mahmood, Syed Enezei, Hamid Hammad Hussain, Siti Aslina Hamad, Hamad Ali Aldoghachi, Ahmed Faris Hagar, Abdullah Doolaanea, Abd Almonem Ibrahim, Wisam Nabeel |
author_facet | Hassani, Abdelkader Mahmood, Syed Enezei, Hamid Hammad Hussain, Siti Aslina Hamad, Hamad Ali Aldoghachi, Ahmed Faris Hagar, Abdullah Doolaanea, Abd Almonem Ibrahim, Wisam Nabeel |
author_sort | Hassani, Abdelkader |
collection | PubMed |
description | The approach of drug delivery systems emphasizes the use of nanoparticles as a vehicle, offering the optional property of delivering drugs as a single dose rather than in multiple doses. The current study aims to improve antioxidant and drug release properties of curcumin loaded gum Arabic-sodium alginate nanoparticles (Cur/ALG-GANPs). The Cur/ALG-GANPs were prepared using the ionotropic gelation technique and further subjected to physico-chemical characterization using attenuated total reflectance–Fourier transform infrared (ATR-FTIR), X-ray diffractometry (XRD), differential scanning calorimetry (DSC), size distribution, and transmission electron microscopy (TEM). The size of Cur/ALG-GANPs ranged between 10 ± 0.3 nm and 190 ± 0.1 nm and the zeta potential was –15 ± 0.2 mV. The antioxidant study of Cur/ALG-GANPs exhibited effective radical scavenging capacity for 1,1-diphenyl-2-picrylhydrazyl (DPPH) at concentrations that ranged between 30 and 500µg/mL. Cytotoxicity was performed using MTT assay to measure their potential in inhibiting the cell growth and the result demonstrated a significant anticancer activity of Cur/ALG-GANPs against human liver cancer cells (HepG2) than in colon cancer (HT29), lung cancer (A549) and breast cancer (MCF7) cells. Thus, this study indicates that Cur/ALG-GANPs have promising anticancer properties that might aid in future cancer therapy. |
format | Online Article Text |
id | pubmed-7249151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72491512020-06-10 Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin Hassani, Abdelkader Mahmood, Syed Enezei, Hamid Hammad Hussain, Siti Aslina Hamad, Hamad Ali Aldoghachi, Ahmed Faris Hagar, Abdullah Doolaanea, Abd Almonem Ibrahim, Wisam Nabeel Molecules Article The approach of drug delivery systems emphasizes the use of nanoparticles as a vehicle, offering the optional property of delivering drugs as a single dose rather than in multiple doses. The current study aims to improve antioxidant and drug release properties of curcumin loaded gum Arabic-sodium alginate nanoparticles (Cur/ALG-GANPs). The Cur/ALG-GANPs were prepared using the ionotropic gelation technique and further subjected to physico-chemical characterization using attenuated total reflectance–Fourier transform infrared (ATR-FTIR), X-ray diffractometry (XRD), differential scanning calorimetry (DSC), size distribution, and transmission electron microscopy (TEM). The size of Cur/ALG-GANPs ranged between 10 ± 0.3 nm and 190 ± 0.1 nm and the zeta potential was –15 ± 0.2 mV. The antioxidant study of Cur/ALG-GANPs exhibited effective radical scavenging capacity for 1,1-diphenyl-2-picrylhydrazyl (DPPH) at concentrations that ranged between 30 and 500µg/mL. Cytotoxicity was performed using MTT assay to measure their potential in inhibiting the cell growth and the result demonstrated a significant anticancer activity of Cur/ALG-GANPs against human liver cancer cells (HepG2) than in colon cancer (HT29), lung cancer (A549) and breast cancer (MCF7) cells. Thus, this study indicates that Cur/ALG-GANPs have promising anticancer properties that might aid in future cancer therapy. MDPI 2020-05-10 /pmc/articles/PMC7249151/ /pubmed/32397633 http://dx.doi.org/10.3390/molecules25092244 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hassani, Abdelkader Mahmood, Syed Enezei, Hamid Hammad Hussain, Siti Aslina Hamad, Hamad Ali Aldoghachi, Ahmed Faris Hagar, Abdullah Doolaanea, Abd Almonem Ibrahim, Wisam Nabeel Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title | Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title_full | Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title_fullStr | Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title_full_unstemmed | Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title_short | Formulation, Characterization and Biological Activity Screening of Sodium Alginate-Gum Arabic Nanoparticles Loaded with Curcumin |
title_sort | formulation, characterization and biological activity screening of sodium alginate-gum arabic nanoparticles loaded with curcumin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249151/ https://www.ncbi.nlm.nih.gov/pubmed/32397633 http://dx.doi.org/10.3390/molecules25092244 |
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