Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth

Despite the advanced development in the field of drug discovery and design, fighting infectious and non-infectious diseases remains a major worldwide heath challenge due to the limited activity of currently used drugs. Nevertheless, in recent years, the approach of designing nanoparticles for therap...

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Main Authors: Husam Qanash, Abdulrahman S. Bazaid, Abdu Aldarhami, Bandar Alharbi, Majed N. Almashjary, Mohannad S. Hazzazi, Hashim R. Felemban, Tarek M. Abdelghany
Format: Article
Language:English
Published: MDPI AG 2023-01-01
Series:Polymers
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Online Access:https://www.mdpi.com/2073-4360/15/2/391
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author Husam Qanash
Abdulrahman S. Bazaid
Abdu Aldarhami
Bandar Alharbi
Majed N. Almashjary
Mohannad S. Hazzazi
Hashim R. Felemban
Tarek M. Abdelghany
author_facet Husam Qanash
Abdulrahman S. Bazaid
Abdu Aldarhami
Bandar Alharbi
Majed N. Almashjary
Mohannad S. Hazzazi
Hashim R. Felemban
Tarek M. Abdelghany
author_sort Husam Qanash
collection DOAJ
description Despite the advanced development in the field of drug discovery and design, fighting infectious and non-infectious diseases remains a major worldwide heath challenge due to the limited activity of currently used drugs. Nevertheless, in recent years, the approach of designing nanoparticles for therapeutic applications has gained more interest and promise for future use. Thus, the current study is focused on the evaluation of <i>A. judaica</i> extract and chitosan nanoparticles loaded extract (CNPsLE) for potential antimicrobial and anticancer activities. The HPLC analysis of the extract has shown the presence of various phenolic and flavonoid compounds, including kaempferol (3916.34 µg/mL), apigenin (3794.32 µg/mL), chlorogenic acid (1089.58 µg/mL), quercetin (714.97 µg/mL), vanillin (691.55 µg/mL), naringenin (202.14 µg/mL), and rutin (55.64 µg/mL). The extract alone showed higher MIC values against <i>B. subtilis</i>, <i>E. coli</i>, <i>S. aureus</i>, <i>K. pneumonia</i>, and <i>C. albicans</i> (62.5, 15.65, 15.62, 31.25, and 31.25 µg/mL, respectively), whereas lower MIC values were observed when the extract was combined with CNPsLE (0.97, 1.95, 3.9, 4.1, and 15.62 µg/mL, respectively). The extract exhibited low cytotoxicity against normal Vero cells with IC<sub>50</sub> 173.74 µg/mL in comparison with the cytotoxicity of the CNPsLE (IC<sub>50</sub>, 73.89 µg/mL). However, CNPsLE showed more selective toxicity against the human prostate cancer cell line (PC3) with IC<sub>50</sub> of 20.8 µg/mL than the extract alone with 76.09 µg/mL. In the docking experiments, kaempferol and apigenin were revealed to be suitable inhibitors for prostate cancer (2Q7L). Overall, the obtained data highlighted the promising potential therapeutic use of CNPsLE as an anticancer and antimicrobial agent.
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spelling doaj.art-3e6949576d6441f790b2a1933c47f37b2023-12-01T00:09:17ZengMDPI AGPolymers2073-43602023-01-0115239110.3390/polym15020391Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial GrowthHusam Qanash0Abdulrahman S. Bazaid1Abdu Aldarhami2Bandar Alharbi3Majed N. Almashjary4Mohannad S. Hazzazi5Hashim R. Felemban6Tarek M. Abdelghany7Department of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi ArabiaDepartment of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi ArabiaDepartment of Medical Microbiology, Qunfudah Faculty of Medicine, Umm Al-Qura University, Al-Qunfudah 21961, Saudi ArabiaDepartment of Medical Laboratory Science, College of Applied Medical Sciences, University of Ha’il, Hail 55476, Saudi ArabiaDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 22254, Saudi ArabiaDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 22254, Saudi ArabiaDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 22254, Saudi ArabiaBotany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo 71524, EgyptDespite the advanced development in the field of drug discovery and design, fighting infectious and non-infectious diseases remains a major worldwide heath challenge due to the limited activity of currently used drugs. Nevertheless, in recent years, the approach of designing nanoparticles for therapeutic applications has gained more interest and promise for future use. Thus, the current study is focused on the evaluation of <i>A. judaica</i> extract and chitosan nanoparticles loaded extract (CNPsLE) for potential antimicrobial and anticancer activities. The HPLC analysis of the extract has shown the presence of various phenolic and flavonoid compounds, including kaempferol (3916.34 µg/mL), apigenin (3794.32 µg/mL), chlorogenic acid (1089.58 µg/mL), quercetin (714.97 µg/mL), vanillin (691.55 µg/mL), naringenin (202.14 µg/mL), and rutin (55.64 µg/mL). The extract alone showed higher MIC values against <i>B. subtilis</i>, <i>E. coli</i>, <i>S. aureus</i>, <i>K. pneumonia</i>, and <i>C. albicans</i> (62.5, 15.65, 15.62, 31.25, and 31.25 µg/mL, respectively), whereas lower MIC values were observed when the extract was combined with CNPsLE (0.97, 1.95, 3.9, 4.1, and 15.62 µg/mL, respectively). The extract exhibited low cytotoxicity against normal Vero cells with IC<sub>50</sub> 173.74 µg/mL in comparison with the cytotoxicity of the CNPsLE (IC<sub>50</sub>, 73.89 µg/mL). However, CNPsLE showed more selective toxicity against the human prostate cancer cell line (PC3) with IC<sub>50</sub> of 20.8 µg/mL than the extract alone with 76.09 µg/mL. In the docking experiments, kaempferol and apigenin were revealed to be suitable inhibitors for prostate cancer (2Q7L). Overall, the obtained data highlighted the promising potential therapeutic use of CNPsLE as an anticancer and antimicrobial agent.https://www.mdpi.com/2073-4360/15/2/391Artemisiachitosan nanoparticlesanticancerantimicrobialbio-efficacy
spellingShingle Husam Qanash
Abdulrahman S. Bazaid
Abdu Aldarhami
Bandar Alharbi
Majed N. Almashjary
Mohannad S. Hazzazi
Hashim R. Felemban
Tarek M. Abdelghany
Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
Polymers
Artemisia
chitosan nanoparticles
anticancer
antimicrobial
bio-efficacy
title Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
title_full Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
title_fullStr Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
title_full_unstemmed Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
title_short Phytochemical Characterization and Efficacy of <em>Artemisia judaica</em> Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth
title_sort phytochemical characterization and efficacy of em artemisia judaica em extract loaded chitosan nanoparticles as inhibitors of cancer proliferation and microbial growth
topic Artemisia
chitosan nanoparticles
anticancer
antimicrobial
bio-efficacy
url https://www.mdpi.com/2073-4360/15/2/391
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