Evaluating the pharmacological activities of Aloe perryi–Silver nanoparticles induced apoptosis against colon cancer cells (HCT‐116)

Aloe perryi has been studied and possesses several activities, including antibacterial, antiparasitic, and anticancer properties. In this study, A. perryi was used as a reducing agent of silver ions into silver nanoparticles. Aloe perryi–silver nanoparticles (APS‐NPs) were characterized and evaluate...

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Veröffentlicht in:Food Science & Nutrition 2024-08, Vol.12 (8), p.5890-5906
Hauptverfasser: Hotan, Omar, Alhaj, Ali, Al‐quhaim, Abdulghfor, Alburaihi, Khaled, Ahmed, Yahya, Munasser, Qassem, Dhufer, Saleh Bin, Nasran, Tammam, Gabir, Mohammed, Ebrahim, Akram, Obadi, Mohammed, Hadi, Maryam, Al‐baity, Hanefa, Ba‐Nafea, Abdulmalek, Qaed, Eskandar, Zaky, Mohamed Y., Okba, Mohammed, Al‐Nasi, Abdullah, Almoiliqy, Marwan
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container_end_page 5906
container_issue 8
container_start_page 5890
container_title Food Science & Nutrition
container_volume 12
creator Hotan, Omar
Alhaj, Ali
Al‐quhaim, Abdulghfor
Alburaihi, Khaled
Ahmed, Yahya
Munasser, Qassem
Dhufer, Saleh Bin
Nasran, Tammam
Gabir, Mohammed
Ebrahim, Akram
Obadi, Mohammed
Hadi, Maryam
Al‐baity, Hanefa
Ba‐Nafea, Abdulmalek
Qaed, Eskandar
Zaky, Mohamed Y.
Okba, Mohammed
Al‐Nasi, Abdullah
Almoiliqy, Marwan
description Aloe perryi has been studied and possesses several activities, including antibacterial, antiparasitic, and anticancer properties. In this study, A. perryi was used as a reducing agent of silver ions into silver nanoparticles. Aloe perryi–silver nanoparticles (APS‐NPs) were characterized and evaluated using characterization techniques. However, the antioxidative, antibacterial, and anticancer assays were studied to evaluate the pharmacological activities of APS‐NPs. APS‐NPs were developed and changed to dark brown and the maximum absorption was 442 nm. SEM (5–583 nm), TEM (4–110 nm), XRD (21.84 nm), and zeta potential analysis (63.39 nm) revealed that the APS‐NPs were nano‐sized, and the APS‐NPs had a cubic crystalline structure, according to the XRD results. FTIR analysis suggested that functional groups of A. perryi metabolites were involved in forming APS‐NPs. The zeta potential indicated that the APS‐NPs were negatively charged (−32 mV), suggesting good stability. APS‐NPs showed significant antioxidative stress activity by reducing DPPH‐free radicles in a dose‐dependent manner. APS‐NPs‐induced antibacterial effect against Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and Acinetobacter baumannii (A. baumannii). APS‐NPs reduced the cell viability and cell migration of the human colon tumor cell line (HCT 116) compared with controls, indicating that APS‐NPs could play a role in reducing metastasis and inducing cell apoptosis against colon cancer. In conclusion, the nanoparticle synthesis from A. perryi extract demonstrated excellent antioxidant, antibacterial, and anticancer activities, thus suggesting that our APS‐NPs have the potential to be used as antioxidative and antibacterial in food and pharmaceutical industries. Synthesis of silver nanoparticles via using Aloe perryi as a reducing agent, and illustrating the characterization studies of Aloe perryi–silver nanoparticles and their pharmacological activity against HCT‐116 colon cancer cells.
doi_str_mv 10.1002/fsn3.4246
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In this study, A. perryi was used as a reducing agent of silver ions into silver nanoparticles. Aloe perryi–silver nanoparticles (APS‐NPs) were characterized and evaluated using characterization techniques. However, the antioxidative, antibacterial, and anticancer assays were studied to evaluate the pharmacological activities of APS‐NPs. APS‐NPs were developed and changed to dark brown and the maximum absorption was 442 nm. SEM (5–583 nm), TEM (4–110 nm), XRD (21.84 nm), and zeta potential analysis (63.39 nm) revealed that the APS‐NPs were nano‐sized, and the APS‐NPs had a cubic crystalline structure, according to the XRD results. FTIR analysis suggested that functional groups of A. perryi metabolites were involved in forming APS‐NPs. The zeta potential indicated that the APS‐NPs were negatively charged (−32 mV), suggesting good stability. APS‐NPs showed significant antioxidative stress activity by reducing DPPH‐free radicles in a dose‐dependent manner. APS‐NPs‐induced antibacterial effect against Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and Acinetobacter baumannii (A. baumannii). APS‐NPs reduced the cell viability and cell migration of the human colon tumor cell line (HCT 116) compared with controls, indicating that APS‐NPs could play a role in reducing metastasis and inducing cell apoptosis against colon cancer. In conclusion, the nanoparticle synthesis from A. perryi extract demonstrated excellent antioxidant, antibacterial, and anticancer activities, thus suggesting that our APS‐NPs have the potential to be used as antioxidative and antibacterial in food and pharmaceutical industries. 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APS‐NPs‐induced antibacterial effect against Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and Acinetobacter baumannii (A. baumannii). APS‐NPs reduced the cell viability and cell migration of the human colon tumor cell line (HCT 116) compared with controls, indicating that APS‐NPs could play a role in reducing metastasis and inducing cell apoptosis against colon cancer. In conclusion, the nanoparticle synthesis from A. perryi extract demonstrated excellent antioxidant, antibacterial, and anticancer activities, thus suggesting that our APS‐NPs have the potential to be used as antioxidative and antibacterial in food and pharmaceutical industries. 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Alhaj, Ali ; Al‐quhaim, Abdulghfor ; Alburaihi, Khaled ; Ahmed, Yahya ; Munasser, Qassem ; Dhufer, Saleh Bin ; Nasran, Tammam ; Gabir, Mohammed ; Ebrahim, Akram ; Obadi, Mohammed ; Hadi, Maryam ; Al‐baity, Hanefa ; Ba‐Nafea, Abdulmalek ; Qaed, Eskandar ; Zaky, Mohamed Y. ; Okba, Mohammed ; Al‐Nasi, Abdullah ; Almoiliqy, Marwan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4016-7adc456078784ca9d6cc469d7251193803ef685b835fe9cf3cf564c90623a7ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>A. perryi</topic><topic>Aloe</topic><topic>Aloe perryi</topic><topic>Antibacterial activity</topic><topic>Antibacterial agents</topic><topic>Antibiotics</topic><topic>Anticancer properties</topic><topic>Antidiabetics</topic><topic>Antiinfectives and antibacterials</topic><topic>Antiparasitic agents</topic><topic>Apoptosis</topic><topic>Bacteria</topic><topic>Cell migration</topic><topic>Cell viability</topic><topic>characterization</topic><topic>Colon cancer</topic><topic>Colorectal cancer</topic><topic>Cosmetics</topic><topic>E coli</topic><topic>Food industry</topic><topic>Functional groups</topic><topic>Fungi</topic><topic>Gram-positive bacteria</topic><topic>Metabolites</topic><topic>Metastases</topic><topic>Microorganisms</topic><topic>Microscopy</topic><topic>Nanoparticles</topic><topic>Nanotechnology</topic><topic>Original</topic><topic>Pharmaceutical industry</topic><topic>pharmacological activities</topic><topic>Pharmacology</topic><topic>Phytochemicals</topic><topic>Reducing agents</topic><topic>Silver</topic><topic>silver nanoparticles</topic><topic>synthesis</topic><topic>Toxicity</topic><topic>Zeta potential</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hotan, Omar</creatorcontrib><creatorcontrib>Alhaj, Ali</creatorcontrib><creatorcontrib>Al‐quhaim, Abdulghfor</creatorcontrib><creatorcontrib>Alburaihi, Khaled</creatorcontrib><creatorcontrib>Ahmed, Yahya</creatorcontrib><creatorcontrib>Munasser, Qassem</creatorcontrib><creatorcontrib>Dhufer, Saleh Bin</creatorcontrib><creatorcontrib>Nasran, Tammam</creatorcontrib><creatorcontrib>Gabir, Mohammed</creatorcontrib><creatorcontrib>Ebrahim, Akram</creatorcontrib><creatorcontrib>Obadi, Mohammed</creatorcontrib><creatorcontrib>Hadi, Maryam</creatorcontrib><creatorcontrib>Al‐baity, Hanefa</creatorcontrib><creatorcontrib>Ba‐Nafea, Abdulmalek</creatorcontrib><creatorcontrib>Qaed, Eskandar</creatorcontrib><creatorcontrib>Zaky, Mohamed Y.</creatorcontrib><creatorcontrib>Okba, Mohammed</creatorcontrib><creatorcontrib>Al‐Nasi, Abdullah</creatorcontrib><creatorcontrib>Almoiliqy, Marwan</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Nutrition</jtitle><addtitle>Food Sci Nutr</addtitle><date>2024-08</date><risdate>2024</risdate><volume>12</volume><issue>8</issue><spage>5890</spage><epage>5906</epage><pages>5890-5906</pages><issn>2048-7177</issn><eissn>2048-7177</eissn><abstract>Aloe perryi has been studied and possesses several activities, including antibacterial, antiparasitic, and anticancer properties. In this study, A. perryi was used as a reducing agent of silver ions into silver nanoparticles. Aloe perryi–silver nanoparticles (APS‐NPs) were characterized and evaluated using characterization techniques. However, the antioxidative, antibacterial, and anticancer assays were studied to evaluate the pharmacological activities of APS‐NPs. APS‐NPs were developed and changed to dark brown and the maximum absorption was 442 nm. SEM (5–583 nm), TEM (4–110 nm), XRD (21.84 nm), and zeta potential analysis (63.39 nm) revealed that the APS‐NPs were nano‐sized, and the APS‐NPs had a cubic crystalline structure, according to the XRD results. FTIR analysis suggested that functional groups of A. perryi metabolites were involved in forming APS‐NPs. The zeta potential indicated that the APS‐NPs were negatively charged (−32 mV), suggesting good stability. APS‐NPs showed significant antioxidative stress activity by reducing DPPH‐free radicles in a dose‐dependent manner. APS‐NPs‐induced antibacterial effect against Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and Acinetobacter baumannii (A. baumannii). APS‐NPs reduced the cell viability and cell migration of the human colon tumor cell line (HCT 116) compared with controls, indicating that APS‐NPs could play a role in reducing metastasis and inducing cell apoptosis against colon cancer. In conclusion, the nanoparticle synthesis from A. perryi extract demonstrated excellent antioxidant, antibacterial, and anticancer activities, thus suggesting that our APS‐NPs have the potential to be used as antioxidative and antibacterial in food and pharmaceutical industries. Synthesis of silver nanoparticles via using Aloe perryi as a reducing agent, and illustrating the characterization studies of Aloe perryi–silver nanoparticles and their pharmacological activity against HCT‐116 colon cancer cells.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>39139937</pmid><doi>10.1002/fsn3.4246</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-9068-5909</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Open Access; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects A. perryi
Aloe
Aloe perryi
Antibacterial activity
Antibacterial agents
Antibiotics
Anticancer properties
Antidiabetics
Antiinfectives and antibacterials
Antiparasitic agents
Apoptosis
Bacteria
Cell migration
Cell viability
characterization
Colon cancer
Colorectal cancer
Cosmetics
E coli
Food industry
Functional groups
Fungi
Gram-positive bacteria
Metabolites
Metastases
Microorganisms
Microscopy
Nanoparticles
Nanotechnology
Original
Pharmaceutical industry
pharmacological activities
Pharmacology
Phytochemicals
Reducing agents
Silver
silver nanoparticles
synthesis
Toxicity
Zeta potential
title Evaluating the pharmacological activities of Aloe perryi–Silver nanoparticles induced apoptosis against colon cancer cells (HCT‐116)
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