<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Antiproliferative Effects of Wild-Type Echovirus in Human Lung Cancer Cells</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1429</FirstPage>
			<LastPage>1438</LastPage>
			<ELocationID EIdType="pii">213588</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2023.400239.1642</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ramazan</FirstName>
					<LastName>Rezaei</LastName>
<Affiliation>Applied Virology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4611-7779</Identifier>

</Author>
<Author>
					<FirstName>Reza</FirstName>
					<LastName>Karbalaei</LastName>
<Affiliation>Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-1134-2287</Identifier>

</Author>
<Author>
					<FirstName>Mahdieh</FirstName>
					<LastName>Farzanehpour</LastName>
<Affiliation>Applied Virology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-2134-1061</Identifier>

</Author>
<Author>
					<FirstName>Ruhollah</FirstName>
					<LastName>Dorostkar</LastName>
<Affiliation>Applied Virology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-2574-1150</Identifier>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Bolouriyan</LastName>
<Affiliation>Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7739-1017</Identifier>

</Author>
<Author>
					<FirstName>Mahdi</FirstName>
					<LastName>Tat</LastName>
<Affiliation>Applied Virology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-3391-2957</Identifier>

</Author>
<Author>
					<FirstName>Mojgan</FirstName>
					<LastName>Saghazadeh</LastName>
<Affiliation>Department of Microbiology, Qom Branch, Islamic Azad University, Qom, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Soleymanitabar</LastName>
<Affiliation>Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-7897-5316</Identifier>

</Author>
<Author>
					<FirstName>Hadi</FirstName>
					<LastName>Esmaeili Gouvarchin Ghaleh</LastName>
<Affiliation>Applied Virology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-8562-2295</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>06</Month>
					<Day>02</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Oncolytic virotherapy is a new method of treating cancer. Various types of viruses have been shown to inhibit the growth of cancer cells due to the high presence of specific receptors on cancer cells. In this study, our aim was to investigate the potential ability of wildtype &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;to suppress the proliferation of A549 cell line as human lung cancer cells.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;In this study, we assessed the effects of treating A549 cells with both wild-type &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;and doxorubicin (DXR). We focused on several key parameters including cell proliferation, reactive oxygen species (ROS) generation, lactate dehydrogenase (LDH) release rate, apoptosis percentage, as well as caspase-8 and caspase-9 activities.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The cytotoxic effects of wild-type &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;were measured on A549 cell lines in all treatment groups by MTT and apoptosis assay. The lowest and highest cytotoxic effects and apoptosis percentage were associated with the 10 and 40 MOIs of &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;treated groups, respectively. Additionally, &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;significantly increased LDH and ROS generation and the activities of caspase-8 and caspase-9 compared with the control group.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Wild-type &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;has the potential to inhibit the proliferation of lung cancer cells and promote apoptosis through both mitochondrial and extracellular apoptotic pathways. This suggests that wild-type &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Echovirus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;could be considered as a possible therapy for human lung cancer in the future.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Oncolytic Virus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Echovirus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">human lung cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis Pathways</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213588_937437eb342b6a01ad104c3902210e33.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Control of the Cyclopiazonic Acid Level in Aspergillus flavus-Contaminated Wheat Flour</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1439</FirstPage>
			<LastPage>1448</LastPage>
			<ELocationID EIdType="pii">213589</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.478289.1784</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ayad</FirstName>
					<LastName>Abdelsalam</LastName>
<Affiliation>Radiology Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, 51001, Babylon, Iraq</Affiliation>
<Identifier Source="ORCID">0009-0002-1117-595X</Identifier>

</Author>
<Author>
					<FirstName>Marwa</FirstName>
					<LastName>Fadhil Alsaffar</LastName>
<Affiliation>Medical Laboratory Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, Babylon, 51001, Iraq</Affiliation>
<Identifier Source="ORCID">0000-0001-7037-4831</Identifier>

</Author>
<Author>
					<FirstName>Zahraa</FirstName>
					<LastName>Hamza Merza</LastName>
<Affiliation>Radiology Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, 51001, Babylon, Iraq</Affiliation>
<Identifier Source="ORCID">0000-0001-6453-7075</Identifier>

</Author>
<Author>
					<FirstName>Rzaq</FirstName>
					<LastName>Shailaan Kaurshead</LastName>
<Affiliation>Radiology Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, 51001, Babylon, Iraq</Affiliation>
<Identifier Source="ORCID">0009-0003-6618-8720</Identifier>

</Author>
<Author>
					<FirstName>Mohamed</FirstName>
					<LastName>Farouk Ghaly</LastName>
<Affiliation>Botany Department, Faculty of Science, Zagazig University, Zagazig, Egypt</Affiliation>
<Identifier Source="ORCID">0000-0002-5977-8269</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>09</Month>
					<Day>23</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Cyclopiazonic acid (CPA) is a mycotoxin produced by various fungal species such as &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Aspergillus flavus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;(&lt;/span&gt;&lt;em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;A. flavus&lt;/span&gt;&lt;/em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;). This study aimed to limit and control the level of CPA production in &lt;/span&gt;&lt;em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;A. flavus&lt;/span&gt;&lt;/em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-contaminated wheat flour.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Wheat flour samples (35 samples) were collected from various locations in Egypt. The fungal contaminations were determined and identified. Pure colonies of &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;A. flavus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;were maintained and tested for CPA production. Different procedures like ultraviolet (UV) treatment, heat treatment, materials adsorption, and biosorption by &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Lactobacilli&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;spp. were applied to control and reduce the CPA level.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Among 24 samples, 14 &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;A. flavus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;isolates (58.33%) were able to produce CPA. Yeast sucrose broth was the most favorable medium for CPA production, yielding 290.6 µg/100 ml dry biomass. UV light had an impact on the synthesis of CPA at different exposure times, decreasing by 45.5% after 60 minutes of exposure. CPA levels decreased with increasing temperature and exposure time, with a maximum reduction of 71.1% achieved at 100 ºC for 30 minutes. Charcoal was the most effective adsorption material, removing 53.3% of CPA. &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Lactobacillus acidophilus&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;(&lt;/span&gt;&lt;em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;L. acidophilus&lt;/span&gt;&lt;/em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;) was the most effective biosorbent, removing over 96.0% of CPA. Increasing the inoculum of &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;L. acidophilus &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;cells by 5×10&lt;sup&gt;7&lt;/sup&gt; reduced CPA levels by 82.1%.&lt;br /&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The diversity of abiotic and biotic control measures and their effectiveness may provide new hope for controlling and reducing CPA levels.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Aspergillus flavus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cyclopiazonic Acid</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Lactobacilli spp</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Ultra Violet</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213589_ddf778dbba94a6e9acc8a28d932887ae.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A Green and Low-Cost Nanocomposite Using Corn Cob Fiber and ZnFe₂O₄ for Pesticide Adsorption from Water</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1449</FirstPage>
			<LastPage>1460</LastPage>
			<ELocationID EIdType="pii">213664</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.487251.1805</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Nazila</FirstName>
					<LastName>Gholipour</LastName>
<Affiliation>Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-0099-5549</Identifier>

</Author>
<Author>
					<FirstName>Moein</FirstName>
					<LastName>Valian</LastName>
<Affiliation>Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Hadi</FirstName>
					<LastName>Baghersad</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-1940-5388</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>11</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;This study synthesized a nanocomposite using corn cob fiber and ZnFe&lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;₂&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;O&lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;₄&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;, characterized by electron microscopy, X-ray diffraction, infrared spectroscopy, and surface porosity analysis. The research focused on evaluating the adsorption capacity and kinetics of this nanocomposite for removing malathion and bendiocarb, representing organophosphate and carbamate pesticides, respectively.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The nanocomposite was prepared and characterized using various techniques. Adsorption experiments assessed the removal efficiency of the pesticides under different conditions, including contact time, initial pollutant concentration, pH, and nanocomposite dosage. Kinetic studies utilized pseudo-first-order (PFO) and pseudo-second-order (PSO) models.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Rapid adsorption occurred within the first 20 minutes, with removal efficiencies of 45.4% for malathion and 40.5% for bendiocarb. Final efficiencies reached 49.3% for malathion and 47.7% for bendiocarb at 85 minutes. Optimal contact times were around 30 minutes for malathion and 40 minutes for bendiocarb. The PSO model provided a better fit, with higher equilibrium adsorption capacities (116.3 mg/g for malathion and 129.9 mg/g for bendiocarb). pH had a positive but minor effect on removal efficiency, and a dosage-dependent increase was observed, with a saturation point beyond 10 mg of nanocomposite.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The corn cob fiber and ZnFe&lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;₂&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;O&lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;₄ &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;nanocomposite effectively removed malathion and bendiocarb from aqueous solutions. Key factors influencing adsorption included contact time, pH, and nanocomposite dosage, highlighting the nanocomposite&#039;s potential for pesticide removal applications.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Pesticides</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Organophosphates</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Carbamates</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nanocomposites, Adsorption</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213664_ce59a9e6583a4db8b71f37204841b25f.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Preparation of Non-Enzymatic Glucose Sensor Using a Free-Standing Electrode Based on Copper Nanoparticles/Electrospun Carbon Nanofibers Composite</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1461</FirstPage>
			<LastPage>1470</LastPage>
			<ELocationID EIdType="pii">213654</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.434297.1697</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Mohammadpoor</LastName>
<Affiliation>Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sharareh</FirstName>
					<LastName>Sajjadi</LastName>
<Affiliation>Department of Biology, Roudehen Branch, Islamic Azad University, Roudehen, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Rasouli</LastName>
<Affiliation>SEM Lab, Central Laboratory, Amirkabir University of Technology, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Amir Homayoun</FirstName>
					<LastName>Keihan</LastName>
<Affiliation>Molecular Biology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-1622-2754</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>01</Month>
					<Day>06</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Diabetes mellitus is known as a public health problem worldwide. Accurate detection of glucose concentration is crucial for managing diabetes mellitus. In this study, a non-enzymatic glucose sensor was fabricated using a free-standing electrode based on a composite of copper nanoparticles and electrospun carbon nanofibers. &lt;/span&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Copper nanoparticles/electrospun carbon nanofibers (Cu/CNFs) nanocomposite was produced using a novel strategy involving electrospinning of polyacrylonitrile/copper acetate (PAN/Cu(OAc)&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;2&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;), followed by thermal treatment to carbonize the PAN nanofibers and reduce Cu. CuO/CNF was also synthesized by post-heating the Cu/CNFs nanocomposite. The morphology of the Cu/CNFs nanocomposite was investigated by field emission scanning electron microscopy (FE-SEM), and its composition and structure were characterized by energydispersive X-ray (EDX) and X-ray diffraction (XRD) analysis, respectively. The Cu precursor content was optimized by comparing the Raman spectra, conductivity test, and TGA analysis. After demonstrating the effective role of Cu in glucose oxidation, the Cu/CNFs and CuO/CNFs nanocomposites were used directly as free-standing working electrodes for non-enzymatic detection of glucose. The electrochemical responses of the electrodes to glucose were examined by cyclic voltammetry and chronoamperometric techniques.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Compared to the Cu/CNF, the CuO/CNFs showed a higher sensitivity of 424.6 µA mM&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-1 &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;cm&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-2 &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;and a lower detection limit of 0.35 mM. Both electrodes exhibited a linear range of 2-10 mM.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Reasonable LOD and sensitivity for glucose detection, good selectivity, reasonable stability of one month, and acceptable reproducibility make the CuO/CNFs nanocomposite a promising candidate for the development of non-enzymatic glucose sensors.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Copper nanoparticles</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Electrospun Carbon Nanofibers</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Non-Enzymatic sensor</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Glucose</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213654_94bfdf1d30c129b4a27dd10932f01ada.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of In Vitro Gastrointestinal Digestion on Monacolin K and α-Glucosidase and α-Amylase Inhibitory Activities of BRTA and Chemometrics Analysis</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1471</FirstPage>
			<LastPage>1478</LastPage>
			<ELocationID EIdType="pii">213658</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.451772.1717</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Narissara</FirstName>
					<LastName>Uthai</LastName>
<Affiliation>Division of Food and Nutrition, Faculty of Home Economics Technology, Rajamangala University of Technology Krungthep, Bangkok 10120, Thailand</Affiliation>
<Identifier Source="ORCID">0009-0004-8398-8882</Identifier>

</Author>
<Author>
					<FirstName>Putkrong</FirstName>
					<LastName>Phanumong</LastName>
<Affiliation>Division of Food Safety Management and Technology, Department of Science, Faculty of Science and Technology, Rajamangala University of Technology Krungthep, Bangkok 10120, Thailand</Affiliation>
<Identifier Source="ORCID">0000-0002-6756-6485</Identifier>

</Author>
<Author>
					<FirstName>Kitisart</FirstName>
					<LastName>Kraboun</LastName>
<Affiliation>Division of Food Safety Management and Technology, Department of Science, Faculty of Science and Technology, Rajamangala University of Technology Krungthep, Bangkok 10120, Thailand</Affiliation>
<Identifier Source="ORCID">0000-0002-5939-5129</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>04</Month>
					<Day>09</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Broken rice tea supplemented with angkak (BRTA) contains monacolin K and Maillard reaction products (MRPs). The dynamic changes in these bioactive compounds and activities of BRTA after &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;in vitro&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gastrointestinal digestion were investigated. &lt;/span&gt;&lt;br /&gt;&lt;strong&gt;&lt;span class=&quot;fontstyle0&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Different ratios of roasted broken rice to angkak were supplemented in BRTA as 25:75, 50:50, 75:25, and 100:0. The colors, water activity (a&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;w&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;), moisture content, monacolin K, inhibition of peroxidation, DPPH radical scavenging assay, chelating ability on Fe&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;sup&gt;2+&lt;/sup&gt;&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;, and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-glucosidase and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-amylase inhibitory properties of BRTA were investigated after &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;in vitro&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gastrointestinal digestion. &lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Monacolin K, antioxidant properties, and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-glucosidase and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-amylase inhibitory abilities of BRTA for all ratios of roasted broken rice to angkak increased after &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;in vitro&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gastric digestion. BRTA activities using a ratio of 25:75 &lt;/span&gt;&lt;span class=&quot;fontstyle4&quot;&gt;(&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;roasted broken rice:angkak&lt;/span&gt;&lt;span class=&quot;fontstyle4&quot;&gt;) &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;were the highest. After &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;in vitro&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gastrointestinal digestion, monacolin K, antioxidant properties, and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-glucosidase and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-amylase inhibitory abilities of BRTA decreased due to the alkaline condition. Principal component analysis (PCA) and Pearson’s correlation coefficient showed that monacolin K was positively correlated with &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-amylase inhibition activity. &lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Changes in monacolin K and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-glucosidase and &lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;α&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;-amylase inhibitory abilities after &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;in vitro&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gastrointestinal digestion of BRTA were investigated. Other experiments using angkak as a main ingredient should be conducted to determine dynamic changes in bioaccessibility.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Angkak</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">antioxidant properties</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PCA</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pearson’s Correlation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DPPH</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213658_f32d230833d03136148c6f937e60fb07.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Production and Evaluation of Uniform Magnetic T-2 Imprinted Polymer from Aqueous Medium</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1479</FirstPage>
			<LastPage>1487</LastPage>
			<ELocationID EIdType="pii">213650</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.423799.1686</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Seyed Javad</FirstName>
					<LastName>Davarpanah</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Science, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-7702-7242</Identifier>

</Author>
<Author>
					<FirstName>Ramin</FirstName>
					<LastName>Karimian</LastName>
<Affiliation>Chemical Injuries Research Center, Systems biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4968-7195</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>11</Month>
					<Day>04</Day>
				</PubDate>
			</History>
		<Abstract> &lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Mycotoxins are harmful secondary metabolites produced by fungi on agricultural products under various climatic conditions. In this study, we developed a method for the extraction and preconcentration of T-2 toxin from aqueous media using magnetic molecular imprinting polymers. This technique involves creating polymers with high recognition properties for specific molecules and has been widely utilized in diverse scientific and technical applications. The objective of the study was to assess the binding properties of the magnetic MIPs for T-2 extraction and determine their potential as an efficient sample preparation technique.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Magnetic T-2 imprinted nanoparticles using T-2 toxin (T-2) as the template, along with Methacrylic acid and ethyleneglycoldimethacrylate as the functional monomer and cross-linker were synthesized in aqueous media and characterized. We investigated their selective adsorption ability, adsorption kinetics, and isotherms. The selective extraction of T-2 toxin from aqueous media was performed.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Our findings showed that under ambient conditions, the magnetic molecularly imprinted polymer nanoparticles (MMIP NPs) successfully extracted 70% to 81% of the T-2 toxin from the aqueous media after three times of recycling.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;This study developed a method to create uniform magnetic T-2 imprinted nanoparticles. The technique holds promise for detecting and analyzing T-2 contamination in food and feed products. Magnetic molecularly imprinted nanoparticles have several advantages, including selective recognition, stability, reusability, and enhanced sensitivity.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Uniform Magnetic Molecularly Imprinted Nanoparticle</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">T-2 toxin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Relative Standard Deviation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Adsorption Kinetic</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Adsorption Isotherm</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213650_3a250d494332149661000330727747f8.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Sequence Identification and Analysis of the 5′ Untranslated Region of UGT76G1 gene in Stevia rebaudiana</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1488</FirstPage>
			<LastPage>1496</LastPage>
			<ELocationID EIdType="pii">213647</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2023.407817.1653</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Atefeh</FirstName>
					<LastName>Amini Neisiani</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, Faculty of Life Sciences &amp; Biotechnology, Shahid Beheshti University, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-3189-2430</Identifier>

</Author>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Saidi</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, Faculty of Life Sciences &amp; Biotechnology, Shahid Beheshti University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Masoud</FirstName>
					<LastName>Tohidfar</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, Faculty of Life Sciences &amp; Biotechnology, Shahid Beheshti University, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-0175-7406</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>07</Month>
					<Day>19</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Stevia rebaudiana&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;contains steviol glycosides responsible for their sweet taste. One of the most important enzymes in the steviol glycosides production pathway in &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Stevia rebaudiana&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;is the UGT76G1 enzyme, which is involved in the conversion of stevioside to rebaudioside A. The aim of this study was to identify the 5&#039;-UTR of the &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;UGT76G1&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;gene and investigate the cis-elements present in this region.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The promoter and gene sequences of this enzyme were obtained from the NCBI database. To identify the 5&#039;-UTR region, a pair of primers was designed. The pure amplified fragment was cloned into the pTG19 vector and transformed into &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;E. coli&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;XL1-Blue bacteria. Sequencing data were analyzed, and a fragment with a length of 944 nucleotides was identified as the 5&#039;-UTR. Then, the cis-elements in this sequence were investigated using PlantCARE and PlantPAN.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The 5&lt;/span&gt;&lt;span class=&quot;fontstyle3&quot;&gt;′&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;UTR sequence has been submitted to the NCBI database with the accession number OP897301. It was found that 65% of the elements in the 5’-UTR are responsible for regulating gene transcription, confirming the regulatory role of this sequence.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The identification of regulatory regions and cis-elements in this region can be used in future research to regulate gene expression.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">5' UTR, Cis-regulatory Elements</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Regulatory Sequences</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">UDP-glycosyltransferase 76G1</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213647_ce0c83d1ce9cccfe20da14686b702ae0.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>11</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2024</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Anticancer properties of nanoniosomes containing ethanolic and methanolic extracts of Citrus limon peel on SKBR-3 breast cancer cells</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1497</FirstPage>
			<LastPage>1505</LastPage>
			<ELocationID EIdType="pii">213667</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2024.422324.1684</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Toktam</FirstName>
					<LastName>Deylami</LastName>
<Affiliation>Department of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-8184-6929</Identifier>

</Author>
<Author>
					<FirstName>Mohammad Mehdi</FirstName>
					<LastName>Yaghoobi</LastName>
<Affiliation>Department of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-1434-6224</Identifier>

</Author>
<Author>
					<FirstName>Masoud</FirstName>
					<LastName>Torkzadeh-Mahani</LastName>
<Affiliation>Department of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-3398-7468</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>10</Month>
					<Day>25</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The adverse effects of chemotherapy in treating breast cancer have prompted research into identifying and using herbal anticancer compounds with suitable carriers. Accordingly, in the current study, we intended to investigate the effects of niosome-formulated methanolic (Nio/ME) and ethanolic (Nio/EE) extracts of &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Citrus limon&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;peel on SKBR-3 breast cancer cells.&lt;/span&gt;&lt;br /&gt;&lt;strong&gt;&lt;span class=&quot;fontstyle0&quot;&gt;Materials and Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span class=&quot;fontstyle2&quot;&gt;The SKBR-3 breast cancer cell line was subjected to niosomal formulation of ethanolic and methanolic extracts of lemon peel and doxorubicin. The effects on cytotoxicity, cell death, and migration via MTT, wound healing assay, and flow cytometry analysis were investigated.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;MTT observations demonstrated that 200 µg/ml of extracts and 0.5 µM doxorubicin were appropriate for loading in the niosome and administered to the cells for 48 hours. In flow cytometry, the apoptosis rate significantly increased for ethanolic and methanolic extract formulations compared to pure extracts. However, encapsulated doxorubicin had a milder toxicity than doxorubicin alone (&lt;/span&gt;&lt;em&gt;&lt;span class=&quot;fontstyle2&quot;&gt;p&lt;/span&gt;&lt;/em&gt;&lt;span class=&quot;fontstyle3&quot;&gt;≤&lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;0.05). Wound healing assay demonstrated significant anti-migratory effects of encapsulated extracts. The extracts had a significant synergistic cytotoxic effect with the drug.&lt;/span&gt;&lt;br /&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Lemon peel extract has anticancer properties similar to doxorubicin. Additionally, the niosomal formulation demonstrated the ability to load and release the extracts and drug efficiently to the breast cancer cell.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Nanoniosome</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Herbal</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cytotoxicity</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">scratch assay</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_213667_c0baadec4f4b86fd22f15766bc91264a.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
