<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2025</year>
	    <month>>Jan-Mar</month>
	    <day></day>
    </pubdate>
    <volume>17</volume>
    <number>1</number>
    <publish_type>online</publish_type>
    <publish_edition>1</publish_edition>
    <article_type>fulltext</article_type>
    <articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed></article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>How are Students Really selected for a PhD? The Impact of the Thesis and Solving the Country&#39;s Problems</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract></abstract>
	<keyword_fa></keyword_fa>
	<keyword></keyword>
	<start_page>1</start_page>
	<end_page>1</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60596</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60596.pdf</pdf_url>
	<author_list><author><first_name>Shahin</first_name><middle_name></middle_name><last_name>Akhondzadeh</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>739</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094097</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Therapeutic Effects of Nanochelating-Based Copper Nanoparticles on Burn Wound Healing in Mouse Model</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;The aim of the present study was to investigate the potential of Nanochelating-based copper to accelerate the wound healing process and prevent infection in burn wounds.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Six to eight-week- old female BALB/c mice were&lt;/span&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;burned with a 1 &lt;em&gt;cm&lt;sup&gt;2&lt;/sup&gt;&lt;/em&gt; heated copper plate on the left flank and then &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;divided into four treatment groups, &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;treated with&lt;/span&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;C8 (nanochelating-based CuNPs), cold cream (supplementary materials) as a control drug,&lt;/span&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;Silver Sulfadiazine and no treatment&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;,&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; respectively&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;. &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Skin tissue samples were taken from the mice on days 0, 3, 8, 15 and 24. One piece was fixed in 10% neutral buffered formalin for pathological examination and the others were stored at -80&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&amp;deg;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;C&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; until used for pro-inflammatory and growth factor gene expression.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;The healing process in the group treated with 10 &lt;em&gt;mg/ml &lt;/em&gt;C8 was significantly faster, and the survival rate of the mice in this group was significantly higher than in the other groups. The pro-inflammatory genes were expressed and down-regulated earlier in the C8 treated mice. Histopathology confirmed the higher cure rate in the group treated with 10 &lt;em&gt;mg/ml&lt;/em&gt; C8 compared to other control groups.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;C8 has beneficial effects on the healing of burn wounds and the effective dose of this compound should be further investigated. The present study demonstrates the anti-inflammatory properties of nano-chelate-based copper particles&amp;#39; on mouse skin burns. This research opens up new possibilities in dermatology and burn therapy and highlights the potential of copper-based formulations in the treatment of burn injuries.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Anti-inflammatory agents, Burns, Copper, Dermatology, Wound healing</keyword>
	<start_page>2</start_page>
	<end_page>13</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60597</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60597.pdf</pdf_url>
	<author_list><author><first_name>Hossein</first_name><middle_name></middle_name><last_name>Rezvan</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92293</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Seyed Masoud</first_name><middle_name></middle_name><last_name>Zolhavarieh</last_name><suffix></suffix><affiliation>Department of Clinical Sciences, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92294</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Alireza</first_name><middle_name></middle_name><last_name>Nourian</last_name><suffix></suffix><affiliation>Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92295</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Elham</first_name><middle_name></middle_name><last_name>Bayat</last_name><suffix></suffix><affiliation>Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92296</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Somayeh</first_name><middle_name></middle_name><last_name>Kalanaky</last_name><suffix></suffix><affiliation>Department of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92297</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Saideh</first_name><middle_name></middle_name><last_name>Fakharzadeh</last_name><suffix></suffix><affiliation>Department of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92298</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Pegah</first_name><middle_name></middle_name><last_name>Karimi</last_name><suffix></suffix><affiliation>Department of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92299</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Maryam</first_name><middle_name></middle_name><last_name>Hafizi</last_name><suffix></suffix><affiliation>Department of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92300</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Sahar</first_name><middle_name></middle_name><last_name>Hamoon Navard </last_name><suffix></suffix><affiliation>Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92302</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mohammad Hassan</first_name><middle_name></middle_name><last_name>Nazaran</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92321</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094092</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Moringa oleifera Docking to Estrogen Receptor α Ameliorates Placental and Brain Damage in Stressed Rats</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Stress during pregnancy significantly impacts offspring early physiological programming. Herbal remedies are frequently used by pregnant women to enhance their wellbeing. &lt;em&gt;Moringa oleifera&lt;/em&gt; Leaf Extract (MoLE) is believed to have both anti-stress and antioxidant properties which can act as a Selective Estrogen Receptor Modulator (SERM) that regulate activities of estrogen, and can have different effects on different tissues. Goal of this study is to compile information on molecular docking analysis of phytochemicals found in MoLE targeting Estrogen Receptor-alpha (ER-&amp;alpha;) and assess effects of MoLE administration on dam&amp;#39;s and fetal brain tissues and placenta, during gestational stress. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Phytochemical study of MoLE was determined using Gas Chromatography-Mass Spectrometry. Molecular docking technique was employed to predict aspects of interaction and binding affinities energy of bioactive phytocompounds in protein site of ER-&amp;alpha; using autodock tools. 30 apparently healthy pregnant Albino-Wistar rats were randomly placed into 6 groups of 5 rats per group and exposed to Chronic Unpredictable Stress (CUS) protocol for two weeks, as follows: Group I (water and normal rat chow &lt;em&gt;ad libitum&lt;/em&gt;), Group II (CUS protocol only), Group III (5 &lt;em&gt;mg/kg &lt;/em&gt;body weight/day of MoLE), Group IV (10 &lt;em&gt;mg/kg &lt;/em&gt;body weight/day of MoLE), Group V (CUS protocol +5 &lt;em&gt;mg/kg &lt;/em&gt;body weight/day of MoLE), Group VI (CUS protocol +10 &lt;em&gt;mg/kg &lt;/em&gt;body weight/ day of MoLE).&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;This study found that 1-Propanol, 3,3&amp;#39;-oxy bis- and 1, 2, 3-Trimethyldiazir-idine are most potent ligands for ER-&amp;alpha; among all 41 compounds. Photomicrograph examination of tissues from stressed rats showed mild to severe alterations in histology. Consumption of MoLE during chronic stress showed mild to moderate protective effects. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; These findings suggest that 1-Propanol, 3,3&amp;#39;-oxy bis- and 1, 2, 3-Trimethyldiaziridine can be further investigated for development of novel therapeutics.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Brain, Estrogens, Moringa, Phytochemicals, Receptors</keyword>
	<start_page>14</start_page>
	<end_page>23</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60598</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60598.pdf</pdf_url>
	<author_list><author><first_name>Odochi</first_name><middle_name></middle_name><last_name>O. Chukwu </last_name><suffix></suffix><affiliation>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike. Abakaliki, Ebonyi State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92273</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Cordilia</first_name><middle_name></middle_name><last_name>Iyare</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92274</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Anthony</first_name><middle_name></middle_name><last_name>C.U. Ezimah </last_name><suffix></suffix><affiliation>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike. Abakaliki, Ebonyi State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92275</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Albert</first_name><middle_name></middle_name><last_name>E. Okorocha </last_name><suffix></suffix><affiliation>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike. Abakaliki, Ebonyi State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92276</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nwaeze</first_name><middle_name></middle_name><last_name>G.  Konyefom</last_name><suffix></suffix><affiliation>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike. Abakaliki, Ebonyi State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92277</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nnaemeka</first_name><middle_name></middle_name><last_name>T. Asogwa </last_name><suffix></suffix><affiliation>Central Research Laboratory, University Road, Tanke Ilorin, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92278</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nancy</first_name><middle_name></middle_name><last_name>P. Igwe</last_name><suffix></suffix><affiliation>Department of Anatomy, Faculty of Basic Medical Sciences, College of Medicine, Alex Ekwueme Federal University, Ndufu-Alike Abakaliki, Ebonyi State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92279</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094094</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Comparison of Anticancer Effects between Platinum Levetiracetam and Platinum  Azidothymidine through the Expression of Biomarker Genes on Cancer Cell Lines</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The utilization of biomarkers is a way to assess the efficacy of recently created anticancer drugs. MiRNAs, telomerase, and Bcl-2 are extensively utilized as biomarkers for this purpose. This study aims to evaluate the comparison of the newly synthesized platinum compounds such as Platinum Azidothymidine (Pt-AZT) with Platinum Levetiracetam (Pt-Lev) on HepG2 cancer cell lines &lt;em&gt;via&lt;/em&gt; the biomarkers. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; In this study, cells were divided into four groups: Group A (HDF cells) were the normal negative control group, group B were HepG2 untreated cancer cells, and groups C and D were treated cancer cells with Pt-AZT and Pt-Lev, respectively. After evaluating the LC&lt;sub&gt;50&lt;/sub&gt; for the drugs by MTT test, the relative gene expression of the biomarkers was determined by qPCR.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The results showed a significant decrease for antiapoptotic genes including miRNA-21 (5.1&amp;plusmn;0.014), telomerase (0.56&amp;plusmn;0.48), Bcl-2 (0.41&amp;plusmn;0.276) in group D, whereas in group C was more than group D for miRNA-21 (6.0&amp;plusmn;0.141), telomerase (3.49&amp;plusmn;0.231), Bcl-2 (4.93&amp;plusmn;0.276) also there was a significant increase in miRNA-122 (33.97&amp;plusmn;0.04) in group D, whereas in group C was (28.36&amp;plusmn;0.007) and so lower than group D. Most of the investigated groups showed a significant difference (p&amp;lt;0.05). In addition, there were widespread apoptotic regions in Pt-Lev treatment compared to Pt-AZT. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;The advantages of using Pt-Lev were more powerful anticancer effects on biomarkers through inhibition of antiapoptotic and stimulation proapoptotic factors and also lower side effects and lower drug resistance than Pt-AZT; therefore, it can be considered a more effective anti-cancer therapy.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Bcl-2, Levetiracetam, miRNAs, Telomerase, Zidovudine</keyword>
	<start_page>24</start_page>
	<end_page>30</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60599</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60599.pdf</pdf_url>
	<author_list><author><first_name>Abdolreza</first_name><middle_name></middle_name><last_name>Sabokrouh</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>793</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nasim</first_name><middle_name></middle_name><last_name>Ghaffari</last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92268</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zahra</first_name><middle_name></middle_name><last_name>Karimi Tafreshi </last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92269</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Freshteh</first_name><middle_name></middle_name><last_name>Atabi</last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92270</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zohreh</first_name><middle_name></middle_name><last_name>Sharifi</last_name><suffix></suffix><affiliation>Blood Transfusion Research Center, High institute for Research and Education in Transfusion Medicine, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>640</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Seyyed Khalil</first_name><middle_name></middle_name><last_name>Shokouhi Mostafavi </last_name><suffix></suffix><affiliation>Department of Microbiology, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92324</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094096</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>The Role of Disulfide Bridges in the Interaction of E. coli -Derived Recombinant SCARB2 and EV-A71&#39;s Capsid</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Hand, Foot, and Mouth disease is an acute infectious disease caused by a group of enteroviruses, including &lt;em&gt;Coxsackievirus A16&lt;/em&gt; and &lt;em&gt;Enterovirus 71&lt;/em&gt;. EV-A71-causing disease can give rise to severe complications in children, leading to meningitis, encephalitis, and even death. A potential approach to prevent the virus spread is inhibiting the invasion of EV-A71 into target cells, thereby helping to prevent not only the spread of EV-A71 in the community but also lessen the risk of outbreaks. EV-A71 cell&amp;rsquo;s receptor, human scavenger receptor class B member 2, SCARB2, was used as a trap to gather the virus and limit its spreading. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; In this study, the recombinant receptor was expressed using &lt;em&gt;Escherichia coli &lt;/em&gt;(&lt;em&gt;E. coli&lt;/em&gt;)&lt;em&gt; &lt;/em&gt;system. SCARB2 proteins expressed from &lt;em&gt;E. coli&lt;/em&gt; BL21(DE3), and &lt;em&gt;E. coli&lt;/em&gt; SHuffle&lt;sup&gt;&amp;reg;&lt;/sup&gt; T7 Express were in inclusion bodies and subsequently refolded into soluble forms with recovery efficiencies of 57.57, and 82.2%, respectively. The presence of intramolecular disulfide bridges in the refolded SCARB2 was examined by SDS-PAGE in combination with Dithiothreitol (DTT). The two proteins were then utilized to evaluate the interaction with EV-A71 capsid by Indirect Enzyme-Linked Immunosorbent Assay (ELISA) at different pH levels to compare the adhesion efficiency. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The results showed that SCARB2 protein expressed from &lt;em&gt;E. coli&lt;/em&gt; SHuffle&lt;sup&gt;&amp;reg;&lt;/sup&gt; T7 Express with disulfide bond modifications had better adhesion to the viral capsid. Notably, when the medium pH was lowered to acidic levels, the binding efficiency of recombinant receptors to the viral capsid increased.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion: &lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;To our knowledge, this study reported for the first time the activity of SCARB2 under extreme pH conditions and also revealed the crucial role of disulfide bridges in the interaction with EV-A71&amp;rsquo;s capsid. This finding contributed to the strategy using recombinant SCARB2 as a viral trap.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Capsid proteins, Enterovirus infections, Escherichia coli (E. coli), Foot and mouth disease</keyword>
	<start_page>31</start_page>
	<end_page>38</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60600</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60600.pdf</pdf_url>
	<author_list><author><first_name>Hai-Vy</first_name><middle_name></middle_name><last_name>Vo-Nguyen </last_name><suffix></suffix><affiliation>Vietnam National University, Ho Chi Minh City, Vietnam</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92280</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Tran</first_name><middle_name></middle_name><last_name>Linh Thuoc</last_name><suffix></suffix><affiliation>Vietnam National University, Ho Chi Minh City, Vietnam</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>71801</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hieu</first_name><middle_name></middle_name><last_name>Tran-Van</last_name><suffix></suffix><affiliation>Vietnam National University, Ho Chi Minh City, Vietnam</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92282</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094089</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>The Induction of L-lysine-α-Oxidase from Trichoderma Harzianum Rifai by  Metabolic Products of Brevibacterium sp. and the Improvement of Its Isolation and  Purification Techniques </title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The enzyme L-Lysine-&amp;alpha;-oxidase from &lt;em&gt;Trichoderma harzianum&lt;/em&gt; Rifai is a promising anticancer, antifungal and antibacterial agent. Intensive exploring of its physico-chemical properties and possible ways of application requires sufficient amounts of the protein which in turn depends on good techniques of cultivation of the micro-organism producer, enzyme soft isolation and purification &amp;quot;and storage&amp;quot;.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; An improved method has been suggested for isolation and purification of the enzyme. A specific combination of column sorbents was adapted and gradient elution with sodium chloride was applied to elevate the yield of the enzyme. The inductive influence of Metabolic Products (MP) of the &lt;em&gt;Brevibacterium&lt;/em&gt; species, along with fungal metabolites of &lt;em&gt;Ulocladium &lt;/em&gt;sp. and &lt;em&gt;Trichoderma&lt;/em&gt; sp. was tested. The enzyme activity assay was based on the detection of oxidized dimethylbenzidine in a peroxidase reaction coupled with an L-lysine-&amp;alpha;-oxidase reaction. Some enzyme properties were additionally explored.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The upgraded technique of isolation and purification resulted in a yield of enzyme of about 79%. All strains of &lt;em&gt;Brevibacterium&lt;/em&gt; sp. proved to be potent enhancers of L-lysine-&amp;alpha;-oxidase activity and concomitant activities. The induced enzyme appeared to be less specific but more thermostable. Possible application scopes for the enzyme with modified properties are discussed. Phosphate buffer solution (pH=5.6) appeared to be the best one for long-term storage of the enzyme.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; A significant inducing effect of MP of &lt;em&gt;Brevibacterium&lt;/em&gt; sp. on L-lysine-&amp;alpha;-oxidase has been detected, and its isolation and purification techniques have been improved.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Antibacterial agent, Antifungal, Antineoplastic agents, Brevibacterium, L-lysine oxidase, Trichoderma, Trichoderma harzianum</keyword>
	<start_page>39</start_page>
	<end_page>46</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60601</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60601.pdf</pdf_url>
	<author_list><author><first_name>Irina</first_name><middle_name></middle_name><last_name>Smirnova</last_name><suffix></suffix><affiliation>T.T. Berezov Department of Biochemistry, Institute of Medicine, Peoples’ Friendship University of Russia (RUDN University), 117198 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92283</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Ekaterina</first_name><middle_name></middle_name><last_name>Neborak </last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92284</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Yuri</first_name><middle_name></middle_name><last_name>Shneyder</last_name><suffix></suffix><affiliation>Federal State Budgetary Institution All-Russian Plant Quarantine Center, 140150 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92287</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Ida</first_name><middle_name></middle_name><last_name>Bashkirova</last_name><suffix></suffix><affiliation>Federal State Budgetary Institution All-Russian Plant Quarantine Center, 140150 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92288</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Elena</first_name><middle_name></middle_name><last_name>Karimova</last_name><suffix></suffix><affiliation>Federal State Budgetary Institution All-Russian Plant Quarantine Center, 140150 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92289</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Daria</first_name><middle_name></middle_name><last_name>Baranova </last_name><suffix></suffix><affiliation>Free University of Bozen-Bolzano, 39100, Bolzano, Italy</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92291</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Maria</first_name><middle_name></middle_name><last_name>Ploskonos </last_name><suffix></suffix><affiliation>Department of Fundamental Chemistry, Astrakhan State Medical University, Astrakhan 414000, Russia</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92292</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Lyudmila</first_name><middle_name></middle_name><last_name>Gavrilyuk</last_name><suffix></suffix><affiliation>T.T. Berezov Department of Biochemistry, Institute of Medicine, Peoples’ Friendship University of Russia (RUDN  University), 117198 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92322</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Valeriy</first_name><middle_name></middle_name><last_name>Shkinev</last_name><suffix></suffix><affiliation>Vernadsky Institute of Geochemistry and Analytical Chemistry, 119991 Moscow, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92323</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Victor</first_name><middle_name></middle_name><last_name>Larichev</last_name><suffix></suffix><affiliation>The Gamaleya National Research Center of Epidemiology and Microbiology, Moscow 123098, Russian Federation</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92286</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094091</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Antidiabetic Activity of Momordica charantia Extracts Through Incretin Pathway in  Streptozotocin-Nicotinamide Induced Diabetic Rat Depends on Dose Differences</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; This study addresses the increasing prevalence of type 2 Diabetes Mellitus (T2DM) and the need for alternative, cost-effective medications. The research problem focuses on the need to further study the dose effectiveness of &lt;em&gt;Momordica charantia&lt;/em&gt; Extracts (MCE) on T2DM parameters, including Glucagon-Like Peptide 1 (GLP-1), &lt;span style=&quot;color:black&quot;&gt;Dipeptidyl Peptidase 4&lt;/span&gt; (DPP-4), alpha glucosidase, glucosetransporter 5 (GLUT5), and pancreatic tissue histopathology.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The methodology employed an experimental research design with 30 Wistar rats divided into six groups, each receiving different inductions and doses. Parameters were measured using Elisa, and histological analysis of pancreatic tissue was conducted using HE staining.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The Kruskal-Wallis test revealed significant differences in each group for the GLP-1 (p=0.003). However, the DPP4 test suggested a lack of significant difference in each group (p=0.192), and the GLUT5 test showed insignificant changes between each group (p=0.119). The ANOVA analysis on alpha-glucosidase revealed no statistically significant differences among the groups (p=0.202). Additionally, a qualitative examination of the histological analysis of pancreatic tissue indicated an improvement in the condition of the pancreatic tissue.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; MCE can increase GLP-1 levels, lower DPP-4, lower alpha-glucosidase, and raise GLUT5. However, there are no significant differences between other groups and the morphology of pancreatic tissue in rat model T2DM at a dose of 300 &lt;em&gt;mg/kg.&lt;/em&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Dipeptidyl peptidase 4, Glucagon-like peptide 1, Momordica charantia extracts, Rats, Type 2 diabetes mellitus</keyword>
	<start_page>47</start_page>
	<end_page>55</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60602</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60602.pdf</pdf_url>
	<author_list><author><first_name>Muhammad</first_name><middle_name></middle_name><last_name>Fadhol Romdhoni </last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92303</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Muchsin</first_name><middle_name></middle_name><last_name>Doewes </last_name><suffix></suffix><affiliation>Department of Pharmacology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92304</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Soetrisno</first_name><middle_name></middle_name><last_name>Soetrisno </last_name><suffix></suffix><affiliation>Department of Obstetrics and Gynaecology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92305</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Ratih</first_name><middle_name></middle_name><last_name>Puspita Febrinasari </last_name><suffix></suffix><affiliation>Department of Pharmacology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92306</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094095</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Repellency Effects, Cytotoxicity Assessment and Chemical Compositions of Citrus  limon Seeds Extracts and Fractions Against Anopheles gambiae sl Mosquitoes</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background: &lt;/span&gt;&lt;/strong&gt;&lt;em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Citrus limon&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; seeds have limited exploration, compared to other parts. The increasing prevalence of mosquito menace prompted the investigation into the repellent effects of the seed n-hexane extract and fractions of &lt;em&gt;Citrus limon&lt;/em&gt; (Rutaceae) against adult &lt;em&gt;Anopheles gambiae sl&lt;/em&gt; mosquitoes. The cytotoxicity and chemical constituents of the 100% n-Hexane Fraction (HF) were also evaluated.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Successive extraction was done with cold-maceration using, n-hexane, Ethyl Acetate (EA) and methanol. The three solvent extracts were screened against &lt;em&gt;Anopheles gambiae sl&lt;/em&gt; mosquitos, using human bait method, at doses, 1.5, 2.5 and 5.0 &lt;em&gt;mg/ml&lt;/em&gt; and with Deet and acetone used as positive and negative controls respectively. The n-hexane extract was further fractionated with column chromatography. Ten fractions (100% n-hexane, 10, 20, 30, 40, 60, 80% EA in n-hexane, 100% EA, 50% methanol in EA, and 100% methanol) were collected, and all tested at a single optimized dose of 5 &lt;em&gt;mg/ml&lt;/em&gt; for 2 &lt;em&gt;hr&lt;/em&gt;. The cytotoxicity and the chemical constituents of HF were determined using brine shrimp lethality test and gas chromatography-mass spectrometry respectively. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; N-hexane extract and HF, both at 5 &lt;em&gt;mg/ml&lt;/em&gt;, showed the most protective effect of 97.52 and 89.40% respectively, compared with standard (Odomos Deet) 100% activity, with no significant difference (p&amp;gt;0.05) between the three. HF was toxic with LC&lt;sub&gt;50&lt;/sub&gt; values of 29.2354 &lt;em&gt;ppm&lt;/em&gt;. Thirty compounds representing 79.25% of HF were identified. Major compounds present in the fraction were heptadecanamine (8.31%), N-(3-methylbutyl) acetamide (7.89%), 2-ethyl- 1-hexanamine (6.65%). &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; This promising repellent activity further justified the traditional usage of &lt;em&gt;Citrus limon&lt;/em&gt; as mosquito repellent.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Anopheles, Citrus, Gas chromatography-mass spectrometry, Insect repellents</keyword>
	<start_page>56</start_page>
	<end_page>63</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60603</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60603.pdf</pdf_url>
	<author_list><author><first_name>Mukaram</first_name><middle_name></middle_name><last_name>Akintunde Adeniyi-Akee </last_name><suffix></suffix><affiliation>Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ibadan, Nigeria, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92307</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Kingsley</first_name><middle_name></middle_name><last_name>Adibe Mbachu </last_name><suffix></suffix><affiliation>Department of Chemistry, Faculty of Science, University of Ibadan, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92308</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Kolade</first_name><middle_name></middle_name><last_name>Ibrahim </last_name><suffix></suffix><affiliation>Department of Zoology, Faculty of Science, University of Ibadan, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92309</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Paul</first_name><middle_name></middle_name><last_name>Matthew Osamudiamen </last_name><suffix></suffix><affiliation>Department of Chemical Sciences, Bells University of Technology, Ota, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92310</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Olapeju</first_name><middle_name></middle_name><last_name>Oluyemisi Aiyelaagbe</last_name><suffix></suffix><affiliation>Department of Chemistry, Faculty of Science, University of Ibadan, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92311</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Sunday</first_name><middle_name></middle_name><last_name>Olakunle Idowu</last_name><suffix></suffix><affiliation>Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ibadan, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92312</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Olajire</first_name><middle_name></middle_name><last_name>Aremu Adegoke</last_name><suffix></suffix><affiliation>Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ibadan, Nigeria, Oyo State, Nigeria</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92313</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094093</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Isolation and Preliminary Characterization of a Novel scFv against SARS-CoV-2: an Experimental and Computational Analysis</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;Since the initial outbreak, the &lt;em&gt;SARS-CoV-2&lt;/em&gt; virus has continued to circulate and mutate, resulting in the emergence of new viral sublineages. Due to the lack of effective protection and therapeutic measures against these new variants, the virus is able to further evolve and diversify. This study aimed to screen a phage antibody library to identify monoclonal antibodies in single-chain variable fragment (scFv) format that target the Receptor Binding Domain (RBD) of different &lt;em&gt;SARS-CoV-2&lt;/em&gt; strains. The newly discovered scFv has the potential for use as a diagnostic or therapeutic option against &lt;em&gt;SARS-CoV-2&lt;/em&gt;.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The RBD protein was produced, purified, and used as an antigen during biopanning. Six rounds of panning enriched RBD-specific phages and the binding affinity of binders were monitored by polyclonal phage ELISA. Subsequently, monoclonal phage ELISA was employed to identify specific binders. After sequence confirmation, the reactivity of the isolated anti-RBD scFv was evaluated. Additionally, bioinformatics tools determined the interaction between selected scFv and &lt;em&gt;SARS-CoV-2&lt;/em&gt; strains.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The ELISA analysis demonstrated that the expressed RBD retains its structural integrity and effectively interacts with antibodies present in the sera of COVID-19 patients. Through screening a phage display library, a strong-binding scFv for RBD was discovered, which can effectively neutralize &lt;em&gt;SARS-CoV-2&lt;/em&gt; and its novel variants.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The findings of this study have led to the discovery of a novel scFv that effectively neutralizes &lt;em&gt;SARS-CoV-2&lt;/em&gt; strains, offering immense potential for research and therapy purposes.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Bioprospecting, COVID-19, Phage display library, Receptor binding domain, Single-chain antibodies</keyword>
	<start_page>64</start_page>
	<end_page>79</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60604</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60604.pdf</pdf_url>
	<author_list><author><first_name>Samaneh</first_name><middle_name></middle_name><last_name>Jahandar-Lashaki</last_name><suffix></suffix><affiliation>Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92316</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Safar</first_name><middle_name></middle_name><last_name>Farajnia</last_name><suffix></suffix><affiliation>Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1278</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Effat</first_name><middle_name></middle_name><last_name>Alizadeh </last_name><suffix></suffix><affiliation>Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92317</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Farzin</first_name><middle_name></middle_name><last_name>Seirafi</last_name><suffix></suffix><affiliation>Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92318</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Asghar</first_name><middle_name></middle_name><last_name>Tanoumand</last_name><suffix></suffix><affiliation>Department of Microbiology, Maragheh University of Medical Sciences, Maragheh, Maragheh, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92319</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mohammad Kazem</first_name><middle_name></middle_name><last_name>Hosseini</last_name><suffix></suffix><affiliation>Faculty of Sciences, Molecular Biology and Genetic, Istanbul University, Istanbul, Turkey</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92320</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094090</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Ethical Considerations Emerge from Artificial Intelligence (AI) in Biotechnology</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;The integration of Artificial intelligence (AI) in biotechnology presents significant ethical challenges that must be addressed to ensure responsible innovations. Key concerns include data privacy and security, as AI systems often handle sensitive genetic and health information, necessitating robust regulations to protect individuals&amp;#39; rights and maintain public trust. Algorithmic bias poses another critical issue; AI can reflect existing biases in training data, leading to inequitable healthcare outcomes. Transparency in AI decision-making is essential, as &amp;quot;black box&amp;quot; models hinder trust, especially in drug discovery and genetics. Ethical implications of genetic manipulation require careful scrutiny to define the limits of human intervention. Additionally, societal impacts must be considered to ensure equitable distribution of AI benefits, preventing the exacerbation of disparities. Engaging diverse stakeholders, including ethicists and policymakers, is vital in aligning these technologies with societal values. Ultimately, prioritizing ethics will allow us to harness AI and biotechnology&amp;#39;s potential while safeguarding human rights and promoting equity.&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Artificial intelligence, Biotechnology, Ethics</keyword>
	<start_page>80</start_page>
	<end_page>81</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60605</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60605.pdf</pdf_url>
	<author_list><author><first_name>Mahintaj</first_name><middle_name></middle_name><last_name>Dara</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92314</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Negar</first_name><middle_name></middle_name><last_name>Azarpira</last_name><suffix></suffix><affiliation>Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>672</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

