<?xml version="1.0" encoding="utf-8"?>
			<journal>
			<title>Nanomedicine Journal</title>
			<title_fa></title_fa>
			<short_title>Nanomed J</short_title>
			<subject>Medical Sciences</subject>
			<web_url>https://nmj.mums.ac.ir/</web_url>
			<journal_hbi_system_id>0</journal_hbi_system_id>
			<journal_hbi_system_user></journal_hbi_system_user>
			<journal_id_issn>2322-3049</journal_id_issn>
			<journal_id_issn_online>2322-5904</journal_id_issn_online>
			<journal_id_pii></journal_id_pii>
			<journal_id_doi></journal_id_doi>
			<journal_id_iranmedex></journal_id_iranmedex>
			<journal_id_magiran></journal_id_magiran>
			<journal_id_sid></journal_id_sid>
			<journal_id_nlai></journal_id_nlai>
			<journal_id_science></journal_id_science>
			<language>en</language>
			<pubdate>
				<type>jalali</type>
				<year>2024</year>
				<month>7</month>
				<day>1</day>
			</pubdate>
			<pubdate>
				<type>gregorian</type>
				<year>2024</year>
				<month>7</month>
				<day>1</day>
			</pubdate>
			<volume>11</volume>
			<number>3</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>A review of topical micro- and nanoemulsions for common skin diseases</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Review Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Microemulsions (MEs) and nanoemulsions (NEs) are dispersions of two immiscible liquids which are usually transparent/translucent. Several reports are available on uses of MEs/NEs to increase efficacy of the loaded active ingredient(s) in topical dosage forms. This review aims to describe brief applications of MEs/NEs in common skin diseases as well as skincare products. Advantages of MEs/NEs in comparison with the traditional bulk form, including their improved efficacy and safety, have been discussed to highlight the importance of use of such delivery systems. The review briefs mechanism of action of MEs/NEs in enhancing delivery of the cargo. Furthermore, applications of MEs/NEs in common skin diseases including infectious rashes, pigmentation disorders (hyperpigmentaion and hypopigmentation), wound healing, skin cancers and scaling patches and plaques/papulosquamous disorders (psoriasis, atopic dermatitis and acne) have been discussed. MEs/NEs in skin care products have also been reviewed here.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Infections, Microemulsion, Nanoemulsion, Skin care, Skin, Topical, Skin disease  </keyword>
				<start_page>205</start_page>
				<end_page>221</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24356.html</web_url>
			<author_list><author>
				<first_name>Yaser</first_name>
				<middle_name></middle_name>
				<last_name>Yousefpoor</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>yousefpoory1@gmail.com</email>
				<code>106825</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Biotechnology, School of Paramedical Sciences, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran|Research Center of Advanced Technologies in Medicine, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Hadi</first_name>
				<middle_name></middle_name>
				<last_name>Baharifar</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>baharifar.h@gmail.com</email>
				<code>106826</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Nanotechnology, Applied Biophotonics Research Center, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Seyedeh Sara</first_name>
				<middle_name></middle_name>
				<last_name>Esnaashari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>sara.esnaashari@gmail.com</email>
				<code>106827</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Nanotechnology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Fatemeh</first_name>
				<middle_name></middle_name>
				<last_name>Gheybi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>gheybi.f@gmail.com</email>
				<code>106828</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Biotechnology and Nanotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran|Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohsen</first_name>
				<middle_name></middle_name>
				<last_name>Mehrabi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mm.nanotech@gmail.com</email>
				<code>106829</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Nanotechnology, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mahmood</first_name>
				<middle_name></middle_name>
				<last_name>Osanloo</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>osanloo_mahmood@yahoo.com</email>
				<code>106830</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Fasa University of Medical Sciences, Fasa, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Vahid</first_name>
				<middle_name></middle_name>
				<last_name>Shirshahi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>shirshahi@gmail.com</email>
				<code>106831</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Medical Nanotechnology, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Amir</first_name>
				<middle_name></middle_name>
				<last_name>Amani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>amani76@gmail.com</email>
				<code>106824</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran</affiliation>
				<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></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 state of the art metal nanoparticles in drug delivery systems: A comprehensive review</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type>Review Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[There has been a growing curiosity and enthusiasm surrounding recent advancements in nanotechnology, electromagnetism, and optics. This interdisciplinary collaboration encompasses fields such as nanomaterials, nanoelectronics, and nanobiotechnology, which often overlap in their applications. One area that has attracted significant attention is the use of metal nanoparticles (MNPs), which has resulted in notable advancements in medicine. MNPs hold the promise of significantly boosting drug delivery efficacy, reducing unwanted side effects, and enhancing delivery precision. They also have applications in diagnostics, the development of biocompatible materials, and the exploration of nutraceuticals. Using metal nanoparticles in drug delivery provides benefits such as increased stability, prolonged circulation time, enhanced distribution, and precise targeting. The field of nanobiotechnnolgy has facilitated the creation of eco-friendly approaches, referred to as green synthesis, for the production of MNPs. MNPs offer improved stability and targeted release in drug delivery, while also providing a more sustainable alternative to chemical synthesis. This review aims to address the challenges and prospects of utilizing MNPs in drug delivery, with a specific focus on sustainable approaches for fabricating and modifying metal nanocarriers. It also explores the application of various MNPs in drug delivery systems (DDSs). ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Antibacterial activity, Drug delivery systems, Green synthesis, Metallic nanoparticles, Nanosystems</keyword>
				<start_page>222</start_page>
				<end_page>249</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24171.html</web_url>
			<author_list><author>
				<first_name>Mohammad Hossein</first_name>
				<middle_name></middle_name>
				<last_name>Karami</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>karami.polymerphd@gmail.com</email>
				<code>105966</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Chemistry, Amirkabir University of Technology, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Majid</first_name>
				<middle_name></middle_name>
				<last_name>Abdouss</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>phdabdouss44@aut.ac.ir</email>
				<code>105967</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Chemistry, Amirkabir University of Technology, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Behrooz</first_name>
				<middle_name></middle_name>
				<last_name>Maleki</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>b.maleki@umz.ac.ir</email>
				<code>105968</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran</affiliation>
				<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></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>Equisetum ramosissimum desf-assisted green synthesis of cerium oxide nanoparticles: Characterization and antimicrobial potential against cariogenic Streptococcus mutans</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): This study explores the biosynthesis of cerium oxide nanoparticles using aqueous extract of Equisetum ramosissimum Desf as both a reducing and stabilizing agent and evaluates its antibacterial activity against cariogenic streptococcus mutans.Materials and Methods: Cerium oxide nanoparticles were synthesized and characterized using UV-VIS, FTIR, XRD, FESEM, EDX, DLS, and Zeta potential analyses. Antibacterial activity against S. mutans was evaluated via the agar well diffusion method.Results: Optical analysis revealed an absorption peak within the 307–314 nm range, suggesting a bandgap value of 3.04–3.37 eV. FTIR analysis confirmed Ce-O stretching vibrations and bonds with phytochemicals from the E.ramosissimum Desf extract on the nanoparticle surfaces. XRD showed a cubic fluorite structure with a crystalline size of 5.99–11.74 nm. FESEM imaging depicted uniform, nearly spherical nanoparticles with estimated sizes ranging from 22 to 31 nm. The EDX spectrum indicated the presence of cerium and oxygen signals, affirming the purity of the fabricated nanoparticles. DLS results corroborated the average nanoparticle size (28.11–54.61 nm), in agreement with FESEM findings and zeta potential values (-11.4 to 29.2 mV) indicating moderate stability of nanoparticles. Antibacterial assays showed significant inhibition zones (20–32 mm) against S. mutans.Conclusion: The green-synthesized CeO2-NPs exhibit promising antimicrobial efficacy against S. mutans, suggesting their potential for dental applications. Furthermore, employing plant extract for cerium salt reduction presents a promising avenue for reducing the environmental impact associated with chemical synthesis. ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Ceric oxide, Dental Caries, Nanoparticles, Phytochemicals Streptococcus mutans</keyword>
				<start_page>250</start_page>
				<end_page>267</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24160.html</web_url>
			<author_list><author>
				<first_name>Mansour</first_name>
				<middle_name>Hadi</middle_name>
				<last_name>Mohammed</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mansour.mohammed@hmu.edu.krd</email>
				<code>105915</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Pedodontic,Orthodontic , Preventive department, college of dentistry, Hawler Medical University, Erbil 44001, Iraq</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Bayan</first_name>
				<middle_name>Abdullah</middle_name>
				<last_name>Hassan</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>bayan.hassan@hmu.edu.krd</email>
				<code>105916</code>
				<coreauthor>No</coreauthor>
				<affiliation>Pedodontic,Orthodontic , Preventive department, college of dentistry, Hawler Medical University, Erbil 44001, Iraq</affiliation>
				<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></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>Plant-mediated synthesis of selenium nanoparticles using Caccinia macranthera extract and assessment of their antioxidant and cytotoxic properties</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): The current study aims to achieve synthesized selenium nanoparticles (Se-NPs) through a green chemistry route using sodium selenite (Na2SeO3) and Caccinia macranthera (C. macranthera) plant extract as stabilizing and reducing agents and to investigate the anticancer effects of the synthesized NPs.Materials and Methods: The outcomes affirmed the successful production of the synthesized Se-NPs, as their spherical framework and particle size scale of 54 to 60 nm were exhibited by the images of FESEM/PSA. This spherical frame was also detected in the TEM images at a size of 11.5 nm. The inhibitory effect of Se-NPs was investigated on the proliferation of human liver cancer cells (Huh-7). Additionally, the effect of Se-NPs was studied on the expression of the implicated genes throughout the cell apoptosis using the Real-Time PCR technique. Also, the percentage of apoptotic cells was obtained using Annexin V/PI and DAPI kits. Finally, flow cytometry was exerted to determine the amount of produced ROS. Results: The results of laboratory studies showed that Se-NPs can significantly reduce the survival of Huh-7 cancer cells in dosage and time-reliant behavior, while they have very little toxicity on normal L929 cells. Also, Se-NPs were able to induce apoptosis in liver cancer cells, which was observed along with the increased expression of Bax, p53, Caspase3, and Caspase 9 genes. In addition, Se-NPs increased the production of ROS in Huh-7 cells and led to an increase in oxidative stress in these cells. Conclusion: Therefore, these NPs can be used in clinical studies of liver cancer.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Antioxidants, Apoptosis, Caccinia macranthera plant, Cytotoxins, Selenium nanoparticles </keyword>
				<start_page>268</start_page>
				<end_page>279</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24132.html</web_url>
			<author_list><author>
				<first_name>Leili</first_name>
				<middle_name></middle_name>
				<last_name>Hosseinpour</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>hosseinpour.62@gmail.com</email>
				<code>105742</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Javad</first_name>
				<middle_name></middle_name>
				<last_name>Baharara</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>baharara78@gmail.com</email>
				<code>105743</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Saeed</first_name>
				<middle_name></middle_name>
				<last_name>Zaker Bostanabad</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>saeedzaker2@yahoo.com</email>
				<code>105744</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Biology, Parand Branch, Islamic Azad University, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Majid</first_name>
				<middle_name></middle_name>
				<last_name>Darroudi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>darroudim@mums.ac.ir</email>
				<code>105745</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Nuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, Iran|Department of Medical Biotechnology and Nanotechnology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<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></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>Preparation and In vitro release of Isoniazid and Rifampicin loaded nanoparticles</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Tuberculosis (TB) is one of the most common infectious diseases in the world and requires novel medications or existing ones should be improved.  Nanotechnology is a modern science that helps to avoid adverse reactions and resistance to drugs. The current regimen for standard therapy calls for routine administration of medications over six months. Since the noncompliance of patients and the emergence of drug-resistant strains, therapies become more challenging. The objective of the current study was to develop Isoniazid-Rifampicin-loaded (INH-RIF-NPs) nanoparticles to improve release properties and drug encapsulation efficiency.Materials and Methods: Box-Behnken Design (BBD) was used for optimizing the nanoparticles. Eudragit was used in the preparations in varying concentrations (1-2% w/v). The compatibility of the drug and excipients was shown. The existence of the nanoparticles was confirmed by the analytical results of the transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). Results: The optimized nanoparticles showed no drug-polymer interaction. The mean size of the INH-RIF-NPs was around 112±8.73 nm, and they were sphere-like, smooth, fairly uniform in size, and well-dispersed, and entrapment efficiencies were high at 98.7±0.68%. Drug release was slow and sustained with 66.91% INH cumulative release and 80.06 of RFP after 24 hr. Conclusion: Significant drug uptake with higher encapsulation efficiency, uniform size, good dispersion, and prolonged release characteristics are all present in INH-RIF-NPs. This suggests the existence of a delivery system capable of effectively encapsulating and delivery of combined drug formulation in polymeric nanoparticles.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Drug Delivery system, Isoniazid, Mycobacterium tuberculosis, Nanoparticles, rifampicin</keyword>
				<start_page>280</start_page>
				<end_page>293</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24257.html</web_url>
			<author_list><author>
				<first_name>Monika</first_name>
				<middle_name></middle_name>
				<last_name>Targhotra</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>monatraghotra@gmail.com</email>
				<code>106336</code>
				<coreauthor>No</coreauthor>
				<affiliation>NDDS Research Laboratory, Department of Pharmaceutics, Delhi Institute of Pharmaceutical Sciences and Research, DPSR-University, Pushp Vihar Sec-3, MB Road, New Delhi, 110017, India</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Meenakshi</first_name>
				<middle_name>Kanwar</middle_name>
				<last_name>Chauhan</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>meenakshikanwar@yahoo.com</email>
				<code>106335</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>NDDS Research Laboratory, Department of Pharmaceutics, Delhi Institute of Pharmaceutical Sciences and Research, DPSR-University, Pushp Vihar Sec-3, MB Road, New Delhi, 110017, India</affiliation>
				<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></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>Green synthesis, characterization, and evaluation of antimicrobial and antioxidant activities of CuO, Co3O4, and CuO-Co3O4 Nano system using Moringa stenopetala plant leaf extracts</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): The purpose of this study was to synthesize copper oxide nanoparticles (CuO NPs), cobalt oxide nanoparticles (Co3O4 NPs), and CuO-Co3O4 nano system using Moringa stenopetala plant leaf extract. These nanoparticles were specifically developed for their antioxidant and antibacterial properties.Materials and Methods: The nanoparticles were synthesized by a green synthesis approach using M. stenopetala leaf extract. Comprehensive characterization using spectroscopic techniques such as X-ray diffraction (XRD), UV-visible spectroscopy, scanning electron microscopy (SEM), Fourier transform infrared (FT-IR), and thermogravimetric analysis (TGA) was executed.Results: UV-Vis analysis revealed an energy bandgap of 3.32 eV for CuO NPs, 3.36 eV for Co3O4 NPs, and 3.66 eV for CuO-Co3O4 nano system. XRD analysis revealed that CuO NPs have a monoclinic crystal structure with an average crystallite size of 11.59 nm, whereas Co3O4 NPs have a cubic crystal structure with an average crystallite size of 12.25 nm. The CuO-Co3O4 nano system exhibited an average crystal size of 9.53 nm. The SEM images showed inhomogeneous composition and large granular particles of CuO NPs, inhomogeneous cubic shape and size with encapsulation and hydrogen bonding aggregation of Co3O4 NPs, and particle heterogeneity. The CuO-Co3O4 nano system. FT-IR analysis confirmed the presence of bioactive molecules such as flavonoids, tannins, terpenoids, steroids, glycosides, saponins, and phenols that actively participate in the synthesis process.Conclusion: The synthesized CuO-Co3O4 nano system showed superior inhibitory effects against the selected bacterial strains compared to CuO NPs and Co3O4 NPs. Furthermore, they showed excellent antioxidant activity. These results highlight the significant potential of CuO-Co3O4 nano system for a wide range of applications due to their remarkable bacterial inhibition and radical scavenging properties. ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Antimicrobial activity, Antioxidant activity, Bacteria, Biosynthesis, Nano system, Phytochemicals</keyword>
				<start_page>294</start_page>
				<end_page>310</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24161.html</web_url>
			<author_list><author>
				<first_name>Desalegn</first_name>
				<middle_name>Tesfa</middle_name>
				<last_name>Tefera</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dtesfa30@gmail.com</email>
				<code>105917</code>
				<coreauthor>No</coreauthor>
				<affiliation>Adama Science and Technology University, School of Applied Natural Science, Department of Applied Chemistry, Adama, Ethiopia</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Tegene</first_name>
				<middle_name>Desalegn</middle_name>
				<last_name>Zeleke</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>tegened@yahoo.com</email>
				<code>105918</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Adama Science and Technology University, School of Applied Natural Science, Department of Applied Chemistry, Adama, Ethiopia</affiliation>
				<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></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>Preparation and transfection evaluation of modified multifunctional envelope-type nano device -DNA nanocomplexes based on low molecular weight protamine</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Gene therapy is a hopeful approach for treatment of a wide range of life threatening disease from infectious and inherited diseases to cancer. Multifunctional Envelope-type Nano Device (MEND) is a new carrier as non-viral genetic vector. Moreover, associating peptide structures with the nuclear localization signals (NLSs), which contains various functional groups enables them to condense DNA and specifically transfer genetic material to the nucleus.Materials and Methods: In this study, two forms of low molecular weight protamine (LMWP) were used for preparation of MEND carrier. The MEND carriers were then targeted with GE11 ligand to obtain T-MEND structure. The size distribution of the resulting nanoparticles, as well as their transfection efficiency and cytotoxicity, were investigated on the A549 cell line.Results: Results demonstrated that the size of polyplex carrier’s formulation by both peptides (VV45 and VV32) was below 200 nm and MEND formulations were between 200-300 nm. T-MEND formulations contained VV32 and VV45 peptides showed slightly higher transfection than similar MEND formulations. Also, MEND formulation showed increased transfection efficiency compared to similar PD complexes. The result of metabolic activity test showed that MEND lipopolyplex did not represent any remarkable cytotoxicity.Conclusion: It can be concluded that multifunctional carriers designed based on LMWP are considered as the safe carrier for gene delivery. Presence of protamine and targeted ligand in the nanoparticulate structure did not increase the risk of cytotoxicity of carriers. So, MEND and T-MEND lipoplexes showed low cytotoxicity and acceptable transfection efficiency at the level of PEI 25 kDa.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Cytotoxicity, Gene delivery, Protamine, Transfection</keyword>
				<start_page>311</start_page>
				<end_page>319</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24318.html</web_url>
			<author_list><author>
				<first_name>Leila</first_name>
				<middle_name></middle_name>
				<last_name>Gholami</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>lagholami86@gmail.com</email>
				<code>106636</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical 
Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Hassan</first_name>
				<middle_name></middle_name>
				<last_name>Zarei</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>zareih1@mums.ac.ir</email>
				<code>106633</code>
				<coreauthor>No</coreauthor>
				<affiliation>School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Fatemeh</first_name>
				<middle_name></middle_name>
				<last_name>Soltani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>soltanif@mums.ac.ir</email>
				<code>106634</code>
				<coreauthor>No</coreauthor>
				<affiliation>School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohammad</first_name>
				<middle_name></middle_name>
				<last_name>Ramezani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>ramezanim@mums.ac.ir</email>
				<code>106635</code>
				<coreauthor>No</coreauthor>
				<affiliation>Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Bizhan</first_name>
				<middle_name></middle_name>
				<last_name>Malaekeh-Nikouei</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>malaekehb@mums.ac.ir</email>
				<code>106632</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
				<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></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>Niosomal tannic acid drug delivery system: An efficient strategy against vancomycin-intermediate Staphylococcus aureus (VISA) infections</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Our study aimed to formulate a niosomal system for enhancing tannic acid’s antibacterial and antibiofilm activities against vancomycin-intermediate staphylococcus aureus (VISA). Materials and Methods: Niosomal tannic acid was formulated by the thin-film hydration technique, which their physicochemical attributes, including drug loading, particle size, zeta potential, morphology, encapsulation efficiency (EE%), polydispersity index (PDI), release profile, were evaluated. To investigate the cell viability of the prepared niosomes, the cytotoxicity effect was analyzed against the human foreskin fibroblast (HFF) cell line. Finally, the antibacterial and anti-biofilm activities of niosomal formulation were examined against VISA strains and compared tothe free drug.Results: Scanning electron microscopy images showed that the niosomal formulation incorporated tannic acid was homogeneous, spherical, and identical in size (151.9 nm). EE% and surface charge of the synthesized niosomes were 68.90% and -60 mV, respectively. The tannic acid-encapsulated niosomes showed a significant antibacterial potential in comparison with the free drug. Furthermore, niosomal tannic acid reduced the biofilm formation ability in all VISA strains and efficiently eradicated the formed bacterial biofilms at the same concentrations of the free drug.Conclusion: Niosomes, as vesicular-based nanoparticles, are known to be potent drug delivery vehicles due to numerous features such as non-toxicity, small size, sustained-release profile, and protection from pharmaceutical degradation. Niosomes have a high capacity to deliver wide range of antimicrobial agents, including natural compounds, which could be presented as a novel approach against bacterial infections, particularly VISA strains.Objective(s): Our study aimed to formulate a niosomal system for enhancing tannic acid’s antibacterial and antibiofilm activities against vancomycin-intermediate staphylococcus aureus (VISA). Materials and Methods: Niosomal tannic acid was formulated by the thin-film hydration technique, which their physicochemical attributes, including drug loading, particle size, zeta potential, morphology, encapsulation efficiency (EE%), polydispersity index (PDI), release profile, were evaluated. To investigate the cell viability of the prepared niosomes, the cytotoxicity effect was analyzed against the human foreskin fibroblast (HFF) cell line. Finally, the antibacterial and anti-biofilm activities of niosomal formulation were examined against VISA strains and compared tothe free drug.Results: Scanning electron microscopy images showed that the niosomal formulation incorporated tannic acid was homogeneous, spherical, and identical in size (151.9 nm). EE% and surface charge of the synthesized niosomes were 68.90% and -60 mV, respectively. The tannic acid-encapsulated niosomes showed a significant antibacterial potential in comparison with the free drug. Furthermore, niosomal tannic acid reduced the biofilm formation ability in all VISA strains and efficiently eradicated the formed bacterial biofilms at the same concentrations of the free drug.Conclusion: Niosomes, as vesicular-based nanoparticles, are known to be potent drug delivery vehicles due to numerous features such as non-toxicity, small size, sustained-release profile, and protection from pharmaceutical degradation. Niosomes have a high capacity to deliver wide range of antimicrobial agents, including natural compounds, which could be presented as a novel approach against bacterial infections, particularly VISA strains. ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Biofilm, Drug Delivery, Niosome, tannic acid, Vancomycin-intermediate Staphylococcus aureus (VISA)</keyword>
				<start_page>320</start_page>
				<end_page>331</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24162.html</web_url>
			<author_list><author>
				<first_name>Jaber</first_name>
				<middle_name></middle_name>
				<last_name>Hemmati</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>jaberhemmati@gmail.com</email>
				<code>105920</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran|Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohsen</first_name>
				<middle_name></middle_name>
				<last_name>Chiani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>m.chiani@gmail.com</email>
				<code>105921</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of NanoBiotechnology, Pasteur Institute of Iran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Babak</first_name>
				<middle_name></middle_name>
				<last_name>Asghari</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>bab.asghari@gmail.com</email>
				<code>105922</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Ghodratollah</first_name>
				<middle_name></middle_name>
				<last_name>Roshanaei</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>gh.roshanaei@umsha.ac.ir</email>
				<code>105923</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Sara</first_name>
				<middle_name></middle_name>
				<last_name>Soleimani Asl</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>sr_soleimani@yahoo.com</email>
				<code>105924</code>
				<coreauthor>No</coreauthor>
				<affiliation>Anatomy Department, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Morvarid</first_name>
				<middle_name></middle_name>
				<last_name>Shafiei</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dr.m.shafiei80@gmail.com</email>
				<code>105925</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mohammad</first_name>
				<middle_name>Reza</middle_name>
				<last_name>Arabestani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>mohammad.arabestani@gmail.com</email>
				<code>105919</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran|Infectious Disease Research Center, Hamadan University of Medical Sciences, Hamadan, Iran</affiliation>
				<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></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>Synthesis, characterization and investigation of biodistribution of dendrimer-amiloride nanoconjugate using single photon computed tomography technique in animal sample</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>مقاله پژوهشی</content_type_fa>
				<content_type>Research Paper</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Objective(s): Amiloride is a pyrazine compound that inhibits the reabsorption of sodium by blocking sodium channels in the cells of the renal cortex. It has demonstrated promising efficacy in the treatment of cancer in recent times. This study assessed the in vivo biodistribution of amiloride conjugated to dendrimer as a targeted agent utilizing SPECT imaging.Materials and Methods: The dendrimer was synthesised using polyethylene glycol and citric acid as precursors, and dicyclohexyl carbodiimide as a zero-order crosslinker. Amiloride was then conjugated to the dendrimer through the terminal amine group, forming an amide bond with the acidic group of the dendrimer. The synthetic particles were assessed by characterization techniques including FTIR, TEM, LC-Mass, and MAP. The response surface optimization method based on the core chemical was employed to achieve maximum labelling efficiency.  The ideal circumstances and biodistribution in the in vivo environment were assessed. Results: TThe characterization findings demonstrated the effective formation and linkage of the nanoconjugate. The Radiochemical purity (RCP) of the dendrimer-amiloride complexes with Technetium-99m, achieved under ideal conditions (28 minutes of incubation, 1.4 units of reduced agent, and 17.5 mg of dendrimer-amiloride), exceeds 90%. This demonstrates the considerable potential of dendrimer-amiloride in forming complexes with Technetium-99m. The results from imaging and biodistribution tests showed that 99mTc-dendrimer–amiloride had a high level of activity (7.8 %ID/g) at the tumor site. This was due to the increased expression of sodium channel. Conclusion: The favorable characteristics and conduct of the produced nanoprobe indicate its potential as an innovative tool for the advancement of radiopharmaceutical-based medication. Furthermore, it has the capacity to envision a broad spectrum of malignancies.]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Amiloride, Biodistribution, Dendrimer, SPECT imaging</keyword>
				<start_page>332</start_page>
				<end_page>341</end_page>
				<web_url>https://nmj.mums.ac.ir/article_24412.html</web_url>
			<author_list><author>
				<first_name>Sheida</first_name>
				<middle_name></middle_name>
				<last_name>Iranpour</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>dr.sh.iranpour@gmail.com</email>
				<code>107043</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Revolution Square, 16 Azar St, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Kimia</first_name>
				<middle_name></middle_name>
				<last_name>Roshani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>k_roshany@ymail.com</email>
				<code>107044</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Revolution Square, 16 Azar St, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Sepehr</first_name>
				<middle_name></middle_name>
				<last_name>Ashrafi</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>sepehrpharmacy@gmail.com</email>
				<code>107045</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Revolution Square, 16 Azar St, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Saeede</first_name>
				<middle_name></middle_name>
				<last_name>Zamani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>zamanisaeede4@gmail.com</email>
				<code>107048</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Medicinal Chemistry, School of Pharmacy and Pharmaceutical Sciences, Lorestan University of Medical Sciences, Khorramabad, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Seyedeh Sayta</first_name>
				<middle_name></middle_name>
				<last_name>Forouzeh Rafiei</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>seyedsyatia@gmail.com</email>
				<code>107046</code>
				<coreauthor>No</coreauthor>
				<affiliation>Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Revolution Square, 16 Azar St, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mehdi</first_name>
				<middle_name></middle_name>
				<last_name>Shafiee Ardestani</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email>shafieeardestani@gmail.com</email>
				<code>107047</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Revolution Square, 16 Azar St, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article>
			</articleset>
			</journal>