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<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Nanoparticles in Vaccine Development</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>125</FirstPage>
			<LastPage>134</LastPage>
			<ELocationID EIdType="pii">69152</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Hajizade</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Firouz</FirstName>
					<LastName>Ebrahimi</LastName>
<Affiliation>Department of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ali-Hatef</FirstName>
					<LastName>Salmanian</LastName>
<Affiliation>Department of Plant biotechnology, National Institute for Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ayyoob</FirstName>
					<LastName>Arpanaei</LastName>
<Affiliation>Department of Industrial and Environmental Bio-technology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Jafar</FirstName>
					<LastName>Amani</LastName>
<Affiliation>Applied Microbiology Research Centre, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5155-4738</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Vaccination has greatly improved human health. Despite of all improvements in this field, there is not an efficient vaccine for many diseases, and of the available ones, some could not produce a long-term immunity. Recently, there have been many researches on the applicability of nanostructures as an efficient system for vaccine delivery, and the initial results have been promising. Their potential adjuvanticity, capability of the stimulation of both humoral and cellular immunity responses, more stability in environmental conditions, possible targeted vaccine delivery, the need for low quantity of proteins (in the case of subunit vaccines), etc., are of the main reasons that this area has gained many interests. Here, we try to review the main nanostructures that could be act as a delivery vehicle in vaccine delivery.</Abstract>
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			<Param Name="value">Nanovaccines</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Vaccine development</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nanoparticles</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Vaccine Delivery</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69152_35ea0e6a8aa9e41d3c1d8377536ec381.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Identification and Distribution of Anaerobic Responsive Elements (AREs) in Genes Functional Categorization of Arabidopsis thaliana</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>135</FirstPage>
			<LastPage>141</LastPage>
			<ELocationID EIdType="pii">69153</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ehsan</FirstName>
					<LastName>Sadeghnezhad</LastName>
<Affiliation>Department of Plant Biology, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hossein</FirstName>
					<LastName>Askari</LastName>
<Affiliation>Department of Biotechnology, Faculty of New Technologies and Energy Engineering, Shahid Beheshti University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sattar</FirstName>
					<LastName>Soltani</LastName>
<Affiliation>Department of Biotechnology, Faculty of New Technologies and Energy Engineering, Shahid Beheshti University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Fatemeh</FirstName>
					<LastName>Honarvar</LastName>
<Affiliation>Department of Biology, Islamic Azad University, Damghan Branch, Damghan, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>The evolution of biota had been tightly linked with formation of atmospheric di-oxygen (O2).Since the shift from anaerobic to aerobic life results in reprogramming gene expression through the regulatory interactions between transcription factors and their target sequences, the anaerobic responsive elements (AREs). The purpose of this study is to consider AREs; the most frequent and divergent motif in comparison to eighty four plant cis-regulatory elements, in order to clarify their biological function in &lt;em&gt;Arabidopsis thaliana&lt;/em&gt;. A genome wide survey revealed the frequency, occurrence number and positional state of each anaerobic element in &lt;em&gt;Arabidopsis&lt;/em&gt; genome. The evidence was obtained that among all AREs, TTCCCTGTT, (A/C/G)AAAAACAAA and AGCAGC &lt;em&gt;in silico&lt;/em&gt; discovered elements, are noteworthy responsive elements in &lt;em&gt;Arabidopsis&lt;/em&gt;. In addition to, our data suggest that the evolutionary process of anaerobic responsive elements may have been directed toward gradual decrease in occurrence numbers of AREs and gradual increase of their ineffectiveness in &lt;em&gt;Arabidopsis&lt;/em&gt; genome. We also classified &lt;em&gt;Arabidopsis&lt;/em&gt; genes according to existence of ARE elements in promoter regions of them to seven main groups including expression, primary metabolism, secondary metabolism, signaling, growth and development, stress and misc.</Abstract>
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			<Param Name="value">Anaerobic Response Element</Param>
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			<Object Type="keyword">
			<Param Name="value">Cis-Regulatory Element</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Gene expression</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Positional Significant Element</Param>
			</Object>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69153_edaea92115915fd2075b53190068f221.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>In Silico Design of a Multimeric Polytope as a Highly Immunogenic DNA Vaccine Against Human Cytomegalovirus</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>143</FirstPage>
			<LastPage>153</LastPage>
			<ELocationID EIdType="pii">69154</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Elaheh</FirstName>
					<LastName>Sabbaghian</LastName>
<Affiliation>Department of Molecular and Cell Biology, Faculty of Basic Science, University of Mazandaran, Babolsar, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Fatemeh</FirstName>
					<LastName>Roodbari</LastName>
<Affiliation>Department of Molecular and Cell Biology, Faculty of Basic Science, University of Mazandaran, Babolsar, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Rafiei</LastName>
<Affiliation>Molecular and Cell Biology Research Center, Hemoglubinopathy Institute, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Jafar</FirstName>
					<LastName>Amani</LastName>
<Affiliation>Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-5155-4738</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Human cytomegalovirus is one of the most common pathogenic viruses all over the world. In congenital infection leads to neurologic severe disorders and even death of fetus and in individuals with immunosuppression may also cause severe clinical symptoms. Multiple evidence indicate that among several strategies, epitope-based vaccine (EVs) that can induce both humoral and cellular immunity responses, are the most important and have numerous potential profits. In this study, we select the viral surface glycoprotein B and phosphoprotein 65 and 150 with the highest antigenic and immunogenic properties, that have the most important role in induce cellular and humoral immune responses. Bioinformatics tools, as a standard and developed approaches use for epitope mapping. Epitope discovery greatly accelerate by in silico prediction methods with in vitro and in vivo verification. Bioinformatics methods and epitopes identification algorithms were used in order to selection of cytomegalovirus immunodominant epitopes, detection of each epitope antigenicity and design chimeric gene construct. The chimeric protein showed high antigenicity in vaxiJen analysis. Also further immunoinformatic analyses in order to predict the discontinuous and continuous B and T cell epitopes and MHC binding peptides affinity were used. The study results show that protein structures were suitable. Therefore it can be expected that construct is proper subject for practical experiments and stimulus for humoral and cellular immune responses.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Cytomegalovirus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Polytope DNA Vaccine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">In silico Study</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Epitope Maping</Param>
			</Object>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69154_3fdbfe846a9b58451c9a4803e77336a4.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Improvement of Thermal Stability of DFPase by In silico Methods</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>155</FirstPage>
			<LastPage>159</LastPage>
			<ELocationID EIdType="pii">69155</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Mirzaei</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ali Mohammad</FirstName>
					<LastName>Latifi</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8952-5174</Identifier>

</Author>
<Author>
					<FirstName>Rahim</FirstName>
					<LastName>Jafari</LastName>
<Affiliation>Department of Nanobiotechnology, Faculty of Bio-logical Sciences, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Efficiency of enzymes which are used in industrial or environmental applications is highly dependent on their thermal stability. In this study, the stability of DFPase has been evaluated after introducing disulfide bonds to the structure. The results obtained from a series of protein design software were subjected to molecular dynamics simulation at different temperature to test the performance of such combinatorial procedure. Amount several designs, mutation M5 showed desirable thermostability via molecular dynamics simulation and normal mode analysis. As it clearly depicted, such in silico structural investigations would be resulted in reducing the numerous choices of experimental options as it was undergone a series of computational evaluation previously.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Rational Design</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DFPase</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Enzyme Stability</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Molecular Dynamics Simulation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nor-mal Mode Analysis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69155_cdde3d4e508d041741794da623dcb393.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Biodecolorization of Textile Effluents by Autochthonous Fungi</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>161</FirstPage>
			<LastPage>165</LastPage>
			<ELocationID EIdType="pii">69156</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Mazaheri Tehrani</LastName>
<Affiliation>Nuclear Biotechnology Laboratory, Nuclear Science Research School, Nuclear Science and Technology Research Institute, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mahnaz</FirstName>
					<LastName>Mazaheri Assadi</LastName>
<Affiliation>Center of Biotechnology, Iranian Research Organization for science and Technology, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hamid</FirstName>
					<LastName>Rashedi</LastName>
<Affiliation>Biotechnology Group, School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Textile effluents contain different kinds of chemical dyes and many mutagenic and carcinogenic substances. Discharge of these effluents into terrestrial and aquatic ecosystems causes harmful effects. In this research, decolorization of a textile effluent by nineteen different strains of fungi was investigated. Removal activity of dyes was in order of Aspergillus&lt;em&gt; &gt; Rhizopus &gt; Fuzarium &gt; Penicillium &gt; Saccharomyces&lt;/em&gt;. The selected fungal strain was capable of decolorizing textile effluent at original pH of effluent (8.5- 9) by adding 0.6 and 0.2 g/L of sucrose and NH&lt;sub&gt;4&lt;/sub&gt;Cl as additional carbon and nitrogen sources respectively at 30&lt;sup&gt;ᵒ&lt;/sup&gt;C. 98 % of dyes were absorbed from effluent during the exponential growth phase in the presence of a biodegradable substrate such as sucrose under shake flask conditions. Dyes strongly bound to the fungal biomass required extraction with methanol for their removal. The dyes pigment yellow (PY 74) and reactive blue (RB 38) were totally decolorized after 6 days at initial concentration of 250 ppm by terrestrial &lt;em&gt;Aspergillus&lt;/em&gt; &lt;em&gt;niger&lt;/em&gt;.</Abstract>
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			<Param Name="value">Biodecolorization</Param>
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			<Object Type="keyword">
			<Param Name="value">Textile Effluent</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Carcinogen</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Aspergillus niger</Param>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69156_a302e3f3e891a1202046b6046d9bc5b8.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effects of Different Concentrations of 2, 4-D and Kinetin on Callogenesis of Taxus Brevifolia Nutt.</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>167</FirstPage>
			<LastPage>170</LastPage>
			<ELocationID EIdType="pii">69158</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ramin</FirstName>
					<LastName>Karimian</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4968-7195</Identifier>

</Author>
<Author>
					<FirstName>Mehrdad</FirstName>
					<LastName>Lahouti</LastName>
<Affiliation>Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Javad</FirstName>
					<LastName>Davarpanah</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>&lt;em&gt;Taxus&lt;/em&gt; is an endangered plant which is the only commercial source of paclitaxel, which is used for treatment of ovary and breast cancer. As production of this valuable drug is a destructive process, other alternatives should be considered for its sustainable production. Plant tissue and cell culture is a promising method for production of secondary metabolites. In order to optimize yew callus culture effects of 16 combinations of two plant growth regulators, 2, 4 dichlorophenoxyacetic acid (0, 0.5, 1 and 1.5 mg/L) and Kinetin (0, 0.1, 0.5 and 1 mg/L) on callogenesis of &lt;em&gt;Taxus brevifolia&lt;/em&gt; twig explants were studied. Considering growth criteria, fresh weight (33.5 mg), dry weight (3.88 mg) and callogenesis ratio (1.45), based on statistical analysis the best plant growth regulators combination for induction and growth of callus of twig explants was appeared to be 1.5 mg/L of 2, 4- dichlorophenoxyacetic acid and 0.1 mg/L of Kinetin.</Abstract>
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			<Param Name="value">Callus</Param>
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			<Object Type="keyword">
			<Param Name="value">Callogenesis</Param>
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			<Object Type="keyword">
			<Param Name="value">PGRs</Param>
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			<Object Type="keyword">
			<Param Name="value">2</Param>
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			<Object Type="keyword">
			<Param Name="value">4-D</Param>
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			<Object Type="keyword">
			<Param Name="value">Kinetin</Param>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69158_54d4a7482b7342bb1abba0e55c521183.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Simultaneous determination of Zinc and Lead in blood samples by Differential Pulse Polarography</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>171</FirstPage>
			<LastPage>174</LastPage>
			<ELocationID EIdType="pii">69160</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Fatemeh</FirstName>
					<LastName>Abolhasani</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Ali</FirstName>
					<LastName>Amani</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hossein</FirstName>
					<LastName>Aghamollaei</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Mirzaei</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ali Mohammad</FirstName>
					<LastName>Latifi</LastName>
<Affiliation>Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8952-5174</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>09</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>In present study we determine the Zinc and Lead levels in human blood samples by differential pulse polarography under optimum experimental conditions (pH=7.5, Scan rate=5mV/S and pulse amplitude=50mV) the polarographic reduction peaks of Zn and Pb were examinedin the -0.72 V and-0.15 respectively. The zinc and lead content can be determined by in comparison with their standard solutions. According to the obtained results differential pulse polarography is more reliable, rapid and sensitive method for determination of zinc and lead levels in the blood than atomic absorption spectroscopy.</Abstract>
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			<Param Name="value">Blood</Param>
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			<Object Type="keyword">
			<Param Name="value">Differential Pulse Polarography</Param>
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			<Param Name="value">zinc</Param>
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			<Object Type="keyword">
			<Param Name="value">Lead</Param>
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<ArchiveCopySource DocType="pdf">https://www.biotechrep.ir/article_69160_826c468eaa57e481357a5b9416513790.pdf</ArchiveCopySource>
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