<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>International Journal of Radiation Research</title>
<title_fa>نشریه پرتو پژوه</title_fa>
<short_title>Int J Radiat Res</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ijrr.com</web_url>
<journal_hbi_system_id>79</journal_hbi_system_id>
<journal_hbi_system_user>journal79</journal_hbi_system_user>
<journal_id_issn>2322-3243</journal_id_issn>
<journal_id_issn_online>2345-4229</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/ijrr</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>1394</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2015</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<volume>13</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Evaluation of MTT and Trypan Blue assays for radiation-induced cell viability test in HepG2 cells</title>
	<subject_fa>Radiation Biology</subject_fa>
	<subject>Radiation Biology</subject>
	<content_type_fa>تحقيق بديع</content_type_fa>
	<content_type>Original Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p dir=&quot;ltr&quot; style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&amp;nbsp;Cell viability is an important factor in radiation therapy and thus is a method to quantify the effect of the therapy. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The viability of human hepatoma (HepG2) cells exposed to radiation was evaluated by both the MTT and Trypan blue assays. The cells were seeded on 96 well-plates at a density of 1 x 10&lt;sup&gt;4 &lt;/sup&gt;cells/well, incubated overnight, and irradiated with 1-100 Gy. &lt;strong&gt;Results:&lt;/strong&gt; The cell viability was decreased in a dose- and time- dependent manner when using the Trypan blue assay, but no significant changes in the response to dose could be detected using the MTT assay. It indicated that the MTT assay was not efficient at a cell density of 1 x 10&lt;sup&gt;4 &lt;/sup&gt;cells/well on 96 well-plates to determine cell viability. Subsequently, the relationship between cell viability and lower cell density (1 x 10&lt;sup&gt;3&lt;/sup&gt;, 3 x 10&lt;sup&gt;3&lt;/sup&gt;, and 5 x 10&lt;sup&gt;3&lt;/sup&gt; cells/well) was investigated. A cell density of 1 x 10&lt;sup&gt;3 &lt;/sup&gt;was found to be the most effective when using the MTT assay. Results show that the cell density is most important when using the MTT assay in 96 well-plates to follow in radiation effects. Furthermore, the radiation-induced cell viability dependent on cell density was confirmed by using the traditional Clonogenic assay. &lt;strong&gt;Conclusion:&lt;/strong&gt; Our results suggest that the MTT and Trypan blue assays are rapid methods to detect radiation-induced cell viability of HepG2 cells in about 3 days as compared with 14 days of assay time in the Clonogenic assay. To obtain accurate cell viability measures using both rapid assays, an incubation time of at least 3 days is needed after irradiation.&lt;/p&gt;

&lt;p&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Cell viability, clonogenic assay, HepG2 cell, MTT, radiation, trypan blue</keyword>
	<start_page>331</start_page>
	<end_page>335</end_page>
	<web_url>http://ijrr.com/browse.php?a_code=A-10-1-580&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>D.M.</first_name>
	<middle_name></middle_name>
	<last_name>Chung</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></email>
	<code>790031947532846007635</code>
	<orcid>790031947532846007635</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Korea Atomic Energy Research Institute</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>J.H.</first_name>
	<middle_name></middle_name>
	<last_name>Kim</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></email>
	<code>790031947532846007636</code>
	<orcid>790031947532846007636</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Korea Atomic Energy Research Institute</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Jin Kyu</first_name>
	<middle_name></middle_name>
	<last_name>Kim</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>jkkim@kaeri.re.kr</email>
	<code>790031947532846007637</code>
	<orcid>790031947532846007637</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Korea Atomic Energy Research Institute</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
