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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2017-03-25</publicationDate>
    
        <volume>14</volume>
        <issue>1</issue>

 
    <startPage>75</startPage>
    <endPage>82</endPage>

	 
      <doi>10.13005/bbra/2419</doi>
        <publisherRecordId>22119</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Cardiotoxicity and Hematoxicity of Sorafenib – Loaded  Nanoemulsion in Ehrlich Ascites Carcinoma &#8211; Bearing Mice</title>

    <authors>
	 


      <author>
       <name>Mayson H. Alkhatib</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Dunya A. Nori</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Maryam A. Al-Ghamdi</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Sorafenib (SOR), a chemotherapeutic agent, is a multikinase inhibitor that has a cardiotoxic and hematoxic effect which could limit its application in cancer therapy. In the current study, SOR was incorporated into a nanoemulsion (NE) containing flaxseed oil (SOR-NE) and its antitumor effect was examined in Ehrlich ascites carcinoma (EAC)-bearing female Swiss Albino mice. Fifty mice were divided into five groups (n =10). Groups I and II served as untreated mice and untreated EAC-bearing mice, respectively, while groups III-V represented the EAC-mice administered orally with blank NE, SOR dissolved in Cremophor (SOR-Chremo) and SOR- NE, respectively. It has been found that SOR-NE group has lesser counts of white blood cells and decreased levels of cardiac enzymes and relatively normal heart tissue when compared to the SOR-Chremo group. Encapsulating SOR in NE has decreased its cytotoxicity on the heart and blood.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol14no1/cardiotoxicity-and-hematoxicity-of-sorafenib-loaded-nanoemulsion-in-ehrlich-ascites-carcinoma-bearing-mice/</fullTextUrl>



      <keywords language="eng">
        <keyword>Chemotherapeutic agents; Cytotoxicity; Cardiac enzymes Flaxseed oil; Nanoparticle;</keyword>
      </keywords>

  </record>
</records>