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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2022-03-31</publicationDate>
    
        <volume>15</volume>
        <issue>1</issue>

 
    <startPage>313</startPage>
    <endPage>320</endPage>

	 
      <doi>10.13005/bpj/2369</doi>
        <publisherRecordId>42675</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Antimalarial Effect of Doxorubicin on Plasmodium Falciparum: an in Vitro Study in FCR-3 Strain</title>

    <authors>
	 


      <author>
       <name>Mutiara Rahmah Amari</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Hesti Lina Wiraswati</name>


		
	<affiliationId>1,2</affiliationId>

      </author>
    

	 


      <author>
       <name>Nisa Fauziah</name>

		
	<affiliationId>2,3 </affiliationId>
      </author>
    

	 


      <author>
       <name>Ilma Fauziah Ma’ruf</name>

		
	<affiliationId>4</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Oncology and Stem Cells Working Group, Faculty of Medicine, Universitas Padjadjaran, Bandung</affiliationName>
    

		
		<affiliationName affiliationId="2">Infections Working Group, Faculty of Medicine, Universitas Padjadjaran, Bandung</affiliationName>
    
		
		<affiliationName affiliationId="3">Parasitology Division, Department of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung</affiliationName>
    
		
		<affiliationName affiliationId="4">Biochemistry Research Group, Department of Chemistry, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Bandung</affiliationName>
    
		
		
	  </affiliationsList>






    <abstract language="eng"><em>Plasmodium falciparum</em> is the most common species of <em>Plasmodium</em> that causes malaria in Southeast Asia. Artemisinin, a drug with the mechanism of action by inducing oxidative stress in infected red blood cells (RBC) is currently used as the main therapy for malaria, after resistance to chloroquine has been found. However, evidence of artemisinin resistance was discovered in several regions in Southeast Asia. Therefore, a research is required to prove the existence of other drugs that have anti-malaria effects. A drug candidate, doxorubicin also can induce the formation of oxidative stress inside the cells. This study aims to determine the activity of doxorubicin to inhibit the development of <em>P. falciparum </em>in vitro. Red blood cell (RBC) infected with <em>P</em><em>. </em><em>falciparum</em> were treated with various concentrations of doxorubicin. Giemsa technique was applied to detect <em>P. falciparum</em> inside RBC. After 48 hours of incubation, the culture was observed to measure the number and the confluence of RBC and <em>P. falciparum</em> in the medium. This study revealed that doxorubicin reduced the number of RBC infected with <em>P. falciparum </em>lysis. The effective dose of doxorubicin-inhibit RBC cell lysis is 0.4 μM, which only reduces 81% RBC cell lysis compared to the control group that reduces 95% RBC cell lysis. At this concentration also found a decrease in the number of <em>P. falciparum</em> cells in the medium. The results proved that doxorubicin has an inhibitory effect on the development of <em>P</em><em>. </em><em>falciparum</em> and can decrease the lysis of RBC due to <em>P</em><em>. </em><em>falciparum</em> infection. This findings provide an insight that doxorubicin is a potential candidate for antimalarial drugs.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol15no1/antimalarial-effect-of-doxorubicin-on-plasmodium-falciparum-an-in-vitro-study-in-fcr-3-strain/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Artemisinin</keyword>
      

      
        <keyword> Antimalaria</keyword>
      

      
        <keyword>  Oxidative Stress</keyword>
      

      
        <keyword> Giemsa</keyword>
      
</keywords>
  </record>
</records>