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  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2023-03-21</publicationDate>
    
        <volume>16</volume>
        <issue>1</issue>

 
    <startPage>573</startPage>
    <endPage>580</endPage>

	 
      <doi>10.13005/bpj/2639</doi>
        <publisherRecordId>48179</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Development and Validation of HPLC Method For the Detection of Fusidic Acid Loaded in Non-ionic and Cationic Nanoemulsion-Based Gels</title>

    <authors>
	 


      <author>
       <name>Ahmed Yaseen</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Mowafaq Mohammed Ghareeb</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>Dania F. Alsaffar</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Toh Seok Ming</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Amirah Mohd Gazzali</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Pharmaceutical Technology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.</affiliationName>
    

		
		<affiliationName affiliationId="2">Department of Pharmaceutics, College of Pharmacy, Baghdad University, Iraq.</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Fusidic acid (FA) is a well-known pharmaceutical antibiotic used to treat dermal infections. This experiment aimed for developing a standardized HPLC protocol to determine the accurate concentration of fusidic acid in both non-ionic and cationic nano-emulsion based gels. For this purpose, a simple, precise, accurate approach was developed. A column with reversed-phase C18 (250 mm x 4.6 mm ID x 5 m) was utilized for the separation process. The main constituents of the HPLC mobile phase were composed of water: acetonitrile (1: 4); adjusted at pH 3.3. The flow rate was 1.0 mL/minute. The optimized wavelength was selected at 235 nm. This approach achieved strong linearity for alcoholic solutions of FA when loaded at a serial concentration ranging from 12.5 to 400 µg/ml. Furthermore, the approach showed good stability and achieved full recovery and an effective separation for FA from the abovementioned formulation. Besides, the protocol validation revealed good robustness at a temperature range of 23 to 27, pH 3.0 to 3.5, detection wavelength 230 to 240 nm, flow rate 0.8 and 1.2 and mobile phase contents of (78:22 to 82:18 acetonitrile/ water). The limit of Detection was obtained 1.33 µg/ml and limit of Quantification was 4.04 µg/ml for FA that uploaded through mentioned formulations. All the validation parameters were within the acceptance criteria, as per ICH , US Pharmacopeia requirements. Overall, an affordable and reproducible method could be achieved for the detection and quantification of fusidic acid within the nano-emulsion based gels formulas.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol16no1/development-and-validation-hplc-method-for-detection-fusidic-acid-loading-in-both-non-ionic-and-cationic-nanoemulsion-based-gels/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Cationic Nanoemulsion</keyword>
      

      
        <keyword> Fusidic Acid</keyword>
      

      
        <keyword> Nanoemulsion</keyword>
      

      
        <keyword> Nanoemulsion Gel</keyword>
      
</keywords>
  </record>
</records>