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  <record>
    <language>eng</language>
    
      <publisher>Oriental Scientific Publishing Company</publisher>
    
    <journalTitle>Material Science Research India</journalTitle>
    
      <issn>0973-3469</issn>
    
    
    <publicationDate>2024-12-15</publicationDate>
    

        <volume>21</volume>

        <issue>3</issue>

 

    <startPage>141</startPage>
    <endPage>150</endPage>

   
      <doi></doi>
    
    <publisherRecordId>23156</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Poly [(maleic acid)-co-(propane-1,2-diol)-ran- (citric acid)] for pH-Responsive Extended Drug Release</title>

    <authors>
	 


      <author>
       <name>Abu Mahmud </name>

 
		

	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Mohammad Abu Bakr</name>


		

	<affiliationId>2</affiliationId>

      </author>
    


	 


      <author>
       <name>Jahanara Nasrin</name>

		

	<affiliationId>1</affiliationId>
      </author>
    


	



	



	

    </authors>
    
	    <affiliationsList>
	    
		

		<affiliationName affiliationId="1">Department of Materials Science and Engineering, University of Rajshahi, Bangladesh</affiliationName>
    


		

		<affiliationName affiliationId="2">Department of Applied Chemistry and Chemical Engineering, University of Rajshahi, Bangladesh</affiliationName>
    

		

		

		

		

	  </affiliationsList>







    <abstract language="eng">The Dean-Stark apparatus was used to synthesize poly[(maleic acid)-co-(propane-1,2-diol)-ran-(citric acid)] in xylene medium in presence of anhydrous FeCl<sub>3</sub> catalyst. FTIR-spectrum, TGA, soil burial biodegradation test, molecular weights, solubility in common organic solvents, elemental analysis and hydrolytic degradation test were performed to characterize the synthesized co-polyester. Soil burial biodegradation study showed nearly complete miscibility of the co-polyester in soil within around 2 months. Hydrolytic degradation study in solutions of different pH values, at room temperature, showed that this co-polyester stayed practically intact in solutions of pH 1.2-6.0, but they steadily degraded in solutions of pH&gt;7.0. Because of such pH-responsive degradation characteristics, this co-polyester was tried as a carrier of oral formulation for non-steroidal anti-inflammatory drugs. In simulated intestinal fluid, a constant rate of drug release (zero order) up to 10 hours from drug-loaded polymer matrix tablets was observed.</abstract>

    <fullTextUrl format="html">https://www.materialsciencejournal.org/vol21no3/poly-maleic-acid-co-propane-12-diol-ran-citric-acid-for-ph-responsive-extended-drug-release/</fullTextUrl>




      <keywords language="eng">
        <keyword>Biodegradability</keyword>
      </keywords>


      <keywords language="eng">
        <keyword> Biodegradable polymer</keyword>
      </keywords>


      <keywords language="eng">
        <keyword> pH-responsive drug release</keyword>
      </keywords>


      <keywords language="eng">
        <keyword> poly[(maleic acid)-co-(propane-1</keyword>
      </keywords>


      <keywords language="eng">
        <keyword>2-diol)-ran-(citric acid)]</keyword>
      </keywords>


      <keywords language="eng">
        <keyword> Polymer matrix tablet</keyword>
      </keywords>

  </record>

</records>