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            <name>Title</name>
            <description>A name given to the resource</description>
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              <elementText elementTextId="3139">
                <text>Faculty Publications</text>
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    <name>Article</name>
    <description>Faculty Publications -Articles</description>
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          <name>Creator</name>
          <description>An entity primarily responsible for making the resource</description>
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              <text>Shinde, Kajal Sunil; Jangme, Chandraprabhu Motichand; Patil, Abhinandan Raosaheb</text>
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          <name>Title</name>
          <description>A name given to the resource</description>
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            <elementText elementTextId="227562">
              <text>RP-HPLC METHOD FOR QUANTITATIVE ESTIMATION OF NAFTIFINE HYDROCHLORIDE IN FORMULATED PRODUCTS: DEVELOPMENT AND VALIDATION</text>
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        <element elementId="40">
          <name>Date</name>
          <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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            <elementText elementTextId="227563">
              <text>01-01-2025</text>
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          <name>Source</name>
          <description>A related resource from which the described resource is derived</description>
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            <elementText elementTextId="227564">
              <text>Journal of Applied Pharmaceutical Research;Volume;13;Issue;4;pp.177-186</text>
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        <element elementId="43">
          <name>Identifier</name>
          <description>An unambiguous reference to the resource within a given context</description>
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            <elementText elementTextId="227565">
              <text>&lt;a href="https://doi.org/10.69857/joapr.v13i4.1115" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.69857/joapr.v13i4.1115&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105016659048?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105016659048?origin=resultslist&lt;/a&gt;</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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            <elementText elementTextId="227566">
              <text>Shinde K.S., Dept. of Pharmaceutical Science, Centre for Interdisciplinary Research, D. Y. Patil Education Society (Deemed to be University), Maharashtra, Kolhapur, 416006, India; Jangme C.M., Department of Pharmacology, D. Y. Patil College of Pharmacy, D. Y. Patil Education Society, Deemed to Be University, Maharashtra, Kolhapur, 416006, India; Patil A.R., Department of Pharmaceutics, D. Y. Patil College of Pharmacy, D. Y. Patil Education Society, Deemed to Be University, Kolhapur, Maharashtra, 416006, India</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Background: Naftifine hydrochloride is an allylamine antifungal agent commonly used to treat dermatophyte infections. It inhibits squalene epoxidase, a key enzyme in ergosterol biosynthesis, thereby disrupting the integrity of the fungal cell membrane. It exhibits broad-spectrum activity against dermatophytes, yeasts, and molds, and is typically formulated as a 1% topical cream or gel. Methodology: A rapid and robust reverse-phase high-performance liquid chromatography (RP-HPLC) method was developed and validated for the estimation of naftifine hydrochloride in a topical cream formulation (2% Naftifast, Zydus), in accordance with ICH and FDA guidelines. Chromatographic separation was achieved on an Inertsil ODS column using an isocratic mobile phase consisting of 35% acetonitrile, 40% methanol, 25% water, and 0.8% triethylamine (pH adjusted to 5.5 with acetic acid) at a flow rate of 1.4 mL/min. Detection was performed at 265 nm. Results and Discussion: Naftifine hydrochloride showed a retention time of approximately 4.0 minutes with a total run time of 6.0 minutes. The method displayed excellent linearity over a concentration range of 20120 g/mL (R &amp;gt; 0.999). Recovery studies indicated a mean recovery of 100.4%. Precision was confirmed by relative standard deviation (RSD) values of less than 2%, demonstrating the methods reproducibility. Conclusion: The proposed RP-HPLC method is simple, precise, and time-efficient. It is suitable for routine quality control of naftifine hydrochloride in pharmaceutical dosage forms due to its short analysis time and strong validation performance.  2025 The authors.</text>
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          <name>Subject</name>
          <description>The topic of the resource</description>
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              <text>Naftifine hydrochloride; pharmaceutical; reversed-phase HPLC; topical antifungal; validation</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
          <elementTextContainer>
            <elementText elementTextId="227569">
              <text>Creative Pharma Assent</text>
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          <name>Relation</name>
          <description>A related resource</description>
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            <elementText elementTextId="227570">
              <text>ISSN: 23480335;</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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            <elementText elementTextId="227571">
              <text>English</text>
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          <name>Type</name>
          <description>The nature or genre of the resource</description>
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            <elementText elementTextId="227572">
              <text>Article</text>
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          <name>Rights</name>
          <description>Information about rights held in and over the resource</description>
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            <elementText elementTextId="227573">
              <text>All Open Access; Gold Open Access; Green Open Access</text>
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          <name>Format</name>
          <description>The file format, physical medium, or dimensions of the resource</description>
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              <text>online</text>
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