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    <timestamp>20250715050210000</timestamp>
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      <depositor_name>Editor</depositor_name>
      <email_address>editor.jddt@gmail.com</email_address>
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    <registrant>Universal Journal of Pharmaceutical Research</registrant>
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      <journal_metadata>
        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
        <issn media_type="print">2831-5235</issn>
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        <publication_date media_type="online">
          <month>07</month>
          <day>15</day>
          <year>2025</year>
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        <titles>
          <title>CHITOSAN COATED ROSUVASTATIN NANOSTRUCTURED LIPID CARRIERS: FORMULATION, IN VITRO CHARACTERIZATION AND STORAGE ASSESSMENTS</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <surname>Walid Anwar</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>El Sayed Gamal E. Shaheen</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Sherif K. Abu-Elyazid</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Mohsen I. Afouna</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>Background and Objective: Rosuvastatin calcium (ROS-Ca) is a synthetic, highly potent third-generation HMG-CoA reductase inhibitor with significant hypocholesterolemic effects. The objective of this study was to develop and characterize nanostructured lipid carriers (NLCs) as a delivery system for the poorly water-soluble drug rosuvastatin calcium (ROS-Ca), with the aim of enhancing its dissolution rate and improving oral bioavailability.
Methods: ROS-NLCs is prepared by hot homogenization–ultrasonication technique then the prepared formulations were further characterized. Finally compare their characteristics to the corresponding a positively charged chitosan coated to develop new CH-ROS-NLCs. In this study, glyceryl monostearate (GMS) was selected as solid lipids and Transcutol® HP as a liquid lipid, to develop ROS-NLC (nanostructured lipid carrier).
Results: The physicochemical properties were achieved. The prepared ROS-NLC formulation was showed in nanometric size (121.6±6.2 nm) with encapsulation efficiency (63±0.2%). Furthermore, ROS-NLC and CH-ROS-NLC appeared almost spherical nanoparticles in morphology under transmission electron microscope (TEM). DSC, XRD and FT-IR analysis showed that ROS was miscible, compatible, and incorporated into NLCs in amorphous form not in native crystalline state.
Conclusion: The previously results showed that ROS-Ca was successfully encapsulated into nanostructured lipid carriers (NLCs) which coated with chitosan CH-ROS-NLC to overcome the above-mentioned defects and, it was ensured that nanostructured lipid carriers have high beneficial effect for enhancing and improving the oral bioavailability of poorly water-soluble drugs such as Rosuvastatin.
                   
Peer Review History: 
Received 9 April 2025;   Reviewed 12 May 2025; Accepted 22 June; Available online 15 July 2025
Academic Editor: Dr. DANIYAN Oluwatoyin Michael, Obafemi Awolowo University, ILE-IFE, Nigeria, toyinpharm@gmail.com
Reviewers:
Dr. Areen Alshweiat, University of Szeged, Hungary, areen.alshweiat@hu.edu.jo
Dr. Awofisayo, O Abosede, University of Uyo, Nigeria, shalomgirl08@yahoo.com</jats:p>
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          <day>15</day>
          <year>2025</year>
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          <doi>10.22270/ujpr.v10i3.1363</doi>
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