﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>
      </PublisherName>
      <JournalTitle>Journal of Biochemicals and Phytomedicine</JournalTitle>
      <Issn>2958-8561</Issn>
      <Volume>4</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2025</Year>
        <Month>12</Month>
        <DAY>15</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Formulation and Design of Antidiabetic Tablets from Eucalyptus camaldulensis Using Wet Granulation and a 2³ Factorial Design</ArticleTitle>
    <FirstPage>34</FirstPage>
    <LastPage>41</LastPage>
    <ELocationID EIdType="doi">10.34172/jbp.2025.15</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Azza Dawoud.</FirstName>
        <LastName>H. Dawoud</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0004-9847-8148</Identifier>
      </Author>
      <Author>
        <FirstName>Daud</FirstName>
        <LastName>Baraka Abdalla</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-8866-0422</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jbp.2025.15</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>04</Month>
        <Day>30</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>10</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Eucalyptus camaldulensis, recognized for its antidiabetic and antimicrobial properties, was formulated into an oral tablet to improve its clinical applicability. This study optimized critical formulation parameters via a 2³ factorial design to produce tablets meeting pharmacopeial standards. Methods: Eight formulations were prepared by wet granulation, evaluating three independent variables: binder (PVP) concentration, disintegrant (croscarmellose sodium) concentration, and kneading time. Tablets were assessed for weight variation, thickness, hardness, friability, disintegration time, and drug release in 0.1N HCl (paddle method, 75 rpm) analyzed at 258 nm. Results: All formulations complied with standard requirements. Tablet hardness ranged from 4.42–5.42 kg, friability was &lt;1%, and disintegration time varied between 0.55–2 minutes. Drug release at 45 minutes exceeded 91.4%, with some formulations reaching 98.8%. Factorial analysis identified optimal variable levels for quality attributes. Conclusion: E. camaldulensis was successfully formulated into rapidly disintegrating tablets with high drug release, suitable for potential use in type 2 diabetes management. Further in vivo and clinical studies are warranted.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Eucalyptus camaldulensis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Antidiabetic agents</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Plant extracts</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Tablets</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Drug formulation</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Factorial design</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>