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  <titleInfo>
    <title>The antiproliferative study of quercus infectoria galls crude and  micelle extract hydrogel beads against selected breast cancer  cells</title>
  </titleInfo>
  <name type="personal">
    <namePart>Wan Nur Suzilla Bt Wan Yusuf</namePart>
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    <dateIssued encoding="marc">2024</dateIssued>
    <copyrightDate encoding="marc">2024</copyrightDate>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <extent>xv, 189 pages : illustration ; 30 cm. + 1 CD-ROM</extent>
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  <abstract>Hydrogel beads are used in scientific studies to investigate the potential of natural extracts  in inhibiting cancer cell growth. They provide stability and transportation by enclosing  the extract within a network, ensuring its antiproliferative properties. They can also be  engineered for controlled release, ensuring consistent antiproliferative effects.  Additionally, they prevent agglutination, ensuring uniform distribution of the extract, and  potentially enhancing its efficacy. Hence, in this study, Quercus infectoria (QI) galls  hydrogel beads incorporated with QI galls crude and micelle extracts were developed to  overcome the micelle aggregation and stability problem as well as a new alternative in  cancer treatment. QI galls crude extract was produced using maceration extraction with  70% aqueous ethanol while QI galls crude extract loaded micelle was formulated using  solvent casting method and then both extracts were characterized for their  physicochemical properties. Then, the QI galls crude and micelle extract were  incorporated into hydrogel beads via crosslinking action between polymer (pectin) and  crosslinker (zinc acetate). All crude extract, micelles and hydrogel beads were tested  against selected breast cancer cells (MCF-7 and MDA-MB-231) to determine the  antiproliferative activity using MTT Assay as well as for apoptosis activity via FITCAnnexin V staining. From the findings, it was observed that the QI galls crude extract,  micelles and hydrogel beads exhibited good antiproliferative activity against breast  cancer cells (MCF-7 and MDA-MB-231) but showed no cytotoxicity against normal cell  line, L929 apart from induced the cell death mechanism through apoptosis. All  formulated micelles showed a good size range (below 20 nm), with polydispersity index  (PDI) value between 0.1-0.4 indicating narrow distribution and negatively charged.  Based on the surface chemistry analysis, it was observed that all formulated micelles, had  almost similar relative ratio amongst the suggested chemical bonds and in accordance  with those reported in pure vitamin E TPGS. For extract loading, it was showed that  Quercus infectoria Vitamin E TPGS (QIT) micelle gave highest loading (110.41 µg/ml)  as compared to other micelles and the surface morphology by Transmission Electron  Microscope (TEM), showed all formulated micelles were in moderate uniformity with  nearly spherical shape. Controlled drug release profile showed all micelles demonstrated  biphasic release pattern while the cellular uptake was increased with prolonged  incubation time. QIT micelle showed highest cytotoxic activity (IC50 8.28±0.82 µg/ml)  against MCF-7 cells with faster onset of action as compared to MDA-MB-231 (IC50 11.09±0.73 µg/ml) and induced apoptotic cell death mechanism with no toxicity effect  against normal cells, L929. For the hydrogel beads formulation, two different hydrogel  beads were formulated, using QI crude (QIC) and micelle (QIM) extract. From the  findings, it was showed both formulated beads, demonstrated good yield, morphology,  swelling ability, swelling time and moisture content (below 20%). As conclusion, a novel  polymeric hydrogel beads incorporated with QI galls crude and micelle extract with good  antiproliferative activity against selected breast cancer cells were successfully formulated  and presents a promising strategy for safeguarding the integrity of extracts by improving  their stability and effectively preventing undesirable aggregation.</abstract>
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  <note type="statement of responsibility">Wan Nur Suzilla Bt Wan Yusuf</note>
  <note>Faculty of Chemical and Process Engineering Technology</note>
  <note>Thesis (Doctor of Philosophy) -- Universiti Malaysia Pahang – 2024</note>
  <note>Includes bibliographical references</note>
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    <name type="corporate">
      <namePart>Faculty of Chemical and Process Engineering Technology</namePart>
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    <topic>Dissertations</topic>
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    <topic>Universities and colleges</topic>
    <topic>Dissertations</topic>
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    <topic>Theses</topic>
    <topic>Dissertations</topic>
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  <identifier type="isbn">THE0009998 (Local)</identifier>
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    <recordCreationDate encoding="marc">250203</recordCreationDate>
    <recordChangeDate encoding="iso8601">20251125111024.0</recordChangeDate>
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      <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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