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  <titleInfo>
    <title>Application of deep eutectic solvent as a green solvent in extracting of phytochemicals compound in phyllanthus niruri</title>
  </titleInfo>
  <name type="personal">
    <namePart>Sabrina Liew, Pui Yee</namePart>
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    <dateIssued encoding="marc">2025</dateIssued>
    <copyrightDate encoding="marc">2025</copyrightDate>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <extent>xiii , 87 pages : illustrations ;</extent>
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  <abstract>A study was performed to extract Phyllanthus Niruri (aerial part of leaves) by using  Ultrasound-assisted Extraction (UAE) and Natural Deep Eutectic Solvent (NaDES) as  extraction solvent and to analyze phytochemical compounds found in the extract using  High Performance Liquid Chromatography (HPLC) and Gas Chromatography-Mass  Spectrometry (GC-MS). NaDES were synthesized by combinations of hydrogen bond  acceptor (HBA): Choline chloride and hydrogen bond donors (HBD): Lactic acid, Oxalic  acid, Citric acid (II) monohydrate, L(+)-Ascorbic acid and L-(+)-Tartaric acid. Both were  stirred in water bath at 80 ºC until a homogenous liquid was formed. FTIR-ATR and KBr  were used to perform analysis of liquid (wavelength 700 and 4000 ��������−1 ) and solid  sample (400 and 4000 ��������−1) respectively. Phyllanthus Niruri was cleaned, dried in oven  and powdered in preparation of extraction. UAE was conducted for 30 minutes at 60 °C  and 200 W using an ultrasonic (Branson ®) machine where 10 mL of NaDES solvent was  used to extract 1.0 g of precisely weighed dry herb powder. HPLC and GC-MS analysis  was conducted for qualitative and quantitative research of the NaDES extract. Results  depicted the NADES-1 was the fastest to form homogenous liquid (10 min) slowest,  NADES-4 (5 hr) Density of NaDES were also calculated and arranged in descending  order, (NADES-3 &gt; NADES-5 &gt; NADES-4 &gt; NADES-2 &gt; NADES-1). Besides, in FTIR  analysis demonstrated the characteristics wavelength of IR for synthesized NADES  according to O-H Stretching, C-H Stretching, C=O Stretching, N-H Bending and C-O  Stretching. The bond shifting of C=O and -OH of FTIR analysis in range of 1650-1750  ��������−1 and 3200–3500 ��������−1 demonstrated that every NADES was successfully prepared.  UAE showed deeper colour of extracts upon complete extraction. HPLC analysis of  extracts found potential compounds: Phyllanthin, hypophyllanthin and niranthin when  referred to previous studies. Finally, in GC-MS analysis, NADES-2 extracts  demonstrated highest abundance achieved by butanedioic acid, 2,3-dihydroxy-, dimethyl  ester. Limited studies showed this compound is a naturally occurring compound. Thus,  benzene, 4-ethyl-1,2-dimethoxy- from analysis of NADES-5 was selected as the most  outperform analysis as this compound is widely found in plant extracts. These findings  gained extra information in identification of new phytochemical compounds that has yet  been explored in analysis of Phyllanthus Niruri as compared to previous studies.  However, more approach has to be conducted in verification of the new compounds  observe. In short, application of deep eutectic solvents in extracting phytochemical  compounds found in Phyllanthus Niruri is achievable.</abstract>
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  <note type="statement of responsibility">Sabrina Liew Pui Yee</note>
  <note>Faculty of Industrial Sciences and Technology</note>
  <note>Final Year Report (Bachelor of Applied Science of Industrial Chemistry) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025</note>
  <note>Include bibliographical reference</note>
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      <namePart>Faculty of Industrial Sciences and Technology</namePart>
    </name>
    <topic>Dissertations</topic>
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  <subject authority="lcsh">
    <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">THE0010484 (Local)</identifier>
  <identifier type="uri">https://umpir.ump.edu.my/id/eprint/46125</identifier>
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    <url>https://umpir.ump.edu.my/id/eprint/46125</url>
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    <recordCreationDate encoding="marc">260421</recordCreationDate>
    <recordChangeDate encoding="iso8601">20260421120706.0</recordChangeDate>
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      <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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