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    <title>DSpace Collection: Bachelor of Science in Biochemistry</title>
    <link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/2823</link>
    <description>Bachelor of Science in Biochemistry</description>
    <pubDate>Wed, 08 Apr 2026 05:11:09 GMT</pubDate>
    <dc:date>2026-04-08T05:11:09Z</dc:date>
    <item>
      <title>The Antimicrobial Property of Psidium guajava Linn. (Guava) Leaf and Fruit on the Periodontopathogen Porphyromonas gingivalis and the Partial Characterization of its Active Component</title>
      <link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3611</link>
      <description>Title: The Antimicrobial Property of Psidium guajava Linn. (Guava) Leaf and Fruit on the Periodontopathogen Porphyromonas gingivalis and the Partial Characterization of its Active Component
Authors: Henson, Karl Evans R.
Abstract: The various components of Psidium guajava Linn. (Guava) leaves and fruit were&#xD;
extracted using a Soxhlet extractor (organic) and by boiling (aqueous). The crude extracts&#xD;
were subjected to further fractionation using organic solvents. The fractions obtained&#xD;
were tested on Porphyromonas gingivalis, one of the major pathogens causing&#xD;
periodontitis. The bioactive fraction, the aqueous water layer of the leaf, was&#xD;
characterized by phytochemical screening. Results showed that guava leaves exhibit&#xD;
antimicrobial effect on P. gingivalis, as shown by the 14-mm zone of inhibition of the&#xD;
crude aqueous extract of the leaf and the 12.33-mm zone of inhibition of the aqueous&#xD;
water layer of the leaf. All other fractions, including all fruit fractions, did not exhibit&#xD;
microbicidal properties. Phytochemical screening revealed that the bioactive fraction&#xD;
contains tannins, plant acids, reducing substances, and flavonoids.</description>
      <pubDate>Fri, 01 Mar 2002 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3611</guid>
      <dc:date>2002-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis and Physico-chemical Characterization of Alkyd Resin from Lumbang Derived Oil</title>
      <link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3103</link>
      <description>Title: Synthesis and Physico-chemical Characterization of Alkyd Resin from Lumbang Derived Oil
Authors: Lola, Lisette Joyce U.
Abstract: Oil was successfully extracted from Lumbang kernels in which it&#xD;
was characterized for its properties. FT-IR spectrum showed pertinent peaks&#xD;
corresponding the presence of functional groups such as ester and sp® C-H&#xD;
stretching. The alkyd resin from Lumbang-derived oil was also successfully&#xD;
synthesized by first undergoing alcoholysis reaction of Lumbang oil and&#xD;
glycerol followed by esterification reaction in the presence of phthalic&#xD;
anhydride. The properties of synthesized alkyd resin were shown in the FT-IR&#xD;
and GC-MS analyses. FT-IR showed pertinent peaks corresponding to the&#xD;
presence of O-H C-O, C=0, C-H and C=C stretching frequencies. GC-MS data&#xD;
confirmed the presence of saturated and unsaturated fatty acid in the&#xD;
structure of the Lumbang oil and alkyd resin. Alkyd resin was also&#xD;
synthesized in which its oil was first purified by deep eutectic solvent (DES,&#xD;
1:2:1 choline chloride:ethylene glycol:glycerol). The synthesized alkyd resins&#xD;
were then characterized based on its adhesive property and chemical&#xD;
resistance. It was found out that presence of alkyd resin with paint leads to&#xD;
longer drying time. In terms of chemical resistance, paint is not chemically&#xD;
resistant to basic and acidic media. Moreover, with the presence of the alkyd&#xD;
resin, paint quality showed to be improved in terms of its adhesive property.&#xD;
Being an additive to paint, results showed that addition of even a small&#xD;
amount of alkyd resin would enhance the quality of the coating. Thus, with all&#xD;
the ratio of alkyd resin to paint that was tested, a ratio of one alkyd resin to five paint possessed the least drying time, most chemical resistant to acidic&#xD;
and basic medium, and have a good adhesive property.</description>
      <pubDate>Sun, 01 Jul 2018 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3103</guid>
      <dc:date>2018-07-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Green and Rapid Synthesis of N-acetyl-L-cysteinecapped ZnSe Quantum Dots in the Aqueous Phase via Microwave Irradiation.</title>
      <link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/2825</link>
      <description>Title: Green and Rapid Synthesis of N-acetyl-L-cysteinecapped ZnSe Quantum Dots in the Aqueous Phase via Microwave Irradiation.
Authors: Estaris, Mylene P.
Abstract: A green and rapid approach was applied in synthesizing water-soluble N-acetyl-Lcysteine&#xD;
(NAC)-capped ZnSe quantum dots (QDs) in the aqueous phase via&#xD;
microwave irradiation. The precursors used were relatively less toxic and did not&#xD;
need pre-treatment prior to reaction. Using IR spectroscopy, NAC molecules&#xD;
were revealed to be successfully mounted on the surface of core ZnSe QDs&#xD;
making the nanoclusters water-soluble. Absorption and emission measurements&#xD;
revealed that the size of the products increases as the duration of reflux&#xD;
increases. The sharp excitonic feature of the absorption spectra was also&#xD;
indicative of the narrow size distribution of the synthesized quantum dots. The&#xD;
as-per synthesized NAC-capped ZnSe QD was determined to possess&#xD;
photoluminescence quantum yield (PLQY) of up to 18% in reference to&#xD;
Rhodamine 6G without post-treatments. Optimum %PLQY was revealed to occur&#xD;
after 60 minutes of reflux. The method employed in synthesizing water-soluble&#xD;
ZnSe quantum dots was proven to be fast and less toxic and showed to improve&#xD;
the optical properties of quantum dots with respect to conventional heating.</description>
      <pubDate>Mon, 01 Apr 2013 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/2825</guid>
      <dc:date>2013-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Cobalamin as Colorimetric Sensor for Gas Pollutants</title>
      <link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/2824</link>
      <description>Title: Cobalamin as Colorimetric Sensor for Gas Pollutants
Authors: Pabilane, Alma L.
Abstract: Cobalamin (Cbl) exposed to gases resulted in color changes visible&#xD;
to the naked eye. These reactions were further analyzed by UV-Vis and IR&#xD;
spectroscopies. Among gases tested, carbon dioxide, sulfur dioxide and nitrogen&#xD;
dioxide, only SO, and NO; induced color changes to the cobalamin. It is&#xD;
proposed that color changes observed were due to metal-gas binding (for NO)&#xD;
and protonation of the benzimidazole group of the cobalamin (for SO,). It was&#xD;
further observed that initial color of cobalamin solution upon introduction of gases&#xD;
changes as time elapses. It is suggested that Cbl-NO; binding, which caused the&#xD;
initial color change from red to yellow-orange is possibly reversible due to&#xD;
photolysis and the color change undergone by cobalamin exposed to SO, that is&#xD;
initially orange and turned yellow afterwards is due to slow protonation of&#xD;
cobalamin, forming a cobalamin species with protonated benzimidazole group&#xD;
which has yellow appearance.</description>
      <pubDate>Mon, 01 Apr 2013 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/2824</guid>
      <dc:date>2013-04-01T00:00:00Z</dc:date>
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