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<title>Information Resources on Zoology</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/1808</link>
<description/>
<pubDate>Thu, 23 Apr 2026 10:59:15 GMT</pubDate>
<dc:date>2026-04-23T10:59:15Z</dc:date>
<item>
<title>Functional and antiglycation properties of cow milk set yogurt enriched with Nyctanthes arbor-tristis L. fower extract</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/12583</link>
<description>Functional and antiglycation properties of cow milk set yogurt enriched with Nyctanthes arbor-tristis L. fower extract
Amadarshanie, D.B.T.; Gunathilaka, T.L.; Silva, R.M.; Navaratne, S.B.; Peiris, L.D.C.
The fortifcation of yogurt with natural herbs to improve its nutritional and health beneft are an emerging trend.&#13;
Hot infusions of Nyctanthes abo-tristis fowers are a traditionally used herb against diabetes. This study was&#13;
designed to develop a novel yogurt fortifed (FY) with 3, 3.5, and 6% N.arbor-tristis fower extract (NFE) to&#13;
determine its suitability as a fortifer en route to innovative functional products. Upon fermentation, the highest&#13;
sensory scores were obtained for the 3.5% NFE-FY with 11-, 6-, 3-fold higher antiglycation (NFE- IC50: 28.04 ±&#13;
1.13 μg/mL and 3.5% NFE-FY IC50: 46.80 ± 0.92 μg/mL) activity, free radical scavenging potentials, and total&#13;
phenolic content, respectively. An improvement of texture profle values was observed in 3.5% NFE-FY compared&#13;
to the control with 3.00 ± 0.1% fat, 3.88 ± 0.23% crude protein, 77.94 ± 0.09 moisture, 14.97 ± 0.27 total&#13;
soluble solids, and 0.7637 ± 0.03 ash. The 3.5%NEF-FY also exhibited a longer shelf life and less microbial&#13;
growth than the control. The GC-MS analysis of the NFE indicated the presence of phytochemicals essential for&#13;
the observed bioactivity. The results confrmed that the N.arbor-tristis fower extract increased the overall quality&#13;
of the yogurt and tested bioactivity. NFE-FY could be used in yogurt production to optimize the health benefts&#13;
with improved functional characteristics to prevent diet-driven glycation activity.
</description>
<pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/12583</guid>
<dc:date>2022-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Integration of in vitro and in‑silico analysis of Caulerpa racemosa against antioxidant, antidiabetic, and anticancer activities</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/12582</link>
<description>Integration of in vitro and in‑silico analysis of Caulerpa racemosa against antioxidant, antidiabetic, and anticancer activities
Dissanayake, I.H.; Bandaranayake, U.; . Keerthirathna, L.R.; Manawadu, C.; Silva, R.M.; Mohamed, B.; Rizwan, A.; Peiris, D.C.
Marine algae are found to be excellent in their nutritional and potential therapeutic properties.&#13;
This study explores the antidiabetic and anticancer potential of fractionated polyphenolic extract&#13;
of Caulerpa racemosa, green macroalgae. Crude polyphenolic extract (CPE) of C. racemosa and its&#13;
fractions (n-hexane, ethyl acetate, chloroform, and distilled water) were tested for its total phenol&#13;
and favonoid contents and antioxidant potential. The ethyl acetate fraction was subjected to gas&#13;
chromatography/mass spectrometry (GC/MS). The in vitro antidiabetic activity was assessed by alphaamylase, glucosidase inhibition and anti-glycation assays. Also, in-silico studies were conducted to&#13;
test the binding afnities between caulerpin with alpha-glucosidase enzyme and estrogen receptor&#13;
(ER) active sites. Each fraction was tested for its in vitroin vitroanticancer activity by CellTiter-Glo and&#13;
MTT cell proliferation assays. The total phenolic and favonoid contents and the antioxidant potential&#13;
of the crude extract were observed to be dose dependent. The GC/MS analysis of the ethyl acetate&#13;
fraction yielded 47 peaks, whereas n-hexadecanoic acid and hexadecanoic acid methyl ester showed&#13;
the highest compatibility percentages of 99% and 96%, respectively. The CPE exhibited a higher&#13;
potential in both alpha-amylase inhibitory and anti-glycation activities. The ethyl acetate fraction&#13;
was more efective against alpha-glucosidase inhibition. Molecular docking revealed a high binding&#13;
afnity between the alpha-glucosidase enzyme and caulerpin and showed high binding afnity toward&#13;
caulerpin, with H-bond interactions. The in vitro anticancer analyses revealed that chloroform fraction&#13;
and CPE exhibited moderate activity on the KAIMRC1 cell line. Also, the CPE exhibited high specifcity&#13;
compared to the standard drug in anticancer studies. Our fndings evidence the pharmacological&#13;
potential of the CPE of C. racemosa, and bioactive compounds of the species may be utilized as lead&#13;
molecules to develop anti-diabetic and anti-cancer drugs.
</description>
<pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/12582</guid>
<dc:date>2022-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>In silico study of SARS‐CoV‐2 spike protein RBD and human ACE‐2 affinity dynamics across variants and Omicron subvariants</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/12581</link>
<description>In silico study of SARS‐CoV‐2 spike protein RBD and human ACE‐2 affinity dynamics across variants and Omicron subvariants
Abeywardhana, S.; Premathilaka, M.; Bandaranayake, U.; Perera, D.; Peiris, L.D.C.
The coronavirus disease 2019 virus outbreak continues worldwide, with many&#13;
variants emerging, some of which are considered variants of concern (VOCs). The&#13;
WHO designated Omicron as a VOC and assigned it under variant B.1.1.529. Here,&#13;
we used computational studies to examine the VOCs, including Omicron&#13;
subvariants, and one variant of interest. Here we found that the binding affinity&#13;
of human receptor angiotensin‐converting enzyme 2 (hACE2) and receptor‐binding&#13;
domain (RBDs) increased in the order of wild type (Wuhan‐strain) &lt; Beta&#13;
&lt; Alpha &lt; OmicronBA.5 &lt; Gamma &lt; Delta &lt; Omicron BA.2.75 &lt; BA.1 &lt; BA.3 &lt; BA.2.&#13;
Interactions between docked complexes revealed that the RBD residue positions&#13;
like 452, 478, 493, 498, 501, and 505 are crucial in creating strong interactions&#13;
with hACE2. Omicron BA.2 shows the highest binding capacity to the hACE2&#13;
receptor among all the mutant complexes. The BA.5's L452R, F486V, and T478K&#13;
mutation significantly impact the interaction network in the BA.5 RBD‐hACE2&#13;
interface. Here for the first time, we report the His505, an active residue on the&#13;
RBD forming a salt bridge in the BA.2, leading to increased mutation stability.&#13;
When the active RBD residues are mutated, binding affinity and intermolecular&#13;
interactions increase across all mutant complexes. By examining the differences in&#13;
different variants, this study may provide a solid foundation for structure‐based&#13;
drug design for newly emerging variants.
</description>
<pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/12581</guid>
<dc:date>2022-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Screening and quantitative analysis of antibiotic resistance genes in hospital and aquaculture effluent in Sri Lanka as an emerging environmental contaminant</title>
<link>http://dr.lib.sjp.ac.lk/handle/123456789/12130</link>
<description>Screening and quantitative analysis of antibiotic resistance genes in hospital and aquaculture effluent in Sri Lanka as an emerging environmental contaminant
Liyanage, G.Y.; Weerasekera, M.M.; Manage, P.M.
</description>
<pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dr.lib.sjp.ac.lk/handle/123456789/12130</guid>
<dc:date>2022-01-01T00:00:00Z</dc:date>
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