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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1075" />
  <subtitle />
  <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1075</id>
  <updated>2026-05-02T22:36:34Z</updated>
  <dc:date>2026-05-02T22:36:34Z</dc:date>
  <entry>
    <title>Cytotoxicity and antioxidant activity of 5-(2,4-dimethylbenzyl)pyrrolidin-2-one extracted from marine Streptomyces VITSVK5 spp.</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1088" />
    <author>
      <name>Kumar, Saurav</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1088</id>
    <updated>2025-10-21T07:32:41Z</updated>
    <published>2011-07-29T00:00:00Z</published>
    <summary type="text">Title: Cytotoxicity and antioxidant activity of 5-(2,4-dimethylbenzyl)pyrrolidin-2-one extracted from marine Streptomyces VITSVK5 spp.
Authors: Kumar, Saurav
Abstract: The aim of the present study was to evaluate the cytotoxicity and antioxidant activity&#xD;
of 5-(2,4-dimethylbenzyl)pyrrolidin-2-one (DMBPO) extracted from marine Streptomyces VITSVK5 spp. The strain was isolated from sediment samples collected at the Marakkanam coast&#xD;
of Bay of Bengal, India. Systematic screening of isolates for anti-Aspergillus activity resulted in&#xD;
the identification of Streptomyces species designated as Streptomyces VITSVK5 spp. Bioactivity&#xD;
guided extraction and purification yielded a compound 5-(2,4-dimethylbenzyl)pyrrolidin-2-one&#xD;
(DMBPO) and was tested for cytotoxicity and antioxidant activity. The structure of the extracted&#xD;
compound was established by spectroscopic studies and identified as 5-(2,4-dimethylbenzyl)pyrrolidin-2-one (DMBPO). DMBPO exhibited cytotoxic activity on HEP 2 and Hep G2 cell lines&#xD;
with the IC50 value of 2.8 lg/ml and 8.3 lg/ml, respectively, as compared to Vero cell line&#xD;
(22.6). DMBPO showed the hemolytic EC50 value of 288 lg/ml on human erythrocytes. DMBPO&#xD;
treatment showed fewer (31.7%) aberrations, gaps and chromatid breaks as compared to&#xD;
untreated controls (27.8%) of human chromosomes. DMBPO also exhibited significant&#xD;
(44.13% at 5 lg/ml DMBPO) DPPH radical scavenging activity and total antioxidant activity&#xD;
(50.10% at 5 lg/ml DMBPO). The results of this study showed that DMBPO is cytotoxic to cancer cells and possesses antioxidant property</summary>
    <dc:date>2011-07-29T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Recent Advances in the Detection of Food Toxins Using Mass Spectrometry</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1076" />
    <author>
      <name>Kumar, Saurav</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/1076</id>
    <updated>2025-10-21T06:54:41Z</updated>
    <published>2023-11-07T00:00:00Z</published>
    <summary type="text">Title: Recent Advances in the Detection of Food Toxins Using Mass Spectrometry
Authors: Kumar, Saurav
Abstract: Edibles are the only source of nutrients and energy&#xD;
for humans. However, ingredients of edibles have undergone many&#xD;
physicochemical changes during preparation and storage. Aging,&#xD;
hydrolysis, oxidation, and rancidity are some of the major changes&#xD;
that not only change the native flavor, texture, and taste of food but&#xD;
also destroy the nutritive value and jeopardize public health. The&#xD;
major reasons for the production of harmful metabolites,&#xD;
chemicals, and toxins are poor processing, inappropriate storage,&#xD;
and microbial spoilage, which are lethal to consumers. In addition,&#xD;
the emergence of new pollutants has intensified the need for&#xD;
advanced and rapid food analysis techniques to detect such toxins.&#xD;
The issue with the detection of toxins in food samples is the&#xD;
nonvolatile nature and absence of detectable chromophores;&#xD;
hence, normal conventional techniques need additional derivatization. Mass spectrometry (MS) offers high sensitivity, selectivity,&#xD;
and capability to handle complex mixtures, making it an ideal analytical technique for the identification and quantification of food&#xD;
toxins. Recent technological advancements, such as high-resolution MS and tandem mass spectrometry (MS/MS), have significantly&#xD;
improved sensitivity, enabling the detection of food toxins at ultralow levels. Moreover, the emergence of ambient ionization&#xD;
techniques has facilitated rapid in situ analysis of samples with lower time and resources. Despite numerous advantages, the&#xD;
widespread adoption of MS in routine food safety monitoring faces certain challenges such as instrument cost, complexity, data&#xD;
analysis, and standardization of methods. Nevertheless, the continuous advancements in MS-technology and its integration with&#xD;
complementary techniques hold promising prospects for revolutionizing food safety monitoring. This review discusses the&#xD;
application of MS in detecting various food toxins including mycotoxins, marine biotoxins, and plant-derived toxins. It also explores&#xD;
the implementation of untargeted approaches, such as metabolomics and proteomics, for the discovery of novel and emerging food&#xD;
toxins, enhancing our understanding of potential hazards in the food supply chain.</summary>
    <dc:date>2023-11-07T00:00:00Z</dc:date>
  </entry>
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