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<title>CSIR-CDRI Theses and Dissertations</title>
<link>http://dkr.cdri.res.in:8080/xmlui/handle/123456789/1177</link>
<description/>
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<rdf:li rdf:resource="http://dkr.cdri.res.in:8080/xmlui/handle/1/1750"/>
<rdf:li rdf:resource="http://dkr.cdri.res.in:8080/xmlui/handle/1/1749"/>
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<dc:date>2026-04-19T12:11:02Z</dc:date>
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<item rdf:about="http://dkr.cdri.res.in:8080/xmlui/handle/1/1751">
<title>Synthesis of Oligosaccharides Related to Bacterial Cell Wall Polysacchairdas Steroidal Glycosides and Blood Group Antigens</title>
<link>http://dkr.cdri.res.in:8080/xmlui/handle/1/1751</link>
<description>Synthesis of Oligosaccharides Related to Bacterial Cell Wall Polysacchairdas Steroidal Glycosides and Blood Group Antigens
Karki, Geeta; Mandal, Pintu Kumar (Guide)
from the Greek word saccharon meaning sugar.3 Carbohydrates that cannot be&#13;
hydrolyzed into simpler compounds are called “monosaccharides” such as glucose,&#13;
fructose etc. and a carbohydrate that can be hydrolyzed to two monosaccharides is&#13;
called a disaccharide. e.g., sucrose, maltose, lactose, melibiose, cellobiose etc. while&#13;
those composed of many monosaccharide units are called polysaccharides.&#13;
Carbohydrates with an aldehydic group are known as “aldoses” and those with a&#13;
ketonic functionality are “ketoses”. Depending upon the number of carbon atoms it&#13;
contains, the monosaccharide is termed as tetrose, pentose, hexose and so on.&#13;
Polysaccharides can also be classified4-6 into homopolysaccharide and&#13;
heteropolysaccharide depending on the monosaccharide units present. The&#13;
carbohydrates those containing only one type of monosaccharide units are called&#13;
homopolysaccharides e.g. glucans, mannans, galactans, arabinans etc. whereas&#13;
heteropolysaccharides contain two or more different monosaccharide units, e.g.&#13;
glucomannans, galactomannans, arabinogalactans etc. Depending upon their&#13;
functional property, polysaccharides can be divided into two parts. One is fibrous&#13;
polysaccharide, e.g. cellulose in higher plants and some algae, chitin in yeast and&#13;
fungi. The other one is the polysaccharide having matrix forming property and is&#13;
characterized by their gel forming characteristics which confer flexibility on the&#13;
structural assembly. Arabinoxylans, galactomannans of plant origin represent this&#13;
group.
Guide- Dr. Pintu Kumar Mandal. PhD Theses Submitted by to AcSIR,Ghaziabad UP in 2019 by Geeta Karki.
</description>
<dc:date>2019-04-16T00:00:00Z</dc:date>
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<item rdf:about="http://dkr.cdri.res.in:8080/xmlui/handle/1/1750">
<title>A STUDY ON NEUROINFLAMMATION AND ITS INFLUENCE ON NMDA RECEPTOR AND SYNAPTIC FUNCTION IN STZ (ICV) INDUCED MEMORY IMPAIRED RATS</title>
<link>http://dkr.cdri.res.in:8080/xmlui/handle/1/1750</link>
<description>A STUDY ON NEUROINFLAMMATION AND ITS INFLUENCE ON NMDA RECEPTOR AND SYNAPTIC FUNCTION IN STZ (ICV) INDUCED MEMORY IMPAIRED RATS
Rai, Shivika; Shukla, Rakesh (Guide)
In the present study the role of glial activation and post synaptic toxicity in ICV Streptozotocin (STZ) induced&#13;
memory impaired rats was explored. In experiment set up 1: Memory deficit was found in Morris water maze&#13;
test on 14–16 days after STZ (ICV; 3 mg/Kg) administration. STZ causes increased expression of GFAP, CD11b&#13;
and TNF-α indicating glial activation and neuroinflammation. STZ also significantly increased the level of ROS, nitrite,&#13;
Ca2+ and reduced the mitochondrial activity in synaptosomal preparation illustrating free radical generation&#13;
and excitotoxicity. Increased expression and activity of Caspase-3 was also observed in STZ treated rat&#13;
which specify apoptotic cell death in hippocampus and cortex. STZ treatment showed decrease expression of&#13;
post synaptic markers CaMKIIα and PSD-95, while, expression of pre synaptic markers (synaptophysin and&#13;
SNAP-25) remains unaltered indicating selective post synaptic neurotoxicity. Oral treatment with Memantine&#13;
(10 mg/kg) and Ibuprofen (50 mg/kg) daily for 13 days attenuated STZ induced glial activation, apoptotic cell&#13;
death and post synaptic neurotoxicity in rat brain. Further, in experiment set up 2: where memory function&#13;
was not affected i.e. 7–9 days after STZ treatment. The level of GFAP, CD11b, TNF-α, ROS and nitrite levels&#13;
were increased. On the other hand, apoptotic marker, synaptic markers, mitochondrial activity and Ca2+ levels&#13;
remained unaffected. Collective data indicates that neuroinflammatory process and oxidative stress occurs earlier&#13;
to apoptosis and does not affect memory function. Present study clearly suggests that glial activation and post&#13;
synaptic neurotoxicity are the key factors in STZ induced memory impairment and neuronal cell death.
Guide- Dr. Rakesh Shukla, PhD Theses Submitted by AcSIR,Ghaziabad UP by Shivika Rai
</description>
<dc:date>2015-08-26T00:00:00Z</dc:date>
</item>
<item rdf:about="http://dkr.cdri.res.in:8080/xmlui/handle/1/1749">
<title>Development and evaluation of Inhalable particdes Containing  kanamycin monosulhate and pyrazinoic acid for the treatment of drug resistant tuberculosis.</title>
<link>http://dkr.cdri.res.in:8080/xmlui/handle/1/1749</link>
<description>Development and evaluation of Inhalable particdes Containing  kanamycin monosulhate and pyrazinoic acid for the treatment of drug resistant tuberculosis.
Srivastava, Ashish; Misra, Amit (Guide)
Tuberculosis (TB) remains a major health problem and a prime cause of global &#13;
patient mortality throughout the world. Even after 90 years of vaccination and 60 &#13;
years of advanced chemotherapy development, we are far away from eradicating the &#13;
disease. All member states of the WHO and the UN pledged to eradicate TB by 2030 &#13;
by reducing all TB deaths by 90% in the 2014 World Health Assembly. In developing &#13;
nations and settings with limited resources, TB poses further challenges.
Guide- Dr. Amit Misra, PhD Thesis Submitted to AcSIR , Ghaziabad, UP  in 2019 by Ashish Srivastava
</description>
<dc:date>2019-08-22T00:00:00Z</dc:date>
</item>
<item rdf:about="http://dkr.cdri.res.in:8080/xmlui/handle/1/1747">
<title>EXPLORING THE FUNCTIONAL SPECTRUM OF HOST DEFENCE PEPTIDES (HDPs)</title>
<link>http://dkr.cdri.res.in:8080/xmlui/handle/1/1747</link>
<description>EXPLORING THE FUNCTIONAL SPECTRUM OF HOST DEFENCE PEPTIDES (HDPs)
Raj, Sneha; Pasupuleti, Mukesh (Guide)
Infectious diseases have been a leading cause of the threat to human existence. Starting&#13;
from early records of 14th century till mid-20th century, a number of severe outbreaks&#13;
have taken thousands of human lives in a very short span of time, e.g. the bubonic&#13;
plague of Europe, which swiped away around one-third of its population, deadly&#13;
massive epidemics of smallpox, influenza, dysentery and typhus that were frequent in&#13;
the medieval era. In fact, the severity is described such that, at times, there was even&#13;
lesser number of survivors in town to bury the dead and harvest crop for the season.&#13;
With gradual learning amongst the people about hygiene and sanitary conditions of&#13;
living, came an improvement and eradication of frequent plague outbreaks.&#13;
Furthermore, several new antimicrobial agents were discovered at an accelerated pace&#13;
and their applicability was found. The first antimicrobial agent in the world was&#13;
Salvarsan which was the most prescribed therapeutic remedy for syphilis until the&#13;
introduction of Penicillin. It was synthesized by Ehrlich, along with Alfred Bertheim&#13;
and Sahachiro Hata in 1907.
Guide- Dr. Mukesh Pasupuleti, PhD Thesis Submitted by Sneha Raj to JNU, New Delhi in 2019
</description>
<dc:date>2019-12-23T00:00:00Z</dc:date>
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