<?xml version='1.0' encoding='utf-8' ?>



<rss version="2.0"
      xmlns:opensearch="http://a9.com/-/spec/opensearch/1.1/"
      xmlns:dc="http://purl.org/dc/elements/1.1/"
      xmlns:atom="http://www.w3.org/2005/Atom">
   <channel>
     <title><![CDATA[NUST Institutions Library Catalogue Search for 'kw,wrdl: su-br:an:&quot;119503&quot;']]></title>
     <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?idx=kw&amp;q=su-br%3Aan%3A%22119503%22&amp;format=rss</link>
     <atom:link rel="self" type="application/rss+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?idx=kw&amp;q=su-br%3Aan%3A%22119503%22&amp;sort_by=relevance_dsc&amp;format=atom"/>
     <description><![CDATA[ Search results for 'kw,wrdl: su-br:an:&quot;119503&quot;' at NUST Institutions Library Catalogue]]></description>
     <opensearch:totalResults>6</opensearch:totalResults>
     <opensearch:startIndex>0</opensearch:startIndex>
     
       <opensearch:itemsPerPage>50</opensearch:itemsPerPage>
     
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Isolation, Phytochemical Analysis and Antibacterial Activity of Rumex  acetosella Plant /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607252</link>
        
       <description><![CDATA[









	   <p>By Abbasi, Zoya Orangzeb . 
	   
                        . 62p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607252">Place Hold on <em>Isolation, Phytochemical Analysis and Antibacterial Activity of Rumex  acetosella Plant /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607252</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Saikosaponin B2 modulate oxidative stress in scopolamine induced murine model of Alzheimer’s Disease /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608656</link>
        
       <description><![CDATA[









	   <p>By Malik, Mehreen Nadeem . 
	   
                        . 80p.
                        , One of the initial pathological hallmarks of Alzheimer's disease is cognitive decline and
memory loss by disruption of cholinergic neurons and oxidative brain damage. A
postsynaptic muscarinic receptor blocker, scopolamine impairs cholinergic
transmission and impairs cognition. Here, we observed the physiological processes
underlying Saikosaponin b2's impact on memory deficits in mice that had been given
scopolamine repeatedly. Scopolamine (1 mg/kg) administration for 15 days caused
severe deficits in working and short-term memory in mice, as determined by the
elevated plus maze, Morris water maze, and novel object recognition tests. However,
scopolamine administered mice who were additionally given Saikosaponin b2 did not
experience either deficit. This effect was associated with an increase in antioxidant
enzymes (superoxide dismutase, Glutathione reductase, glutathione s transferase and
catalase), followed by reduction in lipid peroxidation and myeloperoxidase activity.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608656">Place Hold on <em>Saikosaponin B2 modulate oxidative stress in scopolamine induced murine model of Alzheimer’s Disease /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608656</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Green Synthesized Silver Nanoparticles Enhances Anticancer Activity of HDAC Inhibitor Panobinostat /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608894</link>
        
       <description><![CDATA[









	   <p>By Nawaz, Tayyaba . 
	   
                        . 80p.
                        , Breast cancer is the most common cancer among women even though numerous
treatment options for breast cancer have been documented. Panobinostat, A histone
deacetylase inhibitor, modifies gene expression through epigenetic pathways and
prevents protein breakdown. The focus of this study is to enhance drug distribution to the
tumor site and boost the efficiency of Panobinostat by using silver nanoparticles as
controlled drug delivery system. Here we report the green synthesis of silver
nanoparticles by using Rhazya stricta extract, as a nanocarriers for drug delivery. These
drugs loaded nanoparticles were characterized by UV-Vis spectroscopy, XRD, FTIR,
SEM, and EDX techniques. The overall findings demonstrated that AgNPs synthesized
through Rhazya stricta has the high potential for sustained release of Panobinostat for
cancer therapy. As the successfully synthesized Panobinostat-AgNPs were stable and
exhibited increased in vitro anticancer activity compared with free Panobinostat, our data
demonstrate that the combination of AgNPs with Panobinostat improves the drug's longterm viability, effectiveness, and active targeting as a potential targeted therapeutic
molecule for the treatment of cancer. To strengthen the utilization of this combination
therapy in cancer therapy trials, further research is warranted.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608894">Place Hold on <em>Green Synthesized Silver Nanoparticles Enhances Anticancer Activity of HDAC Inhibitor Panobinostat /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608894</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Liposomal Formulation of Lapatinib for the Treatment of Breast Cancer /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608899</link>
        
       <description><![CDATA[









	   <p>By Idrees, Maria . 
	   
                        . 70p.
                        , Breast cancer is the most common type of cancer among global women, even though
numerous treatment options for breast cancer have been documented. Lapatinib, a tyrosine
kinase inhibitor, modifies the cellular pathways and halts cell proliferation. The focus of
this study includes the distribution of the drug to the tumor site in high amount and boost
the efficiency of Lapatinib-loaded liposomes as a controlled drug delivery system against
breast cancer. The synthesis of liposomes was followed by drug loading. The cargo was
characterized under XRD, FTIR, SEM, EDX, and zeta analysis techniques. The overall
findings demonstrated that the Liposomal formulation of Lapatinib has a high potential for
sustained release of the drug for cancer therapy. As the successfully synthesized Lapatinibliposomes were stable and exhibited increased in vitro anticancer activity as compared to
free Lapatinib. Our study demonstrates that the combination of Lapatinib with liposomes
improves the drug's long-term viability, effectiveness, and active targeting as a potential
targeted therapeutic molecule for breast cancer treatment. To strengthen the utilization of
this combination therapy in cancer therapy trials, further research is warranted.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608899">Place Hold on <em>Liposomal Formulation of Lapatinib for the Treatment of Breast Cancer /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608899</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Endocrine Dysregulation Adversely Effects Female Reproductive Health in South Punjab Pakistan /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=610778</link>
        
       <description><![CDATA[









	   <p>By Rao, Marium Tufail . 
	   
                        . 101p.
                        , Endocrine disorders have severe consequences for reproductive health and, overall, the
woman’s condition. The role of this research is to establish the level of hormonal
imbalance resulting in reproductive and other diseases among women in south Punjab,
Pakistan. Thus, the present study has adopted a cross-sectional, observational research
design in choosing 430 females from Bahawalpur Victoria hospital. Serum samples were
also taken from females and hormonal assays performed on the collected samples in
endocrine lab. The collected data were analyzed statistically to compare hormonal levels
with health status of the women. The findings of the study were that the common
symptoms were fatigue, cravings for food, and the high level of obesity among the
participants. Hormonal level was correlated with amenorrhea, oligomenorrhea, type 2
diabetes, and insomnia at the considerable level. Serum levels of CA- 125 and AFP
were also raised significantly with ovarian cancer. Some other common manifestations
were psychological, such as depression, anxiety, increased, and insomnia. Also, the most
frequent reproductive symptoms identified were pain and swelling of the breasts, benign
breast diseases, and night sweating. The survey work showed high prevalence of hair loss
and hirsutism to above the norms, therefore pointing at dermatological consequences of
hormonal disturbances. Another group of marriage-related problems that were also
identified were fertility problems which were also common affecting a large percentage
of the population. No significant associations were found between hormonal levels and
certain conditions such as cardiovascular disease and liver disease. The hormonal testing
showed dysregulation in FSH and LH and estrogen and progesterone and thyroid
hormones. Women of south Punjab are undergoing hormonal imbalance, which includes
reproductive health problems and other health related concerns. Focused education on
symptoms, early checkups, and encompassing medical approaches are useful in reducing
effects of hormonal fluctuations in this group of ladies.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=610778">Place Hold on <em>Endocrine Dysregulation Adversely Effects Female Reproductive Health in South Punjab Pakistan /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=610778</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    pH-Responsive Aloe Vera Hydrogels Loaded with Imatinib for Targeting Drug Resistance in Cancer /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=611346</link>
        
       <description><![CDATA[









	   <p>By  Hasan Khan ,Aroob. 
	   
                        . 77p. ;
                        , Cancer and its reoccurrence have become a major health problem affecting the
quality of life for millions of individuals every year. The currently available strategies,
radiotherapy, and chemotherapy have non-specific targets, lower solubility, and severe
side effects. Hydrogels are crosslinked polymeric networks with higher swelling
properties, degradation, biocompatibility, and flexibility which can be manipulated based
on the desired application. Incorporating AV can elevate the antioxidant, and anticancer
properties of the hydrogel based drug delivery system (DDS) also warranting enhanced
swelling, drug release, and environmental degradability of the system. Acrylic acid (AA)
induces pH-responsive properties in the hydrogels. The PVA/SA and PVA/SA/AV
hydrogels were synthesized with a pH responsive behavior and investigated at different
pH conditions. The unloaded and loaded PVA/SA and PVA/SA/AV hydrogels with
imatinib (IM) were characterized for their structural morphology, physiochemical
characteristics, and antioxidant and anticancer activity. The IM loaded PVA/SA/AV
hydrogels showed increased pore size in SEM micrographs, enhanced swelling abilities
up to 400%, 100% degradation, 56% encapsulation efficiency, and drug release profiles
of up to 94% in 24 h, compared to PVA/SA hydrogels loaded with IM. Dpph radical
scavenging activity was also observed to be enhanced in PVA/SA/AV hydrogels. Finally,
the cell viability analysis in resistant MCF-7 breast cancer cell lines exhibited 41% cell
viability of the PVA/SA/AV hydrogels loaded with IM implying a promising potential of
AV to be incorporated in a hydrogel based drug delivery system for targeting drug
resistance in cancer. 
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=611346">Place Hold on <em>pH-Responsive Aloe Vera Hydrogels Loaded with Imatinib for Targeting Drug Resistance in Cancer /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=611346</guid>
     </item>
	 
   </channel>
</rss>





