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    <title>DSpace Collection:</title>
    <link>http://localhost:80/xmlui/handle/123456789/13308</link>
    <description />
    <pubDate>Thu, 05 Mar 2026 22:07:18 GMT</pubDate>
    <dc:date>2026-03-05T22:07:18Z</dc:date>
    <item>
      <title>Plasma ApoA-1 and endothelin-1 levels changes in early Parkinson disease and its relationship with cognitive function and cerebral white matter structure change</title>
      <link>http://localhost:80/xmlui/handle/123456789/13507</link>
      <description>Title: Plasma ApoA-1 and endothelin-1 levels changes in early Parkinson disease and its relationship with cognitive function and cerebral white matter structure change
Authors: Yan, Yingying; Fu, Jianjiong
Abstract: The study aimed to investigate the plasma apolipoprotein A-1 (ApoA-1) and endothelin -1 (ET-1) changes in&#xD;
early Parkinson disease (PD), and analyze their relationship with cognitive function and cerebral white matter structure&#xD;
(WMS) change. 76 early PD patients were selected as group PD, and 30 cases of healthy persons were selected as control&#xD;
group. They all scanned with magnetic resonance imaging (MRI) diffusion tensor. The ApoA-1, ET-1, WMS changes,&#xD;
and Montreal Cognitive Assessment (MoCA) scores were recorded in the two groups of subjects. The results revealed&#xD;
that ApoA-1 level and Mo CA score in PD group decreased, FA value in bilateral temporal lobe, left anterior cingulate&#xD;
tract, corpus callosum, and other cerebral WMS area in PD group were also decreased, and ET-1 level in PD group&#xD;
increased (P&lt;0.05). Compared with those of PD group patients with Mo CA≥26, plasma ApoA-1 levels and cerebral&#xD;
WMS FA values of the patients with Mo CA＜26 were decreased, (P&lt;0.05); the MoCA score of PD group was positively&#xD;
correlated with the cerebral WMS FA values (P&lt;0.05). In short, the ApoA-1 level in patients with early PD decreased,&#xD;
while the ET-1 level increased, and both were related to cognitive function and WMS.</description>
      <pubDate>Sat, 16 Jan 2021 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:80/xmlui/handle/123456789/13507</guid>
      <dc:date>2021-01-16T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Therapeutic effect of gefitinib on patients with advanced EGFRmutation NSCLC</title>
      <link>http://localhost:80/xmlui/handle/123456789/13505</link>
      <description>Title: Therapeutic effect of gefitinib on patients with advanced EGFRmutation NSCLC
Authors: Xu, Ailing; Yan, Haixia; Bu, Tongliang
Abstract: This study aims to study the role of gefitinib on patients with advanced EGFR-mutation NSCLC (Non-Small&#xD;
Cell Lung Cancer). Totally 115 patients with advanced EGFR-mutation NSCLC treated in our hospital were enrolled as&#xD;
research objects. They were randomly divided into control group (n=57) applied with cisplatin + pemetrexed and&#xD;
experimental group (n=58) subject to gefitinib+ cisplatin + pemetrexed, both groups were applied with treatment for 4&#xD;
cycles. Clinical efficacy: The disease control rate (DCR) was 72.41% in the experimental group, which was higher than&#xD;
that of the control group (54.39%, p&lt;0.05); Serum CEA, CYFRA21-1, MMP-9 levels: after 2 and 4 cycles of treatment,&#xD;
serum CEA, CYFRA21-1, and MMP-9 levels were lower in the experimental group (p&lt;0.05); Immune function: after 2&#xD;
and 4 cycles of treatment, Th1 cells and Th1/Th2 cell levels were higher in the experimental group, while Th2 cell level&#xD;
was higher in the control group (p&lt;0.05); Angiogenesis related indicators: the levels of VEGF, HIF-1α and sCD105 were&#xD;
lower in the experimental group after 2 and 4 cycles of treatment (p&lt;0.05); (5) Adverse reactions: After 2 and 4 cycles of&#xD;
treatment, the levels of VEGF, HIF-1α, and sCD105 were lower in the experimental group (p&lt;0.05). The application of&#xD;
gefitinib in patients with advanced EGFR-mutation NSCLC can help down-regulate CEA, CYFRA21-1, and MMP-9&#xD;
levels, inhibit angiopoiesis, enhance immune function, and increase disease control rate.</description>
      <pubDate>Sat, 16 Jan 2021 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:80/xmlui/handle/123456789/13505</guid>
      <dc:date>2021-01-16T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Development, characterization and evaluation of in-vitro anti-inflammatory activity of ginger extract based micro emulsion</title>
      <link>http://localhost:80/xmlui/handle/123456789/13497</link>
      <description>Title: Development, characterization and evaluation of in-vitro anti-inflammatory activity of ginger extract based micro emulsion
Authors: Akram, Ayesha; Rasul, Akhtar; Waqas, Muhammad Khurram; Irfan, Muhammad; Khalid, Syed Haroon; Aamir, Muhammad Naeem; Ghulam Murtaza; Kashif Ur Rehman; Iqbal, Muhammad; Khan, Barkat Ali
Abstract: Zingeber officinale is a commonly used plant which has been shown to possess anti-inflammatory activity.&#xD;
The active compounds present in ginger are gingerols, shagaols and paradol. The aim of this study was formulation of&#xD;
topical microemulsion system to enhance the solubility and stability of ginger extract, as it is unstable in the presence of&#xD;
light, air, heat and long term storage, and to evaluate its anti-inflammatory activity. The solubility of ginger extract in&#xD;
different oils, surfactants, and co-surfactants was determined in order to find the optimal components for microemulsion.&#xD;
IPM was selected as oil phase, tween 80 and PEG 400 were selected as surfactant and co-surfactant respectively based&#xD;
on highest solubility values. Pseudo-ternary phase diagram was constructed in order to find out the microemulsion&#xD;
region. The prepared microemulsions were evaluated for pH, viscosity, conductivity, refractive index, globular size, zeta&#xD;
potential, polydispersity index, ginger extract content. The formulation F1 showed best physicochemical properties with&#xD;
smallest globular size. It also showed significant (p&lt;0.05) anti-inflammatory effect as compared to reference piroxicam&#xD;
drug solution. Based on the results, it is concluded that ginger extract can be used to develop stable microemulsion&#xD;
system and promising anti-inflammatory activity.</description>
      <pubDate>Sat, 16 Jan 2021 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:80/xmlui/handle/123456789/13497</guid>
      <dc:date>2021-01-16T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Application effect of tirofiban on percutaneous coronary intervention in patients with acute coronary syndrome and its postoperative effect on C-X-C motif chemokine ligand 16 level and myocardial perfusion</title>
      <link>http://localhost:80/xmlui/handle/123456789/13495</link>
      <description>Title: Application effect of tirofiban on percutaneous coronary intervention in patients with acute coronary syndrome and its postoperative effect on C-X-C motif chemokine ligand 16 level and myocardial perfusion
Authors: Xu, Maoling; Zhang, Cun; Yu, Xiuzhen; Zhu, Lele; Tan, Hong; Wang, Cong; Zhao, Lingshi; Zhao, Zhihua
Abstract: : This study aimed to investigate the application effect of tirofiban on percutaneous coronary intervention (PCI)&#xD;
in patients with acute coronary syndrome (ACS) and its postoperative effect on C-X-C motif chemokine ligand 16&#xD;
(CXCL16) level and myocardial perfusion. A total of 50 cases of patients diagnosed with acute coronary syndrome and&#xD;
treated in Sunshine Union Hospital (Weifang, China) were included in group A and 30 cases of healthy subjects&#xD;
underwent physical examination in our hospital during the same period were enrolled in group B. Tirofiban was used in&#xD;
group A patients during PCI. Clinical efficacy evaluation criteria were used to evaluate the efficacy after treatment. The&#xD;
level of CXCL16 in serum before and after treatment was detected by qRT-PCR. Receiver operating characteristic&#xD;
(ROC) curve was drawn to analyze the value of C-X-C Motif Chemokine Ligand in diagnosing ACS. Before treatment,&#xD;
CXCL16 level in group A was significantly higher than that in group B (p&lt;0.001). After treatment, patients in TMPG&#xD;
grade 3 in group A were significantly increased (p&lt;0.001). Tirofiban could improve myocardial perfusion in patients&#xD;
with ACS after PCI, reduce adverse events and CXCL16 levels. Serum CXCL16 is expected to be a potential diagnostic&#xD;
and therapeutic predictor of ACS.</description>
      <pubDate>Sat, 16 Jan 2021 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:80/xmlui/handle/123456789/13495</guid>
      <dc:date>2021-01-16T00:00:00Z</dc:date>
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