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    <title>DSpace Collection:</title>
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        <rdf:li rdf:resource="http://localhost:80/xmlui/handle/123456789/14821" />
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    <dc:date>2026-04-23T04:59:33Z</dc:date>
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  <item rdf:about="http://localhost:80/xmlui/handle/123456789/14821">
    <title>Formulation development and evaluation of transdermal emulgel using Aloevera extract and natural penetration enhancers</title>
    <link>http://localhost:80/xmlui/handle/123456789/14821</link>
    <description>Title: Formulation development and evaluation of transdermal emulgel using Aloevera extract and natural penetration enhancers
Authors: Javed, Nida; Shah, Syed Nisar Hussain; Saeed, Javaria; Nisar, Memoona; Javed, Hina; Riaz, Rommana; Karim, Khadija
Abstract: This study was to formulate Aloevera extract loaded emulsion (O/W) based gels, by using various&#xD;
concentrations of rose oil, olive oil and Lemon oil as natural penetration enhancers for transdermal effect to treat skin problems. By using RSM, Aloevera emulgels were formulated and then optimized. Stability studies, physico-chemical characteristics, spreadability, skin protection factor, thermal analysis, FTIR, antimicrobial activity, in vitro drug release study (at 37ºC with 100 rpm for 180 minute in release medium at pH 5.5) and in vivo skin evaluation tests were performed. The results were then statistically analyzed. Among all formulations, G12 has shown maximum 93.53% Aloevera release at higher concentration of Olive oil with decreased concentration of Rose oil and Lemon oil. Analysis of variance (ANOVA) was conducted to evaluate the results exhibited independent variables have remarkable effects on dependent variables. Contour plot is also drawn to express the response between independent and dependent variables. All formulations have followed Korsmeyer-Peppas kinetic model. In summary, the combination of penetration enhancers in Aloevera emulgel can be successfully utilized for treatment of mild-moderate acne vulgaris and other skin problems, as optimized emulgel has shown good permeability, prolonged residence time on skin surface and proved good antimicrobial activity.</description>
    <dc:date>2022-05-13T00:00:00Z</dc:date>
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  <item rdf:about="http://localhost:80/xmlui/handle/123456789/14819">
    <title>A combination of tetramethylpyrazine hydrochloride and butylphthalide on serum S100B, CRP, Hcy levels and NIHSS score in patients with acute cerebral infarction: A retrospective study</title>
    <link>http://localhost:80/xmlui/handle/123456789/14819</link>
    <description>Title: A combination of tetramethylpyrazine hydrochloride and butylphthalide on serum S100B, CRP, Hcy levels and NIHSS score in patients with acute cerebral infarction: A retrospective study
Authors: Fu, Beibei; Meng, Shuqing; Gao, Genshan
Abstract: To investigate the effect of tetramethylpyrazine hydrochloride combined with butylphthalide on serum S100B,&#xD;
CRP, Hcy and NIHSS score in patients with acute cerebral infarction. 80 patients with acute cerebral infarction treated in our hospital from February 2019 to February 2021 were selected for retrospective analysis, and according to different treatment methods, the patients were equally divided into control group (conventional treatment) and experimental group (tetramethylpyrazine hydrochloride and butylphthalide). After treatment, the total effective rate of patients in the experimental group was significantly higher than that in the control group (P&lt;0.05); the levels of serum S100B, CRP and Hcy, and NHISS scores in the two groups decreased, and the experimental group was significantly lower than the control group (P&lt;0.05); the ADL scores of the two groups increased and the experimental group witnessed higher score (P&lt;0.05); the number of patients in the experimental group with scores of 0-2 and 5 were significantly larger than that in the control group (P&lt;0.05). The combination of tetramethylpyrazine hydrochloride and butylphthalide emanates a promising result in the treatment of patients with ACI. It reduces serum S100B, CRP and Hcy levels, protects nerve tissue, and improves nerve function, and thus merits clinical application.</description>
    <dc:date>2022-05-12T00:00:00Z</dc:date>
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  <item rdf:about="http://localhost:80/xmlui/handle/123456789/14817">
    <title>Appraisal of the pharmacokinetic profile, histopathology, and stability studies of a fast dissolving oral film based on natural polysaccharide</title>
    <link>http://localhost:80/xmlui/handle/123456789/14817</link>
    <description>Title: Appraisal of the pharmacokinetic profile, histopathology, and stability studies of a fast dissolving oral film based on natural polysaccharide
Authors: Sheikh, Fatima Akbar; Aamir, Muhammad Naeem; Haseeb, Muhammad Tahir; Shah, Muhammad Ajmal; Farid-ul-Haq, Muhammad; Alqarni, Muhammad; Vargas-De-La-Cruz, Celia; Blundell9, Renald
Abstract: The present research is designed to evaluate the pharmacokinetic profile, histological evaluation, and stability&#xD;
studies of an orodispersible film (ODF) of tizanidine (TZ) and meloxicam (MX) prepared from a natural polysaccharide, i.e., xanthan gum. In vivo release study of TZ and MX was performed in rabbits and results indicated the better pharmacokinetics parameters and improved the oral bioavailability when compared to the oral aqueous suspension and solution of TZ and MX, respectively. The intermediate stability studies were performed at 30±2°C and 65±5% RH, whereas, the accelerated stability studies were carried out at 40±2°C and 75±5% RH, respectively for the duration of six months and results indicated that the ODF was stable for six months without any substantial difference in essential physico-chemical parameters, mechanical attributes, and morphological constraints. The toxicity profile of ODF was determined through histopathology of vital organs after administering the ODF to the rabbits. Histopathology revealed that the tissues of all vital organs are normal and did not exhibit any abnormalities, lesions, or hemorrhage. Therefore, the ODF prepared from xanthan gum exhibited a non-toxic and stable formulation with a better pharmacokinetics profile of MX and TZ.</description>
    <dc:date>2022-05-11T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:80/xmlui/handle/123456789/14815">
    <title>Effects of atorvastatin and Zishen Qingqi granules on immune function and liver function of patients with systemic lupus erythematosus with mild and moderate activity</title>
    <link>http://localhost:80/xmlui/handle/123456789/14815</link>
    <description>Title: Effects of atorvastatin and Zishen Qingqi granules on immune function and liver function of patients with systemic lupus erythematosus with mild and moderate activity
Authors: Sun, Yuzi; Yuan, Lili; Liu, Xinrui; Yu, Wenjuan; Li, Jie
Abstract: To explore the effect of atorvastatin combined with Zishen Qingqi Granules on the immune function and liver&#xD;
function of patients with mild to moderate activity systemic lupus erythematosus. The data of 120 patients with mild to moderate activity systemic lupus erythematosus admitted to our hospital from February 2019 to February 2020 were retrospectively analyzed and they were divided into experimental group (n=60) and the control group (n=60) according to the order of admission; the control group was treated with atorvastatin, and the experimental group was treated with Zishen Qingqi Granules plus. The immune function, liver function, TCM syndrome score and systemic lupus erythematosus disease activity index (SLEDAI) were compared between the two groups. The experimental group after treatment was superior to the control group with respect to immune function indexes, liver function indexes, SLEDAI and TCM syndromes (all P&lt;0.001). Atorvastatin combined with Zishen Qingqi Granules can improve the liver function of patients with mild to moderate activity systemic lupus erythematosus, enhance their immunity, and relieve their clinical symptoms.</description>
    <dc:date>2022-05-11T00:00:00Z</dc:date>
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