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    <link>http://localhost:8080/xmlui/handle/123456789/6778</link>
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    <pubDate>Thu, 09 Apr 2026 05:11:37 GMT</pubDate>
    <dc:date>2026-04-09T05:11:37Z</dc:date>
    <item>
      <title>Relationship Between Cephalosporin Use and Increased APTT and PT in Cardiovascular Patients at Government Hospital Bengkulu</title>
      <link>http://localhost:8080/xmlui/handle/123456789/10323</link>
      <description>Title: Relationship Between Cephalosporin Use and Increased APTT and PT in Cardiovascular Patients at Government Hospital Bengkulu
Authors: Laila Ramatillah, Diana; Purba, Rahelia; Rahima Mahyani, Atika; Hassan Elnaem, Mohamed; Ibrahim, Baharudin; Azhar Syed Sulaiman, Syed
Abstract: The interaction that occurs between warfarin and antibiotics is a pharmacokinetic interaction which cause bleeding.&#xD;
This study aims to determine whether there is a relationship between the use of cephalosporins and an increase in APTT and PT&#xD;
in cardiovascular patients. This retrospective observational study employs case-control analysis to examine APTT and PT&#xD;
features in cardiovascular patients receiving single anticoagulant or anticoagulant + cephalosporin therapy for the period July-&#xD;
December 2020. The sampling method used in this study is a convenient sampling method that meets the inclusion and&#xD;
exclusion criteria. Analysis of the data used is Logistic Regression. The study found among 65 male and 15 female, 40&#xD;
patients used anticoagulant, and another 40 patients used anticoagulant and cephalosporine. Among 40 patients who used&#xD;
combination anticoagulant and cephalosporin, 22 of them had experienced of increasing APTT and PT.&#xD;
Cephalosporins showed a significant correlation with APTT and PT, with a P-value of 0.015. From this study, it can be&#xD;
concluded that the use of cephalosporins increases in APTT and PT values in cardiovascular patients who are given&#xD;
anticoagulant drugs and cephalosporins.&#xD;
Keywords: anticoagulants; APTT and PT; cephalosporins</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/10323</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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      <title>Formulation and Antioxidant Activity Test of Gel from Fermented Red Pomegranate Peel Juice (Punica Granatum L)</title>
      <link>http://localhost:8080/xmlui/handle/123456789/10315</link>
      <description>Title: Formulation and Antioxidant Activity Test of Gel from Fermented Red Pomegranate Peel Juice (Punica Granatum L)
Authors: Faizatun, Faizatun; Miftahurrohmah, Nur; Eka Sari, Widya; Rosmawati, Rosmawati
Abstract: Red pomegranate (Punica granatum L.) peel has secondary metabolites such as phenolics, flavonoids, and tannins,&#xD;
which are known to have antioxidant potential. The purpose of this study was to evaluate the comparison of antioxidant activity&#xD;
of juice before and after fermentation and then formulate it into a gel preparation that is physically and chemically stable. Red&#xD;
pomegranate peel juice was dried by freeze drying method and then fermented with Lactobacillus plantarum ATCC 8014 bacteria&#xD;
and measured OD600, pH, and antioxidant activity using DPPH reagent. The results showed that pomegranate peel juice before&#xD;
fermentation had strong antioxidant activity with a value (of IC50 35.64 ± 0.68 ppm) and after fermentation, it was in the very&#xD;
strong category (IC50 8.00 ± 0.01 to 8.11 ± 0.06 ppm); pH before and after (3.96 ± 0.02 and 3.33 ± 0.01). Formula II with juice&#xD;
concentration of 300 x IC50 has the highest antioxidant activity with IC50 values (64.37 ± 1.13 ppm); pH (6.33); spreadability (6.20&#xD;
± 0.07); and viscosity (31333.3 ± 577.35 dPas). There was an increase in antioxidant activity of red pomegranate peel juice after&#xD;
fermentation, the resulting gel is physically and chemically stable based on the results of accelerated stability tests for 4 weeks.&#xD;
Keywords: antioxidant activity; fermentation; Lactobacillus plantarum; pomegranate peel.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/10315</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Synthesis and In Vitro Antimalarial Activity of Amino Chalcone Derivatives Compounds Through Inhibition of Heme Polymerization</title>
      <link>http://localhost:8080/xmlui/handle/123456789/10314</link>
      <description>Title: Synthesis and In Vitro Antimalarial Activity of Amino Chalcone Derivatives Compounds Through Inhibition of Heme Polymerization
Authors: Dona, Rahma; Frimayanti, Neni; Hendra, Rudi; Jasril, Jasril
Abstract: This study aims to investigate the potential of chalcone derivatives as antimalarial agents. The structure of the&#xD;
chalcone derivatives was designed by inserting amino substituents on acetophenone and methoxy variants on benzaldehyde to&#xD;
produce three amino chalcone derivatives (C1, C2, and C3). The synthesis was carried out by carrying out the Claisen-Schmidt&#xD;
condensation reaction with NaOH 40% as catalyst, resulting in compound yields ranging from 66% - 83%. The structure of the&#xD;
three compounds was determined by FTIR, MS, and 1H-NMR spectroscopy techniques, which confirmed that the compounds&#xD;
had structures that were in line with the desired molecular structure. The antimalarial activity test was carried out by inhibiting&#xD;
the heme polymerization process into hemozoin (β-hematin) using hydroxychloroquine sulfate as a positive control. Absorption&#xD;
measurements were carried out at two different wavelengths, namely 415 nm and 630 nm. The results of the IC50 antimalarial&#xD;
activity of the three compounds (C1, C2, C3) were obtained respectively at 227.61; 115.18; 260.01 μg/mL and positive control of&#xD;
184.98 μg/mL. From these results, it was found that compound C2 showed better antimalarial activity compared to the other two&#xD;
compounds and positive control.&#xD;
Keywords: amino chalchone; synthesis; antimalarial; heme polymerization; hemozoin.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/10314</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Development of Coffee Fruit Skin (Coffea canephora) Formula as Antioxidant peel-off Masks</title>
      <link>http://localhost:8080/xmlui/handle/123456789/10311</link>
      <description>Title: Development of Coffee Fruit Skin (Coffea canephora) Formula as Antioxidant peel-off Masks
Authors: Khaira Nursal, Fith; Amalia, Anisa; Nining, Nining; Athaya Putri, Dania; Dara Larasati, Kinanti
Abstract: The outer skin of the robusta coffee bean (Coffea canephora) was a processing waste containing phenolic compounds&#xD;
with an antioxidant role. This activity is relevant when used in cosmetic preparations such as peel-off masks, which form a thin&#xD;
elastic layer on the facial surface and are easy to remove. One of the crucial ingredients of peel-off masks is a plasticizer such as&#xD;
sorbitol, characterized by flexibility, not easily fragile, and elasticity. Therefore, this research aimed to develop a peel-off formula&#xD;
from robusta coffee skin by influencing sorbitol variations on the characteristics of masks in the form of a gel. A total of six gel&#xD;
mask formulas were made with sorbitol variations of 10%, 12.5%, and 15%. The two types of gel base used were Carbopol 940&#xD;
and HPMC (Hydroxy Propyl Methyl Cellulose), at concentrations of 0.25% and 4%, respectively. The results showed that sorbitol&#xD;
variations affected the physical characteristics (p &gt; 0.05) but did not influence the antioxidant activity of robusta coffee skin extract&#xD;
peel-off masks.&#xD;
Keywords: coffe bean skin; peel-off mask; sorbitol; physical characteristics.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/10311</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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