<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/33212">
    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/33212</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/33314" />
      </rdf:Seq>
    </items>
    <dc:date>2026-04-28T04:26:40Z</dc:date>
  </channel>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/33314">
    <title>Investigating pancreatic α-amylase in gastric juice</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/33314</link>
    <description>Title: Investigating pancreatic α-amylase in gastric juice
Abstract: The aims of the study were to develop a method that quantitatively measures P-AM in&#xD;
gastric juice; to differentiate between P-AM and S-AM in gastric juice; to investigate&#xD;
the effect of pH, temperature and time on P-AM detection in gastric juice; to&#xD;
qualitatively analyse P-AM in gastric juice; to investigate the effect of PPI treatment on&#xD;
P-AM.&#xD;
&#xD;
P-AM and AMYL activities were measured at room temperature and on ice. A P-AM&#xD;
pH curve was obtained by testing P-AM activity at different pH values. Different buffer&#xD;
to gastric juice ratio were used to measure P-AM and AMYL activities for an optimum&#xD;
ratio. P-AM and AMYL activities were assayed using the Reflotron® and Phadebas®&#xD;
Amylase test and calibration curves were obtained. Gastric juice from thirteen patient&#xD;
samples on PPT treatment and from four controls was tested for P-AM activity.&#xD;
There was a significant difference between P-AM activity at different time intervals&#xD;
with a P-value of 0.00679 (P&lt;0.05). There was no significant difference between the&#xD;
effect of temperature and time with a P-value of 0.384 (P&gt;0.05). The P-AM calibration&#xD;
curves show lower measured P-AM activity than standard values. A significant&#xD;
correlation was noted with a correlation co-efficient of 0.9998 (P&lt;0.05) using the&#xD;
Reflotron ®.&#xD;
&#xD;
The Reflotron® and the Phadebas® Amylase test can quantitatively analyse P-AM and&#xD;
AMYL activities in gastric juice whereas Iso-Electrofocusing can be used for qualitative&#xD;
analysis. The Hitachi 917 quantitatively analysed AMYL activity and the Agarose&#xD;
method quantitatively analysed P-AM activity in gastric juice. Denaturing of P-AM&#xD;
occurs at a pH &lt; 4.00 and&gt; 10.00. The optimum buffer to gastric juice ratio is 55:45.&#xD;
The time taken from collection to analysis of P-AM activity is critical using the&#xD;
Reflotron® which is not influenced by storage temperature. Hyperamylasemia was&#xD;
present in gastric juice of patients on PPI treatment. No P-AM was found present in the&#xD;
four controls.
Description: M.PHIL.</description>
    <dc:date>2008-01-01T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

