<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>NISCAIR Online Periodicals Repository Collection: JSIR Vol.63(02) [February 2004]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5179</link>
    <description />
    <textInput>
      <title>The Collection's search engine</title>
      <description>Search the Channel</description>
      <name>search</name>
      <link>http://nopr.niscair.res.in/simple-search</link>
    </textInput>
    <item>
      <title>Eighth international congress on plant pathology – solving problems in the real world - A report</title>
      <link>http://nopr.niscair.res.in/handle/123456789/17592</link>
      <description>Title: Eighth international congress on plant pathology – solving problems in the real world - A report
&lt;br/&gt;
&lt;br/&gt;Authors: Johri, J K
&lt;br/&gt;
&lt;br/&gt;Page(s): 187-192</description>
      <pubDate>Thu, 29 Jan 2004 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Characterisation of sapindosides in &lt;i&gt;Sapindus mukorosii &lt;/i&gt;saponin (reetha &lt;span style="font-size:14.0pt;line-height:115%;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";color:black;mso-ansi-language:EN-IN; mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN"&gt;saponin) and quantitative determination of sapindoside B*&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/17591</link>
      <description>Title: Characterisation of sapindosides in &lt;i&gt;Sapindus mukorosii &lt;/i&gt;saponin (reetha &lt;span style="font-size:14.0pt;line-height:115%;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";color:black;mso-ansi-language:EN-IN; mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN"&gt;saponin) and quantitative determination of sapindoside B*&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Saxena, D; Pal, R; Dwivedi, A K; Singh, S
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:14.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN"&gt;High performance thin layer chromatography (HPTLC) method as well as high performance&#xD;
liquid chromatographic (HPLC) method combined with ES-MS are developed and validated&#xD;
for fingerprinting (profiling) &lt;i&gt;Sapindus saponin&lt;/i&gt; and quantitative determination&#xD;
of Sapindoside B in bulk drug samples of &lt;i&gt;Sapindus saponin &lt;/i&gt;and its formulation&#xD;
Consap cream. The separation of saponins using TLC is achieved on precoated silica&#xD;
gel plates using chloroform: methanol: water as mobile phase. Detection of the spots&#xD;
is done at the 630 nm. The identification of saponins is done by LC-MS, using Electro&#xD;
Spray Ionisation [ESI] technique. The HPLC method involves chromatography of the&#xD;
saponins on reverse phase (C-18) column, using acetonitrile-water gradient as mobile&#xD;
phase. The detection is done by UV -visible detector at a wavelength of 215 nm.&#xD;
Calibration graphs are found to be linear over the range 11-220 &lt;span style="font-size:14.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:hiddenhorzocr;color:black;mso-ansi-language:en-in;="" mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;μg &lt;span style="font-size:14.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";color:black;mso-ansi-language:en-in;="" mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;in HPTLC and 30-200 &lt;span style="font-size:14.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:hiddenhorzocr;color:black;mso-ansi-language:en-in;="" mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;μg/mL &lt;span style="font-size:14.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";color:black;mso-ansi-language:en-in;="" mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;in HPLC method. The methods developed&#xD;
are being used for the analysis of the bulk drug samples and Consap cream samples.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 181-186</description>
      <pubDate>Thu, 29 Jan 2004 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Evaluation of a thermal process for bottled watermelon juice</title>
      <link>http://nopr.niscair.res.in/handle/123456789/17590</link>
      <description>Title: Evaluation of a thermal process for bottled watermelon juice
&lt;br/&gt;
&lt;br/&gt;Authors: Ghosh, U; Gangopadhyay, H
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:14.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN"&gt;Process time was determined based on heat inactivation of pectin methyl esterase&#xD;
(PM E) commonly occuring heat resistant enzyme present in watermelon juice. The&#xD;
thermal inactivation time (TIT) of PME was 1 min at 203&lt;sup&gt;o&lt;/sup&gt;F with a z&#xD;
value of 19. The &lt;span style="font-size:14.0pt;line-height:&#xD;
115%;font-family:" times="" new="" roman";mso-fareast-font-family:hiddenhorzocr;="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN"&gt;F&lt;sup&gt;19&lt;/sup&gt;&lt;sub&gt;&lt;span style="font-size:14.0pt;&#xD;
line-height:115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN"&gt;203 &lt;/span&gt;&lt;/sub&gt;&lt;span style="font-size:14.0pt;line-height:115%;&#xD;
font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN"&gt;value is equivalent to 14.2. The process time required to achieve as F value&#xD;
at 203&lt;sup&gt;o&lt;/sup&gt;F was 26 min for bottled watermelon juice.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 177-180</description>
      <pubDate>Thu, 29 Jan 2004 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>New reagent for determination of trace levels of nitrite in environmental samples</title>
      <link>http://nopr.niscair.res.in/handle/123456789/17589</link>
      <description>Title: New reagent for determination of trace levels of nitrite in environmental samples
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, M C Somasekhara
&lt;br/&gt;
&lt;br/&gt;Abstract: A local industrial&#xD;
product an intermediate dye disodium salt of 4,4-diaminostil bene-2,2-disulphonic&#xD;
acid is introduced as a new reagent for a selective and sensitive spectrophotometric&#xD;
determination method of trace levels of nitrite in environmental samples like, water&#xD;
and soil. The method is based on the tetraazo coupling reaction of disodium salt&#xD;
of 4,4-diaminostilbelle-2,2-disulphonic&#xD;
&#xD;
acid with a coupling&#xD;
agent of 2-naphthol. The stable water soluble pink azo dye formed under aqueous&#xD;
alkaline condition has an adsorption maximum at 520 nm. The reaction is fast.&#xD;
The dye formed is stable for more than 48 h. Beer's law is obeyed between 0.04-1.6&#xD;
ppm of nitrite in a final volume of 25 mL. The molar extinction coefficient of&#xD;
the color system is 3.0×10&lt;sup&gt;4  &lt;/sup&gt;L/mole/cm.&#xD;
Sandal sensitivity is 1.5335×10&lt;sup&gt;-3&lt;/sup&gt; ppm/cm&lt;sup&gt;2&lt;/sup&gt; The relative standard&#xD;
deviation is 2.1 per cent for 10 determinations at 10 ppm level. The method is applied&#xD;
to the determi nation of nitrite in water and soil samples and the results are compared&#xD;
with the&#xD;
&#xD;
&lt;span style="font-size:14.0pt;line-height:115%;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";color:black;mso-ansi-language:en-in;="" mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN"&gt;results obtained from the standard&#xD;
method.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 172-176</description>
      <pubDate>Thu, 29 Jan 2004 22:58:59 GMT</pubDate>
    </item>
  </channel>
</rss>

