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    <title>NISCAIR Online Periodicals Repository Collection: IJCT Vol.16(5) [September 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6158</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6170" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6169" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6168" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6167" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6170">
    <title>One–step simple method for the determination of palladium using 3-acetyl- 2-thiohydantoin as a releasing agent</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6170</link>
    <description>Title: One–step simple method for the determination of palladium using 3-acetyl- 2-thiohydantoin as a releasing agent
&lt;br/&gt;
&lt;br/&gt;Authors: Karthikeyan, J; Naik, P Parameshwara; Shetty, A Nityananda
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple, rapid and accurate complexometric method for the&#xD;
determination of palladium(II) is proposed, based on the selective masking&#xD;
property of 3-acetyl-2-thiohydantoin (ATH) towards palladium(II). In the presence&#xD;
of diverse metal ions, palladium(II) is complexed with excess of EDTA and the&#xD;
surplus EDTA is back titrated with standard lead nitrate solution at &lt;i&gt;p&lt;/i&gt;H&#xD;
5-6 (acetic acid – sodium acetate buffer) using xylenol orange as indicator. An&#xD;
excess of a 0.5% solution of ATH is then added to displace EDTA from Pd(II) –&#xD;
EDTA complex. The released EDTA is titrated with the same standard lead nitrate&#xD;
solution as before. Reproducible and accurate results are obtained in the&#xD;
concentration range 0.35–11.00 mg of palladium with relative error of ±0.46%&#xD;
and coefficient of variation not exceeding 0.36%. The effects of diverse ions&#xD;
are studied. The method is used for the determination of palladium in alloys,&#xD;
hydrogenation catalyst and complexes with a fair degree of accuracy.
&lt;br/&gt;
&lt;br/&gt;Page(s): 442-446</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6169">
    <title>Spectrophotometric determination of uranium (VI) via complexation with piroxicam</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6169</link>
    <description>Title: Spectrophotometric determination of uranium (VI) via complexation with piroxicam
&lt;br/&gt;
&lt;br/&gt;Authors: Lutfullah; Khan, Farheen; Rahman, Nafisur; Azmi, Syed Najmul Hejaz
&lt;br/&gt;
&lt;br/&gt;Abstract: An optimized and validated spectrophotometric&#xD;
method has been described for the quantitative analysis of uranyl ion in soil&#xD;
samples. The method is based on the chelation of uranyl ion with piroxicam to&#xD;
produce a yellow complex in 1,4-dioxan–water medium at room temperature which&#xD;
absorbs maximally at 390 nm. Beer’s law is obeyed in the concentration range of&#xD;
6.75 × 10&lt;sup&gt;-2&lt;/sup&gt; – 9.45 × 10&lt;sup&gt;-1&lt;/sup&gt; &lt;img src='/image/spc_char/micro.gif'&gt;g mL&lt;sup&gt;-1&lt;/sup&gt; with apparent molar absorptivity&#xD;
and Sandell’s sensitivity of 4.114 × 10&lt;sup&gt;5 &lt;/sup&gt;L/mol/cm&lt;sup&gt; &lt;/sup&gt;and&#xD;
0.00066 &lt;img src='/image/spc_char/micro.gif'&gt;g/cm&lt;sup&gt;2&lt;/sup&gt;/ 0.001 absorbance unit,&#xD;
respectively. Interference due to various non-target ions was also&#xD;
investigated. The proposed method was successfully applied to the analysis of&#xD;
uranyl ion in synthetic soil samples. The validity of the proposed method was&#xD;
checked by applying the standard addition technique in addition to a comparison&#xD;
with the results obtained from other earlier reported methods.
&lt;br/&gt;
&lt;br/&gt;Page(s): 437-441</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6168">
    <title>New spectrophotometric methods for the estimation of Lercanidipine hydrochloride</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6168</link>
    <description>Title: New spectrophotometric methods for the estimation of Lercanidipine hydrochloride
&lt;br/&gt;
&lt;br/&gt;Authors: Sastry, T Manikya; Ramakrishna, K
&lt;br/&gt;
&lt;br/&gt;Abstract: Three simple and sensitive visible spectrophotometic methods (A-C) have been developed for the assay of Lercanidipine hydrochloride (LER) in bulk and formulations. Method A is based on the formation of colour species by condensation reaction of drug with vanillin (&lt;img src='/image/spc_char/lamda.gif'&gt;&lt;sub&gt;max&lt;/sub&gt;=600). Method B is based on the formation of colour species between the drug and citric acid/acetic anhydride (&lt;img src='/image/spc_char/lamda.gif'&gt;&lt;sub&gt;max&lt;/sub&gt;=555) by means of forming inner salt formation. Method C is based on the formation of colour species by charge transfer complex formation with chloranil-acetaldehyde (&lt;img src='/image/spc_char/lamda.gif'&gt;&lt;sub&gt;max&lt;/sub&gt;=585). The results of analysis have been validated statistically. Recoveries range from 99.4 to 100.5% for the routine assay of LER formulations.
&lt;br/&gt;
&lt;br/&gt;Page(s): 431-436</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6167">
    <title>Estimation of Ibuprofen solubilization in cationic and anionic surfactant media: Application of micelle binding model</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6167</link>
    <description>Title: Estimation of Ibuprofen solubilization in cationic and anionic surfactant media: Application of micelle binding model
&lt;br/&gt;
&lt;br/&gt;Authors: Bhattamishra, S D; Padhy, R K
&lt;br/&gt;
&lt;br/&gt;Abstract: Drug solubility is&#xD;
an important parameter for efficient drug delivery and absorption. Ibuprofen, &lt;img src='/image/spc_char/alpha.gif'&gt;-methyl-4-[2-methyl­propyl] benzene acetic acid is a NSAID group of&#xD;
drug with antipyretic and analgesic properties. It has poor solubility in&#xD;
water. Its solubilisation properties in presence of cetyltrimethylammonium&#xD;
bromide (CTAB) and sodiumdodecyl sulphate (SDS) have been studied. Saturation&#xD;
solubilities in aqueous and aqueous-micellar media have been studied&#xD;
spectrophotometrically by measuring absorbance at 264 nm. Plot of solubility&#xD;
versus [SDS] shows a maximum in the pre-micellar region followed by the linear&#xD;
relationship between the variables in the region past critical micellar&#xD;
concentration (cmc). With CTAB, the solubility- [surfactant] profile shows&#xD;
double maxima, one each in pre- and post- micellar region. Appropriate&#xD;
explanation has been forwarded and the nature of solubilizate-surfactant&#xD;
interaction suggested. The p&lt;i style=""&gt;K&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt;&#xD;
values of ibuprofen determined &lt;i&gt;p&lt;/i&gt;H-metrically in aqueous and aqueous-SDS&#xD;
media have been used to supplement the inference. The association constant&#xD;
values and free energy change of solubilisation are reported.
&lt;br/&gt;
&lt;br/&gt;Page(s): 426-430</description>
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