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    <dc:date>2026-04-16T06:52:49Z</dc:date>
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    <title>DETERMINATION OF THE PHYSICOCHEMICAL PROPERTIES OF PYRONARIDINE – A NEW ANTIMALARIAL DRUG</title>
    <link>http://localhost:80/xmlui/handle/123456789/14403</link>
    <description>Title: DETERMINATION OF THE PHYSICOCHEMICAL PROPERTIES OF PYRONARIDINE – A NEW ANTIMALARIAL DRUG
Authors: A. ADEGOKE, OLAJIRE; P. BABALOLA, CHINEDUM; S. OSHITADE, OLUWASEUN; A. FAMUYIWA, ABIOLA
Abstract: The physicochemical properties of pyronaridine, a new antimalarial drug, have been determined for the first time in this study, since these parameters are comprehensively not available in literature.&#xD;
UV-Vis spectral analysis of both pyronaridine and its tetraphosphate salt were carried out in various solvents, in&#xD;
addition to solubility of the two drugs in these solvents. Partition coefficient was done in n-octanol-water mixture using the Leo-Hansch method as well hydrophobicity index determination. pKa determination was carried out on the tetraphosphate. UV-Vis spectral characteristics showed that both the base and the tetraphosphate salt have significant light absorption in the range 190-380nm. Solubility in different solvents revealed that pyronaridine base is sparingly soluble in chloroform (1.34%) while it is slightly soluble in methanol (0.29%) and ethanol (0.42%) and very slightly soluble in octanol and distilled water. The tetraphosphate salt was sparingly soluble in water (1.46%) while it is only very slightly soluble in other solvents. The higher aqueous solubility of the salt was further revealed by a greater Rm value on extrapolation to 100% water concentration in hydrophobicity index determination. Log P value determination showed that the base (log P of 0.26±0.02) is more liposoluble than the salt {logP of – (1.24±0.21)}. Four prominent pKa values were obtained for the tetraphosphate titrated which when extrapolated to the base gave values of 7.08±0.05, 7.39± 0.05, 9.88± 0.05 and 10.30± 0.10. The results should guide in formulation of appropriate dosage forms to improve bioavailability of the drug especially from oral routes.</description>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
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