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Role of scanning electron microscopy in identifying drugs used in medical practice

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dc.contributor.author Fazil Marickar, Y M
dc.contributor.author Sylaja, N
dc.contributor.author Peter Koshy
dc.date.accessioned 2013-11-13T08:44:41Z
dc.date.available 2013-11-13T08:44:41Z
dc.date.issued 2009
dc.identifier.citation Urological Research 37(5):299-303;Oct 2009 en_US
dc.identifier.issn 0300-5623
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/742
dc.description.abstract Several plant preparations are administered for treatment of stone disease without scientific basis. This paper presents the results of in vitro and animal experimental studies using scanning electron microscopy (SEM) in the identification of the therapeutic properties of trial drugs in medicine. In the first set of the study, urinary crystals namely calcium oxalate monohydrate and calcium oxalate dehydrate were grown in six sets of Hane's tubes in silica gel medium. Trial drugs namely scoparia dulcis Lynn, musa sapiens and dolicos biflorus were incorporated in the gel medium to identify the dopant effect of the trial drugs on the size and extent of crystal column growth. The changes in morphology of crystals were studied using SEM. In the second set, six male Wistar rats each were calculogenised by administering sodium oxalate and ethylene glycol and diabetised using streptozotocin. The SEM changes of calculogenisation were studied. The rats were administered trial drugs before calculogenisation or after. The kidneys of the rats studied under the scanning electron microscope showed changes in tissue morphology and crystal deposition produced by calculogenisation and alterations produced by addition of trial drugs. The trial drugs produced changes in the pattern of crystal growth and in the crystal morphology of both calcium oxalate monohydrate and calcium oxalate dihydrate grown in vitro. Elemental distribution analysis showed that the crystal purity was not altered by the trial drugs. Scoparia dulcis Lynn was found to be the most effective anticalculogenic agent. Musa sapiens and dolicos biflorus were found to have no significant effect in inhibiting crystal growth. The kidneys of rats on calculogenisation showed different grades of crystals in the glomerulus and interstitial tissues, extrusion of the crystals into the tubular lumen, collodisation and tissue inflammatory cell infiltration. Scoparia dulcis Lynn exhibited maximum protector effect against the changes of calculogenisation. Musa sapiens and dolicos biflorus had only minimal effect in preventing crystal deposition, inflammatory cell infiltration and other changes of calculogenisation. SEM was found to be effective in assessing the effect of drugs on crystal growth morphology and tissue histology. en_US
dc.language.iso en en_US
dc.publisher Springer en_US
dc.subject Crystal growth en_US
dc.subject Scoparia dulcis Lynn en_US
dc.subject Musa sapiens en_US
dc.subject Dolicos biflorus en_US
dc.subject Calculogenisation en_US
dc.subject Calcium- oxalate nephrolithiasis en_US
dc.subject Stone formers en_US
dc.subject Urinary stone en_US
dc.title Role of scanning electron microscopy in identifying drugs used in medical practice en_US
dc.type Article en_US


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