1995
DOI: 10.1080/00032719508006405
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Spectrophotometric Determination of Metoclopramide and Oxybuprocaine Through Ion Pair Formation with Thiocyanate and Molybdenum(V) or Cobalt(II)

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Cited by 45 publications
(17 citation statements)
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“…31) The reduction probability of Mo(VI) may occur by ascorbic acid or SCN Ϫ in acidic media 31) and react with thiocyanate to form a red binary Mo(V)-SCN Ϫ complex, non extractable with chloroform.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…31) The reduction probability of Mo(VI) may occur by ascorbic acid or SCN Ϫ in acidic media 31) and react with thiocyanate to form a red binary Mo(V)-SCN Ϫ complex, non extractable with chloroform.…”
Section: Resultsmentioning
confidence: 99%
“…20) For fosinopril with H 2 -receptor antagonists by derivative spectroscopy, 21) UV and third derivative spectrophotometry, 22) microemulsion liquid chromatography, 23) HPLC in the presence of its degradation product fosinoprilate, 24) TLC procedures 25) and reversed-phase ion-pair liquid chromatography. 26) Several colorimetric methods for determination of some drugs in pharmaceutical preparations using molybdenum (V) (Mo(V)) thiocyanate reagent forming ion-pair complex were reported such as; chloroquine and pyrimethamine, 27) ampicillin, dicloxacillin, flucloxacillin and amoxacillin, 28) some piperazine derivatives, 29) trazodone, amineptine and amitriptyline hydrochloride, 30) metoclopramide and oxybuprocaine, 31) and some H 1 -antihistaminics. 32) Although the chromatographic methods are sensitive enough, they are expensive and not easily manageable.…”
mentioning
confidence: 99%
“…The method does not involve any critical reaction conditions and can be compared favourably with other existing methods [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17] . The proposed method can serve as an alternative method for the routine analysis of MCP and DAP in pure drugs and in pharmaceutical formulations.…”
Section: Discussionmentioning
confidence: 99%
“…Several spectrophotometric methods have been reported for the determination of MCP and DAP based on diazotization and coupling with resorcinol or naphtha-2-ol 1 , dibenzoyl methane 2 , chromotropic acid 3 , 3-aminophenol and salbutamol 4 , NEDA 5 , ionassociation complex formation 6,7 , an oxidative coupling reaction 8 , charge-transfer complex formation 9 or through formation of the Schiff 's base with pdimethylaminocinnamaldehyde 10 . Other chromogenic reactions use sodium vanadate 11 , ammonium meta vanadate 12 , 3-methylbenzothiazolin-2-one hydrazone (MBTH) 3 , nitrous acid-cresyl fast-violet acetate (CFVA) 13 , 9-chloroacridine 14 , catechol 15 , sodium 3,4-dioxonaphthalene-1-sulphate 16 and Folin-ciocalteu reagent 17 .…”
Section: Introductionmentioning
confidence: 99%
“…12,13) Thus these methods suffer from strongly interferences of drug excipients and diluents. Spectrophotometric determination of these drugs has been proposed based on diazotization, [14][15][16][17] ion pair complexes, 18) charge transfer complexes, 19,20) and the formation of coloured Schiffs base upon interaction with dimethylaminocinnamaldehyde 21) and use of 9-chloroacridine 22) and sodium 1,2-naphthoquinone-4-sulfonic 23) as chromogenic reagents. These methods involve a time-consuming extraction procedures or heating and require strictly controlled reaction conditions.…”
mentioning
confidence: 99%