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. 2016 Jan 25;6(3):137–149. doi: 10.1016/j.jpha.2016.01.003

Table 2.

Performance characteristics of visible-spectrophotometric and spectrofluorometric methods.

S.No. Reagent Methods Methods Linear range (µg/mL); molar extinction coefficient, Є (L/mol/cm) LOD (µg/mL) LOQ (µg/mL) Application Reference
1 MO TFH-MO ion-pair extracted into CHCl3 and measured at 422 nm. 6–12; 1.89×104 Tablets [17]
2 (a) Mo(V)-SCN TFH-Mo(V)-SCN; TFH-OG; and TFH-ARS ion-pair complexes were extracted into organic solvents and absorbance measured at 470, 500 and 425 nm, respectively 5–75 Bulk drug [18]
(b) OG 10–80 Bulk drug
(c) ARS 5–55 Bulk drug
3 (a) BTB Drug-dye ion pair complexes formed in acid medium extracted into CHCl3 and measured at 410 nm 2–25; 2.0×105 0.24 0.71 Tablets [19]
(b) BPB 2–25; 2.0×105 0.28 0.84 Tablets
(c) BCG 2–25; 2.0×105 0.54 1.62 Tablets
4 (a) CAT-GLN Unbleached dye color measured at 540 nm Bulk drug, tablets [20]
(b) KMnO4-FG FCF Unbleached dye color measured at 620 nm. Bulk drug, tablets
(c) DDQ Charge-transfer complex formed in acetonitrile measured at 450 nm Bulk drug, tablets
5 Iodine Drug-I2 charge-transfer complex formed in chloroform measured at 512 nm 2×10−2–1×10−3 mol/L [21]
6 Spectrofluorimetry-Water Native fluorescence in water was measured at 376 nm after excitation at 275 nm 0.02–0.05 0.0031 0.0094 Tablets, cream, gel and spray, spiked human plasma [22]

MO: Methyl orange; Mo(V)-SCN: Molybdenum (V) thiocyanate; OG: Orange G; ARS: Alizarin red S; BTB: Bromothymol blue; BPB: Bromophenol blue; BCG: Bromocresol green; CAT: Chloramine T; GLN: Gallocyanine; KMnO4: potassium permanganate; FG FCF: fast green FCF; DDQ: 2,3-dichloro-5,6-dicyano-1,4-benzoquinone.