Sl. no. Reagent/s Methodology
, nmBeer’s law range µg mL−1 (ε in L mol−1 cm−1 ) Remarks Reference 1 (a) Brucine-sodium metaperiodate Oxidative coupling product was measured 520 4.0–20.0 NA Less sensitive, multistep reaction
[28 ] (b) Citric acid-acetic anhydride 580 8.0–24.0 NA 2 Sodium nitroprusside acetaldehyde Inner molecular complex formed was measured 552 4.0–20.0 (1.10 × 104 ) Less sensitive, requires rigid pH control [29 ] 3 Cobalt thiocyanate Extracted ternary complex formed by reaction with drug was measured 629.4 16.0–48.0 (3.97 × 103 ) Less sensitive, involves extraction step [30 ] 4 Tropaeolin-OOO Extracted ion-pair complex was measured 482.5 2.0–10.0 (2.08 × 104 ) Requires rigid pH control; involves liquid-liquid extraction; use of organic solvents [31 ] 5 (a) Chloranil in 1,4-dioxane
CT-complex measured 548 5.0–25.0 (1.00 × 104 ) Less sensitive, involves heating step, time consuming
[32 ] (b) Chloranil and acetaldehyde 660 20.0–60.0 (3.19 × 104 ) 6 p-Chloranilic acid CT-complex measured 520 9.28 × 102 20–184 Less sensitive; use of organic solvents [33 ] 7 Folin reagent Chromogen formed by reaction with drug was measured 455.6 16.0–48.0 (3.85 × 103 ) Less sensitive, strict pH control, time consuming [34 ] 8 Folin-Ciocaltaeu reagent Reduced FC-reagent was measured 760 2.0–6.0 NA Narrow linear range, less sensitive [35 ] 9
Bromate-bromide- (a) Methyl orange Unreacted bromine was measured 508 0.2–1.6 (1.90 × 105 ) Narrow linear range, multistep reaction, time consuming
[36 ] (b) Indigo carmine 610 2.0–12.0 (2.71 × 104 ) 10 NBS No rigorous control of experimental conditions, no heating or extraction step, no use of organic solvents or toxic chemicals, and sensitive with wide linear dynamic range Proposed methods (a) Potassium Iodide Tri-iodide ion measured Starch-iodine complex measured 370 0.6–15.0
(b) Potassium Iodide-starch 570 0.2–4.0