Ferrous Gluconate (fer' us gloo' koe nate). C12H22FeO14·2H2O482.17 d-Gluconic acid, iron(2+) salt (2:1), dihydrate; Iron(2+) gluconate (1:2) dihydrate [12389-15-0]. Anhydrous 446.15 [299-29-6]. DEFINITION Ferrous Gluconate contains NLT 97.0% and NMT 102.0% of ferrous gluconate (C12H22FeO14), calculated on the dried basis. IDENTIFICATION • A. Thin-Layer Chromatography Standard solution: 10 mg/mL of USP Potassium Gluconate RS Sample solution: 10 mg/mL of Ferrous Gluconate, heating in a water bath at 60, if necessary, to dissolve Chromatographic system Mode: TLC Adsorbent: 0.25-mm layer of chromatographic silica gel Application volume: 5 µL Developing solvent system: Alcohol, ethyl acetate, ammonium hydroxide, and water (50:10:10:30) Spray reagent: Dissolve 2.5 g of ammonium molybdate in 50 mL of 2 N sulfuric acid in a 100-mL volumetric flask, add 1.0 g of ceric sulfate, swirl to dissolve, and dilute with 2 N sulfuric acid to volume. Analysis Samples: Standard solution and Sample solution Develop the chromatogram until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the chamber, and dry at 110 for 20 min. Allow to cool, and spray with Spray reagent. Heat the plate at 110 for about 10 min. Acceptance criteria: The principal spot of the Sample solution corresponds in color, size, and RF value to that of the Standard solution. • B. Ferrous Ion Sample solution: 5 mg/mL in water Analysis: Add potassium ferricyanide TS to the Sample solution. Acceptance criteria: The solution yields a dark blue precipitate. ASSAY • Procedure Sample: 1.5 g of Ferrous Gluconate Blank: Proceed as directed in the Analysis without the Sample. Titrimetric system (See Titrimetry 541.) Mode: Direct titration Titrant: 0.1 N ceric sulfate VS Endpoint detection: Visual Analysis: Dissolve the Sample in a mixture of 75 mL of water and 15 mL of 2 N sulfuric acid in a 300-mL conical flask. Add 250 mg of zinc dust, close the flask with a stopper containing a Bunsen valve, and allow to stand at room temperature for 20 min or until the solution becomes colorless. Pass the solution through a filtering crucible containing a thin layer of zinc dust, and wash the crucible and contents with 10 mL of 2 N sulfuric acid, followed by 10 mL of water. [NotePrepare and use the filtering crucible in a well-ventilated hood. ] Add orthophenanthroline TS, and immediately titrate the filtrate in the suction flask with Titrant. Perform a Blank determination. Calculate the percentage of ferrous gluconate (C12H22FeO14) in the Sample taken: Result = {[(VS VB) × N × F]/W} × 100
Acceptance criteria: 97.0%102.0% on the dried basis IMPURITIES • Chloride and Sulfate, Chloride 221 Standard solution: 1.0 mL of 0.020 N hydrochloric acid Sample: 1.0 g Acceptance criteria: NMT 0.07% • Chloride and Sulfate, Sulfate 221 Standard solution: 1.0 mL of 0.020 N sulfuric acid Sample: 1.0 g Acceptance criteria: NMT 0.1% • Mercury 261: NMT 3 ppm • Arsenic, Method I 211 Test preparation: Transfer 1.0 g of Ferrous Gluconate to a 100-mL round-bottom flask fitted with a 24/40 standard-taper joint. Add 40 mL of 9 N sulfuric acid and 2 mL of potassium bromide solution (3 in 10). Immediately connect to a suitable distillation apparatus that has a reservoir with a water jacket, cooled with circulating ice water, and heat to dissolve the Ferrous Gluconate. Distill, collect 25 mL of distillate, and transfer the distillate to the arsine generator flask. Wash the condenser and reservoir several times with small portions of water, add the washings to the distillate in the generator flask, add bromine TS until the solution is slightly yellow, and dilute with water to 35 mL. Proceed as directed in the chapter. Acceptance criteria: NMT 3 ppm • Limit of Lead [NoteFor the preparation of all aqueous solutions and for the rinsing of glassware before use, use water that has been passed through a strong-acid, strong-base, mixed-bed ion-exchange resin before use. Select all reagents to have as low a content of lead as practicable, and store all reagent solutions in containers of borosilicate glass. Cleanse glassware before use by soaking in warm 8 N nitric acid for 30 min and by rinsing with deionized water. ] Ascorbic acidsodium iodide solution: 100 mg/mL of ascorbic acid and 192.5 mg/mL of sodium iodide Trioctylphosphine oxide solution: 50 mg/mL of trioctylphosphine oxide in 4-methyl-2-pentanone. [CautionThis solution causes irritation. Avoid contact with eyes, skin, and clothing. Take special precautions in disposing of unused portions of solutions to which this reagent is added. ] Standard solution: Transfer 5.0 mL of Lead Nitrate Stock Solution, prepared as directed in the test for Heavy Metals 231, to a 100-mL volumetric flask, and dilute with water to volume. Transfer 2.0 mL of the resulting solution to a 50-mL volumetric flask, add 10 mL of 9 N hydrochloric acid and 10 mL of water. Add 20 mL of Ascorbic acidsodium iodide solution and 5.0 mL of Trioctylphosphine oxide solution, shake for 30 s, and allow to separate. Add water to bring the organic solvent layer into the neck of the flask, shake again, and allow to separate. The organic layer is the Standard solution, and it contains 2 µg/mL of lead. Sample solution: To a 50-mL volumetric flask add 1.0 g of Ferrous Gluconate, 10 mL of 9 N hydrochloric acid, 10 mL of water, 20 mL of Ascorbic acidsodium iodide solution, and 5.0 mL of Trioctylphosphine oxide solution. Shake for 30 s, and allow to separate. Add water to bring the organic solvent layer into the neck of the flask, shake again, and allow to separate. The organic layer is the Sample solution. Blank: To a 50-mL volumetric flask add 10 mL of 9 N hydrochloric acid, 10 mL of water, 20 mL of Ascorbic acidsodium iodide solution, and 5.0 mL of Trioctylphosphine oxide solution. Shake for 30 s, and allow to separate. Add water to bring the organic solvent layer into the neck of the flask, shake again, and allow to separate. The organic layer is the Blank, and it contains 0 µg/mL of lead. Instrumental conditions Mode: Atomic absorption spectrophotometry Analytical wavelength: 283.3 nm Lamp: Lead hollow-cathode Flame: Airacetylene System suitability Samples: Standard solution and Blank Suitability requirements: The absorbance of the Standard solution and the absorbance of the Blank are significantly different. Analysis Samples: Standard solution, Sample solution, and Blank Concomittantly determine the absorbances of the Blank, Standard solution, and Sample solution. Use the Blank to set the instrument to zero. Acceptance criteria: The absorbance of the Sample solution does not exceed that of the Standard solution (NMT 10 ppm). • Limit of Ferric Iron Sample: 5 g of Ferrous Gluconate Blank: Proceed as directed in the Analysis without the Sample. Titrimetric system (See Titrimetry 541.) Mode: Direct titration Titrant: 0.1 N sodium thiosulfate VS Endpoint detection: Visual Analysis: Dissolve the Sample in a mixture of 100 mL of water and 10 mL of hydrochloric acid, and add 3 g of potassium iodide. Shake, and allow to stand in the dark for 5 min. Titrate any liberated iodine with the Titrant, adding 3 mL of starch TS as the endpoint is approached. Perform a Blank determination. Calculate the percentage of ferric iron in the portion of Ferrous Gluconate taken: Result = {[(VS VB) × N × F]/W} × 100
Acceptance criteria: NMT 2.0% • Oxalic Acid Sample: 1.0 g Analysis: Dissolve the Sample in 10 mL of water, add 2 mL of hydrochloric acid, and transfer to a separator. Extract successively with 50 mL and 20 mL of ether. Combine the ether extracts, add 10 mL of water, and evaporate the ether on a steam bath. Add 1 drop of 6 N acetic acid and 1 mL of a 50 mg/mL solution of calcium acetate. Acceptance criteria: No turbidity is produced within 5 min. • Reducing Sugars Sample: 500 mg Analysis: Dissolve the Sample in 10 mL of water, warm, and render alkaline with 1 mL of 6 N ammonium hydroxide. Pass hydrogen sulfide gas into the solution to precipitate the iron, and allow the solution to stand for 30 min to coagulate the precipitate. Filter, and wash the precipitate with two successive 5-mL portions of water. Acidify the combined filtrate and washings with hydrochloric acid, and add 2 mL of 3 N hydrochloric acid in excess. Boil the solution until the vapors no longer darken lead acetate paper, and continue to boil, if necessary, until it has been concentrated to 10 mL. Cool, add 5 mL of sodium carbonate TS and 20 mL of water, filter, and adjust the volume of the filtrate to 100 mL. To 5 mL of the filtrate add 2 mL of alkaline cupric tartrate TS, and boil for 1 min. Acceptance criteria: No red precipitate is formed within 1 min. SPECIFIC TESTS • Loss on Drying 731: Dry a sample at 105 for 16 h: it loses 6.5%10.0% of its weight. ADDITIONAL REQUIREMENTS • Packaging and Storage: Preserve in tight containers. Auxiliary Information Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 3175 Pharmacopeial Forum: Volume No. 29(3) Page 630Chromatographic Column Chromatographic columns text is not derived from, and not part of, USP 35 or NF 30. |