Limit Tests ppt
Download as PPTX, PDF29 likes19,609 views
The document discusses various limit tests used to detect inorganic impurities in pharmaceutical substances, including tests for chlorides, sulphates, iron, lead, and arsenic. Each test is based on chemical reactions that produce observable changes, allowing for a pass/fail evaluation against standard solutions. It also outlines the procedures for conducting these tests, highlighting the importance of certain reagents and conditions for accurate results.
Limit Tests ppt
- 1. Presented by: Aditya Sharma M.S. (Pharm) Pharmaceutical Analysis NIPER Guwahati
- 2. Content Introduction Limit Test For Chlorides Limit Test For Sulphates Limit Test For Iron Limit Test For Lead Limit Test For Arsenic
- 3. Introduction • Limit means a value or amount that is likely to be present in a substance and test means to examine or to investigate. • Limit test is defined as quantitative or semi quantitative test designed to identify and control small quantities of impurity which is likely to be present in the substance. • Limit test is generally carried out to determine the inorganic impurities present in compound.
- 4. • Limit tests are a category of impurity tests in which a solution of an unknown sample is compared to a standard that contains the impurity at the product limit. Generally this definition applies to limit tests that are in widespread use in various pharmacopoeial compendia, such as United States Pharmacopoeia (USP), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP) and Food Chemicals Codex (FCC). • These tests are used to make a simple pass/fail evaluation of the sample. Typically this category of test relies on the comparison of an unknown sample to a standard solution. • Often these tests rely on a visual evaluation by the technician, though some may rely on instrumental analysis of the sample.
- 5. Limit Test For Chlorides • Principle: Limit test of chloride is based on the reaction of soluble chloride with silver nitrate in presence of dilute nitric acid to form silver chloride, which appears as solid particles (Opalescence) in the solution. NaCl + AgNO3 AgCl + NaNO3 HNO3
- 6. Procedure Test Sample Standard Compound Specific weight of compound is dissolved in water or solution is prepared as directed in the pharmacopoeia and transferred in Nessler cylinder Take 1ml of 0.05845 % W/V solution of sodium chloride in Nessler cylinder Add 1ml of nitric acid Add 1ml of nitric acid Dilute to 50ml in Nessler cylinder Dilute to 50ml in Nessler cylinder Add 1ml of AgNO3 solution Add 1ml of AgNO3 solution Keep aside for 5 min Keep aside for 5 min Observe the Opalescence/Turbidity Observe the Opalescence/Turbidity
- 7. Observation: The opalescence produce in sample solution should not be greater than standard solution. If opalescence produces in sample solution is less than the standard solution, the sample will pass the limit test of chloride and visa versa. Reasons: Nitric acid is added in the limit test of chloride to make solution acidic and helps silver chloride precipitate to make solution turbid at the end of process.
- 8. Limit Test For Sulphates • Principle: Limit test of sulphate is based on the reaction of soluble sulphate with barium chloride in presence of dilute hydrochloric acid to form barium sulphate which appears as solid particles (turbidity) in the solution. SO4 2- + BaCl2 BaSO4 + KClHCl
- 9. Procedure Test Sample Standard Compound Specific weight of compound is dissolved in water or solution is prepared as directed in the pharmacopoeia and transferred in Nessler cylinder Take 1ml of 0.1089 % W/V solution of potassium sulphate in Nessler cylinder Add 2ml of dilute hydrochloric acid Add 2ml of dilute hydrochloric acid Dilute to 45 ml in Nessler cylinder Dilute to 45 ml in Nessler cylinder Add 5ml of barium sulphate reagent Add 5ml of barium sulphate reagent Keep aside for 5 min Keep aside for 5 min Observe the Turbidity Observe the Turbidity
- 10. Observation: The opalescence produce in sample solution should not be greater than standard solution. If opalescence produces in sample solution is less than the standard solution, the sample will pass the limit test of sulphates and visa versa. Reasons: Hydrochloric acid helps to make solution acidic. Potassium sulphate is used to increase the sensitivity of the test by giving ionic concentration in the reagent Alcohol helps to prevent super saturation.
- 11. Limit Test For Iron • Principle: Limit test of Iron is based on the reaction of iron in ammonical solution with thioglycollic acid in presence of citric acid to form iron thioglycolate which is pale pink to deep reddish purple in color. • Fe2+ + CH2SH CH2SH OOC COOH COO Fe HSH2C Thioglycolic acid Ferrous thiogycolate
- 12. Procedure Test Sample Standard Compound Sample is dissolved in specific amount of water and then volume is made up to 40 ml 2 ml of standard solution of iron diluted with water upto 40ml Add 2 ml of 20 % w/v of citric acid (iron free) Add 2 ml of 20 % w/v of citric acid (iron free) Add 2 drops of thioglycollic acid Add 2 drops of thioglycollic acid Add ammonia to make the solution alkaline and adjust the volume to 50 ml Add ammonia to make the solution alkaline and adjust the volume to 50 ml Keep aside for 5 min Keep aside for 5 min Color developed is viewed vertically and compared with standard solution Color developed is viewed vertically
- 13. Earlier amoniumthiocyanate reagent was used for the limit test of iron. Since thioglycolic acid is more sensitive reagent, it has replaced ammonium thiocyanate in the test. Observation: The purple color produce in sample solution should not be greater than standard solution. If purple color produces in sample solution is less than the standard solution, the sample will pass the limit test of iron and vice versa. Reasons: Citric acid helps precipitation of iron by ammonia by forming a complex with it. Thioglycolic acid helps to oxidize iron (II) to iron (III). Ammonia to make solution alkaline.
- 14. Limit Test For Lead • Lead is a most undesirable impurity in medical compounds and comes through use of sulphuric acid, lead lined apparatus and glass bottles use for storage of chemicals. • Principle: Limit test of lead is based on the reaction of lead and diphenylthiocabazone (dithizone) in alkaline solution to form lead dithizone complex which is red in color. Dithizone is green in color in chloroform and lead- dithizone complex is violet in color, so the resulting color at the end of process is red.
- 15. Procedure Test Sample Standard Compound A known quantity of sample solution is transferred in a separating funnel A standard lead solution is prepared equivalent to the amount of lead permitted in the sample under examination Add 6ml of ammonium citrate Add 6ml of ammonium citrate Add 2 ml of potassium cyanide and 2 ml of hydroxylamine hydrochloride Add 2 ml of potassium cyanide and 2 ml of hydroxylamine hydrochloride Add 2 drops of phenol red Add 2 drops of phenol red Make solution alkaline by adding ammonia solution. Make solution alkaline by adding ammonia solution Extract with 5 ml of dithizone until it becomes green Extract with 5 ml of dithizone until it becomes green Combine dithizone extracts are shaken for 30 mins with 30 ml of nitric acid and the chloroform layer is discarded Combine dithizone extracts are shaken for 30 mins with 30 ml of nitric acid and the chloroform layer is discarded To the acid solution add 5 ml of standard dithizone solution To the acid solution add 5 ml of standard dithizone solution Add 4 ml of ammonium cyanide Add 4 ml of ammonium cyanide Shake for 30 mins Shake for 30 mins Observe the color Observe the color
- 16. Observation: The intensity of the color of complex, is depends on the amount of lead in the solution. The color produce in sample solution should not be greater than standard solution. If color produces in sample solution is less than the standard solution, the sample will pass the limit test of lead and vice versa. Reasons: Ammonium citrate, potassium cyanide, hydroxylamine hydrochloride is used to make pH optimum so interference and influence of other impurities have been eliminated. Phenol red is used as indicator to develop the color at the end of process. Lead present as an impurities in the substance, gets separated bye extracting an alkaline solution with a dithizone extraction solution.
- 17. Limit Test For Arsenic • Principle: Limit test of Arsenic is based on the reaction of arsenic gas with hydrogen ion to form yellow stain on mercuric chloride paper in presence of reducing agents like potassium iodide. It is also called as Gutzeit test and requires special apparatus. Arsenic, present as arsenic acid in the sample is reduced to arsenious acid by reducing agents like potassium iodide, stannous acid, zinc, hydrochloric acid, etc. Arsenious acid is further reduced to arsine (gas) by hydrogen and reacts with mercuric chloride paper to give a yellow stain. H3AsO4 + H2SnO2 H3AsO3 + H2SnO3 H3AsO3 + 3H2 AsH3 + 3H2O • The depth of yellow stain on mercuric chloride paper will depend upon the quality of arsenic present in the sample.
- 18. Procedure Test solution: • The test solution is prepared by dissolving specificamount in water and stannated HCl (arsenic free) and kept in a wide mouthed bottle. • To this solution 1 gm of KI, 5 ml of stannous chloride acid solution and 10 gm of zinc is added (all this reagents must be arsenic free). Keep the solution aside for 40 min and stain obtained on mercuric chloride paper is compared with standard solution. Standard solution: • A known quantity of dilute arsenic solution is kept in wide mouthed bottle and rest procedure is followed as described in test solution.
- 19. Reasons: Stannous chloride is used for complete evolution of arsine Zinc, potassium iodide and stannous chloride is used as a reducing agent Hydrochloric acid is used to make the solution acidic Lead acetate pledger or papers are used to trap any hydrogen sulphide which may be evolved along with arsine.
- 20. References • A.H. Beckett and J.B. Stenlake, Practical pharmaceutical chemistry, Part-I. The Athtone press, University of London, London. • P. Gundu Rao, Inorganic Pharmaceutical Chemistry; Vallabh Prakashan, Delhi. • Advanced Inorganic Chemistry by Satya Prakash, G.D. Tuli • J.H Block, E. Roche, T.O Soine and C.O. Wilson, Inorganic Medical and Pharmaceutical Chemistry Lea & Febiger Philadelphia PA.