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This document describes four methods for isolating diosgenin from plant materials:
1) An alcoholic extraction method involving drying, powdering, and extracting tubers with ethanol to produce a concentrated liquid containing crude diosgenin.
2) An acid hydrolysis method involving powdering dried tubers, heating with acid, filtering, and extracting to obtain crude diosgenin.
3) A fermentation and acid hydrolysis method using fresh roots fermented and then subjected to acid hydrolysis and extraction to obtain diosgenin.
4) An incubation and acid hydrolysis method using fresh plant material incubated in water, then subjected to acid hydrolysis and extraction to obtain diosgenin.
This document describes four methods for isolating diosgenin from plant materials:
1) An alcoholic extraction method involving drying, powdering, and extracting tubers with ethanol to produce a concentrated liquid containing crude diosgenin.
2) An acid hydrolysis method involving powdering dried tubers, heating with acid, filtering, and extracting to obtain crude diosgenin.
3) A fermentation and acid hydrolysis method using fresh roots fermented and then subjected to acid hydrolysis and extraction to obtain diosgenin.
4) An incubation and acid hydrolysis method using fresh plant material incubated in water, then subjected to acid hydrolysis and extraction to obtain diosgenin.
This document describes four methods for isolating diosgenin from plant materials:
1) An alcoholic extraction method involving drying, powdering, and extracting tubers with ethanol to produce a concentrated liquid containing crude diosgenin.
2) An acid hydrolysis method involving powdering dried tubers, heating with acid, filtering, and extracting to obtain crude diosgenin.
3) A fermentation and acid hydrolysis method using fresh roots fermented and then subjected to acid hydrolysis and extraction to obtain diosgenin.
4) An incubation and acid hydrolysis method using fresh plant material incubated in water, then subjected to acid hydrolysis and extraction to obtain diosgenin.
The diosgenin tubers are cut into small pieces and dried under sun. The dried tubers are powdered, extracted with ethanol or methanol twice for 6–8 hours. It is filtered and the filtrate is concentrated to a syrupy liquid. The concentrated liquid is then hydrolysed using an acid, hydrochloric acid or sulphuric acid for 2–12 h. About 85% of the crude diosgenin is precipitated. The precipitates are filtered, washed with water and purified with alcohol. Acid hydrolysis method The dried tubers are powdered to a mesh size of 100–200 meshes. It is then refluxed or heated in autoclave with 2–4 N mineral acid for 2–6 h. It is filtered and the crude hydrolyte is washed with water, until neutral. Dried and extracted again for 6 h with hydrocarbon solvent. The liquid is concentrated to about 25 ml. It is allowed to stand for some time in a refrigerator for 1 h. The crystals of diosgenin are filtered out and then it’s washed with acetone. Fermentation cum acid hydrolysis method The fresh green roots are collected and smashed in a hammer mill. The mesh is placed in the fermentation bin and allowed for fermentation for two days. The fermented mesh is dried in sun to reduce the moisture content to 7–8%. It is then subjected to hydrolysis with a mineral acid at reduced temperature. The resulting solution is extracted with heptane to obtain diosgenin. Incubation cum acid hydrolysis method The fresh plant material is incubated in water at 37°C for few days. It is later subjected to acid hydrolysis. The hydrolysed liquid is concentrated and extracted with hydrocarbon solvent to obtain diosgenin. The fresh roots are homogenized with equal weight of water, concentrated acid is added until the required strengthis obtained and then it is extracted with hydrocarbon solvent to obtain diosgenin. Melting point: 204–207°C Thin Layer Chromatography of Diosgenin The sample dissolved in methanol is spotted in Silica gel plates and developed in Toluene: ethyl acetate (7:3). Dark green spot (R f - 0.37) of diosgenin will appear when the dried plate is sprayed with anisaldehyde-sulphuric acid reagent.
(Advances in Experimental Medicine and Biology 338) Wolfgang Pfleiderer (Auth.), Dr. June E. Ayling, M. Gopal Nair, Dr. Charles M. Baugh (Eds.)-Chemistry and Biology of Pteridines and Folates-Springer