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Physical parameters
1.Mosture content
2.Ash values
3.Swelling factor
4.Extractive values
5.Melting point
6.Solubility
7.Optical rotation
8.Viscosity
ASH VALUES

The residue remaining after incineration is the
  ash content of the drug.( inorganic salts of
  carbonates, phosphates, silicates of sodium,
  potassium,   calcium    and   magnesium)     is
  known as ash content.

Ash value is a criterion to judge the identity OR
  purity of the crude drug
TYPES OF ASH VALUES

1.Total ash value

2.Acid insoluble ash value

3.Sulphated ash value

4. Water soluble ash value
Total ash value:

Useful for detecting low grade products

Useful for detecting exhausted products

Useful for detecting   excess of sandy

Useful for detecting   earthy matter with
  drug
DETERMINATION
1.Weigh accurately about 3gms of the powdered drug in a
  tared silica crucible

2.Incinerate the powdered drug by gradually increasing the
  heat until free from carbon and cool. Keep it in
  desiccators

3. Weigh the ash and calculate the % of the total ash with
  reference to the air dried sample
Acid insoluble ash value :
1. Used for the determination of earthy matter present on
  roots, rhizomes, and also on the leaves

2. Crude drugs contain calcium oxalate crystals the amount
  may varies depending on the environmental conditions
DETERMINATION
1. Boil the total ash obtained as above for 5 minutes with
  25ml of dilute HCL

2.Filter and collect the insoluble matter on the ashless filter
  paper , wash the filter paper with hot water, ignite in
  tared crucible, cool and kept in desiccators

3.Weigh the residue and calculate the acid insoluble ash of
  the drug
Sulphated ash value :
Used for the detection of low grade products

Water soluble ash value :

Used to detect either material exhausted by water or not

( Tea leaves, Ginger rhizomes)
SWELLING FACTOR
Significances :

Useful   in the evaluation of crude drugs containing
  mucilage

Useful for the detection of purity of the crude drug
DETERMINATION

1. Transfer 1 gm of the seeds to a 25ml
  stoppered cylinder

2. Fill up to the 20ml mark on the cylinder with
  water. Agitate gently and occasionally during
  24 hours and allowed to stand

3.Measure the volume occupied by the swollen
  seeds
EXTRACTIVE VALUES
Significances :
1.Useful    for the evaluation especially when the
  constituents of the drugs can not be readily estimated
  by any other means
2.It also helps to indicate the nature of chemical
   constituents present in the drug
3. Also helps in the identification of adulterants
TYPES

1.Water soluble extractive values

2.Alcohal soluble extractive values

3.Ether soluble extractive values
1.Water soluble extractive value is applied for
 the   drugs   which   contain   water   soluble
 constituents such as tannins, sugars, plant
 acids and mucilage.

2.Alcohol soluble extractive value is applied
 for the drugs which contain alcohol soluble
 constituents such as tannins, resins and
 alkaloids

    Official method for the assay of myrrh &
 asafoetida
3.Ether soluble extractive value is applied
  for the extraction of volatile oils, fixed oils
  and resins.

1.Volatile ether soluble extractive value

2.Non volatile ether soluble extractive value
DETERMINATION
Water soluble extractive value:

1. Macerate about 5gm of the accurately weighed coarse powder
  with 100ml of chloroform water in a 100ml volumetric flask for
  24 hours .

2. Shake frequently for first 6 hours

3. Filter rapidly through filter paper and evaporate 25ml of water
  extract to dryness in a tared flat-bottomed shallow dish.
4. Dry the residue at 105 and weigh. Keep it in a
  desiccators

5. Dry the extract to constant weight ,finally , calculate
  the % W/W of Water soluble extractive value with
  reference to the air dried drug.
• Alcohol soluble extractive values
• Macerate about 5gm of the accurately weighed coarse
  powder with 100ml of 90% alcohol in a 100ml stoppered
  flask for 24 hours .

• Shake frequently for first 6 hours

• Filter rapidly   through filter paper and collect the filtrate
  evaporate 25ml of alcohol extract to dryness in a tared flat-
  bottomed shallow dish.
• Dry the   residue at 105 and weigh. Keep it in a
  desiccators

• Dry the extract to constant weight ,finally , calculate
  the % w/w of alcohol soluble extractive value with
  reference to the air dried drug.
SIGNIFICANCE:

1.The method is generally used when standardization is not

 done satisfactory by chemical or physical methods

2.When the quantity of the drug /sample are very less then

 the drugs are evaluated by biological methods
These methods are performed on living animals,
isolating living organ and tissue, animal preparation, and
micro-organism

( Bioassay)
Following method is used as

1.Anti inflammatory activity

2.Analgesic activity

3.Antipyretic activity

4.Anti ulcer activity

5.Antidiabetic activity

6.Anthelmintic activity on earth worms
7.Cardiac activity- on frog and pigeon

8.Microbiological methods- living bacteria, yeast, molds are
  used for the assaying vitamins and to determine the
  activity of antibiotic drugs

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D.u.srinivasa

  • 1. F O D O N TH IO E T M A AL ALU IC V S E Y G PH RU D
  • 2. Physical parameters 1.Mosture content 2.Ash values 3.Swelling factor 4.Extractive values 5.Melting point 6.Solubility 7.Optical rotation 8.Viscosity
  • 3. ASH VALUES The residue remaining after incineration is the ash content of the drug.( inorganic salts of carbonates, phosphates, silicates of sodium, potassium, calcium and magnesium) is known as ash content. Ash value is a criterion to judge the identity OR purity of the crude drug
  • 4. TYPES OF ASH VALUES 1.Total ash value 2.Acid insoluble ash value 3.Sulphated ash value 4. Water soluble ash value
  • 5. Total ash value: Useful for detecting low grade products Useful for detecting exhausted products Useful for detecting excess of sandy Useful for detecting earthy matter with drug
  • 6. DETERMINATION 1.Weigh accurately about 3gms of the powdered drug in a tared silica crucible 2.Incinerate the powdered drug by gradually increasing the heat until free from carbon and cool. Keep it in desiccators 3. Weigh the ash and calculate the % of the total ash with reference to the air dried sample
  • 7. Acid insoluble ash value : 1. Used for the determination of earthy matter present on roots, rhizomes, and also on the leaves 2. Crude drugs contain calcium oxalate crystals the amount may varies depending on the environmental conditions
  • 8. DETERMINATION 1. Boil the total ash obtained as above for 5 minutes with 25ml of dilute HCL 2.Filter and collect the insoluble matter on the ashless filter paper , wash the filter paper with hot water, ignite in tared crucible, cool and kept in desiccators 3.Weigh the residue and calculate the acid insoluble ash of the drug
  • 9. Sulphated ash value : Used for the detection of low grade products Water soluble ash value : Used to detect either material exhausted by water or not ( Tea leaves, Ginger rhizomes)
  • 10. SWELLING FACTOR Significances : Useful in the evaluation of crude drugs containing mucilage Useful for the detection of purity of the crude drug
  • 11. DETERMINATION 1. Transfer 1 gm of the seeds to a 25ml stoppered cylinder 2. Fill up to the 20ml mark on the cylinder with water. Agitate gently and occasionally during 24 hours and allowed to stand 3.Measure the volume occupied by the swollen seeds
  • 12. EXTRACTIVE VALUES Significances : 1.Useful for the evaluation especially when the constituents of the drugs can not be readily estimated by any other means 2.It also helps to indicate the nature of chemical constituents present in the drug 3. Also helps in the identification of adulterants
  • 13. TYPES 1.Water soluble extractive values 2.Alcohal soluble extractive values 3.Ether soluble extractive values
  • 14. 1.Water soluble extractive value is applied for the drugs which contain water soluble constituents such as tannins, sugars, plant acids and mucilage. 2.Alcohol soluble extractive value is applied for the drugs which contain alcohol soluble constituents such as tannins, resins and alkaloids Official method for the assay of myrrh & asafoetida
  • 15. 3.Ether soluble extractive value is applied for the extraction of volatile oils, fixed oils and resins. 1.Volatile ether soluble extractive value 2.Non volatile ether soluble extractive value
  • 16. DETERMINATION Water soluble extractive value: 1. Macerate about 5gm of the accurately weighed coarse powder with 100ml of chloroform water in a 100ml volumetric flask for 24 hours . 2. Shake frequently for first 6 hours 3. Filter rapidly through filter paper and evaporate 25ml of water extract to dryness in a tared flat-bottomed shallow dish.
  • 17. 4. Dry the residue at 105 and weigh. Keep it in a desiccators 5. Dry the extract to constant weight ,finally , calculate the % W/W of Water soluble extractive value with reference to the air dried drug.
  • 18. • Alcohol soluble extractive values • Macerate about 5gm of the accurately weighed coarse powder with 100ml of 90% alcohol in a 100ml stoppered flask for 24 hours . • Shake frequently for first 6 hours • Filter rapidly through filter paper and collect the filtrate evaporate 25ml of alcohol extract to dryness in a tared flat- bottomed shallow dish.
  • 19. • Dry the residue at 105 and weigh. Keep it in a desiccators • Dry the extract to constant weight ,finally , calculate the % w/w of alcohol soluble extractive value with reference to the air dried drug.
  • 20.
  • 21. SIGNIFICANCE: 1.The method is generally used when standardization is not done satisfactory by chemical or physical methods 2.When the quantity of the drug /sample are very less then the drugs are evaluated by biological methods
  • 22. These methods are performed on living animals, isolating living organ and tissue, animal preparation, and micro-organism ( Bioassay)
  • 23. Following method is used as 1.Anti inflammatory activity 2.Analgesic activity 3.Antipyretic activity 4.Anti ulcer activity 5.Antidiabetic activity 6.Anthelmintic activity on earth worms
  • 24. 7.Cardiac activity- on frog and pigeon 8.Microbiological methods- living bacteria, yeast, molds are used for the assaying vitamins and to determine the activity of antibiotic drugs