Skip to main content

Renin Angiotensin Mechanism.

Pharmacognosy of Cardiotonics

  • The pharmacological agents which provides strength to the cardiac muscles and improve its force of contraction are called as “Cardiotonics” and are employed in the treatment of CCF “Congestive Cardiac Failure”.
      • e.g.
                     Digitalis
                    Stropanthus.
                     Arjuna.


Digitalis

  • Synonyms: Digitalis Leaves, Foxglove Leaves.
  • Biological Source: Digitalis consists of dried leaves of the plant known as “Digitalis purpurea” belonging to the family “Scrophulariaceae”, leaves are dried below 60 0 C and should contain NMT 5% moisture.
  • Geographical Distribution: Its cultivated majorly in European countries like England, France and also in United States. In India its production is limited to the certain parts of Kashmir.
  • Organoleptic Characters:
Color Dark Greyish Green
Odor Slight
Taste Bitter
Size 10-40 cm L X 4-20 cm W.
Shape Broadly Ovate, irregular crenate margins

Extra Features:  Leaves are pubescent on both the surfaces with pinnate venation and prominent veinlets on lower sides.
  • Chemical Constituents:
    • Digitalis contains “Cardiac Glycosides” (Cadenolides) as active constituents of the drug.
    • The chief active constituents of the Digitalis are,
            • Purpurea Glycoside A
            • Purpurea Glycoside B.
    • Purpurea Glycoside A on enzymatic hydrolysis produce-----> Digitoxin + Glucose, Digitoxin on further hydrolysis produce--------> Digitoxigenin + Digitoxose.
    • Purpurea Glycoside B on enzymatic hydrolysis produce-----> Gitoxin + Glucose, Gitoxin on further hydrolysis produce--------> Gitoxigenin + Digitoxose.
    • Other minor glycosides of Digitalis include,
            • Gitaloxin.
            • Gluco-gitaloxin.
            • Verodoxin.
            • Gluco-verodoxin
            • Odoroside H.
    • Digitalis also contains two saponins,
            • Digitonin.
            • Gitonin.
    • Digitalis also contains certain hydrolytic enzymes. (Hence should contain moisture content NMT 5% to avoid decomposition of the glycosidic activities of the drug.
  • Uses:
  1. As Cardiotonic in treatment of CCF.
  2. As diuretic.
  3. Major Disadvantage: Cumulative effect hence dose monitoring is necessary.

Chemical Tests:

  1. Keller-Killiani Test for Digitoxose:
    1. Boil the powdered drug with 10ml of 70% alcohol for 3 mins.
    2. Extract is filtered.
    3. To the filtrate add 5 ml water and 0.5 ml of Strong Solution of Lead Acetate.
    4. Filter.
    5. To the filtrate add equal volume of Chloroform and evaporate to yield dried extractive.
    6. Dissolve the dried extractive in Glacial Acetic Acid and add few drops of Ferric Chloride Solution to it.
    7. Transfer above content to a test tube containing 2ml Conc. Sulphuric acid.
    8. A reddish brown layer changing to bluish green color on standing is observed.
    9. Digitoxose Confirmed.

Arjuna.

  • Synonyms: Arjun, Arjuna Bark.
  • Biological Source: Arjuna consists of dried bark of the plant known as “Terminalia arjuna” belonging to the family “Combrataceae”.
  • Geographical Distribution: Indigenous to India and is also cultivated in nearby Asian countries. In India most common in Maharashtra particularly in Nagpur and Dehradun.
  • Organoleptic Characters:
.
ColorOuter Side: Greyish Brown.
Inner Side: Reddish Brown with striations.
OdorNone
TasteAstringent
Size Pieces of various size.
ShapeFlat, Fracture Short


  • Chemical Constituents:
    • Arjuna mainly contains Tannins upto 15% and :Triterpenoid saponins as active constituents.
    • The chief active constituents of the drug are,
      • Arjunolic acid.
      • Arjunic acid.
      • Arjunogenin.
    • Other constituents of the drug are,
      • B- Sitosterol.
      • Ellagic acid.
      • Flavonoids.
      • Salts of Aluminium, calcium and magnesium.
    • Starch, proteins and fats are inert constituents of the drug.
  • Uses:
  1. As Cardiotonic
  2. As Diuretic.
  3. Antidysenteric.
  4. Hypotesnsive.
  • Chemical Test:
  • Ether extract shows pinkish fluorescence under UV light.

Popular posts from this blog

Rate of Drying Curve.

  Definition Drying is defined as the removal of liquid from a product usually with application of heat. Rate of Drying Curve. Drying process can be divided into three periods Initial Adjustment Period. Constant drying rate period. First falling drying rate period. Second falling rate period. Initial Adjustment Period (A-B): Also called the “ Heating up” period . In this period the substance gets heat and increases in temperature. Drying has not yet started. Constant drying rate period (B-C): During this period the temperature of the solid and the rate of drying remain constant. The moisture evaporating from the surface is replaced by water diffusing from the interior of the solid at a rate equal t o the rate of evaporation.  The moisture content at the end of constant rate (point C) is referred to as the critical moisture content (CMC).  At CMC, dry spots start appearing and drying rate starts falling . First falling drying rate period (C-D): This period is also called the period of

Heat Exchangers and Heat Interchangers.

  In pharmaceutical industries many types of equipments are used for transfer of heat, they can be classified as follows, Heat Exchangers. Heat Interchangers. Heat Exchangers: These devices are used for transferring heat from a fluid (Hot Gas or Steam) to another fluid (Liquid) through a metal wall. Heat Interchangers: These devices are used for transferring heat from a One liquid to another liquid or one gas to another gas through a metal wall. HEAT EXCHANGERS; The equipment used for heat transferring are known as heat exchangers. Some of the processes that involves heat transfer in pharmaceutical industries are: Preparation of starch paste (in steam jacketed kettle). Crystallization. Evaporation. Distillation.  Classification of heat exchangers On the basis of transfer of heat, heat exchangers are classified as: Direct transfer type:  The hot and cold fluids are separated by a metal wall through which the heat is transferred from hot fluid to cold fluid. E.g. shell and tube heater, 

Flash Distillation.

  Principle: When a hot mixture is allowed to enter from a high-pressure zone into a low pressure zone, the entire liquid mixture is suddenly vaporized. This process is known as flash vaporization .  During this process, the chamber is cooled.  The less volatile fraction is condensed and the more volatile component remains in the vapor phase .  This process requires time, hence liquid and vapor are kept in intimate contact until equilibrium is achieved. Flash distillation is also called equilibrium distillation because separation of two liquids takes place when liquid and vapor phases are at equilibrium. Equipment used for Flash Distillation: Construction: It consists of a pump, which is connected to a feed reservoir.  Pumps help in pumping the feed into the heating chamber.  The heating chamber is heat supplied by steam.  The other end of the pipe is directly introduced into the vapor-liquid separator through a reducing valve.  The vapor outlet is provided at the top of the separato