SlideShare a Scribd company logo
RATNAM INSTITUTE OF PHARMACY
GALENICALS
By,
MR. CH.PRAVEEN KUMAR M.Pharm., (Ph.D)
ASSOCIATE PROFESSOR
DEPARTMENT OF PHARMACEUTICS
 Extraction is defined as the treatment of the plant or animal
tissues with solvent, whereby the medicinally active
constituents or API are dissolved & most of the inert matter
remain undissolved.
 GALEN a Greek pharmacist of Rome who described various
methods of extracting the crude drugs for the first time &
hence the branch dealing with the extraction of plant & animal
drugs is known as Galenical pharmacy & the products as
Galenicals.
INTRODUCTION
2
 Menstruum: solvent used for extraction.
 Marc: the insoluble material that remains extraction.
Various process involved for extraction-
 Infusion
 Decoction
 Maceration
 Percolation
 Continuous hot percolation
Soxhelation process.
 Digestion
or Soxhlet extraction
INTRODUCTION
3
Following solvents are generally used for extraction
 Water & Alcohol
WATER: it is used as a solvent for protein, colouring matter, gums,
glycosides, sugars, alkaloidal salts, enzymes, many organic
acids & most of the organic salts. Waxes, fats, fixed oils & most
alkaloids are insoluble in water.
Disadvantages: fermentation, decomposition of the preparation,
chance to produce undesirable substances & interfere with
clarity of the preparation.
Use of preservatives.
INTRODUCTION
4
 Water causes hydrolysis of many substances.
 Larger amount of heat required compare
aqueous preparations.
with non-
ALCOHOL: it is used as a solvent for alkaloids, alkaloidal salts,
glycosides, volatile oils & resins. It also dissolves many forms of
colouring matter, tannins, many organic acids & salts.
ADVANTAGES: bacterial growth not occurs, if the solution contains
more than 20% alcohol, non-toxic, small amount of heat is
required.
INTRODUCTION
5
 Infusion is pouring water over the drugs and then
allowing it to keep in contact with water for the stated
period, usually 15 minutes, with occasional stirring and
finally filtering off the liquid.
 The marc is not pressed.
 The boiling water is commonly used as a solvent, since it has a
greater solvent action than cold water.
INFUSION
6
 For the preparation of infusions the coffee pots or tea pots or
special infusion pots are used.
 In that, firstly drug is placed in bottom of the pot.
 Then add hot water & stirred three or four times during the
period of infusion.
 Infusion also prepared in muslin cloth. In that drug is placed
in muslin cloth & enclose & then suspending it just below the
level of the water in a beaker.
 For that process stirring is not required.
INFUSION
7
 FRESH INFUSION
 CONCENTRATED INFUSION
FRESH INFUSION
 Aqueous liquid used as a menstruum.
It is prepared by…
 Coarse drug+ Hot water then filter after some time.
 As per pharmacopoeia it is used within 12 Hrs after
formulation.
 e.g. fresh infusion of Quassia.
INFUSION
8
CONCENTRATED INFUSION
 It is eight times stronger than fresh infusion.
 In that 20 to 25 % alcohol conc. used as a menstruum.
 It is prepared by double or triple maceration process.
 It can be stored for a longer time of period.
e.g. Concentrated infusion of Quassia.
INFUSION
9
 In this process, the drug is boiled with water for a stated
period usually 10 minutes.
 After boiling, the liquid is strained and water is passed
through the content of the strainer to make the required
volume.
 This process is mainly used for vegetable drugs of hard and
woody nature having thermostable water soluble
constituents.
DECOCTION
10
 In this process solid ingredients are placed in a stoppered
container with the whole of the solvent and allowed to stand for
a period of at least 3 days (3 - 7 days) with frequent agitation,
until soluble matter is dissolved.
 The mixture is then strained (through sieves / nets), the marc
pressed and the combined liquids clarified (cleaned by
filtration).
MACERATION
11
MACERATION
TYPES OF MACERATION :
 Simple maceration: for organized and unorganized Crude
drug
e.g. i) Tincture of Orange
ii) Tincture of Lemon
 Double maceration : Concentrated infusion of orange
 Triple maceration: The maceration process may
be carried out with help of heat or stirring
12
MACERATION
SIMPLE MACERATION:
 Used for organized drugs e.g. roots, stems, leaves etc.
 Alcohol is used as a menstruum.
 In this process, the drug is placed with the menstruum in a closed
vessel for seven days.
 At this period shaking is done occasionally.
 After seven days, the liquid is strained & marc is pressed.
 The expressed liquid is mixed with strained liquid.
 Then again filter for obtaining the clear liquid.
 The final volume is not adjusted.
13
MACERATION
MODIFIED MACERATION or MACERATION WITH ADJUSTMENT:
 Used for Unorganized drugs e.g. Gum, Resins, Gum-resins, Oleo gum-
resins.
 In this process, the unorganized drug is placed with 4/5th volume of
menstruum in a closed vessel for seven days.
 At this period shaking is done occasionally.
 After the stated period, the liquid is filtered & not necessary to press
the marc.
 After that, the final volume is adjusted with the remaining quantity of
1/5th volume of menstruum through the filter.
14
MACERATION
 It is carried out in the same way as simple maceration process, but
menstruum used in divided into two parts.
 In this process drug is macerated twice by using the menstruum
which is divided into two parts in a such manner that the same
volume is used for each maceration.
 The volume of menstruum required is calculated as follows
Volume of menstruum req. for first maceration
Total Vol.of menstruum - Vol.to be retained by the drug + Vol.to be retained
by the drug
2
Volume of menstruum req. for second maceration
Total vol.of menstrum – Vol. of menstruum used in first maceration
DOUBLE MACERATION PROCESS:
15
MACERATION
 In this process the whole drug is macerated for 48 hrs with
quantity of menstruum for first maceration.
 Strain the liquid & press the marc after 48 hrs.
 Then again macerated for 24 hrs with remaining quty. of menstruum
for second maceration.
 Strain the liquid & press the marc after 24 hrs.
 Then mix the liquids obtained from the two maceration & allows it to
stand for 14 days & then filter.
e.g. Concentrated infusion of orange
Concentrated compound infusion of chirata
16
MACERATION
 It is carried out in the same way as simple maceration process,
but menstruum used in divided into three parts.
 In this process drug is macerated thrice by using the
menstruum which is divided into three parts in a such manner
that the same volume is used for each maceration.
Volume of menstruum req. for first maceration
Total Vol.of menstrum - Vol.to be retained by the drug + Vol. to be retained by the drug
3
Volume of menstruum req. for 2nd & 3rd maceration
Total vol.of menstrum – Vol. of menstrum used in first maceration
2
TRIPLE MACERATION PROCESS:
17
MACERATION
 In this, the drug is macerated for one hour with a part of
menstruum required for first maceration and strained.
 Macerated again for one hour with a part of menstruum for
second maceration & strained.
 Macerated again for one hour with a part of menstruum for
third maceration & strained.
 After that, marc is pressed lightly.
 Then combine the liquids obtained from 2nd & 3rd maceration &
evaporated it to a specified extent.
 Then, mix it with the liquid obtained from 1st maceration & add
alcohol 90% equal to 1/4th of the volume of the finished product.
 Then adjust the volume with water.
 Allow this solution for 14 days & then filter.
e.g. Concentrated infusion of Quassia,
Liquid extract of senna 18
PERCOLATION
Three types of percolation process used for the extraction of drugs
are:
 Simple percolation or percolation process for tinctures.
 Percolation process for concentrated preparations
i) Reverse percolation process
ii) Modified percolation process
 Continuous hot percolation or soxhelation
19
20
PERCOLATION
CONICAL PERCOLATOR
 Comminution: The drug was passed through the sieves for
prevention of lumps & masses. In the percolator, arrange the powder
according to their size i.e coarse powder to fine powder.
 Imbibition: at this stage, the drug was moistened or drug tissue was
swelled before packing it into the percolator.
 Packing of the drug:
 A glass wool was moistened with the solvent and placed at the
bottom of the percolator to prevent the blockage of the outlet trap.
 Then add the moisten drug into the percolator & pressed lightly after
each addition & drug is packed upto 2/3rd or 3/4th of the percolator.
21
PERCOLATION
 Then placed filter paper on the packed drug.
 Place washed sand on filter paper to prevent disturbance of the top
layers of the drug.
 Finally add the menstruum to saturate the material. When liquid
starts coming out from the percolator ,outlet is closed.
 And again add menstruum in the percolator.
 Then allow it to macerate for 24 hrs. The percolator is closed to
prevent evaporation of the solvent.
22
PERCOLATION
 Maceration: after 24 hrs, open the outlet of the percolator and collect
the percolate which measures about 3/4th of the volume required for
the finish product.
 The rate of collection of percolate is generally 10-30 drops per minute.
 Finishing: After collecting the required quantity of percolate, the marc
is taken out from the percolator & it is pressed to recover the solvent.
 Then adjust the final volume with menstruum.
 Then, liquid is filtered in order to free it from other material.
e.g. Tincture of belladona, strong tincture of ginger.
23
PERCOLATION
RESERVE PERCOLATION PROCESS:
 In this process, a part of the percolate, generally 3/4th the volume of the
finished preparation, is reserved.
 Then the percolation process is continued till the drug is completely
exhausted.
 Then the percolate is subjected evaporation or distillation to convert it
into a soft extract.
 This soft extract is dissolved in the reserve portion of the percolate &
then sufficient menstruum is added to produce the required volume.
24
PERCOLATION
CONTINUOUS HOT PERCOLATION:
25
PERCOLATION
CONTINUOUS HOT PERCOLATION:
 This process apply when, the drug is not freely soluble in the solvent.
 The powdered plant material is packed in a thimble.
 The solvent is boiled in a flask. The evaporated solvent passes through
the side tube of the extractor and condensed in the condenser, fitted at
the top of the extractor.
 The condensed hot solvent runs into the thimble and soaks the material
& extracts the constituents.
 When the chamber holding the thimble becomes full the solvent
siphons down to the flask and the process is continuously repeated till
extraction is complete.
26
PERCOLATION
DIGESTION:
 In digestion process, the drug is extracted by heating at a particular
pressure.
 This will increase the penetration power of the menstruum, so that
there is complete extraction of the drug.
 Precautions should be taken so that the increased temperature may not
harm the active constituents of the drug.
27
DIGESTION
DIGESTION:
 The apparatus know as “Digestor” is used for extraction of the drug by
this method.
 It is a vessel made up of metal. The whole of the drug along with the
menstruum is placed in the body of the digestor.
 Place the cover over it and bolt it with the help of nuts.
 The drug is treated with menstruum for a definite period under
specified conditions of temperature and pressure.
28
DIGESTION
29
REFERENCES
1. Handa SS, Khanuja SPS, Longo G, and Rakesh DD. 2008. Extraction
technologies for medicinal and aromatic plants. Trieste: ICS UNIDO.
2. Houghton PJ, Raman A. 1998. Laboratory Handbook for the
Fractionation of Natural Extracts. London: Chapman and Hall.
3. Huie CW. 2002. A review of modern sample-preparation techniques for
the extraction and analysis of medicinal plants. Anal. Bioanal. Chem.
373: 23-30.
30
REFERENCES
THANK YOU

More Related Content

What's hot

Suppository
SuppositorySuppository
Galen, Galenicals, galanical preperations.
Galen, Galenicals, galanical preperations.Galen, Galenicals, galanical preperations.
Galen, Galenicals, galanical preperations.Haris Khan
 
Suspending agents
Suspending agentsSuspending agents
Suspending agents
SILVI SINGH
 
Classical dosage forms-by Amna Saeed
Classical dosage forms-by Amna SaeedClassical dosage forms-by Amna Saeed
Classical dosage forms-by Amna Saeed
Amna Saeed
 
Surface and Interfacial tension [Part-5] (HLB System, Solubilization )
Surface and Interfacial tension [Part-5](HLB System, Solubilization )Surface and Interfacial tension [Part-5](HLB System, Solubilization )
Surface and Interfacial tension [Part-5] (HLB System, Solubilization )
Ms. Pooja Bhandare
 
Solid dosage forms (tablets)
Solid dosage forms (tablets)Solid dosage forms (tablets)
Solid dosage forms (tablets)
Prof. Dr. Basavaraj Nanjwade
 
suspensions
 suspensions suspensions
suspensions
Ravikumar Patil
 
Diffusion principles in biological systems
Diffusion principles in biological systemsDiffusion principles in biological systems
Diffusion principles in biological systems
Mahewash Sana Pathan
 
Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)
Areej Abu Hanieh
 
Physio-chemical processes------(Pharmaceutics)
Physio-chemical processes------(Pharmaceutics)Physio-chemical processes------(Pharmaceutics)
Physio-chemical processes------(Pharmaceutics)
Soft-Learners
 
Pharmaceutical suspension
Pharmaceutical suspensionPharmaceutical suspension
Pharmaceutical suspension
kaleab taye
 
Rheology
RheologyRheology
Rheology
Gourav Singh
 
Pharmaceutical suspensions sb
Pharmaceutical suspensions sbPharmaceutical suspensions sb
Pharmaceutical suspensions sb
Mirza Salman Baig
 
Theories of emulsions
Theories of emulsions Theories of emulsions
Theories of emulsions
ASHOKSHRESHTI
 
Surgical Aids
Surgical AidsSurgical Aids
Surgical Aids
Naresh Gorantla
 
Liquid dosage forms
Liquid dosage formsLiquid dosage forms
Liquid dosage forms
Zahirul Islam
 
emulsion
 emulsion emulsion
emulsion
Ravikumar Patil
 
Pharmaceutical emulsion
Pharmaceutical emulsionPharmaceutical emulsion
Pharmaceutical emulsion
Banaras Hindu University
 
PHARMACEUTICAL INCOMPATIBILITIES
PHARMACEUTICAL INCOMPATIBILITIESPHARMACEUTICAL INCOMPATIBILITIES
PHARMACEUTICAL INCOMPATIBILITIES
Rupali Bhoje
 
Tincture - Pharmaceutical technology-I
Tincture - Pharmaceutical technology-ITincture - Pharmaceutical technology-I
Tincture - Pharmaceutical technology-I
Harish Rahar
 

What's hot (20)

Suppository
SuppositorySuppository
Suppository
 
Galen, Galenicals, galanical preperations.
Galen, Galenicals, galanical preperations.Galen, Galenicals, galanical preperations.
Galen, Galenicals, galanical preperations.
 
Suspending agents
Suspending agentsSuspending agents
Suspending agents
 
Classical dosage forms-by Amna Saeed
Classical dosage forms-by Amna SaeedClassical dosage forms-by Amna Saeed
Classical dosage forms-by Amna Saeed
 
Surface and Interfacial tension [Part-5] (HLB System, Solubilization )
Surface and Interfacial tension [Part-5](HLB System, Solubilization )Surface and Interfacial tension [Part-5](HLB System, Solubilization )
Surface and Interfacial tension [Part-5] (HLB System, Solubilization )
 
Solid dosage forms (tablets)
Solid dosage forms (tablets)Solid dosage forms (tablets)
Solid dosage forms (tablets)
 
suspensions
 suspensions suspensions
suspensions
 
Diffusion principles in biological systems
Diffusion principles in biological systemsDiffusion principles in biological systems
Diffusion principles in biological systems
 
Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)Solubility (Physical Pharmacy)
Solubility (Physical Pharmacy)
 
Physio-chemical processes------(Pharmaceutics)
Physio-chemical processes------(Pharmaceutics)Physio-chemical processes------(Pharmaceutics)
Physio-chemical processes------(Pharmaceutics)
 
Pharmaceutical suspension
Pharmaceutical suspensionPharmaceutical suspension
Pharmaceutical suspension
 
Rheology
RheologyRheology
Rheology
 
Pharmaceutical suspensions sb
Pharmaceutical suspensions sbPharmaceutical suspensions sb
Pharmaceutical suspensions sb
 
Theories of emulsions
Theories of emulsions Theories of emulsions
Theories of emulsions
 
Surgical Aids
Surgical AidsSurgical Aids
Surgical Aids
 
Liquid dosage forms
Liquid dosage formsLiquid dosage forms
Liquid dosage forms
 
emulsion
 emulsion emulsion
emulsion
 
Pharmaceutical emulsion
Pharmaceutical emulsionPharmaceutical emulsion
Pharmaceutical emulsion
 
PHARMACEUTICAL INCOMPATIBILITIES
PHARMACEUTICAL INCOMPATIBILITIESPHARMACEUTICAL INCOMPATIBILITIES
PHARMACEUTICAL INCOMPATIBILITIES
 
Tincture - Pharmaceutical technology-I
Tincture - Pharmaceutical technology-ITincture - Pharmaceutical technology-I
Tincture - Pharmaceutical technology-I
 

Similar to GALENICALS / EXTRACTION PROCEDURES

Extraction
ExtractionExtraction
Extraction
Ravikumar Patil
 
9. extraction processes
9. extraction processes9. extraction processes
9. extraction processes
Gaju Shete
 
Extraction & galenicals
Extraction & galenicalsExtraction & galenicals
Extraction & galenicals
ChandanKumar1979
 
EXTRACTION.pptx
EXTRACTION.pptxEXTRACTION.pptx
EXTRACTION.pptx
vishwapadole
 
Extraction process
Extraction processExtraction process
Extraction process
Dipak Bhingardeve
 
extractionprocess-190307055449.pdf
extractionprocess-190307055449.pdfextractionprocess-190307055449.pdf
extractionprocess-190307055449.pdf
Priyanka Yadav
 
Extraction and Galenical’s.pdf
Extraction and Galenical’s.pdfExtraction and Galenical’s.pdf
Extraction and Galenical’s.pdf
T Reshma
 
Extraction ksa maceratiom.pptx
Extraction   ksa maceratiom.pptxExtraction   ksa maceratiom.pptx
Extraction ksa maceratiom.pptx
kusumAkki1
 
EXTRACTION.pptx
EXTRACTION.pptxEXTRACTION.pptx
EXTRACTION.pptx
PurushothamKN1
 
Extraction
ExtractionExtraction
Extraction
VIKAS MATHAD
 
Basic Extraction methods
Basic Extraction methodsBasic Extraction methods
Basic Extraction methods
Laxmi Singh
 
extraction processes.pptx
extraction processes.pptxextraction processes.pptx
extraction processes.pptx
Harshadaa bafna
 
Unit 4 (1).pptx
Unit 4 (1).pptxUnit 4 (1).pptx
Unit 4 (1).pptx
Yasser Sewilam
 
extraction123456789111111111111111111111
extraction123456789111111111111111111111extraction123456789111111111111111111111
extraction123456789111111111111111111111
afsanamamedova
 
Conventional Extraction Methods.pptx
Conventional Extraction Methods.pptxConventional Extraction Methods.pptx
Conventional Extraction Methods.pptx
Rakesh Barik
 
extraction.pptxajshiqvisqie3iceijc098ehf028hf
extraction.pptxajshiqvisqie3iceijc098ehf028hfextraction.pptxajshiqvisqie3iceijc098ehf028hf
extraction.pptxajshiqvisqie3iceijc098ehf028hf
AkanshaBhatnagar7
 
Alkaloid_drug_assay.pdf
Alkaloid_drug_assay.pdfAlkaloid_drug_assay.pdf
Alkaloid_drug_assay.pdf
UVAS
 
Conventional methods of extraction ppt
Conventional methods of extraction pptConventional methods of extraction ppt
Conventional methods of extraction ppt
PRASHANT SURYAWANSHI
 
Percolation
PercolationPercolation
Percolation
M ArsaLan ChisHti
 
Extraction
ExtractionExtraction
Extraction
Ranajoy Sarkar
 

Similar to GALENICALS / EXTRACTION PROCEDURES (20)

Extraction
ExtractionExtraction
Extraction
 
9. extraction processes
9. extraction processes9. extraction processes
9. extraction processes
 
Extraction & galenicals
Extraction & galenicalsExtraction & galenicals
Extraction & galenicals
 
EXTRACTION.pptx
EXTRACTION.pptxEXTRACTION.pptx
EXTRACTION.pptx
 
Extraction process
Extraction processExtraction process
Extraction process
 
extractionprocess-190307055449.pdf
extractionprocess-190307055449.pdfextractionprocess-190307055449.pdf
extractionprocess-190307055449.pdf
 
Extraction and Galenical’s.pdf
Extraction and Galenical’s.pdfExtraction and Galenical’s.pdf
Extraction and Galenical’s.pdf
 
Extraction ksa maceratiom.pptx
Extraction   ksa maceratiom.pptxExtraction   ksa maceratiom.pptx
Extraction ksa maceratiom.pptx
 
EXTRACTION.pptx
EXTRACTION.pptxEXTRACTION.pptx
EXTRACTION.pptx
 
Extraction
ExtractionExtraction
Extraction
 
Basic Extraction methods
Basic Extraction methodsBasic Extraction methods
Basic Extraction methods
 
extraction processes.pptx
extraction processes.pptxextraction processes.pptx
extraction processes.pptx
 
Unit 4 (1).pptx
Unit 4 (1).pptxUnit 4 (1).pptx
Unit 4 (1).pptx
 
extraction123456789111111111111111111111
extraction123456789111111111111111111111extraction123456789111111111111111111111
extraction123456789111111111111111111111
 
Conventional Extraction Methods.pptx
Conventional Extraction Methods.pptxConventional Extraction Methods.pptx
Conventional Extraction Methods.pptx
 
extraction.pptxajshiqvisqie3iceijc098ehf028hf
extraction.pptxajshiqvisqie3iceijc098ehf028hfextraction.pptxajshiqvisqie3iceijc098ehf028hf
extraction.pptxajshiqvisqie3iceijc098ehf028hf
 
Alkaloid_drug_assay.pdf
Alkaloid_drug_assay.pdfAlkaloid_drug_assay.pdf
Alkaloid_drug_assay.pdf
 
Conventional methods of extraction ppt
Conventional methods of extraction pptConventional methods of extraction ppt
Conventional methods of extraction ppt
 
Percolation
PercolationPercolation
Percolation
 
Extraction
ExtractionExtraction
Extraction
 

Recently uploaded

Synthetic Fiber Construction in lab .pptx
Synthetic Fiber Construction in lab .pptxSynthetic Fiber Construction in lab .pptx
Synthetic Fiber Construction in lab .pptx
Pavel ( NSTU)
 
The French Revolution Class 9 Study Material pdf free download
The French Revolution Class 9 Study Material pdf free downloadThe French Revolution Class 9 Study Material pdf free download
The French Revolution Class 9 Study Material pdf free download
Vivekanand Anglo Vedic Academy
 
Unit 2- Research Aptitude (UGC NET Paper I).pdf
Unit 2- Research Aptitude (UGC NET Paper I).pdfUnit 2- Research Aptitude (UGC NET Paper I).pdf
Unit 2- Research Aptitude (UGC NET Paper I).pdf
Thiyagu K
 
A Strategic Approach: GenAI in Education
A Strategic Approach: GenAI in EducationA Strategic Approach: GenAI in Education
A Strategic Approach: GenAI in Education
Peter Windle
 
The Roman Empire A Historical Colossus.pdf
The Roman Empire A Historical Colossus.pdfThe Roman Empire A Historical Colossus.pdf
The Roman Empire A Historical Colossus.pdf
kaushalkr1407
 
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
siemaillard
 
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdfAdversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
Po-Chuan Chen
 
Unit 8 - Information and Communication Technology (Paper I).pdf
Unit 8 - Information and Communication Technology (Paper I).pdfUnit 8 - Information and Communication Technology (Paper I).pdf
Unit 8 - Information and Communication Technology (Paper I).pdf
Thiyagu K
 
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCECLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
BhavyaRajput3
 
The basics of sentences session 5pptx.pptx
The basics of sentences session 5pptx.pptxThe basics of sentences session 5pptx.pptx
The basics of sentences session 5pptx.pptx
heathfieldcps1
 
1.4 modern child centered education - mahatma gandhi-2.pptx
1.4 modern child centered education - mahatma gandhi-2.pptx1.4 modern child centered education - mahatma gandhi-2.pptx
1.4 modern child centered education - mahatma gandhi-2.pptx
JosvitaDsouza2
 
Palestine last event orientationfvgnh .pptx
Palestine last event orientationfvgnh .pptxPalestine last event orientationfvgnh .pptx
Palestine last event orientationfvgnh .pptx
RaedMohamed3
 
Additional Benefits for Employee Website.pdf
Additional Benefits for Employee Website.pdfAdditional Benefits for Employee Website.pdf
Additional Benefits for Employee Website.pdf
joachimlavalley1
 
Supporting (UKRI) OA monographs at Salford.pptx
Supporting (UKRI) OA monographs at Salford.pptxSupporting (UKRI) OA monographs at Salford.pptx
Supporting (UKRI) OA monographs at Salford.pptx
Jisc
 
The Accursed House by Émile Gaboriau.pptx
The Accursed House by Émile Gaboriau.pptxThe Accursed House by Émile Gaboriau.pptx
The Accursed House by Émile Gaboriau.pptx
DhatriParmar
 
How to Make a Field invisible in Odoo 17
How to Make a Field invisible in Odoo 17How to Make a Field invisible in Odoo 17
How to Make a Field invisible in Odoo 17
Celine George
 
2024.06.01 Introducing a competency framework for languag learning materials ...
2024.06.01 Introducing a competency framework for languag learning materials ...2024.06.01 Introducing a competency framework for languag learning materials ...
2024.06.01 Introducing a competency framework for languag learning materials ...
Sandy Millin
 
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
Nguyen Thanh Tu Collection
 
Operation Blue Star - Saka Neela Tara
Operation Blue Star   -  Saka Neela TaraOperation Blue Star   -  Saka Neela Tara
Operation Blue Star - Saka Neela Tara
Balvir Singh
 
678020731-Sumas-y-Restas-Para-Colorear.pdf
678020731-Sumas-y-Restas-Para-Colorear.pdf678020731-Sumas-y-Restas-Para-Colorear.pdf
678020731-Sumas-y-Restas-Para-Colorear.pdf
CarlosHernanMontoyab2
 

Recently uploaded (20)

Synthetic Fiber Construction in lab .pptx
Synthetic Fiber Construction in lab .pptxSynthetic Fiber Construction in lab .pptx
Synthetic Fiber Construction in lab .pptx
 
The French Revolution Class 9 Study Material pdf free download
The French Revolution Class 9 Study Material pdf free downloadThe French Revolution Class 9 Study Material pdf free download
The French Revolution Class 9 Study Material pdf free download
 
Unit 2- Research Aptitude (UGC NET Paper I).pdf
Unit 2- Research Aptitude (UGC NET Paper I).pdfUnit 2- Research Aptitude (UGC NET Paper I).pdf
Unit 2- Research Aptitude (UGC NET Paper I).pdf
 
A Strategic Approach: GenAI in Education
A Strategic Approach: GenAI in EducationA Strategic Approach: GenAI in Education
A Strategic Approach: GenAI in Education
 
The Roman Empire A Historical Colossus.pdf
The Roman Empire A Historical Colossus.pdfThe Roman Empire A Historical Colossus.pdf
The Roman Empire A Historical Colossus.pdf
 
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
 
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdfAdversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
Adversarial Attention Modeling for Multi-dimensional Emotion Regression.pdf
 
Unit 8 - Information and Communication Technology (Paper I).pdf
Unit 8 - Information and Communication Technology (Paper I).pdfUnit 8 - Information and Communication Technology (Paper I).pdf
Unit 8 - Information and Communication Technology (Paper I).pdf
 
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCECLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
CLASS 11 CBSE B.St Project AIDS TO TRADE - INSURANCE
 
The basics of sentences session 5pptx.pptx
The basics of sentences session 5pptx.pptxThe basics of sentences session 5pptx.pptx
The basics of sentences session 5pptx.pptx
 
1.4 modern child centered education - mahatma gandhi-2.pptx
1.4 modern child centered education - mahatma gandhi-2.pptx1.4 modern child centered education - mahatma gandhi-2.pptx
1.4 modern child centered education - mahatma gandhi-2.pptx
 
Palestine last event orientationfvgnh .pptx
Palestine last event orientationfvgnh .pptxPalestine last event orientationfvgnh .pptx
Palestine last event orientationfvgnh .pptx
 
Additional Benefits for Employee Website.pdf
Additional Benefits for Employee Website.pdfAdditional Benefits for Employee Website.pdf
Additional Benefits for Employee Website.pdf
 
Supporting (UKRI) OA monographs at Salford.pptx
Supporting (UKRI) OA monographs at Salford.pptxSupporting (UKRI) OA monographs at Salford.pptx
Supporting (UKRI) OA monographs at Salford.pptx
 
The Accursed House by Émile Gaboriau.pptx
The Accursed House by Émile Gaboriau.pptxThe Accursed House by Émile Gaboriau.pptx
The Accursed House by Émile Gaboriau.pptx
 
How to Make a Field invisible in Odoo 17
How to Make a Field invisible in Odoo 17How to Make a Field invisible in Odoo 17
How to Make a Field invisible in Odoo 17
 
2024.06.01 Introducing a competency framework for languag learning materials ...
2024.06.01 Introducing a competency framework for languag learning materials ...2024.06.01 Introducing a competency framework for languag learning materials ...
2024.06.01 Introducing a competency framework for languag learning materials ...
 
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
BÀI TẬP BỔ TRỢ TIẾNG ANH GLOBAL SUCCESS LỚP 3 - CẢ NĂM (CÓ FILE NGHE VÀ ĐÁP Á...
 
Operation Blue Star - Saka Neela Tara
Operation Blue Star   -  Saka Neela TaraOperation Blue Star   -  Saka Neela Tara
Operation Blue Star - Saka Neela Tara
 
678020731-Sumas-y-Restas-Para-Colorear.pdf
678020731-Sumas-y-Restas-Para-Colorear.pdf678020731-Sumas-y-Restas-Para-Colorear.pdf
678020731-Sumas-y-Restas-Para-Colorear.pdf
 

GALENICALS / EXTRACTION PROCEDURES

  • 1. RATNAM INSTITUTE OF PHARMACY GALENICALS By, MR. CH.PRAVEEN KUMAR M.Pharm., (Ph.D) ASSOCIATE PROFESSOR DEPARTMENT OF PHARMACEUTICS
  • 2.  Extraction is defined as the treatment of the plant or animal tissues with solvent, whereby the medicinally active constituents or API are dissolved & most of the inert matter remain undissolved.  GALEN a Greek pharmacist of Rome who described various methods of extracting the crude drugs for the first time & hence the branch dealing with the extraction of plant & animal drugs is known as Galenical pharmacy & the products as Galenicals. INTRODUCTION 2
  • 3.  Menstruum: solvent used for extraction.  Marc: the insoluble material that remains extraction. Various process involved for extraction-  Infusion  Decoction  Maceration  Percolation  Continuous hot percolation Soxhelation process.  Digestion or Soxhlet extraction INTRODUCTION 3
  • 4. Following solvents are generally used for extraction  Water & Alcohol WATER: it is used as a solvent for protein, colouring matter, gums, glycosides, sugars, alkaloidal salts, enzymes, many organic acids & most of the organic salts. Waxes, fats, fixed oils & most alkaloids are insoluble in water. Disadvantages: fermentation, decomposition of the preparation, chance to produce undesirable substances & interfere with clarity of the preparation. Use of preservatives. INTRODUCTION 4
  • 5.  Water causes hydrolysis of many substances.  Larger amount of heat required compare aqueous preparations. with non- ALCOHOL: it is used as a solvent for alkaloids, alkaloidal salts, glycosides, volatile oils & resins. It also dissolves many forms of colouring matter, tannins, many organic acids & salts. ADVANTAGES: bacterial growth not occurs, if the solution contains more than 20% alcohol, non-toxic, small amount of heat is required. INTRODUCTION 5
  • 6.  Infusion is pouring water over the drugs and then allowing it to keep in contact with water for the stated period, usually 15 minutes, with occasional stirring and finally filtering off the liquid.  The marc is not pressed.  The boiling water is commonly used as a solvent, since it has a greater solvent action than cold water. INFUSION 6
  • 7.  For the preparation of infusions the coffee pots or tea pots or special infusion pots are used.  In that, firstly drug is placed in bottom of the pot.  Then add hot water & stirred three or four times during the period of infusion.  Infusion also prepared in muslin cloth. In that drug is placed in muslin cloth & enclose & then suspending it just below the level of the water in a beaker.  For that process stirring is not required. INFUSION 7
  • 8.  FRESH INFUSION  CONCENTRATED INFUSION FRESH INFUSION  Aqueous liquid used as a menstruum. It is prepared by…  Coarse drug+ Hot water then filter after some time.  As per pharmacopoeia it is used within 12 Hrs after formulation.  e.g. fresh infusion of Quassia. INFUSION 8
  • 9. CONCENTRATED INFUSION  It is eight times stronger than fresh infusion.  In that 20 to 25 % alcohol conc. used as a menstruum.  It is prepared by double or triple maceration process.  It can be stored for a longer time of period. e.g. Concentrated infusion of Quassia. INFUSION 9
  • 10.  In this process, the drug is boiled with water for a stated period usually 10 minutes.  After boiling, the liquid is strained and water is passed through the content of the strainer to make the required volume.  This process is mainly used for vegetable drugs of hard and woody nature having thermostable water soluble constituents. DECOCTION 10
  • 11.  In this process solid ingredients are placed in a stoppered container with the whole of the solvent and allowed to stand for a period of at least 3 days (3 - 7 days) with frequent agitation, until soluble matter is dissolved.  The mixture is then strained (through sieves / nets), the marc pressed and the combined liquids clarified (cleaned by filtration). MACERATION 11
  • 12. MACERATION TYPES OF MACERATION :  Simple maceration: for organized and unorganized Crude drug e.g. i) Tincture of Orange ii) Tincture of Lemon  Double maceration : Concentrated infusion of orange  Triple maceration: The maceration process may be carried out with help of heat or stirring 12
  • 13. MACERATION SIMPLE MACERATION:  Used for organized drugs e.g. roots, stems, leaves etc.  Alcohol is used as a menstruum.  In this process, the drug is placed with the menstruum in a closed vessel for seven days.  At this period shaking is done occasionally.  After seven days, the liquid is strained & marc is pressed.  The expressed liquid is mixed with strained liquid.  Then again filter for obtaining the clear liquid.  The final volume is not adjusted. 13
  • 14. MACERATION MODIFIED MACERATION or MACERATION WITH ADJUSTMENT:  Used for Unorganized drugs e.g. Gum, Resins, Gum-resins, Oleo gum- resins.  In this process, the unorganized drug is placed with 4/5th volume of menstruum in a closed vessel for seven days.  At this period shaking is done occasionally.  After the stated period, the liquid is filtered & not necessary to press the marc.  After that, the final volume is adjusted with the remaining quantity of 1/5th volume of menstruum through the filter. 14
  • 15. MACERATION  It is carried out in the same way as simple maceration process, but menstruum used in divided into two parts.  In this process drug is macerated twice by using the menstruum which is divided into two parts in a such manner that the same volume is used for each maceration.  The volume of menstruum required is calculated as follows Volume of menstruum req. for first maceration Total Vol.of menstruum - Vol.to be retained by the drug + Vol.to be retained by the drug 2 Volume of menstruum req. for second maceration Total vol.of menstrum – Vol. of menstruum used in first maceration DOUBLE MACERATION PROCESS: 15
  • 16. MACERATION  In this process the whole drug is macerated for 48 hrs with quantity of menstruum for first maceration.  Strain the liquid & press the marc after 48 hrs.  Then again macerated for 24 hrs with remaining quty. of menstruum for second maceration.  Strain the liquid & press the marc after 24 hrs.  Then mix the liquids obtained from the two maceration & allows it to stand for 14 days & then filter. e.g. Concentrated infusion of orange Concentrated compound infusion of chirata 16
  • 17. MACERATION  It is carried out in the same way as simple maceration process, but menstruum used in divided into three parts.  In this process drug is macerated thrice by using the menstruum which is divided into three parts in a such manner that the same volume is used for each maceration. Volume of menstruum req. for first maceration Total Vol.of menstrum - Vol.to be retained by the drug + Vol. to be retained by the drug 3 Volume of menstruum req. for 2nd & 3rd maceration Total vol.of menstrum – Vol. of menstrum used in first maceration 2 TRIPLE MACERATION PROCESS: 17
  • 18. MACERATION  In this, the drug is macerated for one hour with a part of menstruum required for first maceration and strained.  Macerated again for one hour with a part of menstruum for second maceration & strained.  Macerated again for one hour with a part of menstruum for third maceration & strained.  After that, marc is pressed lightly.  Then combine the liquids obtained from 2nd & 3rd maceration & evaporated it to a specified extent.  Then, mix it with the liquid obtained from 1st maceration & add alcohol 90% equal to 1/4th of the volume of the finished product.  Then adjust the volume with water.  Allow this solution for 14 days & then filter. e.g. Concentrated infusion of Quassia, Liquid extract of senna 18
  • 19. PERCOLATION Three types of percolation process used for the extraction of drugs are:  Simple percolation or percolation process for tinctures.  Percolation process for concentrated preparations i) Reverse percolation process ii) Modified percolation process  Continuous hot percolation or soxhelation 19
  • 21.  Comminution: The drug was passed through the sieves for prevention of lumps & masses. In the percolator, arrange the powder according to their size i.e coarse powder to fine powder.  Imbibition: at this stage, the drug was moistened or drug tissue was swelled before packing it into the percolator.  Packing of the drug:  A glass wool was moistened with the solvent and placed at the bottom of the percolator to prevent the blockage of the outlet trap.  Then add the moisten drug into the percolator & pressed lightly after each addition & drug is packed upto 2/3rd or 3/4th of the percolator. 21 PERCOLATION
  • 22.  Then placed filter paper on the packed drug.  Place washed sand on filter paper to prevent disturbance of the top layers of the drug.  Finally add the menstruum to saturate the material. When liquid starts coming out from the percolator ,outlet is closed.  And again add menstruum in the percolator.  Then allow it to macerate for 24 hrs. The percolator is closed to prevent evaporation of the solvent. 22 PERCOLATION
  • 23.  Maceration: after 24 hrs, open the outlet of the percolator and collect the percolate which measures about 3/4th of the volume required for the finish product.  The rate of collection of percolate is generally 10-30 drops per minute.  Finishing: After collecting the required quantity of percolate, the marc is taken out from the percolator & it is pressed to recover the solvent.  Then adjust the final volume with menstruum.  Then, liquid is filtered in order to free it from other material. e.g. Tincture of belladona, strong tincture of ginger. 23 PERCOLATION
  • 24. RESERVE PERCOLATION PROCESS:  In this process, a part of the percolate, generally 3/4th the volume of the finished preparation, is reserved.  Then the percolation process is continued till the drug is completely exhausted.  Then the percolate is subjected evaporation or distillation to convert it into a soft extract.  This soft extract is dissolved in the reserve portion of the percolate & then sufficient menstruum is added to produce the required volume. 24 PERCOLATION
  • 26. CONTINUOUS HOT PERCOLATION:  This process apply when, the drug is not freely soluble in the solvent.  The powdered plant material is packed in a thimble.  The solvent is boiled in a flask. The evaporated solvent passes through the side tube of the extractor and condensed in the condenser, fitted at the top of the extractor.  The condensed hot solvent runs into the thimble and soaks the material & extracts the constituents.  When the chamber holding the thimble becomes full the solvent siphons down to the flask and the process is continuously repeated till extraction is complete. 26 PERCOLATION
  • 27. DIGESTION:  In digestion process, the drug is extracted by heating at a particular pressure.  This will increase the penetration power of the menstruum, so that there is complete extraction of the drug.  Precautions should be taken so that the increased temperature may not harm the active constituents of the drug. 27 DIGESTION
  • 28. DIGESTION:  The apparatus know as “Digestor” is used for extraction of the drug by this method.  It is a vessel made up of metal. The whole of the drug along with the menstruum is placed in the body of the digestor.  Place the cover over it and bolt it with the help of nuts.  The drug is treated with menstruum for a definite period under specified conditions of temperature and pressure. 28 DIGESTION
  • 29. 29 REFERENCES 1. Handa SS, Khanuja SPS, Longo G, and Rakesh DD. 2008. Extraction technologies for medicinal and aromatic plants. Trieste: ICS UNIDO. 2. Houghton PJ, Raman A. 1998. Laboratory Handbook for the Fractionation of Natural Extracts. London: Chapman and Hall. 3. Huie CW. 2002. A review of modern sample-preparation techniques for the extraction and analysis of medicinal plants. Anal. Bioanal. Chem. 373: 23-30.