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ASIAN COLLEGE FOR ADVANCE STUDIES
(ACAS)
(Affiliated by Purbanchal University)
Satdobato, Lalitpur
Project on:
Turmeric powder (Curcuma longa)
Submitted to: Submitted by:
Respected Sir; Pradip Patel
Mr. Ramesh Raj Padhaya Shirsha Upadhyaya
Shivcharan Mandal
……………………………….. Sukesh Kumar Yadav
Signature Susmita Sapkota
4th
semester
Bachelor in pharmacy
Date of submission:
2078/1/8
i
Acknowledgement
Primarily, We would thank god for being able to complete this project successfully.
Then we would like to thanks our Chemistry of Natural Product (CNP) teacher
Mr. Ramesh Raj Padhaya whose valuable guidance has been the once that helped
us patch this project and make it success, his suggestion and instruction has served
as the major contribution towards the completion of the project.
Many Many thanks goes to our friends for their support and valuable suggestions
regarding on this project. Special thanks to Asian College for Advance Studies
which provided a platform for us to study B. Pharmacy and carryout the project.
Last but not the least we would like to thanks our parents, classmates and college for
providing us this opportunity.
ii
Abstract
Turmeric is commonly known as curcuma longa is well known indigenous herbal
medicine traditionally used as spice in Indian and Nepali food. Turmeric is used in
India for thousands of years as a major part of Ayurvedic medicine. It was first used
as a dye and then later for its possible medicinal properties. Turmeric is traditionally
used as a spice and coloring in foods due to curcuminoids curcumin,
demethoxycurcumin, and bis-demethoxycurcumin as important chemical
constituents. Curcuma longa shows wide range of biological activities such as anti-
inflammatory, anticancer, antibacterial, antiviral, antioxidant, antiseptic,
cardioprotective, hepatoprotective and digestive activities. This Review expresses
the development of long from a traditional spice to a modern application in the
present period.
Table of Contents
Acknowledgement.................................................................................................... i
Abstract.................................................................................................................... ii
Introduction..............................................................................................................1
Methodology .............................................................................................................2
Collection and Identification of Plant..............................................................2
Macroscopical character..................................................................................2
Microscopical study.........................................................................................3
Physical evaluation...................................................................................................4
Moisture content..............................................................................................4
Ash value .........................................................................................................5
Extraction..................................................................................................................6
Chemical present:.....................................................................................................7
Phytochemical screening .........................................................................................8
Test for Alkaloids ............................................................................................8
Saponin test......................................................................................................9
Test for Resins .................................................................................................9
Test for Tannins...............................................................................................9
Conclusion...............................................................................................................10
References...............................................................................................................11
1
Introduction
Curcuma longa linn commonly known as besar in local community of hilly reason
of Nepal where as it is also known as haldi or Indian saffron in terai and India.
Turmeric plant is perennial herb 60 to 90 cm height with a short steam and tufted
leaves. The rhizome which are short cultivated in tropical region of Asia. Its
rhizomes is known as turmeric are extensively use for anti-inflammatory, dye and
add flavor to food. Turmeric is also known as the “golden spice” as well as “spice
of life” because of its numerous diverse clinical uses without any adverse effect. The
plant is indigenous to south and south East Asia region. It is cultivated by harappan
civilization.
The derivative of Curcumin is curcuminoids (Curcuminoids is a linear
diarylheptanoid, polyphenolic molecules). The other two main forms of
curcuminoids are desmethoxycurcumin and bis-desmethoxycurcumin and it is
important for the yellow colour of turmeric. Curcumin has two tautomeric compound
form ketonic and enolic. The enolic group has more stability in the solid phase and
solution. Curcumin is a bright yellow colour compound and it is applied as a food
colouring agent. Curcumin has been acquired a wide range of pharmacological and
biological activities including anti-inflammatory, anti-cancer, anti-oxidant, wound
healing, anti-microbial and many others biological properties.
2
Methodology
Methodology is "'a contextual framework' for research, a coherent and logical
scheme based on views, beliefs, and values, that guides the choices researchers [or
other users] make"
Collection and Identification of Plant
Curcuma longa (synonyms besar, haldi), locally called Besar in Nepal It is one of
the widely distributed plants in Nepal. Local people use this plant as spice In addition
to this, plant rhizome is used as anti –inflammatory and dye etc.
For our research we collected the required sample from our college premises and
prepared required parts of the plant for the making of herbarium sheet to get it
identified by Vanaspati Vibhag. Then we simply dried the rhizome of turmeric and
powdered them for the remaining process of identifying the macroscopical character,
Microscopical character, phytochemical screening, chemical evaluation, etc.
Biological source
It is consists of dried as well as fresh rhizomes of curcuma longa belonging to
family Zingibereceae.
Macroscopical character
Colour:
Leaves: green
Rhizomes: brown
Flowers: white, yellow or pink
Powder: yellow
Odour: Aromatic pleasant
Taste: pungent and aromatic
Size: 60-90 cm height
3
Microscopical study
Microscopical study of turmeric powder
Method of evaluation
 Firstly powder sample was taken in a glass slide where one drop of glycerine
reagent was placed.
 The sample was covered with cover slip and was observed under microscope.
Description
The powder is yellow with bitter taste. It includes powder, fibbers and small granules
of vessels.
Microscopic characters
Wet (10 ×) Wet (40 ×) Dry (10 ×)
Parenchyma
Spherical to granular cells in the form of grains.
Oleoresin crystal
Originally impregnated in parenchyma they become free powder and are found in
dispersed.
Vascular element
The large number of vessels elements either entire or in the form of fragments. They
show spiral pitted thickenings most of the elements are of vessel category and
tracheid are few and occasions.
4
Physical evaluation
Moisture content
Presence of moisture in a crude drug can lead to its deterioration due to either
activation of certain enzymes or growth of microbes.
Moisture content can be determined by heating the drug at 150o
c in an
oven to a constant weight and calculating the loss of weight.
Procedures
At first weight of empty petri plate was noted and weight of sample powder was
weighed out. The weighed sample powder was placed into hot air oven for 30
minutes at 150o
c. After 30 minutes the sample was taken out from the hot air oven
and its weight was noted down as fist reading and again the sample was placed in to
hot air oven and after 15 minutes the sample was weight as second reading and at
last again sample was place in the hot air oven and after 30 minute the weight was
taken as third reading. The process was must be continued until the constant reading
not obtained.
Calculation
Weight of petri plate: 45.28 gram
Weight of sample: 3.03 gram
Time Weight (gram)
30 minutes 47.95
15 minutes 47.87
15 minutes 47.87
Now, weight of moisture free powder = 48.31- 47.87
= 0.44 gram
Moisture content =0.44 / 3.03 × 100 %
= 14.52 %
5
Ash value
The total ash is the residue remaining after incineration. The acid insoluble ash is
the part of the total ash which is insoluble in diluted hydrochloric acid. Ash
values are helpful in determining the quality and purity of the crude drugs in powder
form.
Procedure
At first, weight of the empty crucible is noted. About two grams of sample was
weighted and transferred into empty crucible and again transferred them into the
muffle furnace for 2 hours and then the sample was cooled down and weighted out.
Calculation
Weight of empty crucible = 25.23 gram
Weight of sample = 2.02 gram
After incineration,
Weight of crucible + ash = 26.87 gram
Weight of ash = 0.38 gram
Ash content = weight of ash / 2.02 grams of powder × 100
=0.38 / 2.02 × 100
= 18.81 %
6
Extraction
Extraction can be defined as the process of removal of active constituent from plant
sources using suitable solvent.
Extraction of active constituent from turmeric powder using soxhlet apparatus:
Material required:
i. Condenser
ii. Round bottom flask
iii. Stand and clips
iv. Heating mantle
v. Soxhlet apparatus
Chemical required:
i. Sample ( turmeric powder)
ii. Ether
Procedure:
Firstly the soxhlet apparatus was taken, clean
and weight crude drug (turmeric powder) was
packed into thimble.
 Packed in to the central tube of the soxhlet apparatus.
 Known amount of solvent (ether) was poured in to RB flask and in condenser
water inlet and outlet pipe were fitted.
 RB flask was heated until the clear colour found in s-phone.
 After the clear colour was formed solution in RB flask was heated in water
bath until its half concentration.
Calculation:
Weight of sample = 50 gram
Extractive weight = 5 gram
Extractive value = Extractive weight / weight of sample × 100 %
= 5 / 50 × 100 %
= 10 %
Video link: https://youtu.be/narcXVg3xyM
7
Chemical present:
a. Curcumin-I
b. Demethoxy Curcumin
c. Bis-Demethoxy Curcumin
Structures:
8
Phytochemical screening
Phytochemical screening of turmeric powder
Apparatus required
i. Test-tube
ii. Water bath
iii. Dropper
iv. Measuring cylinder
Chemical required
i. Sample (extractive solution)
ii. Wagner reagent
iii. Ferric chlorides
iv. Hanger reagent
v. Molish’s reagent
Phytochemical screening
It refers to the extractive screening and identification of the medicinally active
substance found in the plant. Some of the bioactive substance that can be derived
from plants are flavonoids, alkaloids, carotenoids, tannins and resin.
Test for Alkaloids
Test Observation Result
Wagner reagent +
extracted sample in a test
tube and heated in water
bath
Reddish brown colour
was produced
Test was positive for
presence of Alkaloids
Molish reagent + extracted
sample in a test tube and
heated in water bath
Violet colour ring was
formed
Test was positive for
presence of Alkaloids
9
Saponin test
Test Observation Result
5ml extract was mixed
with 20ml of distilled
water then agitated in
graduated cylinder for 15
minute
Formation of foams was
not observed
Test was negative for
Saponin
Test for Resins
Test (acetone-water test) Observation Result
Extract + acetone + water
was added in test-tube
and was shacked
properly.
Turbidity was seen Test was positive for
Resins
Test for Tannins
Test Observation Result
4 ml extract + 4ml ferric
chloride solution was
taken in test-tube and was
mixed
Green colour was formed Test was positive for
Tannins
Results:
Hence, performing phytochemical screening of turmeric extract, it was found that
the extract contain resins, tannins and alkaloids.
10
Conclusion
From the above project work we conclude that the turmeric powder contain
alkaloids, resins, tannins etc. and also comes to know about their methods of
extraction and their physical as well as morphological characters.
11
References
1. TEXTBOOK OF PHARMACOGNOSY AND PHYTOCHEMISTRY
By; Biren Shah | A. K. Seth; p339-341
2. A Comprehensive Review on Physiological Effects of Curcuma
Article in Drug Research · August 2020
(https://www.researchgate.net/publication/343411049)
3. Curcuma longa Linn. A Phytochemical and Phytopharmacological Review
By; Arjun M. Modi | Prafulla
(Sabalehttps://www.researchgate.net/publication/301644533_Curcuma_long
a_Linn_A_Phytochemical_and_Phytopharmacological_Review)
4. The dictionary definition of turmeric at Wiktionary
(https://en.wikipedia.org/wiki/Turmeric)
5. https://youtu.be/narcXVg3xyM

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Chemistry of Natural Product (CNP) Turmeric powder (Curcuma longa).pdf

  • 1. ASIAN COLLEGE FOR ADVANCE STUDIES (ACAS) (Affiliated by Purbanchal University) Satdobato, Lalitpur Project on: Turmeric powder (Curcuma longa) Submitted to: Submitted by: Respected Sir; Pradip Patel Mr. Ramesh Raj Padhaya Shirsha Upadhyaya Shivcharan Mandal ……………………………….. Sukesh Kumar Yadav Signature Susmita Sapkota 4th semester Bachelor in pharmacy Date of submission: 2078/1/8
  • 2. i Acknowledgement Primarily, We would thank god for being able to complete this project successfully. Then we would like to thanks our Chemistry of Natural Product (CNP) teacher Mr. Ramesh Raj Padhaya whose valuable guidance has been the once that helped us patch this project and make it success, his suggestion and instruction has served as the major contribution towards the completion of the project. Many Many thanks goes to our friends for their support and valuable suggestions regarding on this project. Special thanks to Asian College for Advance Studies which provided a platform for us to study B. Pharmacy and carryout the project. Last but not the least we would like to thanks our parents, classmates and college for providing us this opportunity.
  • 3. ii Abstract Turmeric is commonly known as curcuma longa is well known indigenous herbal medicine traditionally used as spice in Indian and Nepali food. Turmeric is used in India for thousands of years as a major part of Ayurvedic medicine. It was first used as a dye and then later for its possible medicinal properties. Turmeric is traditionally used as a spice and coloring in foods due to curcuminoids curcumin, demethoxycurcumin, and bis-demethoxycurcumin as important chemical constituents. Curcuma longa shows wide range of biological activities such as anti- inflammatory, anticancer, antibacterial, antiviral, antioxidant, antiseptic, cardioprotective, hepatoprotective and digestive activities. This Review expresses the development of long from a traditional spice to a modern application in the present period.
  • 4. Table of Contents Acknowledgement.................................................................................................... i Abstract.................................................................................................................... ii Introduction..............................................................................................................1 Methodology .............................................................................................................2 Collection and Identification of Plant..............................................................2 Macroscopical character..................................................................................2 Microscopical study.........................................................................................3 Physical evaluation...................................................................................................4 Moisture content..............................................................................................4 Ash value .........................................................................................................5 Extraction..................................................................................................................6 Chemical present:.....................................................................................................7 Phytochemical screening .........................................................................................8 Test for Alkaloids ............................................................................................8 Saponin test......................................................................................................9 Test for Resins .................................................................................................9 Test for Tannins...............................................................................................9 Conclusion...............................................................................................................10 References...............................................................................................................11
  • 5. 1 Introduction Curcuma longa linn commonly known as besar in local community of hilly reason of Nepal where as it is also known as haldi or Indian saffron in terai and India. Turmeric plant is perennial herb 60 to 90 cm height with a short steam and tufted leaves. The rhizome which are short cultivated in tropical region of Asia. Its rhizomes is known as turmeric are extensively use for anti-inflammatory, dye and add flavor to food. Turmeric is also known as the “golden spice” as well as “spice of life” because of its numerous diverse clinical uses without any adverse effect. The plant is indigenous to south and south East Asia region. It is cultivated by harappan civilization. The derivative of Curcumin is curcuminoids (Curcuminoids is a linear diarylheptanoid, polyphenolic molecules). The other two main forms of curcuminoids are desmethoxycurcumin and bis-desmethoxycurcumin and it is important for the yellow colour of turmeric. Curcumin has two tautomeric compound form ketonic and enolic. The enolic group has more stability in the solid phase and solution. Curcumin is a bright yellow colour compound and it is applied as a food colouring agent. Curcumin has been acquired a wide range of pharmacological and biological activities including anti-inflammatory, anti-cancer, anti-oxidant, wound healing, anti-microbial and many others biological properties.
  • 6. 2 Methodology Methodology is "'a contextual framework' for research, a coherent and logical scheme based on views, beliefs, and values, that guides the choices researchers [or other users] make" Collection and Identification of Plant Curcuma longa (synonyms besar, haldi), locally called Besar in Nepal It is one of the widely distributed plants in Nepal. Local people use this plant as spice In addition to this, plant rhizome is used as anti –inflammatory and dye etc. For our research we collected the required sample from our college premises and prepared required parts of the plant for the making of herbarium sheet to get it identified by Vanaspati Vibhag. Then we simply dried the rhizome of turmeric and powdered them for the remaining process of identifying the macroscopical character, Microscopical character, phytochemical screening, chemical evaluation, etc. Biological source It is consists of dried as well as fresh rhizomes of curcuma longa belonging to family Zingibereceae. Macroscopical character Colour: Leaves: green Rhizomes: brown Flowers: white, yellow or pink Powder: yellow Odour: Aromatic pleasant Taste: pungent and aromatic Size: 60-90 cm height
  • 7. 3 Microscopical study Microscopical study of turmeric powder Method of evaluation  Firstly powder sample was taken in a glass slide where one drop of glycerine reagent was placed.  The sample was covered with cover slip and was observed under microscope. Description The powder is yellow with bitter taste. It includes powder, fibbers and small granules of vessels. Microscopic characters Wet (10 ×) Wet (40 ×) Dry (10 ×) Parenchyma Spherical to granular cells in the form of grains. Oleoresin crystal Originally impregnated in parenchyma they become free powder and are found in dispersed. Vascular element The large number of vessels elements either entire or in the form of fragments. They show spiral pitted thickenings most of the elements are of vessel category and tracheid are few and occasions.
  • 8. 4 Physical evaluation Moisture content Presence of moisture in a crude drug can lead to its deterioration due to either activation of certain enzymes or growth of microbes. Moisture content can be determined by heating the drug at 150o c in an oven to a constant weight and calculating the loss of weight. Procedures At first weight of empty petri plate was noted and weight of sample powder was weighed out. The weighed sample powder was placed into hot air oven for 30 minutes at 150o c. After 30 minutes the sample was taken out from the hot air oven and its weight was noted down as fist reading and again the sample was placed in to hot air oven and after 15 minutes the sample was weight as second reading and at last again sample was place in the hot air oven and after 30 minute the weight was taken as third reading. The process was must be continued until the constant reading not obtained. Calculation Weight of petri plate: 45.28 gram Weight of sample: 3.03 gram Time Weight (gram) 30 minutes 47.95 15 minutes 47.87 15 minutes 47.87 Now, weight of moisture free powder = 48.31- 47.87 = 0.44 gram Moisture content =0.44 / 3.03 × 100 % = 14.52 %
  • 9. 5 Ash value The total ash is the residue remaining after incineration. The acid insoluble ash is the part of the total ash which is insoluble in diluted hydrochloric acid. Ash values are helpful in determining the quality and purity of the crude drugs in powder form. Procedure At first, weight of the empty crucible is noted. About two grams of sample was weighted and transferred into empty crucible and again transferred them into the muffle furnace for 2 hours and then the sample was cooled down and weighted out. Calculation Weight of empty crucible = 25.23 gram Weight of sample = 2.02 gram After incineration, Weight of crucible + ash = 26.87 gram Weight of ash = 0.38 gram Ash content = weight of ash / 2.02 grams of powder × 100 =0.38 / 2.02 × 100 = 18.81 %
  • 10. 6 Extraction Extraction can be defined as the process of removal of active constituent from plant sources using suitable solvent. Extraction of active constituent from turmeric powder using soxhlet apparatus: Material required: i. Condenser ii. Round bottom flask iii. Stand and clips iv. Heating mantle v. Soxhlet apparatus Chemical required: i. Sample ( turmeric powder) ii. Ether Procedure: Firstly the soxhlet apparatus was taken, clean and weight crude drug (turmeric powder) was packed into thimble.  Packed in to the central tube of the soxhlet apparatus.  Known amount of solvent (ether) was poured in to RB flask and in condenser water inlet and outlet pipe were fitted.  RB flask was heated until the clear colour found in s-phone.  After the clear colour was formed solution in RB flask was heated in water bath until its half concentration. Calculation: Weight of sample = 50 gram Extractive weight = 5 gram Extractive value = Extractive weight / weight of sample × 100 % = 5 / 50 × 100 % = 10 % Video link: https://youtu.be/narcXVg3xyM
  • 11. 7 Chemical present: a. Curcumin-I b. Demethoxy Curcumin c. Bis-Demethoxy Curcumin Structures:
  • 12. 8 Phytochemical screening Phytochemical screening of turmeric powder Apparatus required i. Test-tube ii. Water bath iii. Dropper iv. Measuring cylinder Chemical required i. Sample (extractive solution) ii. Wagner reagent iii. Ferric chlorides iv. Hanger reagent v. Molish’s reagent Phytochemical screening It refers to the extractive screening and identification of the medicinally active substance found in the plant. Some of the bioactive substance that can be derived from plants are flavonoids, alkaloids, carotenoids, tannins and resin. Test for Alkaloids Test Observation Result Wagner reagent + extracted sample in a test tube and heated in water bath Reddish brown colour was produced Test was positive for presence of Alkaloids Molish reagent + extracted sample in a test tube and heated in water bath Violet colour ring was formed Test was positive for presence of Alkaloids
  • 13. 9 Saponin test Test Observation Result 5ml extract was mixed with 20ml of distilled water then agitated in graduated cylinder for 15 minute Formation of foams was not observed Test was negative for Saponin Test for Resins Test (acetone-water test) Observation Result Extract + acetone + water was added in test-tube and was shacked properly. Turbidity was seen Test was positive for Resins Test for Tannins Test Observation Result 4 ml extract + 4ml ferric chloride solution was taken in test-tube and was mixed Green colour was formed Test was positive for Tannins Results: Hence, performing phytochemical screening of turmeric extract, it was found that the extract contain resins, tannins and alkaloids.
  • 14. 10 Conclusion From the above project work we conclude that the turmeric powder contain alkaloids, resins, tannins etc. and also comes to know about their methods of extraction and their physical as well as morphological characters.
  • 15. 11 References 1. TEXTBOOK OF PHARMACOGNOSY AND PHYTOCHEMISTRY By; Biren Shah | A. K. Seth; p339-341 2. A Comprehensive Review on Physiological Effects of Curcuma Article in Drug Research · August 2020 (https://www.researchgate.net/publication/343411049) 3. Curcuma longa Linn. A Phytochemical and Phytopharmacological Review By; Arjun M. Modi | Prafulla (Sabalehttps://www.researchgate.net/publication/301644533_Curcuma_long a_Linn_A_Phytochemical_and_Phytopharmacological_Review) 4. The dictionary definition of turmeric at Wiktionary (https://en.wikipedia.org/wiki/Turmeric) 5. https://youtu.be/narcXVg3xyM