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About OMICS GroupAbout OMICS Group
OMICS Group International is an amalgamation of OMICS Group International is an amalgamation of Open Access publications and worldwide international science and worldwide international science conferences and events. Established in the year 2007 with the sole conferences and events. Established in the year 2007 with the sole aim of making the information on Sciences and technology ‘Open aim of making the information on Sciences and technology ‘Open Access’, OMICS Group publishes 400 online open access Access’, OMICS Group publishes 400 online open access scholarly journals in all aspects of Science, Engineering, Management in all aspects of Science, Engineering, Management and Technology journals. OMICS Group has been instrumental in and Technology journals. OMICS Group has been instrumental in taking the knowledge on Science & technology to the doorsteps of taking the knowledge on Science & technology to the doorsteps of ordinary men and women. Research Scholars, Students, Libraries, ordinary men and women. Research Scholars, Students, Libraries, Educational Institutions, Research centers and the industry are main Educational Institutions, Research centers and the industry are main stakeholders that benefitted greatly from this knowledge stakeholders that benefitted greatly from this knowledge dissemination. OMICS Group also organizes 300 dissemination. OMICS Group also organizes 300 International conferences annually across the globe, where knowledge annually across the globe, where knowledge transfer takes place through debates, round table discussions, poster transfer takes place through debates, round table discussions, poster presentations, workshops, symposia and exhibitionspresentations, workshops, symposia and exhibitions ..
About OMICS Group About OMICS Group ConferencesConferences
OMICS Group International is a pioneer and leading science OMICS Group International is a pioneer and leading science event organizer, which publishes around 400 open access event organizer, which publishes around 400 open access journals and conducts over 300 Medical, Clinical, Engineering, journals and conducts over 300 Medical, Clinical, Engineering, Life Sciences, Phrama scientific conferences all over the globe Life Sciences, Phrama scientific conferences all over the globe annually with the support of more than 1000 scientific annually with the support of more than 1000 scientific associations and 30,000 editorial board members and 3.5 million associations and 30,000 editorial board members and 3.5 million followers to its credit.followers to its credit.
OMICS Group has organized 500 conferences, workshops and OMICS Group has organized 500 conferences, workshops and national symposiums across the major cities including San national symposiums across the major cities including San Francisco, Las Vegas, San Antonio, Omaha, Orlando, Raleigh, Francisco, Las Vegas, San Antonio, Omaha, Orlando, Raleigh, Santa Clara, Chicago, Philadelphia, Baltimore, United Kingdom, Santa Clara, Chicago, Philadelphia, Baltimore, United Kingdom, Valencia, Dubai, Beijing, Hyderabad, Bengaluru and Mumbai.Valencia, Dubai, Beijing, Hyderabad, Bengaluru and Mumbai.
• Economically the Leguminosae (Fabaceae)Leguminosae (Fabaceae) is one
of the most important families of the flowering
plants.
• PterocarpusPterocarpus is a genus representing some of the
most handsome large-crowned trees of the
leguminous family.
• Genus Pterocarpus includes about 60-70 species.60-70 species.
Flowering tree in summer Flowering tree in summer
Pterocarpus dalbergioides (Roxb) is native to
the Andaman islandsAndaman islands in the Indian ocean.
• It has been introduced to EgyptEgypt as an
ornamental plantornamental plant.
• Pterocarpus dalbergioides (Roxb) is known
as:
Andaman padaukAndaman padauk
East Indian mahoganyEast Indian mahogany
Andaman redwoodAndaman redwood
PadaukPadauk.
Phyllum Angiospermae
Subphylum Dicotyledonae
Class Magnoliopsida (Dicotyledons)
Subclass Rosidae
Order Leguminales (fabales)
Family Leguminosae (Fabaceae)
Subfamily Papilionoideae
Tribe Dalbergieae
Genus Pterocarpus
Species dalbergioides (Roxb), Roxb. ex DC.
Outer surface of the stem barkOuter surface of the stem bark Inner surface of the stem barkInner surface of the stem bark
Leaf and flowerLeaf and flower
Compound leafCompound leaf
Axillary panicleAxillary panicle
FlowerFlower
Flowering branchFlowering branch
SeedsSeeds
Fruiting branchFruiting branch
FruitsFruitsFresh Fresh DryDry
• Therefore, it was deemed of interest to
carry out a bioactivity-guided
fractionation study on the different
organs of the Egyptian plant, to choose
the most active organ, which was not
previously investigated.
• A bioactivity-guided screening of the different organs:
Stem barkStem barkFlowerFlowerFruitLeafLeaf
For both antihyperglycemic and anti-inflammatory activies were carried on
050
100150200250300350
Control Alcoholextract of
bark
Alcoholextract of
flower
Alcoholextract of
fruit
Alcoholextract of
leaf
MetforminBlo
od g
luco
se le
vel (
mg/
dl) Zero time After 2 hours After 4hours
0
01020304050607080
Control Alcoholextract of
bark
Alcoholextract of
flower
Alcoholextract of
fruit
Alcoholextract of
leaf
Indometacin
% o
edem
a
Indomethacin
From the previous preliminary From the previous preliminary
Pharmacological screening, one could Pharmacological screening, one could
conclude that the conclude that the alcoholic extracts of the alcoholic extracts of the
bark at a dose of 200 mg/kg b.wt. was the bark at a dose of 200 mg/kg b.wt. was the
most potentmost potent
extract as antihyperglycemic and anti-extract as antihyperglycemic and anti-
inflammatory. inflammatory.
Median lethal dose (LDMedian lethal dose (LD5050) of the alcoholic ) of the alcoholic
extracts ofextracts of Pterocarpus dalbergioides Pterocarpus dalbergioides
(Roxb) of the bark’s alcoholic extract (Roxb) of the bark’s alcoholic extract
was found to be was found to be 6.9 mg/Kg.b.wt.6.9 mg/Kg.b.wt.
Test Bark
Steam volatile substances -
Sterols and/or triterpenes ++
Flavonoidsa.Free
b.Combined
++++
Crystalline sublimate -
Carbohydrates and/or glycosides +
Tanninsa.Catechol
b.Pyrogallol
-++
Saponins -
Alkaloids and/or nitrogenous bases +
Anthraquinonesa.Free
b.Combined
--
Cardiac glycosides -
Were carried on and the obtained ethyl
acetate and butanol extracts of the were
furhtermore subjected to both
antihyperglycemic and anti-inflammatory
investigation.
Antihyperglycemic activity of the ethyl acetate and butanol extracts of the Antihyperglycemic activity of the ethyl acetate and butanol extracts of the
bark, flowers and fruits of bark, flowers and fruits of Pterocarpus dalbergioidesPterocarpus dalbergioides (Roxb) (Roxb)
0
50
100
150
200
250
300
350
Control EtOAc ext.of bark
But. ext.of bark
EtOAc ext. offlowers
But. ext.of flowers
EtOAc ext. offruits
But. ext.of fruits
Metformin
Blo
od
glu
cose
lev
el (
mg/d
l)
Zero time After 2 hours After 4hours
Anti-inflammatory activity of the ethyl acetate and butanol extracts of the Anti-inflammatory activity of the ethyl acetate and butanol extracts of the
bark, flowers and fruits of bark, flowers and fruits of Pterocarpus dalbergioidesPterocarpus dalbergioides (Roxb) (Roxb)
01020304050607080
Control EtOAc ext.of bark
But. ext. ofbark
EtOAc ext.of flowers
But. ext. offlowers
EtOAc ext.of fruits
But. ext. offruits
Indometacin
% o
edem
a
Indomethacin
TLC investigation revealed that the butanol extract of the bark showed more TLC investigation revealed that the butanol extract of the bark showed more spots compared to its corresponding ethyl acetate extract.spots compared to its corresponding ethyl acetate extract.
No. of
spots
Rf in s3
Rf in s4
Ethyl aceta
te bark
Butanol bark
Color of spot in Color with NH3 Color with AlCl3
Color with FeCl3
Color withp-
anisaldehyde
Vis. UV Vis. UV Vis. UV
1 0.9 - - - - - - - - - - violet
2 0.77 - + + - - - - - - - pink
3 0.76 - - - - - - - - - Faint pink
4 0.740.89
+ + - - - - - - - violet
5 0.710.81
+ + - bl. - bl. - - - -
6 0.450.82
- - y. d.y. d.y. d.y. br.y. fl.gr. - green
7 -0.73
+ + f.y.d.pr
.br.y.
d.pr.
y. d.pr. - -
80.71
± + f.y.s.vi.
flbr.
s.vi.fl
Ys.vi.f
lbl. -
9 0.440.72
- - bl. - bl. - - - - -
10 0.420.64
- - f.y.d.pr
.br.y. y. br.y. y. - -
11 -0.66
- - y.d.pr
.y.
d.pr.
y. d.pr. - green
12 0.330.75
- - f.y.d.pr
.br.y. y. br.y. y. - -
13 0.250.68
- - - - - - - - - violet
14 -0.42
- - - bl. - bl. - - - -
15 0.25 0.4 - + f.y.d.pr
.br.
d.pr.
y. d.pr. bl. -
16 0.120.35
- - f.y.d.pr
.br.y. y. br.y. y. - -
17 -0.32
- - - f.br. y. f.y. y. y. - -
18 -0.27
- - - - - - - - - green
Fractionation of the butanol extract of the stem Fractionation of the butanol extract of the stem bark of Pterocarpus dalbergioidesbark of Pterocarpus dalbergioides (Roxb) (Roxb)
10g butanol extract
VLCChloroformChloroform: ethyl acetateEthyl acetate : methanol
FractionsEach 100 ml
TLC monitoring
Fraction I(1-10)
Fraction II(11-18)
CHCl3: EtOAc97:3
85:14780 mg
Fraction III(19-26)
Fraction IV(27-36)
Fraction V(37-44)
CHCl3: EtOAc45:5530:70
330 mg
Fraction VI(45-56)
CHCl3: EtOAc25:75
EtOAc 440 mg
Pulled fractions
(I-VI)
Were screened for
0
50
100
150
200
250
300
350
Control Fraction II Fraction V Fraction VI Metformin
Blo
od g
luco
se le
vel (
mg/
dl)
Zero time After 2 hours After 4hours
0
50
100
150
200
250
300
350
Control Fraction II Fraction V Fraction VI Metformin
Blo
od g
luco
se le
vel (
mg/
dl)
Zero time After 4 weeks After 8 weeks
0
10
20
30
40
50
60
70
80
Control Fraction II Fraction V Fraction VI Indomethacin
% o
edem
a
Fractionation of the butanol extract of the stem Fractionation of the butanol extract of the stem bark of Pterocarpus dalbergioidesbark of Pterocarpus dalbergioides (Roxb) (Roxb)
10g butanol extract
VLCChloroformChloroform: ethyl acetateEthyl acetate : methanol
FractionsEach 100 ml
Pulled together according to similarity
Fraction I(1-10) Fraction II
(11-18)Active
Fraction III(19-26)
Fraction IV(27-36)
Fraction V(37-44)Active
Fraction VI(45-56)Active
P123 mg
P123 mg
P219 mg
P219 mg
F120 mg
CC-Sephadex LH –20MethanolMethanol :waterIncreasing polaritySubfractions Further CC –Sephadex LH-20
Physical Physical characterscharacters
2323 mg off-white needles, mg off-white needles, soluble in methanolsoluble in methanol
Melting pointMelting point 201-203201-203° ° CC
UV λmax nmUV λmax nm MeOHMeOH 259259
M+
M+- H2O
H3
H4H6
H3
H4
H6
O
HO
OH
HO
1
2 3
4
56
Gentisic acid
C1
C6
C3C4C5
C2
COOH
O
HO
OH
HO
1
2 3
4
56
Gentisic acid
O
HO
OH
HO
1
2 3
4
56
Physical Physical characterscharacters
2020 mg yellowish white powder, mg yellowish white powder, soluble in methanolsoluble in methanol . .
Melting pointMelting point 255-258255-258° ° CC
UV λmax nmUV λmax nm MeOHMeOH 272272
H2, H6
OH (3, 4 &5)
O
OH
HO
HO
HO
1
5
23
4
6
Gallic acid
C2, C6
C1
C4
C3, C5
COOH
O
OH
HO
HO
HO
1
5
23
4
6
Gallic acid
O
OH
HO
HO
HO
1
5
23
4
6
Physical Physical characterscharacters
1919 mg yellow powder, soluble in methanolmg yellow powder, soluble in methanol . .
Melting pointMelting point 265-267°C265-267°C
UV λmax nmUV λmax nm MeOHMeOH 260260 , ,329sh (isoflavone)329sh (isoflavone)
NaOMeNaOMe 274274 , ,340340) ) free OH on ring A free OH on ring A & B& B((
AlClAlCl33 271271 , ,300sh, 374 (free OH on 300sh, 374 (free OH on ring A)ring A)
AlClAlCl33/HCl/HCl 270270 , ,305sh, 374 (free OH at 305sh, 374 (free OH at 5 & no ortho-OH in ring B)5 & no ortho-OH in ring B)
NaoAcNaoAc 262262 , ,328sh (occupied OH at 328sh (occupied OH at 7)7)
NaoAc/HNaoAc/H33BoBo33 260260 , ,329sh (no ortho-OH in 329sh (no ortho-OH in ring B)ring B)
H8 H1’’H2', 6'
H2
H6
H3', 5'
C4'C7C4 C9
C2C5 C6''C4''
C5''C3''C8
C10
C3', 5'
C1'C3
C2', 6'
C1’
C6
C2''
O
O
OH
O
OH
O
HO
HO
OH
OH
(1) Vedavanam, K.; Srijayanta, S.; O' Reilly, J.; Raman, A.; Wiseman, H.; "Phytother Res", 13(7),
601-608,1999.
(2) Hung, T.H.W.; Peng, G.; Kota, B.P.; "Toxicology and Applied Pharmacology", 207(2), 160-169,
2005.
• The ethanolic extract of the bark possessed the most
potent antihyperglycemic activity. This effect could be
attributed to the synergistic action of the isoflavone
and phenolic acid content.
• The result of the anti-inflammatory activity showed
promising evidence for the anti-inflammatory effect of
the alcoholic extract of the bark which can be
attributed mainly to the phenolic acid content.
AcknowledgementAcknowledgement
Prof. Dr. Moshera M. El Sherei
Professor of Pharmacognosy – Faculty of Pharmacy
Cairo University
Prof. Dr. Wafaa T. Islam
Professor of Pharmacognosy – Faculty of Pharmacy
Cairo University
Mrs Shimaa Rashad
Assistant lecturer of Pharmacognosy – Faculty of Pharmacy
Cairo University
School of Medicine and Pharmacy School of Medicine and Pharmacy
• was established in Abu Zaabal in was established in Abu Zaabal in
18271827. .
It included 25 students for 5 yearsIt included 25 students for 5 years
• duration study.duration study.
In In 19551955, Faculty of Pharmacy was , Faculty of Pharmacy was
separated as one of the Cairo separated as one of the Cairo
University. University.
In In 19701970, the first internal bylaws , the first internal bylaws
was issued.was issued.
In In 19931993, bylaws was amended to , bylaws was amended to
include two semesters system and include two semesters system and
the cumulative average of the the cumulative average of the
Bachelor.Bachelor.
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Theme: Theme: Advanced trends for the future of Herbal Drugs Advanced trends for the future of Herbal Drugs and Productsand Products
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