Formulation and Evaluation of Gel Containing Barringtonia
Racemosa L.Spreng Kernel Extract for Topical Application
Nur Asnah Sitohang
1
, Effendy De Lux Putra
2
, Musri Musman
3
and Hajjul Kamil
4
1
Lecturer at the Faculty of Nursing, Universitas Sumatera Utara and students of the Study Program Study Doctoral
Mathematics Application Science at the Universitas Syiah kuala
2
Lecturer at the Faculty of Pharmacy, Universitas Sumatera Utara
3
Lecturer at the Faculty of
science teaching, Universitas Syiah kuala
4
Lecturer at the Faculty of Nursing, Universitas Syiahkuala
Keywords: Barringtonia racemosa kernel extract, Carbopol 940, wounds healing.
Abstract: Medicinal plants are now widely used by the community as an effort to tackle health problems amid advances
in science and technology. A natural material that can be used as an alternative biological therapy for wound
management is a putat air (Barringtonia racemosa). The phytochemical content of this plant is in the form of
saponins, flavonoids, and terpenoids. The research objective was obtained physical test data of wound gel
formula with ethanol extract of putat air. The research design is experimental. In this research, four wound
gel formulas containing putat air kernel extract were evaluated for organoleptic, pH, homogeneity and
viscosity. The formula designed was corbopol 940 2% with kernel extract of putat air 1%, 3%, 5% and 7%.
Based on the organoleptic test, the four formulas are semisolid, yellowish-white, thick and odorless.
Homogeneity testing, homogeneous preparations but there are bubbles. The higher the concentration of putat
air (B. racemosa) extract, the more bubbles as well as the color of the yellowish gel. This is also due to high
saponin levels. The pH test shows it is ideal for topical preparations, which is between pH 6-6.2. The highest
pH is found in formulas with a concentration of putat air (B. racemosa) extract 1%. Viscosity measurement
results for the entire formula, resulting in a value that is included in the standard that is 9000-10500 cP. Based
on the physical essence, this gel preparation is still suiTable for treating wounds on the skin.
1 INTRODUCTION
Indonesia has various types of medicinal plants.
Medicinal plants are now widely used by the
community as an effort to tackle health problems
amid advances in science and technology. A natural
material that can be used as an alternative biological
therapy for wound management is a putat air
(Barringtonia racemosa). Based on proven research
that this plant has been prescribed in the Ayurvedic
literature of traditional Indian medicine for the
treatment of dog and snake bite wounds. The
phytochemical content of this plant is in the form of
saponins, flavonoids, and terpenoids (Ojewele et al.,
2004: Gowri.et.al.2009; Musman, 2010). The
B.racemosa plant is a type of local mangrove known
as a putat air. One species in the kingdom of Plantae
of the genus Barringtonia which is classified under
the family Lecythidaceae.
The taxonomic hierarchy of B.racemosa can be
arranged in the following order: Kingdom: Plantae;
Subkingdom: Viridiplantae; Infracingdom:
Streptophyta; Superdivision: Spermatophytina;
Class: Magnoliopsida; Superorder: Asteranae; Order:
Ericales; Family: Lecythidaceae; Genus:
Barringtonia; Species: Barringtonia racemosa (L.).
(Osman et al., 2015).
Phytochemical constituents found in putat air (B.
Racemosa) include saponins, sterols and phenolics.
Saponins for instance are classified as triterpene
glycosides which are very well known to be
inherently present in B. racemosa. The presence of
such compounds had been acknowledged to be the
reason of its suitability to be used as cleaning agents
due to its surface-active properties and may produce
long-lasting foam (Chen.et.all.,2010; Makkar., 2007).
Plant sterols are the components occur in plant
cells which are generally functions to control
membrane fluidity and permeability. The presence of
sterol in plants is associated with a number of benefits
for instance it has the potential to be used as natural
preventive dietary product in lowering plasma
364
Sitohang, N., Putra, E., Musman, M. and Kamil, H.
Formulation and Evaluation of Gel Containing Barringtonia Racemosa L.Spreng Kernel Extract for Topical Application.
DOI: 10.5220/0009515203640370
In Proceedings of the International Conference on Health Informatics and Medical Application Technology (ICHIMAT 2019), pages 364-370
ISBN: 978-989-758-460-2
Copyright
c
2020 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
cholesterol level (Piironen., 2000). Phenolics are
compounds possessing one or more aromatic rings
with one or more hydroxyl groups. They are broadly
diversified ranging from simple molecules to highly
polymerized substances with more than 8000
compounds being categorized into the group. Plant
phenolics can be further classified into several sub-
groups which are phenolic acids, flavonoids, tannins
(non-flavonoid polyphenols), stilbenes and lignans.
Phenolic compounds are frequently associated with
antioxidative properties and being recognized as
natural antioxidants ( Dai and Mumper., 2010).
Flavonoids are reported to have 3 mechanisms of
inhibition of microorganisms, namely by (1)
destruction of the cytoplasmic membrane, (2)
inhibition of nucleic acid synthesis, and (3) inhibition
of metabolic energy (Cushnie, 2011).
Pharmacological activity of B.racemosa contains
antimicrobial, antibacterial against strains of both
gram positive and gram negative bacteria, namely
staphylococcus aureus, staphylococcus epidermidis,
Eschericia coli, shigella dysentriae, vibrio cholerae
and Proteus sp. This plant also contains
antinociceptive (analgesic), antioxidants, anti-
inflammatory and anti-fungal (Khan, 2001).
The various parts of
Barringtonia racemosa
(B. racemosa)
are known to possess multiple
biological activities
.
(Khan and Omoloso., 2002).
Extracts prepared from different parts of
B.
racemosa
possess analgesic, antitumor and
antimicrobial activities (Thomas and Panikkar.,
2002; Muse and Ahmad.,2008). The aqueous
bark extract of
B. racemosa
exerted signicant
and dose-dependent antinociceptive activity in
experimental animals. This activity is attributed
to the presence of opioids or opiodiomimetics as
well as phenolics and steroidal con- stituents in
B.
racemosa
(Husein.at el., 2009). Anti-oxidant and
anti-inammatory ef- fects of
B. racemosa
leaves
ar attributed to its lycopene content . This extract
exerted
in vitro
nitric oxide synthase inhibitory
and antioxidant activity in RAW cells (Muse and
Ahmad., 2008). Methanolic, ethanolic and
boiling water extracts of
B. racemosa
leaves,
sticks and barks at the
concentration of 50 mg/mL
were found to possess antifungal activity against
Fusarium
sp.,
Tricoderma koningii
,
Penicillium
sp.,
Ganoderma
tropicum
,
Ganoderma lucidum
,
Aspergillus
sp. and
Rhizopus
sp
(Osaman.et.al.,2015).
The extracts obtained from the aerial parts of
this plant demonstrated
in vitro
antioxidant
activity
B. racemosa
leaves demonstrated higher
antioxidant activities than the stems, owing to its
antioxidant content (Patil.et.al.,2011).
Effectiveness and comfort in the use of putat air
extract (B.racemosa) on a skin can be improved by
formulating it into gel dosage forms. Topical gel
preparations can increase the effectiveness and
comfort in its use which is able to deliver medicinal
ingredients well, easily spread evenly when applied
to the skin, giving a cold sensation, and does not cause
marks on the skin (Madan and Singh, 2010).
Carbopol is a hydrophilic gel, so it is easily dispersed
in water and in small concentrations can function as a
gel base with a fairly good thickness at pH 6-11.
Carbopol is white, has a texture like feathers, acids,
hygroscopic powder with a slight characteristic odor.
Carbopol is a strong gel base has a high acidity so that
in its use as a gelling agent it only takes around 0.5-
2.0% (Melani et al., 2005; Rowe et al., 2009). This is
the advantage of using carbopol compared to other
ingredients Ideally, gelling agents are the basis of gel
preparations that are inert, safe and not reactive with
other components of the gel formula. The
characteristics of the gelling agent used must be
adjusted to the dosage form. Gel preparations must be
well formulated to meet safe, effective and stable.
Until now there has been no reference that found
wound gel formula using extracts of putat air
(B.racemosa) (Scopus, 2019; Web of Science, 2019;
PubMed, 2019).
2 RESEARCH METHODS
The aim of this study was to conduct a physical test
of a watertight wound gel formula (B. Racemosa).
The research design is experimental. The stages of the
formulation were carried out by designing four types
of formulas, from which the four formulas were tested
physically, namely organoleptic, viscosity,
homogeneity and pH.
Material
Sample Preparation
The putat air fruit (B.racemose) was taken from the
village of Gampong Pulo.Kec. Peudada. Bireuen
Regency. Fruit taken is old and fell on the ground.
The water drops are immediately put into a sealed
plastic bag. Before it is sealed, it expels air from the
plastic bag. Then the plastic bag is placed in a cool
place (4° C) (Table 1).
Formulation and Evaluation of Gel Containing Barringtonia Racemosa L.Spreng Kernel Extract for Topical Application
365
Table 1. Preparation of Carbopol 940 gelling agent formula
The part of the putat air used is the white inside
seeds. The putat air is peeled and the seeds are taken.
Brown seeds are washed without peeling the brown
skin. Brown skin is left to peel itself during drying.
Then the putat air seeds are cut into small pieces and
then dried in a drying chamber at 40 ° C for one week.
Wet material is 4 kg and after drying becomes 1.5 kg.
Simpisia Extraction is removing the first and second
metabolites from putat air tissue cells using solvents.
The solvent used is 70% ethanol. The concentration
of ethanol solvent 70% more dissolved flavonoids
than pure ethanol solvents. Ethanol polarity increases
and more easily penetrates cell membranes with the
addition of 30% water (Musman, 2013).
The extraction method used is homogenization of
sympathies. Dried fruit that has been dried in a dryer
(temperature 40 ° C) is ground in a blender. The putat
flour is stored in a container and 70% ethanol is
poured and 30% water is left for 24 hours. Every 1x24
hours the solvent is replaced until the solvent is no
longer colored. Then the mixture is filtered.
The obtained filtrate is dried with a rotary carrier.
Dehydrated ethanol extract was dissolved in 10 ml of
ethanol and 20 ml of aquades, and placed in a
separating funnel and then mixed with 100 ml of n-
hexane solvent until colorless. The residues were
mixed with ethyl acetate and ethanol, and then the
fraction was evaporated. The resulting solution was
stored in a vial for phytochemical filtration.
2.1 Preparation of Carbopol 940
Gelling Agent Formula
The gel base consisting of carbopol, TEA,
propylenglycol, glycerin and aquades was made into
4 different formulas, namely by varying the
concentration of putat air (B.raccemosa) seed extract
1%, 2%, 3%, 5% and 7%. The gel preparation on the
basis of 940 carbopol is done by means of carbopol
940 developed in 10 parts of distilled water in a
beaker, left to stand for 1 x 24 hours. Then added TEA
then homogenized.
Then propylene glycol and methyl paraben were
added, which were previously dissolved in 900C hot
distilled water, stirring until homogeneous. The
extract was mixed with glycerin, mixed into the base,
added the remaining water to the base, and stirred
until homogeneous.
3 RESULT
3.1 Organoleptic Test
Organoleptic test results of Formula shown on the
Table 2:
Table 2: Organoleptic test results
No Formula Color Smell Consistency
1 F1 Clear Distinctiv
e smell
Thick
2 F2 Yello
wish
white
Typical
odor of
putat air
extract
Thick
3 F3 Yello
wish
white
Typical
odor of
putat air
extract
Thick
4 F4 Yello
wish
white
Typical
odor of
putat air
extract
Thick
5 F5 Yello
wish
white
Typical
odor of
putat air
extract
Thick
Based on Table 2. Data obtained formulas F2, F3, F4
and F5 are yellowish, have a distinctive odor and have
a thick consistency as shown in Figure 1:
Material
Base Formula (% b/b)
F1 F2 F3 F4 F5
Carbopol 2 2 2 2 2
TEA 2 2 2 2 2
Glycerin 1 1 1 1 1
Propylene
Glycol
6 6 6 6 6
Nipagin 0.2 0.2 0.2 0.2 0.2
Aquadest Ad
100
ad
100
Ad
100
Ad
100
Ad
100
Putat extract
(gr)
0 1 3 5 7
ICHIMAT 2019 - International Conference on Health Informatics and Medical Application Technology
366
Figure 1: Result of Homogenity test
3.2 Viscosity Test
Viscosity is a statement of the resistance of a liquid to
flow. The higher the viscosity, the higher the prisoner
(Sinko, 2011). Viscosity of the preparation should not
be too high and should not be too low, because if it is
too high (thick), the gel will be difficult to remove
from the package, whereas if the viscosity is too low
it will reduce the length of time to stay on the skin
when used.
Gel viscosity (Table 3) was measured using a
Brookfiled cone and plate viscometer (Engineering
Laboratories INC, Stoughton MA, USA). Gel flow is
measured at room temperature. The sample is placed
about 1 g in the cone. Measurements are made by
increasing the shear rate from 0.5 / sec to 100 / sec
and viscosity is read at each rotation per minute.
Table 3: Gel Viscosity Test Results
No Formula Viscosity
1 F1 8250 cp
2 F2 9000 cp
3 F3 9500 cp
4 F4 10000 cp
5 F5 10500 cp
3.3 pH of the Preparation
The pH was measured using a pH meter (Schott,
Deutschland, Belgium). 1 g of sample is dissolved in
10 ml of water at room temperature. Furthermore, the
electrode will contact with the surface of the solution
and leave it in balance for 1 minute (Table 4).
Table 4: pH gel test results
N
o Formula pH
1
F1 6,6
2
F2 6,2
3
F3 6,0
4
F4 6,0
5
F5 6,0
Figure 2: pH gel test results
3.4 Homogenity Test
Based on Table 5. the results obtained are all
homogeneous formulas.
Table 5: Homogenecity Test Results Gel wound of putat air
(B.Racemosa) extract
No Formula Results
1
F1 Homogeneous
2
F2 Homogeneous
3
F3 Homogeneous
4
F4 Homogeneous
5
F5 Homogeneous
4 DISCUSSION
Carbopol is a synthetic acrylic acid polymer, a white
powder with a distinctive odor, very easily ionized,
slightly acidic, insoluble in water and most solvents,
and is hygroscopic. In neutral form, carbopol is
soluble in water, alcohol, and glycerin and will form
a clear and sTable gel. In acidic solutions (pH 3.5-4.0)
carbopol dispersions show low to moderate viscosity
and at pH 5.0-10.0 and at temperatures above 750C
will show optimal viscosity. Carbopol functions as a
thickener, surfactant, stabilizer, and thickener. In
cosmetics, carbopol is used in a neutral form at pH
Formulation and Evaluation of Gel Containing Barringtonia Racemosa L.Spreng Kernel Extract for Topical Application
367
7.7 because carbopol is sTable at that pH and is
incompatible with strong acids (Rowe et al., 2009).
Carbopol is a gelling agent that can modify the
flow properties and viscosity and can be a stabilizing
agent for a topical preparation. The use of Carbopol
as a good gelling agent is in the range of 0.5% -2.0%
(Rowe et al., 2009). Propylene glycol is a humectant
that also affects the swelling and viscosity of the gel.
Carbopol formulated in conjunction with humectants
such as propylene glycol and glycerin can produce
good stability at the right ratio.
Humectant propylene glycol is able to bind with
water to form hydrogen bonds so that it can trap
water, therefore the use of these two humectants
should not be too large so that carbopol can still bind
to water and can maintain gel consistency (for
Propylene glycol <30%) (Islam, 2004 ).
According to Bakker (2012), states that gel is a
heterogeneous system. In gel preparations, the solid
phase is in a three-dimensional structure so that
particles in the solid phase cannot move past the
liquid phase. In order for a solid phase to remain
sTable in a three-dimensional structure, solid phase
particles must form secondary bonds with other
particles (Van der Waals bonds). The stability of the
gel preparation depends on the shape of the particles
from the solid phase; physico-chemical
characteristics of the solid phase and its ability to
form secondary bonds; concentration of solid phase;
physico-chemical characteristics of the liquid phase.
Viscosity shows the level of thickness of a gel
preparation. Carbopol 940 in powder form is a
polymer that forms coils so that this will limit its
thickening ability, but if carbopol is dispersed into
water, the carbopol will be hydrated and some of the
coils will be uncoiled (Noveon, 2009). Carbopol will
function well if the constituent polymers are truly
uncoiled. The mechanism is the neutralization of the
carboxylic acid group in the polymer chain with the
appropriate base. This will result in the formation of
negative charges along the polymer chain, where
neutralization is done by adding TEA. The repulsion
between negative charges causes carbopol 940 to
make the coiled structure change to a freer structure
(Garg., Et al., 2002).
Carbopol 940 polymers will be intertwined with
each other by forming cross links so as to produce a
three-dimensional matrix to form a gel that is very
thick in a second, so the higher the viscosity value,
the level of thickness of a preparation is also higher
because of the number of polymers undergoing cross
links and forming more and more gel bases. It cannot
be said that the higher the viscosity, the better the
preparation of the gel, because it will be related to the
spreadability and comfort of the preparation during
use. It should be noted that the value of viscosity is
inversely proportional to the value of the dispersal
power (Garg., Et al., 2002).
The composition of propylene glycol in the
formulation is said to be good at around 15% (Rowe
et.al, 2009). Another opinion states that propylene
glycol can be a good humectant in the composition of
5% of the preparation. The use of humectants that are
too high will cause the water in the preparation to
interact entirely with propylene glycol and form
hydrogen bonds, even skin moisture when applied
can lose moisture and can become dehydrated.
However, if the concentration of propylene glycol is
too small, it can be feared that the water content in the
preparation cannot be maintained (Aulton, 2007).
Based on the theories above, the optimum area of
propylene glycol will be in the range of
approximately 5% -30%. This study uses 6%. Other
materials used this time include glycerin and nipagin
as preservatives, TEA as an alkaline agent,
neutralyzing agent that helps form the gel and
aquadest character (Rowe et.al, 2009). Base
optimization is done by organoleptic test,
homogeneity test, pH test, viscosity test, and
spreadability test.
Organoleptic testing is done by observing the
shape, color, and odor. This test aims to see the
quality and stability of the preparation which includes
the shape, odor, and color of the preparation. If there
is no change in shape, color and odor in the
preparation for 48 hours after the preparation is made,
until during one month of storage, then the
preparation can be categorized as having a fairly good
quality and stability (although it must be tested again
at a later stage).
The results showed that all concentrations of
white, yellowish, thick and odorous putat extract. The
color of the gel is not clear because of the high levels
of saponins. Homogeneity testing was carried out
using two pieces of glass objects.
Homogeneous preparations are preparations in
which there are no beads from the material used. The
test results show that the preparations are
homogeneous but there are bubbles generated during
the manufacturing process using a stirer. The higher
the concentration of putat air extract, the more
bubbles. This is also due to high saponin levels.
The pH test shows that the ideal gel preparation
for topical preparations according to British
Pharmacopeia is between pH 6-8. The highest pH is
found in formulas with a concentration of putat
extract 1%. Formula with a concentration of putat
extract 3%, 5% and 7%, its pH 6. This gel preparation
ICHIMAT 2019 - International Conference on Health Informatics and Medical Application Technology
368
is still suiTable for use in treating wounds on the skin.
If a topical preparation has a pH range that does not
match the pH of the skin, then the preparation has the
potential to cause irritation and erythema to its users.
Gel base viscosity was measured at a speed of 0.1
rpm for 30 seconds. According to Indonesian
National Standars 16-4399-1996, the standard
viscosity value for gel preparations is 6000-50000 cP
or 6-50 Pa.S. Viscosity measurement results for the
entire formula, resulting in a value that is included in
the standard that is 9000-10500 cP. The research of
Srividya et al (2001) describes corbopol 940 as a gel
forming agent oflaxacin antibacterial agent in
combination with hydroxypropyl methylcellulose
(Methocel E50LV) which acts as a viscosity
enhancing agent. The formulation developed is a
therapy that is effective, stable, non-irritating and
provides continuous drug release over an 8 hour
period.
Sari's research (2016), aims to find out the right
comparison between 940 carbohydrate gel base and
hydroxypropyl methylcellulose (HPMC) on the
stability of physical properties of extract gel and
methanol fraction of kesum leaves with Simplex
Lattice Design (SLD) method, there is no significant
difference between the properties physical extract gel
and methanol fraction of kesum leaves (Polygonum
minus Huds.).
5 CONCLUSIONS
Based on the organoleptic test, the four formulas are
semi solid, yellowish-white, thick and odorless.
Homogeneity testing, homogeneous preparations but
there are bubbles The higher the concentration of
putat air (B. racemose) extract, the more bubbles as
well as the color of the yellowish gel. This is also due
to high saponin levels. The pH test shows it is ideal
for topical preparations, which is between pH 6-6.2.
The highest pH is found in formulas with a
concentration of putat air (B. racemose) extract 1%.
Viscosity measurement results for the entire formula,
resulting in a value that is included in the standard that
is 9000-10500 cP. Based on the physical essence, this
gel preparation is still suiTable for treating wounds
on the skin.
ACKNOWLEDGEMENTS
This Research was supported by Universitas
Sumatera Utara in accordance with the USU
TALENTA implementation contract Fiscal Year
2019 ,Number: 439 / UN5.2.3.1 / PPM / KP-
TALENTA USU / 2019 dated April 1, 2019. Thank
you to the chancellor, vice chancellor III and chair of
the USU Research Institute.
REFERENCES
Bakker, P., Herman W., Vincent G., Ben N., Rachel van der
K., Nicolien W. (2012). Dermatological Preparations
for The Tropics. Beta Science Shop. Netherlands.
Cushnie, T.P.T., Lamb, A.J., 2011, Recent Advances in
Understanding the Antibacterial Properties of
Flavonoids, International Journal of Antimicrobial
Agents, (38) 99– 107.
Chen, YF, Yang CH, Chang MS, Ciou, YP, Huang YC.
Foam properties and detergent abilities of the saponins
from Camellia oleifera. Int J Mol Sci. 2010; 11:4417–
25.
Dai J, Mumper RJ. Plant phenolics: Extraction, analysis and
their antioxidant and anticancer properties. Molecules.
2010; 15:7313–52. Garg, A., Aggarwal, D., Garg, S.,
dan Singla, A.K., 2002, Spreading of Semi Solid
Formulation : An Update, Pharmaceutical Technology,
September 2002, 84-102.
Gowri. P.M., Radhakrishnan. S.V.S, Barha. J., Sarma.
A.V.S., Rao.M. (2009). Oleanna- Type Isometric
Triterpenoid From Barrongtoia Racemosa. Journal of
Natural Products. V0. 75(4).
Hussin N, Muse R, Ahmad S, et al. Antifungal activity
of extracts and phenolic compounds from
Barringtonia racemosa
L. (Lecythidaceae).
Afr J
Biotechnol
. 2009;8:2835e2842.
Islam, M. T., Rodriguez-Hornedo, N., Ciotti, S.,
Ackermann, C., 2004, Rheological Characterization of
Topical Carbomer Gels Neutralized to Different pH,
Pharmaceutical Research, Vol. 21, No.7, Plenum
Publishing Corporation, Michigan, pp. 1192-1199
Khan, S., Jabbar, A., Hasan, C. M., & Rashid, M. A. U.
(2001). Antibacterial activity of Barringtonia racemosa.
Fitoterapia, 72 (20010. 162–164.
Khan M, Omoloso A. (2002).Antibacterial,
antifungal activities of
Barringtonia asiatica
.
Fitoterapia
. 2002;73:255e260.
Kong KW, Mat-Junit S, Aminudin N, Ismail A,
Abdul-Aziz A. Antioxidant ac- tivities and
polyphenolics from the shoots of
Barringtonia
racemosa
(L.) Spreng in a polar to apolar medium
system.
Food Chem
. 2012;134:324e332.
Madan, J., Singh, R. 2010. Formulation and Evaluation of
Aloevera Topical Gels. Int.J.Ph.Sci. 2 (2).551-555.
Melani, H.D., Purwanti, T., Soeratri, W., 2005, Korelasi
Kadar Propilen glikol dalam Basis dan Pelepasan
Dietilammonium Diklofenak dari Basis Gel Carbopol
ETD 2020, Majalah Farmasi Aquadestlangga, 5(1), 1.
Makkar HPS, Siddhuraju P, Becker K. Methods in
Molecular Biology: Plant Secondary Metabolites.
Formulation and Evaluation of Gel Containing Barringtonia Racemosa L.Spreng Kernel Extract for Topical Application
369
Totowa, NJ, USA: Humana Press; 2007. p. 93–100.
https://doi. org/10.1007/978-1-59745-425-4_16
Misal G., Dixit G., Gulkari V. (2012). Formulation and
evaluation of herbal gel. Indian Journal of Natural
Product and Resources. 2012;3:501–5.
Muse R, Ramli J, Ahmad S, Mahmood M.
Antioxidant activities of different aerial parts of
putat (
Barringtonia racemosa
L.).
Malays J
Biochem Mol Biol
. 2008;16:15e19
Musman. (2010). Toxicity of Barringtonia racemosa (L.)
Kernel Extract on Pomacea canaliculata
(Ampullariidae). Tropical Life Sciences Research,
21(2), 41–50.
Noveon,( 2009), Neutralizing Carbopol® and Pemulen®
Polymers in queous and Hydroalcoholic system.
Lubrizol Tehchnical data Sheet.
Ojewole.J.A.O., .Nundkumar.,C.O.Adewunmi.(2005).
Molluscicidal,cercariacidal,larvacidaland
antiplasmodial propeeties of barringtonia racemosa
fruit and seed extracts.BLACPMA.Vol.3.no.5:88-92.
Osman..N.I, Sidik.N.J.,Awal Asmah.
(2015).Pharmacological Activities of Barringtonia
Racemosa L. (Putat), A Tropical Medicinal Plant
Species. Journal of Pharmaceutical Sciences and
research.V0l(7)4.2015.185-188.
Patil KR, Patil CR, Jadhav RB, Mahajan VK, Patil
PR, Gaikwad PS(2011) Anti-arthritic activity of
bartogenic acid isolated from fruits of
Barringtonia racemosa
Roxb. (Lecythidaceae).
Evid Based Complement Altern Med
.
2011:2011.
Patil, K. R., Patil, C. R. (2016). Journal of Traditional and
Complementary Medicine Anti-inflammatory activity
of bartogenic acid containing fraction of fruits of
Barringtonia racemosa Roxb . in acute and chronic
animal models of in fl ammation. Journal of Traditional
Chinese Medical Sciences, 4–11.
Piironen, V, Lindsay DG, Miettinen TA, Toivo J, Lampi A-
M. Plant sterols: Biosynthesis, biological function and
their importance to human nutrition. J Sci Food Agric.
2000; 80:939–66.
Rowe, C.R., Sheskey, P.J., Quinn, M.E., 2009, Handbook
of Pharmaceutical Excipients, 6th edition,
Pharmaceutical Press, London, pp. 110-114,. Rowe,
C.R., Sheskey, P.J., Quinn, M.E., 2009, Handbook of
Pharmaceutical Excipients, 6th edition, Pharmaceutical
Press, London, pp. 592-594.
Sari . R., Nurbaeti, S.N., Pratiwi. L. (2016). Optimasi
Kombinasi Karbopol 940 dan HPMC Terhadap Sifat
Fisik Gel Ekstrak dan Fraksi Metanol Daun Kesum
(Polygonum minus Huds.) dengan metode Simplex
Lattice Design. Pharm Sci Res. V0l. 3. No. 2. 72-79.
Sinko PJ (2012). Martin’s Physical Pharmacy and
Pharmaceutical Sciences. 6th edition. Philadelphia:
Lipincott Williams and Walkins; 2012.
Srividya.B., Rita. M., Amin. C P.D. (2001). Sustained
ophthalmic delivery of ofloxacin from a pH triggered
in situ gelling system. Journal of Controlled Release 73.
205–211.
Suhaime, I.H.B., Tripathy, M., Mohamed, M.S., Majeed,
A.B.A., (2012), The Pharmaceutical Applications of
Carbomer, Asian Journal of Pharmaceutical Sciences
and Research, 2 (2), 1-12.
Tanaka O, Tamura Y, Masuda H, Mizutani K. In: Waller
GR, Yamasaki K, editors. Saponins used in food and
agriculture. New York, NY, USA: Plenum Press; 1996.
p. 1–11.
Thomas TJ, Panikkar B, Subramoniam A, Nair MK,
Panikkar K.(2002) Antitumour property and
toxicity of
Barringtonia racemosa
Roxb seed
extract in mice.
J Ethnopharmacol
.
2002;82:223e227.
Tranggono, R.I., Latifah, F., (2007), Buku Pegangan Ilmu
Pengetahuan Kosmetik, PT.Gramedia Pustaka Utama,
Jakarta.
Zocchi., G., (200) , Skin-Feel Agents, in Barrel, Andre
O.,Paye, Marc, dan Maibach, Howard I., Handbook of
Cosmetics Science and Technology, Marcel Dekker
Inc., New York.
ICHIMAT 2019 - International Conference on Health Informatics and Medical Application Technology
370