Formulation
and development of face cream containing natural products
Ram
Kumar Sahu1*, Amit Roy1, Pradeep Kushwah2, Ashmita Sahu2
1Columbia Institute
of Pharmacy, Tekari, Raipur (C.G.)-493111, India.
2Oriental College
of Pharmacy, Raisen Road, Bhopal-462021 (M.P.),
India.
*Corresponding Author E-mail: ramsahu79@yahoo.co.in
ABSTRACT
The aim of
present study was to formulation and development of face cream comprising
extracts of natural products such as Mangifera
indica, Azadirachta indica, Coriandrum sativum, Psoralea corylifolia, Mentha arvensis and Daucus carota and
almond oil. Different types of
formulations oil in water (O/W) base namely F1 to F6 were formulated by
incorporating different concentrations Stearic acid
and Cetyl alcohol. The evaluation of all prepared
base (F1 to F6) were done on different parameters like pH, viscosity, spreadibilty, and stability were examined. The base F3 was found appropriate for the
preparation of cream. The extracts were incorporated in base F3 for the
preparation of herbal face cream. The herbal face cream showed good spreadibilty, good consistency, homogeneity, appearance,
pH, ease of removal and no evidence of phase separation. These herbal face
creams were safe to use for skin.
KEYWORDS: Daucus carota, Azadirachta indica, Psoralea corylifolia, almond oil, herbal cream.
INTRODUCTION:
Today a new hot topic in the cosmetic industry is ‘cosmeceuticals’, which is the fastest growing segment of
the natural personal care industry. The use of plant extracts in cosmetic
formulation is increasing, mostly because of the poor image that animal-derived
extracts have acquired during the past few years. This is due, in part, to news
reports regarding bovine spongiform encephalitis. Some animal derived products
need to be replaced, but synthetic chemicals cannot always do this well.
Natural molecules derived from plant extracts offer a particularly exciting
avenue for further research. Plant extracts, however, are often ill-defined as
to the method of extraction, plant-to-solvent ratio and the content of active
ingredients. Moreover, the stability of the colour, odour, transparency and/or active ingredients with time is
also often a limiting factor. Plant extracts are different in several respects
from purified therapeutic agents. Firstly, they are more dilute than the pure
chemicals that are familiar to us; secondly herbs often contain additional
active principles that may be closely related both chemically and
therapeutically to the constituent primarily responsible for its effects1-3.
The plant used in formulation was selected on the basis
of scientifically reported property. The best cosmetic product must contain
following properties antioxidant property, anti-inflammatory, antibiotic,
whitening agent, moisturizing properties etc. As per this concern we select
following plants Mangifera indica,
Azadirachta indica, Coriandrum sativum, Psoralea corylifolia, Prunus amygdalus, Mentha arvensis and Daucus carota for
the formulation of herbal cosmetic.
Mangifera indica leaves are claimed to possess antibiotic
properties4 and the antibacterial property of Azadirachta indica leaves are reported5. Daucus carota6 contain abundant amount of Vitamin A and Vitamin C. Vitamin A also acts
as a very good anti-oxidant which slows down the
process of aging. Vitamin C produces collagen in the body which is an
essential protein for making our skin elastic. It also prevents wrinkles on the
skin. Moreover Prunus amygdalus is enriched with Vitamin E7. Mentha arvensis were used as cooling and soothing agent8,
while remaining plants produce antioxidant activity9-11. Therefore,
an attempt has been made in this study to combine these plants in preparation
of herbal cosmetic cream and to produce the synergistic effects on skin.
MATERIAL
AND METHODS:
Preparation of extracts
Air dried and coarsely powdered (500 gm) of Mangifera indica leaves, Azadirachta indica leaves, Coriandrum sativum seed, Psoralea
corylifolia seeds, Mentha
arvensis leaves and Daucus
carota were placed in soxhlet
extractor separately, using petroleum ether and then successively with ethanol.
The extracts were then concentrated to dryness under reduced pressure and
controlled temperature, respectively and they were preserved in a refrigerator.
Preparation of cream base: Oil in water (O/W) emulsion-based cream
(semisolid formulation) was formulated. The emulsifier (stearic
acid) and other oil soluble components (Cetyl
alcohol, almond oil) were dissolved in the oil phase (Part A) and heated to 75°
C. The preservatives and other water soluble components (Methyl paraban, Propyl paraban, Triethanolamine,
Propylene glycol) were dissolved in the aqueous phase (Part B) and heated to
75° C. After heating, the aqueous phase was added in portions to the oil phase
with continuous stirring until cooling of emulsifier took place. The formula
for the base is given in table 1.
Table 1: Composition of cream base
Ingredients |
Formula % w/w |
|||||
F1 |
F2 |
F3 |
F4 |
F5 |
F6 |
|
Stearic acid |
15 |
12 |
12 |
10 |
18 |
15 |
Cetyl alcohol |
2 |
3 |
4 |
4 |
3 |
4 |
Almond oil |
4 |
4 |
4 |
4 |
4 |
4 |
Glycerol |
3 |
3 |
3 |
3 |
3 |
3 |
Methyl paraban |
0.02 |
0.02 |
0.02 |
0.02 |
0.02 |
0.02 |
Triethanolamine |
qs |
qs |
qs |
qs |
qs |
qs |
Water, qs, 100 |
qs |
qs |
qs |
qs |
qs |
qs |
Drug formulation: The appropriate base was selected from table
and cream was formulated. The
emulsifier (stearic acid) and other oil soluble
components (Cetyl alcohol, almond oil) were dissolved
in the oil phase (Part A) and heated to 75° C. The preservatives and other
water soluble components (Methyl paraban, Propyl paraban, Triethanolamine, Propylene glycol, all extracts) were
dissolved in the aqueous phase (Part B) and heated to 75° C. After heating, the
aqueous phase was added in portions to the oil phase with continuous stirring
until cooling of emulsifier took place. The composition of cream is given in table
2.
Table 2: pH
of cream base
Formulation |
pH |
F1 |
6.8 |
F2 |
6.9 |
F3 |
6.7 |
F4 |
6.9 |
F5 |
6.6 |
F6 |
6.4 |
Evaluation of cream
pH of the Cream: The pH meter was calibrated using standard buffer
solution. About 0.5g of the cream was weighed and dissolved in 50.0 ml of
distilled water and its pH was measured.
Viscosity: Viscosity of the formulation was determined by
Brookfield Viscometer at 100 rpm, using spindle no 7.
Dye test: The scarlet red dye is mixed with the cream.
Place a drop of the cream on a microscopic slide covers it with a cover slip,
and examines it under a microscope. If the disperse globules appear red the
ground colourless. The cream is o/w type. The reverse
condition occurs in w/o type cream i.e. the disperse globules appear colourless in the red ground.
Homogeneity: The formulations were tested for the
homogeneity by visual appearance and by touch.
Appearance: The appearance of the cream was judged by
its color, pearlscence and roughness and graded.
After feel: Emolliency, slipperiness and amount of residue left
after the application of fixed amount of cream was checked.
Type of smear: After application of cream, the type of film
or smear formed on the skin were checked.
Removal: The ease of removal of the cream applied was
examined by washing the applied part with tap water.
Acid value: Take 10 gm of substance dissolved in
accurately weighed, in 50 ml mixture of equal volume of alcohol and solvent
ether, the flask was connected to reflux condenser and slowly heated, until
sample was dissolved completely, to this 1 ml of phenolphthalein added and
titrated with 0.1N NaOH, until faintly pink color
appears after shaking for 30 seconds.
Acid value
= n*5.61/w
Where, n =
the number of ml of NaOH required.
w = the weigh
of substance.
Saponification
value: Introduce about 2 gm
of substance refluxed with 25 ml of 0.5 N alcoholic KOH for 30 minutes, to this
1 ml of phenolphthalein added and titrated immediately, with 0.5 N HCL.
Saponification value
= (b-a)*28.05/w
Where, The volume in ml of titrant
= a
The volume in ml of titrant
=b
The weigh of substance in gm
= w
Irritancy test: Mark an area (1sq.cm) on the left hand dorsal surface.
The cream was applied to the specified area and time was noted. Irritancy, erythema, edema, was checked if any for regular intervals
up to 24 hrs and reported.
Accelerated stability
testing: Accelerated
stability testing of prepared formulations was conducted for 2 most stable
formulations at room temperature, studied for 7 days. They were formulation
number 4 and 5 at 40 oC ± 1 oC for 20 days. The formulations were kept both
at room and elevated temperature and observed on 0th, 5th, 10th, 15th and 20th
day for the following parameters12-18.
RESULTS:
pH of the Cream: The pH of the cream base was found to be in range of
6-7 which is good for skin pH. All the formulations
of cream base were shown pH nearer to skin required (Table 2).
Viscosity: The viscosity of was cream was in the range of
27021-27053 cps which indicates spreadibilty of
cream. In our study F2, F3 and F4 depicted
easily spreadable by small amounts of shear, while F1, F5
and F6 were not easily spreadable on skin. But F3 shows good
spreadable property than other formulations.
Acid value and Saponification value: The results of acid value and saponification
value of all formulation of cream base were presented in table 3, and showed
satisfactorily values.
Table 3: Test
applied for acid value and saponification
value
Parameter |
Formula |
|||||
F1 |
F2 |
F3 |
F4 |
F5 |
F6 |
|
Acid value |
5.7 |
5.8 |
5.7 |
6.1 |
5.9 |
5.8 |
Saponification value |
26.3 |
26.2 |
25.3 |
27.1 |
26.3 |
26.4 |
Irritancy test: The formulation F3 shows no redness, edema,
Inflammation and irritation during irritancy studies. These formulations are
safe to use for skin (Table 4).
Table 4: Type
of Adverse effect of formulations
Formulation |
Irritant |
Erythema |
Edema |
F1 |
NIL |
NIL |
NIL |
F2 |
NIL |
NIL |
NIL |
F3 |
NIL |
NIL |
NIL |
F4 |
NIL |
NIL |
NIL |
F5 |
NIL |
NIL |
NIL |
F6 |
NIL |
NIL |
NIL |
Dye test: This dye confirms that all formulations were
o/w type emulsion cream. But formulation (F3) shows more stable in o/w type
emulsion. So here we select F3 cream base for further study.
Homogeneity: All formulations produce uniform
distribution of extracts in cream. This was confirmed by visual appearance and
by touch (Table 5).
Appearance: When formulation were kept for long time, it
found that no change in colour of cream (Table 5).
After feel: Emolliency, slipperiness and amount of residue left
after the application of fixed amount of cream was found (Table 5).
Type of smear: After application of cream, the type of
smear formed on the skin were non greasy (Table 5).
Removal: The cream applied on skin was easily removed
by washing with tap water (Table 5).
Cream: From above study, the F3 base was selected
for the preparation of herbal cream, and the composition of cream has
illustrated on table 6. The physical evaluation and stability of herbal has
shown in table 7, and results were considerable and acceptable.
DISCUSSION:
M. indica, A. indica, C. sativum, P. corylifolia, P. amygdalus, M. arvensis and D. carota
are well known for its medicinal value in Indian traditional system of medicine
and in ayurvedic preparations. The active
constituents present in different extracts of plant parts will produce
synergistic and also enhance beautifying property of cream. The herbal face
cream was O/W type emulsion, hence can be easily washed with plane water that
gives better customer compliance. There is a growing demand for herbal
cosmetics in the world market and they are invaluable gifts of nature.
Therefore, we tried to make an herbal face cream containing the extract of M.
indica, A. indica, C. sativum,
P. corylifolia, M. arvensis
and D. carota in different concentration along
with almond oil. Our study indicated that the base F3 found to be more stable,
while remaining base were not stable and resulted in breakdown of the emulsion
when stored for long time. So that base F3 was appropriate for development of
herbal cream, hence we prepared herbal cream by mixing all the extract in this
base. The pH of prepared cream was nearer skin pH, and cream produces
homogeneous, emollient, non-greasy and easily removed properties after the
application. The herbal cream was safe in respect to skin irritation and
allergic sensitization. The prepared herbal face cream is intended for cosmeceutical use rather than as other cosmetic. These
studies suggest that herbal face cream are more stable and also it may produce
synergistic action.
Table 5: Physical
parameter of F4 cream base on room and accelerated temperature
Days |
Temperature |
Parameter |
||||||
pH |
X1 |
X2 |
X3 |
X4 |
X5 |
X6 |
||
0 |
RT |
6.9 |
** |
NCC |
** |
E |
NG |
ES |
40 ºC + 1 ºC |
6.8 |
** |
NCC |
** |
E |
NG |
ES |
|
5 |
RT |
6.7 |
** |
NCC |
** |
E |
NG |
ES |
40 ºC + 1 ºC |
6.8 |
** |
NCC |
** |
E |
NG |
ES |
|
10 |
RT |
6.6 |
** |
NCC |
** |
E |
NG |
ES |
40 ºC + 1 ºC |
6.7 |
** |
NCC |
** |
E |
NG |
ES |
|
15 |
RT |
6.7 |
** |
NCC |
** |
E |
NG |
ES |
40 ºC + 1 ºC |
6.8 |
** |
NCC |
** |
E |
NG |
ES |
|
20 |
RT |
6.7 |
** |
NCC |
** |
E |
NG |
ES |
40 ºC + 1 ºC |
6.7 |
** |
NCC |
** |
E |
NG |
ES |
X1-Homogenity, X2-Appearance, X3-Spreadibility,
X4-After feel, X5-Type of smear, X6-Removal,
**: Good, *: Satisfactory, E: Emollient, NG: Non greasy, ES: Easy,
NCC: Not change in colour
Table 6: Composition of herbal
cream
Ingredients |
Formulation
(% w/w) |
Ethanol extract
of D. carota |
0.75 |
Ethanol extract
of M. indica |
0.20 |
Ethanol extract
of A. indica |
0.30 |
Ethanol extract
of C. sativum |
0.25 |
Ethanol extract
of P. corylifolia |
0.30 |
Ethanol extract
of M. arvensis |
0.20 |
Stearic acid |
12 |
Cetyl alcohol |
4 |
Almond oil |
4 |
Glycerol |
3 |
Methyl paraban |
0.02 |
Triethanolamine |
qs |
Water, qs, 100 |
qs |
Table 7: Evaluation of herbal
cream
Formulation |
pH |
Acid value |
Saponification
value |
Adverse effect |
Physical Parameter |
|
Room Temperature |
Accelerated Temperature |
|||||
Herbal cream |
6.8 |
5.9 |
26.1 |
NIL |
Acceptable |
Acceptable |
ACKNOWLEDGEMENTS:
The authors acknowledge to Director of Oriental College
of Pharmacy, Bhopal (M.P.), India, for providing all the facilities and
successfully completion of work.
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Received on 07.01.2012 Accepted on 20.02.2012
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