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Abstract

Shampoo is a hair care product, that is used for cleaning hair. The aim of the present work was to develop a multipurpose polyherbal powder shampoo. Here the multipurpose means antidandruff action as well as hair dye action. Dandruff is a chronic scalp condition characterized by scaling, itching and redness of the scalp. Hair dye is usually a substance of synthetic or natural origin, which is used to colour the hair as per the desired shade. In this work various plants such as Wrightia tinctoria, Eclipta prostata, Morinda citrifolia, Cyclia peltata, etc were collected, dried, size reduced, weighed, mixed, sieved, packed and labelled. In this work a total of six formulations were made using different ingredients and among these a best formulation were selected. Various evaluation tests were carried out in order to select a best formulation such as stability studies, invitro agar well diffusion method, cleaning action, wetting action, foaming ability, foam stability, dirt dispersion test etc. This work mainly focused to avoid the harmful side effects of the chemically synthesized shampoo and to achieve a better antidandruff as well as hair dye action from a single herbal formulation and from the study such a formulation were made.

Keywords

Dandruff, Scaling, Wrightia tinctoria, Cyclia peltata, Eclipta prostata, Morinda citrifolia.

Introduction

HERBAL MEDICINE

Herbal medicines are used to treat diseases and enhance general health and wellbeing. Herbal medicines are also known as herbal remedies, phytomedicines or phytotherapy. They are still the most widely used system of medicine. Due to its natural origin and less side effects, herbal medicines still flourish and are finding remarkable acceptance in both developed and developing countries. The medicinal plants has a great importance in the human being as it shows various pharmacological properties. Phytochemicals were used by the man for the treatment of various diseases like microbial infections, cardiovascular disorders, carcinogenic complications, metabolic disorders etc. According to the current research, the use of herbal medicines are increasing throughout the world than conventional drugs.

According to World Health Organization, it is determined that 80% of the world population only depends upon herbal medicines for the treatment of various diseases. Plant based medicines are used for the treatment of various diseases such as inflammation, wound healing, skin infections, psoriasis, leprosy, ulcers etc. Today the novel formulations are reported to have more significant advantages over conventional formulations which include enhancement of bioavailability, solubility, pharmacological activity, stability, sustained delivery, protection t from toxicity, physical and chemical degradation.

HERBAL COSMETICS

Herbal cosmetics are also called as natural cosmetics. Herbal cosmetics are defined as the beauty products, which possess desirable physiological activities, such as skin healing, smoothening, to improve appearance, enhancing and conditioning properties with the help of herbal ingredients. Herbal cosmetics are the products which are formulated using various permissible cosmetic ingredients to form the base in which one or more herbal ingredients are used to provide defined cosmetic benefits. The best thing of the herbal cosmetics is that it is purely made by the herbs and shrubs and thus herbal cosmetics are considered as side effects free. The natural contents in the herbs provides nutrients and other useful minerals to the human body. Herbal cosmetics are the products in which herbs are used in crude or extract form. Herbs do not produce instant cure. They offer a way to put the body in proper tune with nature.

HAIR COSMETICS

Hair care products are referred as the formulations meant for cleaning, imparting the color, modifying the texture, nourishing the hair, giving life to the stressed hair and to give healthy looks to the hair. Hair care products include hair oil, shampoo, hair dye, hair strengtheners and depilatories.

ANATOMY OF HAIR

Hair is a keratinous filament growing out of the epidermis. Hair is one of the vital parts of the body and is considered to be the accessory structure of the integuments along with sebaceous gland and sweat gland. They are also known as epidermal derivatives as they originate from the epidermis during embryological development. They can also act as sense organs and the main functions of the hair follicles include regulation of body temperature, protection, evaporation of perspiration and draining of external water from the body.

Hair root:

The hair root is located in the skin and extends down to the deeper layers of the skin. It is surrounded by the hair follicle, which is also connected to the sebaceous gland. Each hair follicle is attached to a tiny muscle called arrector pili that can make the hair stand up. As new hair cells emerge, the old cells move upwards, die slowly and forming hard hair shaft through a process called keratinization. Then, they germinate like seedlings from the epidermis through the dermis.

Hair shaft

Hair shaft is the visible part of the hair that sticks out of the skin. The hair shaft is composed of three concentric layers, the outer cuticle, middle cortex, and inner medulla. They differ from each other in the types of keratin filaments they possess.

Cuticle: It is the outermost part of the hair shaft. It helps to protect the inner layers of  the hair from damage and provides shine. It is comprised of overlapping cells that resemble fish scales. Healthy hair has a smooth, flat cuticle that is translucent and reflects light, making hair feels smooth and look shiny. If the cuticle is damaged, the hair feels rough and becomes vulnerable to chemical and mechanical damage.

Medulla: Medulla is the innermost layer of the hair shaft. It is composed of two or three rows of polyhedral cells containing pigment granules and air spaces. This is the most soft and fragile layer of the hair shaft.

Cortex: It is located between the hair cuticle and medulla and is the thickest hair layer. It contain most of the hair’s pigment. The major pigment in the cortex is melanin which is also present in skin.

DANDRUFF

Dandruff is a common condition that causes the skin on the scalp to flake. It is not contagious or serious. But it can be embarrassing and difficult to treat. It is characterized by presence of corneocytes that form clusters due to their high cohesive power, in the form of flaky white to yellowish scales, accompanied by itching. It has been observed that dandruff occurs mainly between puberty to middle age.

Three factors which is involved in the formation of dandruff are sebaceous gland secretions, Malassezia fungi, individual susceptibility. According to the symptoms, dandruff is classified as follows:

Dry dandruff: It is characterized by excessive formation of white grayish or ashen colored minute scales.

Oily dandruff: It arises on the scalp skin with varied intensity of sebum production.

TREATMENT OF DANDRUFF

Dandruff can be controlled and effectively treated by using various formulations. The formulation must be suitable for the hairy region and it should be compatible with the dandruff condition. There are different types of formulation like creams, shampoos, emulsions, lotions, hair oil and other cosmetic formulation containing anti-dandruff agents are readily available in the market to control dandruff. Out of which shampoos are the most common as well as a worldwide accepted cosmetic product used against dandruff.

A shampoo can be defined as a preparation of soap or detergent used to wash hair and which helps to control and reduce dandruff. Anti-dandruff shampoo is intended to kill dandruff, causing fungi that live on your scalp. The function of shampoo is to remove dirt, surface grease, and skin debris from the hair shaft and scalp without affecting adversely the hair, scalp or health of the user. Surfactants are the main component of shampoo. The raw materials used for the manufacture of shampoos are;

Primary surfactant: Sulfonates, Sulfides

Secondary surfactant: Sulfosuccinates

Anti-dandruff agents: Herbal extracts

Conditioning agent: Glycerin, Propylene glycol

Perfumes: Fruity or floral fragrances

Preservatives: Methyl paraben

ANTI-DANDRUFF SHAMPOO

The anti-dandruff shampoo is a preparation that contains anti-dandruff agents that are intended to reduce and treat the formation of dandruff flakes. Two types of anti-dandruff shampoos are commercially available:

1.Synthetic anti-dandruff shampoos (based on chemical ingredients)

These formulations include therapeutic use of anti-dandruff agents that are classified into three groups according to their mechanism of action:

Keratolytic substances

Cytostatic substances

Fungicidal substances

Some of the marked synthetic anti-dandruff shampoos are All Clear shampoo, Pantene Pro-V shampoo, Head and Shoulders shampoo etc.

DISADVANTAGES OF SYNTHETIC ANTI-DANDRUFF SHAMPOOS

Continuous use of synthetic anti-dandruff shampoos makes hair brittle and causes dryness of the scalp. Anti-dandruff products such as cytostatic and keratolytic agents work only symptomatically, and often reoccurrence of dandruff after stopping treatment is observed.

HERBAL ANTIDANDRUFF SHAMPOO

Herbal anti-dandruff shampoos are the cosmetic preparations or formulations which contain herbal ingredients such as plant extracts and essential oil. These herbal shampoos are generally used to remove the dandruff, to add natural color to the hair, to remove the extra oil content of the hair, to remove the dust, dirt and scales of scalp, for the healthy growth of the hair, to prevent hair falling, to impart softness and smoothness to the hair shaft etc. There are large number of herbs which have beneficial effects on hair and are commonly used in shampoos.

MATERIALS AND METHODS

List of materials:

1: Plant materials used for the formulations


SI.No

Botanical Name

Vernacular Name

Source/supplier

1

Morinda Citrifolia

Noni

Indoor venture

2

Eclipta Prostrata

Brinkaraj

Indoor venture

3

Lawsonia Inermis

Henna

Indoor venture

4

Phyllanthus Emblica

Amla

Indoor venture

5

Cyclea Peltata

Padathali

Indoor venture                                       

6

Clitoria Ternatea

Butterfly Pea

Indoor venture

7

Mussaenda Frondosa

Vellila

Indoor venture

8

Nigella Sativa

Black Cumin

Indoor venture

9

Sida Cordifolia

Kurunthotti

Indoor venture

10

Camellia Sinensis

Tea Powder

Indoor venture

11

Hibiscus Rosa Sinensis

Hibiscus

Indoor venture

12

Plectranthus Barbatus

Panikoorka

Indoor venture

13

Trigonella Foenum Graecum

Fenugreek

Indoor venture

14

Acacia Concinna

Shikakai

Indoor venture

15

Bacopa Monnieri

Brahmi

Indoor venture

16

Sapindus Mukorossi

Reetha

Indoor venture

17

Aloe Barbadensis

Aloe Vera

Indoor venture

18

Xanthomonas Campestris

Xanthan Gum

Crescent biologics private limited


 2: List of chemicals


SI No

Materials/ Solvents

Manufactures/ Suppliers

1

Sabouraud dextrose

AGS Aqua Tech

2

Ethanol

Peer Chemical Industries

3

Molisch’s reagent

Bio Diagnostics

4

Fehling’s reagent

Bio Diagnostics

5

Hager’s reagent

Bio Diagnostics

6

Sudan III

J J Diagnostics


 3: List of equipments


 

SI. No

Equipments

Suppliers/ Manufactures

1

Mortar and pestle

Universal agencies

2

Digital weighing balance

SHIMADZU AY 220

3

PH meter

Jain-LT-10/Labtronics

4

Muffle furnace

Set win

5

Hot air oven

CAT-NO-RHO-14/ROTEK

6

Incubator

Medwin Diagnostics

7

Desiccator

Kawanan international, Kannur


Determination of physicochemical parameters

1.Ash value

A. Total ash: About 2g of the powdered drug were accurately weighed and it is transferred to silica crucible which were previously weighed. It is then heated at a temperature in a muffle furnace until it is carbon free. The silica crucibles were taken out from the muffle furnace and placed in a desiccator. It is then weighed and percentage of total ash with reference to the air dried drug

%Total ash =  Weight of ashWeight of sample

 X 100

 

B. Acid insoluble ash: Total ash obtained were taken in to a beaker and are boiled for about 3minute in 25ml of dilute sulfuric acid and then filtered through a Whatman filter paper and residues were washed with hot water until it is free from chlorides. The residue containing filter paper were taken and placed in different silica crucibles and ignited in muffle furnace 550+20°C for 1 hour. It is then cooled and percentage of acid insoluble ash was calculated with reference to air dried drug.

?id insoluble ash value = weight of total ash-weight of acid insoluble ash Weight of crude drug taken

  X100

 

C.Water soluble ash value: Total ash obtained was taken and it is poured into a beaker and boiled for about 5minute in 25ml of water. It is then filtered and residues were washed with hot water. The residue containing filter paper were then placed in different silica crucibles and ignited in muffle furnace at temperature 450°C to constant weight. It was then cooled and percentage of water soluble ash was calculated with reference to the air dried drug.

water soluble ash value = Weight of total ash-Weight of water souble ashWeight of crude drug taken

 X 100

 

2. Extractive value:

a) Water soluble extractive value

Accurately weighed about 5g of air dried powdered plant material were taken in 100ml chloroform water in a closed flask for 24 hours. During the first 6 hours it was shaken and filtered.25ml of the filtrate were evaporated to dryness in a flat bottomed petridish and dried 105°C and weighed. Then the percentage water soluble extractive values were calculated with reference to the air dried drugs.

b) Alcohol soluble extractive value

 Accurately weighed about 5g of air dried powdered plant material were taken in   closed flask and 100ml of 95% ethanol was added into it. During the first 6 hours it was shaken frequently and filtered. 25ml of the filtrate were evaporated to dryness in a flat bottomed petridish and dried at 105°C and weighed. Then the percentage ethanol soluble extractive values were calculated with reference to the air dried drugs.

FORMULATION OF MULTIPURPOSE POLYHERBAL POWDER SHAMPOO

Formula of the composition of Multipurpose powder shampoo


SI NO

INGREDIENTS

F1(g)

F2(g)

F3(g)

F4(g)

F5(g)

F6(g)

1

Clitoria ternata

_

_

20

_

_

_

2

Plectranthus barbatus

_

_

_

_

_

20

3

Emblica officinalis

_

20

_

_

_

_

4

Camellia sinensis

_

_

_

_

20

_

5

Nigella sativa

_

_

_

20

_

_

6

Eclipta prostata

20

_

_

_

_

_

7

Morinda citifolia

10

_

_

_

_

_

8

Moringa oleifera

_

10

_

_

_

_

9

Cyclea peltata

_

_

10

_

_

_

10

Mussaenda frondose

_

_

_

10

_

_

11

Sida cordifolia

_

_

_

_

10

_

12

Hibiscus rosa sinensis

_

_

_

_

_

10

13

Lowsonia Inermis

10

10

10

10

10

10

14

Trigonella foenum – graecum

10

10

10

10

10

10

15

Acacia concinna

10

10

10

10

10

10

16

Bacopa Monnieri

10

10

10

10

10

10

17

Sapindus Mukorossi

10

10

10

10

10

10

18

Aloe Barbadensis

10

10

10

10

10

10

19

Xanthomonas campestris

10

10

10

10

10

10


PROCEDURE

The multipurpose poly herbal powder shampoo was prepared by simple mixing process. Firstly all the plant materials were collected and dried under shade. After that the materials were size reduced and then sieved using sieve no.120 and weighed the required amount of powdered materials essential for the formulation. All the ingredients are then mixed well and they were finally packed in a suitable container for evaluation.

EVALUATION

Evaluation of shampoo

A. organoleptic evaluation

The developed poly herbal powder shampoo were evaluated for their organoleptic characters like colour, odour, texture.

B. Physico-chemical evaluation

1. pH

The formulated shampoo where diluted  by using distilled water to produce a shampoo of 10%v/v concentration. The pH of the prepared shampoo was determined by using pH paper.

2. Dirt dispersion

Two drops of shampoo were added to a large test tube containing 10ml of distilled water. To this solution, one drop of India ink was added and the test tube was stoppered and shaken 10 times. The amount of ink in the foam was indicated as none, light, moderate or heavy.

 3. Foaming ability and Foam stability

50ml of 1% shampoo solution was put into 250ml graduated cylinder and covered the cylinder with hand and shaken for 10 times. The total volume of the foam contents after 1 minute shaking was recorded. The foam volume was calculated after shaking the volume of the foam at 1 minute interval for 4 minutes were recorded.

 4. Cleaning action

 5g of wool yarn were placed in grease, after that it was placed in 200 ml of water containing of shampoo in a flask. Temperature was maintained at 35°

 celsuis. The flask was shaked for 4 minutes at the rate of 50 times a minute. The solution was removed and sample was taken out, dried and weighed and calculated the amount of grease removed.

 

 5. Determination of percentage solid content

 A china dish was cleaned, dried and weighed. To this, an accurately weighed amount of formulated shampoo(4g) was added and the dish with shampoo was weighted. The china dish with shampoo was placed on a hot plate and heated until the liquid portion was evaporated. The weight of the solid contents of shampoo after complete drying was calculated.

 6. Stability study

 The optimized formulation was subjected to stability studies in accordance with ICH guidelines for accelerated testing with required modification. The sample from each formulation was taken and kept at room temperature for the duration of one month.              

7. Ash value

Total ash: About 2g of the powdered drug were accurately weighed and it is transferred to silica crucible which were previously weighed. It is then heated at a temperature in a muffle furnace until it is carbon free. The silica crucibles were taken out from the muffle furnace and placed in a desiccator. It is then weighed and percentage of total ash with reference to the air dried drug.

%Total ash =  Weight of ashWeight of sample

 X 100

 8. Extractive value

a. Water soluble extractive value

Accurately weighed about 5g of air dried powdered plant material were taken in 100ml chloroform water in a closed flask for 24 hours. During the first 6 hours it was shaken and filtered.25ml of the filtrate were evaporated to dryness in a flat bottomed petridish and dried 105°C and weighed. Then the percentage water soluble extractive values were calculated with reference to the air dried drugs.

 b. Alcohol soluble extractive value

Accurately weighed about 5g of air dried powdered plant material were taken in closed flask and 100ml of 95% ethanol was added into it. During the first 6 hours it was shaken frequently and filtered 25ml of the filterate were evaporated to dryness in a flat bottomed petridish and dried at 105°C and weighed. Then the percentage ethanol soluble extractive values were calculated with reference to the air dried drugs.

9. Wetting time

The canvas was cut into 1 inch diameter discs having an average weight of 0.44g. The disc was floated on the surface of shampoo solution of 1%w/v and the stopwatch started. The time required for the disc to begin to sink was measured accurately and noted as the wetting time.

C. General powder characteristics

1. Angle of repose

The material is poured through a funnel to form a cone. The tip of the funnel should be held close to the growing cone and slowly raised as the pile grows, to minimize the impact of falling particles. Stop pouring the material when the pile reaches a predetermined height or the base a predetermined width.

2.Bulk density

The bulk density of a powder is the ratio of the mass of an untapped powder sample and its volume including the contribution of the interparticulate void volume.

  1. Tapped density

The tapped density is obtained by mechanically tapping a graduated measuring cylinder or vessel containing the powder  sample. After observing the initial powder volume or mass, the measuring cylinder or vessel is mechanically tapped, and volume or mass readings are taken until little further volume or mass change is observed.

 D. Invitro antidandruff activity evaluation (Agar well diffusion method)

  • Preparation of pre-inoculum: Take the loopful of culture of fungus aseptically and transfer to sterilized and cooled 25ml sabouraud dextrose(broth) and mix well. Incubate the broth 25°
    c for 24hrs.
  • Preparation of pour plates: A sabouraud dextrose agar(150ml) is autoclaved and poured to the already autoclaved plate and cooled to room temperature and allowed to solidify. The culture was spread on the agar surface aseptically by using sterilized cotton.
  • Making wells on agar plates: Wells of 6mm in diameter were made aseptically on the agar plate by using a sterilized well digger. The shampoo samples(100ml) were aseptically added into the well by using a micropipette. The petriplates are kept in refrigerator (1hr) for the diffusion of substances from well into surrounding medium. During this time the growth of the organism is reduced. After 1hr, the plates were incubated in inverted condition at 37°
    c for 48hours.
  • Measurement of the zone of inhibition: After 48hours, the plates were observed for the presence of inhibition of fungal growth and it was indicated in the form of a clear zone of inhibition around each well containing different samples. The size of the inhibitory zone was measured in mm.

Evaluation of dye

A. organoleptic evaluation

The developed Multipurpose poly herbal powder shampoo were evaluated for their organoleptic characters like colour, odour, texture.

B. Physico-chemical evaluation

1. pH

The formulated shampoo where diluted by using distilled water to produce a shampoo of 10%v/v concentration. The pH of the prepared shampoo was determined by using pH paper.

 2. Loss on drying

Loss on drying is the loss of mass expressed in present m/m. Two gram of the powder was weighed accurately and transferred into a dry petri dish. The petridish is placed in a dessicator for 2 days over calcium chloride crystals. Then the powder was taken and weighed accurately to find out the weight loss during drying.

3.Ash value

Total ash: About 2g of the powdered drug were accurately weighed and it is transferred to silica crucible which were previously weighed. It is then heated at a temperature in a muffle furnace until it is carbon free. The silica crucibles were taken out from the muffle furnace and placed in a desiccator. It is then weighed and percentage of total ash with reference to the air dried drug.

C. Stability study

The optimized formulation was subjected to stability studies in accordance with ICH guidelines for accelerated testing with required modification. The sample from each formulation was taken and kept at room temperature for the duration of one month. 

D. Phytochemical evaluation

1. Molisch’s test

Add the test sample to the test tube containing water and shake it to dissolve. Add, 2 to 3 drops of the Molisch reagent. Add concentrated sulphuric acid in drops along the sides of the test tube slowly. The formation of a purple ring indicates the presence of carbohydrates.

2.Fehling’s test

Add the sample in a dry test tube. Distilled water should be kept in another tube as control. Fehling's solution is to be added in the tubes. The tubes must be kept in water bath. Make observations and record if there is any development of red precipitate.

3.Hager’s test

Two milliliters of extract were treated with few drops of Hager's reagent. A yellow precipitate was formed, indicating the presence of alkaloids.

4.Volatile oil test

The powder on treatment with alcoholic solution of Sudan III develops red colour in the presence of volatile oils.

E. Rheological evaluation

1.Bulk density

The bulk density of a powder is the ratio of the mass of an untapped powder sample and its volume including the contribution of the interparticulate void volume.

2. Tapped density

The tapped density is obtained by mechanically tapping a graduated measuring cylinder or vessel containing the powder  sample. After observing the initial powder volume or mass, the measuring cylinder or vessel is mechanically tapped, and volume or mass readings are taken until little further volume or mass change is observed.

3.Angle of repose

The material is poured through a funnel to form a cone. The tip of the funnel should be held close to the growing cone and slowly raised as the pile grows, to minimize the impact of falling particles. Stop pouring the material when the pile reaches a predetermined height or the base a predetermined width.

4.Hausner’s ratio

Hausner's ratios (HR = ?TAP/?BULK, where, ?TAP is the tapped density of the powder and ?BULK is the bulk density of the powder) and particle size distribution can be used to measure the flow properties and the size distribution of the particles, respectively.

F.Invitro staining studies

An invitro staining study of an herbal formulation would involve evaluating the dye’s ability to stain hair strands. The main steps include:

  • Sample preparation: Obtain a sample of the formulation and ensure it is standardized and well mixed. It’s important to use a consistent and representative sample throughout the study.
  • Hair strand preparation: Obtain hair samples that are similar in colour, texture, and length. Cut the hair strands into equal lengths to ensure uniformity. If desired, pretreat the hair strands with a standard conditioner to simulate real-world conditions.
  • Application of the powder shampoo: Apply the formulation to the hair strands using a standardized method, such as immersion or brushing. Ensure that the dye is applied uniformly across hair strands.
  • Assesment of staining: The white hair strands were turns into black by the application of the formulation.

RESULTS AND DISCUSSION

Authentication of collected plant materials

The collected plant materials were identified and authenticated by Dr. Delse P Sebastian M.Sc., Ph.D. Assistant Professor of Botany, St. JOSEPH’S COLLEGE ( AUTONOMOUS ), DEVAGIRI CALICUT.

Physicochemical parameters

After the collection of plant materials, they were shade dried and powdered coarsely in an electronic blender and stored in air tight containers until further use. Physicochemical parameters of the plants such as ash value, extractive values are tabulated below:

Physicochemical parameter of Morinda citrifolia, Eclipta prostate, Phyllantus embilica, Lawsonia inermis, Cyclea peltate, Clitoria ternatea


Test

Morinda citrifolia

Eclipta prostate

Phyllantus embilica

Lawsonia inermis

Cyclea peltata

Clitoria ternatea

Total ash (%W/W)

10 %

w/w

 

8 %

w/w

 

6 %

w/w

 

10 %

w/w

 

9 %

w/w

 

9 %

w/w

 

Acid insoluble ash (%W/W)

8  %

w/w

 

6 %

w/w

 

5 %

w/w

 

9 %

w/w

 

6 %

w/w

 

7 %

w/w

 

Water soluble ash (%W/W)

9 %

w/w

 

10 %

w/w

 

8 %

w/w

 

7 %

w/w

 

8 %

w/w

 

9 %

w/w

 

Water soluble extractive value(%W/W)

15 %

w/w

 

13 %

w/w

 

10 %

w/w

 

11 %

w/w

 

12 %

w/w

 

11 %

w/w

 

Alcohol soluble extractive value (%W/W)

14 %

w/w

 

12 %

w/w

 

11 %

w/w

 

10 %

w/w

 

11 %

w/w

 

10 %

w/w

 


 Physicochemical parameters of  Mussaenda frondosa, Nigella sativa, Senegalia rugata, Sida cordifolia, Camelia sinensis and Plectranthus barbatus


Test

Mussaenda frondosa

Nigella sativa

Senegalia rugata

Sida cordifolia

Camelia sinensis

Plectranthus barbatus

Total ash (%W/W)

9%

w/w

 

8%w/w

8%w/w

7%w/w

6%w/w

7%w/w

Acid insoluble ash (%W/W)

7%w/w

6%w/w

7%w/w

5%w/w

4%w/w

5%w/w

Water soluble ash (%W/W)

8%w/w

7%w/w

6%w/w

6%w/w

5%w/w

6%w/w

Water soluble extractive value(%W/W)

14%w/w

12%w/w

13%w/w

11%w/w

10%w/w

11%w/w

Alcohol soluble extractive value (%W/W)

12%w/w

10%w/w

12%w/w

10%w/w

9%w/w

11%w/w


Physicochemical parameters of Hibiscus rosa sinensis, Aloe barbadensis, Trigonella foenum graecum, Sapindus mukorossi and Bacopa monnieri


Test

Hibiscus rosa sinensis

Aloe barbadensis

Trigonella foenum graecum

Sapindus mukorossi

Bacopa monnieri

Acacia concina

Total ash (%W/W)

6%w/w

5%w/w

7%w/w

7%w/w

8%w/w

6%w/w

Acid insoluble ash (%W/W)

8%w/w

7%w/w

9%w/w

8%w/w

9%w/w

9%w/w

Water soluble ash (%W/W)

9%w/w

8%w/w

6%w/w

5%w/w

6%w/w

8%w/w

Water soluble extractive value(%W/W)

15%w/w

16%w/w

14%w/w

13%w/w

15%w/w

14%w/w

Alcohol soluble extractive value (%W/W)

13%w/w

15%w/w

14%w/w

10%w/w

11%w/w

10%w/w


EVALUATION

EVALUATION OF ANTIDANDRUFF SHAMPOO

1 Organoleptic evaluation


SI NO

PARAMETER

F1

F2

F3

F4

F5

F6

1

Colour

Greenish brown

Faint brownish

Grayish brown

Golden brown

Greenish brown

Brownish yellow

2

Odour

Characteristic

Slight

Slight

Characteristic

Characteristic

Slight

3

Texture

Fine

Fine

Fine

Fine

Fine

Fine


Organoleptic evaluation of the formulated powder shampoo were carried out such as colour, odour and texture for all the six formulations and the results was found to be satisfactory.

2 General powder characteristics


SL NO

PARAMETER

F1

F2

F3

F4

F5

F6

1

Angle of repose

19.11°

 

26.46°

 

25.73°

 

30.41°

 

32.43°

 

27.66°

 

2

Bulk density

0.50 g/ml

0.43 g/ml

0.46 g/ml

0.40 g/ml

0.43 g/ml

0.53 g/ml

3

Tapped density

0.12 g/ml

0.13 g/ml

0.14 g/ml

0.16 g/ml

0.11 g/ml

0.12 g/ml

4

Hausner’s ratio

1.10

1.15

1.17

1.2

1.19

1.16


General powder characteristics of all the six formulations were carried out and among that the formulation 1 has excellent flow properties whereas formulations 2, 3 and 6 have good flow and formulation 4 and 5 have moderate flow.

  1. Physicochemical properties

     

SL NO

PARAMETER

F1

F2

F3

F4

F5

F6

1

pH

4.7

5.9

5.1

7

6.9

6.5

2

Dirt dispersion

Good

None

Light

Light

Moderate

None

3

Wetting time

105sec

140sec

115sec

125sec

150sec

162sec

4

Foaming ability

Good

Poor

Moderate

Moderate

Poor

Moderate

5

Ash value

4.88%w/w

4.21%w/w

5.11%w/w

4.45%w/w

4.92%w/w

5.22%w/w

6

Extractive value

18%w/w

14%w/w

12%w/w

17%w/w

19%w/w

15%w/w

7

Stability study

Stable

Stable

Stable

Stable

Stable

Stable

8

Percentage solid content

99.81%

 

99.62%

 

99.32%

 

99.71%

 

99.55%

 

99.69%

 


Various physicochemical parameters of all the six formulations were carried out such as pH ,dirt dispersion, wetting time, foaming ability, ash value, extractive value and percentage solid content. Stability studies of all these formulations were also carried out to check the stability of the  products at various temperature conditions and all of them were found to be stable.

Invitro antidandruff evaluation


SL NO

PARAMETER

F1(mm)

F2(mm)

F3(mm)

F4(mm)

F5(mm)

F6(mm)

1

Zone of inhibition

12mm

10mm

9mm

11mm

9mm

11mm


Invitro antidandruff evaluation were carried out using agar well diffusion method for all the six formulations and among that the formulation 1 shows best antidandruff activity in which the zone of inhibition is 12mm.

EVALUATION OF HAIR DYE

Phytochemical evaluation


SL NO

TEST

F1

F2

F3

F4

F5

F6

1

Molisch’s test

+

+

+

+

+

+

2

Mayer’s test

+

+

+

+

+

+

3

Fehling’s test

+

+

+

+

+

+


Phytochemical evaluation of all the six formulations were carried out such as Molisch’s test, mayer’s test and fehling’s test to determine the presence of sugars, carbohydrates and alkaloids. The results obtained shows that all the six formulations contains sugars, carbohydrates and alkaloids.

Stability study


SL NO

AFTER 1 MONTH

F1

F2

F3

F4

F5

F6

1

Colour

No change

No change

No change

No change

No change

No change

2

Odour

No change

No change

No change

No change

No change

No change

3

Texture

No change

No change

No change

No change

No change

No change

 

The stability studies were carried out for the all the six formulated products and it is noticed that even after a month there is no any change in colour, odour and texture in any of the formulations. This shows that the products are stable.

Invitro staining study

Invitro staining studies were carried out for all the six formulated products by applying them over white hair strands and from this the formulation 1 shows better hair dye action.

CONCLUSION

The ultimate aim of the present work was to formulate multipurpose polyherbal powder shampoo with antidandruff as well as hair colouring activity. Dandruff is a common condition that causes the skin on the scalp to flake. It is caused by Malassezia yeasts and it  affect almost half of the population throughout the world. As a consequence of the use of chemical products an endeavour was made to formulate polyherbal multipurpose powder shampoo which is effective in terms of safety and control the greying and dandruff condition which helps to reduce the adverse effects and toxicity of the chemical drugs.

All the plant materials needed for the formulation were collected from different areas. We have formulated a total of six formulations and the collected plant materials were dried under shade drying before grinding. All these plant materials were also evaluated and then the dried plant materials were grinded thoroughly to form fine powders. After that the powdered materials were passed through sieve no. 120 to make the powder more fine.  The physicochemical parameters like ash vale, extractive vale of the powdered plant material were carried out. The formulations were prepared by simple mixing process of different amount of the plant materials. After formulating, they were evaluated. Evaluation tests such as organoleptic evaluation, physicochemical parameters, rheological properties, invitro staining studies, in vitro antidandruff activity were carried out for all the six formulated products and compared the actions among them. After carrying out all these evaluations it was found to be that the formulation 1 shows better antidandruff as well as hair dye action among the other 5 formulations. We have also carried out stability studies for all these six formulated products to check the stability of the products at different temperatures and it was noticed that all these formulations were stable even after a period of one month. However in the present work, herbal formulations reported to have more significant advantages over synthetic formulations. Hence we concluded that the formulated multipurpose polyherbal powder shampoo offers a natural, safe,effective option for antidandruff action as well as for colouring the hair.

ACKNOWLEDGEMENT

We humbly owe the completion of this dissertation work to the almighty GOD who always guided, protected and least at very moment of our life with our steadfast love. This thesis has been kept on track and seen through to completion with the support and encouragement of numerous people.  The end of our thesis, it is a pleasant task to express our thanks to all those who contributed in many ways for the success of this study and it’s a memorable experience for us. We are grateful to the Management of Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, Trikaripur for supporting us throughout our dissertation period. It is a delightful moment for us to express our heartfelt gratitude and sincere thanks to our esteemed guide Prof. Dr. Roopesh P T, Department of Pharmaceutics, Rajiv Gandhi Institute of Pharmaceutical Sciences and Research for her constant guidance, personal attention valuable suggestions, encouragement, and support throughout our study.  We are deeply indebted to Prof. Dr. M. Paridhavi, M Pharm, Ph.D, FABAP, Principal, Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, for his valuable advice and support to make the study successful. We would like to gratefully thank Prof. Dr. Arun Kumar K.V, M. Pharm, Ph.D, Vice Principal, Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, for his academic support.  We also extent our sincere thanks to Shanthi Mam and other teaching staff, who helped us for the completion of this dissertation.  We also grateful to the Chairman and Directors of Rajiv Gandhi Institute of Pharmaceutical Sciences and Research for providing all necessary facilities for our study and for the constant support and encouragement.  Words cannot express our heartfelt appreciation to our most beloved Parents and Family members for their everlasting love, prayer, lifetime support and encouragement throughout our study. We take pleasure to appreciate the inspiration extended by all our Classmates. We would also like to say thanks to all the non- teaching staffs & library staff for their help in the completion of our study. Last but not least we express our sincere thanks to one and all who gave us constant encouragement and help throughout our educational career.

REFERENCES

  1. Krishnamoorthy JR, Ranganathan S, Gokul SS, Ranjith MS and Dano A, 2006, A herbal solution for Dandruff, African J Biotechnol, 5(10): 960- 962.
  2. Revansiddappa  M,  Sharad ha  R,  Abbulu  K, Formulation  and  Evaluation  of  Herbal  Anti-dandruff Shampoo,  Journal  of  Pharmacognosy  and Phytochemistry, 2018; 7(4); 764-767.
  3. Yateem H, Hanania M, Mosleh N, Formulation and Evaluation  of  Herbal  Shampoo Containing Olive Leaves  Extract , International  Journal  of Development  Research,  October  2018;  8(10); 23173- 23176.
  4. Bhagwat S.S, Formulation and Evaluation of Herbal Shampoo,  International  Journal  of  Creative Research  Th ough ts,  Sep temb er  2020;  8(9); 2860-2869.
  5.  Gubitosa  J,  Rizzi  V,  Fini  P,  Cosma  P,  Hair  Care Cosmetics:  From  Traditional  Shampoo  to  Solid Clay and Herbal Shampoo, Cosmetics, March 2019; 6(1); 13.
  6. Sravanthi  K,  Kavitha  N,  Sowmya  K, Naazneen  S, Vaishnavi  U, Anil  C.H, A  Review  on  Formulation and  Evaluation  of Herbal  Anti-Dandruff Shampoo, International  Journal  of  Pharmaceutical  Research and Applications, June 2021; 6(3); 1300-1311.
  7. Arora  P,  Nanda A,  Karan M,  Shampoos  Based on Synthetic Ingredients vis-a-vis Shampoos Based on Herbal Ingredients: A Review, International Journal of  Pharmaceutical  Sciences  Review and  Research, April 2011; 7(1); 41-46.
  8. Vijaya laks hmi  A,  Sang eeth a  S,  Ranjith  N, Formulation  and  Evaluation  of  Herbal  Shampoo, Asian  Journal  of  Pharmaceutical  and  Clinical Research, 2018; 11(4); 121-124.
  9. Kumar A, Mali R, Evaluation of Prepared Shampoo Formulations and to Compare Formulated Shampoo with  Marketed  Shampoos,  International Journal  of Pharmaceutical  Science  Review  and  Research, August 2010; 3(1); 120-126.
  10. Gaud R.S, Gupta G.D, Practical Physical Pharmacy, 1st  ed,  New  Delhi,  CBS Publisher  and  Distributer, 2001; 81-105.
  11. Barel A. O, Paye M, Maibach H.I,  Handbook  of Cosmetic  Science  and  Technology,  4th  ed,  Boca Raton, CRC press; 2014.
  12. Mainkar  A.R,  Jolly C.I,  Evaluation of  commercial herbal shampoos,  International Journal of Cosmetic Science, October2000; 22(5); 385-391.
  13. Chandran  S,  Vipin  K.V,  Augusthy  AR,  Lindumol K.V, Shirwaikar A, Development  and Evaluation of Antidandruff  Shampoo  Based on  Natural  Sources, Journal  of  Pharmacy  and  Phytotheraputics,  2013; 1(4); 10-14.
  14. Kumar S, Akhila A, Naqvi AA, Farooqi AH, Singh AK, Uniyal G C, et al. Medicinal plants in skin care. Lucknow, India: CIMAP 1994; pp.425-30.
  15. Gulrajani ML. Natural dyes and their applications to textiles. India: IIT New Delhi 1992; page no 1-2.
  16. Ashok D, Vaidya B, Devasagayam T. Current status of herbal drugs in India: An overview. J Clin Biochem Nutr 2007; 41(1): 1-11.
  17. Khare  CP.  Indian  herbal  remedies:  Rational  western  therapy,  ayurvedic,  and  other traditional usage. Botany Springer 2003; p.89.
  18. Brown K. Hair colorants. J Soc Cosmet Chem 1982;33: 375-83.
  19. Balsam MS. Edward sagarin, cosmetics science and technology. John Wiley &Sons 1972.
  20. Kalia AN. Text book of industrial Pharmacognosy, New Delhi: CBS Publishers 2005; page no 264.
  21. Nadkarni KM. Indian material medica. Popular Prakashan 1976; pp.630-680, 1202.
  22. Anjali J.  Hair care formulations. World J Pharm Sci 2016; 5(6):630-48.
  23. Marlen McHugh-Pratt,  Milady's Standard  textbook  of Cosmetology,  Delmer Publishers, USA, 2000, page no 265-304.
  24. Wails  TE,  Textbook  of  Pharmacognosy,  5th  Ed,  CBS  publishers  &  Distributors, Delhi.1997.
  25. Kokate CK, Purohit AP and Gokhale SB, Pharmacognosy, 19th Ed, Nirali Prakashan, pune 2002, page no 220.
  26. Philips I, Steinberg M. Maibach HI and Akers WA, Comparison of Rabbit and human skin responses to certain irritants, Toxicol Appl Pharmacol, 1972, 21, 639.
  27. Koehler Paul  B,  Clinical aspects  of  safety testing of  cosmetic products, J  Soc  Cosmetic Chem, 1980, 31, 213-218.
  28. Kirtikar  KR  and  Basu  BD,  Indian  Medicinal Plants,  3rd  Ed  Vol  2, International  Book Distributors, Dehradun, 1998, p.1361.
  29. Fisher's Contact Dermatitis, Ed. Rietschel RL, Fowler JF, Lippincott Williams & Wilkins, 2001.
  30. M. Thenmozhi et, al., International Journal of Engineering science and Technology,3(1), 2011, 292-298.
  31. Harbone  JB, Phytochemical  method:  A Guide  to  Modern Techniques  of  plant  analysis. Chapman and Hall, London, UK, 1984.
  32. Potts PJ, Webb PC, Waston JS, x -ray Spectrum, 13, 1984, 2.
  33. William Kemp Organic Spectroscopy, ELBS: Hong Kong; 1986.
  34. Natural product Radiance, 7(1), 2008, 45-48.
  35. Jain  U,  1997,  Beauty  through  Herbs, Institute  of  herbal  science  publishers,  1st Edition, 23-27.
  36. Chitravadivu  C  and  Bhoopathi  M,  2009, Antimicrobial activity of Laehiums prepared by  herbal  venders,  South  India, Eurasian Journal  of  Scientific Research,  4(3):  142-147.
  37. Hay  RJ  and Graham  BR,  1997, Dandruff and  Seborrheic  Dermatitis:  Causes  and Management, Clin Exp Dermatol, 22: 3-6.
  38. Mukharjee  PK,  2008,  Quality  Control  of Herbal Drug, An Approach to Evaluation of Botanical, 3: 184, 291.
  39. Subrahmanyam  CVS, 2000, Text  Book of Physical Pharamcy, Vallabh Prakashan, 2nd Edition, 2: 221-224.
  40. Richa  MS,  Kinjal  S  and  Janki  P,  2011, Evaluation  of  prepared  herbal  shampoo formulations  and  to  compare  formulated shampoo  with  marketed  shampoos,  Int  J Pharm Sci, 3: 402-405.
  41. Martin  A,  1993,  Physical  Pharmacy,  4th edition.  London:  Lea  &  Febigen Philadelphia, 431-432.
  42. More  HN  and  Hazare  AA,  Practical Physical Pharmacy, 1st Edition, 114-119.
  43. Naveen  S,  Karthika  S,  Sentila  R, Mahenthiran  R  and  Michael  A,  2012,  In-vitro  evaluation  of  herbal  and  chemical agents  in the  management  of Dandruff, J Microbiol Biotech Res, 2(6): 916-921.
  44. Richa  MS,  Kinjal  S  and  Janki  P,  2011, Evaluation  of  Prepared  Herbal  Shampoo Formulations and To Compare Formulated Shampoo  with Marketed  Shampoos, Int  J Pharm Sci, 3(4): 402-405.
  45. Sagar R  and Dixit  VK, 2005,  Formulation and  evaluation  herbal  anti-dandruff shampoo, Nig J Nat Prod Med, 09: 55-60
  46. Krishnamoorthy JR, Ranganathan S, Gokul SS, Ranjith MS and Dano A, 2006, A herbal solution for Dandruff, African J Biotechnol, 5(10): 960- 962.
  47. Maniker AR, Jolly CI. Formulation of natural shampoo. Int J Cosm Sci. 2001; 23(1):59-62.
  48. Aghel N, Moghimipour B, Dana RA. Formulation of a herbal shampoo using total saponins of Acanthophyllum squarrosum. Iran J Pharm Res. 2007; 6:167-72.
  49. Potluri A, Asma SS, Rallapally N, DurrivelS, Harish GA. Review on herbs used in antidandruff shampoo and its evaluation parameters. Indo Am J Pharm Res. 2013; 3:3266-3278.
  50. Chandrani D, Lubaina SZ, Soosamma M. A review of antifungal effect of plant extract..

Reference

  1. Krishnamoorthy JR, Ranganathan S, Gokul SS, Ranjith MS and Dano A, 2006, A herbal solution for Dandruff, African J Biotechnol, 5(10): 960- 962.
  2. Revansiddappa  M,  Sharad ha  R,  Abbulu  K, Formulation  and  Evaluation  of  Herbal  Anti-dandruff Shampoo,  Journal  of  Pharmacognosy  and Phytochemistry, 2018; 7(4); 764-767.
  3. Yateem H, Hanania M, Mosleh N, Formulation and Evaluation  of  Herbal  Shampoo Containing Olive Leaves  Extract , International  Journal  of Development  Research,  October  2018;  8(10); 23173- 23176.
  4. Bhagwat S.S, Formulation and Evaluation of Herbal Shampoo,  International  Journal  of  Creative Research  Th ough ts,  Sep temb er  2020;  8(9); 2860-2869.
  5.  Gubitosa  J,  Rizzi  V,  Fini  P,  Cosma  P,  Hair  Care Cosmetics:  From  Traditional  Shampoo  to  Solid Clay and Herbal Shampoo, Cosmetics, March 2019; 6(1); 13.
  6. Sravanthi  K,  Kavitha  N,  Sowmya  K, Naazneen  S, Vaishnavi  U, Anil  C.H, A  Review  on  Formulation and  Evaluation  of Herbal  Anti-Dandruff Shampoo, International  Journal  of  Pharmaceutical  Research and Applications, June 2021; 6(3); 1300-1311.
  7. Arora  P,  Nanda A,  Karan M,  Shampoos  Based on Synthetic Ingredients vis-a-vis Shampoos Based on Herbal Ingredients: A Review, International Journal of  Pharmaceutical  Sciences  Review and  Research, April 2011; 7(1); 41-46.
  8. Vijaya laks hmi  A,  Sang eeth a  S,  Ranjith  N, Formulation  and  Evaluation  of  Herbal  Shampoo, Asian  Journal  of  Pharmaceutical  and  Clinical Research, 2018; 11(4); 121-124.
  9. Kumar A, Mali R, Evaluation of Prepared Shampoo Formulations and to Compare Formulated Shampoo with  Marketed  Shampoos,  International Journal  of Pharmaceutical  Science  Review  and  Research, August 2010; 3(1); 120-126.
  10. Gaud R.S, Gupta G.D, Practical Physical Pharmacy, 1st  ed,  New  Delhi,  CBS Publisher  and  Distributer, 2001; 81-105.
  11. Barel A. O, Paye M, Maibach H.I,  Handbook  of Cosmetic  Science  and  Technology,  4th  ed,  Boca Raton, CRC press; 2014.
  12. Mainkar  A.R,  Jolly C.I,  Evaluation of  commercial herbal shampoos,  International Journal of Cosmetic Science, October2000; 22(5); 385-391.
  13. Chandran  S,  Vipin  K.V,  Augusthy  AR,  Lindumol K.V, Shirwaikar A, Development  and Evaluation of Antidandruff  Shampoo  Based on  Natural  Sources, Journal  of  Pharmacy  and  Phytotheraputics,  2013; 1(4); 10-14.
  14. Kumar S, Akhila A, Naqvi AA, Farooqi AH, Singh AK, Uniyal G C, et al. Medicinal plants in skin care. Lucknow, India: CIMAP 1994; pp.425-30.
  15. Gulrajani ML. Natural dyes and their applications to textiles. India: IIT New Delhi 1992; page no 1-2.
  16. Ashok D, Vaidya B, Devasagayam T. Current status of herbal drugs in India: An overview. J Clin Biochem Nutr 2007; 41(1): 1-11.
  17. Khare  CP.  Indian  herbal  remedies:  Rational  western  therapy,  ayurvedic,  and  other traditional usage. Botany Springer 2003; p.89.
  18. Brown K. Hair colorants. J Soc Cosmet Chem 1982;33: 375-83.
  19. Balsam MS. Edward sagarin, cosmetics science and technology. John Wiley &Sons 1972.
  20. Kalia AN. Text book of industrial Pharmacognosy, New Delhi: CBS Publishers 2005; page no 264.
  21. Nadkarni KM. Indian material medica. Popular Prakashan 1976; pp.630-680, 1202.
  22. Anjali J.  Hair care formulations. World J Pharm Sci 2016; 5(6):630-48.
  23. Marlen McHugh-Pratt,  Milady's Standard  textbook  of Cosmetology,  Delmer Publishers, USA, 2000, page no 265-304.
  24. Wails  TE,  Textbook  of  Pharmacognosy,  5th  Ed,  CBS  publishers  &  Distributors, Delhi.1997.
  25. Kokate CK, Purohit AP and Gokhale SB, Pharmacognosy, 19th Ed, Nirali Prakashan, pune 2002, page no 220.
  26. Philips I, Steinberg M. Maibach HI and Akers WA, Comparison of Rabbit and human skin responses to certain irritants, Toxicol Appl Pharmacol, 1972, 21, 639.
  27. Koehler Paul  B,  Clinical aspects  of  safety testing of  cosmetic products, J  Soc  Cosmetic Chem, 1980, 31, 213-218.
  28. Kirtikar  KR  and  Basu  BD,  Indian  Medicinal Plants,  3rd  Ed  Vol  2, International  Book Distributors, Dehradun, 1998, p.1361.
  29. Fisher's Contact Dermatitis, Ed. Rietschel RL, Fowler JF, Lippincott Williams & Wilkins, 2001.
  30. M. Thenmozhi et, al., International Journal of Engineering science and Technology,3(1), 2011, 292-298.
  31. Harbone  JB, Phytochemical  method:  A Guide  to  Modern Techniques  of  plant  analysis. Chapman and Hall, London, UK, 1984.
  32. Potts PJ, Webb PC, Waston JS, x -ray Spectrum, 13, 1984, 2.
  33. William Kemp Organic Spectroscopy, ELBS: Hong Kong; 1986.
  34. Natural product Radiance, 7(1), 2008, 45-48.
  35. Jain  U,  1997,  Beauty  through  Herbs, Institute  of  herbal  science  publishers,  1st Edition, 23-27.
  36. Chitravadivu  C  and  Bhoopathi  M,  2009, Antimicrobial activity of Laehiums prepared by  herbal  venders,  South  India, Eurasian Journal  of  Scientific Research,  4(3):  142-147.
  37. Hay  RJ  and Graham  BR,  1997, Dandruff and  Seborrheic  Dermatitis:  Causes  and Management, Clin Exp Dermatol, 22: 3-6.
  38. Mukharjee  PK,  2008,  Quality  Control  of Herbal Drug, An Approach to Evaluation of Botanical, 3: 184, 291.
  39. Subrahmanyam  CVS, 2000, Text  Book of Physical Pharamcy, Vallabh Prakashan, 2nd Edition, 2: 221-224.
  40. Richa  MS,  Kinjal  S  and  Janki  P,  2011, Evaluation  of  prepared  herbal  shampoo formulations  and  to  compare  formulated shampoo  with  marketed  shampoos,  Int  J Pharm Sci, 3: 402-405.
  41. Martin  A,  1993,  Physical  Pharmacy,  4th edition.  London:  Lea  &  Febigen Philadelphia, 431-432.
  42. More  HN  and  Hazare  AA,  Practical Physical Pharmacy, 1st Edition, 114-119.
  43. Naveen  S,  Karthika  S,  Sentila  R, Mahenthiran  R  and  Michael  A,  2012,  In-vitro  evaluation  of  herbal  and  chemical agents  in the  management  of Dandruff, J Microbiol Biotech Res, 2(6): 916-921.
  44. Richa  MS,  Kinjal  S  and  Janki  P,  2011, Evaluation  of  Prepared  Herbal  Shampoo Formulations and To Compare Formulated Shampoo  with Marketed  Shampoos, Int  J Pharm Sci, 3(4): 402-405.
  45. Sagar R  and Dixit  VK, 2005,  Formulation and  evaluation  herbal  anti-dandruff shampoo, Nig J Nat Prod Med, 09: 55-60
  46. Krishnamoorthy JR, Ranganathan S, Gokul SS, Ranjith MS and Dano A, 2006, A herbal solution for Dandruff, African J Biotechnol, 5(10): 960- 962.
  47. Maniker AR, Jolly CI. Formulation of natural shampoo. Int J Cosm Sci. 2001; 23(1):59-62.
  48. Aghel N, Moghimipour B, Dana RA. Formulation of a herbal shampoo using total saponins of Acanthophyllum squarrosum. Iran J Pharm Res. 2007; 6:167-72.
  49. Potluri A, Asma SS, Rallapally N, DurrivelS, Harish GA. Review on herbs used in antidandruff shampoo and its evaluation parameters. Indo Am J Pharm Res. 2013; 3:3266-3278.
  50. Chandrani D, Lubaina SZ, Soosamma M. A review of antifungal effect of plant extract..

Photo
Dr Roopesh P. T.
Corresponding author

Department of Pharmaceutics, Rajiv Gandhi institute of Pharmaceutical Sciences and Research Thrikkaripur Kasaragod India

Photo
Anjali p.
Co-author

Bachelor of pharmacy Rajiv Gandhi institute of Pharmaceutical Sciences and Research, Thrikkaripur, Kasaragod, India

Photo
Aishwarya Lakshmi T.
Co-author

Bachelor of pharmacy, Rajiv Gandhi institute of Pharmaceutical Sciences and Research, Thrikkaripur Kasaragod India

Photo
Suhana Muhammad Kunji
Co-author

Bachelor of pharmacy, Rajiv Gandhi Institute of pharmaceutical sciences and research, Thrikkaripur, Kasaragod, India

Photo
Jumana Haseen
Co-author

Bachelor of Pharmacy, Rajiv Gandhi Institute of Pharmaceutical Sciences and Research Trikkaripur, Kasargod, India

Dr. Roopesh P. T.*, Anjali P.*, Aiahwarya Lakshmi T., Suhana Muhammed Kunhi, Jumana Haseen, Formulation And Evaluation of Multipurpose Polyherbal Powder Shampoo, Int. J. of Pharm. Sci., 2024, Vol 2, Issue 12, 529-543. https://doi.org/10.5281/zenodo.14276667

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