Pawan Kumar Final Project
Pawan Kumar Final Project
BACHELOR OF PHARMACY
By
PAWAN KUMAR
Roll no: 21109168003
(Assistant Professor)
to the
FACULTY OF PHARMACY
ARYABHATTA KNOWLEDGE UNIVERSITY, PATNA, BIHAR
SESSION 2021-2025
i
RAJENDRA KISHORI PHARMACY COLLEGE
DISSERTATION
STUDENT NAME
(ROLL NO) PAWAN KUMAR (21109168003)
SESSION 2021-2025
SIGNATURE OF DIRECTOR
DATE OF SUBMISSION
ii
CERTIFICATE BY THE SUPERVISOR
This is to certify that Mr. PAWAN KUMAR (Roll no. 21109168003),) has carried out
the project report presented in this project entitled “FORMULATION AND
EVALUATION OF POLYHERBAL COOKIES FOR DIABETIC PATIENT” for
the award of Bachelor of Pharmacy from Rajendra Kishori Pharmacy College,
Aryabhatta Knowledge University; Siwan Under my supervision.
The project report embodies results of original work, and studies are carried out by the
student herself/himself and the contents of the thesis do not form the basis for the award
of any other degree to the candidate or to anybody else from this or any other
University/Institution.
Signature
Date:
Mr .Sudhanshu Mishra
Assistant Professor
Rajendra Kishori Pharmacy college
Siwan ,Bihar
iii
DECLERATION BY CANDIDATE
I hereby proclaim that the thesis for the project work entitled “FORMULATION AND
EVALUATION OF POLYHERBAL COOKIES FOR DIABETIC PATIENT” submitted
to the ARYABHATTA KNOWLEDGE UNIVERSITY, is a record of an inventive work
prepared by me under the guidance of Mr.Sudhanshu Mishra, Assistant professor, RKPC, the
project work is submitted in the partial fulfillment of the requirement for the award of the degree
of Bachelors of Pharmacy. It is further stated that no part of such project work has been submitted
either partially or fully, for the award of any degree by me to this or any former university.
PAWAN KUMAR
Bachelors of Pharmcy
iv
INDEX
Abstract 1
1. Introduction 2-3
2. Review Article 4
5. Plan of work 17
9. Conclusion 28
List of Table:
List of Abbreviations:
ABSTRACT
Most of the people consume cookies during their breakfast, snacks and leisure time to regulate
their hunger and get some energy, in market there are varieties of cookies which are available, and
the main components are refined flour, sugar and butter. Hence, are generally avoided by obese
and diabetic patients as they lead to high sugar level in blood. Therefore, in this recent
investigation, we have formulated Polyherbal cookies using oats, wheat flour and different
Ayurveda herb. Diverse varieties were formulated using different plant to find out the best
composition for cookies on the basis of palatability. After selection, cookies were formulated for
the physiochemical, sensory and their nutritional analysis. Sensory analysis was evaluated based
on organoleptic characteristics: color, taste, aroma and overall acceptability on the basis of 9-
paledonic scale. Physiochemical evaluation including: total ash value, total moisture content total
water and alcoholic extraction, total moisture content. On the basis of its nutritional value
comparison, it was found that the protein content is higher in our formulation than the other
marketed preparation.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
1. INTRODUCTION
Plants have provided a source of inspiration for novel drug compounds, as plant derived medicines
have made large contributions of human health and well-being. Traditional medicine using plant
extract continues to provide health coverage for over 80% of the world’s population, especially in
the developing world. Plants are used medicinally in different countries and are a source of many
potent and powerful drugs.
Medicinal plants provide good remedies for human diseases and play a vital role in our day-to-day
life. Indian systems of medicines are all based on the knowledge of drugs from plants. Higher
plants, as sources of medicinal compounds, have continued to play a dominant role in the
maintenance of human health since ancient time. Over 50% of all modern clinical drugs are natural
product origin and natural products play an important role in drug development programs in the
pharmaceutical industry. In India people have been used plants and natural products for the
treatment of various diseases from ancient time. In the last two decades of the century the scientists
are sincerely trying to evaluate many plant drugs used in traditional system of medicine. [1]
Diabetes- common, non-communicable metabolic disorder mostly occurring in young ones and
are associated with other diseases like kidney disease, cardiovascular diseases etc. It occurs when
pancreas does not produce insulin or is not properly consumed by body. According to the WHO
survey report globally, it is estimated that 422 million adults were suffering in 2014 and rate of
increment is about from 4.7% to 8.5%. Diabetes mellitus, a chronic metabolic disease condition
enounces by the elevated glucose level in blood (Hyperglycemia), hyperlipidemia, negative
nitrogen balance, glycosuria and sometimes ketonemia. Basically, it is grouped in three main
types: Type-1 diabetes mellitus / Insulin dependent diabetes mellitus/Juvenile onset diabetes
mellitus, which are mostly caused by the T-cell mediated autoimmune devastation of islets of
insulin secretion Beta cells. Type-2diabetes mellitus /Non-Insulin Dependent diabetes mellitus
occurs due to the moderate reduction in β cell mass or the low circulation of insulin due to the
interaction of genetic or metabolic factor. Nearly 90% of diabetes patients are suffering from type-
2 diabetes. And Type-3 occurred during pregnancy when insulin is not produced properly or the
cells become resist to insulin.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Insulin is a hypoglycemic hormone with two polypeptide 51amino acid chains. 1U insulin is
secreted per hour by the human pancreas but maximum amount is being secreted after meal and
are controlled by chemical, hormonal and neural mechanism. Insulin is site specific and is present
on all cell membrane but more densely depends on the cell type: liver and fat cells are rich in its
presence. Some of the secondary messenger like PIP3 activate PI3 kinase also facilitates the action
of insulin on metabolism enzymes. Insulin activates glucose transport through the cell membrane
by ATP dependent transfer of glucose transporter (GLUT-4) to plasma membrane.
The secondary messenger PIP3 and certain tyrosine phosphorylated guanine exchanger protein
help GLUT-4 to move from cytosol to the plasma membrane. Recent drugs which are used to
treat diabetes worldwide are in effect, but some natural therapies, natural foods and various
changes in the lifestyle would be a wise act to treat and control diabetes and its associated disease.
Various plants, its part or products (more than 1200) are identified as hypoglycemic with fewer
side effect. [2]
Polyherbal antidiabetic cookies are the combination of various herbs and cereals that have a great
power to stimulate insulin secretion by countless mechanism of action. These cookies contain oats,
Tecoma stans leaves, Tulsi leaves, ashwagandha, honey, artificial sugar (sucralose) etc., which is
tasty,healthy as well as beneficial for a diabetic patient of all age group and as the product contains
herbs and cereals it has less adverse effect on ones body. According to WHO report, 2016 it was
made an action plan for the year from 2013-2020 in which it involved various action plans and
suggested natural food products which can decrease or regularise the blood glucose level in blood
should be develop more. [3]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
2. REVIEW ARTICLE
2.1 A Complete Review on Avena sativa
2.2 Evaluation of the Cookies Formulated with Costus igneus Plant Material for Antidiabetic
Activity
A Rajani Chowdary et al, (2020),
The present research work aimed to formulate a nutritionally rich cookie with Costus igneus
leaf extract and to determine the effect of cookie consumption on decreasing blood glucose
level in type 2 Diabetic patient.
Aim
The aim of the present study is to design and formulate a cookie formulation as a drug delivery
system for diabetic patients.
Objective
The objective of the study is to design polyherbal cookies containing Tecoma stans, Tulsi leaves
and ashwagandha.
The essential target of the study was to formulate and evaluate antidiabetic polyherbal cookies that
will have to work on antidiabetic enhancing property.
Polyherbal formulation has wide therapeutic range, pure side effects, cheaper eco-friendly and
rapidly available
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
4. DRUG PROFILE
Oats (Avena sativa) belongs to family Poaceae. It has soluble fibre known as beta glucan is
polysaccharides which containing glucose residue binds with 1, 3 and 1, 4 bonds. Products that
have β glucan have been used from thousands of years for human health, but β glucans has been
recently scrutinized as active ingredient. Since then, they have been studied extensively for immune
stimulation effects and developed for the treatment of various diseases including cancer, infectious
diseases. Oat β glucan have been used for several clinical trials to reduce glucose. Studies showed
that oat β glucan lowered postprandial glycemia. The effect of β glucans to reduce blood glucose
could be mediated possibly by delaying stomach emptying so that dietary glucose is absorbed more
gradually. After ingestion of oats (bran flour or crisp), the blood glucose level was lower at 15, 30
and 45 min but higher at 90 min after 12.5g glucose loading. Thus, the peak level is much smoothed
and the shape of the plasma glucose response curve is flatter. These changes reduce the feeling of
hunger caused by rapid decrease in blood glucose. Thus, β glucan may reduce appetite and reduce
food intake. [4]
Tecoma stans is commonly planted as an ornamental in warmer climates throughout the world
because of its showy yellow flowers and pinnate foliage. Tecoma stans is an important medicinal
plant. The major bioactive compounds like alkaloids, phenols, terpenoids, glycosides, flavonoids,
saponins had been isolated from this plant. The leaves, bark and roots contain biologically active
chemicals, and extracts from those tissues are in use as traditional folk medicines. The presence of
phytoconstituents like phytosterol, triterpene, glycosides, phenols, flavonoids, saponins, and
tannins either individually or combined together may exhibit the synergistic effect towards healing
of wounds. [6]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Description
Tecoma stans is a promising species in the trumpet vine family, Bignoniaceae. The common names
are yellow trumpet bush, yellow bells, yellow elder and Esperanza. It is a flowering perennial shrub
or small tree, 5-7.6 m in height. Bark is pale brown to grey and roughens with age. Leaves are
opposite, compound and imparipinnate with 2 to 5 pairs of leaflets and a larger single terminal
leaflet.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Flowers occur in clusters at the ends of the branches and are trumpet shaped with 5 rounded lobes,
6 cm long, pale to bright yellow, with faint orange stripes at the throat. Stamens 4, attached at
summit of tube in 2 unequal pairs, filaments pilose at base, curved above, anthers versatile, linear,
yellow, pilose and 6 mm long; Fruits are narrow, slightly flattened to pointed capsules, up to 20 cm
long, containing many winged seeds; green when young, pale brown on ripening and remain on the
tree in untidy clusters for many months. [7]
Phytochemical properties
Tecoma stans leaves bark, and roots contain many biologically active chemicals, and extracts from
those tissues have been used in traditional folk medicine to treat many diseases and conditions. The
major bio active compounds like alkaloids, phenols, terpenoids, glycosides, flavonoids, saponins
have been isolated. These bioactive compounds contain various phytoconstituents. The
phytochemical screening of the Tecoma stans plants varied according to the solvents used for the
extraction of the leaves. Therapeutically important active principle of Tecoma stan is Tecomine
(the alkaloids isolated from the plant harvested in Egypt) was shown to be one of the compounds
responsible for the hypoglycemic action given the interest in substances able to treat type II
diabetes. The Tecoma stans leaves and barks both shows the anti-inflammatory activity. The
biosynthesis of monoterpene alkaloids in callus tissues of Tecoma stans has been studied, together
with the identification of the presence of lapachol and other primary and secondary plant
metabolites such as: sugars (glucose, fructose, sucrose and xylose), triterpenoids (ursolic and
oleanolic acids and α- amyrine), p-sitosterol and phenolics (chlorogenic, caffeic, vanillic, o-
ceramics and sinapicnacids). Alkaloids namely 5β Hydroxyskitanthine, early called Base C, and
boschniakine were inactive both in vivo and in vitro assays. Other chemical constitutes are
phytosterols, alkaloids, quinones, amino acids, monoterpenes, triterpene, glycosides, phenols,
flavonoids, saponins, and tannins. Recently the presence of iridoid glycosides, indolic compounds
in the leaves has been identified from this plant. [8]
Pharmacological activities
Tecoma stans have various pharmacological activities like antidiabetic, anti-inflammatory, wound
healing, antimicrobial, antioxidant, cytotoxic, antifungal and anti-proliferative activity.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Anti-Diabetic activity
Antidiabetic effect of Tecoma stans was attributed to alkaloids denominated tecomine and
tecostanine. It has been reported that sub chronic and acute administration of the alkaloid tecomine
diminished plasmatic cholesterol and triglycerides levels without modifying fasting glucose.
Tecoma stans aqueous extract of leaves exert its antidiabetic effects by stimulating glucose uptake
in both insulin-sensitive and insulin-resistant murine and human adipocytes without significant
proadipogenic or antiadipogenic side effects.[9]
In another study it has been reported that the ethanolic extract of Tecoma stans stem (200 mg/kg)
showed statistically more significant in decrease blood glucose level. The ethanolic extract shows
(147.5±4.4) more significant value, when compared to positive control group and near to standard
group (124.6±3.9). The antidiabetic activity of ethanolic extract of Tecoma stans stem may be due
to potentiation of insulin secretion from β-cells of pancreas. The potential antidiabetic activity
may be due to the actions of phytochemicals such as flavonoids, saponins and alkaloids present in
ethanolic extract of Tecoma stans stem. [10]
Anti-Inflammatory activity
The methanol, ethanol and water extracts of T. stans showed anti-inflammatory activity by
inhibiting the heat induced albumin denaturation and red blood cells membrane stabilization. In
another studies administration of alcohol extract at 250 and 500 mg/kg inhibited the edema from
the 3h after carrageenan challenge, and aqueous extract at dose of 250 and 500 mg/kg inhibited
the edema from 4h after carrageenan challenge, which probably inhibits the different aspects and
chemical mediators of inflammation. [11]
phytosterols, triterpenes, glycosides, phenols, flavonoids, saponins, and tannins either individually
[12]
or combined together may exhibit the synergistic effect towards healing of wounds.
Antimicrobial Activity
The alcoholic and aqueous extract of T. stans exhibited the antibacterial activity and the growth of
E. coli and B. subtilis was inhibited at different concentrations. The methanol extracts of leaves and
stem bark of Tecoma stans was studied for their antimicrobial activity using a wide range of Gram-
positive and Gram-negative bacteria and fungi. It was observed that the extracts of stem bark
generally showed better antimicrobial activity than those of the leaves. In another study, the
ethanol, methanol and water leaf extracts of Tecoma stans was tested on various bacteria
(Pseudomonas fluorescens, Clavibacter michiganensis, Staphylococcus aureus, E. coli,
Pseudomonas aeruginosa and Klebsiella pneumonia) and was found to be effective. Phytochemical
analysis revealed the presence of alkaloids, flavonoids, saponins, phenols, steroids, anthraquinones
and tannins.
The three extract fractions have showed highest total phenolic content (177-216mg gallic acid
equivalent/g) which may be attributed to its antimicrobial activity. Flavonoids also have been
proven to display a wide range of pharmacological and biochemical actions, like antimicrobial
activities. [13]
Antioxidant Activity
Plants are primary resources for antioxidants like carotenes, phenolic acids, etc., the phytochemical
analysis 0f Tecoma stans revealed that the plant has alkaloids, steroids, glycosides and
carbohydrates. Flavonoids can act as free radical scavengers and terminate the radical chain
reactions that occur during the oxidation of triglycerides in the food systems. [14]
The presence of tannins in the extracts may explain its potent bioactivities known to possess potent
antioxidants. The antioxidant activity of methanolic and ethanolic extract of Tecoma stans plants
parts was measured by the capability of DPPH free radicles scavenging in comparison to the
standards, ascorbic acid and butylated hydroxytoulene. DPPH assay results show that methanolic
extract of T. stans in higher concentration show better antioxidant potential than the standard L-
ascorbic acid. They exhibited strong antioxidant potential at 20 μg/mL concentration. [15]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Cytotoxic Activity
Cytotoxic effects of Tecoma stans were found to be concentration and time-dependent in the
presence and absence of fetal bovine serum (FBS). Cytotoxicity was determined
spectrophotometrically by MTT and reported in terms of % cell viability. In another study the
cytotoxicity effects of different concentrations of alcoholic and aqueous extracts 100000(A),
50000(B), 25000(C), 12500(D), 6250(E), 3125(F), 1562.5(G), 781.2(H) μg mL-1 were tested on
normal mouse embryo fibroblast cell line (MEF) and treated cell line. The higher concentrations of
the plant extracts had a significant cytotoxic effect than lower concentrations on the MEF cell line.
Morphological assessment using inverted microscopy of the cultured cells indicated that cell death
occurred in the treated cell lines. The active constitutes in the plant extract causes morphological
changes and cell death. [16]
Antifungal activity
Antifungal activities were tested by the drop diffusion method. Tecoma stans differ significantly in
their activities against the microorganisms tested and most of the extracts showed antifungal
activity against Candida albicans, Cryptococcus neoformans and Microsporum gypseum. Tecoma
stans found to give the best zone of inhibition against the fungal activity. In another study Tecoma
stans was tested against two species of subcutaneous fungi: Sporothrix schenckii and Fonsecaea
pedrosoi by the agar dilution method at a concentration of 100 μ/mL. Tecoma stans, showed
effective activity against F. pedrosoi at MIC 12.5 μg/mL. [17]
Anticancer activity
Natural products derived from medicinal plants have gained significance in the treatment of
cancer. Compounds which are derived from plants one or another way constitutes more than 50%
of antiproliferative agents. Traditionally flowers and bark of Tecoma stans are used for treatment
of various cancers. Tecoma stans leaves and bark shows anti proliferative activity. Report
suggested that the hydroxyl groups of the aromatic rings (acteoside) appear to play an essential
role in the antiproliferative effect. A novel monoterpene alkaloid, 5- hydroxy-skytanthine
hydrochloride isolated from Tecoma stans Juss. fruits and flowers are effective as an anti-
proliferative against MCF-7 and as a NO inhibitor. The invitro anti- proliferative activity of the
various parts of the Tecoma stans was studied in the Breast cancer. MCF-7 cell lines by MTT
assay. The stem, root, bark and flower extracts showed significant anti-proliferative action on the
cell line (MCF-7) but extreme action was found to be in extract stem bark of Tecoma stans.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Another study shows a dramatic invitro anticancer activity of ethanolic leaf extract of Tecoma
stans on human breast cancer cell line (MCF-7) at increasing concentrations with Inhibitory
concentration 64.5μg/ml. [18-19]
It is in use for a very long time for all age groups and both sexes and even during pregnancy without
any side effects. Historically, the plant has been used as an antioxidant, adaptogen, aphrodisiac,
liver tonic, anti-inflammatory agent, astringent and more recently to treat ulcers, bacterial infection,
venom toxins and senile dementia.
Clinical trials and animal research support the use of WS for anxiety, cognitive and neurological
disorders, inflammation, hyperlipidaemia and Parkinson’s disease. WS chemo preventive
properties make it a potentially useful adjunct for patients undergoing radiation and chemotherapy.
Recently WS is also used to inhibit the development of tolerance and dependence on chronic use
of various psychotropic drugs.
WS is a small, woody shrub in the Solanaceae family that grows about two feet in height. It can be
found growing in Africa, the Mediterranean, and India. An erect, evergreen, tomentose shrub, 30-
150 cm high, found throughout the drier parts of India in waste places and on bunds. Roots are
stout fleshy, whitish brown; leaves simple ovate, glabrous, those in the floral region smaller and
opposite; flowers inconspicuous, greenish or lubrid-yellow, in axillary, umbellate cymes; berries
small, globose, orange-red when mature, enclosed in the persistent calyx; seeds yellow, reniform.
The roots are the main portions of the plant used therapeutically. The bright red fruit is harvested
in the late fall and seeds are dried for planting in the following spring. Parts used: Whole plant,
roots, leaves, stem, green berries, fruits, seeds, bark are used. [20]
Pharmacological Activity
Antidiabetic Activity
The use of Ashwagandha is also considered in the context of anti-diabetic effects. However, there
are relatively few reports on this issue. The antidiabetic properties of the raw material were
interestingly described in a review paper by Drug. The results of the preclinical studies were
promising. Animal studies have shown its ability to lower blood glucose levels. Withaferin A can
effectively control induced type 1 diabetes in rats through modulation of Nrf2/NFκB signaling and
therefore has significant potential for therapy. In silico studies have also confirmed withaferin A’s
potential using molecular docking. However, only one clinical study from the year 2000 showed a
direct blood-glucose-lowering effect. On the other hand, many studies have shown a beneficial
effect on the lipidemic profile. In a study conducted on white albino rats with hypercholesterolemia,
a reduction in cholesterol levels and also in the antioxidant effects of Withania somnifera were
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
observed. In the case of clinical trials on diabetes, despite not showing an effect on blood sugar
levels, interesting results were achieved in improving the lipidemic profile, body weight, and blood
pressure, showed an improvement in the lipidemic profile and patient assessment with the DDS17
scale assessing patients’ distress scale. The administration of a standardized Ashwagandha extract
under the name SENSORIL improved antioxidant parameters and the lipidemic profile and
demonstrated the tolerability and safety of the raw material. In site of its tolerability and safety,
demonstrated an effect on lipidemic profile and a change in the reflection index. [21-22]
Species A. Sativa
Common Names Oat, Cultivated Oat, Oats, Side Oat, Tree Oat, Red Oat
Description:
The word Avena originated from the Sanskrit word “avi,” which means sheep, or “avasa” means
food material. The Indian variety is equated with A. byzantina C. Koch., Avena sativa L. known as
oat or common oat is associate degree annual grass concerning 1.5 meters high, culms tufted or
solitary, erect or bent at the bottom. The leaves are non-articulate, green; the ligules are blunt and
membranous. The inflorescence may be a diffuse raceme with 2–3 florets, all bisexual or the distal
one or 2 could also be reduced and male or sterile; glumes sub-equal 7–11 patterned, longer glumes
17–30 mm; lemmas 7–9 patterned, either divided or with a mind their apex; lowest lemma is 12–
25 metric linear unit. The rachilla of the cultivated oat doesn't disjoint at maturity (that of many
weed species do). Its lemmas are seldom awed. The grain is tightly enveloped by the exhausting
lemma and palea. Seed size is found to vary with the variety. [23]
Pharmacological Activities
Antidiabetic Activity
Foods yielding low postprandial glycemic responses have been suggested to be beneficial for the
dietary prevention of type 2 diabetes. The soluble fibre β-glucan from the oats can decrease the
glycemic response. The high molecular weight of β-glucan increases the fluid viscosity in the
intestine, it is crucial for obtaining the positive effect of β-glucan on the peak blood glucose level.
It has been reported that the inclusion of oat β-glucan into breakfast cereals could reduce the
postprandial glycemic response up to 50%. At low levels (below 5%) the response was dose
dependent whereas at the levels above 5% it did not show significant reductions in the glycemic
response. These findings will be of importance for deciding the appropriate levels of β-glucan
inclusion in food systems. Studies to evaluate the effect of inclusion of β-glucan enriched cereal in
foods was carried out in Type 2 diabetic patients and their glycemic indices (GI) were found to be
significantly lower than the GI of the group with white bread.
The results of the study suggest that the blood glucose levels of diabetic and pre-diabetic individuals
can be moderated by using β-glucan rich foods and so oat has great potential. Oats are a rich source
of magnesium which acts as a co-factor for more than 300 enzymes, including enzymes involved
in the body’s use of glucose and insulin secretion.
Foods containing at least 51% whole grains by weight (and are also low in fat, saturated fat, and
cholesterol) are permitted by FDA to display a health claim stating that its consumption is linked
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
to lower risk of heart disease and certain cancers. The data of an 8-year trial, involving 41,186
participants of the Black Women’s Health Study, revealed inverse associations between
magnesium, calcium, and major food sources in relation to type 2 diabetes Risk of type 2 diabetes
was 31% lower in the group of black women frequently eating whole grains as compared to those
eating the lesser quantity of those magnesium-rich foods. When the women’s dietary intake of
magnesium in take was considered by itself, a beneficial, but lesser-19%-reduction in risk of type
2 diabetes was found, indicating that whole grains offer special benefits in promoting healthy blood
sugar control. Daily consumption of low-fat dairy foods was also helpful in lowering the risk of
type 2 diabetes by 13%. [24]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
5. PLAN OF WORK
5.1. Comprehensive literature
5.2. Collection of crude drugs
5.3. Phytochemical screening
Carbohydrates
Alkaloids
Tannins
Glycosides
Saponins
Flavonoids
Steroids (LB test)
Proteins
Amino acids
Phenolic compounds
Gums and Mucilage
5.4. Formulation of polyherbal antidiabetic cookies
5.5. Evaluation of physical properties of polyherbal antidiabetic cookies
Phytochemical evaluation of powdered flower extract of Tecoma stans.
Physiochemical properties of cookies.
Nutritional analysis.
5.6. Results and discussion
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
Collection of Sample
Fresh aerial parts of Tecoma stans (leaves), Ashwagandha (bark), and Tulsi (leaves) were collected
from local areas of Chandrapur city. The collected plants were washed properly and sun dried. The
dried plant was ground into coarse powder material and in sunlight container till future. Milk,
Flavoring agent (vanilla and cocoa), salt, baking powder, baking soda, butter, were purchased from
local market of Chandrapur and Artificial sugar (Diabliss sugar) was procured from its online store.
[25]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
6.2. Methods
Preparation of Cookies
Different compositions of cookies were formulated using different ratios of Oats, wheat flour,
roasted black-gram flour, Tecoma stans leaves powder, Ashwagandha powder, Tulsi powder,
Milk, Flavoring agent (vanilla and cocoa), salt, baking powder, baking soda, butter, artificial sugar
(sugar free Natura), and based on the palatability and visual appealing final product were selected
for sensory evaluation and nutritional value analysis.
7. EVALUATION PARAMETERS
7.1. Phytochemical Evaluation of Powdered Flower Extract of Tecoma stans
The powdered flower sample of Tecoma stans was taken and phytochemical screening was done
to check the phytoconstituents present using standard reagents.
a) Carbohydrates
Molisch's test:
About 2ml of powdered flower extract was mixed with 0.2 ml of alcoholic solution of α- naphthol
10% in addition to 2 ml of sulphuric acid, a bluish violet zone is formed this indicates the presence
of carbohydrates and /or glycosides.
b) Alkaloids
About 0.2 g of the powdered flower extracts was warmed with 2% H2S04 for two minutes. It was
filtered and few drops of Dragendroff’s reagent were added. Orange red precipitate indicates the
presence of alkaloids.
c) Tannins
Small quantity of powdered flower extract was mixed with water and heated on water bath. The
mixture was filtered and ferric chloride was added to the filtrate. A dark green solution indicates
the presence of tannins.
d) Glycosides
The powdered flower extract was hydrolysed with HCl solution and neutralized with NaOH
solution. A few drops of Fehling’s solution A and B were added. Red precipitate indicates the
presence of glycosides.
e) Saponins
About 0.2 g of the powdered flower extract was shaken with 5ml of distilled water and then heated
to boil. Frothing (Appearance of creamy miss of small bubbles) shows the presence of saponins.
f) Flavonoids
Powdered flower extract of about 0.2 g was dissolved in diluted NaOH and HCl was added. A
yellow solution that turns colourless, indicates the presence of flavonoids.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
h) Proteins
To the powdered flower extract, 5%NaOH and 1% copper sulphate solution were added. Violet
color produced shows the presence of proteins.
i) Amino acids
The powdered flower was treated with Million’s reagent. Red colour showed the presence of amino
acids.
j) Phenolic compounds
Small quantities of powdered flower samples were taken separately in water and test for the
presence of phenolic compounds was carried out by using reagents like 5%ferric chloride solution,
1%gelatin solution containing 10% NaCl and 10%lead acetate.
Where,
W1 = Weight of moisture dish with sample before drying;
W2 = Weight of moisture dish with sample after drying;
W = Weight of moisture dish.
b) Ash value:
Total ash content of the prepared cookies was determined by the following procedure.
According to the given procedure 1 gm of cookie sample was taken in a tarred crucible and it
was burnt on the Bunsen burner until all the carbon was burnt. Then Sample was let to be
cooled, weighed and then again the procedure was repeated until the weight became constant.
After that the total Ash value were calculated based on the equation given below:
Where,
W2 = Weight of empty dish;
W = Weight of sample taken;
W1=Weight of crucible with sample after complete burn.
were taken in porcelain dishes. All the samples of alcoholic and water extracts were heated at
the temperature of 100°C for evaporation, following samples were cooled down and advance
calculations were done by the following method.
Calculation: 5 gm of sample gives 4x of alcohol extract so 100 gm of sample gives = 80 × x/4
Where, x=Sample after drying. [2]
b) Fat content:
According to the given procedure, 2 gm of the cookie sample was kept in Soxhlet apparatus
with diethyl alcohol and petroleum ether in the ratio of 1:1 for 6 hours then ether was removed
by the process of distillation and were dried in hot air oven at 110 ± 1°C and later on was cooled
in a desiccator. Taken dried sample was weighed again. The left Residue was washed with 2
to 3 ml of diethyl ether and the same process was repeated until the weight became constant.
c) Carbohydrate estimation:
Carbohydrate estimation was done by the procedure given in DGHS Manual. For estimation of
carbohydrate 2 gm of cookie sample powder was taken in a 200 ml of volumetric flask and
then 50 ml of lead acetate was added. 6 ml of 0.5 N HCl was added and heated on hot water
bath. After heating, the sample was cooled and neutralized with 6 ml of 0.5 N NaOH, lastly the
sample volume was makeup upto 200 ml using distilled water, Invert sugar was determined
before inversion by Lane and Eynon method.
According to this method 10 ml of mixed Fehling A and B solution was taken in the conical
flask and titration was passed out with sample solution within 3 min without inversion by using
1% aqueous Methylene Blue as an indicator.
d) Total Energy
Total energy was valued on the basis of carbohydrates, proteins and fats content of cookie
sample.
Energy (Kcal) = Fat×4+ Protein×9+ Carbohydrates×4
e) Sensory Analysis
Sensory attributes such as flavor, aroma, taste, appearance and odor were evaluated by 9- point
hedonic scale, total 64 people participated in this survey. Questionnaires and mouth rinsing
water were conferred to taste panelist, through the session product was introduced and
questions were explained to the volunteers. The obtained data were analyzed by Microsoft
Excel on the basis of age group. [27]
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
By above mentioned Table 1 of results shown, those Cookies were spanking in nutritional values
with controlled fat and carbohydrate and high rich in protein content which have made it
acceptable among the health-conscious people, growing people and case of malnutrition.
Comparative studies of different parameters of sensory evaluation exhibited that use of curry
leaves as an active ingredient has given an appetizing and flavoring effect. Selected composition
of cookies has made it acceptable around 90-96% that will give us a hope to convert this
formulation into large scale production. In terms of physiochemical properties, nutrition value,
sensory evaluation and comparison with other marketed product were in acceptable range.
Taste is a strategic parameter of sensory evaluation. The product might be captivating and having
an eminent energy but sans of righteous taste it is likely to unaccepted. So, on the basis of sensory
evaluation, it is found that due to use of Tecoma stans leaves its mean score was 90-95% among
the age group of 18-40. Graph of taste has been depicted below (Figure No. 6).
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
8.2. Flavour
Flavour is an integral part of taste that plays a vital role in the acceptance of any food material.
Used flavour of Tecoma stans leaves and coco was found to be highly appreciable among all the
volunteer of sensory evaluation because its smell act as an appetizer, because of that it means score
on excel was found to be 90-95% (Figure No. 7).
9. CONCLUSION
Based on statistical data it was found that herbal cookies have high amount of protein, controlled
amount of fat and carbohydrate in compared to other marketed product. Presence of Tecoma stans
leaves and ashwagandha bark have given a new direction to convert home remedies into a marketed
preparation which gives the highest acceptance in terms of flavor as well as the ingredients used in
formulation has already proven significant role to control non-insulin dependent diabetes mellitus
and other health issue. So, it could be serviceable in the manufacturing of highly nutritious cookies
with low cost and high efficiency.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
10. REFERENCE
1. Jeo A V and Raj J S. “Therapeutic Properties and Applications of Tecoma stansLinn”. Int. J.
Pharm. Sci. Rev. Res. 63(1), 2020; 19: 111-115.
2. Pathak K, Khan S, Sen S., et al. “Formulation of Polyherbal Antidiabetic Cookies”. J. Chem.
Pharm. Res., 2018; 10(2): 91-97.
3. Pratley RE. “The early treatment of type 2 diabetes”. Am J Med. 2013; 126: S2-S9.
4. Ewenighi C, Dimkpa U, Onyeanusi J., et al. “Responses to glycemic control therapy according
to age, gender, level of adiposity, and duration of diabetes in type 2 diabetic patients”. Ultas Med
J. 2015; 1(2): 26-30.
5. Tappy L, Gugolz E and Wursch P., et al. “Effects of Breakfast Cereals Containing Various
Amounts of β-Glucan Fibers on Plasma Glucose and Insulin Responses in NIDDM Subjects”.
Diabetes Care. 1996; 19: 83-84.
6. Saris WH. Carbohydrate, memory, and mood Nutr Rev. 2003; 61(5 Pt 2): S10-S16.
7. Das C, Dash S, Sahoo DC., et al. “Evaluation of methanolic bark extract of Tecoma stans linn,
for wound healing in albino rats”. International Journal of Pharmacy & Technology. 2010; 2: 735-
42.
9. Castroa A J A, Bustosa R Z, Yaneza J R., et al. “The antidiabetic plants Tecoma stans (L.) Juss.
ex Kunth (Bignoniaceae) and Teucrium cubense Jacq (Lamiaceae) induce the incorporation of
glucose in insulinsensitive and insulin-resistant murine and human adipocytes”. Journal of
Ethnopharmacology, 2010; 127: 1–6.
10. Elosh G, Palanivel V and Senthil Kumar KL. “Evaluation of antidiabetic activity of Tecoma
stans stem extract in induced diabetic albino rats”. International Journal of Innovative
Pharmaceutical Research. 2013; 4(3): 337-341.
11. Prasanna LV, Lakshman K, Hegde MM., et al. “Antinociceptive and anti-inflammatory activity
of Tecoma stans leaf extracts”. Indian Journal of Research in Pharmacy and Biotechnology. 2013;
1(2): 156 -160.
12. Das C, Dash S, Sahoo DC., et al. “Evaluation of methanolic bark extract of Tecoma stans linn,
for wound healing in albino rats”. International Journal of Pharmacy & Technology. 2010; 2: 735-
742.
13. Gharib N, Moghaddam A and Bahadoram S. “Antispasmodic effect of Tecoma stans (L.) Juss
leaf extract on rat ileum”. Der Pharmacia Lettre. 2007; 3: 123-128.
Formulation And Evaluation of Polyherbal Cookies For Diabetic Patient
15. Roedig-Penman A and Gordon MH. “Antioxidant properties of myricetin and quercetin in oil
and emulsions”. J. Am. Oil Chem. Soc. 1998; 75: 169-180.
16. Robinson JP, Kumaresan S, Ramasamy S., et al. “Antioxidant and cytotoxic activity of Tecoma
stans against lung cancer cell line (A549)”. Braz J Pharm Sci. 2017; 53: 1-5.
17. Al-Azzawi AM. “Genotoxic and Cytotoxic Study of Tecoma stans Bignoniaceae”. Pakistan
Journal of Biological Sciences. 2012; 15: 92-97.
18. Govindappa M, Sadananda TS, Channabasava R., et al. “Raghavendra, in vitro anti-
inflammatory, lipoxygenase, xanthine Oxidase and acetycholinesterase inhibitory activity of
Tecoma stans”. Juss. Ex kunth, International Journal of Pharma and Bio Sciences. 2011; 2(2): 275-
85.
19. Thirumal M, Kishore G and Srimanthula S. “Invitro anticancer activity of Tecoma stans (L.)
Ethanolic leaf extract on human breast cancer cell line (MCF-7)”. 2012; 2(4): 488-493.
21. Tekula S, Khurana A, Anchi P., et al. 1’Withaferin-A attenuates multiple low doses of
Streptozotocin (MLD-STZ) induced type 1 diabetes”. Biomed. Pharmacother. 2018; 106: 1428–
1440.
22. Usharani P, Fatima N, Kumar C U., et al. “Evaluation of a highly standardized Withania
somnifera extract on endothelial dysfunction and biomarkers of oxidative stress in patients with
type 2 diabetes mellitus: A randomized, double blind, placebo controlled study”. Int. J. Ayurveda
Pharma Res. 2014; 2: 22–32.
23. Singh R, De S, Belkheir A., et al. “Avena sativa (Oat), A Potential Neutraceutical and
Therapeutic Agent: An Overview Avena sativa (Oat)”. Crit Rev Food Sci Nutr 2013; 8398.
24. Rani K U and Shaheen Begum. “A Complete Review on Avena sativa”. Research &
Reviews: Journal of Pharmacognosy and Phytochemistry. 2021; 9(3): 27-41.
25. Srivastava S, Genitha TR and Yadav V. “J Food Process Technol”. 2012; 3(12): 1-5.
26. D Pearson. “The Chemical Analysis of Food”. T&A Cost. Ltd, Edinburgh, UK. 1970; 6: 4-
13.
27. “Food Safety and Standards Authority of India”. Manual of Methods of Analysis of Foods,
Lab Manual 4, FDA Bhawan, Kotla Road, New Delhi, India, 2105: 32-35, 68-71.