Mid Term Presentation Zoya Aditi Aditya-1
Mid Term Presentation Zoya Aditi Aditya-1
1. Introduction
2. Literature Review
4. Plan of Work
5. References
Introduction
• Mammals' hair displays diverse forms, hues, and growth patterns, serving functions
such as sensory stimulation, thermal insulation, and protection.
• Human hair goes beyond protection, embodying aesthetic, cultural, and attractiveness
ideals, often symbolizing youth, vigor, and health.
• While not a vital organ, hair significantly influences cosmetic appearance, impacting
how individuals perceive themselves.
• Characteristics like length, color, texture, and shape play crucial roles in this
perception, affecting self-esteem and confidence levels.
• The cultural significance of hair extends to various rituals and practices worldwide,
illustrating its profound impact on human societies throughout history.
Herbal formulations are those formulations with active ingredients made from plant or
plant parts such as leaves, flowers, fruits, etc. As they are know to have the least side effects
doesn’t mean that we should use them carelessly. As we are working on hair damage
repairing activity (anti-oxidant) we have chosen :
3. Sharma Pushpam et al International journal The medicinal herb bhringraj, often known as fake daisy, increases hair growth.
Formulation and evaluation of of Creative It's an ayurvedic substance that promotes hair growth . It improves blood
herbal hair pack. Research circulation to the scalp by encouraging and activating hair growth that has been
Thoughts lost due to a variety of factors, including dandruff. It also helps to prevent
(IJCRT) dandruff and irritation on the scalp, which can lead to hair loss.
[June ,2022]
Warintorn Ruksiriwanich et al
4. uava (Psidium guajava L.) Leaf MDPI In Plants Leaves of guava (Psidium guajava L.) have been used in Thai folk medicine without any
Extract as Bioactive Substances [2022, supporting evidence as a traditional herbal remedy for hair loss. Androgenetic alopecia
for AntiAndrogen and Antioxidant 11 ] ,3514 (AGA) is
Activities chronic hair loss caused by effects of androgens in those with a genetic predisposition,
resulting in
hair follicle miniaturization. Our objectives were to provide the mechanistic assessment of
guava
leaf extract on gene expressions related to the androgen pathway in well-known in vitro
models, hair follicle dermal papilla cells (HFDPC), and human prostate cancer cells (DU-
145), and to determine its bioactive constituents and antioxidant activities. Our study
reveals new perspectives on guava leaf extract’s anti-androgen properties. This extract
could be
developed as alternative products or therapeutic adjuvants for the treatment of AGA and
other
androgen-related disorders.
AIM:
OBJECTIVES:-
• Conduct a thorough analysis of the body of knowledge on each of the botanical ingredients or individual herbs suggested for the
polyherbal cream.
• To better understand the potential advantages, synergistic effects, and restrictions of polyherbal formulations, analyze earlier studies
on the subject.
• Formulate and evaluate the hair cream for hair damage repair.
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NEED OF RESEARCH:
The study of polyherbal cream formulation and evaluation fills several vital needs and advances knowledge in several fields, including
medicine, science, and consumer health. These are some of the main justifications for performing such research:
Natural Approaches:
Polyherbal creams are in line with the rising popularity of natural practices. These formulations provide alternatives to synthetic or
chemical-based goods, appealing to people looking for more natural skincare and therapeutic solutions.
Evaluation of Extracts.
Characterization of Nanoparticles
1
1
Authentication of the Plants
0.5 ml of ethanolic solution of extract (1mg/ml) and 2.5 ml of 10% Folin-Ciocalteu’s reagent
The same procedure for Gallic acid at a concentration range of 100 - 1000 µg/ml,
flask & 4 ml distilled water was added along with 0.3ml 5% NaNO 2.
After 5 min add 0.3 ml f 10% AlCl3 & further after 5-6 min add 2ml 1M
NaOH.
After the addition of NaOH, the solution turns red color. Incubate/keep at
E.g.
Solvent Evaporation
◦ Using Rota-Evaporator
Salting Out.
Anti Solvent Precipitation
Add 20 ml Of Hexane with continuous stirring. Pass through #100 mesh size
Filter it and collect in vacuum desiccator. Up to Dryness and Break into Mortar
Solvent Evaporation
Using Rota-Evaporator
Soya-phosphatidylcholine + span 80 (90:10)+ Drug
dissolved in ethanol/alcohol.
Multilamellar lipid vesicles (MLV) are then Then the solution was put in a
sonicated at room temperature. round bottom flask.
Final traces are removed under vacuum. The These were then dissolved by shaking. Thin film was
deposited lipid film is hydrated with the then formed by keeping it in a rotator vacuum
appropriate buffer by rotation at 60rpm for 1 hr at evaporator at 40°
room temperature.
Results of Rota Evaporator
Again this method was not used because the desired results were not obtained and the results were unsatisfactory.
Solvent Evaporation
Using Magnetic Stirrer
Preparation of Nanoparticles
a. Place the required amount of lecithin (1-4% w/v) into a small round bottom flask.
b. Add the ethanol (10-50% v/v) containing the drug to the flask.
c. Start the magnetic stirrer to solubilize the lecithin and the drug in the ethanol. Ensure thorough
mixing.
d. Cover the round bottom flask with its lid or an appropriate cover to prevent ethanol evaporation
during stirring.
e. Slowly add distilled water to the mixture while maintaining continuous stirring. This step is crucial to
obtain the colloidal suspension.
Fig:- Magnetic stirrer
f. Continue stirring for a sufficient time until the nanoparticle are formed. This usually takes around 30
minutes at room temperature.
g. After 30 minutes, stop the stirring and let the final nanoparticle suspension sit at room temperature.
1 7 ml 50 ml 10 g 20 ml 1018.6 nm
3 1 ml 15 ml 1g 10 ml 224.4 nm
Results
Trial and error methodology was employed to develop the described procedure for the preparation of colloidal suspensions,
using lecithin, ethanol, and distilled water.
1 1 ml 15 ml 1g 10 ml 491.6 nm
3 1 ml 15 ml 1g 10 ml 252.9 nm
Results for Flavonoid Content for
Hibiscus sabdariffa
0.80 mg/ml
Results Flavonoid Content for
Murraya koenigii
µg of QE /mg of extract.
Therefore the total flavonoid content
observed was 5.55. QE /mg of extract
0.83 mg/ml
Characterization of Nanoparticles
1. SEM
2. DSC
3. ZETA POTENTIAL
4. FTIR
5. NUTRITIONAL EVALUATION
THESE ARE SENT FOR THE EVALUATION RESULTS ARE PENDING.
REFERENCES:-