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DELHI PHARMACEUTICAL SCIENCES AND
RESEARCH UNIVERSITY
FORMULATION AND EVALUATION OF ANTIAGING PHYTOSOMAL GEL
SUPERVISED BY :- PRESENTED BY :-
Dr. MINAKSHI GARG KUMARI SUPRIYA
ASSOCIATE PROFESSOR M.PHARMA COSMECEUTICS
72/MPH/DPSRU/19
IMPACT FACTOR –1.23
CONTENT
 ABSTRACT
 INTRODUCTION OF AGING
 PHYTOSOMES
 MATERIAL & METHODS
 PROCEDURE
 COMPOSITION
 EVALUATION
 RESULTS
 CONCLUSION
 REFERENCES
ABSTRACT
AIM – To prepare and evaluate antiaging phytosomal gel.
METHOD – Coconut water – Cytokinins, Grape seed Extract – Polyphenols and
proanthocyanidin
Aloe Vera Extract – Vitamin C and phenols,
Vitamin E and Jojoba Oil – Antioxidant and Moisturizing properties
Phytosome was prepared by binding herbal extracts to phosphatidylcholine (acts as a carrier
and nourishes the skin). They had a phospholipid molecular structure which included a water-
soluble head and two fat-soluble tails, and due to this dual solubility, it was better absorbed and
so it was used for the treatment of skin disorders, antiaging.
RESULT - F2 containing both tender coconut water and A. Vera extract was chosen as the optimized
formula. Optimization was done on the basis of in vitro antioxidant studies and physicochemical
parameters. F2 acts as a potent free radical scavenger and inhibits oxidation by free radicals.
CONCLUSION - From the present study, it can be concluded that the prepared antiaging phytosomal
gel was safe, convenient, and efficient carrier to deliver the herbal extracts. It also showed better
penetration into the skin. Hence, the desired antiaging property was obtained. Hence, the desired
antiaging property was obtained and is used in skin care cosmetics.
INTRODUCTION
 Aging is the process of becoming older. In humans, ageing represents the accumulation of
changes in a human being over time and can encompass physical, psychological, and social
changes.
 It is signified by progressive deterioration and degeneration of cells and organs.
 According to biologists, aging is a sum of all changes that occur in a living being with the
passage of time and lead to a decreasing ability to survive stress, to functional impairment, and
finally to death.
AETIOLOGY OF SKIN AGING
CLASSIFICATION OF AGING
7 SIGNS OF AGING
PATHOPHYSIOLOGY OF AGING
PHYTOSOMAL ANTIAGING GEL –
Phytosomes are very recent introduction into herbal formulation as they are better absorbed and have higher
bioavailability. The term phyto means “plant” while “some” means cell like. These are advanced forms of herbal
formulation that contains bioactive phyto constituents of herbal extract surrounded by a lipid. Antiaging cream
reduces the wrinkles and blemishes on the skin. Gel is a semisolid preparation with two interpenetrating phases:
A gelling phase and a liquid.
ADVANTAGES OF PHYTOSOMES
1
2
4
3
5
Increases bioavailability
Optimum entrapment efficiency
Efficient nutrient safety
Hepatoprotective
Better stability
MATERIALS AND METHODS
MATERIALS - Tender coconut water was obtained from CDB lab, South Ernakulum. Aloe vera extract was
obtained from Elixir Extracts, Nellad Kochi.
METHODS –
i. Phytosomes are prepared by reacting the herbal extract in an aprotic solvent such as methylene chloride,
dioxane, and ethyl acetate with the phospholipid such as phosphatidylcholine, phosphatidyl ethanolamine,
or phosphatidylserine dissolved in the same solvent.
ii. After solubilization has completed, the complex compounds are isolated by removing the solvent
under vacuum, by freeze drying or by precipitation with non-solvents such as n-hexane.
iii. The obtained complexes are lipophilic in character and soluble in a polar and aprotic solvent, in
which the individual components of the complex are normally insoluble
FORMULATION OF PHYTOSOMES
Phosphatidylcholine
Dissolved in organic solvent containing drug
Hydration
Solution of phospholipid in organic solvent
Solvent evaporation
Formation of thin film
Formation of phytosomal suspension
SOLVENT EVAPORATION METHOD
Drug and Soya Lecithin
Concentrated mixture to 5-10 ml
Obtain the precipitate
Filter and collect
Phytosomes obtained
Refluxed with 20 ml of acetone at a temperature 50-60℃ for 24
hr
FORMULATION OF PHYTOSOMAL GEL
Carbopol 934 was dissolved in distilled water and stored overnight for
complete hydration
Active ingredients are dissolved in propylene glycol
Preservatives are added slowly with continuous stirring
Prepared phytosomes were incorporated into gel.
COMPOSITION
S.No
.
Ingredients F1 F2 F3 F4
1 Carbopol 934 1gram 1gram 1gram 1gram
2 Methyl Paraben 0.2ml 0.2ml 0.2ml 0.2ml
3 Propyl Paraben 0.1ml 0.1ml 0.1ml 0.1ml
4 Propylene Glycol
400
5ml 5ml 5ml 5ml
5 Triethanolamine 1.2ml 1.2ml 1.2ml 1.2ml
6 Tender Coconut
Water
10ml 10ml 10ml 10ml
7 Aloe vera extract 1ml 1ml - -
8 Grape seed extract 0.2gram - 0.2gram -
9 Vitamin E 0.1ml - - 0.1ml
10 Jojoba Oil 0.05ml 0.05ml 0.05ml 0.05ml
EVALUATION
 General Characterisation
I. In-vitro antioxidant studies
II. pH
III. Viscosity
IV. Spreadibility
V. Extrudability
VI. Vesicle Size and Zeta potential
VII. Stability Studies
I. In Vitro Antioxidant Studies
20
mcg/ml
40
mcg/ml
60
mcg/ml
80
mcg/ml
100
Mcg/ml
In Methanol
0.002% DPPH in methanol was used as free radical
Equal volume of different concentrations and
DPPH was mixed
Incubated at room temperature in dark for 30 min
Absorbance was measured at 517 nm
DPPH DPPHH
Yellow indicate scavenging efficiency
Percentage inhibition = [(Abs control – Abs sample) * 100 / (Abs control)]
II. pH of formulation –
1 % solution was made and pH was measured
III. Viscosity
Viscosity was determined by using Brookfield
viscometer at 100 rpm.
IV. Spreadalibity
Two glass slides of 20 cm × 20 cm were selected
A small amount of sample was sandwiched between the two glass slides.
A 100 gram of gel was placed uniformly between two slides
The weight was removed without any disturbance and upper slide was
removed slowly
Time taken in separation of two slides was observed using stop clock
CALCULATION –
S = m × L / T
Where,
S = Spreadability
m = Weight tied to the upper slide
L = Length of the glass
T = Time taken in seconds
V. Extrudability
The gel was filled in collapsible tube and sealed, weight recorded
Weight was done of extruded gel and percentage was calculated
500 gram weight was placed on tube and amount to gel extrude was
collected
VI. Vesicle Size & Zeta Potential
The particle size and zeta potential can be determined by dynamic light scattering (DLS) using a computerized
inspection system and photon correlation spectroscopy.
VII. Stability Studies A/c to ICH Guidelines for Cosmetics
8℃±1℃ 25℃±1℃ 45℃±1℃ 60℃±1℃
75% Relative Humidity
Observed for 60 days
RESULTS
I. In vitro Antioxidant Studies –
II. pH of phytosomal gel –
S.No. Formulations pH
1 F1 6.5
2 F2 6.4
3 F3 6.2
4 F4 6.3
III. Viscosity
IV. Spreadability
V. Extrudability
VII. Vesicle Size & Zeta Potential
VII. Stability Studies
Days Temperature Formulat-
ion
Parameters
pH Viscosity Spreadability Extrudability
0 8 F1 6.5 23108± 32.4±0.2 90.7±0.6
25 F2 6.4 27634± 35.7±0.2 90.9±0.9
45 F3 6.2 30192± 31.2±0.1 92.8±1.1
60 F4 6.3 35628± 35±0.8 92.9±1.3
20 8 F1 6.7 23106± 32.9±0.2 91.7±0.6
25 F2 6.4 27634± 35.8±0.2 90.2±0.9
45 F3 6.4 30195± 31.9±0.1 92.6±1.1
60 F4 6.5 35629± 35±5.8 93.6±1.3
40 8 F1 6.6 23108± 32.4±0.2 90.9±0.6
25 F2 6.4 27634± 35.7±0.2 90.8±0.9
45 F3 6.4 30195± 31.2±0.1 92.9±1.1
60 F4 6.5 35626± 35±0.8 92.1±1.3
60 8 F1 6.6 23109± 32.4±0.2 90.9±0.6
25 F2 6.4 27634± 35.7±0.2 90.9±0.9
45 F3 6.5 30195± 31.2±0.1 93.1±1.1
60 F4 6.5 35628± 35±0.8 93.5±1.3
CONCLUSION
 Antioxidants are the major ingredients present in antiaging cosmetics. The antioxidants
chosen for this study were tender coconut water, A. vera extract, grape seed extract, and
Vitamin E.
 F2 containing both tender coconut water and A. vera extract was chosen as the optimized
formula.
 Characterization studies of the optimized formulation such as vesicle size, size
distribution, and stability were performed, and it was identified that the prepared
antiaging phytosomal gel had all the parameters as optimum.
 Phytosomal gel having coconut water and aloe vera extract has better absorption and
bioavailability in skin.
REFERENCES
 https://www.researchgate.net/publication/323659309_Formulation_and_evaluation_of_antiaging_phyt
osomal_gel.
 https://link.springer.com/article/10.1208/s12249-015-0386-x
 http://repository-tnmgrmu.ac.in/6486/1/260107917_261510901.pdf
 https://rjptonline.org/HTMLPaper.aspx?Journal=Research%20Journal%20of%20Pharmacy%20and%2
0Technology;PID=2013-6-11-15.
 https://ijpsr.com/bft-article/phytosomes-a-novel-drug-delivery-for-herbal-extracts/?view=fulltext
 https://www.longdom.org/open-access/phytosomes-a-modernistic-approach-for-novel-herbal-drug-
delivery-enhancing-bioavailability-and-revealing-endless-frontier-ofphytop-44058.html
 https://www.longdom.org/open-access/phytosomes-a-modernistic-approach-for-novel-herbal-drug-
delivery-enhancing-bioavailability-and-revealing-endless-frontier-ofphytop-44058.html
Antiaging phytosomal gel

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Antiaging phytosomal gel

  • 1. DELHI PHARMACEUTICAL SCIENCES AND RESEARCH UNIVERSITY FORMULATION AND EVALUATION OF ANTIAGING PHYTOSOMAL GEL SUPERVISED BY :- PRESENTED BY :- Dr. MINAKSHI GARG KUMARI SUPRIYA ASSOCIATE PROFESSOR M.PHARMA COSMECEUTICS 72/MPH/DPSRU/19
  • 3. CONTENT  ABSTRACT  INTRODUCTION OF AGING  PHYTOSOMES  MATERIAL & METHODS  PROCEDURE  COMPOSITION  EVALUATION  RESULTS  CONCLUSION  REFERENCES
  • 4. ABSTRACT AIM – To prepare and evaluate antiaging phytosomal gel. METHOD – Coconut water – Cytokinins, Grape seed Extract – Polyphenols and proanthocyanidin Aloe Vera Extract – Vitamin C and phenols, Vitamin E and Jojoba Oil – Antioxidant and Moisturizing properties Phytosome was prepared by binding herbal extracts to phosphatidylcholine (acts as a carrier and nourishes the skin). They had a phospholipid molecular structure which included a water- soluble head and two fat-soluble tails, and due to this dual solubility, it was better absorbed and so it was used for the treatment of skin disorders, antiaging.
  • 5. RESULT - F2 containing both tender coconut water and A. Vera extract was chosen as the optimized formula. Optimization was done on the basis of in vitro antioxidant studies and physicochemical parameters. F2 acts as a potent free radical scavenger and inhibits oxidation by free radicals. CONCLUSION - From the present study, it can be concluded that the prepared antiaging phytosomal gel was safe, convenient, and efficient carrier to deliver the herbal extracts. It also showed better penetration into the skin. Hence, the desired antiaging property was obtained. Hence, the desired antiaging property was obtained and is used in skin care cosmetics.
  • 6. INTRODUCTION  Aging is the process of becoming older. In humans, ageing represents the accumulation of changes in a human being over time and can encompass physical, psychological, and social changes.  It is signified by progressive deterioration and degeneration of cells and organs.  According to biologists, aging is a sum of all changes that occur in a living being with the passage of time and lead to a decreasing ability to survive stress, to functional impairment, and finally to death.
  • 9. 7 SIGNS OF AGING
  • 11. PHYTOSOMAL ANTIAGING GEL – Phytosomes are very recent introduction into herbal formulation as they are better absorbed and have higher bioavailability. The term phyto means “plant” while “some” means cell like. These are advanced forms of herbal formulation that contains bioactive phyto constituents of herbal extract surrounded by a lipid. Antiaging cream reduces the wrinkles and blemishes on the skin. Gel is a semisolid preparation with two interpenetrating phases: A gelling phase and a liquid.
  • 12. ADVANTAGES OF PHYTOSOMES 1 2 4 3 5 Increases bioavailability Optimum entrapment efficiency Efficient nutrient safety Hepatoprotective Better stability
  • 13. MATERIALS AND METHODS MATERIALS - Tender coconut water was obtained from CDB lab, South Ernakulum. Aloe vera extract was obtained from Elixir Extracts, Nellad Kochi. METHODS – i. Phytosomes are prepared by reacting the herbal extract in an aprotic solvent such as methylene chloride, dioxane, and ethyl acetate with the phospholipid such as phosphatidylcholine, phosphatidyl ethanolamine, or phosphatidylserine dissolved in the same solvent.
  • 14. ii. After solubilization has completed, the complex compounds are isolated by removing the solvent under vacuum, by freeze drying or by precipitation with non-solvents such as n-hexane. iii. The obtained complexes are lipophilic in character and soluble in a polar and aprotic solvent, in which the individual components of the complex are normally insoluble
  • 15. FORMULATION OF PHYTOSOMES Phosphatidylcholine Dissolved in organic solvent containing drug Hydration Solution of phospholipid in organic solvent Solvent evaporation Formation of thin film Formation of phytosomal suspension
  • 16. SOLVENT EVAPORATION METHOD Drug and Soya Lecithin Concentrated mixture to 5-10 ml Obtain the precipitate Filter and collect Phytosomes obtained Refluxed with 20 ml of acetone at a temperature 50-60℃ for 24 hr
  • 17. FORMULATION OF PHYTOSOMAL GEL Carbopol 934 was dissolved in distilled water and stored overnight for complete hydration Active ingredients are dissolved in propylene glycol Preservatives are added slowly with continuous stirring Prepared phytosomes were incorporated into gel.
  • 18. COMPOSITION S.No . Ingredients F1 F2 F3 F4 1 Carbopol 934 1gram 1gram 1gram 1gram 2 Methyl Paraben 0.2ml 0.2ml 0.2ml 0.2ml 3 Propyl Paraben 0.1ml 0.1ml 0.1ml 0.1ml 4 Propylene Glycol 400 5ml 5ml 5ml 5ml 5 Triethanolamine 1.2ml 1.2ml 1.2ml 1.2ml 6 Tender Coconut Water 10ml 10ml 10ml 10ml 7 Aloe vera extract 1ml 1ml - - 8 Grape seed extract 0.2gram - 0.2gram - 9 Vitamin E 0.1ml - - 0.1ml 10 Jojoba Oil 0.05ml 0.05ml 0.05ml 0.05ml
  • 19. EVALUATION  General Characterisation I. In-vitro antioxidant studies II. pH III. Viscosity IV. Spreadibility V. Extrudability VI. Vesicle Size and Zeta potential VII. Stability Studies
  • 20. I. In Vitro Antioxidant Studies 20 mcg/ml 40 mcg/ml 60 mcg/ml 80 mcg/ml 100 Mcg/ml In Methanol 0.002% DPPH in methanol was used as free radical Equal volume of different concentrations and DPPH was mixed
  • 21. Incubated at room temperature in dark for 30 min Absorbance was measured at 517 nm DPPH DPPHH Yellow indicate scavenging efficiency Percentage inhibition = [(Abs control – Abs sample) * 100 / (Abs control)]
  • 22. II. pH of formulation – 1 % solution was made and pH was measured
  • 23. III. Viscosity Viscosity was determined by using Brookfield viscometer at 100 rpm.
  • 24. IV. Spreadalibity Two glass slides of 20 cm × 20 cm were selected A small amount of sample was sandwiched between the two glass slides. A 100 gram of gel was placed uniformly between two slides The weight was removed without any disturbance and upper slide was removed slowly Time taken in separation of two slides was observed using stop clock
  • 25. CALCULATION – S = m × L / T Where, S = Spreadability m = Weight tied to the upper slide L = Length of the glass T = Time taken in seconds
  • 26. V. Extrudability The gel was filled in collapsible tube and sealed, weight recorded Weight was done of extruded gel and percentage was calculated 500 gram weight was placed on tube and amount to gel extrude was collected
  • 27. VI. Vesicle Size & Zeta Potential The particle size and zeta potential can be determined by dynamic light scattering (DLS) using a computerized inspection system and photon correlation spectroscopy.
  • 28. VII. Stability Studies A/c to ICH Guidelines for Cosmetics 8℃±1℃ 25℃±1℃ 45℃±1℃ 60℃±1℃ 75% Relative Humidity Observed for 60 days
  • 29. RESULTS I. In vitro Antioxidant Studies –
  • 30. II. pH of phytosomal gel – S.No. Formulations pH 1 F1 6.5 2 F2 6.4 3 F3 6.2 4 F4 6.3
  • 34. VII. Vesicle Size & Zeta Potential
  • 35.
  • 36. VII. Stability Studies Days Temperature Formulat- ion Parameters pH Viscosity Spreadability Extrudability 0 8 F1 6.5 23108± 32.4±0.2 90.7±0.6 25 F2 6.4 27634± 35.7±0.2 90.9±0.9 45 F3 6.2 30192± 31.2±0.1 92.8±1.1 60 F4 6.3 35628± 35±0.8 92.9±1.3 20 8 F1 6.7 23106± 32.9±0.2 91.7±0.6 25 F2 6.4 27634± 35.8±0.2 90.2±0.9 45 F3 6.4 30195± 31.9±0.1 92.6±1.1 60 F4 6.5 35629± 35±5.8 93.6±1.3 40 8 F1 6.6 23108± 32.4±0.2 90.9±0.6 25 F2 6.4 27634± 35.7±0.2 90.8±0.9 45 F3 6.4 30195± 31.2±0.1 92.9±1.1 60 F4 6.5 35626± 35±0.8 92.1±1.3 60 8 F1 6.6 23109± 32.4±0.2 90.9±0.6 25 F2 6.4 27634± 35.7±0.2 90.9±0.9 45 F3 6.5 30195± 31.2±0.1 93.1±1.1 60 F4 6.5 35628± 35±0.8 93.5±1.3
  • 37. CONCLUSION  Antioxidants are the major ingredients present in antiaging cosmetics. The antioxidants chosen for this study were tender coconut water, A. vera extract, grape seed extract, and Vitamin E.  F2 containing both tender coconut water and A. vera extract was chosen as the optimized formula.  Characterization studies of the optimized formulation such as vesicle size, size distribution, and stability were performed, and it was identified that the prepared antiaging phytosomal gel had all the parameters as optimum.  Phytosomal gel having coconut water and aloe vera extract has better absorption and bioavailability in skin.
  • 38. REFERENCES  https://www.researchgate.net/publication/323659309_Formulation_and_evaluation_of_antiaging_phyt osomal_gel.  https://link.springer.com/article/10.1208/s12249-015-0386-x  http://repository-tnmgrmu.ac.in/6486/1/260107917_261510901.pdf  https://rjptonline.org/HTMLPaper.aspx?Journal=Research%20Journal%20of%20Pharmacy%20and%2 0Technology;PID=2013-6-11-15.  https://ijpsr.com/bft-article/phytosomes-a-novel-drug-delivery-for-herbal-extracts/?view=fulltext  https://www.longdom.org/open-access/phytosomes-a-modernistic-approach-for-novel-herbal-drug- delivery-enhancing-bioavailability-and-revealing-endless-frontier-ofphytop-44058.html  https://www.longdom.org/open-access/phytosomes-a-modernistic-approach-for-novel-herbal-drug- delivery-enhancing-bioavailability-and-revealing-endless-frontier-ofphytop-44058.html