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Formulation and Evaluation of
Herbal Transdermal Patches
By:-SAILI .P. RAJPUT
Guided By:-RUPESH .B. KHALSE
CONTENT
1. Introduction and History of Transdermal
Drug Delivery System
2. Introduction to Anatomy of Skin
3. Transdermal Patches
4. Components of Transdermal Patches
5. Types of Transdermal Patches
6. Factors Affecting the T D Patches
7. Mechanism of Drug Release From
Transdermal Patches
8. Advantages and Disadvantages of TD
Patches
9. New Approaches in Transdermal Drug
Delivery System
10. Introduction to Wound Healing
11. Role of Herbal Plants in Wound Healing
12. Formulation Of Herbal Transdermal
Patches
13. Evaluation Test For Formulated Patches
14. Results
15. Conclusion
Introduction and History of Transdermal Drug
Delivery System
• The Transdermal Drug Delivery System Aims in Drug Targeting and Controlled Release of Drug.
• Transdermal Drug Delivery system of Novel Drug Delivery System which also involves various drug
delivery systems like Sustain Release system , Delayed release System, Targeted release system,
Modified release system, Extended release system and many more.
• The Transdermal drug delivery system is used to produce clinical effects like local anesthesia and anti-
inflammatory activities.
• TDDS has a very wide scope now-a-days because it has many advantages over old and traditional drug
delivery systems.
• There are wide scope for new innovations in TDDS as is its developing in medical field
• TDDS tends to enhance the Bioavailability of and drug and also Bypass the First Pass Metabolism.
• TDDS helps to maintain the drug concentration in given therapeutic window for the Prolonged effect of
desired drug.
Continued…
• GALEN a Greek physician introduced the compounding of herbal drugs and other excipients in
dosage form.
• He is widely considered to be “FATHER OF PHARMACY”. And his work and practices are
called as “GALEN PHARMACY”.
• The concept that certain drugs cross the skin appears to have been applied by Ibn Sina (AD 980-
1037) a Persian physician.
• In 1904, Schwenkenbecker generalized that skin was relatively permeable to lipid soluble
substance but not to water and electrolytes.
• Dale Wruster and his student Sherman Kramer stated that the absorption can be enhanced or
modified by varying the diffusion area of cell by changing the level of skin hydration.
• Scopolamine (Hyoscine) patch for treatment of motion sickness was the First Transdermal Patch to
reach the market.
• Then after scopolamine Nitro-glycerine patches for Angina pectoris were evolved.
• Before marketing the transdermal scopolamine patches the nitro-glycerine ointments was the only
transdermal product of nitro-glycerine.
INTRODUCTION TO SKIN ANATOMY
• EPIDERMIS:- It is a keratinized stratified
squamous epithelial layer which is derived from
ectoderm and forms outermost layer of skin.
Epidermis is composed of various layers like
stratum corneum, stratum lucidium, stratum
granulosum, stratum spinosum.
1. STRATUM CORNEUM: - It is the outermost layer
of epidermis. The stratum corneum layer
prevents both penetration of substance from
environment and insensible loss of body water
from surface to the environment.
2. STRATUM LUCIDIUM: -This layer contains of
translucent thin zone between stratum
granulosum and corneum layer.
3. STRATUM GRANULOSUM: - This layer contains
3-5 layers of flat cells and also has irregular
shaped, non-membrane bound granules
4. STRATUM SPINOSUM: - This has several layers
of irregular polyhedral shaped cells
• DERMIS:- Dermis is composed of network of
collagen and elastin fibres embedded in
mucopolysaccharides matrix which contains
blood vessels, lymphatic nerve endings, etc.
Dermis is a mesodermal in origin which support
to epidermis. Dermis is approx. 3-5 mm thick
layer.
TRANSDERMAL PATCHES
• Transdermal patches are a mediated adhesive patch which have coating of drug and is then placed on skin to
deliver the drug in the blood stream through the skin.
• The delivery technology like TDDS helps to enhance the convenience for patients and also increases their
effectiveness and protection of drug.
• Transdermal patches are formulated mainly to deliver drug through skin which diffuse through various skin
layer and reach systemic circulation i.e., blood.
• To resolve and address the various problems generated by use of old conventional methods the controlled
release of drug delivery and novel drug delivery systems are evolved.
• TDDS patches are defined as self-contained dosage form which when applied to the skin and deliver the
drug through the skin and drug reach the systemic circulation at the controlled rate for prolonged period.
COMPONENTS OF
TRANSDERMAL PATCHES
Sr
No.
Components Role Example
1. Polymer
Matrix
To release drug from
patches
PVP,PVC,Star
ch
2. Active agent Therapeutic Effect Any desired
drug
3. Penetration
Enhancer
Enhance permeation
enhancing skin
function
SLS, Ethanol
etc.
4. Plasticizer Reduce Brittleness of
Patches
Propylene
Glycol
5. Drug
Reservoir
Its combination of
polymers
1-2 polymers
6. Backing
Membrane
Gives strength and
support
Aluminum
Foil
7. Adhesive layer Helps adhere to skin -
8. Release Liner Act as Protective
Layer
Teflon, silicon
etc.
TYPES OF TRANSDERMAL PATCHES
1. SINGLE LAYER PATCHES :- Here the adhesive layer not only serves to adhere the various
layers together along entire system to skin but also helps and is responsible for drug release from the
patch. This adhesive is also surrounded by the backing laminate and release liner.
2. MULTI LAYER PATCHES:- These patches are similar to single layer patches. It consists more
than one layer. One of the layers is for immediate release of the drug and other one is for control
release of the drug
3. RESERVOIR:- In this patch there is a separated drug layer. The drug layer is a liquid compartment
containing a drug solution or suspensions. Here the drug compartment is totally encapsulated in
shallow compartment
4. MATRIX:- The Matrix system has a drug layer of semisolid matrix which contains drug in solution
or suspension form. This is also called as monolithic device.
5. VAPOUR PATCH:- In this patch the adhesive layer carries out two roles one to adhere the various
layers and other one to release the vapours. This vapour patches are mainly and widely used for
decongestion. Other vapour patches are formulated to enhance the quality of sleep and as an aid for
smoking cessation.
FACTORS AFFECTING TD PATCHES
A. Physiochemical
properties of
penetrant
• Partition Coefficient
• Ph condition
• Composition of
Drug
A.B. Physiochemical
properties of delivery
system
• Affinity of vehicle
and drug molecule
• Composition of drug
delivery system
• Enhancement of TD
Permeation
A.C. Physiological
and pathological Skin
conditions
• Skin Age
• Lipid Film
• Skin Hydration
• Skin Temperature
• Species Difference
MECHANISM OF DRUG RELEASE FROM
TRANSDERMAL PATCHES
ADVANTAGES AND DISADVANTAGES OF TD
PATCHES
ADVANTAGES
1. Maintain Steady Infusion of Drug for prolonged time.
2. Alternate dosage form for patient who cant tolerate oral
dosage from.
3. Increase Therapeutic Value of Drug.
4. Helps to Increase Patient Compliance.
5. Bypass the First Pass Metabolism.
6. Helps to minimize the Fluctuation in Physiological and
pharmacological response.
7. Helps in Easy termination of drug Therapy.
8. Provide Extended Therapy with Single Application.
9. Helps to reduce Side Effects associated with Parenteral
Dosage Form.
DISADVANTAGES
1. Drug with High Molecular weight is difficult to
penetrate stratum corneum.
2. In TDDS the Drug Dose is a Limitation Factor.
3. If Drug which metabolize in liver and if given
through Transdermal route then results in Low
Bioavailability.
4. Drug which cause Local or Systemic Irritations
are not suitable for Transdermal drug delivery
system.
5. Only Potent drugs can be Incorporated through
Transdermal Drug Delivery System.
DIFFERENCE BETWEEN TRANSDERMALAND
TOPICAL FORMULATIONS
Topical Formulation
1. This works on Surface of Skin and do not reach
Blood Stream or Systemic Circulation.
2. For Example:- Hydrocortisone Ointment For Skin
Rashes.
3. Topical Formulation Are Creams, Ointments,
Lotions, Sprays, Foam, Powder etc.
4. These Formulation Cant Avoid First Pass
Metabolism.
5. There are some chances for Occurrence of Skin
Irritations and Rashes.
6. Drug Given through Topical route Show
Superficial Action.
7. This Drug Absorbed do not reach systemic
circulation so do not show a prolonged action.
Transdermal Formulation
1. Transdermal Medication Penetrates The Skin and
Enters Blood and also Distribute Through Whole
Bloodstream.
2. For Example:- Nitro-Glycerin Patches to treat Chest
Pain.
3. Transdermal Formulation are Patches, Nanogels,
Pastes.
4. Transdermal Formulation Bypass and Avoid First Pass
Metabolism.
5. It Helps to maintain Adverse drug reaction due to Low
Drug Concentration.
6. Here Drug Penetrates Deep Inside The Layers of
Tissues.
7. Patches do not Enhance Drug Molecule But Increase
Drug Absorption by Prolong Application of patches.
New Approaches in Transdermal Drug Delivery System
1. IONTOPHORESIS: - Iontophoresis is defined as facilitation of drug
permeation across skin by applying electrode.
2. ELECTROPORATION: - There is formation of small pores with the help
of electric pulses in stratum corneum through which drug is transported.
3. PHOTOMECHANICAL WAVE: - This wave makes stratum corneum
permeable to drug by developing transient channel.
4. MEDICATED TATTOOS: - This are also called as Med-Tats. Med-Tats
contains active drug substance. So, manufacturer gives colour chart which is
then compared with patients tattoo to analyse when tattoo is to be removed.
5. MICRONEEDLE: -This was seen or observed first in 1976. Microneedle
which are 50-100mm long are used.
6. SKIN ABRASSION: - Here there is removal and destruction of upper layer
of skin to enhance the permeation of medicament.
7. LASER RADIATION: - In this there is a direct use and exposure of laser to
skin which results in ablation of stratum corneum without any damage
caused to epidermis this is beneficial for lipophilic or hydrophilic drugs
delivery.
8. ULTRASOUND: - Here there is use of low frequency ultrasound for
average 15 seconds to enhance the permeation of skin.
INTRODUCTION TO WOUND HEALING
1. Wound is Defined as Lesions on skin or Rupture of Skin Surface which
is caused by Various Physical and Thermal Trauma.
2. Skin Wounds are typically of 2 types and they are Acute Wounds and
Chronic Wounds .
3. Acute wounds are traumatic or surgical wounds which normally heal due
to normal healing procedure.
4. Wound Healing involves 4 main steps i.e. HAEMOSTASIS,
INFAMATION, PROLIFERATION and REMODELLING.
5. Skin serves as protective barrier against Physical and chemical threats.
The Wound site is under pressure and thus superficial skin wound is
practically never sterile.
6. The paramount cellular signaling in wound healing are controlled by
different types of growth factors.
7. There are many factors which affects the quality of wound healing and
they are Blood flow in that particular area, Wound size, Microbial attack,
Age and nutrition related patient.
Steps of Wound Healing
1. Haemostasis: - Haemostasis is process of the wound healing closed by clotting. Haemostasis
starts when blood leaks out of the body. The first step of haemostasis is when blood vessels
constrict to restrict the blood flow. Next, platelets stick together in order to seal the break in the
wall of blood vessels. The haemostasis stage of wound healing happens very quickly.
2. Inflammation: - Inflammation controls both bleeding and prevents infection. The fluid
engorgement allows healing and repairs cells to move to site of wound. During this phase
damaged cells, pathogens and bacteria are removed from wound area. Prolonged inflammation
retards healing due to excessive level of protease and reactive oxygen that destroy essential
factors.
3. Proliferation: - Proliferative phase of wound healing is when the wound is rebuilt with new
tissues made up of collagen and matrix. A new network of blood vessels must be constructed.
Fibroblasts supported by new capillaries, proliferate and synthesize disorganized ECM.
4. Remodelling: - Also called as maturation phase. In this phase collagen is remodelled from
type 3 to type1 and wound fully closes. During maturation phase collagen is aligned along
tension lines and water is reabsorbed so that collagen fibres can lie and cross link.
ROLE OF HERBAL PLANTS IN WOUND
HEALING
TULSI[Ocimum Sanctum]
1. The chemical composition of tulsi is complex
due to Prescence of many nutrients.
2. The stem and leaves contains saponin,
Flavonoids, Tannins and Volatile oils.
3. The tulsi extract increase the wound healing
breaking strength and wound contraction is also
increased.
4. Tulsi also shows Anti-oxidant property which is
helpful in wound healing. Leaves of tulsi shows
Anti-inflammatory and Analgesic Action.
5. Tulsi extract also shows Anti-Bacterial, Anti-
Fungal, Anti-Inflammatory Actions which is
Beneficial in wound healing.
6. Volatile oils like eugenol has enzyme inhibitory
action and strengthen the Immune System.
ALOEVERA[Aloe Barbadense]
1. Aloe vera is known for its Anti-Tumor , Anti-
inflammatory, Anti-Viral, Anti-Bacterial, Wound
healing actions.
2. Aloe vera is beneficial in treating wounds like
Psoriasis, Mouth sire, burn wounds.
3. Aloe vera is effective in inhibiting inflammatory
reaction by inhibiting the IL-6 and IL-8 and also
reduce the adhesion of WBC and Decrease the
TNF-α Levels.
4. The mucopolysaccharides along with amino acods
present in aloe results in Skin integrity, Moisture
retention, and helps to prevent skin ulcers.
5. The mucilage of aloe vera consist some
glycoproteins which stimulate skin growth and
also healing process of wounds.
FORMULATION OF HERBAL TRANSDERMAL
PATCHES
1. Initially weigh the required ingredients for the formulation.
2. Then add 8 ml chloroform and 4 ml methanol in the beaker and
mix them properly using the electric stirrer or Magnetic stirrer.
3. Then add 2.5 ml Propylene Glycol and 2.5 ml Polyethylene
Glycol and again stir it continuously using electric or magnetic
stirrer.
4. Each medicinal plant extract i.e., 5 ml Tulsi extract and 5 ml Aloe
vera extract were added with constant stirring for 10-15 minutes.
5. Now then add HPMC with constant stirring using electric stirrer.
But Add 1 gm HPMC at the Time Interval of 1 minute.
6. After time period of 10-15 minutes when the formulation becomes
viscous then was added to the glass petri plates which were coated
using the Aluminium Foil.
7. Then the petri plate was placed in the Hot Air Oven at 50 degrees
for certain time period for the Evaporation of solvent.
Sr
No.
NAME OF INGRIDIENTS QUANTITY REQUIRED
1. Aloe Vera Extract 5 ml
2. Tulsi Extract 5ml
3. Polyethylene Glycol-400 2.5 ml
4. Propylene Glycol 2.5 ml
5. HPMC 5 gm
6. Chloroform 8 ml
7. Methanol 4 ml
EVALUATION TEST FOR TRANSDERMAL
PATCHES
• The various evaluation test was being performed on laboratory level for
the evaluation of formulated transdermal patches. Following are the Test
performed: -
1. Organoleptic Characteristics
2. Surface Ph Determination
3. Phytochemical Screening of Tulsi
4. Phytochemical Screening of Aloe vera
5. Measurement Of Thickness of patches
6. UV Spectroscopy
7. % Moisture content
RESULTS
SR.NO CHARECTERISTIC OBSERVATION
1. COLOUR Whitish cream
2. TEXTURE Smooth and
Uniform
3. APPEREANCE Turbid
4. ODOUR Herbal
Extract
5. PH 5-9
6. THICKNESS 0.22mm
7. MOISTURE
CONTENT
50%
8. UV
ABSORBANCE
2.25Abs
CONCLUSION
• The Transdermal patches with the incorporation of herbal extract of Ocimum Sanctum
and Aloe barbadense were Formulated.
• The Herbal transdermal Patches including aloe and tulsi were aimed to heal the wound or
any type of injury or the skin infection like eczema etc.
• The Evaluation studies states that the patches have the optimum thickness and is within
the suitable range of Ph.
• In the various research its seen that transdermal drug delivery system has great scope in
future for developing drug delivery system in NDDS.
• Transdermal drug delivery system is widely accepted now-a-days because it causes the
drug penetration through skin layers and reach systemic circulation without causing any
damage to skin or rupturing it. TDDS also benefits for controlled release of drug for
prolonged period of time.
• More research and innovation will bring the wide acceptance in the use of various other
transdermal drug delivery system like iontophoresis, Ultrasound technology, Med Tat etc.
HERBAL TRANSDERMAL PATCHES By SAILI. P. RAJPUT

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HERBAL TRANSDERMAL PATCHES By SAILI. P. RAJPUT

  • 1. Formulation and Evaluation of Herbal Transdermal Patches By:-SAILI .P. RAJPUT Guided By:-RUPESH .B. KHALSE
  • 2. CONTENT 1. Introduction and History of Transdermal Drug Delivery System 2. Introduction to Anatomy of Skin 3. Transdermal Patches 4. Components of Transdermal Patches 5. Types of Transdermal Patches 6. Factors Affecting the T D Patches 7. Mechanism of Drug Release From Transdermal Patches 8. Advantages and Disadvantages of TD Patches 9. New Approaches in Transdermal Drug Delivery System 10. Introduction to Wound Healing 11. Role of Herbal Plants in Wound Healing 12. Formulation Of Herbal Transdermal Patches 13. Evaluation Test For Formulated Patches 14. Results 15. Conclusion
  • 3. Introduction and History of Transdermal Drug Delivery System • The Transdermal Drug Delivery System Aims in Drug Targeting and Controlled Release of Drug. • Transdermal Drug Delivery system of Novel Drug Delivery System which also involves various drug delivery systems like Sustain Release system , Delayed release System, Targeted release system, Modified release system, Extended release system and many more. • The Transdermal drug delivery system is used to produce clinical effects like local anesthesia and anti- inflammatory activities. • TDDS has a very wide scope now-a-days because it has many advantages over old and traditional drug delivery systems. • There are wide scope for new innovations in TDDS as is its developing in medical field • TDDS tends to enhance the Bioavailability of and drug and also Bypass the First Pass Metabolism. • TDDS helps to maintain the drug concentration in given therapeutic window for the Prolonged effect of desired drug.
  • 4. Continued… • GALEN a Greek physician introduced the compounding of herbal drugs and other excipients in dosage form. • He is widely considered to be “FATHER OF PHARMACY”. And his work and practices are called as “GALEN PHARMACY”. • The concept that certain drugs cross the skin appears to have been applied by Ibn Sina (AD 980- 1037) a Persian physician. • In 1904, Schwenkenbecker generalized that skin was relatively permeable to lipid soluble substance but not to water and electrolytes. • Dale Wruster and his student Sherman Kramer stated that the absorption can be enhanced or modified by varying the diffusion area of cell by changing the level of skin hydration. • Scopolamine (Hyoscine) patch for treatment of motion sickness was the First Transdermal Patch to reach the market. • Then after scopolamine Nitro-glycerine patches for Angina pectoris were evolved. • Before marketing the transdermal scopolamine patches the nitro-glycerine ointments was the only transdermal product of nitro-glycerine.
  • 5. INTRODUCTION TO SKIN ANATOMY • EPIDERMIS:- It is a keratinized stratified squamous epithelial layer which is derived from ectoderm and forms outermost layer of skin. Epidermis is composed of various layers like stratum corneum, stratum lucidium, stratum granulosum, stratum spinosum. 1. STRATUM CORNEUM: - It is the outermost layer of epidermis. The stratum corneum layer prevents both penetration of substance from environment and insensible loss of body water from surface to the environment. 2. STRATUM LUCIDIUM: -This layer contains of translucent thin zone between stratum granulosum and corneum layer. 3. STRATUM GRANULOSUM: - This layer contains 3-5 layers of flat cells and also has irregular shaped, non-membrane bound granules 4. STRATUM SPINOSUM: - This has several layers of irregular polyhedral shaped cells • DERMIS:- Dermis is composed of network of collagen and elastin fibres embedded in mucopolysaccharides matrix which contains blood vessels, lymphatic nerve endings, etc. Dermis is a mesodermal in origin which support to epidermis. Dermis is approx. 3-5 mm thick layer.
  • 6. TRANSDERMAL PATCHES • Transdermal patches are a mediated adhesive patch which have coating of drug and is then placed on skin to deliver the drug in the blood stream through the skin. • The delivery technology like TDDS helps to enhance the convenience for patients and also increases their effectiveness and protection of drug. • Transdermal patches are formulated mainly to deliver drug through skin which diffuse through various skin layer and reach systemic circulation i.e., blood. • To resolve and address the various problems generated by use of old conventional methods the controlled release of drug delivery and novel drug delivery systems are evolved. • TDDS patches are defined as self-contained dosage form which when applied to the skin and deliver the drug through the skin and drug reach the systemic circulation at the controlled rate for prolonged period.
  • 7. COMPONENTS OF TRANSDERMAL PATCHES Sr No. Components Role Example 1. Polymer Matrix To release drug from patches PVP,PVC,Star ch 2. Active agent Therapeutic Effect Any desired drug 3. Penetration Enhancer Enhance permeation enhancing skin function SLS, Ethanol etc. 4. Plasticizer Reduce Brittleness of Patches Propylene Glycol 5. Drug Reservoir Its combination of polymers 1-2 polymers 6. Backing Membrane Gives strength and support Aluminum Foil 7. Adhesive layer Helps adhere to skin - 8. Release Liner Act as Protective Layer Teflon, silicon etc.
  • 8. TYPES OF TRANSDERMAL PATCHES 1. SINGLE LAYER PATCHES :- Here the adhesive layer not only serves to adhere the various layers together along entire system to skin but also helps and is responsible for drug release from the patch. This adhesive is also surrounded by the backing laminate and release liner. 2. MULTI LAYER PATCHES:- These patches are similar to single layer patches. It consists more than one layer. One of the layers is for immediate release of the drug and other one is for control release of the drug 3. RESERVOIR:- In this patch there is a separated drug layer. The drug layer is a liquid compartment containing a drug solution or suspensions. Here the drug compartment is totally encapsulated in shallow compartment 4. MATRIX:- The Matrix system has a drug layer of semisolid matrix which contains drug in solution or suspension form. This is also called as monolithic device. 5. VAPOUR PATCH:- In this patch the adhesive layer carries out two roles one to adhere the various layers and other one to release the vapours. This vapour patches are mainly and widely used for decongestion. Other vapour patches are formulated to enhance the quality of sleep and as an aid for smoking cessation.
  • 9. FACTORS AFFECTING TD PATCHES A. Physiochemical properties of penetrant • Partition Coefficient • Ph condition • Composition of Drug A.B. Physiochemical properties of delivery system • Affinity of vehicle and drug molecule • Composition of drug delivery system • Enhancement of TD Permeation A.C. Physiological and pathological Skin conditions • Skin Age • Lipid Film • Skin Hydration • Skin Temperature • Species Difference
  • 10. MECHANISM OF DRUG RELEASE FROM TRANSDERMAL PATCHES
  • 11. ADVANTAGES AND DISADVANTAGES OF TD PATCHES ADVANTAGES 1. Maintain Steady Infusion of Drug for prolonged time. 2. Alternate dosage form for patient who cant tolerate oral dosage from. 3. Increase Therapeutic Value of Drug. 4. Helps to Increase Patient Compliance. 5. Bypass the First Pass Metabolism. 6. Helps to minimize the Fluctuation in Physiological and pharmacological response. 7. Helps in Easy termination of drug Therapy. 8. Provide Extended Therapy with Single Application. 9. Helps to reduce Side Effects associated with Parenteral Dosage Form. DISADVANTAGES 1. Drug with High Molecular weight is difficult to penetrate stratum corneum. 2. In TDDS the Drug Dose is a Limitation Factor. 3. If Drug which metabolize in liver and if given through Transdermal route then results in Low Bioavailability. 4. Drug which cause Local or Systemic Irritations are not suitable for Transdermal drug delivery system. 5. Only Potent drugs can be Incorporated through Transdermal Drug Delivery System.
  • 12. DIFFERENCE BETWEEN TRANSDERMALAND TOPICAL FORMULATIONS Topical Formulation 1. This works on Surface of Skin and do not reach Blood Stream or Systemic Circulation. 2. For Example:- Hydrocortisone Ointment For Skin Rashes. 3. Topical Formulation Are Creams, Ointments, Lotions, Sprays, Foam, Powder etc. 4. These Formulation Cant Avoid First Pass Metabolism. 5. There are some chances for Occurrence of Skin Irritations and Rashes. 6. Drug Given through Topical route Show Superficial Action. 7. This Drug Absorbed do not reach systemic circulation so do not show a prolonged action. Transdermal Formulation 1. Transdermal Medication Penetrates The Skin and Enters Blood and also Distribute Through Whole Bloodstream. 2. For Example:- Nitro-Glycerin Patches to treat Chest Pain. 3. Transdermal Formulation are Patches, Nanogels, Pastes. 4. Transdermal Formulation Bypass and Avoid First Pass Metabolism. 5. It Helps to maintain Adverse drug reaction due to Low Drug Concentration. 6. Here Drug Penetrates Deep Inside The Layers of Tissues. 7. Patches do not Enhance Drug Molecule But Increase Drug Absorption by Prolong Application of patches.
  • 13. New Approaches in Transdermal Drug Delivery System 1. IONTOPHORESIS: - Iontophoresis is defined as facilitation of drug permeation across skin by applying electrode. 2. ELECTROPORATION: - There is formation of small pores with the help of electric pulses in stratum corneum through which drug is transported. 3. PHOTOMECHANICAL WAVE: - This wave makes stratum corneum permeable to drug by developing transient channel. 4. MEDICATED TATTOOS: - This are also called as Med-Tats. Med-Tats contains active drug substance. So, manufacturer gives colour chart which is then compared with patients tattoo to analyse when tattoo is to be removed. 5. MICRONEEDLE: -This was seen or observed first in 1976. Microneedle which are 50-100mm long are used. 6. SKIN ABRASSION: - Here there is removal and destruction of upper layer of skin to enhance the permeation of medicament. 7. LASER RADIATION: - In this there is a direct use and exposure of laser to skin which results in ablation of stratum corneum without any damage caused to epidermis this is beneficial for lipophilic or hydrophilic drugs delivery. 8. ULTRASOUND: - Here there is use of low frequency ultrasound for average 15 seconds to enhance the permeation of skin.
  • 14. INTRODUCTION TO WOUND HEALING 1. Wound is Defined as Lesions on skin or Rupture of Skin Surface which is caused by Various Physical and Thermal Trauma. 2. Skin Wounds are typically of 2 types and they are Acute Wounds and Chronic Wounds . 3. Acute wounds are traumatic or surgical wounds which normally heal due to normal healing procedure. 4. Wound Healing involves 4 main steps i.e. HAEMOSTASIS, INFAMATION, PROLIFERATION and REMODELLING. 5. Skin serves as protective barrier against Physical and chemical threats. The Wound site is under pressure and thus superficial skin wound is practically never sterile. 6. The paramount cellular signaling in wound healing are controlled by different types of growth factors. 7. There are many factors which affects the quality of wound healing and they are Blood flow in that particular area, Wound size, Microbial attack, Age and nutrition related patient.
  • 15. Steps of Wound Healing 1. Haemostasis: - Haemostasis is process of the wound healing closed by clotting. Haemostasis starts when blood leaks out of the body. The first step of haemostasis is when blood vessels constrict to restrict the blood flow. Next, platelets stick together in order to seal the break in the wall of blood vessels. The haemostasis stage of wound healing happens very quickly. 2. Inflammation: - Inflammation controls both bleeding and prevents infection. The fluid engorgement allows healing and repairs cells to move to site of wound. During this phase damaged cells, pathogens and bacteria are removed from wound area. Prolonged inflammation retards healing due to excessive level of protease and reactive oxygen that destroy essential factors. 3. Proliferation: - Proliferative phase of wound healing is when the wound is rebuilt with new tissues made up of collagen and matrix. A new network of blood vessels must be constructed. Fibroblasts supported by new capillaries, proliferate and synthesize disorganized ECM. 4. Remodelling: - Also called as maturation phase. In this phase collagen is remodelled from type 3 to type1 and wound fully closes. During maturation phase collagen is aligned along tension lines and water is reabsorbed so that collagen fibres can lie and cross link.
  • 16. ROLE OF HERBAL PLANTS IN WOUND HEALING TULSI[Ocimum Sanctum] 1. The chemical composition of tulsi is complex due to Prescence of many nutrients. 2. The stem and leaves contains saponin, Flavonoids, Tannins and Volatile oils. 3. The tulsi extract increase the wound healing breaking strength and wound contraction is also increased. 4. Tulsi also shows Anti-oxidant property which is helpful in wound healing. Leaves of tulsi shows Anti-inflammatory and Analgesic Action. 5. Tulsi extract also shows Anti-Bacterial, Anti- Fungal, Anti-Inflammatory Actions which is Beneficial in wound healing. 6. Volatile oils like eugenol has enzyme inhibitory action and strengthen the Immune System. ALOEVERA[Aloe Barbadense] 1. Aloe vera is known for its Anti-Tumor , Anti- inflammatory, Anti-Viral, Anti-Bacterial, Wound healing actions. 2. Aloe vera is beneficial in treating wounds like Psoriasis, Mouth sire, burn wounds. 3. Aloe vera is effective in inhibiting inflammatory reaction by inhibiting the IL-6 and IL-8 and also reduce the adhesion of WBC and Decrease the TNF-α Levels. 4. The mucopolysaccharides along with amino acods present in aloe results in Skin integrity, Moisture retention, and helps to prevent skin ulcers. 5. The mucilage of aloe vera consist some glycoproteins which stimulate skin growth and also healing process of wounds.
  • 17. FORMULATION OF HERBAL TRANSDERMAL PATCHES 1. Initially weigh the required ingredients for the formulation. 2. Then add 8 ml chloroform and 4 ml methanol in the beaker and mix them properly using the electric stirrer or Magnetic stirrer. 3. Then add 2.5 ml Propylene Glycol and 2.5 ml Polyethylene Glycol and again stir it continuously using electric or magnetic stirrer. 4. Each medicinal plant extract i.e., 5 ml Tulsi extract and 5 ml Aloe vera extract were added with constant stirring for 10-15 minutes. 5. Now then add HPMC with constant stirring using electric stirrer. But Add 1 gm HPMC at the Time Interval of 1 minute. 6. After time period of 10-15 minutes when the formulation becomes viscous then was added to the glass petri plates which were coated using the Aluminium Foil. 7. Then the petri plate was placed in the Hot Air Oven at 50 degrees for certain time period for the Evaporation of solvent. Sr No. NAME OF INGRIDIENTS QUANTITY REQUIRED 1. Aloe Vera Extract 5 ml 2. Tulsi Extract 5ml 3. Polyethylene Glycol-400 2.5 ml 4. Propylene Glycol 2.5 ml 5. HPMC 5 gm 6. Chloroform 8 ml 7. Methanol 4 ml
  • 18. EVALUATION TEST FOR TRANSDERMAL PATCHES • The various evaluation test was being performed on laboratory level for the evaluation of formulated transdermal patches. Following are the Test performed: - 1. Organoleptic Characteristics 2. Surface Ph Determination 3. Phytochemical Screening of Tulsi 4. Phytochemical Screening of Aloe vera 5. Measurement Of Thickness of patches 6. UV Spectroscopy 7. % Moisture content
  • 19. RESULTS SR.NO CHARECTERISTIC OBSERVATION 1. COLOUR Whitish cream 2. TEXTURE Smooth and Uniform 3. APPEREANCE Turbid 4. ODOUR Herbal Extract 5. PH 5-9 6. THICKNESS 0.22mm 7. MOISTURE CONTENT 50% 8. UV ABSORBANCE 2.25Abs
  • 20. CONCLUSION • The Transdermal patches with the incorporation of herbal extract of Ocimum Sanctum and Aloe barbadense were Formulated. • The Herbal transdermal Patches including aloe and tulsi were aimed to heal the wound or any type of injury or the skin infection like eczema etc. • The Evaluation studies states that the patches have the optimum thickness and is within the suitable range of Ph. • In the various research its seen that transdermal drug delivery system has great scope in future for developing drug delivery system in NDDS. • Transdermal drug delivery system is widely accepted now-a-days because it causes the drug penetration through skin layers and reach systemic circulation without causing any damage to skin or rupturing it. TDDS also benefits for controlled release of drug for prolonged period of time. • More research and innovation will bring the wide acceptance in the use of various other transdermal drug delivery system like iontophoresis, Ultrasound technology, Med Tat etc.