SEMI SOLID DOSAGE
FORMS
INTRODUCTION
Pharmaceutical semisolid dosage preparations include :
ointments,
pastes, cream,
plasters,
gels and
rigid foams.
They contain one or more active ingredients dissolved or
uniformly dispersed in a suitable base and any suitable excipients
such as emulsifiers, viscosity increasing agents, anti microbial
agents, antioxidants, or stabilizing agents etc..
Definition
Semi solids are the topical dosage form
used for the therapeutic, protective or cosmetic
function. They may be applied to the skin, or
used nasally, vaginally, or rectally…
ADVANTAGES
 It is used externally
 Probability of side effect can be reduce
 First pass gut and hepatic metabolism is avoided.
 Local action and Site specific action of drug on
affected area.
 Convenient for unconscious patient or
patienthaving difficulty on oral administration.
 Suitable dosage form for bitter drugs.
 More stable than liquid dosage form
DISADVANTAGES
 There is no dosage accuracy in this type of dosage
form
 The base which is used in the semi-solid dosage form
 can be easily oxidized.
 May cause staining.
 They are bulky to handle.
 Application with finger may cause contamination.
 Physico-chemically less stable than solid dosage
form.
 May cause irritation or allergy to some patients
IDEAL PROPERTIES OF SEMISOLIDS
PHYSICAL PROPERTIES:
Smooth texture
Elegant in appearance
Non dehydrating
 Non gritty
Non greasy and non staining
Non hygroscopic
IDEAL PROPERTIES OF SEMISOLIDS
PHYSIOLOGICAL PROPERTIES
 Non irritating
Do not alter membrane / skin functioning
Miscible with skin secretion
Have low sensitization index
APPLICATION PROPERTIES
Easily applicable with efficient drug release.
High aqueous wash ability.
MECHANISMS & FACTORS INFLUENCING
DERMAL PENETRATION OF DRUG
Absorption of substances through the skin
depends on a number of factors:
• Concentration
• Molecular Weight of the molecule
• Duration of contact
• Solubility of medication
• Physical condition of the skin
• Part of the body exposed including the amount of
hair on the skin.
• Small amounts of chemicals may enter the body
rapidly through the glands or hair follicles, they
are primarily absorbed through the epidermis.
• The stratum corneum is the outermost layer of the
epidermis and the rate-limiting barrier in
absorption of an agent.
• Once a substance passes through stratum
corneum, then its no significant further hindrance
to penetration of the remaining epidermal layer &
corium.
• The stratum corneum is primarily composed of
lipophilic cholesterol, cholesterol ester and
ceramides (fatty acids).
• Thus lipid-soluble chemicals make it through the
layer and into the circulation faster, however
nearly all molecules penetrate it to some minimal
degree.
• Also, penetration depending upon effective blood
flow, interstitial fluid movement.
BIOAVABILITY OF DRUG
For bioavailability there are two factors
are most important
1. Choice of vehicle (Base).
2. Maximizing movement (partitioning) of drug
from vehicle to stratum corneum.
PREPARATION OF SEMISOLID DOSAGE FORMS
INGREDIENTS USED IN PREPARATION:
• Bases
• Preservative
• Humectants
• Antioxidants
• Emulsifier
• Gelling agent
• Permeation enhancer
• Buffers
BASES
It is one of the most important ingredient used in
formulation of semisolid dosage form. Ointment
bases do not merely act as the carriers of the
medicaments, but they also control the extent of
absorption of medicaments incorporated in them.
IDEAL PROPERTIES OF A BASE
They should be
 Inert, non-irritating and non-sensitizing.
 Compatible with skin pH and the drug.
 Good solvent and/or emulsifying agent.
 Emollient, protective, non-greasy and easily
removable.
 Release medicament readily at the site of application.
 Pharmaceutically elegant and possess good stability
ANTIOXIDANTS
Oxygen is a highly reactive atom that is capable
of becoming part of potentially damaging
molecules commonly called “free radicals.”
Free radicals are capable of attacking the healthy
cells of the body, causing them to lose their
structure and function.
To prevent this an antioxidants are added.
E.g. Butylated hydroxy anisole,
Butylatedhydroxy toluene
PERMEATION ENHANCERS
Skin can act as a barrier. With the
introduction of various penetration enhancers,
penetration of the drug through the skin can be
improved.
Eg: Oleic acid
EMULSIFIER
• An emulsifier (emulgent) is a substance that
stabilizes an emulsion by increasing its kinetic
stability.
• Must reduce surface tension for proper
emulsification.
• Prevents coalescence.
• Ability to increase the viscosity at low concentration.
HUMECTANT
A humectant is a hygroscopic substance,
Humectants are used to :
increase the solubility of the active ingredient
to elevate its skin penetration.
elevate the hydration of the skin.
BUFFERS
Buffers are added for various purpose such as :
• Compatibility with skin.
• Drug solubility.
• Drug stability.
• Influence ionization of drug.
• Skin, due to its weak acidic nature, tolerates weak
acidic preparations.
E.g. sodium acetate, sodium citrate, potassium
Antimicrobial preservatives
To inhibit the growth of contaminating
microorganisms,
So require the addition of chemical
antimicrobial preservatives to the formulation
E.G. para-hydroxybenzoates (parabens),
phenols, benzoic acid, sorbic acid, quaternary
ammonium salts and other compounds.
1- Ointments
DEFINITION
Ointments are homogenous, translucent, viscous
semi-solid preparations, most commonly a greasy,
thick oil (oil 80% - water 20%) intended for external
application to the skin or mucous membrane. They
are used as:
• Emollients
• Protective
• Therapeutic
• Prophylactic purpose
Classification of ointments
A- Epidermic ointments
 These ointments are intended to produce their action on the
surface of the skin and produce local effect,they are not
absorbed.
 They acts as protectives, antiseptics and parasiticides.
B- Endodermic ointments
 These ointments are intended to release the medicaments
that penetrate into the skin. They are partially absorbed
and acts as emollients, stimulants and local irritants.
C- Diadermic ointments
 These ointments are intended to release the medicaments
that pass through the skin and produce systemic effects.
CLASSIFICATION OF OINTMENTS
BASES
 Oleaginous bases or hydrocarbon bases
 Absorption bases
 Water-miscible bases/removable bases/emulsifying
bases
 Water-soluble bases
Oleaginous bases are non-aqueous
 Oleaginous bases are non-aqueous formulations
which provides emollient & protective properties.
 It is difficult to remove hydrocarbon bases from skin
due to their oily nature.
 These are water insoluble hydrocarbons, vegetable
oils, animal fats and waxes.
E.G. Hard paraffin, white or yellow soft, Paraffin,
liquid paraffin, mineral oil etc
Absorption bases
• In the absorption bases contains small amt. Of water
& they provide relatively less emollient properties
than hydrocarbon bases.
• These bases are generally anhydrous substances
which have the property of absorbing considerable
quantity. Of water but still retaining their ointment
like consistency.
• They have 2 types :
• 1. Non-emulsified bases
• 2. Water in oil emulsion bases
Non-emulsified bases: Those bases absorb
water & aqueous solution producing W/O
emulsion.
e.g. Wool fat, Wool alcohol, Bees Wax etc..
Water in oil emulsion bases: Those bases
have the capability of absorbing more water &
have the properties of non- emulsified bases.
e.g. Hydrous wool fat (Lanolin)
WATER-MISCIBLE BASES/REMOVABLE
BASES/ EMULSIFYING BASES
 These are anhydrous, hydrophilic, absorbs water with low
thermal conductivity.
 It is easy to remove these bases from the skin due to their
hydrophilic nature.
 These are used to form oil in water emulsion for topical
 Applications.
 They have the same properties as the absorption bases.
 They are used as emollients, cleansing creams, vehicle for
solid, liquid drugs.
E.G. Cold cream type, hydrous lanoline, rose water ointment
etc.
WATER SOLUBLE BASES
• In that bases does not contain oily substances & are called
greaseless bases & completely soluble in water.
• Those are prepared using mixtures of different molecular weights of
polyethylene glycol (macrogols).
• Peg are mixture of poly condensation product of ethylene oxide &
water.
• Lower m.W of this polymers (200,400 & 600g/mol) are liquids &
the average M.W increases of this polymers changes from liq. To a
waxy solid but not greater than 1000g/mol.
Preparation of Ointments
Both on a large and a small scale,
ointments are prepared by three general
methods:
• Incorporation method / trituration method
• Fusion method
• Chemical reaction
The method for a particular preparation
depends primarily upon the nature of the
ingredients
INCORPORATION METHOD /
TRITURATION METHOD
This method is when the base is soft and medicament is
insoluble in the base.
 Powders pass out from mesh no. 250 or 180 or 125.
 Then apply levigation process with small amt. Of base.
 Then add remaining quantity of base.
 Finally add liquid ingredients & mix well.
(1) incorporation
- The components of the ointment are mixed together by various
means until a uniform preparation has been attained.
- On a small scale, the pharmacist may mix the components of an
ointment in a mortar with a pestle, or a spatula and an ointment
slab may be used to rub the ingredients together
E.G whitfield ointment
FUSION METHOD
 When an ointment base contains a number of solid
ingredients such as white bees wax, cetyl alcohol,
stearyl alcohol, hard paraffin etc.
 By the fusion method, all or some of the components
of an ointment are combined by being melted
together and cooled with constant stirring until
congealed.
 Naturally, heat-labile substances and any volatile
components are added last when the temperature of
the mixture is low enough not to cause decomposition
of volatilization of the components.
OINTMENT CONTAINING FREE IODINE
 Iodine is slightly soluble in most fats & oil but very
readily soluble in conc. Aq.Solution of potassium
iodide due to formation of molecular complex.
 E.G. Strong iodine ointment B.Vet.C is used to treat
ringworm in cattle. At one time this type ointment
used on humans for counter-irritants but they were
not popular bec. They remain stain on skin a deep red
colour.
OINTMENT CONTAINING COMBINED IODINE
• Fixed oils & many vegetable & animal fats absorb iodine
which combines with the double bounds of the
unsaturated constitutes. Oleic acid + iodine = di-iodo
stearic acid
• E.g. Non-staining Iodine Ointment BPC
• In the preparation of ointments having an emulsion type
of formula, the general method of manufacture involves a
melting process as well as an emulsification process.
EMULSIFICATION

Semi solid dosage forms

  • 1.
  • 2.
    INTRODUCTION Pharmaceutical semisolid dosagepreparations include : ointments, pastes, cream, plasters, gels and rigid foams. They contain one or more active ingredients dissolved or uniformly dispersed in a suitable base and any suitable excipients such as emulsifiers, viscosity increasing agents, anti microbial agents, antioxidants, or stabilizing agents etc..
  • 3.
    Definition Semi solids arethe topical dosage form used for the therapeutic, protective or cosmetic function. They may be applied to the skin, or used nasally, vaginally, or rectally…
  • 4.
    ADVANTAGES  It isused externally  Probability of side effect can be reduce  First pass gut and hepatic metabolism is avoided.  Local action and Site specific action of drug on affected area.  Convenient for unconscious patient or patienthaving difficulty on oral administration.  Suitable dosage form for bitter drugs.  More stable than liquid dosage form
  • 5.
    DISADVANTAGES  There isno dosage accuracy in this type of dosage form  The base which is used in the semi-solid dosage form  can be easily oxidized.  May cause staining.  They are bulky to handle.  Application with finger may cause contamination.  Physico-chemically less stable than solid dosage form.  May cause irritation or allergy to some patients
  • 6.
    IDEAL PROPERTIES OFSEMISOLIDS PHYSICAL PROPERTIES: Smooth texture Elegant in appearance Non dehydrating  Non gritty Non greasy and non staining Non hygroscopic
  • 7.
    IDEAL PROPERTIES OFSEMISOLIDS PHYSIOLOGICAL PROPERTIES  Non irritating Do not alter membrane / skin functioning Miscible with skin secretion Have low sensitization index APPLICATION PROPERTIES Easily applicable with efficient drug release. High aqueous wash ability.
  • 8.
    MECHANISMS & FACTORSINFLUENCING DERMAL PENETRATION OF DRUG Absorption of substances through the skin depends on a number of factors: • Concentration • Molecular Weight of the molecule • Duration of contact • Solubility of medication • Physical condition of the skin • Part of the body exposed including the amount of hair on the skin.
  • 9.
    • Small amountsof chemicals may enter the body rapidly through the glands or hair follicles, they are primarily absorbed through the epidermis. • The stratum corneum is the outermost layer of the epidermis and the rate-limiting barrier in absorption of an agent. • Once a substance passes through stratum corneum, then its no significant further hindrance to penetration of the remaining epidermal layer & corium.
  • 10.
    • The stratumcorneum is primarily composed of lipophilic cholesterol, cholesterol ester and ceramides (fatty acids). • Thus lipid-soluble chemicals make it through the layer and into the circulation faster, however nearly all molecules penetrate it to some minimal degree. • Also, penetration depending upon effective blood flow, interstitial fluid movement.
  • 11.
    BIOAVABILITY OF DRUG Forbioavailability there are two factors are most important 1. Choice of vehicle (Base). 2. Maximizing movement (partitioning) of drug from vehicle to stratum corneum.
  • 12.
    PREPARATION OF SEMISOLIDDOSAGE FORMS INGREDIENTS USED IN PREPARATION: • Bases • Preservative • Humectants • Antioxidants • Emulsifier • Gelling agent • Permeation enhancer • Buffers
  • 13.
    BASES It is oneof the most important ingredient used in formulation of semisolid dosage form. Ointment bases do not merely act as the carriers of the medicaments, but they also control the extent of absorption of medicaments incorporated in them.
  • 14.
    IDEAL PROPERTIES OFA BASE They should be  Inert, non-irritating and non-sensitizing.  Compatible with skin pH and the drug.  Good solvent and/or emulsifying agent.  Emollient, protective, non-greasy and easily removable.  Release medicament readily at the site of application.  Pharmaceutically elegant and possess good stability
  • 15.
    ANTIOXIDANTS Oxygen is ahighly reactive atom that is capable of becoming part of potentially damaging molecules commonly called “free radicals.” Free radicals are capable of attacking the healthy cells of the body, causing them to lose their structure and function. To prevent this an antioxidants are added. E.g. Butylated hydroxy anisole, Butylatedhydroxy toluene
  • 16.
    PERMEATION ENHANCERS Skin canact as a barrier. With the introduction of various penetration enhancers, penetration of the drug through the skin can be improved. Eg: Oleic acid
  • 17.
    EMULSIFIER • An emulsifier(emulgent) is a substance that stabilizes an emulsion by increasing its kinetic stability. • Must reduce surface tension for proper emulsification. • Prevents coalescence. • Ability to increase the viscosity at low concentration.
  • 18.
    HUMECTANT A humectant isa hygroscopic substance, Humectants are used to : increase the solubility of the active ingredient to elevate its skin penetration. elevate the hydration of the skin.
  • 19.
    BUFFERS Buffers are addedfor various purpose such as : • Compatibility with skin. • Drug solubility. • Drug stability. • Influence ionization of drug. • Skin, due to its weak acidic nature, tolerates weak acidic preparations. E.g. sodium acetate, sodium citrate, potassium
  • 20.
    Antimicrobial preservatives To inhibitthe growth of contaminating microorganisms, So require the addition of chemical antimicrobial preservatives to the formulation E.G. para-hydroxybenzoates (parabens), phenols, benzoic acid, sorbic acid, quaternary ammonium salts and other compounds.
  • 21.
    1- Ointments DEFINITION Ointments arehomogenous, translucent, viscous semi-solid preparations, most commonly a greasy, thick oil (oil 80% - water 20%) intended for external application to the skin or mucous membrane. They are used as: • Emollients • Protective • Therapeutic • Prophylactic purpose
  • 22.
    Classification of ointments A-Epidermic ointments  These ointments are intended to produce their action on the surface of the skin and produce local effect,they are not absorbed.  They acts as protectives, antiseptics and parasiticides. B- Endodermic ointments  These ointments are intended to release the medicaments that penetrate into the skin. They are partially absorbed and acts as emollients, stimulants and local irritants. C- Diadermic ointments  These ointments are intended to release the medicaments that pass through the skin and produce systemic effects.
  • 23.
    CLASSIFICATION OF OINTMENTS BASES Oleaginous bases or hydrocarbon bases  Absorption bases  Water-miscible bases/removable bases/emulsifying bases  Water-soluble bases
  • 24.
    Oleaginous bases arenon-aqueous  Oleaginous bases are non-aqueous formulations which provides emollient & protective properties.  It is difficult to remove hydrocarbon bases from skin due to their oily nature.  These are water insoluble hydrocarbons, vegetable oils, animal fats and waxes. E.G. Hard paraffin, white or yellow soft, Paraffin, liquid paraffin, mineral oil etc
  • 25.
    Absorption bases • Inthe absorption bases contains small amt. Of water & they provide relatively less emollient properties than hydrocarbon bases. • These bases are generally anhydrous substances which have the property of absorbing considerable quantity. Of water but still retaining their ointment like consistency. • They have 2 types : • 1. Non-emulsified bases • 2. Water in oil emulsion bases
  • 26.
    Non-emulsified bases: Thosebases absorb water & aqueous solution producing W/O emulsion. e.g. Wool fat, Wool alcohol, Bees Wax etc.. Water in oil emulsion bases: Those bases have the capability of absorbing more water & have the properties of non- emulsified bases. e.g. Hydrous wool fat (Lanolin)
  • 27.
    WATER-MISCIBLE BASES/REMOVABLE BASES/ EMULSIFYINGBASES  These are anhydrous, hydrophilic, absorbs water with low thermal conductivity.  It is easy to remove these bases from the skin due to their hydrophilic nature.  These are used to form oil in water emulsion for topical  Applications.  They have the same properties as the absorption bases.  They are used as emollients, cleansing creams, vehicle for solid, liquid drugs. E.G. Cold cream type, hydrous lanoline, rose water ointment etc.
  • 28.
    WATER SOLUBLE BASES •In that bases does not contain oily substances & are called greaseless bases & completely soluble in water. • Those are prepared using mixtures of different molecular weights of polyethylene glycol (macrogols). • Peg are mixture of poly condensation product of ethylene oxide & water. • Lower m.W of this polymers (200,400 & 600g/mol) are liquids & the average M.W increases of this polymers changes from liq. To a waxy solid but not greater than 1000g/mol.
  • 29.
    Preparation of Ointments Bothon a large and a small scale, ointments are prepared by three general methods: • Incorporation method / trituration method • Fusion method • Chemical reaction The method for a particular preparation depends primarily upon the nature of the ingredients
  • 30.
    INCORPORATION METHOD / TRITURATIONMETHOD This method is when the base is soft and medicament is insoluble in the base.  Powders pass out from mesh no. 250 or 180 or 125.  Then apply levigation process with small amt. Of base.  Then add remaining quantity of base.  Finally add liquid ingredients & mix well. (1) incorporation - The components of the ointment are mixed together by various means until a uniform preparation has been attained. - On a small scale, the pharmacist may mix the components of an ointment in a mortar with a pestle, or a spatula and an ointment slab may be used to rub the ingredients together E.G whitfield ointment
  • 32.
    FUSION METHOD  Whenan ointment base contains a number of solid ingredients such as white bees wax, cetyl alcohol, stearyl alcohol, hard paraffin etc.  By the fusion method, all or some of the components of an ointment are combined by being melted together and cooled with constant stirring until congealed.  Naturally, heat-labile substances and any volatile components are added last when the temperature of the mixture is low enough not to cause decomposition of volatilization of the components.
  • 34.
    OINTMENT CONTAINING FREEIODINE  Iodine is slightly soluble in most fats & oil but very readily soluble in conc. Aq.Solution of potassium iodide due to formation of molecular complex.  E.G. Strong iodine ointment B.Vet.C is used to treat ringworm in cattle. At one time this type ointment used on humans for counter-irritants but they were not popular bec. They remain stain on skin a deep red colour.
  • 35.
    OINTMENT CONTAINING COMBINEDIODINE • Fixed oils & many vegetable & animal fats absorb iodine which combines with the double bounds of the unsaturated constitutes. Oleic acid + iodine = di-iodo stearic acid • E.g. Non-staining Iodine Ointment BPC • In the preparation of ointments having an emulsion type of formula, the general method of manufacture involves a melting process as well as an emulsification process. EMULSIFICATION