NIOSOMES 1ST M.PHARM PHARMACEUTICS

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NIOSOMES

1ST M.PHARM

PHARMACEUTICS

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DEFINATION

 Niosomes are synthetic microscopic vesicles consisting of an
aqueous core enclosed in a bi layer consisting of cholesterol
and one or more nonionic surfactants.

 Vesicles are prepared from self assembly of hydrated non
ionic surfactants molecules

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STRUCTURE OF NIOSOMES
 A typical Niosomal vesicle consist of a vesicle forming

amphiphile i.e. a non-ionic surfactant such as Span-60, which
is usually stabilized by the addition of cholesterol and a small
amount of anionic surfactant such as dicetyl phosphate, which
also helps in stabilizing the vesicle.

 Niosomes are microscopic lamellar structures, which are
formed on the admixture of non-ionic surfactant of the alkyl
or dialkyl polyglycerol ether class and cholesterol with
subsequent hydration in aqueous media

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COMPOSITIONS OF NIOSOMES
 The two major ingredients or components are used for the

preparation of niosomes:

1. Cholesterol: – It provides rigidity and proper shape,
conformation to the niosomes preparations.

2. Non-ionic surfactants:-Surfactants play an important role
in the preparation of niosomesThe following non-ionic
surfactants are generally used for the preparation of niosomes.
e.g. 1. Spans (span 60, 40, 20, 85, 80) 2. Tweens (tween 20,
40, 60, 80) and 3. Brijs (brij 30, 35, 52, 58, 72, 76)

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TYPES OF NIOSOMES
 The niosomes are classified as a function of the number of bilayer

and size as
i) Multi lamellar vesicles (MLV),
ii) Large unilamellar vesicles (LUV),
iii) Small unilamellar vesicles (SUV).
Multilamellar vesicles (mlv):
It consists of a number of bilayer surrounding the aqueouslipid
compartment separately. The approximate size of these vesicles is
0.5-10 µm diameter. Multilamellar vesicles are the most widely
used niosomes. It is simple to make and are mechanically stable
upon storage for long periods. Thesevesicles are highly suited as
drug carrier for lipophilic compounds.

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Large unilamellar vesicles (luv):

Niosomes of this type have a high aqueous/lipid compartment
ratio, so that larger volumes of bio-active materials can be
entrapped with a very economical use of membrane lipids.

Small unilamellar vesicles (suv):

These small unilamellar vesicles are mostly prepared from
multilamellar vesicles by sonication method, French press
extrusion electrostatic stabilization is the inclusion of diacetyl
phosphate in 5(6)-carboxyfluorescein (CF) loaded Span 60 based
niosomes

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METHOD OF PREPARATION
1. Ether injection method

2. The ‘bubble’ method

3. Reverse phase evoparation method

4. Hand shanking method

5. Sonication

6. Microfludization method

7. Transmembrane pH gradient uptake

8. Multiple membrane extrusion metod

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The “Bubble” Method
 It is novel technique for the one step preparation of liposomes

and niosomes without the use of organic solvents

 The bubbling unit consists of round-bottom flask with three
necks positioned in water bath to control the temperature

 Water-cooled reflux and thermometer is positioned in the first
and second neck and nitrogen supply through the third neck

 Cholesterol and surfactant are dispersed together in this buffer
(pH 7.4)at 70°C, the dispersion mixed for 15 seconds with high
shearhomogenizer and immediately afterwards “bubbled at 70°C
usingnitrogen gas 25

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REVERSE PHASE EVAPORATION
TECHNIQUE
 Cholesterol and surfactant (1:1) are dissolved in a mixture of

ethe rand chloroform

 An aqueous phase containing drug is added to this and the
resulting two phases are sonicated at 4-5°C. The clear gel
formed is further sonicated after the addition of a small
amount of phosphate buffered saline (PBS)

 The organic phase is removed at 40°C under low pressure.
The resulting viscous niosome suspension is diluted with PBS
and heated on a water bath at 60°C for 10 min to yield
niosomes

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MULTIPLE MEMBRANE EXTRUSION
METHOD

 In this method, a mixture of surfactant,
cholesterol and diacetyl phosphate is prepared
and then solvent is evaporated using rotary
vacuum evaporator to leave a thin film. The
film is then hydrated with aqueous drug
solution and the suspension thus obtained
isextruded through the polycarbonate
membrane (mean pore size 0.1 mm) and
thenplaced in series up to eight passages to
obtain uniform size niosomes

 Good method of controlling niosome size

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Trans membrane pH gradient Drug
Uptake Process

 Surfactant and cholesterol are dissolved in chloroform
 The solvent is then evaporated under reduced pressure to get a

thin film on thewall of the round bottom flask
 The film is hydrated with 300 mM citric acid (pH 4.0) by vortex

mixing
 The multilamellar vesicles are frozen and thawed 3 times and later

sonicated. To this niosomal suspension, aqueous solution
containing 10 mg/ml of drug is added and vortexed

 The pH of the sample is then raised to 7.0-7.2 with 1M disodium
phosphate

 This mixture is later heated at 60°C for 10 minutes to give
niosomes

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REFERENCE
 Gandhi, M., Sanket, P. and Mahendra, S., 2014. Niosomes:

novel drug delivery system. International Journal of Pure &
Applied Bioscience, 2(2), pp.267-274.

 Shakya, V. and Bansal, B.K., 2014. Niosomes: a novel trend in
drug delivery. International Journal of Research And Development
In Pharmacy And Life Sciences, 3(4), pp.1036-1041.

 Tangri, P. and Khurana, S., 2011. Niosomes: formulation and
evaluation. International Journal, 2229, p.7499.

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Thank you

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