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A SEMINAR ON
NANOPARTICLES
Presented by
NIVEDITHA G
NARGUND COLLEGE OF PHARMACY
Niveditha G 1
SEMINAR OUTLINE
 DEFINATION
 ADVANTAGES, LIMITATIONS
 NOVEL NANOPARTICULATE SYSTEMS
 CHARACTERIZATION OF NANOPARTICLES
 THERAPEUTIC APPLICATIONS
Niveditha G 2
NOVEL NANOPARTICULATE SYSTEMS
ADVANTAGES OF NANOPARTICLES.
 Biodegradable,
 Nontoxic,
 Site specific,
 Longer shelf life,
 High carrier capacity,
 Feasibility of incorporation of both hydrophilic and
hydrophobic substances and
 Feasibility of variable routes of administration.
LIMITATIONS
 Drugs can be targeted only to RES or organs which are
phagocytically active. Niveditha G 3
NOVEL NANOPARTICULATE SYSTEMS
SOLID LIPID NANOPARTICLES (SLNs)
 The SLNs are submicron colloidal carriers having size
range of 50–1000 nm.
 They are composed of physiological lipid, dispersed in
water or in an aqueous surfactant solution.
 These are colloidal drug carrier combines the
advantages of polymeric nanoparticles, fat emulsion
and liposomes simultaneously and avoiding some of
their disadvantages.
 Here, to overcome the problems associated with the
liquid state of the oil droplets, the liquid lipid was
replaced by a solid lipid,
Niveditha G 4
NOVEL NANOPARTICULATE SYSTEMS
Advantages of SLNs
 small size and relatively narrow size distribution which
provide biological opportunities for site-specific drug
delivery,
 controlled release of the drug over a prolonged period
can be achieved,
 protection of incorporated drug against chemical
degradation,
 possible sterilization by autoclaving or  irradiation,
 no toxic metabolites are produced,
 relatively cheaper and stable and
 ease of large scale production.
Niveditha G 5
NOVEL NANOPARTICULATE SYSTEMS
Preparation Methods of SLNs
 High pressure homogenization technique
- Hot homogenization technique
- Cold homogenization technique
 Microemulsion technique
Niveditha G 6
NOVEL NANOPARTICULATE SYSTEMS
Homogenization Techniques
1. Hot homogenization technique
 involves homogenization of melted lipids at elevated
temperature.
 applied to lipophilic and insoluble drugs.
 many heat sensitive drugs can also be safely processed
because the exposure time to high temperatures is
relatively short.
Niveditha G 7
SLN Preparation using SLN Preparation using
Hot Homogenization Tech Cold Homogenization Tech
MOP of SLNs:-
Niveditha G 8
Niveditha G 9
NOVEL NANOPARTICULATE SYSTEMS
Homogenization Techniques
2. Cold homogenization technique
 involves homogenization of a suspension of solid lipid
at room temperature or below.
 applied to hydrophilic drugs.
 avoids and minimizes melting process of lipid and
 hence it is suitable for thermosensitive drugs.
Niveditha G 10
NOVEL NANOPARTICULATE SYSTEMS
SYNTHETIC NANOPARTICLES USING MICROEMULSIONS
AS NANO-SIZE REACTORS.
Niveditha G 11
CHARACTERIZATION
 The nanoparticles are characterized for size, density,
electrophoretic mobility, angle of contact and specific
surface area.
Niveditha G 12
CHARACTERIZATION
Niveditha G 13
CHARACTERIZATION
Size and Morphology
 Freeze-fracture technique
- a very good technique
- size evaluation
- morphological determination of inner structure of
particles
 Electron microscopy
- measures individual particles for size and its
distribution
- relatively less time consuming
 TEM AND SEM
- permits differentiation among nanocapsules and
nanoparticles
- SEM is relatively less time consuming
Niveditha G 14
CHARACTERIZATION
Atomic Force Microscopy (AFM)
- Using the AFM, individual particles and groups of particles
can be resolved
- applied for characterization of nanospheres and SLNs
- an effective means for the investigation of nanoparticle
behaviour in biological environment
AFM Images : Particle Visualization Display
Niveditha G 15
CHARACTERIZATION
 Specific Surface
- sorptometer is used
- the specific surface area is calculated by the following
equation:
A = 6 / d . D
where,
A = specific surface area
d = density
D= diameter of the particle
Niveditha G 16
THERAPEUTIC APPLICATIONS
Niveditha G 17
 Acne medications from antimicrobial nanoparticles,
 For improved stability –Influenza vaccine,
 Superficial and systemic Staph infections could be
managed via nanoparticles, and
 As a diagnostic agents :
colloidal preparations are used as carriers of radio
isotopes for study of morphology, blood flow and function
of various organs in the body.
THERAPEUTIC APPLICATIONS
Niveditha G 18
Niveditha G 19

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introduction of nanoparticles, advantages and disadvantages, characterization and applications

  • 1. A SEMINAR ON NANOPARTICLES Presented by NIVEDITHA G NARGUND COLLEGE OF PHARMACY Niveditha G 1
  • 2. SEMINAR OUTLINE  DEFINATION  ADVANTAGES, LIMITATIONS  NOVEL NANOPARTICULATE SYSTEMS  CHARACTERIZATION OF NANOPARTICLES  THERAPEUTIC APPLICATIONS Niveditha G 2
  • 3. NOVEL NANOPARTICULATE SYSTEMS ADVANTAGES OF NANOPARTICLES.  Biodegradable,  Nontoxic,  Site specific,  Longer shelf life,  High carrier capacity,  Feasibility of incorporation of both hydrophilic and hydrophobic substances and  Feasibility of variable routes of administration. LIMITATIONS  Drugs can be targeted only to RES or organs which are phagocytically active. Niveditha G 3
  • 4. NOVEL NANOPARTICULATE SYSTEMS SOLID LIPID NANOPARTICLES (SLNs)  The SLNs are submicron colloidal carriers having size range of 50–1000 nm.  They are composed of physiological lipid, dispersed in water or in an aqueous surfactant solution.  These are colloidal drug carrier combines the advantages of polymeric nanoparticles, fat emulsion and liposomes simultaneously and avoiding some of their disadvantages.  Here, to overcome the problems associated with the liquid state of the oil droplets, the liquid lipid was replaced by a solid lipid, Niveditha G 4
  • 5. NOVEL NANOPARTICULATE SYSTEMS Advantages of SLNs  small size and relatively narrow size distribution which provide biological opportunities for site-specific drug delivery,  controlled release of the drug over a prolonged period can be achieved,  protection of incorporated drug against chemical degradation,  possible sterilization by autoclaving or  irradiation,  no toxic metabolites are produced,  relatively cheaper and stable and  ease of large scale production. Niveditha G 5
  • 6. NOVEL NANOPARTICULATE SYSTEMS Preparation Methods of SLNs  High pressure homogenization technique - Hot homogenization technique - Cold homogenization technique  Microemulsion technique Niveditha G 6
  • 7. NOVEL NANOPARTICULATE SYSTEMS Homogenization Techniques 1. Hot homogenization technique  involves homogenization of melted lipids at elevated temperature.  applied to lipophilic and insoluble drugs.  many heat sensitive drugs can also be safely processed because the exposure time to high temperatures is relatively short. Niveditha G 7
  • 8. SLN Preparation using SLN Preparation using Hot Homogenization Tech Cold Homogenization Tech MOP of SLNs:- Niveditha G 8
  • 10. NOVEL NANOPARTICULATE SYSTEMS Homogenization Techniques 2. Cold homogenization technique  involves homogenization of a suspension of solid lipid at room temperature or below.  applied to hydrophilic drugs.  avoids and minimizes melting process of lipid and  hence it is suitable for thermosensitive drugs. Niveditha G 10
  • 11. NOVEL NANOPARTICULATE SYSTEMS SYNTHETIC NANOPARTICLES USING MICROEMULSIONS AS NANO-SIZE REACTORS. Niveditha G 11
  • 12. CHARACTERIZATION  The nanoparticles are characterized for size, density, electrophoretic mobility, angle of contact and specific surface area. Niveditha G 12
  • 14. CHARACTERIZATION Size and Morphology  Freeze-fracture technique - a very good technique - size evaluation - morphological determination of inner structure of particles  Electron microscopy - measures individual particles for size and its distribution - relatively less time consuming  TEM AND SEM - permits differentiation among nanocapsules and nanoparticles - SEM is relatively less time consuming Niveditha G 14
  • 15. CHARACTERIZATION Atomic Force Microscopy (AFM) - Using the AFM, individual particles and groups of particles can be resolved - applied for characterization of nanospheres and SLNs - an effective means for the investigation of nanoparticle behaviour in biological environment AFM Images : Particle Visualization Display Niveditha G 15
  • 16. CHARACTERIZATION  Specific Surface - sorptometer is used - the specific surface area is calculated by the following equation: A = 6 / d . D where, A = specific surface area d = density D= diameter of the particle Niveditha G 16
  • 18.  Acne medications from antimicrobial nanoparticles,  For improved stability –Influenza vaccine,  Superficial and systemic Staph infections could be managed via nanoparticles, and  As a diagnostic agents : colloidal preparations are used as carriers of radio isotopes for study of morphology, blood flow and function of various organs in the body. THERAPEUTIC APPLICATIONS Niveditha G 18