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 
MUDASIR MALIK
 Introduction
 Drug vehicles
 Ideal characteristics of nanoparticles
 Drug release mechanisms
 Diseases controlled using nanoparticles
 Modes of administration
 Advantages
 Limitations
3
 Particle size ranges from 10-1000nm in
diameter
 Particulate dispersions or solid particles
 A drug may be adsorbed or covalently
attached to the nanocarriers surface or it
can be encapsulated into it
4
 Liposomes
 Polymeric nanoparticles
 Nanoparticles based on
solid lipids
 Silica nanoparticles
 Gold nanoparticles
5
 Usually with 80-300 nm size range
composed of phospholipids and
cholestrol
 Drug is encapsulated
 Examples in liposomal formulations,
such as anticancer drugs,
neurotransmitters (serotonin),
antibiotics, anti-inflammatory etc
6
 Diameter ranging from 10 to 100 nm
 These may be biodegradable and
non-biodegradable
 Drug may b on the surface or
incorporated
 Drug release by desorption and
diffusion
7
 A core, dendrons and surface
active groups
 Surface functional groups
enables the interaction
 Drug may be encapsulated or
adsorbed on the surface
 Polyvalency
8
 Solid lipid nanoparticles(SLN)
o Size 100-500nm
o Delivery medium for lipophilic
drugs
o Loading capacity limited by the
solubility of drug in lipid
9
 Nanostructured lipid carriers (NLC)
o Imperfect type NLC
o Multiple type NLC
o Amorphous type NLC
 Lipid drug conjugates (LDC)
o For lipophobic drug molecules
10
 < 50nm
 Highly porous framework
 Invading deeper parts of body
 Phenytoin, cisplatin, diclofenac,
heparin are examples of drugs
delivered by silica materials
11
 Size 130nm
 Use for cancer treatment
 Relay on enhanced permeability and
retention effect
 Suitable for delivering enzymatic
degradation susceptible materials
12
 Small particle size
 Controlled drug release rate
 High drug loading capacity
 Biochemically inert and non toxic
 Physically and chemically stable
 Restricted drug distribution to
normal cells
13
 Active targeting
o Drug targeting by ultrasonic
energy and magnetic field
o Cell surface antigen should be
expressed
o Antibody and ligand as
targeting moiety
o Receptor-mediated endocytosis
14
 Passive targeting
o Physical targeting
o Direct drug injection and
catheterization
o Spontaneous drug
accumulation in areas with
leaky vasculature
15
16
 Cancer
o Ethylene glycol molecules attach to
nanoparticles that deliver therapeutic
drugs
o Or coating nanoparticles with
membrane from RBCs
o Photosensitizing agents
17
 Heart diseases
o Clot busting
o Inflamed tissue such as arterial plaque
 Diabetic mellitus
o Nanoparticles contain both insulin and an
enzyme
 Autoimmune diseases
o Nanoparticles deliver antigens
18
 Neurologic disorders
o Cross the blood brain barrier(BBB)
 Aging
o The contents of the nanoparticle released
when an enzyme found in aging cells is
present
19
 Oral
 Intravenous
 Transdermal
 Pulmonary
20
 Controlled and sustained release
 No wastage of drug
 No side effects
 Provide comfort and compliance
 Longer circulation half-lives
 High cell uptake
21
 Expensive
 Small size and large surface area can
lead to particle aggregation
 Limited drug loading
 Highly sophisticated technology
22
23

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USES OF NANO PARTICLES IN DRUG DELIVERY

  • 1. 1
  • 3.  Introduction  Drug vehicles  Ideal characteristics of nanoparticles  Drug release mechanisms  Diseases controlled using nanoparticles  Modes of administration  Advantages  Limitations 3
  • 4.  Particle size ranges from 10-1000nm in diameter  Particulate dispersions or solid particles  A drug may be adsorbed or covalently attached to the nanocarriers surface or it can be encapsulated into it 4
  • 5.  Liposomes  Polymeric nanoparticles  Nanoparticles based on solid lipids  Silica nanoparticles  Gold nanoparticles 5
  • 6.  Usually with 80-300 nm size range composed of phospholipids and cholestrol  Drug is encapsulated  Examples in liposomal formulations, such as anticancer drugs, neurotransmitters (serotonin), antibiotics, anti-inflammatory etc 6
  • 7.  Diameter ranging from 10 to 100 nm  These may be biodegradable and non-biodegradable  Drug may b on the surface or incorporated  Drug release by desorption and diffusion 7
  • 8.  A core, dendrons and surface active groups  Surface functional groups enables the interaction  Drug may be encapsulated or adsorbed on the surface  Polyvalency 8
  • 9.  Solid lipid nanoparticles(SLN) o Size 100-500nm o Delivery medium for lipophilic drugs o Loading capacity limited by the solubility of drug in lipid 9
  • 10.  Nanostructured lipid carriers (NLC) o Imperfect type NLC o Multiple type NLC o Amorphous type NLC  Lipid drug conjugates (LDC) o For lipophobic drug molecules 10
  • 11.  < 50nm  Highly porous framework  Invading deeper parts of body  Phenytoin, cisplatin, diclofenac, heparin are examples of drugs delivered by silica materials 11
  • 12.  Size 130nm  Use for cancer treatment  Relay on enhanced permeability and retention effect  Suitable for delivering enzymatic degradation susceptible materials 12
  • 13.  Small particle size  Controlled drug release rate  High drug loading capacity  Biochemically inert and non toxic  Physically and chemically stable  Restricted drug distribution to normal cells 13
  • 14.  Active targeting o Drug targeting by ultrasonic energy and magnetic field o Cell surface antigen should be expressed o Antibody and ligand as targeting moiety o Receptor-mediated endocytosis 14
  • 15.  Passive targeting o Physical targeting o Direct drug injection and catheterization o Spontaneous drug accumulation in areas with leaky vasculature 15
  • 16. 16
  • 17.  Cancer o Ethylene glycol molecules attach to nanoparticles that deliver therapeutic drugs o Or coating nanoparticles with membrane from RBCs o Photosensitizing agents 17
  • 18.  Heart diseases o Clot busting o Inflamed tissue such as arterial plaque  Diabetic mellitus o Nanoparticles contain both insulin and an enzyme  Autoimmune diseases o Nanoparticles deliver antigens 18
  • 19.  Neurologic disorders o Cross the blood brain barrier(BBB)  Aging o The contents of the nanoparticle released when an enzyme found in aging cells is present 19
  • 20.  Oral  Intravenous  Transdermal  Pulmonary 20
  • 21.  Controlled and sustained release  No wastage of drug  No side effects  Provide comfort and compliance  Longer circulation half-lives  High cell uptake 21
  • 22.  Expensive  Small size and large surface area can lead to particle aggregation  Limited drug loading  Highly sophisticated technology 22
  • 23. 23