introduction of nanoparticles, advantages and disadvantages, characterization and applications

660 views 19 slides Feb 16, 2024
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About This Presentation

Nanoparticles, advantages and disadvantages, characterization and applications


Slide Content

A SEMINAR ON
NANOPARTICLES
Presented by
NIVEDITHA G
NARGUND COLLEGE OF PHARMACYNiveditha G 1

SEMINAROUTLINE
DEFINATION
ADVANTAGES, LIMITATIONS
NOVELNANOPARTICULATE SYSTEMS
CHARACTERIZATION OFNANOPARTICLES
THERAPEUTICAPPLICATIONS
Niveditha G 2

NOVEL NANOPARTICULATE SYSTEMS
ADVANTAGES OF NANOPARTICLES.
Biodegradable,
Nontoxic,
Sitespecific,
Longershelflife,
Highcarriercapacity,
Feasibilityofincorporationofbothhydrophilicand
hydrophobicsubstancesand
Feasibilityofvariableroutesofadministration.
LIMITATIONS
DrugscanbetargetedonlytoRESororganswhichare
phagocyticallyactive.
Niveditha G 3

NOVEL NANOPARTICULATE SYSTEMS
SOLID LIPID NANOPARTICLES (SLNs)
TheSLNsaresubmicroncolloidalcarriershavingsize
rangeof50–1000nm.
Theyarecomposedofphysiologicallipid,dispersedin
waterorinanaqueoussurfactantsolution.
Thesearecolloidaldrugcarriercombinesthe
advantagesofpolymericnanoparticles,fatemulsion
andliposomessimultaneouslyandavoidingsomeof
theirdisadvantages.
Here,toovercometheproblemsassociatedwiththe
liquidstateoftheoildroplets,theliquidlipidwas
replacedbyasolidlipid,
Niveditha G 4

NOVEL NANOPARTICULATE SYSTEMS
Advantages of SLNs
smallsizeandrelativelynarrowsizedistributionwhich
providebiologicalopportunitiesforsite-specificdrug
delivery,
controlledreleaseofthedrugoveraprolongedperiod
canbeachieved,
protectionofincorporateddrugagainstchemical
degradation,
possiblesterilizationbyautoclavingorirradiation,
notoxicmetabolitesareproduced,
relativelycheaperandstableand
easeoflargescaleproduction.
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
involveshomogenizationofmeltedlipidsatelevated
temperature.
appliedtolipophilicandinsolubledrugs.
manyheatsensitivedrugscanalsobesafelyprocessed
becausetheexposuretimetohightemperaturesis
relativelyshort.
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
involveshomogenizationofasuspensionofsolidlipid
atroomtemperatureorbelow.
appliedtohydrophilicdrugs.
avoidsandminimizesmeltingprocessoflipidand
henceitissuitableforthermosensitivedrugs.
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 beresolved
-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

Acnemedicationsfromantimicrobialnanoparticles,
Forimprovedstability–Influenzavaccine,
SuperficialandsystemicStaphinfectionscouldbe
managedviananoparticles,and
Asadiagnosticagents:
colloidalpreparationsareusedascarriersofradio
isotopesforstudyofmorphology,bloodflowandfunction
ofvariousorgansinthebody.
THERAPEUTIC APPLICATIONS
Niveditha G 18

Niveditha G 19