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- Part I. General subjects
-
1. Need for drug delivery systems 1
- Prof. Ana Catarina Silva
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2. Need for drug delivery systems 2
- Prof. João Nuno Moreira
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3. Routes of drug delivery
- Prof. Dr. Sven Stegemann
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4. Transporters in drug delivery
- Dr. Pravin Shende
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5. The theory and applications of controlled release principles
- Dr. Michael J. Rathbone
- Part II. Routes for drug delivery
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6. Oral drug delivery
- Dr. Vineet Kumar Rai
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7. Transdermal drug delivery
- Prof. Sabine Szunerits
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8. Pulmonary drug delivery
- Prof. Anthony J. Hickey
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9. Gastrointestinal drug delivery
- Prof. Susan Hua
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10. Mucoadhesive drug delivery systems
- Dr. Panoraia I. Siafaka
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11. Ocular drug delivery
- Prof. Emily Dosmar
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12. Vaginal and uterine drug delivery
- Prof. José Luis Arias Mediano
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13. Drug-eluting implants
- Dr. Aliasger K. Salem
- Part III. Materials for drug delivery
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14. Polymers as nanocarriers for controlled drug delivery
- Prof. Dr. Marcelo Calderón
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15. Polymeric gels for drug delivery
- Dr. G. Roshan Deen
- Ms. Dora Safar
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16. Liposomes as a drug delivery system
- Dr. G. Roshan Deen
- Ms. Bushra Hasan
- Ms. Renad AlAnsari
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17. Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC)
- Prof. Ana Catarina Silva
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18. Micellar drug delivery
- Prof. Francesco Cellesi
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19. Nanocrystals in drug delivery
- Prof. Eliana Souto
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20. Layer-by-layer assemblies for drug delivery
- Prof. Szczepan Zapotoczny
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21. Inorganic nanostructured interfaces for therapeutic delivery
- Prof. Tejal Desai
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22. Inorganic porous drug delivery carriers
- Prof. Jessica Rosenholm
- Part IV. Specifics of drug delivery
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23. Delivery of genes and nucleotides
- Prof. Esam Yahya
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24. Vaccine delivery
- Prof. Sevda Şenel
- Part V. Drug delivery in various diseases
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25. Drug delivery for cancer therapeutics
- Prof. Tejraj Aminabhavi
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26. Nanomedicines for brain diseases
- Prof. Giovanni Tosi
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27. Drug delivery to the colon
- Prof. Susan Hua
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28. Role of the lymphatic system in drug absorption
- Dr. Kishor M. Wasan
Printable Handouts
Navigable Slide Index
- Introduction
- Outline
- Layer-by-Layer (LbL) assembly
- Preparation of multilayer films
- Fabrication of capsules by LbL
- Encapsulation and release
- LbL assemblies for drug delivery
- Capsules carrying proteins
- Multilayer films for drug release
- NIR-triggered release
- LbL nanoparticles
- Oil core capsules
- Cellular uptake of nanocapsules
- Biodistribution in vivo
- LbL capsules for drug delivery
- Thank you for your attention!
Topics Covered
- Layer-by-Layer (LbL) deposition techniques
- Drug delivery systems
- Fabrications of multilayer films and capsules using the LbL approach
- Capsules on a solid core template
- Capsules with liquid oil cores
- Encapsulation and releasing mechanisms
- Nano-emulsions
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Zapotoczny, S. (2023, September 28). Layer-by-layer assemblies for drug delivery [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/RYEI3657.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Szczepan Zapotoczny has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Pharmaceutical Sciences
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, my name is
Szczepan Zapotoczny,
I work as a professor heading
the Group of Nanotechnology
of Polymers and
Biomaterials at
the Agilonian University
Faculty of Chemistry
in Krakow, Poland.
I'm going to talk about
the formation of layer
by layer assemblies,
such as films, capsules,
and their applications
in drug delivery.
0:25
I'm going to start
with the introduction
to the layer by
layer assembly as
the position technique enabling
fabrication of multi
layer films and capsules.
I will particularly focus on
capsules that can
be formed using
solid micro particles as well as
liquid nano droplets
serving as templates.
Then encapsulation of drugs and
their release from the capsules
and films will be addressed,
I will complete the talk
with some examples of
drug delivery systems
based on LbL assemblies.
1:03
LbL assembly based on
sequential absorption
of oppositely charged polymers
was introduced by
Professor Decher
in the 90s, but
some first attempts
with application of
charge microparticles
were already reported
30 years earlier.
In a classical approach,
polyelectrolytes are absorbed on
oppositely charged surfaces by
simple immersion
of a substrate in
an aqueous solution
of polyelectrolyte,
for example, poly-anion,
followed by washing
the coating to
remove loosely bound
macro-molecules,
and subsequent deposition
of another
polyelectrolyte layer,
in this case, polyketile.
By repeating this procedure,
a number of times
multi layer films of desired
thickness are formed,
such a sequential absorption
of thin layers of
oppositely charged
polyelectrolytes relies
mainly on electrostatic
forces acting
cooperatively for high
molecular weight compounds.
This technique has a
number of advantages
with respect to other
film fabrication methods.
It is relatively simple
and inexpensive,
it can be applied on
various charged substrates,
both flat and curved,
such as micro or nano particles.
Importantly, various
synthetic and natural
polyelectrolytes
can be used in LbL
approach that is
crucial for their potential
biomedical applications.
Thus typical synthetic
polyelectrolytes such as
poly(sodium-4-styrenesulfonate)
abbreviated PSS,
or poly(allylamine
hydrochloride) PAH,
but also biocompatible
polysaccharides
such as hyaluronic
acid, chitosan,
as well as charged
polypeptides can be
used in preparation
of LbL coatings.
LbL offers also
high control over
film thickness down to about
one nanometer per layer,
as well as its related
properties such
as permeability and
density of the coating.
Such coatings are pretty
robust also in aqueous media,
but can be further strengthened
by cross linking of
the polymer layers.
The methodology
is not limited to
polyelectrolytes only since
other charged objects,
such as nanoparticles,
nanotubes,
or nanoplates can be applied.
LbL can also be driven by
other types of interactions,
such as hydrogen bondings,
host gas interactions
that significantly
broaden application of this
film fabrication method.