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- Part I. General subjects
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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
- Aim (1)
- Side effects associated with chemotherapy
- Lipid-based nanotechnologies: a clinical reality (1)
- Lipid-based nanotechnologies: a clinical reality (2)
- Caelyx®
- Aim (2)
- Thermosensitive pegylated liposomes
- Thermodox delivers more doxorubicin into tumors
- survival benefit in the HEAT subgroup analysis
- HEAT study phase III by Celsion
- OPTIMA study (NCT02112656)
- Aim (3)
- Ligand-mediated target lipid-based nanotechnology
- Targeting the tumor microenvironment
- The different roles of nucleolin
- pH-sensitive liposomes (PEGASEMP™)
- Suppression of tumor invasion to adjacent tissues
- Relevance
- PEGASEMP™ as treatment for mesothelioma
- Aim (4)
- Abraxane™
- Abraxane & metastatic breast cancer
- Abraxane is used to treat other cancers
- Paclitaxel and immunotherapy
- Aim (5)
- Thank you!
- Acknowledgments
Topics Covered
- The need for delivery system in oncology
- Lipid-based nanotechnologies: a clinical reality
- Improving biodistribution and pharmacokinetics and safety
- Improving therapeutic outcome upon increasing drug release at target organ
- Targeting tumor microenvironment at two different cell levels
- Improving formulation
Talk Citation
Moreira, J.N. (2019, October 31). Need for drug delivery systems 2 [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/BUPE7855.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. João Nuno Moreira has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Need for drug delivery systems 2
Published on October 31, 2019
28 min
A selection of talks on Oncology
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. My name is João Nuno Moreira,
I work at the Center for Neuroscience and Cell Biology and at
the Faculty of Pharmacy at University of Coimbra in Portugal.
0:12
The goal of my talk today will be to answer this simple question,
why do we need drug delivery systems specifically within the field of oncology?
So I'm going through several examples that will help us out
to answer in a very simple manner to this very simple question.
0:31
We have a summary of the main side effects that
oncological patients go through when they are treated with conventional chemotherapy.
Now, the problem of conventional chemotherapy upon
intravenous injection results from the fact that
these drugs have a very high volume of distribution,
meaning that these drugs once injected in the blood,
they are rapidly redistributed throughout the body and so they tend to accumulate in
healthy organs where there are a number of
different cells that they have a very high rate of proliferation.
For example in the bone marrow,
GI tract or hair follicles.
It is the accumulation and these chaotic biodistribution of
these drugs that leads to a number of side effects that are
summarized on this slide like for example
mouth sores and this can be something in a very high extent that might lead
to the inability of the patient to actually be
fat in a regular manner or alopecia, so hair falling.
So this means that under these circumstances,
oncologists have two choices;
either they stopped treatment or they must give
the patient suboptimal doses and often these ends up in treatment failure.