Nanomaterial Drug Delivery

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Nanomaterial Drug Delivery Group 5: Daniel Ehlers Daniel Barnes Ann-Marie Scarborough Nguyen Lam Featuring: Nanomaterials For Drug Delivery https://encrypted- tbn1.gstatic.com/images? q=tbn:ANd9GcSh0iVqg8Z7WUm1a_XO7uTQ QpHl67Lz1El1kl2YHlNy4qkCEz2KBQ http:// research.mdhs.unimelb.e du.au/event/nano- medicine-bio21-cluster- symposium

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Nanomaterial Drug Delivery. http://research.mdhs.unimelb.edu.au/event/nano-medicine-bio21-cluster-symposium. https://encrypted-tbn1.gstatic.com/images?q=tbn:ANd9GcSh0iVqg8Z7WUm1a_XO7uTQQpHl67Lz1El1kl2YHlNy4qkCEz2KBQ. Group 5: Daniel Ehlers Daniel Barnes Ann-Marie Scarborough Nguyen Lam. - PowerPoint PPT Presentation

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Page 1: Nanomaterial Drug Delivery

Nanomaterial Drug Delivery

Group 5:Daniel EhlersDaniel Barnes

Ann-Marie ScarboroughNguyen Lam

Featuring:Nanomaterials For Drug Delivery

https://encrypted-tbn1.gstatic.com/images?q=tbn:ANd9GcSh0iVqg8Z7WUm1a_XO7uTQQpHl67Lz1El1kl2YHlNy4qkCEz2KBQ

http://research.mdhs.unimelb.edu.au/event/nano-medicine-bio21-cluster-symposium

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Interactive Presentation

• To view an interactive version of this presentation, visit the link below (recommended):

• http://prezi.com/qa0bx-dztksu/untitled-prezi/

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http://nextbigfuture.com/2011/01/nanorattle-drug-delivery.html

http://mayoresearch.mayo.edu/dev_lab/images/single_drug.gif

Nanomaterials are the future of drug delivery

Drugs are able to reach their site of action more effectively

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http://onlinelibrary.wiley.com/store/10.1002/mabi.201100419/asset/image_m/mcontent.jpg?v=1&s=2899b61a4ddaff99e1b18b7a79ea871a7f4eaabc

Bodily system barriers are able to be broken with nanocarriers

http://ultraphyte.com/2012/02/26/nanorobot-detects-cancer/

Advanced materials can target various cells, such as cancer cells.

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http://sina.sharif.edu/~adeli/?view=Synthesis_of_Hybrid_Nano_Structures&id=15

http://www.azonano.com/images/news/NewsImage_23414.jpg

Drugs with different molecular shapes and chemical properties can be synthesized

Different properties results in greater possibilities

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Background Information

• All drugs face several transport barriers

o Plasma membraneo The acidic environment of endolysosomeso Nuclear membraneo Multiple drug resistance mechanism

from their site of introduction to their molecular site of action.

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Background Information

https://dl-web.dropbox.com/Articles/1-s2.0-S0169409X1200021X-main.pdf?w=AACRdlAYxdLRb6iZvjRVrMMwvLN-ChawIar3xGlbaupaGw

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Advantages1. Very small size

2.High surface-to-volume ratio

High-resolution image of detonation nanodiamonds

http://nanoall.blogspot.com/2012/01/synthesis-of-metallic-nanoparticles.html

3. One or more therapeutic drugs can be attached to

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Advantages4.Attach to specific target cells and organs with selected binding agents5.Helps to avoid the fluctuations of drug (by using time-release)

https://dl-web.dropbox.com/Articles/1-s2.0-S0169409X1200021X-main.pdf?w=AACRdlAYxdLRb6iZvjRVrMMwvLN-ChawIar3xGlbaupaGw

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Polymers and Cancer Cells

• Other polymers allow for easy binding to tumor sites

• At the correct pH and/or [Cl-] of a tumor site, the drug can be released

• Certain polymers allow for delivery past protective DNA barriers in a tumor cell

http://static5.businessinsider.com/image/500ff7b2eab8ea2b60000001-590/this-mix-of-polymers-and-cancer-medicines-would-then-attach-to-nanoparticles.jpg

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Cylindrical Miccles• Initially block polymers• Hydrophillic end –

causes them to form miccle shape with water

• Hydrophobic end – Keeps them from being easily bound/absorbed to other things

• Benefits:o Prolonged circulationo Reduction of off-target toxicity

(less side effects)o Can be formed using existing

drugs

http://news.rice.edu/images/media/2006RiceNews/1130_gold_nano.jpg

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PEGylation of Drugs• Adding PEG

(Polyethylene glycol) polymer to existing drug molecular structure

• Benefits:o Increases drug half lifeo Increases drug solubility at

site of actiono Increases drug stabilityo Slows down drug

metabolism through kidneys, etc.

http://www.peg-drug.com/images/peg-top_photo2.jpg

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Ideal siRNA Cancer Drug

• siRNA – Small Interfering RNA can be inserted into a tumor cell to cause it to malfunction

• Problem: Needs to be delivered to tumor site and not to healthy cells

• In figure, nanomaterial (green) is attached to siRNA drug (purple ring)

http://www.sciencemag.org/content/337/6092/303/F1.large.jpg

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Ideal siRNA Cancer Drug

• Nanomaterial is PEGylated:o Increases drug half lifeo Increases drug solubility at

site of actiono Decreases interaction

outside target side (and therefore side effects)

o Increases drug stabilityo Slows down drug

metabolism through kidneys, etc.

http://www.sciencemag.org/content/337/6092/303/F1.large.jpg

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Ideal siRNA Cancer Drug

• Nanomaterial searches for biological signals of a cancer cello Certain peptides have this

ability

• Nanomaterial is engineered to bind to the unique receptors on the cancer cell

http://www.alternative-cancer.net/images/cell_attack.jpg

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Ideal siRNA Cancer Drug

• Another problem: Overcome defenses in cytoplasm of cancer cell

• Nanomaterial overcomes defenses and rapidly delivers siRNA drug into cell

• siRNA modifies the cancer cell DNA and causes it to die http://www.sciencemag.org/content/337/6092/303/F1.large.jpg

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Specific Cancer Drug Design: Carbon

Nanotubes• Antibodies are

designed that will fight cancer cells

• Carbon Nanotube carriers have molecular strands that contain the antibodies and a link system to cancer cells

• Recognize cancer cells by pH, biological markers

http://www.ncbi.nlm.nih.gov/pubmed/23143677

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Specific Cancer Drug Design: Carbon

Nanotubes• Carbon Nanotubes can

be PEGed and attached with antibodies to bring it specifically to a cancer cell

• The drugs inside the nanotube can be released in the presence RF frequencies

• Metal nanotubes also heat in presence of RF waves, and “burn up” cancer cells

http://www.ncbi.nlm.nih.gov/pubmed/23143677

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Specific Cancer Drug Design:

Nanodiamonds• Drug can be placed in

nanodiamonds• Nanodiamonds contain

receptors that allow them only to bind and react with tumor cells

• Nanodiamonds release drug into tumor cell and result in highly effective treatment http://www.sciencedaily.com/releases/2013/04/130415172308.htm

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Assessment of Work• The use of Nano-Diamonds and their effects on the PH increase

solubility in the solution for several types of deliveries by making the pH closer to that of the natural body levels

• Table 1• Plotted n value of the release of RB from carbon nanomaterials at

pH 7.4 and pH 4.5.• n value at pH 7.4 n value at pH 4.5 Drug release mode• CB–RB 0.39 0.32 Fickian diffusion• CNT–RB 0.42 0.64 Fickian diffusion at pH 7.4,• anomalous transport at pH 4.5• f-CNT–RB 0.5 0.64 Anomalous transport• GO–RB 1 0.63 Case II transport at pH7.4,• anomalous transport at pH 4.5• Zhang and Olin Pg. 1251

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Assessment of Work• In addition, they allow for a controlled time

release of the drug for consistant delivery

• Zhang and Olin pgl. 1250Time (min)

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Assessment of Work• Allows better ability to

Penetrate the Plasma wall of the cells

• Can release on correct rNA code recognition for needed antigen.

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Conclusions• The use of Nano-

Diamonds allows the Pharmicutical Industry to be much more presice in drug delivery due too pH Controlo Time Release Controlo rNA Release Control

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Conclusion• It also allows a larger range of effective drugs to

be administered fromo Size Controlo pH Control

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Further Research Suggested

• Hazards/toxicity of particles• Cancer research

http://research.mdhs.unimelb.edu.au/event/nano-medicine-bio21-cluster-symposium

http://www.healingrosacea.com/images/nanomaterial-in-cancer-therapy1.jpeg

http://www.dddmag.com/sites/dddmag.com/files/legacyimages/Articles/2009_09/pnp.jpg

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References1. Nanomaterials for Drug Delivery. Jeffrey A. Hubbell and Ashutosh Chilkoti. Science 20 July 2012: 337 (6092), 303-305.

[DOI:10.1126/science.1219657]2. Nanodiamonds as novel nanomaterials for biomedical applications: drug delivery and imaging systems.

Badea, Ildiko and Kaur, Randeep. International Journal of Nanomedice. 8. Jan 2013. Web. 2 April 20133. Computational design of a CNT carrier for a high affinity bispecific anti-HER2 antibody based on trastuzumab

and pertuzumab Fabs. Salazar-Salinas Karim, Kubli-Garfias, Carlos, and Seminario, Jorge M. Springer-Verlag.