recent advances in micro and nano drug delivery systems

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RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS M ROSHINI 13PN02

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RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS

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Page 1: RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS

RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS

M ROSHINI

13PN02

Page 2: RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS
Page 3: RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS

Targetted Drug Delivery

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Nano Drug-delivery

• Nanomedicine uses nanoscale technologies (≤100 nm) for the diagnosis, treatment and/or prevention of diseases

• It includes sustained delivery of Therapeutic Agents, Targeted Delivery Of DrugsReduced Side Effects

Page 5: RECENT ADVANCES IN MICRO AND NANO DRUG DELIVERY SYSTEMS

Drug delivery carriers

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Nanoparticles in drug delivery

• Metal-based nanoparticles – Au, Ag, Cd-Se, Zn-S etc

• Lipid-based nanoparticles – Liposome & Neosome based….

• Polymer-based nanoparticles – Dendrimer,chitosen Micelle based…

• Biological nanoparticles – RGD based…

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Metal based nanoparticles

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Gold Nanoparticles

• Plasmonic Vesicles of Amphiphilic Gold Nanocrystals: Self-Assembly and External-Stimuli-Triggered Destruction

• Plasmonic vesicular nanostructures assembled from amphiphilic gold nanocrystals with mixed polymer brush coatings.

• Analogous to block copolymers,the disruption of the plasmonic vesicles can be triggered by stimulus mechanisms

• The development of multifunctional vesicles containing stimuli-responsive polymers applications in theragnostic nanomedicine

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Self-Assembly and External-Stimuli-Triggered Destruction

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Thermal ablation of cancer cells by ‘Silica-gold’ nano shells

• Thermal ablation of cancer cells by nanoshells coated with metallic layer and by applying an external energy source to kill them

• Gold nps absorb light in the near infra red region becomes hot and can kill the cells in their proximity

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Lipid based nps

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Liposomes

• Liposomes are small spherical vesicles, composed of lipid bilayers surrounding aqueous inner phase.

• Reservoir (i.e) Bilayers - hydrophobic drugs and inner aqueous phase - hydrophilic drugs

• Liposomes -ocular drug delivery• Encapsulation of idoxuridine into liposomes increased the corneal penetration of

the drug• Variety of biomaterials for ocular drug delivery including

polymeric nanoparticles dendrimers hydrogels

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Lipid Nanoparticle Drug Delivery System

• Major problem with IV administration of colloidal particles is interaction with reticulo-endothelial system (RES)

• Any foreign material, biological response to administered nanoparticle, coated by proteins called opsonins, enhance uptake of coated material by RES

• Opsonins on particle surface creates a “molecular signature” recognized by immune cells

• Lipid nanoparticles engineered to evade RES cells by limiting particle sizes to 200 nm or less.

• It is believed that these cells do not recognise low nanometer-sized particles as foreign.

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Drug Delivery To BBB

• The BBB is single layer of endothelial cells in inner surfaces of capillaries in the brain

• The endothelial cells fit tightly together and substances cannot pass out of the bloodstream

• The mechanism for transport is endocytosis • Endothelial cells with lipoprotein receptor transports the lipoprotein with

nanoparticle from the blood plasma.

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Polymer based nps

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Polymeric Nanoparticles On Drug Delivery

• Polymeric nps from natural and synthetic polymers have stability and ease of surface modification

• Polymeric materials-biocompatible and biodegradable • The polysaccharides polymeric materials to prepare nps for drug delivery. • Biodegradable nanoparticles

nanocapsulenanosphere

• The drug molecules are either entrapped inside or adsorbed on the surface.

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Chitosan Carrier In Nano Drug Delivery System

• Chitosan (CS) is abundant naturally occurring polysaccharide• Chitosan is made of randomly distributed β-(1-4)-linked D-glucosamine (deacetylated unit)

and N-acetyl-D-glucosamine (acetylated unit) • It is produced by deacetylation of chitin extracted from shells of crabs, shrimps and krill. • Chitosan attracted as

Matrix for controlled release due to its reactive functionalities Easily degradation by enzymes Non-toxic degradation products

• Hydrophobic interactions enhance stability of substituted CS by reducing hydration of matrix ,resisting degradation by gastric enzymes

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Polymeric Nanoparticles On Drug Delivery

Chemical Structure Of Chitosan

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Biological nanoparticles

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TREATING CANCER WITH NANOPARTICLES

• Cancer therapeutics,chemotherapy serious side effects –Devastation of healthy tissueSome cancerous tissue survives after radiation

• Nanoparticles -targeted drug delivery systems  • Nps with UV-sensitive proteins,assemble with drug and cancer cell-

targeting protein fragment when exposed to UV.• Nanoparticle-drug complex that specifically attaches to cancerous cells.  

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Reference

• [1] Maeda, H., Wu, J., Sawa, T., Matsumura, Y., and Hori, K. (2000) Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J. Controlled Release 65, 271-84.

• [2] Palmer, T. N., Caride, V. J., Caldecourt, M. A., Twickler, J., and Abdullah, V. (1984) The mechanism of liposome accumulation in infarction. Biochim. Biophys. Acta 797, 363-8.

• [3] Jaracz, S., Chen, J., Kuznetsova, L. V., and Ojima, I. (2005) Recent advances I tumortargeting anticancer drug conjugates. Bioorg. Med. Chem. 13, 5043-54.

• [4] Torchilin, V. P. (2004) Targeted polymeric micelles for delivery of poorly soluble drugs. Cell Mol. Life Sci. 61, 2549-59.

• [5] Gabizon, A., Shmeeda, H., Horowitz, A. T., and Zalipsky, S. (2004) Tumor cell targeting of liposome-entrapped drugs with phospholipid- anchored folic acid-PEG conjugates. AdV. Drug DeliVery ReV.56, 1177-92.

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Thank you!!!