nanomedicine 1, 2 Flashcards

1
Q

what is nanotechnology

A

study of things that when reduced in size they display unique different physiochemical properties than when compared to bulk material

or

creation of useful/functional devices or material through control/manipulation of matter on nanometre length scale

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2
Q

what is nanomedicine

A

use of nanotechnology to treat disease

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3
Q

ways nanoparticles treat cancer

A

lipid based nanocarriers- high degree of biocompatibility, encapsulates wide range

polymer based nanocarriers- suitable for development due to ease and adaptability, eg. polymeric NP, dendrimers, polymer micelles

inorganic nanoparticles- diagnosis/treatment due to superior physiochemical properties like magnetic, thermal, optical, catalytic, excellent functions like imaging, targeted delivery and controlled release

viral nanoparticles-plant virus nanoparticles can be functionalised to be taken up by cancer cells

drug conjugates- class of biopharmaceutical drugs designed to enhance efficacy of therapeutic targeting by allowing for targeting enhanced dose delivery

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4
Q

name 6 nanoparticle types

A

liposomes, gold nanoparticles, carbon nanotubes, iron oxide nanoparticles, quantum dots, polymer micelles

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5
Q

describe the characteristics of liposomes

A

present high loading efficacy ensuring a high dose delivered, encapsulates drugs by protecting them and designed to release on a stimulus like pH or light

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6
Q

describe the characteristics of gold nanoparticles

A

display unique optical characteristics at nanoscale, due to interactions with light photons giving the nanoparticle different colours depending on size

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7
Q

describe the characteristics of carbon nanotubes

A

display unique electrical properties compared to bulk material of carbon which doesnt display it, used to conjugate with drugs so they release drug on electrical stimulation

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8
Q

describe the characteristics of iron oxide nanoparticles

A

superior magnetic and thermal characteristics at nanoscale, used to develop imaging and thermal stimulated killing of cancer cells

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9
Q

describe the characteristics of quantum dots/semi conducting crystals

A

develop theranostics due to their unique optical properties, when exposed to light a unique light is produced depending on their nanoscale size and material properties, results from an electron being excited and forming a valent bond to a conduction band, energy required to do this is called a band gap, band gap=distance between valence band of electrons and the conduction band, band gap is minimum energy required to excite and electron up to a state in the conduction band where it can participate in conduction

-when bandgap lies in visible spectrum, a change in bandgap with size means change in colour

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10
Q

describe the characteristics of polymer micelles

A

unique mechanical and chemical phenomena at nanoscale, used to develop advanced drug delivery systems eg. swelling causes release of an encapsulated drug

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11
Q

main aims of nanotechnology

A

-create new properties- to understand control and create nanostructures

-improve ability to image/measure/manipulate matter on nanoscale to exploit those properties and functions

-ability to integrate those properties and functions into systems spanning nano to macroscopic scales

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12
Q

benefits of nanotechnology based drug delivery systems

A

-improved drug absorption
-reduced side effects
-targeted drug delivery
-controlled drug release
-creates more efficient/targeted/controlled systems

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13
Q

limitations of current drug delivery systems

A

-low drug absorption
-quick metabolism and excretion
-side effects

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14
Q

name different physical and chemical properties depending on size

A

optical properties, band gap energy, melting point, specific heat capacity, surface reactivity

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15
Q

advantages of nanoscale devices in medicine

A

-devices smaller than 50nm can easily enter most cells
-devices smaller than 20nm can transit out of blood vessels
-devices are capable of holding thousands of small molecules like drugs and contrast agents

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16
Q

major areas of development of nanomedicine

A

-prevention and control
-early detection
-imaging diagnostics
-multifunctional therapeutics

17
Q

chemotherapy non targeted delivery, what pathway is used, what is it formulated with

A

uses endogenous albumin pathways, formulated with albumin obviates the need for toxic solvents, increase drug delivery initiating albumin receptor mediated transcytosis

18
Q

what is transcytosis

A

type of transcellular transport in which various macomolecules are transported across the interior of a cell

-macromolecules captured in vesicles on one side, drawn across cell and ejected onto the other side

19
Q

challenges/problems with cancer therapeutics in nanomedicine

A

delivery-nanoparticles difficult to deliver to tumours in the body, can be intercepted by immune system or other organs

targeting-difficult to target to specific cancer cells, can be taken up by healthy cells

toxicity-toxic to healthy cells causes side effects

cost-expensive to produce, makes them inaccessible to some patients

regulatory hurdles-regulatory process still in development, difficult to get new products approved for clinical use

20
Q

binding strategies(?)

A

hydrophobic/hydrophilic drug, PEG, transferrin, cell penetrating peptide, fibronectin (ligand for integrin receptor), folate, fibroblast growth factor, matrix metalloproteinase ligand, antibody, genetic material, antibody fragment

21
Q

stimuli responsive delivery in chemotherapy-cancer characteristics can be taken advantage of when developing drug delivery systems eg:

A
  1. leaky vascular system- enhanced permeability and retention effect
  2. cell surface receptors/markers
  3. inside tumour differences eg. reduced pH compared to healthy tissues
22
Q

what is ROS mediated killing stimulated by and what is ROS

A

stimulated by: light, radiation, electric fields
-causes mediated ROS production via nano particles

ROS=toxic to cells in high concentrations due to high reactivity

23
Q

gene/RNA therapy

A

causes detrimental effects to cancer, eg. stops key protein from being synthesised

24
Q

nanoparticle physical properties

A

size, geometry, surface charge, porosity, elasticity, surface hydrophobicity, roughness, curvature, electronic, magnetic, optical

25
Q

nanoparticle structure/chemical composition

A

liposomes, polymeric NOs, micelles, dendrimers, protein NPs, viral NPs, exosomes, metal and metal derived NPs, carbon nanomaterials

26
Q

nanoparticle targeting ligands

A

small molecules, antibodies and fragments aptamers and nucleic acids, proteins and peptides, sugars

27
Q

problems with cancer therapeutics in standard delivery systems

A

limited targeting, biodegradation of drug, rapid drug clearance, low specificity

28
Q

vectors in nanomedicine (1st 2nd 3rd gen)

A

1st generation=nanospheres and nanocapsules

2nd generation=nanoparticles coated with hydrophilic polymers (PEG)

3rd generation=biodegradable core and polymer coating with a membrane recognition ligand

29
Q

why nanoparticle is good for cancer

A

delivers directly to tumour, protects drug from being degraded, enhances drug delivery into diseased tissue, controls cell uptake allowing oncologists more control on determining how effective treatment is, prevents drug from interacting with normal cells

30
Q

things that trigger nanoparticles to destroy tumours from within

A

thermo, magnetic, pH, light, electrical

31
Q

difference between active and passive targeting

A

active targeting receptor makes it selective
passive targeting- shape/charge/lipophilicity makes it more likely to pass membrane of diseased cell

32
Q

types of nanotheranostics being developed

A

liposomes-spherical vesicles of lipid bilayer, delivers variety of drugs, imaging agents, heat

polymeric nanoparticles- made from synthetic polymers, delivers drugs, imaging agents, genes

gold nanoparticles- delivers drugs, imaging agents, heat

magnetic nanoparticles- delivers drugs, imaging agents, heat, used to guide nanoparticles to tumours using magnetic fields