Nanotechnology Flashcards

1
Q

Name 3 advantages of micro needles

A

1) Painless and easy to use
2) Safe needle disposal
3) Eliminate spread of pathogens

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2
Q

Name 2 reasons why drugs can’t always be oral

A

1) Poor absorption

2) Drug degradation in GI tract and Liver

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3
Q

Where do micro needles penetrate the skin

A

Stratum corner into viable epidermis avoiding contact with nerve fibres and blood belles that reside in german layer

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4
Q

Describe the process of photolithography

A

1) Silicon Wafer
2) Layer of oxide and nitrate
3) Layer of photo resist
4) UV shine
5) Photoresist developed to remove area exposed to UV
6) Reactive ion etching with KOH removes oxide and nitrate

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5
Q

Describe the process of sacrificial micromolding and selective electrodeposition

A

1) Fabrication of master structure with laser ablated cavity
2) Micromold created featuring protruding pillow that will become lumen exit hole
3) Creation of replica
4) Sputting a gold seed layer onto replica
5) Electrodeposition of metal everywhere except cavity - dissolving sacrificial base material to release metal hollow microneedle

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6
Q

Describe how solid micro needles work

A

Skin pretreatment
Insert and remove micro needles to form micro scale pores in surface
Drug formulation applied to skin for slow diffusion of drug through pores into body

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7
Q

Drug coated micro needles - expectations

A

Dipping or spray
Controlled wetting/spreading
Should be water soluble for coating and dissolution
Adhesion between dried drug coating and micro needle
Coating excipient and solvent safe and compatible

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8
Q

Explain and describe Drug Encapsulated microneedles

A

Rapid dissolving - water soluble sugars and polymers, photopolymerisable liquid monomers. - PLGA
Thermo -sensitive - moderate conditions
Speed of dissolution decides time of insertion

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9
Q

Hollow Microneedles
What are they
Advantages
Requirements

A

Infusion of liquid formulations or diffusion through needle
Great control over amount/timing
Separation of micro needles during manufacturing
Already existing drug liquid formulations
Requires drug reservoir, pump, microfluidic networks

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10
Q

A small molecule is how big

A

~1nm

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11
Q

Basic structure of insulin

A

Six insulin molecules assembled in a hexameter ~6kda

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12
Q

Size of trastuzumab

A

Herceptin (breast cancer) ~160kda with 10nm radius

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13
Q

Advantage and disadvantage of proteins

A

Highly specific and potent, low permeability across biological barriers so injection route

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14
Q

Structure of nucleic acids

A

Negatively charged due to phosphate group in backbone and hydrophilic due to sugar-phosphate backbone

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15
Q

Disadvantages of antibodies

A

Low cell uptake, short blood circulation time, rapid degradation and lack of cell specificity

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16
Q

What are the four viral vector types

A

1 - Adenovirus (non-enveloped, without outer layer)
2 - Adeno-associated virus
3 - Retrovirus
4 - Lentivirus

17
Q

Advantages and disadvantages of viral vectors

A

Efficient cell uptake, endosomal escape

Immunogenicity, low cell specificity, limited packaging ability and difficult to produce

18
Q

Advantages of non-viral vectors

A

Lower immunogenicity, no pre-existing immunity, larger pay load and easier to synthesise

19
Q

Advantages of degradable (PGLA)

A

Long term delivery, can affect pharmacokinetics by enabling sustained release

20
Q

Nanoparticles role in cancer

A

Usually larger than 10nm impedes diffusion through small vascular pores, leaky in tumours so up to 700nm can penetrate through endothelium

21
Q

How can we increase serum 1/2 life

A

Fc fusion proteins fuse with drug.
DNA recombinant technologies can endow proteins with IG like property by utilising neonatal Fc receptor recycling pathway

22
Q

Major Components of liposome

DOTMA

A

Phosphatidylcholine and phosphatidylserine

Ampiphillic molecule for making liposome

23
Q

Define ampiphillic

A

Both hydrophilic and lipophilic

Hydrophobic tails face inwards away from aqueous solution while hydrophilic heads are in contact with solution

24
Q

How do polymerosomes work

A

Polymeric versions of liposome (nitrogen = hydrophilic) self assemble into vesicle

25
Q

How do cationic polymers work

A

PE1 (Polyethyenimine) for delivering nucleic acids, positively charged so can condense negatively charged nucleic acids to form polyplexes.
Also helps binding to negative cell membrane

26
Q

Describe cell-penetrating peptides

A

Transactivator of transcription (TAT) protein from HIV virus could directly enter cells

27
Q

Describe pegylation

A

1) Highly hydrated which increase hydrodynamic radius of conjugate, reduce renal filtration
2) Prevents uptake and clearance by mononuclear phagocyte system
3) Decreases formation of neutralising antibodies against a protein drug by masking antigenic sites
4) Protection from proteolytic enzymes and proteases

28
Q

Three types of endocytosis

A

1) Phagocytosis
2) Pinocytosis
3) Receptor-mediated endocytosis

29
Q

Drug loading efficiency =

Loading capacity =

A
DLE = (drug added-free)/drug added
LC = (encapsulated drug/ nanoparticle mass) X 100
30
Q

Principle of 3D printing

A

Complex structures difficult to make using subtractive, additive can make within limited timeframe

31
Q

Problems with bioprinting

A

1) High temp - fuse deposition and selective laser sintering
2) Long UV exposure time - stereolithography
3) 3D printing - toxic binders

32
Q

Describe process of selective laser sintering

A

1) Lay an even layer of powders using roller
2) Laser beam scanned at pre-decided positions to fuse/melt powders together
3) Stage lowered and second layer laid
METAL, POLYMER, CERAMIC

33
Q

Describe process of 3D printing

A

1) Lay even layer of powder using roller
2) Binder jetted onto positions to fuse powders - adhesive
3) repeated then put in oven to make mechanically strong
METAL, POLYMER, CERAMIC

34
Q

Describe Inkjet printing

A

1) Piezoelectric actuator generates picoliter drop
2) Drop ejects and reaches substrate
3) Solidification - UV
PHOTOPOLYMERISABLE MONOMERS or cell suspension

35
Q

Describe the process of Stereolithography

A

1) UV laser scanned across layer of photopolymerisable monomers (reservoir of liquid monomers)
2) monomers polymerise and solidify
PHOTOPOLYMERISABLE MONOMERS

36
Q

Describe process of Fused Deposition Modelling

A

1) feed polymer into heater
2) Melt polymer
3) Extrude polymer through nozzle whilst stage moved in x,y,z direction
4) Cools and solidified
THERMOPLASTIC MONOMERS - Polyetherether ketone

37
Q

Describe Laser assisted printing

A

1) Laser beam shines upon energy absorbing layer
2) Shockwave generated resulting in ejection of drop which reaches substrate
3) Energy absorbing layer expands when UB light shone, expelling drop

38
Q

Describe Microextrusion bioprinting

A

1) Hydrogel with suitable viscosity range loaded into cartridge
2) Material extruded through nozzle by pressure
3) Hydrogel strand forms 3D structure

39
Q

What is a hydrogel

A

Non-fluidic colloidal network/polymer networks that ar physically or chemically cross-linked and contain a large amount of water. (shear thinning)