CNTs Flashcards

1
Q

define the structure of CNTs?

A

strip of a graphene sheet rolled into a tube

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2
Q

how are CNTs made?

A
  1. arc discharge - using graphite
  2. chemical vapor deposition (CVD) - using hydrocarbon and metal catalysts
  3. laser ablation - graphite + laser - SWNT
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3
Q

what are the type of CNTs?

A

single-walled CNTs (SWNT) - one layer graphite
multi-walled CNTs (MWNT) - several graphite concentric layers

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4
Q

describe CNT properties

A

ordered structure
extraordinary mechanical properties
electrostatic properties
metallic
semiconducting-insulating

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5
Q

what are the main issues with CNTs?

A

insoluble in any organic solvent or aqueous solution

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6
Q

what is CNT functionalism?

A

addition of functional groups to CNTs

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7
Q

why do we use CNT functionalism?

A
  1. increase the hydrophilicity to allow increase aqueous dispersion
  2. stops aggregation of CNTs
  3. allows further modifications by electrostatic and covalent bonds
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8
Q

what is the difference between a covalent and non-covalent bond CNT?

A

covalent bonds- incorporated with the CNT structure
non-covalent bonds- coat the CNT

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9
Q

what is the nanoneedle theory?

A

insertion of a functionalised hydrophobic nanotube into a membrane spontaneously (no energy needed)

parallel CNT into a perpendicular CNT

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10
Q

what can SWNTs do?

A

enter the nucleus via nuclear pores

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11
Q

how can CNTs be used?

A
  1. radiolabelling
  2. fluorescence intensity analysis
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12
Q

what is radio labelling?

A

allows visualisation of CNT uptake for CT imaging

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13
Q

how are CNTs removed from the body?

A

urinary excretion

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14
Q

how are CNTs excreted from the kidney?

A

functionalised CNTs stop aggregation

aggregated non functionalised CNTs are too big = can’t fit the pores and cannot be excreted

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15
Q

what type of CNTs are excreted faster?

A

highly functionalised CNTs

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16
Q

how can CNTs be used in fluorescence intensity analysis?

A

by detecting the pi-pi interactions between chromophores and CNT surface= larger AUC

17
Q

what is MTX?

A

an antimetabolite and antifolaxe drug

competitively and reversibly inhibits the enzyme DHFR responsible for folic acid metabolism

18
Q

what does folic acid do?

A

synthesis of nucleoside thyme required for DNA synthesis and purine base synthesis

19
Q

what is a PK set back of MTX?

A

cellular resistance
low uptake
and therefore low efficacy

20
Q

explain the mechanism of CNT- MTX

A
  1. CNT-MTX enters cell via nano needle hypothesis
  2. no cell death as MTX cannot be released from the CNT
21
Q

how can we control the release of CNT-MTX?

A

addition of proteases/esterases

22
Q

why are CNT-MTX used?

A

The CNT in the hydrogel allows a slower and more controllable release behavior of MTX cellular uptake