Drug delivery Flashcards

1
Q

Give examples of applications of nanotechnology in life sciences which use the iv delivery route.

A
  • treatment of cancer, siRNA and gene delivery, intracellular infections.
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2
Q

Give examples of applications of nanotechnology in life sciences which use the oral delivery route.

A

improvement of solubility, delivery of peptides, proteins and vaccin

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3
Q

describe the evolution of drug delivery systems since the 1970s

A

sof natural organic drug carriers, soft synthetic drug carriers, hard inorganic particles for imaging and drug delivery

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4
Q

Mention 5 forms in which can you deliver a drug using nanomaterials.

A

as a nanocrystal of the active substannce or embeded in nanocarriers (depo, matrix, dendrimer, layer-by-layer)

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5
Q

What are the possible benefits of using nanomaterials in drug delivery?

A

-tissue targetting (efficiency, toxicity), protection against degradation (clearance, dosing frequency), use of enhanced permeability and retention effect (EPR)

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6
Q

Which pre-requisits must be fulfilled before a drug can be abosrbed into the blood?

A

the active substance needs to have solubility and permeability

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7
Q

What are the consequences when a drug is poorly soluble?

A
  • poor and variable bioavailability, no dose-response, slow onset of action
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8
Q

How are poorly soluble compounds being called?

A

brick dust, grease balls

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9
Q

The Lipinski rule of 5 is used for the selection of candidate drugs for further development. Which type of drugs?

A

drugs to be given orally, absorbed via passive diffusion.

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10
Q

Give the rules of Lipinski.

A

-

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11
Q

What does the Ostwald-Freundlich equation describe?

A
  • the relationshipe between solubility and particle size, in similarity to the Kelvin equation for the condensation of gasses. - smallest particles dissolve first
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12
Q

Why is the solubility of irregular particles underestimated by Ostwald - Freundlich?

A

xx

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13
Q

What is supersaturation and how can you prolong this?

A
  • more dissolved than in equilibrium situation. rate nucleation and rate of crystal growth.
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14
Q

Describe 5 models of nucleation and growth

A

LaMer burst nucleation, Ostwald and digestive ripening, coalescence and oriented attachment, finke-watzky 2 step mechanism, intraparticle growth

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15
Q

What is nucleation?

A
  • Wikipedia: Nucleation is typically defined to be the process that determines how long an observer has to wait before the new phase or self-organised structure appears.
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16
Q

What are the benefits of using nanosusspensions, and challenges?

A
  • higher bioavailbility, less variability due to food, increased rate of absoprtion, improved absorption of higher doses (tox testing), rapid formulation development ? - agglomeration
17
Q

Mention characteristics of an amorphous state

A

short-range order (?), low enthalpy of dissolution, metastable, recrystalise at varying T, rel humidity, p and agitation.

18
Q

How can you stabilise an amorphous compound using nanotechnology. Give an example.

A
  • Pb in carbon nanotubes. amorphous compound in a poreous nanomaterial Study with CaCO3; amorpheous, vaterite (poreous), aragonite (non-poreous), calcite (non-poreous) ibuprofen in upsalite
19
Q

Cancer treatment. Why may NPs be a good tool for the passive targetting of tumor tissue?

A
  • poor lymfatic draining, high vascularisation, leaky vessels. EPR effect
20
Q

What are the important physicochemical characteristics of rigid core nanoparticles to enable an optimal bioavailability?

A
  • zeta-potential (neg); size (100-200 nm); hydrophylicity (high) ; these characteristics are good for Enhanced Permeability and Retention.
21
Q

How do you avoid RES (?, immune response)?

A
  • polyethylene glycol of brush type (vs mushroon type (intermediate PEG density) and pancake type)
22
Q

Describe 2 examples of the use of nanothechnologically-induced hyperthemia.

A
  • photothermal plasmon resonance (Au nanorods); magnetic hyperthermia through Néel or Brownian relaxation.
23
Q

You want to develop a treatment to eradicate a tumor by hyperthermia induced by Au nanorods. At which wavelength should the rods preferably absorb?

A

NIR (650 - 900 nm) because hemoglobin has minimal absorption below that and water above that.

24
Q

What are today’s challenges for the use of nanotechnology in cancer treatment?

A
  • variable EPR effect, rapid clearance, drug resistance, inefficient cargo delivery (?)