Past Paper Questions Flashcards

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1
Q

Name 4 types of Biomaterials

A

pacemaker, skin graft, hip replacement, ocular implant

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2
Q

What is a phospholipid?

A

has a polar head group (phosphate) and a hydrophobic tail. They form a bilayer with the polar head group (hydrophillic) pointing outwards towards the aqueous surrounding.

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3
Q

What are the 3 main functions of phospholipids?

A

Building blocks of biological membranes. Hormones and intracellular membranes. Energy storage.

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4
Q

What are the 4 main nanostructrues formed by phospholipids

A

Bilayer, Micelle, Liposome, Lipid monolayer.

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5
Q

Describe two methods for surface tension measurement of a peptide solution

A

Wilhelmy Plate Method. (suspended ring on surface of water) Du Noüy ring (slowly lifting ring out of the water).

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6
Q

Explain the meanings of primary sequence, and secondary, tertiary and quaternary structures of a protein.

A

Primary sequence is the linear order of amino acids. Secondary is local folded structures. Tertiary is 3D shape of whole molecule. Quanternary refers to the arrangement of peptide chains.

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7
Q

Describe the non-covelant forces involved in the stabalisation of proteins.

A

Hydrogen bonds (alpha and beta), ionic bonds (inside and outside of proteins), Van der Waals force, Hydrophobic interaction (folding of proteins)

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8
Q

How can you stabilise a bioengineered antibody.

A

pH adjustment and buffering. Addition of stabilising. Control temperature.

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9
Q

What are the key properties of hydrogels that can be used to spread onto wounds.

A

Semi-permeable. Strong. anti bacterial properties.Biodegradable

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10
Q

Describe two structural features and two physical characteristics of a surfactant.

A

Structural: Hydrophobic tail, hydrophilic head. Physical: Amphiphilic, leads to interfacial adsorption lowering surface tension and allowing water to spread. - Antimicrobial negative charge bacterial cell membranes get broken down.

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11
Q

Describe how cationic surfactants and peptides work to kill pathogenic bacteria.

A

Disrupt the bacterial cell membrane.

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12
Q

Explain why a cationic surfactant may not achieve as high selectivity as a cationic
peptide.

A

cationic peptides can specifically target bacterial cell components.

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13
Q

What factors affect the minimum inhibition concentration.

A

Ph, Ionic strength, aggregation somehow….

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14
Q

Describe a method, and key processes involved, in producing lipid nanoparticles
for the delivery of RNA. Justify the lipid components you use.

A

Cholesterol: structure builder. DLin-MC3-DMA (cationic surfactant): charge neutralisation. Helper lipid: flexibility. DMG-PEG-2000 (outer surface cover) strong steric stabilisation.

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15
Q

Give 5 reasons for development of biomedical materials.

A

Ageing/diseases/cancers, Birth defect, Accidents, War casualties, Beauty

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16
Q

Describe the main four structural features of collagens and how these features affect their mechanical behaviour

A

Amino acid sequence: -Gly-Pro-Hyp-Gly-X. X is any other amino acid. 3 left-handed helical peptide chains coiled together to give aright handed coiled tropocollagen superhelix with periodicity of 2.86 nm. Hydrogen bonding between the glycine residues and the OH groups of hydroxyproline

17
Q

Describe the mechanical behaviour of self-assembled hydrogels. Outline the main
characteristic features desired for topical wound treatment.

A

They are viscoelastic. Biocompatibility, permeable to oxygen, strong against friction.

18
Q

Why is neutron reflection good for studying buries interfaces?

A

Nuetrons are uncharged so highly penetrative. Stable. eg (imaging on plane for damage)

19
Q

Give three main properties of biomaterials

A

Viscoelastic (mechanical), transparant (optical), biocompatible

20
Q

Draw three types of hydrogen bonds

A

Acceptor H2O—H-OH donor; HO—H-NH-R; R1-H2N—H-NH-R2

21
Q

write the equation for the reaction between 2 amino acids to form a dipeptide

A

week 6 long qesutions 2

22
Q

Why is tha charge on a protein pH dependent?

A

Proteins contain charged amino acids, which can dissociate depending on the pH solution, createing different charges

23
Q

Describe a process for measuring the isoelectric point

A

Measuring the zeta potential. Isoelectric focussing (IEF). Separates charged molecules, carried out in gel with pH gradient.

24
Q

What secondary structure would peptide GIIIQGK-NH2 prefer to adopt.

A

Anti parallel B sheet.

25
Q

5 main differences in NR and X-ray reflection

A

Isotopic variateions make it easier to study structures in more detail by parallel runs. NR has less resolution than X-ray. NR is better at resolving complex interfaces. NR avoids contribution of water from NRW by mixing 8.1vol% D2O with H2O0 scattering density. X-ray is better for electron, NR is better for nuclei.

26
Q

What are the key features of viscoelasticity

A

time dependent deformation, stress relaxatio, strain and rate dependence

27
Q

Sketch temperature, composition diagram for copper and nickle (nickle has a higher melting point. Write equation for amount of liquid in L+a phase.

A

(Calp - C_A)/Calp - CL) = L /(alp + L)

28
Q

Sketch temperature, composition diagram for copper and Ag

A
29
Q

Write down equation for strain of a dashpot and how strain is in the maxwell and voight models

A

maxwell: et = e_spring + e_dash
voight: et = e_spring = e_dash
sigma = visx de/dt

30
Q

What are the hume rothery rules?

A

To form a solid solution: substitutional solids. -r difference less than 15% - Same crystal - same valance - same electronegativity. Interstitial solid: solute atoms smaller than sites - same electrognegativity - same valence.

31
Q

name two charactersitic properties of hydrogels

A
  • phase difference between stress and strain. - shear storage and shear loss moduli. G’ = (sigma0/eps0)cosPhi.G’‘=sigma0/eps0)cosPhi
32
Q

write equation for debye length, bjerrum length and ionic strength

A

I = 0.5sum c z^2. Lambda b = e^2/(4pi eps0 epsr kB T). k-1 = 1/sqrt(8pi lambda b N_A *10^3 I)