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Name 4 types of Biomaterials
pacemaker, skin graft, hip replacement, ocular implant
What is a phospholipid?
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.
What are the 3 main functions of phospholipids?
Building blocks of biological membranes. Hormones and intracellular membranes. Energy storage.
What are the 4 main nanostructrues formed by phospholipids
Bilayer, Micelle, Liposome, Lipid monolayer.
Describe two methods for surface tension measurement of a peptide solution
Wilhelmy Plate Method. (suspended ring on surface of water) Du Noüy ring (slowly lifting ring out of the water).
Explain the meanings of primary sequence, and secondary, tertiary and quaternary structures of a protein.
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.
Describe the non-covelant forces involved in the stabalisation of proteins.
Hydrogen bonds (alpha and beta), ionic bonds (inside and outside of proteins), Van der Waals force, Hydrophobic interaction (folding of proteins)
How can you stabilise a bioengineered antibody.
pH adjustment and buffering. Addition of stabilising. Control temperature.
What are the key properties of hydrogels that can be used to spread onto wounds.
Semi-permeable. Strong. anti bacterial properties.Biodegradable
Describe two structural features and two physical characteristics of a surfactant.
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.
Describe how cationic surfactants and peptides work to kill pathogenic bacteria.
Disrupt the bacterial cell membrane.
Explain why a cationic surfactant may not achieve as high selectivity as a cationic
peptide.
cationic peptides can specifically target bacterial cell components.
What factors affect the minimum inhibition concentration.
Ph, Ionic strength, aggregation somehow….
Describe a method, and key processes involved, in producing lipid nanoparticles
for the delivery of RNA. Justify the lipid components you use.
Cholesterol: structure builder. DLin-MC3-DMA (cationic surfactant): charge neutralisation. Helper lipid: flexibility. DMG-PEG-2000 (outer surface cover) strong steric stabilisation.
Give 5 reasons for development of biomedical materials.
Ageing/diseases/cancers, Birth defect, Accidents, War casualties, Beauty