Week 1 - Intro To Semi-solid Formulations Flashcards
Describe the Structure of the Skin
3 Layers:
1. Epidermis
- has NO blood flow BUT has live cells undergoing mitosis = these cells get O2, H2O, nutrients etc,
- protects skin = also a barrier to drug delivery
- drug needs to be carried through epidermis into dermis (to enter body)
- has layer of dead cells (flattened cells)
- Dermis
- Hypodermis
- subcutaneous injections are injected into this layer
Other:
- Hair folicles affect drug delivery
- Sweat glands secrete sweat onto skin which maintains low pH
- Have sensory cells in skin e.g. merkel cells
List potential ways of drug delivery through skin
- Oral
- Topical
- Nasal
- Occular (eye)
- Rectal
- Aural (ear)
ALL routes EXCEPT RESPIRATORY (NO inhaled semi-solds)
What is Transdermal Drug Delivery
Transdermal = delivery through the skin
- Sometimes we DONT want drugs to enter circulation, want to use the drug locally (NOT systemically)
- But some drugs can pass through skin
- Transdermal routes have a lag time (time depends on the route drug has to take)
- skin saturates with drug = will see movement of drug into body even if drug has been removed / wiped off
- lag time is realted to membrane thickenss + diffusion co-efficient
TYPES of Delivery Routes
1. Intracellular route - drug travels through matrix between dead vells
2. Follicular Route = drug goes through hair
3. Ecrine route - along sweat glands
How does the resistance model explain transdermal drug delivery and formulation
4 Types of Resistance
R1 = vehicle resistance (drug diffusing out of the vehicle)
R2 and R3 = 2 diff. pathways / routes drug can go down
- R2 has small fractional area = high ressistance
- R3 = stratum corneum resistance
- stratum corneum is defining capacity
R4 = Drug diffusing to where we want it to be
If route has large fractional area = resistance is low
List the possible Adminstration routes for semi-solids
- Oral
- Nasal
- Topical
- Rectal
- Occular
- Aural
ALL ROUTES except respiratory = NO INHALED SEMI-SOLIDS
semi solids can be used locally or transdermally
List the 4 topical semi-solid preparations
- Ointments
- Creams
- Gels
- Pastes
Also includes: foams, lotions, plasters, suppositories
What characteristics, application and excipients apply to OINTMENTS formulation
- Are single phase preparations, consisting of matrix former + liquid component
- can be transparent or coloured
- drug can be dissolved in base OR disperesed throughout base
4 Types of bases:
1. Hydrocarbon
- C30 and C50 hydrocarbon mixture
- shorter hydrocarbons (C16 to C30) are usually liquid
- are hydrophobic bases = occlusive
- Other Hydrophobic / lipophilic
- barrier to moisture = keeps moisture out = good emollient (keeps everything within skin)
- greasy + difficult to remove
- used on dry lesions but NOT wounds etc.
- may have lower bioavaiability due to solubility of drug in highly lipophilic ointment
- e.g. silicone - Hydrophillic
- Miscible with water (base contains water as part of liquid component)
- e.g. macrogols (polyethene glycol)
- can be applied to wounds
- bioavailability barely affected due to low vechile resistance - Water-emulsifying
- have emulsifying excipients e.g.wool fat, wool alcohol, fatty alcohols, monoglyceridies, polysorbates
- may have water incorporated into base (dispersed)
- can be used on wounds as liquid / what is excreted from wounds will be emulsified
What characteristics, application and excipients apply to PASTE formulation
- stiffer than ointments
- less greasy than ointment
- have high loading of insoluble solid
- solid includes talc, starch, zinc oxide, sulfur - generate protective barrier
- dry opaque
What characteristics, application and excipients apply to CREAM formulation
- Are multiphase preparations (2 phases) ~ lipophilic and aqueous (hydrophillic)
- less greasy + easy to wash off (compared to ointment)
Liphophilic cream = w/o emulsion
Hydrophillic cream = o/w emulsion
Aqueous = dissolved in water
What characteristics, application and excipients apply to GEL formulation
- Has 2 inter-penetrating networks ~ solid and liquid network
- liquid phase is held by surface tension, immobilised by platelets or capillary forces
- Has sheer thinning = will breakdown into liquid at specific strength but may reform back into gel
Have many application routes:
- patches
- gel in tube
What factors affect percutaneous absorption
Percutaneous Absorption - amount of substance that passes theough stratum corneum compared with the amount applied
Skin Factors:
- skin hydration (thiock water layer = easier to get drug through)
- skin age
- ethnicity
- skin temp. (hydration benefits)
- skin health
- occlusion
Drug Factors:
- drug conc.
- partition coefficient
- degree of ionisation (ionised drug wont go through skin)
- solubility (insoluble drug wont pass through)
- chemical structure