The drugs must be absorbed to the systemic circulation.
Uptake can be through:
Passive diffusion depends on lipophilicity Active transport When the drug passes through the stomach, this is classed as the first pass metabolism and this limits the bioavailability of the drug (this only happens for oral administrated drugs). Since the small intestine has a pH of 5.3 this is where most the drugs are absorbed.
Type of administration Advantages Disadvantages
Oral Cheap Fraction of dose is lost due Easy to do to the first pass metabolism GI diseases can prevent absorption (such as vomiting) Not all drugs can be formulated into oral form Intravenous 100% bioavailability Risk of serious ADR’s can be useful for patients Not suitable for insoluble that struggle with oral substances delivery Rectal Avoids first pass metabolism Reduced bioavailability compared to oral Intramuscular Prompt absorption Painful Formulation can modify Danger of nerve damage release kinetics Subcutaneous Prompt absorption Not good for large volumes Modify release kinetics Pain or necrosis (kills cells) from irritating substances Intrathecal Bypasses BBB (blood brain Skilled staff barrier) Sterility essential Direct access to the CNS Not suitable for many drugs
Challenges with antibiotics?
Site of infection Microorganism responsible? Susceptibility? Pharmacokinetic limitations? Status of patient?