Phosphate binder
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Through Medication, Gastrointestinal tract and Aluminium
Mechanism of action
These agents work by binding to phosphate in the GI tract, thereby making it unavailable to the body for absorption. Hence, these drugs are usually taken with meals to bind any phosphate that may be present in the ingested food. Phosphate binders may be simple molecular entities (such as magnesium, aluminium, calcium, or lanthanum salts) that react with phosphate and form an insoluble compound.
Calcium carbonate
Calcium-based phosphate binders, such as calcium carbonate, directly decrease phosphate levels by creating insoluble calcium–phosphate complexes which gets eliminated in the feces.
Lanthanum carbonate
Non-calcium-based phosphate binders, including lanthanum carbonate, form insoluble complexes with phosphates in food, thereby reducing the amount of phosphate in the body.
Sevelamer carbonate
Sevelamer is an insoluble polymeric amine, which is protonated once in the intestines and this allows it to bind dietary phosphate. Phosphates are eliminated along with sevelamer, leading to a decrease in the body's phosphate levels.
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Medical use
For people with chronic kidney failure, controlling serum phosphate is important because it is associated with bone pathology and regulated together with serum calcium by the parathyroid hormone (PTH).
Adverse effects
Calcium carbonate
- GI effects (nausea, vomiting, constipation)
- Risk of cardiovascular calcification
- Risk of hypercalcemia
Lanthanum carbonate
- GI obstruction
- Bile duct obstruction
- Hepatic impairment
- No hypercalcemia risk
Sevelamer carbonate
- GI effects (nausea, vomiting, constipation, flatulence)
- No hypercalcemia risk
Choice of agent
There have been limited trials comparing phosphate binders to placebo in the treatment of hyperphosphatemia in people with chronic kidney disease. When compared with people receiving calcium-based binders, people taking sevelamer have a reduced all-cause mortality.
Types
- Calcium acetate/magnesium carbonate

