In one sentence A concentration states how much drug is dissolved in a given volume, written as an amount per volume such as 500 mg/5 mL.
Concentration is an amount of drug inside a stated volume
A stock label does not tell you how much drug the bottle holds in isolation; it tells you how much drug sits in the volume printed beside it. The form is always amount per volume: 500 mg/5 mL, 250 mg/1 mL, 1 g/10 mL. The first number is a mass of drug and the second is the volume of liquid that contains it. Because both numbers matter, the same bottle can be described in two ways: 500 mg/5 mL and 100 mg/mL are the same strength, since 500 ÷ 5 = 100. Reading the label as a rate — this many milligrams in every millilitre — is what lets you scale it to any volume you need. Before any calculation, write the strength as a fraction, with the drug above the line and the volume below it, so that the units can cancel later.
A vial is labelled 500 mg/5 mL. Dividing both numbers by 5 gives 100 mg/mL, so every millilitre contains 100 mg; two millilitres therefore contain 200 mg.
A vial is labelled 1 g/10 mL. What is its concentration in mg/mL, and how much drug is in 4 mL?
Show the answer
1 g = 1,000 mg, so the concentration is 1,000 ÷ 10 = 100 mg/mL. Four millilitres therefore contain 4 × 100 = 400 mg of drug.
Read detailed explanations
- What a strength statement really says: weight/volume, volume/volume and the ratio convention
A strength statement is a small specification, and the sign that introduces it decides which quantities are being compared. A percentage of a solid dissolved in a liquid is a weight/volume strength: the drug is weighed in grams and the liquid is measured up to 100 mL. That is why 5% glucose holds 5 g of glucose in every 100 mL of solution, and not 5 g of glucose in 100 g of fluid. When both components are liquids, the same sign usually means volume/volume instead: 70% alcohol is 70 mL of alcohol made up with water to a final volume of 100 mL. Creams and ointments are different again, because they are weighed rather than poured, so 1% hydrocortisone cream means 1 g of drug in 100 g of cream. There the density of the base is needed before any mg/mL figure can be produced, and the arithmetic of a dilution no longer applies unchanged. Ratio strengths follow the weight/volume convention whenever the drug is a solid: 1:1000 means 1 g made up to 1,000 mL of solution, which is 1 mg/mL, and 1:10,000 means 0.1 mg/mL. The notation is a survival from apothecary practice, when a grain of a substance was dissolved in an ounce of liquid, and it still appears on adrenaline, lidocaine and potassium permanganate labels today. Its danger is ambiguity: 1:1000 can be read as one part of drug in one thousand parts of the finished product, which for a dilute solid gives the same answer because the dissolved solid adds almost no volume, but for two concentrated liquids 1:1 means equal volumes rather than one part in one part. Convert every ratio strength into milligrams per millilitre before you calculate, and say the units out loud; reading the 1 of 1:1000 as one milligram instead of one gram understates the dose a thousandfold.
- Making up a dilution safely: dilute to a final volume, then let the arithmetic follow
Every dilution question hides a wording decision, and the decision is whether the figure in the prescription is the volume you end up with or the volume you pour in. “Dilute 10 mL to 100 mL” fixes the final volume at 100 mL, so the denominator of the new concentration is known. “Add 100 mL of saline to 10 mL” fixes only the volume added, so the final volume is 110 mL and the concentration is lower than the prescriber may have expected. Read the verb: make up to, dilute to and bring to volume all fix the final figure, while add and dilute with fix only the diluent. The arithmetic itself starts from conservation of mass. The amount of drug in the stock is C1 × V1 and the amount in the finished solution is C2 × V2; because no drug is created or lost, the two expressions are equal. Rearranged, V1 = (C2 × V2) ÷ C1 gives the volume of stock to withdraw, and V2 = (C1 × V1) ÷ C2 gives the final volume that produces a wanted strength. A practical difficulty appears when V1 is larger than the container of stock: 100 mL of 5 mg/mL needs 500 mg, which is two 5 mL ampoules of 50 mg/mL, so either more ampoules are opened or a more concentrated presentation is requested. The opposite difficulty appears when V1 is too small to measure accurately, for instance 0.02 mL. Then a serial dilution is used: a first dilution of 1 in 100 is prepared, and a measured portion of that is diluted again by 1 in 10, so the overall dilution is 1 in 1,000 and every step stays within the range of a syringe. Accuracy decides the equipment, because 0.1 mL read in a 10 mL syringe is a poor measurement; choose the smallest syringe that comfortably holds the volume. Two further cautions belong with the method. Volumes are not perfectly additive — ethanol and water contract slightly when mixed — which is why a pharmacy specifies a final volume instead of assuming that millilitres simply add. And the diluent is not interchangeable: some drugs precipitate or are inactivated in the wrong fluid, so the name of the diluent is part of the order. Finish by labelling the container with the drug, the total amount, the final volume, the resulting strength, the time and your initials; a diluted product is less stable than the concentrate and should not be kept beyond its stated expiry.
- Concentration inside the patient: why serum levels are measured
Concentration is not only a property of bottles; it is the quantity clinicians measure inside the patient. The plasma concentration of a drug is the amount circulating in the blood divided by the volume it appears to occupy, and that apparent volume is called the volume of distribution. It is a mathematical volume rather than an anatomical one: a drug that leaves the blood and dissolves in fat has a large apparent volume and therefore a low plasma concentration, even though the body has not become larger. The rule concentration = amount ÷ volume then does real work at the bedside. To reach a target concentration quickly, a loading dose is given, calculated from the target concentration multiplied by the volume of distribution and corrected for how much of the dose survives absorption. It is larger than the maintenance dose because it must fill the whole apparent volume, not merely replace what the body has already removed. Elimination normally removes a constant fraction of the drug per unit time — a first-order process — and the time needed to remove half of the amount present is the half-life. Because of this, a continuous infusion climbs until the rate of drug entering the body equals the rate being removed; that plateau is steady state, and it is reached after roughly four to five half-lives. Doubling the infusion rate doubles the steady-state concentration, which is the same proportionality that governs a dilution. Laboratories exploit all of this by reporting a serum concentration against a therapeutic range, the interval between the level below which the drug does not work and the level above which it becomes toxic. Nursing actions keep those numbers meaningful: give the infusion at the prescribed rate and check the pump setting, and draw a trough level just before the next dose and a peak level at the interval the protocol names, because a sample taken at the wrong moment produces a concentration that looks dangerous or useless when neither is true. Never adjust a rate on the basis of a level drawn at the wrong time; report the value and the timing to the prescriber.