💊 Tablet dissolution test (dissolution)

Pharma Ph.Eur. 2.9.3

Determination of dissolution rate of active substance from tablets and capsules in simulated gastrointestinal environment. Key bioequivalence test for generic drugs.

Overview

Dissolution test is one of the most important pharmaceutical tests, allowing assessment of active substance release from solid dosage forms (tablets, capsules) in vitro. Results correlate with drug bioavailability in vivo — drug must dissolve before being absorbed.

The test is performed in basket apparatus (apparatus 1, Ph.Eur./USP) or paddle apparatus (apparatus 2) in 500–1000 mL dissolution medium (buffer pH 1.2 / 4.5 / 6.8 or 0.1 M HCl). Samples are taken at specified time points and active substance concentration is determined (HPLC or UV). Acceptance criterion: Q = 80% in 30–45 min (immediate release) or profile according to specification.

Method principle

Tablet/capsule is placed in basket (apparatus 1, 100 rpm) or on vessel bottom with paddle (apparatus 2, 50–75 rpm) in 500–1000 mL dissolution medium thermostated at 37.0 ± 0.5°C. Medium samples are taken at specified time points (e.g., 5, 10, 15, 30, 45, 60 min), filtered, and analyzed spectrophotometrically (UV) or chromatographically (HPLC). Result: dissolution profile — plot of % released active substance vs. time.

Applications

Key parameters

ParameterValue
ApparatusApparatus 1 (basket), Apparatus 2 (paddle)
Medium volume500, 900, or 1000 mL
Temperature37.0 ± 0.5°C
Rotation speed100 rpm (basket), 50–75 rpm (paddle)
Q criterion≥80% in 30–45 min (typically)
Number of units6 (S1), 12 (S2), 24 (S3) per USP

Standard

Standard number
European Pharmacopoeia 2.9.3
Title (PL)
Badanie szybkości rozpuszczania tabletek i kapsułek
Title (EN)
Dissolution test for solid dosage forms

Step-by-step procedure

1. Medium preparation

Prepare 6×900 mL medium (e.g., 0.1 M HCl). Degas under vacuum or ultrasound 15 min. Heat to 37°C.

⏱ Time: 30 min • 🌡 Temperature: 37°C

2. Vessel filling

Fill 6 vessels with 900 mL medium each. Check temperature (37.0 ± 0.5°C). Set rotation speed (50 or 100 rpm).

⏱ Time: 10 min

3. Test start

Place 1 tablet in each vessel/basket. Start stirring. Start timer.

⏱ Time: 1 min

4. Sample collection

Collect 5–10 mL medium at: 5, 10, 15, 30, 45, 60 min. Filter through 0.45 µm. Replace volume with fresh medium.

⏱ Time: 5 min/point

5. UV/HPLC analysis

Measure absorbance (UV) or concentration (HPLC) of active substance in collected samples.

⏱ Time: 30–60 min

6. Calculations and evaluation

Calculate % release at each point. Check Q criterion. Evaluate compliance with specification (S1/S2/S3).

⏱ Time: 15 min

Required equipment and apparatus

EquipmentExampleIndicative price
Dissolution apparatus (6 or 8 positions)Agilent 708-DS, Sotax AT 7smart, Erweka DT 82660 000–180 000 PLN
UV-VIS spectrophotometerAgilent Cary 60, Shimadzu UV-1900i, Thermo Evolution 20125 000–60 000 PLN
HPLC (if required)Agilent 1260, Shimadzu Nexera200 000–400 000 PLN
Syringe filtersPVDF 0.45 µm, Full Flow, 25 mm1–3 PLN/pc
Automatic pipettesEppendorf Research Plus 1–5 mL800–2 000 PLN

Reagents, media and consumables

ReagentCASDetails
Hydrochloric acid 0.1 mol/L7647-01-0Medium pH 1.2 (stomach simulation without enzymes)
Acetate buffer pH 4.5Sodium acetate + acetic acid, per Ph.Eur.
Phosphate buffer pH 6.8KH₂PO₄ + NaOH, per Ph.Eur. (intestine simulation)
SLS (sodium lauryl sulfate)151-21-3Surfactant 0.5–2%, for poorly soluble substances
Active substance standardCertified CRM (Ph.Eur. Reference Standard)

Health and safety (OHS)

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