

Dual-Basket Disintegration Tester
双吊篮崩解时限测试仪
- SKU DIT-0002
- Disintegration Testers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Number of baskets | 2 |
|---|---|
| Tubes per basket | 6 |
| Stroke length | 55 ± 2 mm |
| Frequency | 29–32 cycles/min |
| Mesh aperture | 2.0 mm |
| Bath temperature range | Ambient +5 to 45 °C |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <701>, Ph. Eur. 2.9.1, JP 6.09
What is the Dual-Basket Disintegration Tester?
A dual-basket disintegration tester drives two basket-rack assemblies in separate beakers, each with independent temperature or medium. It is used where two test groups or acid and buffer stages run in parallel.
What is the Dual-Basket Disintegration Tester?
A dual-basket disintegration tester drives two basket-rack assemblies in separate beakers, each with independent temperature or medium. It is used where two test groups or acid and buffer stages run in parallel.
Overview
A dual-basket tester has two stations on one frame, each with its own beaker held in a common or independently controlled water bath. Both baskets may be driven by a single motor at the same stroke and frequency, or by separate drives with independent start and stop. This arrangement doubles throughput and supports staged tests, for example 0.1 M hydrochloric acid for the gastric stage in one beaker and pH 6.8 phosphate buffer in the other for the intestinal stage. It also allows comparison of two lots or formulations under the same conditions. Independent timers and, in some models, independent temperature controllers give flexibility, but they add cost and calibration work. The unit is wider than a single-basket model and needs more bench area and more medium per run.
How does it work?
A disintegration tester consists of a basket-rack assembly, a motor-driven mechanism, and a thermostatic bath. The basket-rack holds six transparent tubes with a stainless steel mesh (typically 2.0 mm aperture) at the bottom. The mechanism moves the assembly vertically through a distance of 53 to 57 mm at 29 to 32 cycles per minute, while the immersion fluid, usually water, 0.1 M hydrochloric acid or phosphate buffer, is held at 37 ± 2 °C. A dosage unit is placed in each tube, optionally with a perforated disc that adds gentle mechanical action. The test ends when no residue, other than fragments of insoluble coating or capsule shell, remains on the mesh. The operator records the time of complete disintegration, which is compared with the monograph limit, commonly 15 to 60 minutes.
What are the key features?
- Two stations with independent beakers for parallel or staged testing
- Independent timers and start-stop control for each basket
- Optional independent temperature control for each bath
- Same stroke and frequency on both stations for comparability
- Lift mechanism for each basket to ease inspection
What are the technical specifications?
A typical dual-basket disintegration tester configuration offers number of baskets of 2, tubes per basket of 6, stroke length of 55 ± 2 mm, frequency of 29–32 cycles/min, mesh aperture of 2.0 mm and bath temperature range of Ambient +5 to 45 °C. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Dual-Basket Disintegration Tester is used in acid and buffer staged testing, comparing two batches in parallel, high-volume QC laboratories and enteric-coated dosage forms. Across the wider Disintegration Testers class, laboratories also deploy it for tablet and capsule release testing, formulation development and stability studies.
Which standards and certifications apply?
Relevant standards and methods include USP <701>, Ph. Eur. 2.9.1, JP 6.09 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the tester on a stable bench with a level water bath and access to clean water. Calibrate stroke length, frequency and temperature at installation and at defined intervals, using an independent thermometer and a ruler or gauge. Replace the immersion medium frequently and clean tubes, mesh and discs to prevent residue build-up that blocks the mesh. Use deaerated medium if required by the method, because air bubbles can lift tablets. Check the mesh for distortion, since a damaged screen changes the test outcome. Record lot numbers of medium, bath temperature and operator. Under GMP, document IQ, OQ and PQ, and verify the system with a suitable reference tablet where practical.
How do I select the right Dual-Basket Disintegration Tester?
Select the dual-basket model when staged or parallel testing is routine. If you only test one group at a time, a single-basket model costs less. In an RFQ, state whether independent temperature control, independent timers and lift mechanisms are required, together with stroke, frequency and mesh details.
How does it compare with other Disintegration Testers variants?
Choose according to sample throughput, temperature control and data requirements. A two-basket tester allows two test groups in parallel and is often chosen where stage testing is performed, for example acid stage followed by buffer stage for enteric products. Single-basket units are adequate for routine release. Confirm stroke length, frequency and basket dimensions against the target pharmacopoeia, and check that the bath can hold 37 °C within ±1 °C. Automatic endpoint detection reduces subjectivity, which matters for opaque or colored dosage forms where visual judgment is difficult. Laboratories under GMP should look for software with audit trails and probe-based temperature recording. A portable or benchtop size matters if bench space is limited, and a bath with a cooling or sealed circulation option helps in warm climates.
Full specifications
| Number of baskets | 2 |
|---|---|
| Tubes per basket | 6 |
| Stroke length | 55 ± 2 mm |
| Frequency | 29–32 cycles/min |
| Mesh aperture | 2.0 mm |
| Bath temperature range | Ambient +5 to 45 °C |
| Temperature accuracy | ± 0.5 °C |
| Timer | 2 independent, 0–99 min |
| Beaker volume | 2 × 1000 mL |
| Power supply | 220 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Acid and buffer staged testing
- Comparing two batches in parallel
- High-volume QC laboratories
- Enteric-coated dosage forms
Key features
- Two stations with independent beakers for parallel or staged testing
- Independent timers and start-stop control for each basket
- Optional independent temperature control for each bath
- Same stroke and frequency on both stations for comparability
- Lift mechanism for each basket to ease inspection
Frequently asked questions about Dual-Basket Disintegration Tester
Yes, each basket sits in its own beaker, so different media can be used, such as acid in one and phosphate buffer in the other. Verify that the shared bath temperature suits both media.
Usually yes, although some models offer independent start and stop for each station. Check that stroke and frequency are identical on both stations so that results can be compared directly.
Yes, two beakers of about 1 L each are needed per run, so medium preparation and waste volumes double. Plan for enough prepared medium and a consistent warming step before starting.
A disintegration tester is a pharmacopoeial apparatus that moves tablets or capsules up and down in a heated fluid and measures how long they take to break apart. It is used as a quick quality test for oral solid dosage forms.
The standard temperature is 37 ± 2 °C, representing body temperature. The bath must hold this range throughout the test, and many laboratories check it with a calibrated independent thermometer rather than relying solely on the display.
Disintegration measures when a dosage form breaks into particles, while dissolution measures the rate and extent to which the drug enters solution. A tablet can disintegrate quickly and still dissolve slowly, so the two tests are complementary.
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