DISSOLUTION RATE TEST EQUIPMENT

Tablets or capsules taken orally remain one of the most effective
means of treatment available even today. Tablet Dissolution is a
standardized method for measuring the rate of drug release from a
dosage form.
• Extremely Useful for Pharmaceutical Labs Demonstration
• Accurate with Digital Temperature , RP.M Panel and Easy to
Operate
• Easy to Empty & Clean the Water bath with Bottom Drainage
1,2,3,6 ,8 Station Model
Apparatus consists of A water bath with 500 W heater covered
1000 ml glass vessel and a digital temperature controller. Variable
speed motor, with 30 cm. long 6 mm. dia. Stainless steel shaft. A
cylindrical stainless steel basket and a membrane fixing
attachment, water bath of thick acrylic sheet with transparent
cover at top. Temperature of the bath is maintained at 37°C with an
accuracy of +/-_ 1°C. A cylindrical glass vessel of capacity 1000 ml
with slightly concave bottom has a flanged edge at the top to
accept a fitted cover having four holes. One hole is in the center.
The shaft of motor fitted on an upright and has an electronic
speed regulating device that allows the speed to be varied from 25
to 250 R.P.M. The shaft, with basket fitted at the end rotates
smoothly and without any perceptible wobble. Basket consist of
two parts, one of which is to be attached to the shaft of solid metal
except for 2 mm vent and is fitted with three springs clips that
allows removal of the lower part of the basket to admit the test
samples, the detachable part of basket is of stainless steel mesh
formed into cylindrical 3.6 x 2.5 cm dia. Works 220 volts 50 Hz A.
C. Available models are
( i ) Single Stage (ii) D ouble Stage (iii) Three Stage (iv) Six Stage
(iv) Eight Stage (b) same as above but analog type single stage.

SKU: NPH- 28 DISSOLUTION RATE TEST EQUIPMENT

Description

DISSOLUTION RATE TEST APPARATUS

Dissolution Tests are conducted to determine the drug release patterns, physiological availability and bioavailability of formulated drug products i.e for the determination of active drug ingredient in any pharmaceutical formulation – tablet or capsule.

Dissolution apparatus are used throughout the product development life cycle, from Product release to stability testing and study of the product data from product to product. Then after passing or approval from the Quality control and Quality assurance, drugs are sent to markets.

Dissolution test apparatus working principle: The dissolution test apparatus checks how fast a drug dissolves in your body. A tablet or capsule is put in a container that has a medium that is prepared and operated just like the stomach or intestines functions (physiochemical conditions of the body). The container spins or moves around, and samples are taken to see how much of the medicine has dissolved over time. This helps to know how that drug works in a body. It also ensures the quality and efficacy of a product.

The high head dissolution testing apparatus can be configured for1,2,3, 6 or 8 vessel configuration.

Easy to operate, Accurate with Digital Timers and Digital RPM Controls.

Easy to clean the bath with bottom drainage.

Used in Analytical and Pharmaceutical industries.

Apparatus Powder coated Mild steel body with front panel controls and a constant temperature water bath made of transparent acrylic. The round bottom glass jar of capacity 1000 ml are placed inside the bath. The jar are with acrylic lid which allow passing of stirring shaft. The shaft is suspended from the top and is operated by the motor. The motor is electronically controlled to give speed precisely within ±1 RPM. The RPM is controlled digitally and is indicated on a digital display. Temperature is controlled by a fully solid state controller within ± 0.5°C. which maintains temperature at 37 Deg C with + 0.5 Deg C variations or Digital temperature controller. The basket assemblies and stirring paddles are of stainlesssteel.Power required is 230 V ± 10% AC, 50 Hz