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NPH-27 TABLET DISINTEGRATION TEST APPARATUS SIX BASKET

  • NPH-28 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
  • The instrument is designed to test two batches of six tablets, simultaneously. The unit is extremely useful for pharmaceutical industries. Extremely useful for pharmaceutical labs   It is used in quality control and R & D to determine compliance with the disintegration requirement of the tablet and capsule as per required standards. Instrument uses the latest microprocessor technology and advanced engineering techniques so as to give enhanced accuracy and reproducibility.   Microprocessor based, easy to use,With long trouble free life. Seven segment LED display Supports Two baskets assemblies. Temperature is controlled digitally so produces accurate results. The Tablet Disintegration Double Test Apparatus with a capacity of 1000 ml is usedfor testing the disintegration properties of tablets. Allows for simultaneous testing of multiple tablets, offering a high capacity of 1000ml for conducting disintegration tests. The apparatus consists of multiple test stations or Two baskets that can hold tablets during the disintegration process. The apparatus features a water bath or reservoir with temperature control to maintain the desired testing conditions. Measures Disintegration time of 12 tablets at one time. Disintegration time is displayed on Seven Segment LED display. Electrically operated,Robust powder coated Mild steel body.Front panel provided with all main controls.Supplied complete with all accessories and working manual.

With six disc. With six removable glass vessels of size 7.5 x 20 mm.
diameter, have a stainless steel wire mesh bottom, which dips in
water in a beaker of 1000 ml. capacity kept on the hot plate,
temperature of which is maintained at 37°C with an accuracy of
+_1° C.

SKU: NPH-27 TABLET DISINTEGRATION TEST APPARATUS SIX BASKET Category: Pharmacy Apparatus
  • NPH-28 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
  • The instrument is designed to test two batches of six tablets, simultaneously. The unit is extremely useful for pharmaceutical industries. Extremely useful for pharmaceutical labs   It is used in quality control and R & D to determine compliance with the disintegration requirement of the tablet and capsule as per required standards. Instrument uses the latest microprocessor technology and advanced engineering techniques so as to give enhanced accuracy and reproducibility.   Microprocessor based, easy to use,With long trouble free life. Seven segment LED display Supports Two baskets assemblies. Temperature is controlled digitally so produces accurate results. The Tablet Disintegration Double Test Apparatus with a capacity of 1000 ml is usedfor testing the disintegration properties of tablets. Allows for simultaneous testing of multiple tablets, offering a high capacity of 1000ml for conducting disintegration tests. The apparatus consists of multiple test stations or Two baskets that can hold tablets during the disintegration process. The apparatus features a water bath or reservoir with temperature control to maintain the desired testing conditions. Measures Disintegration time of 12 tablets at one time. Disintegration time is displayed on Seven Segment LED display. Electrically operated,Robust powder coated Mild steel body.Front panel provided with all main controls.Supplied complete with all accessories and working manual.
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NPH-27 TABLET DISINTEGRATION TEST APPARATUS SIX BASKET

The instrument is designed to test Six batches of six tablets, simultaneously.

Required for pharmaceutical industries where several batches are to be tested.

  • Measures Disintegration time of 36 tablets at one time.
  • Supports Six baskets assemblies.
  • Seven segment LED display for each basket
  • Temperature is controlled digitally so produces accurate results.
  • Measures Disintegration time of 36 tablets at one time.
  • Disintegration time of each basket is displayed on Seven Segment LED display.

Electrically operated, Strong powder coated Mild steel body. Front panel provided with all main controls. Supplied complete with all accessories and working manual.

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NPH-28 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
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