Disintegration Test Apparatus

The HTLP Double Basket Tablet Disintegration Machine HTLP-074 is a workhorse in the pharmaceutical industry. The machine uses an auger system to break down tablets, which is then followed by a flotation recovery system that allows for easy removal of excess fines and recycle of plastic baskets. The machine also has an integrated waste feeder for easy disposal of material that does not fit in the basket.This machine has been designed to help people dissolve tablets or capsules quickly and easily. The machine has a touch screen interface and can be set to automatically turn on at specific times during the day, or it can be used manually.This machine is designed to continuously disintegrate tablets in a basket that can be repeatedly filled and emptied. The machine is an improvement over existing tablet disintegration machines because it does not require the use of a hammer or pestle to break up tablets for easier swallowing.The machine's basket will hold up to 12 tablets at once, and it features an adjustable timer that allows users to choose the amount of time they want their medicines dissolved for. It is recommended that people set the timer between 15 minutes and 60 minutes, depending on the tablet they're dissolving. After the timer reaches zero, the machine will automatically shut off so that users don't have to worry about forgetting it in the morning.

The SND Bharat Mild Steel Single Basket Disintegration Test Apparatus DI-105 is a crucial equipment used in laboratories to determine the disintegration time of tablets and capsules. It is an essential test to evaluate the quality and effectiveness of pharmaceutical products. This apparatus is designed to simulate the disintegration process that occurs in the human body, ensuring that the medication is released and absorbed properly.
The disintegration test apparatus consists of a water bath, a set of glass tubes, and a motor-driven basket rack. The water bath is filled with a suitable medium, usually water or a simulated gastric fluid, which is maintained at a specific temperature. The glass tubes, also known as disintegration tubes, are placed in the water bath and hold the tablets or capsules being tested. The motor-driven basket rack holds the disintegration tubes and provides the necessary agitation to mimic the movement in the gastrointestinal tract.
To perform the test, the tablets or capsules are placed in the disintegration tubes, and the tubes are then positioned in the basket rack. The rack is lowered into the water bath, ensuring that the tablets or capsules are fully immersed in the medium. The motor is then activated, causing the basket rack to move up and down, creating a reciprocating motion. This motion promotes the disintegration of the tablets or capsules, allowing the release of the active ingredients.
The disintegration time is determined by observing the tablets or capsules in the disintegration tubes. The disintegration is considered complete when no residue of the tablets or capsules remains, and the particles are small enough to pass through a mesh screen. The time taken for this complete disintegration is recorded as the disintegration time.
The disintegration test apparatus is designed to meet the specifications outlined in pharmacopoeial standards, ensuring accurate and reliable results. It is essential for pharmaceutical manufacturers to comply with these standards to ensure the quality and efficacy of their products. The disintegration test is particularly important for immediate-release dosage forms, as it ensures that the medication is released within a specified time frame for optimal absorption.
In conclusion, the disintegration test apparatus is a vital tool in pharmaceutical laboratories for evaluating the disintegration time of tablets and capsules. It simulates the disintegration process that occurs in the human body, providing valuable information about the quality and effectiveness of pharmaceutical products. By following the specified procedures and standards, this apparatus ensures accurate and reliable results, contributing to the development of safe and efficient medications.

Programmable time with digital display, Auto stop after the set time with audio alarm for enteric coated tablet.
Facility to hold and resume the time and motor movement for quickly disintegrating tablets.
Manual mode of operation in case digital system fails.
Special low RPM motor means less noise and constant speed even at very low/high voltage (160-260).
Heating control through regulator with indicator, Electric Motor-Low rpm A.C. Motor, Operation Time-Programmable.
Type of Heating- Hot Plate, Temperature Control - Energy Regulator.

Programmable time with digital display, Auto stop after the set time with audio alarm for enteric coated tablet.
Facility to hold and resume the time and motor movement for quickly disintegrating tablets.
Manual mode of operation in case digital system fails.
Special low RPM motor means less noise and constant speed even at very low/high voltage (160-260).
Heating control through regulator with indicator, Electric Motor-Low rpm A.C. Motor, Operation Time-Programmable.
Type of Heating- Hot Plate, Temperature Control - Energy Regulator.

Tablet Disintegration Single Basket Used For Determination of Disintegration of Time of Tablets.
The Test Equipment Consist Of 1 Litre Beaker, Tablet can be Tested Simultaneously
Through Motorized Shaft Moves Up And Down Direction Of 30 R.P.M Approx.;
Carrying A Rigid Basket Rack Assembly. On The Upper End Of The Shaft Is Fitted
A Horizontal Strip To Support Cylindrical Standard Size Glass Tubes With Stainless Steel
Wire Gauge Bottom. Cylindrical Basket Moves Up And Down With Standard Perforated
Made of Acrylic Sheet Inside In One Litre Glass Beaker Of Distilled Water. Unit Having
Hot Plate Rating 125 Watts Fixed On The Top For Beaker. Temperature can be maintained.
Disclaimer: Product may differ (eg. colour) from the product Image displayed on website. Kindly check the technical specifications provided in description to make better purchase decision.

The Labtronics Digital Tablet Disintegration Test Apparatus, model LT-74, is an advanced instrument designed for assessing the disintegration time of tablets in pharmaceutical quality control and research applications. The disintegration test is a critical parameter to evaluate the effectiveness of tablet formulations, ensuring that the tablets break down appropriately in the digestive system for optimal drug absorption.
Key features of the LT-74 include its digital functionality and the inclusion of two baskets. The digital interface allows for precise control and monitoring of the disintegration test process, ensuring accurate and repeatable results. The inclusion of two baskets enhances the efficiency of testing by allowing simultaneous evaluation of two different tablet samples, increasing throughput in pharmaceutical laboratories.
The apparatus operates by immersing the tablet samples into individual baskets, which are then moved up and down in a standardized manner within the dissolution medium. The digital controls enable users to set specific parameters, such as the immersion depth and frequency, ensuring compliance with pharmacopoeial standards.
The digital display provides real-time information about the disintegration process, allowing users to monitor the time it takes for tablets to break apart. This information is crucial for assessing the quality and performance of the tablets, especially in formulations where a specific disintegration time is critical for therapeutic efficacy.
The LT-74 is likely constructed with materials suitable for pharmaceutical applications, ensuring durability and resistance to corrosion from the dissolution medium. The design of the apparatus meets industry standards, making it a reliable tool for pharmaceutical laboratories that require accurate and reproducible disintegration testing.
In summary, the Labtronics Digital Tablet Disintegration Test Apparatus with 2 Baskets (LT-74) is an advanced instrument designed for pharmaceutical quality control. With its digital controls, dual-basket configuration, and real-time monitoring capabilities, it offers a reliable solution for evaluating the disintegration time of tablets, contributing to the assessment of their effectiveness and compliance with regulatory standards.

The Labcare Tablet Disintegration Double Test Apparatus LB-TD2JN is designed to test the dissolution of tablets, capsules, and sugar granules in different liquids. The apparatus comprises of a central reaction tube, an observation tube, and a valve for acidity control.
This is a benchtop apparatus that's been designed with the intention of testing the disintegration rate of tablets. The apparatus has two chambers: one to hold the tablets, and one to hold the dissolution medium. The medium chamber is fitted with an agitator and thermometer, so it's capable of mixing and measuring temperatures. Also, it comes in a plastic housing that's easy to clean, allowing for quick maintenance and sanitation.
This is a tablet disintegration tester that has been designed to measure the disintegration time of tablets with a diameter of 6.0mm or less using a double dissolution method. The apparatus is composed of two tablet disintegrator compartments, which are separated by a partition. Each compartment has an opening for adding tablets. The number of tablets added can be set between 1 and 100 in increments of 10, and the time between 0 and 120 minutes can also be set in increments of 10.
Each tablet disintegrator compartment contains an agitator, which moves up and down to ensure an even distribution of the water around each tablet during the test period. The amount of water used is adjustable from 50-300 ml in increments of 5 ml. At the end of the test period, the saturated solution is removed from both compartments and measured for turbidity, which is then recorded on a graph for analysis.

The LABCARE LB-940 Up-Down: 30 rpm- 2 rpm Disintegration Test Apparatus is a test apparatus used to determine the disintegration time of tablet dosage forms under specified conditions. The test apparatus is used as an in vitro method to predict drug release rates in vivo. It provides a basic comparative evaluation of the tablet disintegration rate and thus can be used to compare different dosage forms and batches of tablets. It is a device that measures the disintegration time of tablets from the point at which they are placed into the device until no tablet remains. This test is used to determine whether a tablet is suitable for human consumption. It is comprised of a Plexiglass tube fitted with a grinding disk, turned by a motor at 30rpm, to mimic the action of chewing. The grinding disk is coated with the sample of anti-grinding agent and an agitator turns inside the tube to disperse the product as if it were in saliva. The agitator is driven by an electric motor at 2rpm and ensures that there is always agitation within the tube to guarantee that the sample remains dispersed. The result is measured by measuring the time it takes for the sample to break down into its composite components, expressed in milliliters per minute (ml/min).

NSAW DTA-1 30 rpm Single Basket Analog Disintegration Test Apparatus NSAW-1680 is a device used in the pharmaceutical industry to determine the disintegration time of solid dosage forms such as tablets, capsules, and granules. The apparatus evaluates the ability of a dosage form to break down and disintegrate into smaller particles when exposed to simulated physiological conditions.
The disintegration test is an essential quality control test to ensure that a medication will dissolve and release its active ingredients in a timely manner, allowing for proper absorption in the body. The apparatus typically consists of the following components:
Basket or tube assembly: This component holds the dosage form during the test. It can be a wire mesh basket or a tube with open ends, depending on the type of dosage form being tested.
Temperature control: Some disintegration test apparatus includes a temperature control feature to maintain the test medium at a specified temperature, typically 37°C, to simulate body conditions.
Test medium: The apparatus uses a suitable liquid medium, such as water or simulated gastric fluid, to immerse the dosage form during the test. The medium should mimic the physiological environment in which the dosage form will be exposed.
Impeller or paddle: The apparatus includes a mechanism, usually an impeller or paddle, to provide mechanical agitation to the test medium. This agitation ensures that the dosage form is constantly in motion, aiding in disintegration.
During the test, the dosage form is placed in the basket or tube assembly and immersed in the test medium. The apparatus is then set to agitate the test medium at a specified speed. The disintegration time is measured as the time required for the dosage form to completely disintegrate, i.e., when no residue is visible or when the particles are small enough to pass through the mesh of the basket.
The disintegration test apparatus is widely used in pharmaceutical manufacturing to assess the quality and performance of solid dosage forms. It helps ensure that medications are properly formulated, allowing for effective drug release and absorption. The results obtained from the disintegration test can guide manufacturers in optimizing their formulations and processes, as well as ensure compliance with regulatory requirements.
In summary, a disintegration test apparatus is a vital tool in the pharmaceutical industry to evaluate the disintegration time of solid dosage forms. It aids in quality control and helps ensure that medications provide the desired therapeutic effects by properly disintegrating and releasing their active ingredients.

Lab Junction Single Basket Digital Tablet Disintegration Apparatus LJ-904 is a laboratory instrument used to assess the disintegration time of tablets and other solid dosage forms in a controlled and standardized manner. It is an essential tool in pharmaceutical quality control and research to ensure that tablets disintegrate properly and release their active ingredients effectively.
The disintegration of a tablet refers to the process of breaking down and dispersing the tablet into smaller particles when exposed to a specific medium, typically simulated gastric fluid or simulated intestinal fluid. The disintegration time is a critical parameter that determines how quickly the tablet dissolves and allows the active ingredients to become available for absorption in the body.
The digital tablet disintegration apparatus consists of a water bath with multiple test stations, each equipped with a mesh basket or assembly that holds the tablets during the test. The apparatus maintains the temperature and agitation conditions according to pharmacopeial standards or specific test protocols. It also incorporates a digital display or timer to accurately measure and record the disintegration time.
During the test, the tablets are placed in the mesh baskets and immersed in the dissolution medium. The water bath is set to the specified temperature, usually 37°C, to simulate physiological conditions. The apparatus then applies a controlled vertical up-and-down movement to the mesh baskets, creating agitation that mimics the peristaltic action of the gastrointestinal tract. The tablets gradually disintegrate, and the time taken for complete disintegration is recorded.
The digital aspect of the tablet disintegration apparatus allows for precise timing and automated data recording. It ensures accuracy and consistency in measuring the disintegration time of tablets across multiple test stations. The digital display or timer provides real-time monitoring and allows users to easily track the progress of the disintegration test.
The results obtained from the digital tablet disintegration apparatus are crucial in pharmaceutical quality control. They provide information about the tablet's ability to break down into smaller particles, which is essential for drug release and absorption. The disintegration time can be compared against specified limits or pharmacopeial standards to ensure product quality and batch-to-batch consistency.
In research and development, the digital tablet disintegration apparatus is used to evaluate the performance of different formulations and optimize tablet design. It allows researchers to assess the effect of various factors, such as excipients, coating, and manufacturing techniques, on the disintegration behavior of tablets.
In summary, a digital tablet disintegration apparatus is a laboratory instrument used to determine the disintegration time of tablets and other solid dosage forms. It provides controlled conditions of temperature and agitation to mimic physiological environments. The digital display and timer enable precise timing and automated data recording. The apparatus plays a critical role in pharmaceutical quality control and research, ensuring that tablets disintegrate properly and release their active ingredients effectively.

The Labtronics Microprocessor Disintegration Test Apparatus, model LT-731, is a specialized instrument designed for pharmaceutical quality control to assess the disintegration time of solid dosage forms such as tablets and capsules. This apparatus is crucial in ensuring that pharmaceutical formulations meet regulatory standards and dissolve properly for effective drug delivery.
**1. Disintegration Test:** The primary function of the LT-731 is to perform disintegration tests on pharmaceutical products. Disintegration time is a critical parameter that indicates how quickly a solid dosage form breaks down into smaller particles or dissolves in a simulated physiological environment. This information is vital for predicting the drug's release and absorption in the body.
**2. Microprocessor Control:** The microprocessor technology integrated into the LT-731 ensures precise control over the disintegration testing process. This feature allows for accurate timing, data recording, and automated operation, enhancing the reliability and reproducibility of the test results.
**3. Two Baskets:** The inclusion of two baskets in the apparatus allows for simultaneous testing of two samples, increasing the efficiency of the testing process. This is particularly beneficial in pharmaceutical laboratories where multiple samples need to be assessed concurrently.
**4. Compliance with Pharmacopeia Standards:** The LT-731 is likely designed to comply with pharmacopeia standards, such as the United States Pharmacopeia (USP) or other relevant regulatory guidelines. Adhering to these standards ensures that the disintegration tests are conducted in a standardized and accepted manner, providing consistency and comparability of results.
**5. User-Friendly Interface:** The instrument is likely equipped with a user-friendly interface for easy operation, parameter setting, and data retrieval. This is important for laboratory technicians and pharmaceutical quality control professionals who may use the apparatus regularly.
**6. Applications:** The LT-731 is specifically tailored for use in pharmaceutical quality control laboratories. It is employed to assess the disintegration characteristics of various solid dosage forms, helping pharmaceutical manufacturers ensure the efficacy and safety of their products.
In summary, the Labtronics Microprocessor Disintegration Test Apparatus (LT-731) is a sophisticated tool designed for pharmaceutical quality control. Its microprocessor control, ability to test two samples simultaneously, and adherence to pharmacopeia standards make it an essential instrument for ensuring the quality and performance of solid dosage forms in the pharmaceutical industry.

Salient Features: Used for determination of disintegration time of tablets. The test equipment consist of 1 litre beaker. Tablet can be tested simultaneously through motorized shaft moves up and down direction of 30 R.P.M approx.; carrying a rigid basket rack assembly. Unit having hot plate rating 125 watts fixed on the top for beaker. Temperature can be maintained by thermostat in between 35 ⁰c to 37⁰c. Digital timer can be fixed with the machine. Optional Accessories DT Basket Complete DT Disc DT Plate IQ, OQ, PQ Documents

Electronic India Digital Tablet DisintegrationApparatus
Key Features :
Digital time output with I second resolution
Accurate time output provided by microprocessor based time totalizer
Baskets move 'Up and Down' as per IP/USP test specifications
Temperature controlled by sensitive thermostat
Please Note: Image displayed on the website is a reference , the product specifications will be same however the actual product colour might differ. Kindly check the technical specifications provided in the description to make the better purchase decision.

Electronic India µP Disintegration Test Appartus
Key Features :
Complies with USp,IP specifications
Extremely useful for pharmaceutical lab
Highly Accurate and Easy to Operate
Continuation of Last Test Run in case of Power Failure.
Baskets 'Up' & 'Down' movement as per 'IP/USP Specifications
20 x 4 Line LCD with Backlit
10 Setups Storage Facility
200 Samples Storage Facility
Printer Attachment Facility
Audio Visual Indicators for System Status
Technical Specifications
Keyboard :15 soft touch membrane keys
LED's :4 LED's available for different status indications. 3 LED's for Test status like Run,Alarm, End and one LED for heater on/off status.
Setup Data :Facility for 10 different test setups available
Printer : Provision for the attachment of dot-matrix printer with centronics parallel port interface available
Temperature Control :Microprocessor based using PT I00/ Semiconductor Sensor
Heater :1 KW
Please Note: Image displayed on the website is a reference , the product specifications will be same however the actual product colour might differ. Kindly check the technical specifications provided in the description to make the better purchase decision.

Digital Tablet Disintegration Apparatus Model-904 is designed for accurate estimation of disintegration time of tablets as per IP/USP standards. The instrument is designed to test tow batches of six tablets, simultaneously. The unit consists of two beakers having capacity of 1000 cc each. In these beakers, suitable disintegration media can be taken. These can be temperature controlled using a in-built heater and a highly thermostat fitted inside the instrument. Microprocessor based time totalizer is provided for accurate time readout.

Salient Features: Used for determination of disintegration time of tablets. The test equipment consist of 1 litre beaker. Tablet can be tested simultaneously through motorized shaft moves up and down direction of 30 R.P.M approx.; carrying a rigid basket rack assembly. Unit having hot plate rating 125 watts fixed on the top for beaker. Temperature can be maintained by thermostat in between 35 ⁰c to 37⁰c. Digital timer can be fixed with the machine. Optional Accessories DT Basket Complete DT Disc DT Plate IQ, OQ, PQ Documents

Salient Features: Used for determination of disintegration time of tablets. The test equipment consist of 1 litre beaker. Tablet can be tested simultaneously through motorized shaft moves up and down direction of 30 R.P.M approx.; carrying a rigid basket rack assembly. Unit having hot plate rating 125 watts fixed on the top for beaker. Temperature can be maintained by thermostat in between 35 ⁰c to 37⁰c. Digital timer can be fixed with the machine. Optional Accessories DT Basket Complete DT Disc DT Plate IQ, OQ, PQ Documents

Salient Features: Used for determination of disintegration time of tablets. The test equipment consist of 1 litre beaker. Tablet can be tested simultaneously through motorized shaft moves up and down direction of 30 R.P.M approx.; carrying a rigid basket rack assembly. Unit having hot plate rating 125 watts fixed on the top for beaker. Temperature can be maintained by thermostat in between 35 ⁰c to 37⁰c. Digital timer can be fixed with the machine. Optional Accessories DT Basket Complete DT Disc DT Plate IQ, OQ, PQ Documents