Disintegration Test Apparatus

The HTLP Basket Type Tablet Disintegration Machine HTLP-074 is a crucial instrument used in pharmaceutical quality control laboratories to assess the disintegration time of tablets and capsules. Disintegration testing is essential to ensure that oral dosage forms break down properly in the gastrointestinal tract, allowing for efficient drug absorption. This machine employs a basket method, where tablets or capsules are placed in individual mesh baskets immersed in a dissolution medium, typically water or a simulated gastric fluid. The baskets are then oscillated up and down at a constant rate, simulating the mechanical forces encountered in the digestive system. The disintegration process is monitored visually, with the operator observing when each tablet or capsule disintegrates, signified by the absence of remaining particles or fragments. The HTLP-074 disintegration machine is designed for accuracy, reliability, and ease of use. It features precise temperature control to maintain the dissolution medium at the required temperature, ensuring consistency in testing conditions. The oscillation mechanism operates smoothly and consistently, facilitating uniform disintegration testing across multiple samples. Furthermore, the machine offers adjustable parameters, such as oscillation speed and temperature, allowing users to customize testing conditions according to pharmacopeial standards or specific product requirements. This flexibility ensures compliance with regulatory guidelines and facilitates optimization of testing protocols for different formulations. The HTLP-074 disintegration machine also incorporates safety features to protect both operators and samples during testing. These may include automatic shut-off mechanisms in case of malfunction or overheating, as well as protective enclosures to prevent accidental contact with moving parts. Overall, the HTLP Basket Type Tablet Disintegration Machine HTLP-074 plays a crucial role in pharmaceutical quality assurance, enabling manufacturers to evaluate the performance of oral dosage forms accurately. Its precision, reliability, and user-friendly design make it an indispensable tool for ensuring the safety, efficacy, and consistency of pharmaceutical products.

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 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).

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 NSAW Disintegration Test Apparatus NSAW-1680 is a specialized instrument used in pharmaceutical quality control laboratories to assess the disintegration time of solid dosage forms such as tablets, capsules, and suppositories. Disintegration testing is an essential step in the evaluation of pharmaceutical products, ensuring that they will properly disintegrate and release their active ingredients within the gastrointestinal tract for effective absorption. The NSAW-1680 apparatus typically consists of a set of test stations, each equipped with a basket rack or a tube rack where individual dosage units are placed. These racks are immersed in separate beakers filled with a suitable disintegration medium, such as water or simulated gastric fluid, maintained at a specified temperature. During testing, the dosage units are subjected to agitation or reciprocating motion within the disintegration medium, simulating the conditions encountered in the gastrointestinal tract. The disintegration time is determined by observing the complete breakdown of the dosage unit into smaller particles or dissolution of its components.

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.

The Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC is a laboratory instrument designed to test the disintegration time of pharmaceutical tablets under controlled conditions. The Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC ensures precise and consistent results by providing uniform immersion and agitation of tablets in a liquid medium, simulating physiological conditions. Operable on a standard 220/230 V AC power supply, this machine is compatible with a wide range of laboratory environments without requiring additional modifications. The robust construction and user-friendly design of the Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC allow for easy handling, reliable operation, and accurate monitoring, making it an essential tool for pharmaceutical research, quality control, and formulation development. Engineered for efficiency and precision, the Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC provides consistent immersion cycles and controlled temperature conditions to ensure reproducible disintegration measurements. The machine’s 220/230 V AC compatibility allows seamless integration into standard laboratory setups, while its durable build ensures long-lasting performance. The Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC is ideal for pharmaceutical laboratories focused on quality assurance, regulatory compliance, and formulation testing. With accurate timing, uniform operation, and reliable construction, the Vesca VSLI-280 Tablet Disintegration Machine Workable on 220/230 V AC guarantees dependable results, helping researchers and quality control professionals maintain high standards in tablet evaluation.

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.

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.

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

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