Superex Scientific Private Limited

The Dissolution Tester is a critical laboratory instrument used to measure the rate at which an active pharmaceutical ingredient (API) is released from a solid dosage form—such as tablets or capsules—into a dissolution medium under standardized conditions. This process simulates how the drug dissolves in the gastrointestinal tract and is essential for evaluating the performance, consistency, and bioavailability of oral medications.

Designed in compliance with major pharmacopeial standards (USP, IP, BP, EP), the Dissolution Tester is a staple in pharmaceutical R&D, quality control, and regulatory testing. With multiple test stations, precise temperature control, and programmable settings, it provides reliable and reproducible results for both routine and advanced dissolution testing.

The Dissolution Tester is widely used in:

• Pharmaceutical R&D – Formulation development and drug release profiling

• Quality Control Laboratories – Batch release and regulatory compliance testing

• Bioequivalence Studies – Comparing generic and innovator drug products

• Stability Testing – Monitoring changes in dissolution over product shelf life

• Academia & Training – Educational institutions for pharmaceutical sciences

• Test Stations: Typically available in 6, 7, or 8 positions; allows parallel testing of multiple samples

• Drive Mechanism: Motorized shaft to rotate paddles or baskets at a controlled RPM (usually 50–100 rpm)

• Dissolution Vessels: 1000 ml capacity, made of borosilicate glass, with precision alignment

• Temperature Control: Integrated water bath or heating system with a digital temperature sensor (usually 37.0°C ± 0.5°C)

• Control Panel: Digital or touch screen interface with programmable test parameters

• Compliance: USP <711>, IP, BP, and EP specifications

• Accessories: Paddles (Apparatus 2), Baskets (Apparatus 1), sampling probes, and validation tools

The Sieve Shaker is a high-performance, mechanical sieving instrument designed to deliver accurate and reproducible particle size analysis for a wide range of materials. Built for efficiency and durability, this shaker is suitable for laboratory and industrial applications where quality control and material classification are critical.

This device automates the manual sieving process, reducing operator workload while ensuring consistent results. With adjustable time and amplitude settings, the Universal Sieve Shaker accommodates different material types and testing standards, making it a versatile solution for any testing environment.

The Sieve Shaker is widely used in:

• Pharmaceutical Industry – Granule and powder size classification

• Chemical Industry – Raw material quality control

• Food & Beverage – Particle size distribution in flour, grains, and powders

• Mining & Metallurgy – Ore and mineral analysis

• Environmental Science – Soil and sediment particle size testing

Semi-Automatic Tablet Hardness Tester is a precision laboratory instrument used to measure the mechanical strength of pharmaceutical tablets. It determines the force required to break a tablet across its diameter, a critical parameter in ensuring tablet integrity during handling, packaging, and transportation.

Combining digital accuracy with user-guided operation, this semi-automatic tester offers consistent results with minimal operator influence. It is ideal for R&D labs, production quality control, and compliance testing, adhering to international pharmacopoeial standards (USP, IP, BP, and EP).

• Measurement Range: Typically 2–500 Newtons (or up to 50 kgf)

• Display: Digital LCD/LED screen showing hardness value clearly

• Operation Type: Semi-automatic — operator positions the tablet, and the device applies force and records the result automatically

• Accuracy: ± 1 Newton or better

• Units of Measurement: Selectable (N, Kgf, or lbf)

• Test Speed: Fixed or adjustable depending on model; optimized to minimize tablet deformation

• Tablet Size Compatibility: Suitable for a range of shapes and sizes (usually 2 mm to 30 mm diameter)

• Data Output: USB or RS-232 for data transfer (optional)

• Construction: Rugged stainless steel or coated metal housing for lab-grade durability

• Compliance: Conforms to USP <1217> and other international standards

The Friability Tester is a precision laboratory instrument designed to evaluate the durability and mechanical strength of pharmaceutical tablets during handling, packaging, and transportation. It determines the tablets' friability — their tendency to crumble, chip, or break under stress — by rotating them in a standardized drum that simulates real-world conditions.

Engineered for compliance with major pharmacopeial standards (USP, IP, BP, and EP), the Friability Tester is essential for quality control and R&D in pharmaceutical manufacturing. It features user-friendly controls, digital timers, and transparent drums for easy observation of the testing process.

The Friability Tester is used primarily in:

• Pharmaceutical Manufacturing – To assess the physical integrity of uncoated tablets.

• Quality Control Laboratories – Ensuring products meet compliance and regulatory standards.

• Research & Development – Evaluating formulations and the effect of different excipients.

• Educational Institutions – Teaching tablet testing and quality assurance procedures.

• Testing Capacity: Typically 1 or 2 drums; can test multiple tablets per cycle (standard: 10 tablets)

• Drum Specifications: Made of transparent acrylic with a beveled edge, rotating at 25 ± 1 rpm

• Test Duration: Adjustable digital timer (typically up to 999 seconds or rotations)

• Speed Control: Fixed or variable rotation speed as per pharmacopeial guidelines

• Display: Digital LCD/LED for time, rotation count, and sometimes speed

• Construction: Durable, chemical-resistant housing with compact footprint

• Standards Compliance: Meets USP <1216>, IP, BP, and EP friability testing requirements

• Optional Features:

  • Dual drum operation for simultaneous testing

  • Automatic stop at preset time or rotation count

  • Detachable drums for easy cleaning

The Disintegration Tester is a critical laboratory device used to determine the disintegration time of tablets and capsules under standardized conditions. This test simulates the environment of the human gastrointestinal tract to assess how quickly and completely a dosage form breaks down, ensuring proper drug release and absorption.

• Test Stations: Typically available in single, double, or triple basket configurations (1–3 stations)

• Basket Rack Assembly: Holds 6 tubes per basket with standard mesh size (usually 2 mm)

• Stroke Frequency: Approximately 30 cycles per minute, as per pharmacopoeial requirements

• Heating System: Digital water bath maintains temperature at 37.0°C ± 0.5°C

• Control Panel: Digital or touchscreen interface with programmable timers

• Automatic Lift Mechanism: Raises basket rack automatically at the end of the test

• Beaker Capacity: Typically 1000 mL, made of heat-resistant glass

• Construction: Stainless steel or chemically resistant body for long-term durability

• Compliance: Meets USP <701>, IP, BP, and EP standards