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Pharmaceutical Dissolution Media

Drug Dissolution Media serves as an essential method for controlling API release throughout pharmaceutical product formulations based on requirements of Chinese, U.S., and EU Pharmacopoeia standards and 21 CFR Part 11. The system fulfills the standards established by the Pharmacopoeia from Chinese, the U.S., and the EU as well as satisfying 21 CFR Part 11 requirements. The device operates on all USP 1 to USP 4 equipment including mechanical test kits and solvent handling equipment. The system's intuitive design improves both precision level and operational speed along with adaptable attachments which enable smooth laboratory implementation.  

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Features

This dissolution testing system adheres to strict pharmaceutical quality control standards, meeting Chinese, U.S., and EU Pharmacopoeia regulations. The solution implements 21 CFR Part 11 specifications to provide data security and maintain traceable records which helps organizations pass global audit assessments.

 

Multi-channel Synchronized Testing

Supports simultaneous dissolution testing of multiple samples, improving efficiency.

Automated Temperature Control System

Automatically adjusts temperature, ensuring consistent testing conditions.

High-Precision Data Acquisition

High-precision data acquisition involves collecting and analyzing data accurately and in real time

Intelligent Analysis Software

Provides data acquisition, comparison, and visualization, simplifying analysis.

Compliant with GMP and GLP Standards

Meets pharmaceutical industry compliance requirements, ensuring data reliability.

Complies with 21 CFR Part 11

meets audit trails to ensure data security


Resources

PDF

12 Positions Automated Dissolution tester Leaflet

pdf 3.46MB

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PDF

Flow-through cell dissolution system Leaflet

pdf 4.45MB

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RT612-ST Automatic Sampling General Dissolution System


Cases

This system performs USP 1, USP 2, USP 3, and USP 4 dissolution exams with its components which include mechanical test systems and solvent control solutions. The system delivers three key benefits through its precise operation while attaining maximum efficiency and producing reliable drug formulation analysis results for pharmaceutical needs.

 

Drug Patch
Dissolution apparatus RT612-ST  12 Positions Automated Dissolution tester Method USP <724> DRUG RELEASE: Apparatus 6 (Cylinder) Temperature 37℃ ± 0.5℃ Speed 50 RPM
Enteric-Coated Tablet
Dissolution apparatus RT3 Reciprocating Cylinder Apparatus Temperature 37℃ ± 0.5℃ Medium Volume 200 mL Reciprocating stroke 10 mm Reciprocating rate 10 DPM Medium  0-60 min (pH 1.2 HCl)/ 60-75 min (pH 6.5 PBS)/ 75-90min (pH 6.8 ...
Liposome-Based Drug Delivery
Liposome-Based Drug Delivery
Dissolution apparatus RT7 Flow-through Cell Dissolution System Temperature 37℃± 0.5℃ Model Closed-loop
Suspending Eye Drops
Suspending Eye Drops
Dissolution apparatus RT7 Flow-through Cell Dissolution System Temperature 37℃± 0.5℃ Model Closed-loop
Nanocrystal Injection
Nanocrystal Injection
Dissolution apparatus RT7 Flow-Through Cell Dissolution System Type of Flow-Through Cell Cell for 22.6mm Temperature 37℃± 0.5℃ Velocity 4/ 8/ 16 mL/min Model Closed-loop Medium Volume 500 mL
Albumin-Bound Injections
Albumin-Bound Injection
Dissolution apparatus RT7 Flow-Through Cell Dissolution System Type of Flow-Through Cell Cell for 22.6mm Temperature 37℃± 0.5℃ Sample volume 1 mL Model Closed-loop Pulse 0 Hz
Sustained-Release Tablet
Sustained-Release Tablet
Dissolution apparatus RT7 Flow-Through Cell Dissolution System Type of Flow-Through Cell Cell for 22.6mm Temperature 37℃± 0.5℃ Model Closed-loop
Softgel Capsules
Softgel Capsules
Dissolution apparatus RT7 Flow-Through Cell Dissolution System Type of Flow-Through Cell Cell for suppositories and gelatin capsules Temperature 37℃± 0.5℃ Pulse 0 Hz

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The device provides a user-friendly interface that reduces operator mistakes as well as simplifies all processes for dissolution testing. The machine-driven system improves workflow precision along with accuracy and repeatability to advance general laboratory operations.

 

The solution contains multiple accessories to build diverse testing setups for dissolution tests. The system offers rapid customization services that support pharmaceutical research laboratories as well as quality control labs through its capability to work with various testing needs.