Pharmaceutical Bioavailability Testing A Dissolution Test Apparatus is a critical instrument in pharmaceutical quality control and R&D, designed to measure the rate and extent of drug release from solid dosage forms like tablets and capsules. By simulating the human gastrointestinal environment, it provides essential data on how quickly a medication becomes available for absorption. At Labend Scientific, we provide high-precision 6 and 8-station systems that ensure rigorous adherence to international Pharmacopeial standards. Our dissolution systems are often used in a sequence of physical evaluations. Before dissolution, tablets undergo testing with the ESAW Tablet Hardness Tester to ensure structural integrity. Following the dissolution process, the concentration of the released active pharmaceutical ingredient (API) is typically quantified using precision analyzers such as the ESAW Spectrophotometer 3375 or the ESAW 2306 UV-VIS models. Advanced features of our apparatus include precise RPM control, temperature uniformity across all vessels, and vibration-free operation. For moisture-sensitive formulations, validation with the ESAW Moisture Titrator 761 and density checks using the ESAW Tap Density Tester are recommended to complete the stability profile. Our systems are built for 24/7 laboratory operations, ensuring long-term durability and repeatable results. System Specifications 🔘 Vessel Stations: 6 / 8 / 14🔘 Speed Range: 25 - 250 RPM🔘 Temp Range: 25.0°C - 45.0°C🔘 Accuracy: ±0.2°C🔘 Bath MOC: High-Grade Acrylic🔘 Shaft/Paddle: SS 316L Mirror Finish *Compliant with 21 CFR Part 11 for data integrity and secure login. Integrated Pharmaceutical Catalog • Dissolution Test Apparatus • ESAW Spectrophotometer 3375 • ESAW Spectrophotometer 2377 • ESAW Tap Density Tester 1951 • Tablet Hardness Tester 3956 • ESAW Moisture Titrator 761 • ESAW Spectrophotometer 2306 • ESAW Spectrophotometer 2375 • ESAW Spectrophotometer 1371 • ESAW Tap Density Tester 951 • ESAW Moisture Titrator 1760 • ESAW Spectrophotometer 302 Technical Support & FAQ Q1: What is the difference between Paddle and Basket? A: Apparatus 1 (Basket) is typically for capsules, while Apparatus 2 (Paddle) is used for standard tablets, per USP guidelines. Q2: How is temperature uniformity maintained? A: Our systems use a specialized water bath circulator that ensures all 8 vessels remain within ±0.2°C of the target temperature. Q3: Does the apparatus support auto-sampling? A: Yes, our high-end models can be integrated with automated manifold systems for precise sampling intervals. Q4: Are these keywords optimized for search? A: Yes: Dissolution Test Apparatus Price, 8 Station Dissolution Tester, Tablet Dissolution USP, Pharma QC Instruments India. RELEVANT SEARCHES: Automatic Dissolution Tester, Tablet Release Testing Machine, Pharmacopeia Compliant Dissolution Unit, Digital Pharma Tester, Dissolution Vessel SS 316, 6 Station Dissolution Apparatus, Drug Bioavailability Equipment, Labend Dissolution Series, #DissolutionTest #PharmaQC #DrugDevelopment #TabletTesting #LabendScientific Global Export & Distribution Markets USA | UK | Germany | United Arab Emirates | Saudi Arabia | Singapore | Malaysia | Australia | Canada | India | South Africa | Brazil | Qatar | Oman | France | Italy | Spain | New Zealand | Ireland | Netherlands | Thailand | Indonesia | Vietnam | South Korea | Mexico | Philippines | Egypt