Dissolution Apparatus DP-6
Introdution:
the DP-6 Dissolution Apparatus is a precision instrument designed for performing dissolution tests on pharmaceutical formulations. It provides controlled conditions for simulating drug release in the human body, with accurate temperature and speed adjustments. Ideal for evaluating the dissolution profiles of tablets, capsules, and other solid dosage forms, the DP-6 ensures reliable and reproducible results, meeting industry standards for pharmaceutical testing.
Applications:
The DP-6 Dissolution Apparatus is used for:
Dissolution Testing: Assessing drug release from tablets, capsules, and solid dosage forms.
Quality Control: Ensuring consistency and compliance with regulatory standards.
Formulation Development: Optimizing drug formulations for better bioavailability.
Regulatory Testing: Meeting pharmacopoeia requirements (USP, EP, BP).
The DP-6 ensures precise and reliable dissolution testing for pharmaceutical applications.
Specification :
| Model NO. | DP-6 |
| Number of baskets | 6 |
| Basket Paddle (Axis) Verticality | ≤0.5° From The Vertical Direction |
| Coaxiality of The Vessel and The Basket | off-Axis ≤1.0mm |
| Dissolution cup verticality | ≤1° deviation from the vertical direction |
| Basket (paddle) shaft swing | swing ≤ 0.3mm |
| Basket (paddle) depth | 25 ± 1mm |
| Medium temperature in each vessel | 37oC ± 0.3 oC |
| Speed range | 25-250 rpm |
| Speed accuracy resolution | 0.1 rev / min |
| Water bath temperature range | 5oC -50oC |
| Temperature control accuracy | ≤ ± 0.3oC |
| Cumulative time | 99 hours, 59 minutes and 59 seconds. (Basic experiment timing) |
| Continuous working time | 100h |
| Electric heating power | 1500W |
| Voltage | 220V |
Reliable Performance for Pharmaceutical Dissolution Testing: Dissolution Apparatus DP-6
The Dissolution Apparatus DP-6 is a dependable laboratory instrument designed for conducting standardized dissolution tests on pharmaceutical dosage forms such as tablets, capsules, and granules. Widely used in quality control, formulation development, and regulatory compliance, it supports pharmacopeial methods including USP <711> and EP 2.9.3.
This apparatus provides consistent, reproducible testing conditions by precisely controlling vessel temperature, paddle or basket rotation speed, and test duration. Its robust build and user-friendly operation make it suitable for routine dissolution profiling in pharmaceutical labs, ensuring accurate assessment of drug release characteristics and batch-to-batch consistency.
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