Disolution Tester United Pharmatek home >> Disolution Tester United Pharmatek

DT-8D-Dissolution-Tester

Product Name

Disolution Tester United Pharmatek

Product Category

Disolution Tester United Pharmatek

DISULUTION TESTER

DT Series Tablet Dissolution Tester is the requisite instrument in detecting dissolution of tablets, capsule etc. All of our lab instruments are designed and manufactured in accordance with USP Specifications. The units come with 6 or 8 vessels; the 2 additional vessels can be used for blank, standard or media replacement. The USP dissolution apparatus consist of a control system, electric system, dissolution bath, transmission system, lifting system, transducer unit, paddle unit, and rotating basket unit.

Gallery of Product

Information of Product

Description

Disolution Tester United Pharmatek

DISULUTION TESTER

DT Series Tablet Dissolution Tester is the requisite instrument in detecting dissolution of tablets, capsule etc. All of our lab instruments are designed and manufactured in accordance with USP Specifications. The units come with 6 or 8 vessels; the 2 additional vessels can be used for blank, standard or media replacement. The USP dissolution apparatus consist of a control system, electric system, dissolution bath, transmission system, lifting system, transducer unit, paddle unit, and rotating basket unit.

Additional information

Application & Information

Dissolution Tester Principle

Dissolution testing is the most important way to study, under in vitro conditions, the release of a drug from a solid dosage form, and thus represents an important tool to assess factors that affect the bioavailability of a drug from a solid preparation. During a dissolution test the cumulative amount of drug that passes into solution is studied as a function of time. The test thus describes the overall rate of all the processes involved in the release of the drug into a bioavailable form.

Dissolution studies are carried out for several reasons:

To evaluate the potential effect of formulation and process variables on the bioavailability of a drugTo ensure that preparations comply with product
specifications. To indicate the performance of the preparation under in vivo conditions.Dissolution is accomplished by locating the tablet in a chamber containing a flowing dissolution media. So that the method is reproducible, all factors that can affect the dissolution process must be standardized. Details on approved
test methods and official monographs can be found in the European or US Pharmacopoeias.

Reviews

There are no reviews yet.

Be the first to review “Disolution Tester United Pharmatek”

Your email address will not be published.

Feel Free to Contact Us

× Ada yang bisa saya bantu?