Dissolution method development for Immediate Release (IR) drug product 

Your videos have a great impact on the future of juniors in the pharma industry....

Hi sir Iam fresher, iam starting my learning with this video, it helps me a lot, thank you so much sir...🙏

Very use full topic tq sir

Good lesson. Can you please make a session on dissolution method development for Modified release dosage?

Nav varsh ki subh kamna sir....nice one as usual...

Iam 1st Viewer

THANKS A LOT SIR ,

Is it OK to prepare final dilution of standard using a dissolution media containing a higher percentage of surfactant compared to the dissolution media?? (Media has a 0.2% surfactant whereas final dilution with same pH media but a higher concentration of surfactant, how will this be justified?)

1st is it same for both assay and dissolution. 2nd how I would perform dissolution accuracy for different concentration of finished tablet. As we take one tablet for each disolution vessel. for validation purpose

Hi sir, thanks for the information. We getting 85% of the dissolution if we add enzyme for accelerated condition. But for long term no need of adding enzyme. Then what will be the final dissolution media.

Dear Bhaskar Sir, Plan 2week training with online mode after few days

On what basis you are selecting 900 mL as your Dissolution media volume. Could you explain it?

Sir. Why do IR tablets have a dissolution time point in 15, 30, 45, and 60 mins... Why don't we have 20, 35,50 mintus ??

Whether release media and discrimination media r same.. or different..?

how much active atleast should be present in tablet for dissolution test requirement? if tablet contain 5 or 25 mg active ingredient should we perform dissolution test on it or not require?

0.01N hcl pH2.0 0.1NHCL pH1.2

Hi, is it possible to contact you on phone for some training requirement? Kindly share the contract details. Thanks

Hello, in this video selection of dissolution media and volume not clear. ...