Golgappa.net | Golgappa.org | BagIndia.net | BodyIndia.Com | CabIndia.net | CarsBikes.net | CarsBikes.org | CashIndia.net | ConsumerIndia.net | CookingIndia.net | DataIndia.net | DealIndia.net | EmailIndia.net | FirstTablet.com | FirstTourist.com | ForsaleIndia.net | IndiaBody.Com | IndiaCab.net | IndiaCash.net | IndiaModel.net | KidForum.net | OfficeIndia.net | PaysIndia.com | RestaurantIndia.net | RestaurantsIndia.net | SaleForum.net | SellForum.net | SoldIndia.com | StarIndia.net | TomatoCab.com | TomatoCabs.com | TownIndia.com
Interested to Buy Any Domain ? << Click Here >> for more details...

What is the reason for using the 900ml of dissolution medium

Answer Posted / amit

Selection of disoslution media depends on the sink
condition which means, three time the highest dose of drug
dissolving in 250 ml of media. So, if your drug diosslves
in 250ml you can select 250ml as mediavolume or depending
on the solubiliy you can go upto 2 lts with proper
justification.
Remember the selection of dissolution media volume is only
to get whole amount of drug dissolved and sholud be able to
quantifiy it.

Is This Answer Correct ?    33 Yes 6 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

why require the ph, buffer during hplc mobile phase?

874


what is mean by extactable and leachable study?

1185


Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?

2741


Why Ethanol is Used for Standardization of GC Head space?

4235


in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?

737


why require to add enzymes in capsules dissolution only? is it require to tablet also?

686


If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?

813


we can use expired sample for validation and analyst qualification?

824


USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...

2023


What are modes of quantification in related substances

2176


Basic principle of ESI?

2160


Principle of single pan analytical balance

5153


How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.

2591


using gradient pressure in gas chromatography are not ?using gradient pressure why

3398


What is shaking level in GC?

803