what is sink condition in Dissolution?
Answer Posted / ganesh parsewar
One of the requirements to conduct an appropriate drug
dissolution test is to use a sufficient volume of
dissolution medium, which should be able to dissolve the
expected amount of drug released from a product. This
ability of the medium to dissolve the expected amount of
drug is known as a “sink condition”.It is important to note
that a dissolution test should not be conducted in a volume
of the medium which would not dissolve the expected amount
of the drug completely and freely.
Is This Answer Correct ? | 22 Yes | 11 No |
Post New Answer View All Answers
What do you mean by Bracketing and Matrixing in stability?
How can you fix the known and unknown impurity limit for any drug substance?
the international interview procedure for a job.
i like to know when is drug inspector exam 2009.and plz send me da question paper, interviev questions,and other details on my mail.id. shubhg2009@gmail.com. plz
How would you make a physician to prescribe your medicine rather than that of the competitor?
How do you balance the benefits and risks of Alprazolam treatment when considering its prescription for an elderly patient with multiple comorbidities?
hello,am milan mohite,i have completed B.PHARM,in 2008.and now do M.B.A from ignou,and D.P.P.M,from IPER{PUNE},please suggest me best coaching institute in pune for drug inspector,and send me model question paper for prepration of D.I. on my e.mail id - milan_mohite@yahoo.in Thanks.
if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration
How would you stay updated with the latest guidelines and recommendations for prescribing medications like Alprazolam in your practice?
What is validation, validation protocol and validation master plan?
what is difference between temporary change control and deviation
If granules are over lubricated what defect arises in tablet compression how we solve this problem.
solubility of drug in penetration enhancers is affected to the transdermal penetration of any drug yes or not? increase penetration with solubility or not?
What is limit of cleaning validation?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?