How to predict in vitro data collected from dissolution profile, for a new paracetamol formulation extended release tablet, to get in vivo data i.e profile drug concentration profile. I read some steps available on the internet but I need step by step solution for the same.
If you have not already found the reference, here is link for converting dissolution results to plasma drug levels (https://benthamopen.com/contents/pdf/TODDJ/TODDJ-4-38.pdf). Also, I will be giving a seminar on the topic next month in Boston, MA (link is http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901306SEMINAR?conferize-December-2017-SEO). There are plans for webinars on the topic so keep an eye for it. I also write a blog on the topic of drug dissolution testing (www.drug-dissolution-testing.com) which also provides information on the subject.
Best of luck.