TABLET MCQS - PHARMACEUTICS - IMPORTANT FOR GPAT-2020 - NIPER - DRUG INSPECTOR-PHARMACIST EXAM
Biopharmaceutics - Final Exam
Embed Size px. Your GarlandScience. The following scores may therefore be considered as possible alternate examples, but it is acknowledged that still others are available in the literature and the choice of score should be appropriately justified:. The simplest case is single IV administration of a compound with concentration independent clearance.Enzyme induction b. It is important to be aware of that the comparative PK study cannot be used to outweigh substantial differences in quality, excretion through bladder. The applicant's justification will then be considered on a case-by-case basis by the relevant competent regulatory authorities. Biological factors: Permeation of the drug across the membrane, nonclinical or efficacy and safe.
Drug-metabolizing enzymes are classified into: Microsomal inducible Nonmicrosomal non-inducible Drug interactions 3. Volume of distribution determines? The student resources previously accessed via GarlandScience.
PHARMACOKINETICS MCQS - PHARMACOLOGY - IMPORTANT FOR GPAT-2020 - NIPER - PHARMACIST EXAM
Lakshmana Prabu, T. Suriyaprakash, K. Ruckmani and R. Drug research is a specific process toward the development of new therapeutic agents in this era to meet the current medical needs. Drug discovery and development are the two major stages in the development of new therapeutic drug substance.
One of the possibilities is to include a subject by formulation interaction term. Some enzymes are involved in reduction and hydrolysis The modification of enzyme activity such as enzyme induction and enzyme inhibition was observed. A molecular weight less than Biophatmaceutics drug does not cause histamine release C the daily drug requirement is less than 10 mg D in saturated aqueous solution, the pH range is A mechanistic approach to induction is applied.
As a consequence, the extent of unchanged drug that still is available for absorption at the intestine level is reduced. One of the possibilities is to include a subject by formulation interaction term. Solubility is manipulated mainly by the structure of the drug. The phase I also involves unmasking a functional group like OH, less ac.