R Ranjeet π Tutor III β 34.60K Points π Biopharmaceutics and Pharmacokinetic Q. The Binding Order of drug to tissue is………………… (A) Kidney > Liver > Lungs > Muscle (B) Muscle > Kidney > Lungs > Liver (C) Liver > Kidney > Lungs > Muscle (D) Liver > Lungs > Kidney > Muscle ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (C) Liver > Kidney > Lungs > Muscle
R Rakesh Kumar π Hard Worker β 28.44K Points π Biopharmaceutics and Pharmacokinetic Q. ……………is located at the sertoli-sertoli cell junction. (A) Blood testis barrier (B) Blood CSF barrier (C) Blood cellular barrier (D) All of the above ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (A) Blood testis barrier
R Ranjeet π Tutor III β 34.60K Points π Biopharmaceutics and Pharmacokinetic Q. Displacement is significant when, the displaced drug is more than protein bound. (A) 50% (B) 95% (C) 10% (D) 1% ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (B) 95%
R Ranjeet π Tutor III β 34.60K Points π Biopharmaceutics and Pharmacokinetic Q. Fat is act as reservoir for……………………… Drugs (A) Highly water soluble (B) Lower lipid soluble (C) Highly lipid soluble (D) Lower lipid soluble ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (C) Highly lipid soluble
P Praveen Singh π Tutor III β 36.81K Points π Biopharmaceutics and Pharmacokinetic Q. The drugs having molecular size …………..easily cross capillary membrane. (A) <500-600d (B) < 100-200 d (C) <300-600d (D) <90M600d ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (A) <500-600d
V Vinay π Mover β 28.75K Points π Biopharmaceutics and Pharmacokinetic Q. It is defined as the distribution of a drug between plasma and the rest of the body after oral or parenteral dosing. (A) Volume of distribution (VD) (B) Apparent volume of drug distribution (C) Phagocytosis (D) None of the above ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (B) Apparent volume of drug distribution
P Praveen Singh π Tutor III β 36.81K Points π Biopharmaceutics and Pharmacokinetic Q. …………..it represents the degree to which a drug is distributed in body tissue rather than (A) Volume of distribution (YD) (B) Effect of distribution (C) Area of distribution (D) None of the above ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (A) Volume of distribution (YD)
V Vijay Sangwan π Mover β 28.62K Points π Biopharmaceutics and Pharmacokinetic Q. The procedure of transporting a drug from the bloodstream to tissues is called as (A) Absorption (B) Dissolution (C) Distribution (D) Elimination ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (C) Distribution
P Priyanka Tomar π Tutor III β 35.28K Points π Biopharmaceutics and Pharmacokinetic Q. The formula to calculate half life (t1/2) is (A) 0.693 *Vd / C1 (B) 0.693 *Cl / Vd (C) 0.693 / Cl * Vd (D) 0.693 / Cl ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (A) 0.693 *Vd / C1
V Vijay Sangwan π Mover β 28.62K Points π Biopharmaceutics and Pharmacokinetic Q. The rate of drug transport across a cell membrane by lipid diffusion depends on all of the following except (A) Drug size (diffusion constant) (B) Surface area of absorption (C) Lipid partition coefficient (D) Density of tr ποΈ Show Answer π¬ Discuss π Share β‘Menu β Correct Answer: (A) Drug size (diffusion constant)