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Graduate Pharmacy Aptitude Test
>
Biopharmaceutics and Pharmacokinetics
List of top Biopharmaceutics and Pharmacokinetics Questions asked in Graduate Pharmacy Aptitude Test
Which of the following is an example of physical incompatibility:
GPAT - 2024
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Histogram can be drawn only for:
GPAT - 2024
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which type of in-vitro-in-vivo correlation compares % drug released vs % drug absorbed?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Which of the following is true for bone tissue cell differentiation and maturation?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
A hypertensive patient receiving a drug ‘Y’for managing BP was prescribed a tricyclic antidepressant. As a result, there was an abolition of the antihypertensive action of‘Y’. Which of the following drug could be ‘Y’?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
A 70 kg woman was administered 1000 mg of the drug as i.v. bolus. After its uniform distribution in the body, the plasma concentration of the drug was found to be 50 mg/L. What is its volume of distribution?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Which of the following levels of IVIVC is represented by “the relatinship between one dissolution time point(e.g., t 50%) and one mean pharmacokinetic parameter, such as AUC, T
max
or C
max
”?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Under which of the following conditions in-vitro-in-vivo correlation for a drug fails?
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
In pharmacokinetic models, the term “compartment” means:
GPAT - 2023
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
Decrease in effective surface area available to the dissolution medium leading to a fall in the dissolution rate, may happen due to which one of the following reasons?
GPAT - 2022
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Match List I with List II
List I
List II
A
When two dosage forms have equal t max
I
When their total body clearance is constant.
B
AUC values of the two analogs can be compared to measure relative bioavailability
II
Absorption rate constants are equal
C
Urinary data is valid to measure bioavailability. III. W
III
When fraction absorbed and elimination rate is constant.
D
C max is proportional to the rate of absorption
IV
Excretion of drug and/or metabolite is related to the bioavailable dose.
Choose the correct answer from the options given below:
GPAT - 2022
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
For depot injections, in which drug is slowly released over weeks or months, which bioequivalence study design is used?
GPAT - 2021
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
For solid oral drug products, a change in the concentration of which of the following excipients is more likely to influence the bioavailability of a drug.
GPAT - 2021
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Name the popular system for ocular delivery of pilocarpine, based on membrance -controlled reservoir systems
GPAT - 2021
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Chitosan possesses which of the following property?
GPAT - 2021
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Method of Study Drug Distribution pattern is:
GPAT - 2020
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
For drug substances with highly variable pharmacokinetic characteristics the following Bioequivalence study design is used
GPAT - 2019
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
A material which is insoluble and inert and used in matrix tablet formulation is:-
GPAT - 2018
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
IVIVC utilizes the principles of statistical moment analysis:-
GPAT - 2018
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
When Ke is constant and Ka is larger:-
GPAT - 2018
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
In relation to buccal and sublingual route of administration which of the following statement is incorrect
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
To rule out the probability of dose dumping from an oral CR dosage form, USP hasincluded which sampling time point for in vitro dissolution test where D is normal dosing interval
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Type IV dissolution apparatus as per USP is
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
The useful variable from in vitro dissolution test data for IVIVC includes
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-availability & Bio-equivalence
Diazepam is not suitable for peroral sustained release form since
GPAT - 2017
GPAT
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics
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