Name: Thakur Biopharmaceutics and Pharmacokinetics For B Pharmacy Semester 6th PTU
Brand: Amit Book Depot
Availability: OutOfStock

Thakur Biopharmaceutics and Pharmacokinetics For B Pharmacy Semester 6th PTU

by Madhurima

₹0 ₹0.00(-/ off)

Rating & Reviews

23 Customer Review

Have Doubts Regarding This Product ? Ask Your Question

Q1

Is this book strictly aligned with the Punjab Technical University (PTU) Semester 6 syllabus?

A1

Yes, this textbook is meticulously crafted to cover 100% of the prescribed syllabus for the subject Biopharmaceutics and Pharmacokinetics (BP 604 T) for B. Pharmacy Semester VI under PTU. The chapters and units correspond directly to the official curriculum.
Q2

Does the book cover both biopharmaceutics and pharmacokinetics in equal detail?

A2

Absolutely. The book is structured in two integrated parts. The first half provides a comprehensive foundation in biopharmaceutics (absorption, distribution, elimination), while the second half delves deeply into pharmacokinetics, including compartment models, parameter calculations, and non-linear kinetics, as per the syllabus.
Q3

Are topics like bioavailability and bioequivalence included, which are important for modern pharmacy?

A3

Yes, Chapter 4 is entirely dedicated to Bioavailability and Bioequivalence. It covers definitions, measurement methods, IVIVC (In Vitro-In Vivo Correlation), and the significance of bioequivalence studies, which are crucial for generic drug development and regulatory science.
Q4

Does it include numerical problems or methods for calculating pharmacokinetic parameters?

A4

While the book focuses on conceptual clarity and theory as per the PTU syllabus, it outlines the methods and principles for determining pharmacokinetic parameters from plasma and urinary data following different routes of administration (IV bolus, infusion, extravascular).
Q5

Are the mechanisms of drug absorption explained comprehensively?

A5

Yes, Chapter 1 provides a detailed breakdown of all mechanisms of drug absorption through the GIT, including passive diffusion, active transport, facilitated diffusion, pore transport, and endocytosis, along with factors affecting each.
Q6

Is protein binding of drugs, a commonly challenging topic, well covered?

A6

Chapter 2 offers an in-depth analysis of protein binding of drugs, covering plasma protein binding, tissue binding, factors affecting it, kinetics of protein binding, and, most importantly, its clinical significance in drug therapy.
Q7

Does the book discuss methods to improve the solubility and bioavailability of drugs?

A7

Yes, a dedicated section (4.2) covers various methods to enhance dissolution rates and bioavailability. It includes both traditional methods like salt formation and particle size reduction and modern approaches like nanotechnology and co-crystallization.
Q8

Are multicompartment models and multiple dosing kinetics included?

A8

Certainly. Chapter 6 is dedicated to Multicompartment Models, specifically the two-compartment open model, and includes the kinetics of multiple dosing, steady-state levels, and the calculation of loading and maintenance doses.
Q9

Does the book cover drug absorption from routes other than oral?

A9

Yes, Section 1.4 extensively covers extra-absorption of drugs from non-peroral routes, including intravenous, intramuscular, transdermal, inhalational, rectal, and ocular routes, explaining their absorption characteristics.
Q10

Is there any content on non-linear pharmacokinetics?

A10

Yes, the final chapter (Chapter 7) provides an introduction to non-linear pharmacokinetics, discusses factors causing non-linearity, and explains the Michaelis-Menten method for estimating parameters.

0.00

0 Overall Rating

5

0
4

0
3

0
2

0
1

0

Try this product & share your review & thoughts

No Description Added

No Table Content Added

Have Doubts Regarding This Product ? Ask Your Question

Q1

Is this book strictly aligned with the Punjab Technical University (PTU) Semester 6 syllabus?

A1

Yes, this textbook is meticulously crafted to cover 100% of the prescribed syllabus for the subject Biopharmaceutics and Pharmacokinetics (BP 604 T) for B. Pharmacy Semester VI under PTU. The chapters and units correspond directly to the official curriculum.
Q2

Does the book cover both biopharmaceutics and pharmacokinetics in equal detail?

A2

Absolutely. The book is structured in two integrated parts. The first half provides a comprehensive foundation in biopharmaceutics (absorption, distribution, elimination), while the second half delves deeply into pharmacokinetics, including compartment models, parameter calculations, and non-linear kinetics, as per the syllabus.
Q3

Are topics like bioavailability and bioequivalence included, which are important for modern pharmacy?

A3

Yes, Chapter 4 is entirely dedicated to Bioavailability and Bioequivalence. It covers definitions, measurement methods, IVIVC (In Vitro-In Vivo Correlation), and the significance of bioequivalence studies, which are crucial for generic drug development and regulatory science.
Q4

Does it include numerical problems or methods for calculating pharmacokinetic parameters?

A4

While the book focuses on conceptual clarity and theory as per the PTU syllabus, it outlines the methods and principles for determining pharmacokinetic parameters from plasma and urinary data following different routes of administration (IV bolus, infusion, extravascular).
Q5

Are the mechanisms of drug absorption explained comprehensively?

A5

Yes, Chapter 1 provides a detailed breakdown of all mechanisms of drug absorption through the GIT, including passive diffusion, active transport, facilitated diffusion, pore transport, and endocytosis, along with factors affecting each.
Q6

Is protein binding of drugs, a commonly challenging topic, well covered?

A6

Chapter 2 offers an in-depth analysis of protein binding of drugs, covering plasma protein binding, tissue binding, factors affecting it, kinetics of protein binding, and, most importantly, its clinical significance in drug therapy.
Q7

Does the book discuss methods to improve the solubility and bioavailability of drugs?

A7

Yes, a dedicated section (4.2) covers various methods to enhance dissolution rates and bioavailability. It includes both traditional methods like salt formation and particle size reduction and modern approaches like nanotechnology and co-crystallization.
Q8

Are multicompartment models and multiple dosing kinetics included?

A8

Certainly. Chapter 6 is dedicated to Multicompartment Models, specifically the two-compartment open model, and includes the kinetics of multiple dosing, steady-state levels, and the calculation of loading and maintenance doses.
Q9

Does the book cover drug absorption from routes other than oral?

A9

Yes, Section 1.4 extensively covers extra-absorption of drugs from non-peroral routes, including intravenous, intramuscular, transdermal, inhalational, rectal, and ocular routes, explaining their absorption characteristics.
Q10

Is there any content on non-linear pharmacokinetics?

A10

Yes, the final chapter (Chapter 7) provides an introduction to non-linear pharmacokinetics, discusses factors causing non-linearity, and explains the Michaelis-Menten method for estimating parameters.

No Syllabus Added

0.00

0 Overall Rating

5

0
4

0
3

0
2

0
1

0

Try this product & share your review & thoughts