Bioavailability & Bioequivalance in Pharmaceutical Technology (PB)
Bioavailability & Bioequivalance in Pharmaceutical Technology (PB)
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The concept of bioavailability and its study methodology in human volunteers have been discussed in detail with a special emphasis on protocol preparation, volunteer screening, informed consent, inclusion and exclusion criteria and study of pathological parameters prior to undertaking any bioequivalence study. Various methods of sample preparation and extraction of drug from plasma have been illustrated by different methods. The sophisticated techniques of solid phase extraction (SPE) system have been proved to be most simple, sensitive and time-saving. The different dimensions of its application and procedures have been highlighted. The procedures for evaluation of pharmacokinetic parameters (Cmax, Tmax & AUC) and their interpretation have been illustrated with methodical approach. The application of microdialysis in bioavailability study as well as ocular kinetics and drug delivery system of ophthalmic medicines have also been discussed in this book.
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Carefully structured with updated medical advancements, evidence-based guidelines, and detailed illustrations, this edition helps simplify complex topics while improving clinical understanding. Whether you are preparing for exams, enhancing your medical expertise, or building a strong foundation in medicine, Davidson’s remains one of the most reliable and respected resources in the healthcare field.
Carefully structured with updated medical advancements, evidence-based guidelines, and detailed illustrations, this edition helps simplify complex topics while improving clinical understanding. Whether you are preparing for exams, enhancing your medical expertise, or building a strong foundation in medicine, Davidson’s remains one of the most reliable and respected resources in the healthcare field.
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