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PRESENTATION
ON
Application of biopharmaceutics
in Pharmaceutical field
 It must be transported by the body fluids.
 It must traverse the required biologic
membrane barriers.
 It must escape widespread distribution to
unwanted areas.
 It must endure metabolic attack.
 It must penetrate in adequate concentration
to the sites of action.
 Extensive bioavailability testing is carried out by
drug manufacturers because of an enlightened
self-interest to ensure the quality of its products
.
 It is important to the manufacturer that drug
product is appropriate to its side of action.
 Bioavailability testing is also carried out by
academic and government research institution to
study ADME.
 Biopharmaceutical principal can provide a
sound basis for rational drug product
selection.
 Drug product from different manufacturers
may perform differently in patient .
 Proper selection of drug product is a major
role and responsibility of the pharmacist
 This phase is the longest one in drug
development from 2-10 year
 used to determine
I. Pharmacokinetics data
II. Pharmacodynamics data
III. Max. tolerated dose
IV. Adverse reactions profile
 To understand process administration of drug , which
affects onset and intensity of biological response.
 To access plasma drug concentration response to
given dose which is now considered as more
appropriate parameter then intrinsic pharmacological
activity .
 In design and utilization of in vitro model system
 In design and development of new drug and their
appropriate dosage regimen.
 Drug Development
 Formulation Development
 Deciding Dosage Regimen
 Designing Rational Dose, Frequency and Duration
 Rational Drug Design
 Clinical Pharmacy
 ADME study, Bioavailability and Bioequivalence studies
 Pharmacokinetics, Pharmacodynamics Relationship
From toxicological and pharmacological points of view, it is
desirable to design a “safer” drug that undergoes no metabolism.
Hard drugs: The concept of nonmetabolisable drugs called hard
drugs. Drugs are excreted primarily through either bile or kidney.
Eg: Bisphosphonates, enalaprilat, lisinopril
Soft drugs: It is pharmacologically active,itundergoes
a predictable and controllablemetabolism tonontoxic
and inactive metabolites
Cont…
 The main concept is to avoid oxidative metabolism as much as
possible and to use hydrolytic enzymes to achieve predictable
and controllable drug metabolism.
Eg: Atracurium, Remifentanil etc.
 Active metabolites: The metabolites of some drugs are
pharmacologically active being used as a source of new drug
candidates.
Eg: Acetaminophen which is an O-deethylated metabolite of
Phenacetin.
Application of biopharmaceutics in pharmaceutical field.siam(ppt file)
Application of biopharmaceutics in pharmaceutical field.siam(ppt file)
Application of biopharmaceutics in pharmaceutical field.siam(ppt file)

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Application of biopharmaceutics in pharmaceutical field.siam(ppt file)

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  • 4.  It must be transported by the body fluids.  It must traverse the required biologic membrane barriers.  It must escape widespread distribution to unwanted areas.  It must endure metabolic attack.  It must penetrate in adequate concentration to the sites of action.
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  • 13.  Extensive bioavailability testing is carried out by drug manufacturers because of an enlightened self-interest to ensure the quality of its products .  It is important to the manufacturer that drug product is appropriate to its side of action.  Bioavailability testing is also carried out by academic and government research institution to study ADME.
  • 14.  Biopharmaceutical principal can provide a sound basis for rational drug product selection.  Drug product from different manufacturers may perform differently in patient .  Proper selection of drug product is a major role and responsibility of the pharmacist
  • 15.  This phase is the longest one in drug development from 2-10 year  used to determine I. Pharmacokinetics data II. Pharmacodynamics data III. Max. tolerated dose IV. Adverse reactions profile
  • 16.  To understand process administration of drug , which affects onset and intensity of biological response.  To access plasma drug concentration response to given dose which is now considered as more appropriate parameter then intrinsic pharmacological activity .  In design and utilization of in vitro model system  In design and development of new drug and their appropriate dosage regimen.
  • 17.  Drug Development  Formulation Development  Deciding Dosage Regimen  Designing Rational Dose, Frequency and Duration  Rational Drug Design  Clinical Pharmacy  ADME study, Bioavailability and Bioequivalence studies  Pharmacokinetics, Pharmacodynamics Relationship
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  • 19. From toxicological and pharmacological points of view, it is desirable to design a “safer” drug that undergoes no metabolism. Hard drugs: The concept of nonmetabolisable drugs called hard drugs. Drugs are excreted primarily through either bile or kidney. Eg: Bisphosphonates, enalaprilat, lisinopril Soft drugs: It is pharmacologically active,itundergoes a predictable and controllablemetabolism tonontoxic and inactive metabolites
  • 20. Cont…  The main concept is to avoid oxidative metabolism as much as possible and to use hydrolytic enzymes to achieve predictable and controllable drug metabolism. Eg: Atracurium, Remifentanil etc.  Active metabolites: The metabolites of some drugs are pharmacologically active being used as a source of new drug candidates. Eg: Acetaminophen which is an O-deethylated metabolite of Phenacetin.