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Pharmaceutical and
Formulation Considerations
What is Pharmaceutical
technology?
• Pharmaceutical Technology is the discipline of
pharmacy that deals with the process of turning a
new chemical entity (NCE) into a medication to be used
safely and effectively by patients.
• It is also called the science of dosage form design.
• It deals with the formulation of a pure drug substance
into a dosage form
Drug and medicine
• Medicine is actually the drug delivery system
• That is, they are means of introducing drugs to the body
in safe, efficacious, reproducible and convenient ways
• Medicines are rarely drugs alone, but requires excipients
or additives or pharmaceutical ingredients to be
formulated into dosage forms
Different Dosage Forms
Pharmaceutical ingredients or excipients
• The non-medicinal agents that are given as parts of a
formulation in combination with a drug substance to
produce a final dosage form and serve varied and
specialized pharmaceutical functions are known as
pharmaceutical ingredients or excipients.
• Examples:
For solutions- solvents, flavors, sweeteners, colorants,
preservatives, stabilizers etc.
For tablets- diluents or fillers, binders, lubricants,
disintegrating agents etc.
What are the purposes of formulating
different types of dosage forms?
• In order to provide the safe and appropriate dose of a
drug to the patient, drug substances are formulated in a
dosage forms
• Selective use of different excipients produces dosage
forms of various types
• Besides providing the safe and convenient delivery of
accurate dosage, there are different purposes for which
different dosage forms are designed.
These are :
1) To protect the drug substance from the destructive
influences of atmospheric oxygen or humidity (coated
tablets, sealed ampuls)
Sealed ampoules and coated
tablets
The purposes …
2) To protect the drug substance from the destructive
influences of gastric acid after oral administration
( enteric coated tablets)
The purposes …
3) To conceal the bitter, salty or offensive taste or odor of
a drug substance (capsules, coated tablets, flavored
syrups)
4) To provide liquid preparations of substances that are
either insoluble or unstable in the desired vehicle
( suspensions)
The purposes …
5) To provide clear liquid dosage forms of substances
( syrups, solution)
6) To provide rate-controlled drug action ( various
controlled release tablets, capsules and suspensions)
7) To

provide optimal drug action from topical administration
sites ( ointments, creams, transdermal patches and
ophthalmic ear & nasal preparations)
The purposes …
8) To provide for insertion of a drug into one of body’s
orifices ( rectal or vaginal suppositories)
The purposes …
9) To provide for placement of drugs directly in the
bloodstream or body tissues (injections)

10) To provide for optimal drug action through inhalation
therapy ( inhalants and inhalation aerosols)
Major considerations in dosage form design
• Three major things should be considered before
designing a dosage form :
-The physicochemical considerations
- The biochemical considerations
- Determination of the desired product type and
establishment of a framework for product development
Major considerations ….
• Then, various initial formulations of the product are
developed and examined for desired features (e.g., drug
release profile, bioavailability, clinical effectiveness etc.)
• The formulation that best meets the goals for the product
is selected as “master formula”.
Major considerations ….
• Then a pilot batch and subsequently large scale
production is carried on
• Each of the subsequently prepared batch of the product
must meet the specifications established in the master
formula
• Most commonly a manufacturer prepares a drug
substance in several dosage forms and strengths for the
efficacious and convenient treatment of disease
Major considerations….
• Some therapeutic matters are also considered before
formulating different kinds of dosage forms like- nature of illness ( whether emergency or not)
- manner of treatment ( whether local or systemic action)
- the age and anticipated condition of the patient ( for
infants and children liquid preparation is preferred, for
young patient with cough & vomiting injections or
suppositories are preferred)
Major considerations….
- in case of swallowing problem, chewable tablet or
capsules may be prepared
-

to reduce the frequency of administration, sustained
release or extended released form is preferred

- Thus the therapeutic considerations, in turn helps to
decide the suitable dosage form, the appropriate route of
administration, suitable duration and dose frequency if
the drug in question

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Dosage form design

  • 2. What is Pharmaceutical technology? • Pharmaceutical Technology is the discipline of pharmacy that deals with the process of turning a new chemical entity (NCE) into a medication to be used safely and effectively by patients. • It is also called the science of dosage form design. • It deals with the formulation of a pure drug substance into a dosage form
  • 3. Drug and medicine • Medicine is actually the drug delivery system • That is, they are means of introducing drugs to the body in safe, efficacious, reproducible and convenient ways • Medicines are rarely drugs alone, but requires excipients or additives or pharmaceutical ingredients to be formulated into dosage forms
  • 5. Pharmaceutical ingredients or excipients • The non-medicinal agents that are given as parts of a formulation in combination with a drug substance to produce a final dosage form and serve varied and specialized pharmaceutical functions are known as pharmaceutical ingredients or excipients. • Examples: For solutions- solvents, flavors, sweeteners, colorants, preservatives, stabilizers etc. For tablets- diluents or fillers, binders, lubricants, disintegrating agents etc.
  • 6. What are the purposes of formulating different types of dosage forms? • In order to provide the safe and appropriate dose of a drug to the patient, drug substances are formulated in a dosage forms • Selective use of different excipients produces dosage forms of various types • Besides providing the safe and convenient delivery of accurate dosage, there are different purposes for which different dosage forms are designed. These are : 1) To protect the drug substance from the destructive influences of atmospheric oxygen or humidity (coated tablets, sealed ampuls)
  • 7. Sealed ampoules and coated tablets
  • 8. The purposes … 2) To protect the drug substance from the destructive influences of gastric acid after oral administration ( enteric coated tablets)
  • 9. The purposes … 3) To conceal the bitter, salty or offensive taste or odor of a drug substance (capsules, coated tablets, flavored syrups) 4) To provide liquid preparations of substances that are either insoluble or unstable in the desired vehicle ( suspensions)
  • 10. The purposes … 5) To provide clear liquid dosage forms of substances ( syrups, solution) 6) To provide rate-controlled drug action ( various controlled release tablets, capsules and suspensions) 7) To provide optimal drug action from topical administration sites ( ointments, creams, transdermal patches and ophthalmic ear & nasal preparations)
  • 11. The purposes … 8) To provide for insertion of a drug into one of body’s orifices ( rectal or vaginal suppositories)
  • 12. The purposes … 9) To provide for placement of drugs directly in the bloodstream or body tissues (injections) 10) To provide for optimal drug action through inhalation therapy ( inhalants and inhalation aerosols)
  • 13. Major considerations in dosage form design • Three major things should be considered before designing a dosage form : -The physicochemical considerations - The biochemical considerations - Determination of the desired product type and establishment of a framework for product development
  • 14. Major considerations …. • Then, various initial formulations of the product are developed and examined for desired features (e.g., drug release profile, bioavailability, clinical effectiveness etc.) • The formulation that best meets the goals for the product is selected as “master formula”.
  • 15. Major considerations …. • Then a pilot batch and subsequently large scale production is carried on • Each of the subsequently prepared batch of the product must meet the specifications established in the master formula • Most commonly a manufacturer prepares a drug substance in several dosage forms and strengths for the efficacious and convenient treatment of disease
  • 16. Major considerations…. • Some therapeutic matters are also considered before formulating different kinds of dosage forms like- nature of illness ( whether emergency or not) - manner of treatment ( whether local or systemic action) - the age and anticipated condition of the patient ( for infants and children liquid preparation is preferred, for young patient with cough & vomiting injections or suppositories are preferred)
  • 17. Major considerations…. - in case of swallowing problem, chewable tablet or capsules may be prepared - to reduce the frequency of administration, sustained release or extended released form is preferred - Thus the therapeutic considerations, in turn helps to decide the suitable dosage form, the appropriate route of administration, suitable duration and dose frequency if the drug in question