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  • Faculty of Pharmacy
  • Course Structure Diagram with Credits
  • Pharmaceutical Technology IV
  • Learning Outcomes
  • Description
  • Content
  • Learning Outcomes
  • Learning Activities and Teaching Methods
  • Course's Contribution to Prog.
  • Assessment Methods

  • Will be able to explain general information about granules.
  • Defines the relationship between powder, granules, and tablets.
  • Defines granules.
  • Compares the use of granules and powders in tablet preparation.
  • Will be able to explain granule preparation methods.
  • Defines granule preparation methods.
  • Defines the components used in granule preparation
  • Defines effervescent granules.
  • Compares dry, wet, and effervescent granules.
  • Will be able to explain granule control.
  • Defines the controls performed on granules.
  • Interprets the results obtained from granule controls.
  • Will be able to explain general information about tablets.
  • Defines tablets.
  • Lists the general characteristics of tablets.
  • Will be able to define tablet formulation.
  • Lists the excipients used in tablet formulation.
  • Knows the preparation of tablet formulation.
  • Will be able to explain tablet preparation methods.
  • Classifies tablet preparation methods.
  • Explains the factors to be considered in selecting a tablet preparation method.
  • Explains the direct compression tablet preparation method.
  • Explains tablet preparation after dry granulation.
  • Explains tablet preparation after wet granulation.
  • Will be able to explain tablet compression.
  • Explains the purpose of tablet machines.
  • Explains situations in which tablet hardness, weight, and shape need to be changed.
  • Explains the compression cycle of a conventional rotary tablet press.
  • Explains the effect of the preparation method on tablet compression.
  • Will be able to explain tablet control.
  • Explains the importance of tablet control.
  • Evaluates tablet control as pre-production, in-production, and post-production.
  • Explains the importance of raw material control in tablet production.
  • Explains the importance of in-process control in tablet production.
  • Explains the importance of finished product control in tablet production.
  • Explains the official sources used in the evaluation of finished product control of tablets.
  • Will be able to define coated tablets.
  • Explains the purpose of tablet coating.
  • Explains the types of tablet coating.
  • Explains the properties the core tablet should possess for coating.
  • Explains tablet coating methods.
  • Explains the advantages and disadvantages of tablet coating methods.
  • Explains the controls performed on coated tablets.
  • Explains the equipment used for the coating process.
  • Will be able to provide general information about modified drug delivery systems.
  • Classifies systems with modified release.
  • Explains the concept of modified drug release.
  • Explains the advantages and disadvantages of modified drug release systems.
  • Compares modified drug release systems with conventional systems.
  • Explains the properties the active ingredient should have for modified drug release systems.
  • Will be able to explain the structural classification of modified drug delivery systems.
  • Classifies modified drug release systems based on their structure.
  • Explains particulate drug delivery systems.
  • Will be able to explain the classification of modified drug delivery systems based on their method of application.
  • Classifies controlled drug delivery systems by the route of administration.
  • Explains the characteristics of oral modified release systems.
  • Lists the key parameters that are important for the effectiveness of oral modified release systems.
  • Classifies oral modified release systems.
  • Will be able to explain targeting in modified drug delivery systems.
  • Explains the purpose of targeting in modified release systems.
  • Explains the reasons for pharmaceutical and biopharmaceutical targeting.
  • Explains the reasons for targeting from a pharmacokinetic and pharmacodynamic perspective.
  • Explains the reasons for targeting from a clinical perspective.
  • Explains the reasons for targeting from a commercial perspective.
  • Will be able to explain bioavailability in modified drug delivery systems.
  • Explains bioavailability studies in modified drug delivery systems.
  • Will be able to explain the stages of bioavailability and bioequivalence in modified drug delivery systems.
  • Explains the relationship between bioavailability and the active ingredient in modified drug delivery systems.
  • Explains the relationship between bioavailability and dosage form in modified drug delivery systems.
  • Will be able to explain the characteristics of agricultural chemicals.
  • Defines agricultural chemicals.
  • Explains the purpose of agricultural chemicals.
  • Classifies the active ingredients used in agricultural chemicals according to their purpose.
  • Will be able to explain the use, storage, and packaging of agricultural chemicals.
  • Explains the important points to consider when preparing agricultural chemicals.
  • Describes the label color and its characteristics for agricultural chemicals.
  • Explains the points to consider when using agricultural chemicals.
  • Explains the points to consider when storing agricultural chemicals.
  • Will be able to give examples of agricultural chemicals.
  • Gives an example of herbicides.
  • Gives an example of pesticides.
  • Gives an example of plant growth regulators.
  • Will be able to explain the characteristics of veterinary drugs.
  • Defines veterinary drugs.
  • Explains the purpose of veterinary drugs.
  • Will be able to explain the use, storage, and packaging of veterinary drugs.
  • Explains the animal species to which veterinary drugs are applied.
  • Explains the routes of administration for veterinary drugs.
  • Explains the points to consider when using veterinary drugs.
  • Lists veterinary drug carrier systems.
  • Will be able to explain the prescription and prospectus for veterinary drugs.
  • Explains the prescription used for veterinary drugs.
  • Explains prescription and non-prescription veterinary drugs.
  • Evaluates the effect of veterinary drug residues in food in terms of negative impact.
  • Explains the reason for off-label use of veterinary drugs.
  • Will be able to define GLP/GMP terminology.
  • Explains the importance of GLP and GMP in pharmaceutical technology.
  • Explains the relationship between the drug production stage and quality.
  • Explains the concept of quality in pharmaceuticals.
  • Will be able to explain validation.
  • Defines validation.
  • Explains the importance of validation in pharmaceuticals.
  • Explains the FDA’s dosage form priority in process validation.
  • Will be able to explain production.
  • Explains the documentation requirements in GMP.
  • Explains the concept of quality in industrial production processes.
  • Explains the characteristics that the production site must have.
  • Explains the health conditions that must be adhered to in the production site.
  • Will be able to explain quality.
  • Lists the topics to be followed for quality control in production.
  • Explains the structure of the quality assurance system.
  • Defines quality management.
  • Defines quality assurance.
  • Will be able to explain the basic concepts of granules.
  • Defines granule.
  • Lists the properties that granules must have.
  • Lists the steps for preparing a granule formulation.
  • Will be able to explain the application of granules.
  • Explains how to prepare granules using wheat starch.
  • Prepares normal granules using wheat starch and delivers them in suitable packaging.
  • Explains how to prepare effervescent granules containing sodium bicarbonate and tartaric acid.
  • Prepares effervescent granules containing sodium bicarbonate and tartaric acid and delivers them in suitable packaging.
  • Explains how to prepare effervescent granules containing sodium bicarbonate and sodium dihydrogen phosphate.
  • Prepares effervescent granules containing sodium bicarbonate and sodium dihydrogen phosphate and delivers them in suitable packaging.
  • Explains how to prepare effervescent granules containing magnesium citrate.
  • Prepares effervescent granules containing magnesium citrate and delivers them in suitable packaging.
  • Will be able to explain granule controls.
  • Classifies the controls performed on granules.
  • Performs the necessary quality control work on granules.
  • Will be able to explain the basic concepts of tablets.
  • Defines a tablet.
  • Classifies different types of tablets.
  • Lists the general characteristics of tablets.
  • Lists the steps for preparing a tablet formulation.
  • Will be able to explain tablet preparation methods.
  • Lists tablet preparation methods.
  • Explains the direct compression method for tablet preparation.
  • Explains the compression method after granulation for tablet preparation.
  • Will be able to explain tablet application.
  • Explains how to prepare aspirin tablets using the dry granulation method.
  • Prepares aspirin tablets using the dry granulation method and delivers them in suitable packaging.
  • Explains how to prepare APC tablets using the dry granulation method.
  • Prepares APC tablets using the dry granulation method and delivers them in suitable packaging.
  • Explains how to prepare tablets containing vitamin C and lactose starch granules using the dry granulation method.
  • Prepares tablets containing vitamin C and lactose starch granules using the dry granulation method and delivers them in suitable packaging.
  • Explains how to prepare pastille tablets using the dry granulation method.
  • Prepares pastille tablets using the dry granulation method and delivers them in suitable packaging.
  • Explains how to prepare tablets containing sodium bicarbonate using the wet granulation method.
  • Prepares tablets containing sodium bicarbonate using the wet granulation method and delivers them in suitable packaging.
  • Explains how to prepare combination tablets using the wet granulation method.
  • Prepares combination tablets using the wet granulation method and delivers them in suitable packaging.
  • Explains how to prepare research tablets containing saccharin using the wet granulation method.
  • Prepares research tablets containing saccharin using the wet granulation method and delivers them in suitable packaging.
  • Explains how to prepare tablets containing novalgin (metamizole sodium) using the wet granulation method.
  • Prepares tablets containing novalgin (metamizole sodium) using the wet granulation method and delivers them in suitable packaging.
  • Explains how to prepare tablets containing betamethasone using the wet granulation method.
  • Prepares tablets containing betamethasone using the wet granulation method and delivers them in suitable packaging.
  • Explains how to prepare tablets containing sulfamethoxazole-trimethoprim using the wet granulation method.
  • Prepares tablets containing sulfamethoxazole-trimethoprim using the wet granulation method and delivers them in suitable packaging.
  • Will be able to explain the basic concepts of effervescent tablets.
  • Defines the terms monohydrate, dihydrate, and trihydrate.
  • Defines the equivalent calculation required for effervescent tablets.
  • Will be able to explain the application of effervescent tablets.
  • Explains how to prepare effervescent tablets containing aspirin.
  • Prepares effervescent tablets containing aspirin and delivers them in suitable packaging.
  • Explains how to prepare effervescent tablets containing vitamin C.
  • Prepares effervescent tablets containing vitamin C and delivers them in suitable packaging.
  • Will be able to explain the basic concepts of modified-release tablets.
  • Defines modified-release tablets.
  • Lists types of modified-release tablets.
  • Will be able to explain the application of modified-release tablets.
  • Explains how to prepare ketorolac tromethamine-carbopol tablets with controlled release using direct compression.
  • Prepares ketorolac tromethamine-carbopol tablets with controlled release using direct compression and delivers them in suitable packaging.
  • Explains how to prepare dimenhydrinate-HEC tablets with controlled release using wet granulation.
  • Prepares dimenhydrinate-HEC tablets with controlled release using wet granulation and delivers them in suitable packaging.
  • Explains how to prepare diclofenac sodium tablets with controlled release using wet granulation.
  • Prepares diclofenac sodium tablets with controlled release using wet granulation and delivers them in suitable packaging.
  • Will be able to explain the basic concepts of bioadhesive tablets.
  • Defines bioadhesive dosage forms.
  • Lists the advantages of bioadhesive dosage forms.
  • Lists the characteristics of bioadhesive tablets.
  • Lists the steps involved in preparing bioadhesive tablets.
  • Will be able to explain the application of bioadhesive dosage forms.
  • Explains how to prepare acyclovir-HPMC vaginal bioadhesive tablets.
  • Prepares acyclovir-HPMC vaginal bioadhesive tablets and delivers them in suitable packaging.
  • Explains how to prepare acyclovir-Carbopol® 934 vaginal bioadhesive tablets.
  • Prepares acyclovir-Carbopol® 934 vaginal bioadhesive tablets and delivers them in suitable packaging.
  • Explains how to prepare acyclovir-MC vaginal bioadhesive tablets.
  • Prepares acyclovir-MC vaginal bioadhesive tablets and delivers them in suitable packaging.
  • Explains how to prepare miconazole-HPMC buccal bioadhesive tablets.
  • Prepares miconazole-HPMC buccal bioadhesive tablets and delivers them in suitable packaging.
  • Explains how to prepare miconazole-carbomer buccal bioadhesive tablets.
  • Prepares miconazole-carbomer buccal bioadhesive tablets and delivers them in suitable packaging.
  • Explains how to prepare miconazole-HPMC-carbomer buccal bioadhesive tablets.
  • Prepares miconazole-HPMC-carbomer buccal bioadhesive tablets and delivers them in suitable packaging.
  • Will be able to explain the basic concepts of tablet control.
  • Explains the importance of tablet control.
  • Classifies and defines the finished product controls in tablets.
  • Will be able to explain the application of tablet control.
  • Performs resistance to breakage determination.
  • Explains how to perform mass uniformity determination in tablets.
  • Explains how to perform content uniformity determination in tablets.
  • Performs dissolution rate determination in tablets.
  • Will be able to explain the basic concepts of coated tablets.
  • Defines coated tablets.
  • Lists the materials used in tablet coating.
  • Will be able to explain the control of coated tablets.
  • Lists the controls performed on coated tablets.
  • Defines the controls performed on coated tablets.
  • Will be able to explain the basic concepts of microcapsules.
  • Defines microcapsules.
  • Lists the uses of microcapsules.
  • Lists the methods of preparing microcapsules.
  • Will be able to explain the control of microcapsules.
  • Lists the controls performed on microcapsules.
  • Defines the controls performed on microcapsules.
  • Will be able to explain the application of distilled water control.
  • Performs ion control in distilled water.
  • Performs heavy metal control in distilled water.
  • Performs control of oxidizable substances in distilled water.
  • Will be able to explain the application of glass control.
  • Performs ampoule glass control.
  • Performs control of pharmaceutical bottles.
  • Will be able to explain the application of cotton control.
  • Determines the sinking time of cotton.
  • Performs ion control in cotton.
  • Performs control of reducing substances in cotton.
  • Will be able to explain the application of gauze control.
  • Performs yarn count control in gauze.
  • Performs ion control in gauze.
  • Performs control of reducing substances in gauze.

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