PHARMACEUTICAL TECHNOLOGY IV

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Learning Outcomes

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.