Faculty of Pharmacy

pharmaceutical preparations, microbiological limit tests of preparations that do or don’t have to be
sterilized.
(ECZ524) INDUSTRIAL MICROBIOLOGY (T)
HOUR/WEEK : 2, ECTS: 2
Industrial microbiology, utilized microorganisms and their manufacture, ındustrial fermentation, the
utilized microorganisms, gene engineering in ındustrial microbiology, bacterial metabolism and its
enzymes, manufacture of some products by fermentation and techniques used in industrial
microbiology.
(ECZ525) DETERMINATION of DISSOLUTION RATE on THE EVALUATION of
DRUG FORMULATION and QUALITY CONTROLS and ITS IMPORTANCE (T)
HOUR/WEEK : 1, ECTS: 1
Dissolution rate, definion and mechanisms, officinal methods given in pharmacopoeial monographs
non-officinal methods, ımportance of dissolution rate from the point of bioequivalance, ımportance
of dissolution methods on the evaluation of formulations, dissolution methods from the point of
finished product quality control, classical dosage forms, controlled release dosage forms, evaluation
of dissolution rate data, alternative methods in bioavailability/bioequivalance determinations.
(ECZ533) DESIGN and APPLICATION on BIOAVAILABILITY/
BIOEQUIVALANCE (T)
HOUR/WEEK : 1 , ECTS: 1
Pharmacokinetics, design of bioavailability practice, statistical methods and average bioavailability,
ıntra- and ınter- subject variabilities, cross experimental designs between two formulations,
bioequivalance, chemical equivalance, pharmaceutical-generic equivalance and therapeutical,
equivalance, therapeutical alternative and pharmaceutical alternative.
(ECZ534) DRUG PREPARATION on HOSPITAL SCALE (T)
HOUR/WEEK : 1, ECTS: 1
Preparation of Internally given drugs, preparation of externally applied drugs, preparation of
parenterally applied drugs, serums, plasma expanders and large volume parenteral preparations
(LVP), surgical and medicinal materials used in hospital practice and their controls
(ECZ535) SYSTEMS for CONTROLLED DRUG DELIVERY and DELIVERY
MECHANISMS (T)
HOUR/WEEK : 2, ECTS: 2
Terminology, ınvestigations of active agent properties choosen for the controlled release,
ınvestigations on the physicochemical properties of active agent, ınvestigations on the
biopharmaceutical-pharmacokinetic properties of active agent, determination of dosage forms for