BP
303 T. PHARMACEUTICAL MICROBIOLOGY (Theory)
Unit I
· History of microbiology, its
branches, scope and its importance.
· Introduction to Prokaryotes and
Eukaryotes
· Study of ultra-structure and morphological classification of bacteria,
· Raw materials used for culture median physical parameters for growth,
· Isolation and preservation methods
for pure cultures,
· Cultivation of anaerobes,
· Quantitative measurement of bacterial
growth (total & viable count).
· Study of different types of phase
constrast microscopy,
· Dark field microscopy and electron
microscopy.
Unit II
· Identification of bacteria using
staining techniques (simple, Gram’s &Acid fast staining) and biochemical
tests (IMViC).
· Study of principle, procedure,
merits, demerits and applications of physical,
· chemical gaseous, radiation and
mechanical method of sterilization.
· Evaluation of the efficiency of
sterilization methods.
· 79 Equipments employed in large scale
sterilization.
· Sterility indicators.
Unit III
· Study of morphology,
· classification,
· reproduction/replication and
cultivation of Fungi and Viruses.
· Classification and mode of action of
disinfectants Factors influencing disinfection,
· antiseptics and their evaluation.
· For bacteriostatic and bactericidal
actions Evaluation of bactericidal & Bacteriostatic.
· Sterility testing of products
(solids, liquids, ophthalmic and other sterile products) according to IP, BP
and USP.
Unit IV
· Designing of aseptic area, laminar
flow equipments;
· study of different sources of
contamination in an aseptic area and methods of prevention,
· clean area classification.
· Principles and methods of different
microbiological assay.
· Methods for standardization of
antibiotics,
· vitamins and amino acids.
· Assessment of a new antibiotic.
Unit V
· Types of spoilage,
· factors affecting the microbial
spoilage of pharmaceutical products,
· sources and types of microbial
contaminants,
· assessment of microbial contamination
and spoilage.
· Preservation of pharmaceutical
products using antimicrobial agents,
· evaluation of microbial stability of
formulations.