GPAT 2021 Syllabus

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GPAT 2021 Syllabus

GPAT 2021 Application Form has been released on 23rd December 2020. It is organized by the National Testing Agency (NTA). GPAT (Graduate Pharmacy Aptitude Test) is conducted once in every year for admission to various M. Pharma or its equivalent courses across the country. On qualifying this national level examination, the candidates will get admission to 24000 seats in nearly 841 participating pharmacy institutions.

Physical Chemistry

Intermolecular forces & their impact on the state of the matter. Various physical properties of matter, dipole moment, dielectric constant, Van Der Waal’s equation & critical phenomenon, liquefaction of gases, aerosols.

The liquid state, vapor pressure, ideal & real solutions. Raoult’s law, elevation of boiling point, depression of freezing point, osmotic pressure, determination of molecular weight based on colligative properties.

First, second & third law of thermodynamics, Thermochemical laws, isothermic & adiabatic processes, reversible processes, work of expansion, heat content, enthalpy, heat capacity. Gibb’s & Helmholtz equation & chemical potential.

Refractive index, specific refractivity, molar refractivity, refractometers.

Solubility, factors affecting solubility, solubility curves. Types of solutions, effect of co-solvency, pH & other factors on solubility. Solubility of gases in liquids, liquids in liquids, & solids in liquids, critical solution temperature, law of partitioning & its applications. Solute-solvent interactions. Expression of the concentration of pharmaceutical solutions & calculations. Molarity, molality, mole fraction & percentage expressions.

Properties of electrolyte solutions, electrolysis. Faraday’s law of electrolysis, electron transport, electrical cell, single electrode potential, concentration cells, half-cells & half-cell potential, types of half cells, sign convention, Nernst equation, salt bridge, electromotive series, standard potential, SHE. Measuring the relative voltage of half cells, Calculation of standard potential. Reference & indicator electrodes. Standard oxidation-reduction potential.

Theory of conductivity, equivalent conductance, mobility of ions, specific conductance. 8. Kinetics Order of reactions, derivation & internal form of rate laws, molarities of reaction, derivation of rate constants.

Physical Chemistry

States of matter, change in the state of matter, latent heat and vapor pressure, sublimationcritical point, eutectic mixtures, gases, aerosols- inhalers, relative humidity, liquid complexes, liquid crystals, glasses state, solid crystalline and amorphous polymorphism.

Particle size and distribution, average particle size number and weight distribution, particle number, methods of determining particle size and volume, optical microscopy, sieving, sedimentation, determining surface areas, permeability, adsorption, derived properties of powders, porosity, packing arrangement densities, bulkiness and flow properties.

Liquid interface, surface and interfacial tensions, surface free energy, measurement of surface and interfacial tension, spreading coefficient, adsorption and liquid interfaces, surface active agents, HLB classification, solubilization, detergency, absorption at solid interfaces, solid gas and solid-liquid interfaces, complex films, electrical properties of interfaces.

Newtonian systems, law of flow, kinematics viscosity, effect of temperature, non- Newtonian systems, pseudoplastics, dilatant, plastic, thixotropy in formulations, determination of viscosity and thixotropy by capillary, falling ball, rotational viscometer, application of theology in pharmacy

Classification of complexes, methods of preparations and analysis, applications.

Buffer equations and buffer capacity in general. Buffers in pharmaceutical systems, preparations and stability, buffered isotonic solutions. Measurements of tonicity calculations and methods of adjusting isotonicity.

Organic Chemistry

A brief review of classification & sources of organic compounds, sp3 , sp 2 , sp hybridization, sigma & pi- bonds, bond lengths, bond angles & bond energies along with their significance in reactions should be carried out. An overview of bond polarization, hydrogen bonds, inductive effects, resonance, and hyperconjugation be taken. Concept of homolytic & heterolytic bond fission, acidity & basicity with different theories should be covered briefly. Ease of formation & order of stabilities of electron deficient & electron rich species along with the reasons for the same should be covered. Relationships between energy content, stability, reactivity & their importance in chemical reactions should be covered. Calculations for determining empirical & molecular formula should be covered.

The following classes of compounds should be taught in detail with respect to their IUPAC / systematic nomenclature, industrial [wherever applicable] & laboratory methods of preparations, physical properties & chemical reactions with emphasis on reaction mechanisms [arrow based] & stereochemistry [wherever applicable].

Introduction to protection & deprotection of functional groups. Two examples each for amino, hydroxyl, & carbonyl groups. The significance of these in syntheses should be explained.

Concept of aromaticity, Huckel’s rule & its use in determining the aromatic/non-aromatic character of a compound. A brief coverage of structure of benzene. Detailed coverage of electrophilic & nucleophilic aromatic substitution reactions. Reactivity & orientation in these reactions. Reactivity & orientation in mono- & disubstituted benzenes. Benzyne mechanism.

The following classes of compounds with respect to their IUPAC / systematic nomenclature, industrial [wherever applicable] & laboratory methods of preparations, physical properties & chemical reactions with emphasis on reaction mechanisms [arrow based] & stereochemistry [wherever applicable].

Syntheses & reactions with mechanisms of bi & tricyclic fused carbocyclic rings like naphthalene, anthracene, & phenanthrene.

Carbonyl chemistry involving group conversions & their reaction mechanisms along with stereochemistry wherever applicable.

IUPAC Nomenclature of heterocyclic rings [3-10 membered] containing O, S, & N atoms. Nomenclature of above rings containing mono-, di-, & multiple [same or different] heteroatoms should also be covered. Nomenclature of 2 & 3 fused rings containing mono-, di-, & multiple heteroatoms [same or different] should also be covered. Syntheses & reactions of three to sixmembered rings in detail. Syntheses of five & six-membered rings containing mono- or any diheteroatoms [O, S, & N]. Syntheses of quinoline, isoquinoline, benzoxazole, benzothiazole, & benzimidazole, benzotriazole, and benzothiazole.

Bridged ring systems & their nomenclature.C8, C9, C11 bridged bicyclic alkanes. Chemistry of hexamine, morphan, biperiden, amantadine, diazabicyclo[2.2.2] octane

Kinetic & thermodynamic control of sulfonation, enolate anion formation & alkylation of enamine reactions.

Chirality & asymmetry [introduction of the same to S, P, & N]. Definition & classification [different types of isomerisms]. Enantiomers, diastereomers. Enantiomerism & diastereomerism. Meso compounds & their optical activity. Stereochemistry in acyclic compounds. Newman projection formulae & their significance. Conformational analysis of nbutane. Absolute & relative configuration. Assigning R & S configuration based on Cahn Ingold & Prelog system. Racemic mixture- its definition & resolution. Definitions of terms stereoselective, stereospecific, Enantiomeric excess & diastereomeric excess. Stereochemistry in cyclic systems. Conformations of cyclohexane. Cis-trans relationship in cyclohexane. Prediction of stability of different conformations of 1, 2- 1,3- & 1,4- disubstituted cyclohexanes. Effect of multiple substitutions on the stability of cyclohexane conformations. Chair conformations of cis-, & trans-decalins, perhydrophenanthrenes, & a tetracyclic steroidal nucleus. An introduction to atropisomerism.

Carbohydrates. Definition & classification. D & L nomenclature in sugars. Different ways of drawing / representing a sugar molecule [including cyclic Structure], interconversion of these representations. Anomers & epimers. Mutarotation. Reactions of glucose. Chain extension & chain reduction of a sugar.

Amino acids & proteins. Definition & classification. D & L Amino acids, natural, essential, & nonessential amino acids. Denaturation, Strecker, Gabriel phthalimide methods for the preparation of amino acids. Peptide bond & its formation. Two protective groups each, for -NH2 & -COOH functionalities during protein synthesis. Sequencing of a protein by chemical & enzymatic methods.

Pericyclic reactions. Concept of HOMO & LUMO. Drawing of HOMO & LUMO of 1, 3-butadiene, allylic cation, radical & anion, & 1, 3, 5-hexatriene, Diel’s-Alder & retro Diel’s Alder reaction.

Pharmaceutical Chemistry I

1. Pharmaceutical Inorganic Chemistry

2. Medicinal Chemistry

A detailed study of the following classes with respect to drug nomenclature, classification, physicochemical properties, mode of action [MOA], structure-activity relationships [SAR], wherever applicable, synthesis of simple & prototype molecules, drug metabolism, therapeutic uses & side effects. Drug resistance, wherever applicable, should be covered in respective classes of drugs.

  1. (a) Sedative-hypnotics,  (b) Antiepileptic agents, (c) Neuroleptics, (d) Anti-anxiety drugs.
  2. Antibiotics:. Penicillins, cephalosporins & other beta-lactam antibiotics like imipenem & aztreonam. Beta-lactamase inhibitors such as clavulanic acid & sulbactam. Chloramphenicol. Tetracyclines. Aminoglycoside antibiotics. Macrolide antibiotics. Lincomycins. Polypeptide antibiotics. Anticancer antibiotics.
  3. Steroids: Corticosteroids [gluco- & mineralocorticoids] & anti-inflammatory steroids. Sex steroids. Male & female contraceptive agents. Anabolic steroids. Anticancer agents.
  1. Narcotic [centrally acting] analgesics [analgetics]. Morphine & all its structural modifications [peripheral & nuclear]. Narcotic agonists & antagonists [dual & pure]. Non-narcotic analgesics [NSAIDS]. Difference between narcotic & non-narcotic agents.
  2. Adrenergic drugs. Neurotransmitters & their role. General & specific adrenergic agonists & antagonists [up to alpha-2 & beta-2 only].
  3. III. Cholinergic agents. Muscarinic & nicotinic cholinergic agonists & antagonists [up to M2 & N2]. Neuronal [transmission] blockers.
  4. Drugs used in neuromuscular disorders. Drugs used in the treatment of Parkinson’s disease. Central & peripheral muscle relaxants.
  5. Hypertensive, antihypertensive, & antianginal agents.
  6. Diuretics.
  7. Eicosanoids. Prostaglandins, prostacyclins, & thromboxanes. Their biochemical role, biosynthesis, & inhibitors. 9. Introduction to quantitative structure-activity relationship. [QSAR]. Linear free energy relationship. Hammett’s equation. Use of substituent constants such as π, σ, Es, & physicochemical parameters such as pKa, partition coefficient, Rm, chemical shifts, molar refractivity, simple & valance molecular connectivity to indicate electronic effects, lipophilic effects, & steric effects. Introduction, methodology, advantages & disadvantages/limitations of Hansch analysis.

Pharmaceutics

Pharmacology

Pharmacognosy

Pharmaceutical Analysis

Calculation of equivalent weight of oxalic acid, KMnO4, FeSO4, permanganate & I2 from halfreactions. Calculation of factors for titrations mentioned in a, b & c.

Biochemistry

Biotechnology

  1. Plant Cell and Tissue Culture

Structure of plant cell, DNA, Genes and chromosomes.

  1. Cell and tissue culture
    1. Requirements.
    2. Callus culture, suspension culture, batch culture.
    3. The concept of somatic hybridization, somatic embryogenesis.
  2. Processes and applications
    1. Isolation and immobilization of enzymes and plant cells and application.
    2. Protoplast and cell fusion.
    3. Germplasm conservation.
    4. Production of secondary metabolites by plant tissue culture.
    5. Gene transfer techniques.
  1. Animal Cell Culture: Introduction to animal cell culture, medium used in ATC. Use of FCS, primary culture, secondary culture, cell line. Cloning: concept and application with technical hurdles. Transgenic animals as a source of food, organs and tissues, concept of xeno transplant.
  2. Fermentation Technology and Industrial Microbiology:1. Fermentation as a biochemical process, types of fermentation.2. Fermenter – working and construction, accessory components, modification.3. Fermentation monitoring and in situ recovery of products.
  3. Recombinant DNA Technology Basic concepts
    • Introduction.
    • Role of a restriction endonuclease, DNA ligase, DNA polymerase, Reverse transcriptase.
  4. Process and Applications

a) Constructing Recombinant DNA molecules.

b) PCR and applications.

c) Drug delivery systems in gene therapy.

Physical Chemistry

Physical Pharmacy

Organic Chemistry

Pharmaceutical Chemistry

Pharmaceutics

Pharmacology

Pharmacognosy

Pharmaceutical Analysis

Biochemistry

Biotechnology

Microbiology

Pathophysiology

Biopharmaceutics and Pharmacokinetics

Human Anatomy and Physiology

Pharmaceutical Engineering

Pharmaceutical Management

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