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Home » Gate Sample Papers » Pharmaceutical Sciences Sample Papers » GATE Pharmacy Question Paper 2008

GATE Pharmacy Question Paper 2008

1. An antidiabetic drug Piogliazone used in Type 2 diabetes acts by
(A) Decrease of glucose uptake in muscles
(B) Increasing insulin sensitivity
(C) Inhibiting intestinal n-glucosidase    
(D) Stimulating insulin secretion

2. An angiotensin-II receptor blocker useful in treating hypertension is
(A) Enalaprilat      
(B) Valsartan         
(C) Atenolol       
(D) Amiodipine

3.Co-administration of NSAIDs with Warfarin may often lead to
(A) Antagonistic interaction
(B) Interaction to change in drug transport
(C) Interaction due to disturbances in electrolyte balance
(D) Additive or synergistic interaction

4. Laminaria and Kelp are the principal genera, currently used for the industrial
   production of
(A) Carrageenans                        
(B) Agar
(C) Fucans                              
(D) Alginic acid and alginates

5. A transverse section of the root fo Glycyrrhiza glabra when treated with 80%
   sulphuric acid gave
(A) Deep yellow colour                   
(B) No reaction, but only charring
(C) Deep blue colour                    
(D) Deep red colour

6. Microscopy of the bulbs of Urginea Indica family Liliaceae shows
(A) Prisms of calcium oxalate              
(B) Calcium carbonate and silica
(C) Rosettes of calcium oxalate            
(D) Raphides of calcium oxalate

7. Streptomycin is a
(A) di-acidic base possessing an aldehydic carbonyl group
(B) tri-acidic base possessing an aldehydic carbonyl group
(C) neutral compound possessing a ketonic group
(D) acidic compound possessing a carboxylic group

8. The antihistamine with diphenyl methyl group is
(A) Methdilazine                          
(B) Cyclizine hydrochloride
(C) Pheniramine                          
(D) Phenindamine

9. Heterocyclic rings present in pilocarpine are
(A) Imidazole and Quinoline                  
(B) Imidazole and Thiazole
(C) Quinoline and Phenanthrene               
(D) Imidazole and Dihydrofuran

10. The most important microbial virulence factor in the etiology of bacterial
    meningitis is
(A) Exotoxin                          
(B) Components of the capsule
(C) Coagulase                         
(D) Hyaluronidase

11. Commonly used tetanus vaccine is produced by
(A) treatment of the causative organism with heat or UV light and finally
    obtaining the toxoid
(B) sub-culuring the virus at pH 10.4
(C) artificially generating antibodies to viral glycoproteins
(D) isolating the antigenicity genes from the causative organism

12. Which of the following equations is valid for standard B-DNA?
(A) A+T=G+C          
(B) A+T=2(G+C)
(C) 2(A+T)=3(G+C)
(D) A+G=T+C

13. Clinical jaundice, typified by yellowing of the tissues is associated with elevated
    levels of
(A) serum lysozyme                            
(B) serum bilirubin
(C) serum creatinine
(D) serum γ-glutamyl transferase

14.In NMR spectrometry, the chemical shift ( δ ) is expressed in
(A) Parts per million
(B) Gauss             
(C) Tesla       
(D) Hertz

15. In chromatographic separation, the different species in the sample, undergo the
    process of
(A) chemical interaction
(B) partition     
(C) volatilization
(D) ionization

16. A target material used in the production of X-rays is
(A) potassium        
(B) copper            
(C) aluminium
(D) sodium

17. The requirements and guidelines for clinical trials, import and manufacture of
    new drugs as per the Drugs & Cosmetics Rules is given under Schedule
(A)  N              
(B) Y               
(B) A              
(D) B

18. The growth of large particles at the expense of smaller ones, as a result of a
    difference in the solubility of the particles of varying sizes, is termed as
(A)   Interfacial phenomenon                   
(B) Partitioning
(C)   Erosive formulation                      
(D) Oswald ripening

19. Cyclic oligomers of glucose that form water soluble inclusion complexes, which
    are biocompatible and improve the bioavailability of drugs
(A)   chlorophyll                           
(B) polyethylene glycol
(C)   cross povidone                        
(D) cyclodextrin

20. 'Draves test' is associated with measuring the efficiency of
(A) Detergents                              
(B) Wetting agents
(C)   Suspending agents                     
(D) Adsorbent

21. Effects of fibrates on blood lipids are mediated by
(A) Inhibiting both synthesis and esterification of fatty acids
(B) Their interaction with peroxisome proliferators-activated receptors (PPARs)
(C) Reducing the conversion of HMG-CoA to mevalonate
(D) Sequestering bile acids

22. A cardioselective beta blocker with vasodilating properties is
(A) Pindolol           
(B) Atenolol         
(C) Bisoprolol    
(D) Nebivolol

24. (-) � Hyoscyamine is
(A) 15-20 times more active as a mydriatic than (+)- hyoscyamine
(B) Inactive as a mydriatic
(C) 3-5 times less active as a mydriatic than (+)- hyoscyamine
(D) 100 times more active as a mydriatic than (+)- hyoscyamine

26. In thiazole diuretics, the position 7 is very important and is occupied by a
(A) CH3 group                                 
B) Free sulphamoyl group
(C) Chloro group                              
(D) Free � NH2 group

28. A mass spectrum is obtained by plotting
(A) Molecular weight versus peak height
(B) Concentration versus peak height
(C) Concentration versus degree of deflection of ions
(D) Abundance of ions versus their m/e ratio

29. Aldehydes can be distinguished from other C=O containing compounds by IR,
    due to
(A) The low frequency of absorption of aldehydes
(B) The alkyl or aryl group is attached to >C=O
(C) The double bond present
(D) The double at the C-H-stretching region

30. A super disintegrant in tablet formulation is
(A)  sodium starch glycollate                
(B) starch
(C)  PVP                                     
(D) Mg-Aluminium silicate

31. A drug was administered to 30 subjects as a tablet (30 mg), an oral aqueous
    solution (30 mg) and as an intravenous infusion (0.3 mg). Mean AUC's
    (ng.hr/mL), dose normalized to 1 mg, for tablet, oral solution and IV were 0.91,
    0.87 and 103.0 respectively.
    Calculate the relative bioavailability of the drug in tablet compared to the oral
    solution and the absolute bioavailability of tablet form
(A)   104.6%, 0.883%
(B) 81%,5.6%
(C)   10.46%, 8.83%                           
(D) 19%, 56%

32. When ammonium chloride is gradually and slowly incorporated into an emulsion
    stabilized with ammonium oleate,
(A)   Emulsion will crack immediately
(B)   It will invert from o/w to w/o type
(C)   It will invert from w/o to o/w type
(D)   There will be no impact on its physical stability

 33.   A prescription requires 4 mEq/ liter of hydrogen phosphate ion HPO4-2. How many
    milligrams of dibasic potassium phosphate K2HPO4 (molecular weight 174) be
    required?
(A)   174 mg/litre      
(B) 30.5 mg/litre   
(C) 522 mg / litre
(D) 348 mg/ litre

34. Gram positive bacteria typically contain
(A) cell walls that lack peptidoglycans
(B) repeating units of arabinogalactan and mycolates in their cell walls
(C) Peptidoglycan containing muramic acid and D-amino acids in their cell walls
(D) cell walls containing predominantly polysaccharides and glycoprotein

35. Quaternary structure of a protein molecule refers to
(A) Specific association of two or more copies of a polypeptide chain to result in
         a biologically active molecule
(B) Regularly seen local structures within a polypeptide chain
(C) The portion of the polypeptide chain that comes into contact with another
         protein molecule
(D) The portion of the structure that gets stabilized upon binding to nucleic acids

36. A blood sample is treated with alkaline phosphotungestic acid to from tungsten
    blue, which is estimated colorimetric ally to give a positive reaction. The sample
    contains
(A) Protien                                  
(B) Serum creatinine
(C) Serum Phenylalanine                      
(D) Uric acid

37. Two important steps for plant regeneration by organogenesis are
                                                    (Q) Initiation of somatic embryogenesis
    (P) Establishment of callus cultures
    (R) Germination of seeds                        (S) Initiation of cell suspensions
(A) Q, S                 
(B) P, R             
(C) P, S             
(D) Q, R

38. Two tests for ephedrine are
    (P) A solution in dilute HCl, treated with copper sulphate and sodium hydroxide
         gives a violet colour
    (Q) An alcoholic solution gives a red colour with FeCl3
    (R) On shaking with solvent ether, the organic layer shows purple while the
         aqueous layer becomes blue in colour
    (S) A solution of vanillin gives a violet-red colour
(A) Q, S                 
(B) P, S             
(C) P, R             
(D) Q, R

39. Dried fruits of sweet fennel has two of the following properties
    (P) 80% of E-anethole, 10% of methyl chavicol and 5% (+) � fenchone as
         constitutents
    (Q) 65-75% (+)- Linalool as a constitutent
    (R) The fruit is a diakene, almost cylindrical and surrounded by large stylopod
    (S) The fruit is elongated and surrounded by calyculus
(A) P, R                 
(B) Q, S             
(C) P, S             
(D) Q, R

40. Dihydroxy acetone phosphate is involved in the biosyntheses of two of the
    following
    P: serotonin              Q: triacylglycerol    R:  pyruvate          S: methionine
(A) P, Q                 
(B) P, R             
(C) Q, S             
(D) Q, R

41. The virus responsible for SARS can be described by two of the following features
    P:   It contains double-stranded DNA and requires two complementary strands to
         be synthesized to serve as mRNA
    Q: It has distinctive club-shaped particles projecting from the surface, appearing
         like a crown.
    R:   It contains plus-strand RNA that can serve directly as mRNA
    S:   It is retrovirus and requires extra cellular DNA for replication
(A) P, Q                 
(B) P, S             
(C) Q, R             
(D) R, S

42.    Two of the following facts are associated with Ethylene oxide gas
           It is non toxic and non inflammable and used for sterilization
    (P)
    (Q)    It is a colourless inflammable gas, toxic in nature and used for sterilization
    (R)    It is diluted with CO2
    (S)    It cannot penetrate plastic and paper packaging
(A)    P, R              
(B) P, S             
(C) R, S             
(D) Q, R

44. Tranexamic acid is
    P   trans-4-amino methyl cyclohexane carboxylic acid
    Q   a polypeptide
    R   an inhibitor pf proteolytic enzymes including plasmin
    S   used for the prophylaxis of hemorrhage associated with excessive fibrinolysis
(A) P, S              
(B) P, R             
(C) Q, R         
(D) R, S

45. Prostaglandins are derivatives of
    P   C25 acid
    Q   7-(2 cyclohexyl) pentenoic acid
    R   C20 prostanoic acid
    S   7-(2 octyl cyclopentyl) heptanoic acid
(A) P, Q              
(B) R, S             
(C) P, R         
(D) Q, S

46. Two ex-officio members of the Drugs Technical Advisory Board under Drugs and
    Cosmetics Act are
    (P)  The Drugs Controller General of India
    (Q)  The President, Medical Council of India
    (R)  The Secretary, Pharmacy Council of India
    (S)  The Director, National Institute of Pharmaceutical Education and Research,
         India
(A)  P, Q             
(B) P, R             
(C) R, S         
(D) P, S

47. Calfactant is
    P   a sterile non-pyrogenic lung surfactant intended for intracgeal instillation to
        premature infants
    Q   a synthetic surfactant popularly used to prepare total parental nutrition
    R   a potent chelating agent used to prevent metal induced oxidation process
    S   an extract of natural surfactant from calf lungs
(A) P, Q             
(B) R, S              
(C) P, S          
(D) Q, R

48. In cross-over bioavailability studies, in which the subjects must be rested for
    sufficient time between each drug administration to ensure that 'washout' is
    complete. Practically, wash-out is deemed complete, when
    (P)   95% is washed out                       (Q) 100% is washed out
    (R)   5 biological half-lives have elapsed    (S) 2 biological half-lives have elapsed
(A)   P, R             
(B) P, S             
(C) Q, R             
(D) Q, S

49. Two reference electrodes are
P.    Glass membrane electrodes              
Q.  Sb/Sb2O3 electrodes
R.    Calomel electrode                      
S.  Silver/Silver-chloride electrode
(A)   P, Q             
(B) Q, S             
(C) R, S             
(D) P, R

50. Polarography can be used for the
P     simultaneous determination of several analytes
Q     study of resistance of a solution
R     study of current potential relationship
S     study of optical activity of organic compounds
(A)   P, S             
(B) Q, S             
(C) P, R             
(D) P, Q

51. Primary amines show
          Two N-H stretching bands in the range of 3500 � 3300cm-1
    P
          Only one band in the region 3500 � 3300 cm-1
    Q
    R     -NH band in primary amine results in a broad band in the region 1640 �
          1560 cm-1
          the typical �NH2 stretching value at 1715 cm-1
    S
(A)   Q, R             
(B) P, R             
(C) P, S             
(D) Q, S

52. The drug disulfiram is
         known to inhibit dopamine β-hydroxylase and cause noradrenaline depletion
    P
    Q    a substance that produces aversive reaction to alcohol
         known to stimulate dopamine β-hydroxylase
    R
    S    used in barbiturate poisoning
(A) P, S               
(B) Q, R             
(C) R, S             
(D) P, Q

53. Two important attributes associated with L- asparaginase
    P:   an enzyme obtained from E.Coli and is administered paranterally
    Q: an enzyme obtained from Streptococcus caespitosus and is administered
         orally
    R:   used in acute lymphocytic leukemia
    S:   used as fibrinolytic
(A) P, S               
(B) P, R             
(C) Q, R             
(D) Q, S

54. Amikacin is
    P   a semisynthetic aminoglycoside and a derivative of kanamycin
    Q   a semisynthetic aminoglycoside and a derivative of tobramycin
    R   it is administered parenterally and does not cause nephrotoxicity and
        otooxicity
    S   it is administered parenterally and is both nephrotoxic and ototoxic
(A) P, Q              
(B) P, R             
(C) P, S           
(D) Q, S

55. Matching exercises. Match Group I and Group-II and identify the correct
    combinations
        Group-I                              Group-II
        Plant                                Source
    (P) Thorn apple                      (1) Dried leaves and flowering
                                             tops of Hyoscyamus niger
    (Q) Henbane                          (2) Dried leaves and flowering
                                             tops of Datura Stramonium
    (R) Deadly nightshade                (3) Leaves of Digitalis purpurea dried
                                             at a temperature below 60oC
    (S) Foxglove leaves                  (4) Dried leaves and other aerial
                                             parts of Atropa acuminate
(A) P - 2 Q - 1 R - 4 S - 3         
(B) P - 1 Q - 2 R - 3 S - 4
(C) P - 3 Q - 4 R - 2 S - 1         
(D) P - 2 Q - 3 R - 4 S - 1

58. Derivatives of cortisol and their structural modifications are
        Group I                 Group II
        Derivative              Structural modification
    P.  Prednisolone        1.  1, 2-dehydro, 9α-fluoro, 16α-methyl
    Q.  Dexamethasone 2.        1, 2-dehydro
    R.  Betamethasone       3.  1, 2- dehydro, 9α-fluoro, 16β-methyl
    S.  Triamcinolone       4.  1, 2-dehydro, 9α-fluoro, 16α-hydroxy

(A) P-2 Q-1 R-3 S-4                          
(B) P-2 Q-1 R-3 S-4
(C) P-2 Q-4 R-3 S-1                          
(D) P-3 Q-2 R-1 S-4

59.     Group I          Group II
        Drugs            Starting material for synthesis
    P.  Clofazimine   1. p-chloronitro benzene
    Q.  Ketoconazole  2. L-phenyl alanine
    R.  Melphalan     3. -N-(4-chlorophenyl)-O-phenylenediamine
    S.  Dapsone       4. 2, 4-dichloro phenylbromide and glycerine
(A) P-1 Q-2 R-3 S-4                   
(B) P-4 Q-3 R-1 S-2
(C) P-3 Q-4 R-2 S-1                   
(D) P-2 Q-1 R-4 S-3

72. Nifedipine when exposed to day light and artificial light, is readily converted to a
    derivative of
(A) 4-Phenyl pyridine                    
(B) Nitrosophenyl pyridine
(C) Diazophenyl pyridine                 
(D) Nitrobenzene

73. The B.P.assay of Nifedipine is by titration of a
(A) Solution in anhydrous acetic acid with 0.1M perchloric acid
(B) Solution in previously neutralized acetone with 0.1N sodium hydroxide; end
        point by potentiometry
(C) Solution in previously neutralized acetone against standard potassium
        dichromate solution
(D) A solution in 2 methyl -2 propanol and perchloric acid with 0.1M cerium
        sulphate using ferroin as indicator

 74.   Tenoposide is a natural product used for the management of certain diseases.
 It is derived form
     (A) Flavonolignans form Silybum marianum
     (B) Lignans from Podophyllum peltatum
     (C) Lignans from Schizandra chinensis
     (D) Neolignans from Piper futokadsura

75. This drug is used in the management of
(A) Candidiasis                       
(B) Trypanosomiasis
(C) Cardiac arrhythmia                
(D) Acute leukemia in children

    Extracts of Chondrodendron tomentosum, family menispermaceae contains
    several alkaloids
76. One of the important alkaloid is
(A) (-) Phyllandrene                
(B) (+) Holarrhenine
(C) (+) Tubocurarine                
(D) (�) Colchicine

77. This alkaloid has
(A) Bis benzyl tetrahydro isoquinoline ring
(B) Quinoline ring
C) Phenanthrene ring                      
(D) Pyrido pyrimidine ring

78.    Several drugs are used for migraine
 Acute migraine is treated with
(A) Prazosin         
(B) Formeterol
(C) Sumatriptan
(D) Dopamine

79. The drug chosen is an agonist of
(A) α1 adrenoceptor             
B) α2 adrenoceptor
(C) M3 receptor
(D) 5 − HTID receptor

82.  A 250 mg dose of a drug was administered to a patient by rapid IV injection. The
    initial plasma concentration was 2.50μg/mL. After 4 hours, the plasma
    concentration was 1.89μg/mL. Assuming that the drug was eliminated by a
    pseudo first order process and the body behaves as one compartment model
Kel is
(A) 0.0699 h−1    
(B) 0.0349 h−1      
(C) 1.623h−1      
(D) 0.699 h−1
 
















































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