Current Advances of Novel Drug Delivery System Mock Test

Refer to Current Advances of Novel Drug Delivery System Mock Test below. Students of BSc Pharmaceutical Science Current Advances of Novel Drug Delivery System can do the below online test and refer to the full list of free Current Advances of Novel Drug Delivery System BSc Pharmaceutical Science Mock Online Test provided below. These online Mock tests for BSc Pharmaceutical Science Current Advances of Novel Drug Delivery System have been designed based on the pattern of questions expected to come in the upcoming examinations and the latest syllabus. This Current Advances of Novel Drug Delivery System Mock Test is a free online mock practice test based on the important multiple choice questions (MCQs) from your BSc Pharmaceutical Science syllabus. The test for the topic Current Advances of Novel Drug Delivery System includes a series of carefully selected questions with four options each as you can see below. Whether you’re a first-year, second-year, or final-year BSc Pharmaceutical Science student, this test will help you revise key questions that are likely to appear in your semester exams or university assessments.

Online Mock Test for BSc Pharmaceutical Science Current Advances of Novel Drug Delivery System

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BSc Pharmaceutical Science Current Advances of Novel Drug Delivery System Mock Test

1. Liposomes consists of a bilayer of

Hydrophobic molecules Hydrophilic molecules Both Hydrophilic molecules and Hydrophobic molecules None of the options

2. To produce a microemulsion of small vesicles at least _______ circulations are required

10 circulations at least 2 circulations but not greater than 10 at least 20 circulation but not greater than 200 at least 200 circulation but not greater than 2000

3. Solvent vaporization is also known as

Ether injection Double emulsification Reverse-phase evaporation Ethanol injection

4. Liposome phospholipids undergoes

Oxidation Hydrolysis Both Oxidation and Hydrolysis Acetylation

5. If further electrophoresis is used for recovery of DNA from gels, the method is termed as ____________

electro-elution denaturing electrophoresis secondary electrophoresis recovery electrophoresis

6. Tranfersome belongs to the classification according to

Composition Function Application None of the options

7. Self micro emulsifying drug delivery systems (SMEDDSs) form transparent micro emulsions with droplet size of less than__________.

50 nm 70 nm 200 nm 100 nm

8. Which one of the following will travel fastest through the gel if the amount of DNA present is same in all?

Supercoiled and circular will move at same speed and faster than nicked Nicked Supercoiled Circular

9. Amphotericin B liposomes are given

Oral Transdermal Intravenous Lungs

10. The separation of charged molecules under the influence of electric current is called

Dot Blot Hybridization Western Blotting Colony Hybridization Electrophoresis

11. Liposomes with ___________number of lamella are called as 'pauci -lamellar liposomes'.

Lower Higher Single None of the options

12. Ketoconazole liposomes are given by

Oral Transdermal Intravenous Lungs

13. The greatest separation is obtained in which portion of the gel?

It varies according to the quantity of the size of the molecules to be separated The separation is uniform all over Lower portion where the cathode is Lower portion where the anode is

14. Which of the following is false in regarding reservoir devices?

The drug is contained in a powder from floating on liquid These devices are used when the drug permeation rate is rapid Suitable for low therapeutic index The release of the drug is controlled

15. SEDDSs produce emulsion with droplet size between ____________.

100 to 300nm 1000nm 200 to 400nm 10 to 100nm

16. How is the size of molecules under analysis measured?

By measuring the amount of visualising dye used There is no exact criterion for doing so By running a standard molecule, whose size is known in parallel By measuring the distance moved through a ruler

17. The absorption of the ophthalmic drug does not depend on which of the following?

Output of tears Physicochemical properties of permeating molecule Size of the eyeball Drainage of tears

18. In the use of TDDS for drug application ? size has to be considered reasonable?

Film size Strip size Diskette size Patch size

19. Gel matrices are generally of two types Agarose and Polyacrylamide. Which of the statements is correct with respect to agarose gels.

Agarose is a polysaccharide obtained from fungus Agarose is a polysaccharide which is obtained from red algae It is composed of glucose residues It is obtained via dissolving in its water by boiling in water and then cooling it

20. How many layer are seen in membrane-controlled system?

6 4 3 5

21. Which of the following characteristics is suitable for transdermal drug?

Drugs with narrow therapeutic index Large molecular size Large drug dose Drug which are metabolized in the skin

22. Which of the following is true for monolithic devices?

Suitable for drugs with large therapeutic index These devices are used when the drug permeation rate is rapid The drug is contained in a powder form floating on liquid The release of the drug is controlled

23. Which theory use for Physical entanglement of Mucin strands and flexible polymer chains.

Wetting theory Fracture theory Diffusion theory Adsorption theory

24. A method of permeation enhancement that involves the use of charged chemical components across the skin membrane using an electric field.

Ion exchange Electrophoresis Iontophoresis Sonophoresis

25. Which of the following is false for monolithic devices?

1st type has the drug dissolved in the polymer matrix The drug used for these devices has large therapeutic index 2nd type has drug delivery There are three categories of matrix devices

26. What is the largest organ of the body?

Liver Lungs Brain Skin

27. Which of the following can be incorporated into a liposome?

Only drugs and viruses Only viruses Drugs, peptides, viruses, bacteria Only Peptides and viruses due to similar characteristics

28. If the amount of agarose added is more, the molecular under analysis should have the following characteristic

small size the amount of molecules under analysis matters size has no relation with the amount of agarose large size

29. Which of the following is false for Merits of the TDDS.

Avoidance of the First pass effect A stable and controlled blood level Skin irritation and allergic response Termination at any time is conceivable

30. What are the characteristics of the monolithic devices?

Aqueous solution The drug has a large therapeutic index Administration of emulsion Control drug release by partitioning the drug from oil

31. How many layer are seen in monolithic TDDS design?

5 4 2 3

32. Which route is not use for MDDS?

Rectal Oral Buccal Nasal

33. In niosomes phospholipids are

Present Absent Both Present or Absent None of the options

34. Which polymers are not having charge?

Amino dextran Pectin Sodium CMC Starch

35. The rate at which monolithic devices transfer drug the patient body is proportional to________ of time.

Twice the time Half the time The square root of time Square of time

36. Which of the following drugs can not be given as transdermal administration?

Drugs with very short half life Drugs with narrow therapeutic index Drug against peptic ulcer Easy removal and termination

37. Which polymers is not soluble in water?

PEG HPMC CMC PVP

38. Liposomes have half-life

Longer Shorter Intermediate Both Longer and Shorter

39. Pharmacosome belongs to the classification according to

Composition Application Function None of the options

40. Which polymers is not included in the semisynthetic class?

Carbopol Chitosan Gelatin Pectin

41. In the case of electrophoresis of single stranded DNA or RNA, which type of gels are used?

The routine polyacrylamide gel The routine agarose gel Denaturing Renaturing

42. How are OLV liposomes made?

2-10 bilayers of lipid 100 bilayer of lipid A single bilayer of lipid Series of concentric bilayers of lipid

43. What are the characteristics of the mixed monolithic reservoir devices?

The drug has a large therapeutic index Drug permeation rate is high The drug polymer matrix is layered by rate controlling membrane Administration of emulsion

44. The technique used to located specific genes in chromosomes is

Colony Hybridization Dot Blot Hybridization Western Blotting In situ Hybridization

45. How are MLV liposomes made?

2-10 bilayers of lipid Series of concentric bilayers of lipid The single bilayer of lipid 100 bilayer of lipid

46. What are the characteristics of the reservoir or membrane devices?

Drug permeation rate is high The drug has a large therapeutic index Administration of emulsion Control drug release by partitioning the drug from oil

47. Which of the following is a characteristic of the parental controlled drug release system by liposomes?

Aqueous solutions Lipid bilayer enclosing the drug Administration of emulsions Free flowing powders

48. Loading of the entrapped agents before/during the manufacture procedure is known as

Active loading Passive loading Both Active loading and Passive loading none of the options

49. Which sentence is false in merits of MDDS?

Painless administration Low enzymatic activity & avoid of first pass metabolism Some patient suffers unpleasant feeling Targeting & localization of the dosage form at a specific site

50. Howmany nontechnology based product approved for clinical use?

30 24 20 10

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BSc Pharmaceutical Science Mock online test Current Advances of Novel Drug Delivery System

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