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USP DISSOLUTION STUDIES
DISSOLUTION A process in which a solid substance solubilizes in a given solvent. i.e. mass transfer from the solid surface to the liquid phase. USP DISSOLUTION APPARATUS • 	Apparatus 1 - Basket (37º) • 	Apparatus 2 - Paddle (37º) • 	Apparatus 3 - Reciprocating Cylinder (37º) • 	Apparatus 4 – Flow-Through Cell (37º)
• 	Apparatus 5 – Paddle over Disk (32º), Transdermal Delivery   	System, use paddle and vessel from Apparatus 2 with a    	stainless steel disk assembly to hold the transdermal on the    	bottom of vessel. • 	Apparatus 6, Cylinder (32º), Transdermal Delivery System,    	use Apparatus 1 except replace the basket shaft with a stainless     	steel cylinder element. • 	Apparatus 7, Reciprocating Holder, for transdermal delivery    	systems and also a variety of dosage forms
APPARATUS 1: The assembly consists of the following : A covered vessel, Transparent material, A motor, A metallic drive shaft, A cylindrical basket, The water bath permits the holding of temp inside vessel at  37±0.5  ̊C   The vessel is a cylindrical with hemispherical bottom with dimension and capacity of.
[object Object]
Use 40mm mesh cloth.
A basket having a gold coating 0.0001 inch  thick may be used.                  The dosage unit is place in a dry basket at the beginning of each test. The distance between  the inside bottom of the vessel and the basket is maintained  at 25± 2mm. APPARATUS  2 ,[object Object], Except paddle formed from a blade.   a shaft is used as the stirring element   The vertical center line of the blade is flush with the bottom        of the shaft.  The distance of 25±2 mm between the blade and the inside bottom of the vessel.
[object Object]
The dosage unit is allowed to sink to the bottom of the vessel before rotation of the blade.
A small, loose piece of nonreactive material such as wire helix may be attached to dosage units in order to prevent floating. ,[object Object]
If two or more times are specified, specimen are to be withdrawn only at the stated times within a tolerance of ±2 % PROCEDURES ,[object Object]
Equilibrate the dissolution medium to 37±o.5  ̊c
Place 1 tablet or 1 capsule in the apparatus.,[object Object]
Within the time interval, withdraw a specimen from zone midway between the surface of the dissolution medium and the top of the rotating basket or blade , not less than 1cm from vessel wall.
Replace the aliquots withdrawn for analysis with equal volume of dissolution medium at 37 ̊c.  ,[object Object]
APPARATUS 3 The assembly consists of: 	a set of cylindrical, 	flat-bottomed glass vessels; 	a set of glass reciprocating 	cylindrical; 	stainless steel fitting;  	screen; 	a motor and drive.  ,[object Object],    bath holding temp at 37± 0.5 ̊
PROCEDURE: ,[object Object]
Equilibrate the dissolution medium to 37 + 0.5°
Place 1 dosage-form unit in each of the six reciprocating cylinders.
Operate the apparatus
During the upward and downward stroke, the reciprocating cylinder moves through a total distance of 9.9 to 10.1 cm

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Usp dissolution studies

  • 2. DISSOLUTION A process in which a solid substance solubilizes in a given solvent. i.e. mass transfer from the solid surface to the liquid phase. USP DISSOLUTION APPARATUS • Apparatus 1 - Basket (37º) • Apparatus 2 - Paddle (37º) • Apparatus 3 - Reciprocating Cylinder (37º) • Apparatus 4 – Flow-Through Cell (37º)
  • 3. • Apparatus 5 – Paddle over Disk (32º), Transdermal Delivery System, use paddle and vessel from Apparatus 2 with a stainless steel disk assembly to hold the transdermal on the bottom of vessel. • Apparatus 6, Cylinder (32º), Transdermal Delivery System, use Apparatus 1 except replace the basket shaft with a stainless steel cylinder element. • Apparatus 7, Reciprocating Holder, for transdermal delivery systems and also a variety of dosage forms
  • 4. APPARATUS 1: The assembly consists of the following : A covered vessel, Transparent material, A motor, A metallic drive shaft, A cylindrical basket, The water bath permits the holding of temp inside vessel at 37±0.5 ̊C The vessel is a cylindrical with hemispherical bottom with dimension and capacity of.
  • 5.
  • 7.
  • 8.
  • 9. The dosage unit is allowed to sink to the bottom of the vessel before rotation of the blade.
  • 10.
  • 11.
  • 12. Equilibrate the dissolution medium to 37±o.5 ̊c
  • 13.
  • 14. Within the time interval, withdraw a specimen from zone midway between the surface of the dissolution medium and the top of the rotating basket or blade , not less than 1cm from vessel wall.
  • 15.
  • 16.
  • 17.
  • 18. Equilibrate the dissolution medium to 37 + 0.5°
  • 19. Place 1 dosage-form unit in each of the six reciprocating cylinders.
  • 21. During the upward and downward stroke, the reciprocating cylinder moves through a total distance of 9.9 to 10.1 cm
  • 22. Within the time interval specified withdraw a portion of the solution under test from a zone midway between the surface of the dissolution medium and the bottom of each vessel.
  • 23.
  • 24. The pump forces the dissolution medium upwards through the flow-through cell.
  • 25. The pump has a delivery range between 240 and 960 mL per hour, with standard flow rates of 4, 8, and 16 mL per minutes.
  • 26. The cell is immersed in a water bath and the temperature is maintained at 37 + 0.5°
  • 27.
  • 28. Place 1 dosage form unit on top of the beads.
  • 29. Assemble the filter head and fix the parts together by means of a suitable clamping device.
  • 30. Introduce by the pump the dissolution medium warmed to 37 + 0.5° through the bottom of the cell.
  • 31. Collect the eluate by fractions at each of the times stated.
  • 32.
  • 33. The temperature is maintained at 32 + 0.5°C
  • 34. A distance of 25 + 2 mm between the paddle blade and the surface the disk assembly is maintained during the test.
  • 35.
  • 36. Apply the transdermal system disk assembly.
  • 37. The system may be attached to the disk by a suitable adhesive.
  • 38. Place the disk assembly flat at the bottom of the vessel with the release surface facing up and parallel to of the paddle blade and surface of the dissolution medium.
  • 40. At each sampling time interval, withdraw a sample from a zone midway between the surface of the dissolution medium and the top of the blade, not less than 1 cm from the vessel wall.
  • 41.
  • 42. The dosage unit is placed on the cylinder at the beginning of each test.
  • 43.
  • 44. Equilibrate the dissolution medium to 32 + 0.5°C
  • 45. Prepare the test system prior to test as follows.
  • 46. Remove the protective liner from the system and place the adhesive side on a piece of cuprophan.
  • 47.
  • 48. Press the cuprophan covering to remove trapped air bubbles.
  • 49. Place the cylinder in the apparatus and immediately rotate at the rate specified
  • 50. Within the time interval specified, withdraw a quantity of dissolution medium for analysis from a zone midway between the surface of the dissolution medium and the top of the rotating cylinder, not less than 1 cm from the vessel wall.
  • 51.
  • 52. A motor and drive assembly to reciprocate the system vertically
  • 53. A set of suitable sample holders.
  • 54.
  • 55. Taking care to eliminate air bubbles between the substrate release surface
  • 56. Attach the system to a suitable sized sample holder with a suitable O-ring.
  • 57.
  • 58. Reciprocating a frequency of about 30 cycles per minutes with an amplitude of about 2 cm.
  • 59. Remove solution containers from the bath, cool to room temperature.
  • 60.

Notes de l'éditeur

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