Standard Practice for Qualification of Basket and Paddle Dissolution Apparatus

SIGNIFICANCE AND USE
2.1 This practice outlines a procedure for the mechanical calibration of paddle and basket dissolution units to ensure reproducibility of results.  
2.2 Once a unit meets all of the mechanical specifications included in this practice, it is considered calibrated and further calibration with dissolution calibrator tablets is not required.
SCOPE
1.1 This practice covers the set-up and calibration of the paddle and basket dissolution apparatus.  
1.2 Use of this practice may be applied to apparatus that have been modified to enable automatic dissolution testing (that is, a valve in the bottom of the vessel or sampling through the shaft).  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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Publication Date
31-Jan-2013
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Standards Content (Sample)

NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation:E2503 −13
StandardPractice for
1
Qualification of Basket and Paddle Dissolution Apparatus
This standard is issued under the fixed designation E2503; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope 4.2 Wherever possible, tools shall be traceable to an ac-
cepted standard calibration source from a national or interna-
1.1 This practice covers the set-up and calibration of the
tional calibration laboratory.
paddle and basket dissolution apparatus.
4.3 ApparatusSet-up—Duringapparatusinstallationorafter
1.2 Use of this practice may be applied to apparatus that
replacement of parts or components, verify that the description
have been modified to enable automatic dissolution testing
and critical dimensions for each part meets the original
(that is, a valve in the bottom of the vessel or sampling through
description and dimension.
the shaft).
4.3.1 VesselDimensions—In the absence of a COAor COC,
1.3 The values stated in SI units are to be regarded as
the vessel’s internal dimensions should be measured with an
standard. No other units of measurement are included in this
appropriate measuring device and vessel shape and condition
standard.
should be noted. For example, for a cylindrical, hemispherical
1.4 This standard does not purport to address all of the
vessel, the vessel’s sides must be cylindrical, the internal
safety concerns, if any, associated with its use. It is the
dimension should be measured, and the vessel bottom should
responsibility of the user of this standard to establish appro-
be smooth and without defects. The vessel must fit within the
priate safety and health practices and determine the applica-
apparatus in such a manner as to ensure stable operation and
bility of regulatory limitations prior to use.
centering of the shaft in the vessel.
4.3.2 Basket/ShaftDimensions—In the absence of a COAor
2. Significance and Use
COC, an appropriate measuring device is used to measure the
2.1 This practice outlines a procedure for the mechanical relevant basket dimensions. Critical dimensions to be mea-
calibration of paddle and basket dissolution units to ensure suredoneachbasketshouldincludebutarenotlimitedto:shaft
reproducibility of results. diameter, vent hole diameter, thickness of wide portion of the
basket-to-shaft adaptor, total basket height, internal diameter at
2.2 Once a unit meets all of the mechanical specifications
the top of the basket, outer diameter of the screen, height of the
included in this practice, it is considered calibrated and further
open screen, outer diameter of bottom, diameter of screen on
calibration with dissolution calibrator tablets is not required.
the bottom, and screen mesh number.
4.3.3 Paddle Dimensions—In the absence of a COA or
3. Analyst Responsibilities
COC, an appropriate measuring device is used to measure the
3.1 Verify the vessel, basket, and paddle dimensions on
relevant dimensions of the paddle. Examples of dimensions to
receipt through measurement or Certificate ofAnalysis (COA)
be determined on each paddle should include but are not
or Certificate of Conformity (COC).
limited to: shaft diameter, blade height, blade thickness, total
3.2 Ensure the instrument is calibrated and fit for perform-
blade length, length of flat portion on bottom of blade, radius
ing dissolution analysis.
of the angle on the top outer edge of the top of the blade, radius
of the outside edge of the blade, difference between the
4. Procedure
distance from the midline of the shaft to the top outer edge for
the two sides, and difference between the heights of both sides
4.1 Background—The set-up, mechanical, and operational
of the paddles at the outside top.
checks are used to minimize variability during dissolution
testing to ensure the reproducibility of dissolution results.
4.4 Maintenance—Consult the manufacturer’s maintenance
recommendations and maintenance schedule to establish an
appropriate maintenance program based on the frequency of
1
This practice is under the jurisdiction of ASTM Committee E55 on Manufac-
apparatus use and quality system requirements.
ture of Pharmaceutical Products and is the direct responsibility of Subcommittee
E55.03 on General Pharmaceutical Standards.
4.5 Mechanical Calibration—Perform these tests on the
Current edition approved Feb. 1, 2013. Published March 2013. Originally
frequency determined by the quality system or after repair or
approved in 2007. Last previous edition approved in 2007 as E2503 – 07. DOI:
10.1520/E2503-13. move. If the instrument is not in routine use, the mechanical
Copyright © ASTM International, 100 Barr
...

This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation: E2503 − 07 E2503 − 13
Standard Practice for
1
Qualification of Basket and Paddle Dissolution Apparatus
This standard is issued under the fixed designation E2503; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope
1.1 This practice covers the set-up and calibration of the paddle and basket dissolution apparatus.
1.2 Use of this practice may be applied to apparatus that have been modified to enable automatic dissolution testing (that is,
a valve in the bottom of the vessel or sampling through the shaft).
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility
of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory
limitations prior to use.
2. Significance and Use
2.1 This practice outlines a procedure for the mechanical calibration of paddle and basket dissolution units to ensure
reproducibility of results.
2.2 Once a unit meets all of the mechanical specifications included in this practice, it is considered calibrated and further
calibration with dissolution calibrator tablets is not required.
3. Analyst Responsibilities
3.1 Verify the vessel, basket, and paddle dimensions on receipt through measurement or Certificate of Analysis (COA) or
Certificate of Conformity (COC).
3.2 Ensure the instrument is calibrated and fit for performing dissolution analysis.
4. Procedure
4.1 Background—The set-up, mechanical, and operational checks are used to minimize variability during dissolution testing to
ensure the reproducibility of dissolution results.
4.2 Wherever possible, tools shall be traceable to an accepted standard calibration source from a national or international
calibration laboratory.
4.3 Apparatus Set-up—During apparatus installation or after replacement of parts or components, verify that the description and
critical dimensions for each part meets the original description and dimension.
4.3.1 Vessel Dimensions—In the absence of a COA or COC, the vessel’s internal dimensions should be measured with an
appropriate measuring device and vessel shape and condition should be noted. For example, for a cylindrical, hemispherical vessel,
the vessel’s sides must be cylindrical, the internal dimension should be measured, and the vessel bottom should be smooth and
without defects. The vessel must fit within the apparatus in such a manner as to ensure stable operation and centering of the shaft
in the vessel.
4.3.2 Basket/Shaft Dimensions—In the absence of a COA or COC, an appropriate measuring device is used to measure the
relevant basket dimensions. Critical dimensions to be measured on each basket should include but are not limited to: shaft diameter,
vent hole diameter, thickness of wide portion of the basket-to-shaft adaptor, total basket height, internal diameter at the top of the
basket, outer diameter of the screen, height of the open screen, outer diameter of bottom, diameter of screen on the bottom, and
screen mesh number.
1
This practice is under the jurisdiction of ASTM Committee E55 on Manufacture of Pharmaceutical Products and is the direct responsibility of Subcommittee E55.03 on
General Pharmaceutical Standards.
Current edition approved March 15, 2007Feb. 1, 2013. Published April 2007 March 2013. Originally approved in 2007. Last previous edition approved in 2007 as E2503
– 07. DOI: 10.1520/E2503-07.10.1520/E2503-13.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

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E2503 − 13
4.3.3 Paddle Dimensions—In the absence of a COA or COC, an appropriate measuring device is used to measure the relevant
dimensions of the paddle. Examples of dimensions to be determined on each paddle should include but are not limited to: shaft
diameter, blade height, blade thickness, total blade length, length of flat portion on bottom of blade, radius of the angle on the top
outer edge of the top of the blade, radius of the outside edge of the blade, difference between the distance from the midline of the
shaft to the top outer edge for the t
...

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