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  • ASTM
    F1984-99(2013) Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials
    Edition: 2013
    $93.60
    Unlimited Users per year

Description of ASTM-F1984 2013

ASTM F1984-99-Reapproved2013

Historical Standard: Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials




ASTM F1984

Scope

1.1 This practice provides a protocol for rapid, in vitro screening for whole complement activating properties of solid materials used in the fabrication of medical devices that will contact blood.

1.2 This practice is intended to evaluate the acute in vitro whole complement activating properties of solid materials intended for use in contact with blood. For this practice, the words “serum” and “complement” are used interchangeably (most biological supply houses use these words synonymously in reference to serum used as a source of complement).

1.3 This practice consists of two procedural parts. Procedure A describes exposure of solid materials to a standard lot of human serum, using a 0.1-mL serum/13 x 100-mm disposable test tube. Cellulose acetate powders and fibers are used as examples of test materials. Procedure B describes assaying the exposed serum for significant functional whole complement depletion as compared to control samples.

1.4 This practice does not address function, elaboration, or depletion of individual complement components, nor does it address the use of plasma as a source of complement.

1.5 This practice is one of several developed for the assessment of the biocompatibility of materials. Practice F748 may provide guidance for the selection of appropriate methods for testing materials for other aspects of biocompatibility.

1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.


Keywords

biocompatibility; blood compatibility; whole complement testing


ICS Code

ICS Number Code 11.100.30 (Analysis of blood and urine)


DOI: 10.1520/F1984-99R13

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