Significance of HRBC membrane stabilization
HRBC membrane stabilization is a technique used to evaluate the protective effects of substances against hemolysis of red blood cells, serving as an important indicator of anti-inflammatory activity. This method assesses the ability of various extracts, such as Sivathai chooranam and Coldenia procumbens, to stabilize human red blood cell membranes. By measuring the prevention of lysis under stress conditions, HRBC membrane stabilization correlates with the effectiveness of extracts in exhibiting anti-inflammatory properties, demonstrating their potential therapeutic benefits.
Synonyms: Membrane protection
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The concept of HRBC membrane stabilization in scientific sources
HRBC membrane stabilization is a method to evaluate anti-inflammatory activity by measuring the prevention of human red blood cell lysis, serving as an indicator of the effectiveness of various extracts in reducing inflammation.
From: World Journal of Pharmaceutical Research
(1) A technique used to assess the protective effects of substances against heat-induced hemolysis of red blood cells.[1] (2) A laboratory method used to assess the protective effects of substances on red blood cell membranes, used to evaluate the anti-inflammatory properties of extracts.[2] (3) A measure of the ability of a substance to protect human red blood cells (HRBC) from lysis under stress conditions, which serves as an indicator of anti-inflammatory activity.[3] (4) A method used to assess the anti-inflammatory activity of compounds by preventing hypotonicity induced lysis of human red blood cells.[4] (5) A method used to test the protective effect of Coldenia procumbens extracts against damage to human red blood cell membranes, indicating its potential anti-inflammatory action.[5]
From: Ancient Science of Life
(1) A method used to evaluate the protective effects of substances on human red blood cell membranes against hemolysis.[6]
From: Ayushdhara journal
(1) A method used to assess the ability of Sivathai chooranam to stabilize human red blood cell membranes as an indicator of anti-inflammatory activity.[7]