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Process / pipelineBlood compatibility testing

Kipimo cha Hemolysis

Kipimo cha hemolysis ni njia sanifu ya kutathmini utangamano wa damu wa biomaterials kwa kupima kiwango ambacho nyenzo au dutu huharibu chembechembe nyekundu za damu (RBCs) na kusababisha kutolewa kwa hemoglobini. Kikiwa kimesanifishwa katika viwango kama vile ASTM F756 na ISO 10993-4, kipimo cha hemolysis ni muhimu kwa idhini ya udhibiti wa vifaa vinavyogusana na damu kama vile stenti, katheta, vali bandia za moyo, na utando wa hemodialysis. Kipimo hutoa kipimo rahisi, cha kiasi cha uwezo wa hemolytic unaohusiana na usalama wa kimatibabu.

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Vyanzo

  1. ASTM F756-17 (2017). Standard Practice for Assessment of Hemolytic Properties of Materials. ASTM International. link
  2. ISO 10993-4:2017. Biological Evaluation of Medical Devices. Part 4: Selection of tests for interactions with blood. link
  3. Tomos, M. S., Morrison, S., & Williams, D. F. (2012). Comparison of hemolytic methods for assessing the blood compatibility of biomaterials. Journal of Biomedical Materials Research, 105(7), 1926-1933. link

Jinsi ya kunukuu ukurasa huu

ScholarGate. (2026, June 3). Hemolysis Assay Red Blood Cell Toxicity Evaluation. ScholarGate. https://scholargate.app/sw/biomaterials/hemolysis-assay

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ScholarGateHemolysis Assay (Hemolysis Assay Red Blood Cell Toxicity Evaluation). Imepatikana 2026-06-17 kutoka https://scholargate.app/sw/biomaterials/hemolysis-assay · Seti ya data: https://doi.org/10.5281/zenodo.20539026