{"title":"同步辐射成像对血液透析膜形态及人血清蛋白沉积的研究","authors":"A. Abdelrasoul","doi":"10.11159/icbes21.117","DOIUrl":null,"url":null,"abstract":"Extended Abstract End stage renal disease (ESRD) affects ~10% of the world’s population. Hemodialysis (HD) is a life-sustaining extracorporeal blood purifying method for patients with ESRD or kidney failure. This membrane-based therapy is associated with acute side effects, life-threatening chronic conditions, and unacceptably high morbidity and mortality rates. Due to the lack of endothelium functionality of the polymeric surfaces of HD membranes, their interaction with human serum proteins induces an inflammatory response and leads to numerous long-term clinical consequences that are in part determined by the degree of membrane biocompatibility[1]. Blood–membrane interactions trigger a multifaceted series of events of protein adsorption, in addition to the activation blood cells such as leukocytes, platelets, and red blood cells (RBCs) or indirectly activate them through a pathway that activates the complement system or coagulation factors [2,3]. Therefore, protein adsorption provokes a series of biochemical reactions that can lead to serious longand short-term side effects in HD patients [4]. In addition, the attachment of human serum proteins on membrane surface would significantly reduce uremic toxins clearance efficiency, especially protein bound uremic toxins and middle molecules. Membrane characteristics such as chemical composition, hydrophilicity, surface roughness, pore size and binding affinity influence the interactions and the attachments between human serum proteins and HD membranes hence they can impact the inflammatory response experienced by HD patients. This study highlighted an innovative investigation on the common HD membrane morphology available in Canadian hospitals, and its affinity for human serum protein attachment. Synchrotron based X-ray imaging techniques available at the Biomedical Imaging and Therapy (BMIT) beamline at the Canadian Light Source (CLS) has answered key questions of HD membrane morphology layer-by-layer and human serum protein transport in membrane channels. This study will highlight the proof that Synchrotron imaging techniques are effective for membrane characterization and protein deposition assessment through both qualitative and quantitative analyses.","PeriodicalId":433404,"journal":{"name":"Proceedings of the 7th World Congress on Electrical Engineering and Computer Systems and Science","volume":"49 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigation on Hemodialysis Membranes Morphology and Human Serum Proteins Depositions Using Synchrotron-based Imaging\",\"authors\":\"A. Abdelrasoul\",\"doi\":\"10.11159/icbes21.117\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Extended Abstract End stage renal disease (ESRD) affects ~10% of the world’s population. Hemodialysis (HD) is a life-sustaining extracorporeal blood purifying method for patients with ESRD or kidney failure. This membrane-based therapy is associated with acute side effects, life-threatening chronic conditions, and unacceptably high morbidity and mortality rates. Due to the lack of endothelium functionality of the polymeric surfaces of HD membranes, their interaction with human serum proteins induces an inflammatory response and leads to numerous long-term clinical consequences that are in part determined by the degree of membrane biocompatibility[1]. Blood–membrane interactions trigger a multifaceted series of events of protein adsorption, in addition to the activation blood cells such as leukocytes, platelets, and red blood cells (RBCs) or indirectly activate them through a pathway that activates the complement system or coagulation factors [2,3]. Therefore, protein adsorption provokes a series of biochemical reactions that can lead to serious longand short-term side effects in HD patients [4]. In addition, the attachment of human serum proteins on membrane surface would significantly reduce uremic toxins clearance efficiency, especially protein bound uremic toxins and middle molecules. Membrane characteristics such as chemical composition, hydrophilicity, surface roughness, pore size and binding affinity influence the interactions and the attachments between human serum proteins and HD membranes hence they can impact the inflammatory response experienced by HD patients. This study highlighted an innovative investigation on the common HD membrane morphology available in Canadian hospitals, and its affinity for human serum protein attachment. Synchrotron based X-ray imaging techniques available at the Biomedical Imaging and Therapy (BMIT) beamline at the Canadian Light Source (CLS) has answered key questions of HD membrane morphology layer-by-layer and human serum protein transport in membrane channels. This study will highlight the proof that Synchrotron imaging techniques are effective for membrane characterization and protein deposition assessment through both qualitative and quantitative analyses.\",\"PeriodicalId\":433404,\"journal\":{\"name\":\"Proceedings of the 7th World Congress on Electrical Engineering and Computer Systems and Science\",\"volume\":\"49 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the 7th World Congress on Electrical Engineering and Computer Systems and Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11159/icbes21.117\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the 7th World Congress on Electrical Engineering and Computer Systems and Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11159/icbes21.117","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Investigation on Hemodialysis Membranes Morphology and Human Serum Proteins Depositions Using Synchrotron-based Imaging
Extended Abstract End stage renal disease (ESRD) affects ~10% of the world’s population. Hemodialysis (HD) is a life-sustaining extracorporeal blood purifying method for patients with ESRD or kidney failure. This membrane-based therapy is associated with acute side effects, life-threatening chronic conditions, and unacceptably high morbidity and mortality rates. Due to the lack of endothelium functionality of the polymeric surfaces of HD membranes, their interaction with human serum proteins induces an inflammatory response and leads to numerous long-term clinical consequences that are in part determined by the degree of membrane biocompatibility[1]. Blood–membrane interactions trigger a multifaceted series of events of protein adsorption, in addition to the activation blood cells such as leukocytes, platelets, and red blood cells (RBCs) or indirectly activate them through a pathway that activates the complement system or coagulation factors [2,3]. Therefore, protein adsorption provokes a series of biochemical reactions that can lead to serious longand short-term side effects in HD patients [4]. In addition, the attachment of human serum proteins on membrane surface would significantly reduce uremic toxins clearance efficiency, especially protein bound uremic toxins and middle molecules. Membrane characteristics such as chemical composition, hydrophilicity, surface roughness, pore size and binding affinity influence the interactions and the attachments between human serum proteins and HD membranes hence they can impact the inflammatory response experienced by HD patients. This study highlighted an innovative investigation on the common HD membrane morphology available in Canadian hospitals, and its affinity for human serum protein attachment. Synchrotron based X-ray imaging techniques available at the Biomedical Imaging and Therapy (BMIT) beamline at the Canadian Light Source (CLS) has answered key questions of HD membrane morphology layer-by-layer and human serum protein transport in membrane channels. This study will highlight the proof that Synchrotron imaging techniques are effective for membrane characterization and protein deposition assessment through both qualitative and quantitative analyses.