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Accurate and sensitive low-density lipoprotein (LDL) detection based on the proximity ligation assisted rolling circle amplification (RCA).
Zhang, Xingyu; Li, Jie; Yang, Mei; Huang, Hong; Wang, Hao; Zhang, Hongmin.
Afiliação
  • Zhang X; Department of Endocrinology, People's Hospital of Chongqing Liang Jiang New Area, No. 199, Renxing Road, Chongqing, China 401121. zhanghongmin@stu.cqmu.edu.cn.
  • Li J; Department of Clinical Biochemistry, The Key Laboratory of Laboratory Medical Diagnostics in the Ministry of Education, College of Laboratory Medicine, Chongqing Medical University, Chongqing, China 400016.
  • Yang M; Department of Endocrinology, People's Hospital of Chongqing Liang Jiang New Area, No. 199, Renxing Road, Chongqing, China 401121. zhanghongmin@stu.cqmu.edu.cn.
  • Huang H; Department of Clinical Laboratory, People's Hospital of Chongqing Liang Jiang New Area, Chongqing, China 401121.
  • Wang H; Department of Endocrinology, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China 400016.
  • Zhang H; Department of Endocrinology, People's Hospital of Chongqing Liang Jiang New Area, No. 199, Renxing Road, Chongqing, China 401121. zhanghongmin@stu.cqmu.edu.cn.
Anal Methods ; 16(13): 1894-1900, 2024 Mar 28.
Article em En | MEDLINE | ID: mdl-38482952
ABSTRACT
Metabolic-associated fatty liver disease (MAFLD) is one of the leading causes of mortality from chronic diseases worldwide, and it is strongly linked to dyslipidemia. Dyslipidemia typically presents as an elevated concentration of low density lipoprotein (LDL). Hence, accurate quantification of LDL particles is crucial for predicting the risks of cardiovascular illnesses. Nevertheless, conventional techniques can merely provide indirect measurements of LDL particle concentrations through the detection of cholesterol or proteins within LDL particles, and they often require significant effort and time. Therefore, an accurate and effective method for identifying intact LDL particles is highly desired. We have devised a method that allows for the measurement of LDL concentration without the need for isolation. This method relies on proximity ligation rolling circle amplification (RCA). This technique enables the direct and precise measurement of the concentration of "actual" LDL particles, rather than measuring the cholesterol content inside LDL. It has a detection limit of 7.3 µg dL-1, which also meets the requirements for analyzing lipoproteins in clinical samples. Hence, this platform exhibits immense potential in clinical applications and health management.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dislipidemias / Lipoproteínas LDL Limite: Humans Idioma: En Revista: Anal Methods Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dislipidemias / Lipoproteínas LDL Limite: Humans Idioma: En Revista: Anal Methods Ano de publicação: 2024 Tipo de documento: Article