Affiliations 

  • 1 Advanced Membrane Technology Research Centre (AMTEC), Universiti Teknologi Malaysia, 81310 Skudai, Johor, Malaysia
  • 2 Advanced Membrane Technology Research Centre (AMTEC), Universiti Teknologi Malaysia, 81310 Skudai, Johor, Malaysia. Electronic address: juhana@utm.my
  • 3 Institute of Medical Molecular and Biotechnology (IMMB), Faculty of Medicine, Universiti Teknologi MARA (UiTM), 47000 Sungai Buloh, Selangor, Malaysia
  • 4 Membrane Science and Technology Research Group (MSTRG), Chemistry Department, Faculty of Science and Technology, Universitas Airlangga, Surabaya 60115, Indonesia
Int J Biol Macromol, 2025 Feb 17;305(Pt 2):141231.
PMID: 39971062 DOI: 10.1016/j.ijbiomac.2025.141231

Abstract

The study aims to enhance the biocompatibility of haemodialysis membranes to reduce mortality risks in end-stage renal disease (ESRD) patients by addressing oxidative stress and thrombus formation. A novel Chitosan Diallyl Disulfide Nanoparticle (CNP/DADS) complex was immobilised into PSF membranes at various concentrations. The most optimal membrane, with 0.3 wt% CNP, demonstrated the highest KUF of 116 mL/m2.h.mmHg, 95.7 % BSA rejection, and significant urea, creatinine, and lysozyme clearance rates. This was attributed to increased hydrophilicity, improved morphological structure with higher porosity, and a thinner membrane skin layer. However, CNP/DADS-immobilised PSF HFM showed reduced performance due to denser morphological structures. Despite this, CNP/DADS-immobilised membranes met high-flux standards and exhibited enhanced biocompatibility, low haemolysis percentage, reduced protein adsorption and platelet adhesion, and less complement activation. They also significantly prolonged clotting times (P 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.