Polyamide 6 composite membranes: Properties and in vitro biocompatibility evaluation

• Published in: Journal of biomaterials science. Polymer ed. 2001-01, Vol.12 (1), p.125-136
• Main Authors: V.Risbud, Makarand, Bhonde, Ramesh R.
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Animals; Antigens, CD - biosynthesis; B7-2 Antigen; BIOCOMPATIBILITY; Biocompatible Materials; Caprolactam - analogs & derivatives; Caprolactam - chemistry; Cell Division; Cell Membrane - chemistry; Cell Separation; CHARACTERIZATION; CHONDROITIN SULFATE; Chondroitin Sulfates - chemistry; Coloring Agents - pharmacology; COMPOSITE; DNA Damage; Flow Cytometry; Gelatin - chemistry; Humans; Leukocyte Common Antigens - biosynthesis; Lipopolysaccharide Receptors - biosynthesis; Lymphocytes - metabolism; Macrophage-1 Antigen - biosynthesis; Membrane Glycoproteins - biosynthesis; Membranes, Artificial; Mice; Mice, Inbred BALB C; Microscopy, Confocal; Neutral Red - pharmacology; POLYAMIDE & GELATIN; Polymers - chemistry; Spleen - metabolism; Tetrazolium Salts - pharmacology; Thiazoles - pharmacology
• ISSN: 0920-5063; 1568-5624
• DOI: 10.1163/156856201744498

The aim of the present study was to develop polyamide 6 membrane blended with gelatin and chondroitin sulfate using the phase precipitation method and evaluate its in vitro biocompatibility. Morphology of membranes was studied by laser scanning confocal microscopy which allowed the nondestructive visualization of internal bulk morphology of membranes. Membranes exhibited porous morphology with pores spanning across the membrane width with interconnections at various depths. Membranes showed adequate mechanical properties with tensile strengths of 20.10 ± 0.64 MPa, % strain of 3.01±0.07, and modulus of 1082.50±23.50 MPa. In vitro biocompatibility of membranes by direct contact test did not show degenerative effects on NIH3T3 cells and also its leach-out products (LOP), as determined by tetrazolium (MTT) and neutral red uptake (NRU) assay. Mouse peritoneal macrophage cultured in contact with membranes and PTFE control showed comparable expression of activation markers such as CD11b/CD18, CD45, CD14, and CD86 suggesting the membranes' non-activating nature. Membrane LOP did not induce excessive proliferation of mouse splenocytes suggesting its non-antigenic nature. Preliminary blood compatibility of membranes was observed with no detectable hemolysis in static incubation assay. Taken collectively, the present data demonstrate that polyamide 6 composite membranes are biocompatible and prospective candidates for tissue engineering applications.