The effect of phagocytosis of poly(L‐lactic acid) fragments on cellular morphology and viability
- 1 December 1993
- journal article
- research article
- Published by Wiley in Journal of Biomedical Materials Research
- Vol. 27 (12) , 1569-1577
- https://doi.org/10.1002/jbm.820271214
Abstract
The aim of this study was to investigate the effect of phagocytosed poly(L-lactic acid) particles on the morpholgy and viability of phagocytes, mainly macrophages. Therefore, predegraded poly(L-lactic acid) (P-PLLA) and nontreated PLLA (N-PLLA) particles, both having diameters not exceeding 38 μm, were injected intraperitoneally in mice. P-PLLA particles were obtained by 25 kGy γ-irradiation of N-PLLA particles. N-PLLA and P-PLLA particles were injected using an 0.3% ethanol/0.9% saline solution intraperitoneally to the mice. We also studied the release of the absorbed ethanol as a possible model for the release of low molecular weight, potentially toxic products. As control, nondegradable polytetrafluoroethylene (PTFE) particles and the carrier solution were used. After 1, 2, 3, 4, 5, and 7 days, the cells of the abdominal cavity were harvested to study the effect of phagocytosis of polymer particles on phagocytic cell morphology and viability. Studies with transmission electron microscopy indicated that, upon injection of particles in the peritoneal cavity, macrophages demonstrated signs of cell damage, cell death, and cell lysis due to phagocytosis of a large amount of P-PLLA particles. The morphology of the cells that had phagocytosed the N-PLLA and PTFE particles did not differ substantially from those of control animals in which only the solution was injected. Also, in the controls, hardly any cell death and no debris was observed. When the PLLA particles were injected as a suspension in a 0.3% ethanol/0.9% saline solution, no difference was observed between N-PLLA and P-PLLA. After phagocytosis, both cause cell damage, sometimes leading to cell death. The highest numbers of necrotic cells were observed on day 2. The effects could be caused by the (peak) release of degradation products from P-PLLA fragments or by the release of the absorbed ethanol when the 0.3 ethanol/0.9 saline solution was used to administer the particles. In conclusion, it can be stated that cell damage, sometimes leading to cell death, may be caused by phagocytosed poly(L-lactic acid) particles. © 1993 John Wiley & Sons, Inc.Keywords
This publication has 23 references indexed in Scilit:
- In vivo degradation of processed dermal sheep collagen evaluated with transmission electron microscopyBiomaterials, 1991
- In vivo and in vitro degradation of glycine/DL‐lactic acid copolymersJournal of Biomedical Materials Research, 1989
- Improved Epon embedding for biomaterialsBiomaterials, 1989
- Murine hematopoietic cell surface antigen expressionImmunology Today, 1988
- Interleukin 4 induces cultured monocytes/macrophages to form giant multinucleated cells.The Journal of Experimental Medicine, 1988
- Effect of implantation site on phagocyte/polymer interaction and fibrous capsule formationBiomaterials, 1988
- In vivo biocompatibility studies. VII. Inflammatory response to polyethylene and to a cytotoxic polyvinylchlorideJournal of Biomedical Materials Research, 1986
- Macrophage PolykaryaCRC Critical Reviews in Toxicology, 1979
- Role of phagocytosis in the activation of macrophagesThe Journal of Experimental Medicine, 1978
- Lymph macrophages enter the germinal center of lymph nodes of guinea pigsCells Tissues Organs, 1977