Transmission electron microscopy of intracellular particles of polyethylene from joint replacement prostheses: size distribution and cellular response

Citation
Eb. Benz et al., Transmission electron microscopy of intracellular particles of polyethylene from joint replacement prostheses: size distribution and cellular response, BIOMATERIAL, 22(21), 2001, pp. 2835-2842
Citations number
27
Categorie Soggetti
Multidisciplinary
Journal title
BIOMATERIALS
ISSN journal
01429612 → ACNP
Volume
22
Issue
21
Year of publication
2001
Pages
2835 - 2842
Database
ISI
SICI code
0142-9612(200111)22:21<2835:TEMOIP>2.0.ZU;2-0
Abstract
The objectives of this transmission electron microscopy study of peri-impla nt tissues retrieved at revision arthroplasty were to (1) determine the siz e distribution of intracellular polyethylene particles, and (2) assess the cellular response to phagocytosed polyethylene particles as revealed by the condition of the cellular organelles. The frequency distributions of intra cellular polyethylene particle sizes for 15 cases of total hip replacement showed that more than 75% of the particles had lengths of less than 0.5 mum . More than 90% of the particles were less than 1.0 mum in size. In compari son, the frequency distribution for the particles in cells comprising tissu e retrieved from three total knee replacement prostheses showed that only 4 3% of the particles were less than 0.5 mum in length and 72% were less than 1 mum in size. There was no statistically significant difference in the me an particle length between the specimens from the hip and knee patients. Th e majority of the cells containing polyethylene were without signs of degen eration. The cytoplasmic and nuclear membranes were intact. Several electro n lucent voids which once contained polyethylene particles were seen surrou nded by several healthy appearing mitochondria, which displayed sharp membr anes and intact cristae. There were no signs of a cytotoxic response to pol yethylene at the ultrastructural level. (C) 2001 Elsevier Science Ltd. All rights reserved.