The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria

Abstract Background Prosthetic joint infection (PJI) is a serious complication of orthopedic implant surgery. Treatment often includes the use of an antibiotic-loaded Polymethyl methacrylate (PMMA) bone cement spacer. Several antibiotics are commonly used for the preparation of these spacers, but du...

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Main Authors: Matthias Schmid, Oliver Steiner, Lisa Fasshold, Walter Goessler, Anna-Maria Holl, Klaus-Dieter Kühn
Format: Article
Language:English
Published: BMC 2020-08-01
Series:European Journal of Medical Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40001-020-00428-z
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spelling doaj-7a8f22bfb4db47648e5b86bd55c631372020-11-25T03:01:41ZengBMCEuropean Journal of Medical Research2047-783X2020-08-0125111010.1186/s40001-020-00428-zThe stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteriaMatthias Schmid0Oliver Steiner1Lisa Fasshold2Walter Goessler3Anna-Maria Holl4Klaus-Dieter Kühn5Department of Orthopaedics and Orthopaedic Surgery, Medical University GrazInstitute of Chemistry, Analytical Chemistry for Health and Environment, University of GrazInstitute of Chemistry, Analytical Chemistry for Health and Environment, University of GrazInstitute of Chemistry, Analytical Chemistry for Health and Environment, University of GrazClinical Affairs, Heraeus Medical GmbHDepartment of Orthopaedics and Orthopaedic Surgery, Medical University GrazAbstract Background Prosthetic joint infection (PJI) is a serious complication of orthopedic implant surgery. Treatment often includes the use of an antibiotic-loaded Polymethyl methacrylate (PMMA) bone cement spacer. Several antibiotics are commonly used for the preparation of these spacers, but due to the increasing number of infections with resistant Gram-negative bacteria, there is a need for the use of carbapenem antibiotics such as meropenem and imipenem as drugs of last resort. Unfortunately, the reaction heat generated during the preparation of the bone cement can be a major problem for the stability of these antibiotics. In the present study, the stability of meropenem and imipenem was tested before and after the admixture to PMMA bone cements. Methods High-performance liquid chromatography with ion-pairing reversed-phase separation and spectrophotometric detection was used for analysis. Stability tests with meropenem and imipenem were performed with antibiotics in solution and solid form at different temperatures (37 °C, 45 °C, 60 °C, 90 °C) and times (30 min, 60 min, 120 min). To test the stability of both antibiotics in PMMA after exposure to the reaction heat during polymerization, three different bone cements were used to generate specimens that contained defined amounts of antibiotics. Reaction heat was measured. The form bodies were mechanically crushed and aliquots were dissolved in ethyl acetate. Samples were prepared for HPLC DAD analysis. Results Meropenem and imipenem showed the highest degradation levels after heat stressed in solution, with maximum levels of 75% and 95%, respectively. In solid form, degradation levels decreased dramatically for meropenem (5%) and imipenem (13%). Stability tests of both carbapenems in bone cement showed that they remained largely stable during PMMA polymerization, with retrieved amounts of about 70% in Palacos® R and Copal® G+V, and between 80 and 90% in Copal® spacem. Conclusions In contrast to the results of meropenem and imipenem in solution, both antibiotics remain stable in solid form and mostly stable in the cement after PMMA polymerization. The low degradation levels of both antibiotics after exposure to temperatures > 100 °C allow the conclusion that they can potentially be used for an application in PMMA cements.http://link.springer.com/article/10.1186/s40001-020-00428-zImipenemMeropenemCarbapenemsPMMA cementPeriprosthetic joint infectionLocal antibiotic therapy
collection DOAJ
language English
format Article
sources DOAJ
author Matthias Schmid
Oliver Steiner
Lisa Fasshold
Walter Goessler
Anna-Maria Holl
Klaus-Dieter Kühn
spellingShingle Matthias Schmid
Oliver Steiner
Lisa Fasshold
Walter Goessler
Anna-Maria Holl
Klaus-Dieter Kühn
The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
European Journal of Medical Research
Imipenem
Meropenem
Carbapenems
PMMA cement
Periprosthetic joint infection
Local antibiotic therapy
author_facet Matthias Schmid
Oliver Steiner
Lisa Fasshold
Walter Goessler
Anna-Maria Holl
Klaus-Dieter Kühn
author_sort Matthias Schmid
title The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
title_short The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
title_full The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
title_fullStr The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
title_full_unstemmed The stability of carbapenems before and after admixture to PMMA-cement used for replacement surgery caused by Gram-negative bacteria
title_sort stability of carbapenems before and after admixture to pmma-cement used for replacement surgery caused by gram-negative bacteria
publisher BMC
series European Journal of Medical Research
issn 2047-783X
publishDate 2020-08-01
description Abstract Background Prosthetic joint infection (PJI) is a serious complication of orthopedic implant surgery. Treatment often includes the use of an antibiotic-loaded Polymethyl methacrylate (PMMA) bone cement spacer. Several antibiotics are commonly used for the preparation of these spacers, but due to the increasing number of infections with resistant Gram-negative bacteria, there is a need for the use of carbapenem antibiotics such as meropenem and imipenem as drugs of last resort. Unfortunately, the reaction heat generated during the preparation of the bone cement can be a major problem for the stability of these antibiotics. In the present study, the stability of meropenem and imipenem was tested before and after the admixture to PMMA bone cements. Methods High-performance liquid chromatography with ion-pairing reversed-phase separation and spectrophotometric detection was used for analysis. Stability tests with meropenem and imipenem were performed with antibiotics in solution and solid form at different temperatures (37 °C, 45 °C, 60 °C, 90 °C) and times (30 min, 60 min, 120 min). To test the stability of both antibiotics in PMMA after exposure to the reaction heat during polymerization, three different bone cements were used to generate specimens that contained defined amounts of antibiotics. Reaction heat was measured. The form bodies were mechanically crushed and aliquots were dissolved in ethyl acetate. Samples were prepared for HPLC DAD analysis. Results Meropenem and imipenem showed the highest degradation levels after heat stressed in solution, with maximum levels of 75% and 95%, respectively. In solid form, degradation levels decreased dramatically for meropenem (5%) and imipenem (13%). Stability tests of both carbapenems in bone cement showed that they remained largely stable during PMMA polymerization, with retrieved amounts of about 70% in Palacos® R and Copal® G+V, and between 80 and 90% in Copal® spacem. Conclusions In contrast to the results of meropenem and imipenem in solution, both antibiotics remain stable in solid form and mostly stable in the cement after PMMA polymerization. The low degradation levels of both antibiotics after exposure to temperatures > 100 °C allow the conclusion that they can potentially be used for an application in PMMA cements.
topic Imipenem
Meropenem
Carbapenems
PMMA cement
Periprosthetic joint infection
Local antibiotic therapy
url http://link.springer.com/article/10.1186/s40001-020-00428-z
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