2021
DOI: 10.3390/ijms222111503
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Hyaluronic Acid as a Carrier Supports the Effects of Glucocorticoids and Diminishes the Cytotoxic Effects of Local Anesthetics in Human Articular Chondrocytes In Vitro

Abstract: The current study aimed to investigate the cytotoxicity of co-administrating local anesthetics (LA) with glucocorticoids (GC) and hyaluronic acid (HA) in vitro. Human articular cartilage was obtained from five patients undergoing total knee arthroplasty. Chondrocytes were isolated, expanded, and seeded in 24-well plates for experimental testing. LA (lidocaine, bupivacaine, ropivacaine) were administered separately and co-administered with the following substances: GC, HA, and GC/HA. Viability was confirmed by … Show more

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Cited by 7 publications
(6 citation statements)
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“…A number of studies have noted significantly higher cell viability in cultured human chondrocytes after exposure to ropivacaine 1%, similar to control levels, than what was seen after exposure to either bupivacaine 0.25% or lidocaine 1% for 1 h. 57 Shaw et al 58 compared the chondrotoxicity of bupivacaine (0.5%), ropivacaine (0.5%), and 1.3% liposomal bupivacaine on bovine chondrocyte derived cells. Cells were plated and exposed to each solution without dilution for 1 h, then were washed and allowed to incubate in medium for an additional 23 h. Liposomal bupivacaine had the highest cell viability (as assessed by flow cytometry) of all treatment groups, followed by ropivacaine and bupivacaine, which had the lowest chondrocyte viability of the anaesthetic solutions tested.…”
Section: In Vitro Studies Of Toxicitymentioning
confidence: 88%
See 1 more Smart Citation
“…A number of studies have noted significantly higher cell viability in cultured human chondrocytes after exposure to ropivacaine 1%, similar to control levels, than what was seen after exposure to either bupivacaine 0.25% or lidocaine 1% for 1 h. 57 Shaw et al 58 compared the chondrotoxicity of bupivacaine (0.5%), ropivacaine (0.5%), and 1.3% liposomal bupivacaine on bovine chondrocyte derived cells. Cells were plated and exposed to each solution without dilution for 1 h, then were washed and allowed to incubate in medium for an additional 23 h. Liposomal bupivacaine had the highest cell viability (as assessed by flow cytometry) of all treatment groups, followed by ropivacaine and bupivacaine, which had the lowest chondrocyte viability of the anaesthetic solutions tested.…”
Section: In Vitro Studies Of Toxicitymentioning
confidence: 88%
“…Cell density and synoviocyte viability were further reduced ex vivo in the methylprednisolone/lidocaine group at day seven, leading the authors to conclude there is potential for cytotoxicity to both chondrocytes and synoviocytes treated with a corticosteroid/LA combination; however, the individual contributions of LA versus steroids was not investigated. Moser et al 57 investigated in vitro the effects of various LA (lidocaine, bupivacaine, ropivacaine) combined with glucocorticoids (GC), hyaluronic acid (HA) or both using cultured human chondrocytes. When examined under a microscope, chondrocytes had increased branching and enhanced attachment when exposed to HA and GC/HA compared to local anaesthetics alone or local anaesthetics with glucocorticoids.…”
Section: Additives To Local Anaesthetic Injectionsmentioning
confidence: 99%
“…[32] Therapeutic trajectory following intra-articular hyaluronic acid injection in KOA - meta-analysis yielded the same conclusion, namely that IAHA is efficacious at 4 weeks, reaches maximum efficacy at 8 weeks, and exerts detectable residual effects at 24 weeks. [33] In addition, a number of studies [34] have investigated whether HA can attenuate the cytotoxic effects of glucocorticoids and anesthetics. One study examined the efficacy and safety of Diclofenac-Hyaluronate (DF-HA) Conjugate (Diclofenac Etalhyalu-rate) in the treatment of KOA utilizing DF covalently linked to a high molecular weight fermented HA.…”
Section: Discussionmentioning
confidence: 99%
“…Cell isolation from shavered or scalpel minced cartilage fragments was performed overnight via enzymatic release using Liberase™ (0.2 WU/mL, Roche Diagnostics GmbH, Mannheim, Germany) in a shaker at 30 rpm at 37 °C, as previously described [ 17 ]. On the second day, 1*10 5 cells were resuspended in 100 µl annexin staining buffer (10 mM CaCl 2 , HEPES) and stained with 5 µl PE-labeled annexin V and 1 µl 7-Aminoactinomycin (7-AAD) from an apoptosis detection kit (BD Pharmingen, #559793).…”
Section: Methodsmentioning
confidence: 99%