AI Article Synopsis

  • The Bioartificial Liver (BAL) is an extracorporeal support system designed for patients with liver dysfunction, utilizing alginate encapsulated liver spheroids (AELS).
  • A study evaluated the toxicity of the cryoprotectant DMSO on AELS during cryopreservation, finding that a 12% DMSO concentration was safe while exposure to 40% DMSO was toxic at higher temperatures.
  • The research also established an effective washing process to remove DMSO after thawing, ensuring the BAL is safe and viable for clinical use.

Article Abstract

The Bioartificial Liver (BAL) is an extra-corporeal liver support designed to support the function of the Liver in patients with impaired liver function. The BAL biomass consists of alginate encapsulated liver spheroids (AELS). To facilitate rapid delivery of a BAL to patients the AELS are cryopreserved using a DMSO-containing cryoprotectant solution. This study assesses toxicity of DMSO in AELS at concentrations and temperatures relevant to the cryopreservation and recovery process of a cellular biomass. Additionally, it develops a process to remove DMSO from AELS before delivery of cell product to patients. Exposure of AELS to DMSO, at a concentration of 12% (v/v) for 10 min did not have a negative effect on the viability of the AELS up to 24 h after exposure, irrespective of the exposure temperature between 37 C and 0 C. Evidence of toxicity was only seen with exposure to 40% (v/v) DMSO, which was more notable at warm temperatures. Post-Thaw removal of DMSO was measured by determining the DMSO concentration of the post-thaw washes using refractometry. Washing AELS 3 times in tapering concentrations of Glucose supplemented DMEM at an AELS:wash ratio of 1:2 was sufficient to reduce DMSO to undetectable levels (<1%). The study demonstrated that the thawing method minimised DMSO toxicity to the BAL biomass, and the post-thaw washing protocol successfully removed all the DMSO present in the cryopreserved BAL. Thereby enabling effective cryopreservation of the BAL for future clinical translation.

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http://dx.doi.org/10.1016/j.cryobiol.2022.03.007DOI Listing

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