Nguyen Alexander K, Goering Peter L, Elespuru Rosalie K, Sarkar Das Srilekha, Narayan Roger J
Joint UNC/NCSU Department of Biomedical Engineering, North Carolina State University, Raleigh, NC 27695, USA.
Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 20993, USA.
Polymers (Basel). 2020 Jul 3;12(7):1489. doi: 10.3390/polym12071489.
Lithium phenyl (2,4,6-trimethylbenzoyl) phosphinate (LAP) is a free radical photo-initiator used to initiate free radical chain polymerization upon light exposure, and is combined with gelatin methacryloyl (GelMA) to produce a photopolymer used in bioprinting. The free radicals produced under bioprinting conditions are potentially cytotoxic and mutagenic. Since these photo-generated free radicals are highly-reactive but short-lived, toxicity assessments should be conducted with light exposure. In this study, photorheology determined that 10 min exposure to 9.6 mW/cm 405 nm light from an LED light source fully crosslinked 10 wt % GelMA with >3.4 mmol/L LAP, conditions that were used for subsequent cytotoxicity and mutagenicity assessments. These conditions were cytotoxic to M-1 mouse kidney collecting duct cells, a cell type susceptible to lithium toxicity. Exposure to ≤17 mmol/L (0.5 wt %) LAP without light was not cytotoxic; however, concurrent exposure to ≥3.4 mmol/L LAP and light was cytotoxic. No condition of LAP and/or light exposure evaluated was mutagenic in bacterial reverse mutation assays using strains TA98, TA100 and WP2 uvrA. These data indicate that the combination of LAP and free radicals generated from photo-excited LAP is cytotoxic, but mutagenicity was not observed in bacteria under typical bioprinting conditions.
苯基(2,4,6-三甲基苯甲酰基)次膦酸锂(LAP)是一种自由基光引发剂,用于在光照下引发自由基链式聚合反应,并与甲基丙烯酰化明胶(GelMA)结合以制备用于生物打印的光聚合物。生物打印条件下产生的自由基可能具有细胞毒性和致突变性。由于这些光生自由基具有高反应活性但寿命较短,因此毒性评估应在光照条件下进行。在本研究中,光流变学测定,用LED光源发出的9.6 mW/cm 405 nm光照射10分钟,可使10 wt%的GelMA与>3.4 mmol/L的LAP完全交联,这些条件用于后续的细胞毒性和致突变性评估。这些条件对M-1小鼠肾集合管细胞具有细胞毒性,该细胞类型对锂毒性敏感。在无光照条件下暴露于≤17 mmol/L(0.5 wt%)的LAP不会产生细胞毒性;然而,同时暴露于≥3.4 mmol/L的LAP和光照则具有细胞毒性。在使用TA98、TA100和WP2 uvrA菌株的细菌回复突变试验中,所评估的LAP和/或光照条件均未显示出致突变性。这些数据表明,LAP与光激发产生的自由基的组合具有细胞毒性,但在典型的生物打印条件下,未在细菌中观察到致突变性。