Biagiotti Marco, Bassani Giulia Alessandra, Chiarini Anna, Vincoli Valentina Teodolinda, Dal Prà Ilaria, Cosentino Cesare, Alessandrino Antonio, Taddei Paola, Freddi Giuliano
Silk Biomaterials S.r.l, Lomazzo, Italy.
Department of Surgery, Dentistry, Pediatrics and Gynecology, Human Histology and Embryology Unit, Medical School, University of Verona, Verona, Italy.
Front Bioeng Biotechnol. 2022 Jan 27;10:833157. doi: 10.3389/fbioe.2022.833157. eCollection 2022.
The dissolution of silk fibroin (SF) films in formic acid (FA) for the preparation of electrospinning dopes is widely exploited to produce electrospun SF scaffolds. The SILKBridge nerve conduit is an example of medical device having in its wall structure an electrospun component produced from an FA spinning dope. Though highly volatile, residual FA remains trapped into the bulk of the SF nanofibers. The purpose of this work is to investigate the type and strength of the interaction between FA and SF in electrospun mats, to quantify its amount and to evaluate its possible toxicological impact on human health. The presence of residual FA in SF mats was detected by FTIR and Raman spectroscopy (new carbonyl peak at about 1,725 cm) and by solid state NMR, which revealed a new carbonyl signal at about 164.3 ppm, attributed to FA by isotopic C substitution. Changes occurred also in the spectral ranges of hydroxylated amino acids (Ser and Thr), demonstrating that FA interacted with SF by forming formyl esters. The total amount of FA was determined by HS-GC/MS analysis and accounted for 247 ± 20 μmol/g. The greatest part was present as formyl ester, a small part (about 3%) as free FA. Approximately 17% of the 1,500 μmol/g of hydroxy amino acids (Ser and Thr) theoretically available were involved in the formation of formyl esters. Treatment with alkali (NaCO) succeeded to remove the greatest part of FA, but not all. Alkali-treated electrospun SF mats underwent morphological, physical, and mechanical changes. The average diameter of the fibers increased from about 440 nm to about 480 nm, the mat shrunk, became stiffer (the modulus increased from about 5.5 MPa to about 7 MPa), and lost elasticity (the strain decreased from about 1 mm/mm to about 0.8 mm/mm). Biocompatibility studies with human adult dermal fibroblasts did not show significant difference in cell proliferation (313 ± 18 and 309 ± 23 cells/mm for untreated and alkali-treated SF mat, respectively) and metabolic activity. An in-depth evaluation of the possible toxicological impact of residual FA was made using the SILKBridge nerve conduit as case study, following the provisions of the ISO 10993-1 standard. The Potential Patient Daily Intake, calculated from the total amount of FA determined by HS-GC/MS, was 2.4 mg/day and the Tolerable Exposure level was set to 35.4 mg/day. This allowed to obtain a value of the Margin of Safety of 15, indicating that the amount of FA left on SF mats after electrospinning does not raise concerns for human health.
丝素蛋白(SF)膜在甲酸(FA)中溶解以制备静电纺丝原液,这一方法被广泛用于生产静电纺丝SF支架。SILKBridge神经导管就是一种医疗设备,其壁结构中含有由FA纺丝原液制成的静电纺丝组件。尽管FA极易挥发,但仍有残留被困在SF纳米纤维的主体中。本工作的目的是研究静电纺丝垫中FA与SF之间相互作用的类型和强度,量化其含量,并评估其对人体健康可能产生的毒理学影响。通过傅里叶变换红外光谱(FTIR)和拉曼光谱(约1725 cm处出现新的羰基峰)以及固态核磁共振检测到SF垫中存在残留FA,固态核磁共振显示在约164.3 ppm处有一个新的羰基信号,通过同位素碳取代确定其归属于FA。羟基化氨基酸(丝氨酸和苏氨酸)的光谱范围也发生了变化,表明FA通过形成甲酰酯与SF相互作用。通过顶空-气相色谱/质谱(HS-GC/MS)分析确定FA的总量为247±20 μmol/g。其中大部分以甲酰酯形式存在,一小部分(约3%)为游离FA。理论上可利用的1500 μmol/g羟基氨基酸(丝氨酸和苏氨酸)中约17%参与了甲酰酯的形成。用碱(碳酸钠)处理成功去除了大部分FA,但并非全部。碱处理后的静电纺丝SF垫发生了形态、物理和机械变化。纤维的平均直径从约440 nm增加到约480 nm,垫子收缩,变得更硬(模量从约5.5 MPa增加到约7 MPa),并失去弹性(应变从约1 mm/mm降低到约0.8 mm/mm)。对人类成人皮肤成纤维细胞的生物相容性研究表明,细胞增殖(未处理和碱处理的SF垫分别为313±18和309±23个细胞/mm²)和代谢活性没有显著差异。以SILKBridge神经导管为例,按照ISO 10993-1标准的规定,对残留FA可能产生的毒理学影响进行了深入评估。根据HS-GC/MS测定的FA总量计算出的潜在患者每日摄入量为2.4 mg/天,可耐受暴露水平设定为35.4 mg/天。由此得出安全系数为15,表明静电纺丝后留在SF垫上的FA量不会对人体健康造成担忧。