Nelson S K, Wataha J C, Lockwood P E
Department of Oral Rehabilitation, Medical College of Georgia, School of Dentistry, Augusta, GA 30912-1260, USA.
J Prosthet Dent. 1999 Jun;81(6):715-20. doi: 10.1016/s0022-3913(99)70112-5.
Short-term (72-168 hours) in vitro testing of dental casting alloys for cytotoxicity may not reflect in vivo biocompatibility. An accelerated test for evaluation of dental casting alloy cytotoxicity could help screen newly developed alloys more rapidly and accurately.
This study evaluated a method of accelerating alloy cytotoxicity by short-term conditioning of alloys. Cytotoxicity and mass release of these conditioned alloys were compared with alloys conditioned for 10 months or unconditioned alloys. The hypothesis was that a short-term conditioning procedure could be developed that would give cytotoxicity and mass release values similar to alloys exposed to a biologic solution for 10 months.
Dental casting alloys were conditioned in either saline, cell-culture medium, or a saline/bovine serum albumin (BSA) solution for 168 hours before standard in vitro cytotoxicity testing. Eight types of casting alloys with a range of nobilities (98% to 0%) were tested (n = 6). Controls were Teflon (Tf). Conditioned alloys were placed in direct contact with Balb/c fibroblasts for 72 hours, and cell viability was measured by succinic dehydrogenase activity (MTT method) relative to Tf controls. Elements released into the conditioning solutions were measured by atomic absorption spectroscopy. The cytotoxicities of conditioned alloys and total mass released were compared with unconditioned alloys (0 month) and alloys that were exposed to cell culture medium for 10 months. ANOVA and Tukey multiple comparison intervals (alpha =. 05) were used to compare mass released and cytotoxicity.
Conditioning for 168 hours altered the cytotoxicity of the alloys. The saline/BSA conditioning solution reduced cytotoxicity of the alloys compared with unconditioned alloys, except for the Ni-Cr alloy. Other conditioning solutions were not as uniform in their effects, some increasing toxicity, others decreasing it. Overall, the saline/BSA solution was the most effective at changing alloy cytotoxicity from the unconditioned (0 month) toward the 10-month values. Mass loss during saline/BSA conditioning most closely approximated 10-month loss for most alloys.
Conditioning of casting alloys appeared to be a useful method for predicting long-term cytotoxicity with a short-term in vitro test, but all conditioning solutions were not equivalent.
牙科铸造合金的细胞毒性短期(72 - 168小时)体外测试可能无法反映体内生物相容性。一种用于评估牙科铸造合金细胞毒性的加速测试方法有助于更快速、准确地筛选新开发的合金。
本研究评估了一种通过对合金进行短期预处理来加速合金细胞毒性的方法。将这些预处理合金的细胞毒性和质量释放与预处理10个月的合金或未处理合金进行比较。假设是可以开发一种短期预处理程序,其细胞毒性和质量释放值与暴露于生物溶液10个月的合金相似。
在进行标准体外细胞毒性测试前,将牙科铸造合金在生理盐水、细胞培养基或生理盐水/牛血清白蛋白(BSA)溶液中预处理168小时。测试了八种不同贵金属含量范围(98%至0%)的铸造合金(n = 6)。对照组为聚四氟乙烯(Tf)。将预处理合金与Balb / c成纤维细胞直接接触72小时,并通过相对于Tf对照组的琥珀酸脱氢酶活性(MTT法)测量细胞活力。通过原子吸收光谱法测量释放到预处理溶液中的元素。将预处理合金的细胞毒性和总质量释放与未处理合金(0个月)和暴露于细胞培养基10个月的合金进行比较。使用方差分析和Tukey多重比较区间(α = 0.05)来比较质量释放和细胞毒性。
168小时的预处理改变了合金的细胞毒性。与未处理合金相比,生理盐水/BSA预处理溶液降低了合金的细胞毒性,但镍铬合金除外。其他预处理溶液的效果不太一致,有些增加毒性,有些降低毒性。总体而言,生理盐水/BSA溶液在将合金细胞毒性从未处理(0个月)转变为10个月的值方面最有效。对于大多数合金,生理盐水/BSA预处理期间的质量损失最接近10个月的损失。
铸造合金的预处理似乎是一种通过短期体外测试预测长期细胞毒性的有用方法,但并非所有预处理溶液都等效。