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Comparison of mammalian cell suspension culture methods using poly(lactic-co-glycolic acid) nanospheres and dextran microcarriers

机译:使用聚乳酸-乙醇酸纳米球和葡聚糖微载体的哺乳动物细胞悬浮培养方法的比较

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Previously, we have developed a novel method for suspension culture of anchorage-dependent animal cells using biodegradable polymer nanospheres. In this study, we compared the polymer nanosphere culture method to dextran microcarrier culture method, which is a conventional suspension culture method. Most of human dermal fibroblasts (91 ± 5 %) cultured with polymer nanospheres formed aggregates on day 2. Most of cells (92 ± 7 %) attached onto microcarriers by 4 h. Microcarrier culture method had a lower apoptotic activity (3.4 folds on day 4), compared to the nanosphere culture. The microcarrier culture method had a higher cell growth (2.4-fold versus 1.7-fold growth on day 4) than the nanosphere culture. Although the polymer nanosphere culture method did not yield better outcomes than the microcarrier culture, the polymer nanosphere culture method may offer advantages over the microcarrier culture method with respect to cell protection from the shear stress during agitation at high speed and cell transplantation without enzyme digestion process to harvest cultured cells.
机译:以前,我们已经开发了一种使用可生物降解的聚合物纳米球悬浮培养锚定依赖性动物细胞的新方法。在这项研究中,我们将聚合物纳米球培养方法与葡聚糖微载体培养方法进行了比较,后者是常规的悬浮培养方法。与聚合物纳米球一起培养的大多数人类皮肤成纤维细胞(91±5%)在第2天形成聚集体。大多数细胞(92±7%)在4 h时附着在微载体上。与纳米球培养相比,微载体培养法具有较低的凋亡活性(第4天为3.4倍)。与纳米球培养相比,微载体培养方法的细胞生长更高(第4天的生长速度是2.4倍,而第4天是1.7倍)。尽管聚合物纳米球培养方法没有比微载体培养方法产生更好的结果,但是在高速搅拌和不进行酶消化过程的细胞移植过程中,细胞纳米保护方法免受微切应力的影响,聚合物纳米球培养方法可能比微载体培养方法更具优势。收获培养的细胞。

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