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

机译:哺乳动物细胞悬浮培养方法使用聚(乳酸 - 共乙醇酸)纳米球和葡聚糖微载体的比较

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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的锚固依赖性动物细胞悬浮培养的新方法。在该研究中,我们将聚合物纳米培养方法与葡聚糖微载体培养方法进行比较,这是常规悬浮培养方法。用聚合物纳米球培养的大多数人的皮肤成纤维细胞(91±5%)在第2天形成聚集体。大部分细胞(92±7%)通过4小时连接到微载体上。与纳米培养相比,微载体培养方法具有较低的凋亡活动(第4天折叠)。微载体培养方法具有比纳米培养物的细胞生长更高(第4天的1.7倍)。虽然聚合物纳米培养方法没有比微载体培养更好的结果,但是聚合物纳米培养方法可以在高速和细胞移植期间对微载体培养方法提供微载体培养方法的优点,但在没有酶消化过程的情况下收获培养的细胞。

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