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Primary porcine hepatocytes with portal vein serum cultured on microcarriers or in spheroidal aggregates

机译:在微载体或球状聚集体上培养门静脉血清的原代猪肝细胞

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摘要

AIM To develop a culture model providing durable biomaterials with high yields and activities used in bioartificial liver. METHODS Hepatocytes were isolated from a Whole pig liver by Seglen's method of orthotopic Prfusion with collagenase. In culture on Microcarriers, primary porcine hepatocytes Were inoculated at a concentration of 5 × 10~7 /mL Into the static culture systems containing 2 g/L Cytodex-3, then supplemented with 100 Ml/l Fetal calf serum (FCS) or 100 mL/L porcine Portal vein serum (PPVS) respectively.
机译:目的开发一种培养模型,为生物人工肝提供高产量和高活性的耐用生物材料。方法采用Seglen原位灌注胶原酶法从全猪肝脏中分离肝细胞。在微载体培养中,将原代猪肝细胞以5×10〜7 / mL的浓度接种到含有2 g / L Cytodex-3的静态培养系统中,然后补充100 Ml / l胎牛血清(FCS)或100毫升/升猪门静脉血清(PPVS)。

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