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2.9. Cell culture
Human mesenchymal stem cells (hMSCs) were a kind gift donated by the Second Affiliated Hospital of Sun Yat-Sen University and were propagated in Dulbecco¡¯s Modified Eagle¡¯s Medium (DMEM) with supplements of 1.5 mg$ml-1 sodium bicarbonate,4.5 mg ml-1 glucose, 10% (v/v) fetal bovine serum (FBS), 3 mg ml-1 4-(2- hydroxyerhyl)piperazine-1-erhanesulfonic acid (HEPES). The cells were kept in a humidified incubator at 37¡æand5%CO2, and themediumwas changed every 3 days.

2.10. Cell seeding on the scaffolds
PLGA/PHBV scaffolds were cut into disks of 6mmin diameter and 2mmin height and sterilized by exposing to gamma radiation (15 kGy). The pure PLGA scaffolds of the same size as that of PLGA/PHBV were immersed in 75% (v/v) ethanol aqueous solution for 2 h and followed by ultraviolet radiation for 30 min to sterilize. All the scaffolds were prewet in the DMEM solution for 24 h. Fifteen microlitres of passage 6 cells in suspension (7.5¡Á104 cells/well) were seeded on each scaffold. 2 h later, 700 ¦Ìl of culture medium was added into each well. The cells/scaffold constructs were incubated at 37¡æ in a humidified incubator of 5% CO2 for pre-set days.

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ÈËÀà¼ä³äÖʸÉϸ°û(hMSCs)ÊÇÒ»ÖÖÀñÎïÓÉÖÐɽ´óѧµÚ¶þ¸½ÊôÒ½ÔºµÄ¾èÔùºÍÔÚDulbeccoÐÞ¸ÄÓ¥µÄ´«²¥Ã½½é(DMEM)²¹³ä1.5ºÁ¿Ëml-1ÃÀԪ̼ËáÇâÄÆ,4.5ºÁ¿Ëml-1ÆÏÌÑÌÇ,10%(v / v)̥ţѪÇåµÄ±ßºóÎÀ,3ºÁ¿Ëml-1 4 -(2 - hydroxyerhyl)piperazine-1-erhanesulfonicËá(õ¹å)¡£ÕâЩϸ°û±»±£´æÔÚÒ»¸öʪÈó·õ»¯Æ÷ÔÚ37¡æand5%CO2,ºÍthemediumwasÿ3Ìì»»Ò»´Î¡£


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PLGA / PHBVÖ§¼Ü±»ÇгɴÅÅÌ6 mminÖ±¾¶ºÍ2 mmin¸ß¶ÈºÍÏû¶¾±©Â¶Ù¤Âí·øÉä(15 kGyµÄ)¡£Ïàͬ´óСµÄ´¿PLGAÖ§¼ÜµÄPLGA / PHBV³Á½þÔÚ75%(v / v)ÒÒ´¼Ë®ÈÜҺΪ2 h,½ôËæÆäºóµÄÊÇ×ÏÍâÏßÏû¶¾30·ÖÖÓ¡£ËùÓеÄÖ§¼Ü¶¼ÊÇÁ½¸ßÒ»µÍµÄDMEM 24 h¡£15ºÁÉýͨµÀ½â¾ö·½°¸6ϸ°ûÐü¸¡(7.5¡Á104ϸ°û/)±»²¥ÖÖÔÚÿ¸öÖ§¼Ü¡£2 hºó,700¦ÌlÅàÑø»ùÌí¼Óµ½Ã¿¸ö¡£Ï¸°û/Ö§¼Ü½á¹¹ÔÚ37¡æÊªÈó·õ»¯Æ÷·õ»¯Ô¤ÉèÌì5%µÄ¶þÑõ»¯Ì¼¡£
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