Durkut Serap, Elçin Y Murat, Elçin A Eser
Ankara University, Faculty of Science and Biotechnology Institute, Tissue Engineering and Biomaterials Laboratory, Ankara, Turkey.
Artif Cells Blood Substit Immobil Biotechnol. 2006;34(2):263-76. doi: 10.1080/10731190600581866.
In this study, chitosan [(1 --> 4) linked 2-amino-2-deoxy-beta-D-glucopyranose] beads were prepared by interacting this polycation (> 90% deacetylated) with the tripolyphosphate (TPP) polyanion. The resulting chitosan-TPP beads (C) were modified either by coating with sodium alginate (CA) or by cross-linking with glutaraldehyde (CGA). The in vitro degradation of C beads was found to be faster than its CA and CGA counterparts. C beads degraded faster at pH 6.5, compared to pH 7.4 conditions. At pH 7.4, about 41%, 37% and 10% of dry mass loss after 12 months was determined for C, CA and CGA, respectively. At pH 6.5, the dry mass loss of CA and CGA after the same period of time was found to be 73% and 37%, respectively. However, C beads completely degraded at pH 6.5 after 8 months of in vitro incubation. The in vivo biodegradation experiments were performed on Wistar rats (n = 24) for a duration of 6 months. No sign of fibrotic capsule formation was observed around any of the implanted beads at 2 and 6 months post-transplantation. At 2 months, the in vivo-degradation was slow-going and the beads in all groups were intact; CGA beads had more tissue reaction than C and CA beads at this time point. While the C beads had almost completely degraded after 6 months, the biodegradation process in CA and CGA beads was progressing. Histomorphometric analysis revealed that the in vivo biodegradation was in the order of C (approximately 85%) > CA (approximately 50%) > CGA (approximately 25%) after 6 months. Neovascularization was observed at the vicinity of the bead implants close to major blood vessels, both at 2 and 6 months time-points.
在本研究中,壳聚糖[(1→4)连接的2-氨基-2-脱氧-β-D-吡喃葡萄糖]珠粒是通过使这种聚阳离子(脱乙酰度>90%)与三聚磷酸(TPP)聚阴离子相互作用制备而成。所得的壳聚糖-TPP珠粒(C)通过用海藻酸钠包被(CA)或与戊二醛交联(CGA)进行改性。发现C珠粒的体外降解速度比其CA和CGA对应物更快。与pH 7.4条件相比,C珠粒在pH 6.5时降解更快。在pH 7.4时,12个月后C、CA和CGA的干质量损失分别约为41%、37%和10%。在pH 6.5时,相同时间段后CA和CGA的干质量损失分别为73%和37%。然而,C珠粒在体外培养8个月后在pH 6.5时完全降解。在Wistar大鼠(n = 24)上进行了为期6个月的体内生物降解实验。移植后2个月和6个月时,在任何植入的珠粒周围均未观察到纤维化包膜形成的迹象。在2个月时,体内降解进展缓慢,所有组的珠粒均完整;此时CGA珠粒比C和CA珠粒有更多的组织反应。虽然C珠粒在6个月后几乎完全降解,但CA和CGA珠粒的生物降解过程仍在进行。组织形态计量学分析显示,6个月后体内生物降解顺序为C(约85%)>CA(约50%)>CGA(约25%)。在2个月和6个月时间点,在靠近主要血管的珠粒植入部位附近均观察到了新血管形成。