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具有定制大孔形成速率的用于骨再生的快速凝固磷酸钙支架。

Fast-setting calcium phosphate scaffolds with tailored macropore formation rates for bone regeneration.

作者信息

Xu Hockin H K, Takagi Shozo, Quinn Janet B, Chow Laurence C

机构信息

Paffenbarger Research Center, American Dental Association Foundation, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA.

出版信息

J Biomed Mater Res A. 2004 Mar 15;68(4):725-34. doi: 10.1002/jbm.a.20093.

Abstract

Calcium phosphate cement (CPC) is highly promising for craniofacial and orthopedic repair because of its ability to self-harden in situ to form hydroxyapatite with excellent osteoconductivity. However, its low strength, long hardening time, and lack of macroporosity limit its use. This study aimed to develop fast-setting and antiwashout CPC scaffolds with high strength and tailored macropore formation rates. Chitosan, sodium phosphate, and hydroxypropyl methylcellulose (HPMC) were used to render CPC fast-setting and resistant to washout. Absorbable fibers and mannitol porogen were incorporated into CPC for strength and macropores for bone ingrowth. Flexural strength, work-of-fracture, and elastic modulus were measured vs. immersion time in a physiological solution. Hardening time (mean +/- SD; n = 6) was 69.5 +/- 2.1 min for CPC-control, 9.3 +/- 2.8 min for CPC-HPMC-mannitol, 8.2 +/- 1.5 min for CPC-chitosan-mannitol, and 6.7 +/- 1.6 min for CPC-chitosan-mannitol-fiber. The latter three compositions were resistant to washout, whereas the CPC-control paste showed washout in a physiological solution. Immersion for 1 day dissolved mannitol and created macropores in CPC. CPC-chitosan-mannitol-fiber scaffold had a strength of 4.6 +/- 1.4 MPa, significantly higher than 1.2 +/- 0.1 MPa of CPC-chitosan-mannitol scaffold and 0.3 +/- 0.2 MPa of CPC-HPMC-mannitol scaffold (Tukey's). The strength of CPC-chitosan-mannitol-fiber scaffold was maintained up to 42 days and then decreased because of fiber degradation. Work-of-fracture and elastic modulus showed similar trends. Long cylindrical macropore channels were formed in CPC after fiber dissolution. The resorbable, fast-setting, anti-washout and strong CPC scaffold should be useful in craniofacial and orthopedic repairs. The novel method of combining fast- and slow-dissolution porogens/fibers to produce scaffolds with high strength and tailored macropore formation rates to match bone healing rates may have wide applicability to other biomaterials.

摘要

磷酸钙骨水泥(CPC)因其能够在原位自硬化形成具有优异骨传导性的羟基磷灰石,在颅面和骨科修复方面极具前景。然而,其低强度、长硬化时间以及缺乏大孔隙率限制了其应用。本研究旨在开发具有快速凝固、抗冲刷性能、高强度且大孔隙形成率可定制的CPC支架。壳聚糖、磷酸钠和羟丙基甲基纤维素(HPMC)被用于使CPC快速凝固并抗冲刷。将可吸收纤维和甘露醇致孔剂加入CPC中以增强强度并形成利于骨长入的大孔隙。测量了弯曲强度、断裂功和弹性模量与在生理溶液中浸泡时间的关系。CPC对照组的硬化时间(平均值±标准差;n = 6)为69.5±2.1分钟,CPC-HPMC-甘露醇组为9.3±2.8分钟,CPC-壳聚糖-甘露醇组为8.2±1.5分钟,CPC-壳聚糖-甘露醇-纤维组为6.7±1.6分钟。后三种组合物抗冲刷,而CPC对照组糊剂在生理溶液中出现冲刷现象。浸泡1天可溶解甘露醇并在CPC中形成大孔隙。CPC-壳聚糖-甘露醇-纤维支架的强度为4.6±1.4 MPa,显著高于CPC-壳聚糖-甘露醇支架的1.2±0.1 MPa和CPC-HPMC-甘露醇支架的0.3±0.2 MPa(Tukey检验)。CPC-壳聚糖-甘露醇-纤维支架强度可维持42天,之后因纤维降解而下降。断裂功和弹性模量呈现相似趋势。纤维溶解后在CPC中形成了长圆柱形大孔隙通道。这种可吸收、快速凝固、抗冲刷且强度高的CPC支架在颅面和骨科修复中应具有实用性。将快速和缓慢溶解的致孔剂/纤维相结合以生产具有高强度且大孔隙形成率可定制以匹配骨愈合速率的支架的新方法可能广泛适用于其他生物材料。

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