• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过挤出工艺制造用于引导组织再生的多孔可生物降解聚合物导管。

Manufacture of porous biodegradable polymer conduits by an extrusion process for guided tissue regeneration.

作者信息

Widmer M S, Gupta P K, Lu L, Meszlenyi R K, Evans G R, Brandt K, Savel T, Gurlek A, Patrick C W, Mikos A G

机构信息

Department of Chemical Engineering and Institute of Biosciences and Bioengineering, Rice University, Houston, TX 77251-1892, USA.

出版信息

Biomaterials. 1998 Nov;19(21):1945-55. doi: 10.1016/s0142-9612(98)00099-4.

DOI:10.1016/s0142-9612(98)00099-4
PMID:9863528
Abstract

We have fabricated porous, biodegradable tubular conduits for guided tissue regeneration using a combined solvent casting and extrusion technique. The biodegradable polymers used in this study were poly(DL-lactic-co-glycolic acid) (PLGA) and poly(L-lactic acid) (PLLA). A polymer/salt composite was first prepared by a solvent casting process. After drying, the composite was extruded to form a tubular construct. The salt particles in the construct were then leached out leaving a conduit with an open-pore structure. PLGA was studied as a model polymer to analyze the effects of salt weight fraction, salt particle size, and processing temperature on porosity and pore size of the extruded conduits. The porosity and pore size were found to increase with increasing salt weight fraction. Increasing the salt particle size increased the pore diameter but did not affect the porosity. High extrusion temperatures decreased the pore diameter without altering the porosity. Greater decrease in molecular weight was observed for conduits manufactured at higher temperatures. The mechanical properties of both PLGA and PLLA conduits were tested after degradation in vitro for up to 8 weeks. The modulus and failure strength of PLLA conduits were approximately 10 times higher than those of PLGA conduits. Failure strain was similar for both conduits. After degradation for 8 weeks, the molecular weights of the PLGA and PLLA conduits decreased to 38% and 43% of the initial values, respectively. However, both conduits maintained their shape and did not collapse. The PLGA also remained amorphous throughout the time course, while the crystallinity of PLLA increased from 5.2% to 11.5%. The potential of seeding the conduits with cells for transplantation or with biodegradable polymer microparticles for drug delivery was also tested with dyed microspheres. These porous tubular structures hold great promise for the regeneration of tissues which require tubular scaffolds such as peripheral nerve, long bone, intestine, or blood vessel.

摘要

我们采用溶剂浇铸和挤出相结合的技术,制备了用于引导组织再生的多孔、可生物降解的管状导管。本研究中使用的可生物降解聚合物为聚(DL-乳酸-乙醇酸共聚物)(PLGA)和聚(L-乳酸)(PLLA)。首先通过溶剂浇铸法制备聚合物/盐复合材料。干燥后,将复合材料挤出形成管状结构。然后将结构中的盐颗粒浸出,留下具有开孔结构的导管。以PLGA作为模型聚合物,分析盐重量分数、盐粒径和加工温度对挤出导管孔隙率和孔径的影响。发现孔隙率和孔径随盐重量分数的增加而增加。增大盐粒径会增大孔径,但不影响孔隙率。较高的挤出温度会减小孔径,但不改变孔隙率。在较高温度下制造的导管观察到分子量有更大的降低。在体外降解长达8周后,对PLGA和PLLA导管的力学性能进行了测试。PLLA导管的模量和断裂强度比PLGA导管高约10倍。两种导管的断裂应变相似。降解8周后,PLGA和PLLA导管的分子量分别降至初始值的38%和43%。然而,两种导管都保持了其形状,没有塌陷。PLGA在整个时间过程中也保持无定形,而PLLA的结晶度从5.2%增加到11.5%。还用染色微球测试了在导管中接种细胞进行移植或接种可生物降解聚合物微粒进行药物递送的潜力。这些多孔管状结构对于需要管状支架的组织再生,如周围神经、长骨、肠道或血管,具有很大的前景。

相似文献

1
Manufacture of porous biodegradable polymer conduits by an extrusion process for guided tissue regeneration.通过挤出工艺制造用于引导组织再生的多孔可生物降解聚合物导管。
Biomaterials. 1998 Nov;19(21):1945-55. doi: 10.1016/s0142-9612(98)00099-4.
2
Hydroxyapatite fiber reinforced poly(alpha-hydroxy ester) foams for bone regeneration.用于骨再生的羟基磷灰石纤维增强聚(α-羟基酯)泡沫材料。
Biomaterials. 1998 Nov;19(21):1935-43. doi: 10.1016/s0142-9612(98)00097-0.
3
A biodegradable vascularizing membrane: a feasibility study.一种可生物降解的血管化膜:可行性研究。
Acta Biomater. 2007 Sep;3(5):631-42. doi: 10.1016/j.actbio.2007.03.003. Epub 2007 May 15.
4
Control of pore size and structure of tissue engineering scaffolds produced by supercritical fluid processing.通过超临界流体加工控制组织工程支架的孔径和结构。
Eur Cell Mater. 2007 Dec 17;14:64-77. doi: 10.22203/ecm.v014a07.
5
Manufacture of porous polymer nerve conduits through a lyophilizing and wire-heating process.通过冻干和线加热工艺制造多孔聚合物神经导管。
J Biomed Mater Res B Appl Biomater. 2005 Jul;74(1):659-64. doi: 10.1002/jbm.b.30267.
6
Poly(alpha-hydroxyl acids)/hydroxyapatite porous composites for bone-tissue engineering. I. Preparation and morphology.用于骨组织工程的聚(α-羟基酸)/羟基磷灰石多孔复合材料。I. 制备与形态
J Biomed Mater Res. 1999 Mar 15;44(4):446-55. doi: 10.1002/(sici)1097-4636(19990315)44:4<446::aid-jbm11>3.0.co;2-f.
7
In vivo evaluation of poly(L-lactic acid) porous conduits for peripheral nerve regeneration.聚(L-乳酸)多孔导管用于周围神经再生的体内评估。
Biomaterials. 1999 Jun;20(12):1109-15. doi: 10.1016/s0142-9612(99)00010-1.
8
Effects of unidirectional permeability in asymmetric poly(DL-lactic acid-co-glycolic acid) conduits on peripheral nerve regeneration: an in vitro and in vivo study.不对称聚(DL-乳酸-共-乙醇酸)导管中单向通透性对周围神经再生的影响:一项体外和体内研究。
J Biomed Mater Res B Appl Biomater. 2007 Oct;83(1):206-15. doi: 10.1002/jbm.b.30785.
9
Influence of the microencapsulation method and peptide loading on poly(lactic acid) and poly(lactic-co-glycolic acid) degradation during in vitro testing.微囊化方法和肽负载对聚乳酸和聚乳酸-乙醇酸共聚物体外测试期间降解的影响。
J Control Release. 1998 Feb 12;51(2-3):327-41. doi: 10.1016/s0168-3659(97)00188-0.
10
Fabrication of biodegradable polymer scaffolds to engineer trabecular bone.用于构建小梁骨的可生物降解聚合物支架的制备
J Biomater Sci Polym Ed. 1995;7(1):23-38. doi: 10.1163/156856295x00805.

引用本文的文献

1
Potentially commercializable nerve guidance conduits for peripheral nerve injury: Past, present, and future.用于周围神经损伤的潜在可商业化神经导向导管:过去、现在和未来。
Mater Today Bio. 2025 Feb 5;31:101503. doi: 10.1016/j.mtbio.2025.101503. eCollection 2025 Apr.
2
Protective vs. Therapeutic Effects of Mitochondria-Targeted Antioxidant MitoTEMPO on Rat Sciatic Nerve Crush Injury: A Comprehensive Electrophysiological Analysis.线粒体靶向抗氧化剂MitoTEMPO对大鼠坐骨神经挤压伤的保护作用与治疗作用:全面的电生理分析
Biomedicines. 2023 Dec 14;11(12):3306. doi: 10.3390/biomedicines11123306.
3
Fabrication of initial trabecular bone-inspired three-dimensional structure with cell membrane nano fragments.
利用细胞膜纳米片段制备初始小梁骨启发的三维结构
Regen Biomater. 2022 Nov 2;10:rbac088. doi: 10.1093/rb/rbac088. eCollection 2023.
4
3D Printed Personalized Nerve Guide Conduits for Precision Repair of Peripheral Nerve Defects.3D 打印个性化神经导管引导精准修复周围神经缺损。
Adv Sci (Weinh). 2022 Apr;9(12):e2103875. doi: 10.1002/advs.202103875. Epub 2022 Feb 18.
5
Potential Therapeutic Strategies and Substances for Facial Nerve Regeneration Based on Preclinical Studies.基于临床前研究的面神经再生的潜在治疗策略和物质。
Int J Mol Sci. 2021 May 6;22(9):4926. doi: 10.3390/ijms22094926.
6
Effects of Two Melt Extrusion Based Additive Manufacturing Technologies and Common Sterilization Methods on the Properties of a Medical Grade PLGA Copolymer.两种基于熔融挤出的增材制造技术及常用灭菌方法对医用级聚乳酸-羟基乙酸共聚物性能的影响
Polymers (Basel). 2021 Feb 14;13(4):572. doi: 10.3390/polym13040572.
7
A new engineering process of biodegradable polymeric solid implants for ultra-long-acting drug delivery.一种用于超长效药物递送的可生物降解聚合物固体植入物的新型工程工艺。
Int J Pharm X. 2020 Dec 25;3:100068. doi: 10.1016/j.ijpx.2020.100068. eCollection 2021 Dec.
8
High Throughput Manufacturing of Bio-Resorbable Micro-Porous Scaffolds Made of Poly(L-lactide-co-ε-caprolactone) by Micro-Extrusion for Soft Tissue Engineering Applications.通过微挤压技术高通量制造用于软组织工程应用的聚(L-丙交酯-共-ε-己内酯)生物可吸收微孔支架
Polymers (Basel). 2019 Dec 24;12(1):34. doi: 10.3390/polym12010034.
9
Engineering Porous Poly(lactic acid) Scaffolds with High Mechanical Performance via a Solid State Extrusion/Porogen Leaching Approach.通过固态挤出/致孔剂浸出法制备具有高机械性能的多孔聚乳酸支架
Polymers (Basel). 2016 May 31;8(6):213. doi: 10.3390/polym8060213.
10
Effect of Exosomes from Rat Adipose-Derived Mesenchymal Stem Cells on Neurite Outgrowth and Sciatic Nerve Regeneration After Crush Injury.脂肪间充质干细胞来源的外泌体对挤压伤后轴突生长和坐骨神经再生的影响。
Mol Neurobiol. 2019 Mar;56(3):1812-1824. doi: 10.1007/s12035-018-1172-z. Epub 2018 Jun 21.