• 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

使用可生物吸收的植入物进行无额外细胞或生长因子的新生脂肪生成。

De novo adipogenesis using a bioabsorbable implant without additional cells or growth factors.

机构信息

Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyoto University, Sakyou-ku, Kyoto, Japan.

Department of Plastic and Reconstructive Surgery, National Hospital Organization Kyoto Medical Center, Fushimiku, Kyoto, Japan.

出版信息

J Tissue Eng Regen Med. 2020 Jul;14(7):920-930. doi: 10.1002/term.3041. Epub 2020 Jun 3.

DOI:10.1002/term.3041
PMID:32293793
Abstract

Adipose tissue regeneration in breast cancer patients without additional growth factors or adipose-tissue-derived stromal cells is desirable because of the possibility of recurrence and metastasis. We report that a poly-L-lactic acid (PLLA) mesh implant containing a collagen sponge (CS) maintained the internal space in vivo for up to 12 months and substituted for adipose tissue. We developed a PLLA capsule that maintained the internal space longer than that of PLLA mesh and compared adipose tissue formation at 12 and 24 months after implantation between the PLLA mesh with CS implant and the PLLA capsule implant with or without CS in a rabbit model. After 12 months, all implants maintained the internal space, and the adipose tissue that formed in all implant groups was larger than that in the control group. At 24 months, PLLA mesh maintained the internal space just as well as that at 12 months, while the PLLA capsule collapsed and accumulated a large number of macrophages. The formed adipose tissue in the PLLA mesh group was maintained up to 24 months; however, those in two PLLA capsule groups decreased and showed no difference from the control group. In conclusion, the internal space of the PLLA mesh implant with CS was substituted for adipose tissue at 12 months and sustained the formed adipose tissue after 24 months. The PLLA mesh implant containing CS is a desirable bioabsorbable implant that can be replaced by autologous adipose tissue after implantation in vivo without using any growth factors or cells.

摘要

在乳腺癌患者中,不添加额外的生长因子或脂肪组织来源的基质细胞即可实现脂肪组织再生,这是因为存在复发和转移的可能性。我们报告称,一种含有胶原海绵(CS)的聚 L-乳酸(PLLA)网片植入物可在体内维持内部空间长达 12 个月,并替代脂肪组织。我们开发了一种 PLLA 胶囊,其维持内部空间的时间长于 PLLA 网片,并在兔模型中比较了植入 PLLA 网片加 CS 植入物与植入 PLLA 胶囊加或不加 CS 之间在植入后 12 个月和 24 个月时的脂肪组织形成情况。12 个月后,所有植入物均维持了内部空间,所有植入物组形成的脂肪组织均大于对照组。24 个月时,PLLA 网片维持内部空间的效果与 12 个月时相同,而 PLLA 胶囊则塌陷并积聚了大量巨噬细胞。PLLA 网片组形成的脂肪组织可维持至 24 个月,但两个 PLLA 胶囊组的脂肪组织减少,与对照组无差异。总之,CS 与 PLLA 网片植入物的内部空间在 12 个月时被脂肪组织替代,并在 24 个月后维持已形成的脂肪组织。含有 CS 的 PLLA 网片植入物是一种理想的可生物吸收植入物,可在体内植入后无需使用任何生长因子或细胞即可被自体脂肪组织替代。

相似文献

1
De novo adipogenesis using a bioabsorbable implant without additional cells or growth factors.使用可生物吸收的植入物进行无额外细胞或生长因子的新生脂肪生成。
J Tissue Eng Regen Med. 2020 Jul;14(7):920-930. doi: 10.1002/term.3041. Epub 2020 Jun 3.
2
Development of a novel bioabsorbable implant that is substituted by adipose tissue in vivo.研发一种新型可生物吸收的植入物,该植入物在体内可被脂肪组织替代。
J Tissue Eng Regen Med. 2018 Mar;12(3):633-641. doi: 10.1002/term.2482. Epub 2017 Sep 28.
3
Development of new bioabsorbable implants with de novo adipogenesis.具有新生脂肪形成功能的新型生物可吸收植入物的研发。
Regen Ther. 2023 Aug 12;24:311-317. doi: 10.1016/j.reth.2023.07.008. eCollection 2023 Dec.
4
Preliminary report of de novo adipogenesis using novel bioabsorbable implants and image evaluation using a porcine model.新型可吸收植入物诱导脂肪生成的初步报告及猪模型的影像学评估
J Artif Organs. 2022 Sep;25(3):245-253. doi: 10.1007/s10047-022-01313-8. Epub 2022 Mar 2.
5
Long term observation of adipogenesis using novel bioabsorbable implants with larger size in a porcine model.在猪模型中使用更大尺寸的新型生物可吸收植入物对脂肪生成进行长期观察。
Regen Ther. 2023 Aug 24;24:324-331. doi: 10.1016/j.reth.2023.08.004. eCollection 2023 Dec.
6
Evaluation of adipogenesis over time using a novel bioabsorbable implant without the addition of exogenous cells or growth factors.使用一种新型生物可吸收植入物对脂肪生成进行长期评估,该植入物不添加外源性细胞或生长因子。
Regen Ther. 2024 Jan 4;25:220-228. doi: 10.1016/j.reth.2023.12.015. eCollection 2024 Mar.
7
Adipose tissue regeneration in a 3D-printed poly(lactic acid) frame-supported space in the inguinal region of rats.大鼠腹股沟区域内 3D 打印聚乳酸框架支撑空间中的脂肪组织再生。
Biomed Mater Eng. 2020;31(4):203-210. doi: 10.3233/BME-201103.
8
Long-term tissue response to bioabsorbable poly-L-lactide and metallic screws: an experimental study.生物可吸收聚左旋乳酸与金属螺钉的长期组织反应:一项实验研究。
Bone. 2006 Oct;39(4):932-7. doi: 10.1016/j.bone.2006.04.009. Epub 2006 Jun 5.
9
Tissue response to poly(L-lactic acid)-based blend with phospholipid polymer for biodegradable cardiovascular stents.组织对聚(L-乳酸)基共混物与磷脂聚合物的反应用于可生物降解心血管支架。
Biomaterials. 2011 Mar;32(9):2241-7. doi: 10.1016/j.biomaterials.2010.11.067. Epub 2010 Dec 24.
10
Engineered adipose tissue formation enhanced by basic fibroblast growth factor and a mechanically stable environment.碱性成纤维细胞生长因子和机械稳定环境促进工程化脂肪组织形成。
Cell Transplant. 2007;16(4):421-34. doi: 10.3727/000000007783464795.

引用本文的文献

1
Adipogenesis of bioabsorbable implants under irradiation in a rodent model.啮齿动物模型中生物可吸收植入物在辐射下的脂肪生成
Regen Ther. 2024 Oct 30;26:990-998. doi: 10.1016/j.reth.2024.10.002. eCollection 2024 Jun.
2
Unveiling the Mechanism: Injectable Poly-L-Lactic Acid's Evolving Role-Insights From Recent Studies.揭示机制:可注射聚左旋乳酸不断演变的作用——来自近期研究的见解
J Cosmet Dermatol. 2025 Jan;24(1):e16635. doi: 10.1111/jocd.16635. Epub 2024 Oct 16.
3
Long term observation of adipogenesis using novel bioabsorbable implants with larger size in a porcine model.
在猪模型中使用更大尺寸的新型生物可吸收植入物对脂肪生成进行长期观察。
Regen Ther. 2023 Aug 24;24:324-331. doi: 10.1016/j.reth.2023.08.004. eCollection 2023 Dec.
4
Development of new bioabsorbable implants with de novo adipogenesis.具有新生脂肪形成功能的新型生物可吸收植入物的研发。
Regen Ther. 2023 Aug 12;24:311-317. doi: 10.1016/j.reth.2023.07.008. eCollection 2023 Dec.