4.6 Article

Blending with Poly(L-lactic acid) Improves the Printability of Poly(L-lactide-co-caprolactone) and Enhances the Potential Application in Cartilage Tissue Engineering

期刊

ACS OMEGA
卷 6, 期 28, 页码 18300-18313

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c02190

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资金

  1. National Natural Science Foundation of China [81972043, 81501578]
  2. CAMS Innovation Fund for Medical Sciences [CAMS-2017-I2M-1007]
  3. Fundamental Research Funds for the Central Universities [3332019102]
  4. Key Project of GuangDong Basic and Applied Basic Research Foundation [2020B1515120091]

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Blending PLLA with PLCL improves the rigidity and viscoelasticity of the blends for cartilage tissue engineering applications. 3D-printed PLCL/PLLA scaffolds exhibit good thermal stability and toughness, with mechanical properties similar to native cartilage. The addition of PLLA also enhances the printability of PLCL and promotes chondrogenic behavior in vitro.
Poly(L-lactide-co-caprolactone) (PLCL, 50:50) has been used in cartilage tissue engineering because of its high elasticity. However, its mechanical properties, including its rigidity and viscoelasticity, must be improved for compatibility with native cartilage. In this study, a set of PLCL/poly(L-lactic acid) (PLLA) blends was prepared by blending with different mass ratios of PLLA that range from 10 to 50%, using thermoplastic techniques. After testing the properties of these PLCL/PLLA blends, they were used to fabricate scaffolds by the 3D printing technology. The structures and viscoelastic behavior of the PLCL/PLLA scaffolds were determined, and then, the potential application of the scaffolds in cartilage tissue engineering was evaluated by chondrocytes culture. All blends demonstrate good thermal stability for the 3D printing technology. All blends show good toughness, while the rigidity of PLCL is increased through PLLA blending, and Young's modulus of blends with 10-20% PLLA is similar to that of native cartilage. Furthermore, blending with PLLA improves the processability of PLCL for 3D printing, and the compression modulus and viscoelasticity of 3D-printed PLCL/PLLA scaffolds are different from that of PLCL. Additionally, the stress relaxation time (t(1/2)) of the PLCL/PLLA scaffolds, which is important for chondrogenesis, is dramatically shortened compared with the pure PLCL scaffold at the same 3D-printing filling rate. Consistently, the PLCL90PLLA10 scaffold at a 70% filling rate with much shorter t(1/2) is more conducive to the proliferation and chondrogenesis of in vitro seeded chondrocytes accompanied by upregulated expression of SOX9 than the PLCL scaffold. Taken together, these results demonstrate that blending with PLLA improves the printability of PLCL and enhances its potential application, particularly PLCL/PLLA scaffolds with a low ratio of PLLA, in cartilage tissue engineering.

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