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Poly(ε-caprolactone) Dendrimer Cross-Linked via Metal-Free Click Chemistry: Injectable Hydrophobic Platform for Tissue Engineering.
Liu, Xifeng; Miller, A Lee; Fundora, Kevin A; Yaszemski, Michael J; Lu, Lichun.
Afiliação
  • Liu X; Departments of Physiology and Biomedical Engineering and ‡Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
  • Miller AL; Departments of Physiology and Biomedical Engineering and Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
  • Fundora KA; Departments of Physiology and Biomedical Engineering and Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
  • Yaszemski MJ; Departments of Physiology and Biomedical Engineering and Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
  • Lu L; Departments of Physiology and Biomedical Engineering and Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
ACS Macro Lett ; 5(11): 1261-1265, 2016 Nov 15.
Article em En | MEDLINE | ID: mdl-35614737
The fabrication of injectable self-cross-linkable hyperbranched poly(ε-caprolactone) (hyPCL) formulation using metal-free click chemistry was reported. The cross-linking between hyPCL32-(1R,8S,9s)-bicyclo[6.1.0]non-4-yn-9-ylmethanol (hyPCL32-BCN) and hyPCL32-azide (hyPCL32-N3) components was proceeded via strain-promoted alkyne-azide cycloaddition (SPAAC) click reaction. Cross-linking was tested to proceed effectively with the exclusion of any toxic cross-linking agents. Strong mechanical properties and excellent biocompatibility were demonstrated for the cross-linked substrates. These newly synthesized dendrimers may have broad applications in tissue engineering such as bone defect repair. In addition, the introduction of metal-free click chemistry to hydrophobic polymers provides an attractive new strategy for developing injectable stiff polymer formulations besides hydrogels for biomedical applications.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Macro Lett Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Macro Lett Ano de publicação: 2016 Tipo de documento: Article