María Ayala-Velásquez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
María Ayala-Velásquez has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Alejandro Velandia-Sánchez
Vascular and Endovascular Surgery Research Group, Fundación Cardioinfantil-Instituto de Cardiología, Bogotá, Colombia
1 shared publication - Andrés M. Aragón-Rivera
Department of Biomedical Engineering, Universidad de los Andes, Bogotá 111711, Colombia
1 shared publication - Camilo A. Polanía-Sandoval
Vascular and Endovascular Surgery Research Group, Fundación Cardio Infantil—Instituto de Cardiología, Bogotá 111711, Colombia
1 shared publication - Carolina Muñoz-Camargo
Universidad de los Andes
1 shared publication - Daniel Buitrago
Department of Biomedical Engineering, Universidad de los Andes, Bogotá 111711, Colombia
1 shared publication - Gabriela Peralta Peluffo
Department of Biomedical Engineering, Universidad de los Andes, Bogotá 111711, Colombia
1 shared publication
Latest Publications
- Open Access
Small Diameter Cell-Free Tissue-Engineered Vascular Grafts: Biomaterials and Manufacture Techniques to Reach Suitable Mechanical Properties
Vascular grafts (VGs) are medical devices intended to replace the function of a blood vessel. Available VGs in the market present low patency rates for small diameter applications setting the VG failure. This event arises from the inadequate response of the cells interacting with the biomaterial in the context of operative conditions generating chronic inflammation and a lack of regenerative signals where stenosis or aneurysms can occur. Tissue Engineered Vascular grafts (TEVGs) aim to induce the regeneration of the native vessel to overcome these limitations. Besides the biochemical stimuli, the biomaterial and the particular micro and macrostructure of the graft will determine the specific behavior under pulsatile pressure. The TEVG must support blood flow withstanding the exerted pressure, allowing the proper compliance required for the biomechanical stimulation needed for regeneration. Although the international standards outline the specific requirements to evaluate vascular grafts, the challenge remains in choosing the proper biomaterial and manufacturing TEVGs with good quality features to perform satisfactorily. In this review, we aim to recognize the best strategies to reach suitable mechanical properties in cell-free TEVGs according to the reported success of different approaches in clinical trials and pre-clinical trials.
Open AccessSmall Diameter Cell-Free Tissue-Engineered Vascular Grafts: Biomaterials and Manufacture Techniques to Reach Suitable Mechanical Properties
Vascular grafts (VGs) are medical devices intended to replace the function of a blood vessel. Available VGs in the market present low patency rates for small diameter applications setting the VG failure. This event arises from the inadequate response of the cells interacting with the biomaterial in the context of operative conditions generating chronic inflammation and a lack of regenerative signals where stenosis or aneurysms can occur. Tissue Engineered Vascular grafts (TEVGs) aim to induce the regeneration of the native vessel to overcome these limitations. Besides the biochemical stimuli, the biomaterial and the particular micro and macrostructure of the graft will determine the specific behavior under pulsatile pressure. The TEVG must support blood flow withstanding the exerted pressure, allowing the proper compliance required for the biomechanical stimulation needed for regeneration. Although the international standards outline the specific requirements to evaluate vascular grafts, the challenge remains in choosing the proper biomaterial and manufacturing TEVGs with good quality features to perform satisfactorily. In this review, we aim to recognize the best strategies to reach suitable mechanical properties in cell-free TEVGs according to the reported success of different approaches in clinical trials and pre-clinical trials.