TU Darmstadt / ULB / TUbiblio

Biosynthetic, biomimetic, and self-assembled vascularized Organ-on-a-Chip systems

Fritschen, Anna ; Blaeser, Andreas (2023)
Biosynthetic, biomimetic, and self-assembled vascularized Organ-on-a-Chip systems.
In: Biomaterials, 2021, 268
doi: 10.26083/tuprints-00024336
Artikel, Zweitveröffentlichung, Postprint

WarnungEs ist eine neuere Version dieses Eintrags verfügbar.

Kurzbeschreibung (Abstract)

Organ-on-a-Chip (OOC) devices have seen major advances in the last years with respect to biological complexity, physiological composition and biomedical relevance. In this context, integration of vasculature has proven to be a crucial element for long-term culture of thick tissue samples as well as for realistic pharmacokinetic, toxicity and metabolic modelling. With the emergence of digital production technologies and the reinvention of existing tools, a multitude of design approaches for guided angio- and vasculogenesis is available today. The underlying production methods can be categorized into biosynthetic, biomimetic and self-assembled vasculature formation. The diversity and importance of production approaches, vascularization strategies as well as biomaterials and cell sourcing are illustrated in this work. A comprehensive technological review with a strong focus on the challenge of producing physiologically relevant vascular structures is given. Finally, the remaining obstacles and opportunities in the development of vascularized Organ-on-a-Chip platforms for advancing drug development and predictive disease modelling are noted.

Typ des Eintrags: Artikel
Erschienen: 2023
Autor(en): Fritschen, Anna ; Blaeser, Andreas
Art des Eintrags: Zweitveröffentlichung
Titel: Biosynthetic, biomimetic, and self-assembled vascularized Organ-on-a-Chip systems
Sprache: Englisch
Publikationsjahr: 2023
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 2021
Verlag: Elsevier
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Biomaterials
Jahrgang/Volume einer Zeitschrift: 268
Kollation: 34 ungezählte Seiten
DOI: 10.26083/tuprints-00024336
URL / URN: https://tuprints.ulb.tu-darmstadt.de/24336
Zugehörige Links:
Herkunft: Zweitveröffentlichungsservice
Kurzbeschreibung (Abstract):

Organ-on-a-Chip (OOC) devices have seen major advances in the last years with respect to biological complexity, physiological composition and biomedical relevance. In this context, integration of vasculature has proven to be a crucial element for long-term culture of thick tissue samples as well as for realistic pharmacokinetic, toxicity and metabolic modelling. With the emergence of digital production technologies and the reinvention of existing tools, a multitude of design approaches for guided angio- and vasculogenesis is available today. The underlying production methods can be categorized into biosynthetic, biomimetic and self-assembled vasculature formation. The diversity and importance of production approaches, vascularization strategies as well as biomaterials and cell sourcing are illustrated in this work. A comprehensive technological review with a strong focus on the challenge of producing physiologically relevant vascular structures is given. Finally, the remaining obstacles and opportunities in the development of vascularized Organ-on-a-Chip platforms for advancing drug development and predictive disease modelling are noted.

Status: Postprint
URN: urn:nbn:de:tuda-tuprints-243367
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 620 Ingenieurwissenschaften und Maschinenbau
Fachbereich(e)/-gebiet(e): 16 Fachbereich Maschinenbau
16 Fachbereich Maschinenbau > Institut für Druckmaschinen und Druckverfahren (IDD)
16 Fachbereich Maschinenbau > Institut für Druckmaschinen und Druckverfahren (IDD) > Biomedizinische Drucktechnologie (BMT)
Hinterlegungsdatum: 17 Jul 2023 12:09
Letzte Änderung: 18 Jul 2023 05:28
PPN:
Export:
Suche nach Titel in: TUfind oder in Google

Verfügbare Versionen dieses Eintrags

Frage zum Eintrag Frage zum Eintrag

Optionen (nur für Redakteure)
Redaktionelle Details anzeigen Redaktionelle Details anzeigen