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1.
ACS Nano ; 18(22): 14388-14402, 2024 Jun 04.
Artículo en Inglés | MEDLINE | ID: mdl-38775287

RESUMEN

Organ-on-a-chip, which recapitulates the dynamics of in vivo vasculature, has emerged as a promising platform for studying organ-specific vascular beds. However, its practical advantages in identifying vascular-targeted drug delivery systems (DDS) over traditional in vitro models remain underexplored. This study demonstrates the reliability and efficacy of the organ-on-a-chip in screening efficient DDS by comparing its performance with that of a conventional transwell, both designed to simulate the blood-brain barrier (BBB). The BBB nanoshuttles discovered through BBB Chip-based screening demonstrated superior functionality in vivo compared to those identified using transwell methods. This enhanced effectiveness is attributed to the BBB Chip's accurate replication of the structure and dynamics of the endothelial glycocalyx, a crucial protective layer within blood vessels, especially under shear stress. This capability of the BBB Chip has enabled the identification of molecular shuttles that efficiently exploit the endothelial glycocalyx, thereby enhancing transendothelial transport efficacy. Our findings suggest that organ-on-a-chip technology holds considerable promise for advancing research in vascular-targeted DDS due to its accurate simulation of molecular transport within endothelial systems.


Asunto(s)
Barrera Hematoencefálica , Dispositivos Laboratorio en un Chip , Barrera Hematoencefálica/metabolismo , Animales , Sistemas de Liberación de Medicamentos , Glicocálix/metabolismo , Glicocálix/química , Humanos , Ratones , Sistemas Microfisiológicos
2.
Tissue Eng Regen Med ; 17(6): 747-757, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-32329023

RESUMEN

BACKGROUND: Brain organoids are self-organized from human pluripotent stem cells and developed into various brain region following the developmental process of brain. Brain organoids provide promising approach for studying brain development process and neurological diseases and for tissue regeneration. METHODS: In this review, we summarized the development of brain organoids technology, potential applications focusing on disease modeling for regeneration medicine, and multidisciplinary approaches to overcome current limitations of the technology. RESULTS: Generations of brain organoids are categorized into two major classes by depending on the patterning method. In order to guide the differentiation into specific brain region, the extrinsic factors such as growth factors, small molecules, and biomaterials are actively studied. For better modelling of diseases with brain organoids and clinical application for tissue regeneration, improvement of the brain organoid maturation is one of the most important steps. CONCLUSION: Brain organoids have potential to develop into an innovative platform for pharmacological studies and tissue engineering. However, they are not identical replicas of their in vivo counterpart and there are still a lot of limitations to move forward to clinical applications.


Asunto(s)
Organoides , Células Madre Pluripotentes , Encéfalo , Diferenciación Celular , Humanos , Ingeniería de Tejidos
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