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Unlocking the Gates: Therapeutic Agents for Noninvasive Drug Delivery Across the Blood-Brain Barrier.
Culkins, Courtney; Adomanis, Roman; Phan, Nathan; Robinson, Blaise; Slaton, Ethan; Lothrop, Elijah; Chen, Yinuo; Kimmel, Blaise R.
Afiliação
  • Culkins C; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Adomanis R; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Phan N; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Robinson B; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Slaton E; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Lothrop E; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Chen Y; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
  • Kimmel BR; Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
Mol Pharm ; 21(11): 5430-5454, 2024 Nov 04.
Article em En | MEDLINE | ID: mdl-39324552
ABSTRACT
The blood-brain barrier (BBB) is a highly selective network of various cell types that acts as a filter between the blood and the brain parenchyma. Because of this, the BBB remains a major obstacle for drug delivery to the central nervous system (CNS). In recent years, there has been a focus on developing various modifiable platforms, such as monoclonal antibodies (mAbs), nanobodies (Nbs), peptides, and nanoparticles, as both therapeutic agents and carriers for targeted drug delivery to treat brain cancers and diseases. Methods for bypassing the BBB can be invasive or noninvasive. Invasive techniques, such as transient disruption of the BBB using low pulse electrical fields and intracerebroventricular infusion, lack specificity and have numerous safety concerns. In this review, we will focus on noninvasive transport mechanisms that offer high levels of biocompatibility, personalization, specificity and are regarded as generally safer than their invasive counterparts. Modifiable platforms can be designed to noninvasively traverse the BBB through one or more of the following pathways passive diffusion through a physio-pathologically disrupted BBB, adsorptive-mediated transcytosis, receptor-mediated transcytosis, shuttle-mediated transcytosis, and somatic gene transfer. Through understanding the noninvasive pathways, new applications, including Chimeric Antigen Receptors T-cell (CAR-T) therapy, and approaches for drug delivery across the BBB are emerging.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Barreira Hematoencefálica / Sistemas de Liberação de Medicamentos Limite: Animals / Humans Idioma: En Revista: Mol Pharm Assunto da revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Barreira Hematoencefálica / Sistemas de Liberação de Medicamentos Limite: Animals / Humans Idioma: En Revista: Mol Pharm Assunto da revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos