Your browser doesn't support javascript.
loading
Electrokinetic convection-enhanced delivery for infusion into the brain from a hydrogel reservoir.
Cruz-Garza, Jesus G; Bhenderu, Lokeshwar S; Taghlabi, Khaled M; Frazee, Kendall P; Guerrero, Jaime R; Hogan, Matthew K; Humes, Frances; Rostomily, Robert C; Horner, Philip J; Faraji, Amir H.
Afiliação
  • Cruz-Garza JG; Department of Neurosurgery, Houston Methodist Research Institute, Houston, TX, USA. jgcruzgarza@houstonmethodist.org.
  • Bhenderu LS; Center for Neural Systems Restoration, Houston Methodist Research Institute, Houston, TX, USA. jgcruzgarza@houstonmethodist.org.
  • Taghlabi KM; Department of Neurosurgery, Houston Methodist Research Institute, Houston, TX, USA. lokeshwar.bhenderu@houstonmethodist.org.
  • Frazee KP; Center for Neural Systems Restoration, Houston Methodist Research Institute, Houston, TX, USA. lokeshwar.bhenderu@houstonmethodist.org.
  • Guerrero JR; Texas A&M University College of Medicine, Houston, TX, USA. lokeshwar.bhenderu@houstonmethodist.org.
  • Hogan MK; Department of Neurosurgery, Houston Methodist Research Institute, Houston, TX, USA.
  • Humes F; Center for Neural Systems Restoration, Houston Methodist Research Institute, Houston, TX, USA.
  • Rostomily RC; Department of Neurosurgery, Houston Methodist Research Institute, Houston, TX, USA.
  • Horner PJ; School of Engineering, Texas A&M, College Station, TX, USA.
  • Faraji AH; Department of Neurosurgery, Houston Methodist Research Institute, Houston, TX, USA.
Commun Biol ; 7(1): 869, 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-39020197
ABSTRACT
Electrokinetic convection-enhanced delivery (ECED) utilizes an external electric field to drive the delivery of molecules and bioactive substances to local regions of the brain through electroosmosis and electrophoresis, without the need for an applied pressure. We characterize the implementation of ECED to direct a neutrally charged fluorophore (3 kDa) from a doped biocompatible acrylic acid/acrylamide hydrogel placed on the cortical surface. We compare fluorophore infusion profiles using ECED (time = 30 min, current = 50 µA) and diffusion-only control trials, for ex vivo (N = 18) and in vivo (N = 12) experiments. The linear intensity profile of infusion to the brain is significantly higher in ECED compared to control trials, both for in vivo and ex vivo. The linear distance of infusion, area of infusion, and the displacement of peak fluorescence intensity along the direction of infusion in ECED trials compared to control trials are significantly larger for in vivo trials, but not for ex vivo trials. These results demonstrate the effectiveness of ECED to direct a solute from a surface hydrogel towards inside the brain parenchyma based predominantly on the electroosmotic vector.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Sistemas de Liberação de Medicamentos / Convecção / Hidrogéis Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Sistemas de Liberação de Medicamentos / Convecção / Hidrogéis Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article