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Therapeutic luminal coating of the intestine.
Lee, Yuhan; Deelman, Tara E; Chen, Keyue; Lin, Dawn S Y; Tavakkoli, Ali; Karp, Jeffrey M.
Afiliación
  • Lee Y; Engineering in Medicine, Department of Medicine, Center for Regenerative Therapeutics, Brigham and Women's Hospital, Harvard Medical School, Harvard Stem Cell Institute, Harvard-MIT, Division of Health Sciences and Technology, Boston, MA, USA. ylee21@bwh.harvard.edu.
  • Deelman TE; Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Chen K; Department of Surgery, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Lin DSY; Laboratory for Surgical and Metabolic Research, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Tavakkoli A; Engineering in Medicine, Department of Medicine, Center for Regenerative Therapeutics, Brigham and Women's Hospital, Harvard Medical School, Harvard Stem Cell Institute, Harvard-MIT, Division of Health Sciences and Technology, Boston, MA, USA.
  • Karp JM; Engineering in Medicine, Department of Medicine, Center for Regenerative Therapeutics, Brigham and Women's Hospital, Harvard Medical School, Harvard Stem Cell Institute, Harvard-MIT, Division of Health Sciences and Technology, Boston, MA, USA.
Nat Mater ; 17(9): 834-842, 2018 09.
Article en En | MEDLINE | ID: mdl-29891893
The gastrointestinal tract is the site of most drug delivery and therapeutic interventions for the management and treatment of numerous diseases. However, selective access to its mucosa, especially in the small bowel, is challenging. Here we develop an orally administered gut-coating formulation that provides a transient coating of the bowel. Through a materials screening campaign, we identified a sucrose octasulfate aluminium complex and further engineered the pH-dependent material into a complex coacervate formulation linked via pH-independent electrostatic interaction, which allowed an effective transient physical coating on the gastrointestinal mucosa, independent of gastric acid exposure. We tested the therapeutic values of this technology in two settings. Oral administration of this gut-coating formulation modulated the nutrient contact with bowel mucosa, which lowered the glucose responses in rodent models indicating a potential therapeutic utility in diabetes. Furthermore, the formulation protected biological agents from gastric acid exposure and degradation, which enabled oral delivery to the small bowel mucosa.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mucosa Intestinal Límite: Animals Idioma: En Revista: Nat Mater Asunto de la revista: CIENCIA / QUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mucosa Intestinal Límite: Animals Idioma: En Revista: Nat Mater Asunto de la revista: CIENCIA / QUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
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