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Development of a Nanoparticle-Embedded Chitosan Sponge for Topical and Local Administration of Chemotherapeutic Agents.
Goldberg, Manijeh; Manzi, Aaron; Aydin, Erkin; Singh, Gurtej; Khoshkenar, Payam; Birdi, Amritpreet; LaPorte, Brandon; Krauskopf, Alejandro; Powell, Geralle; Chen, Julie; Langer, Robert.
Afiliação
  • Goldberg M; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Manzi A; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Aydin E; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Singh G; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Khoshkenar P; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Birdi A; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • LaPorte B; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Krauskopf A; Massachusetts Institute of Technology , Cambridge, MA 02139.
  • Powell G; Wellesley College , Department of Biology, Wellesley, MA 02481.
  • Chen J; University of Massachusetts Lowell , Department of Mechanical Engineering, Lowell, MA 01854.
  • Langer R; Massachusetts Institute of Technology , Cambridge, MA 02139.
J Nanotechnol Eng Med ; 5(4): 0409051-4090511, 2014 Nov.
Article em En | MEDLINE | ID: mdl-26336575
ABSTRACT
The following work describes the development of a novel noninvasive transmucosal drug delivery system, the chitosan sponge matrix (CSM). It is composed of cationic chitosan (CS) nanoparticles (NPs) that encapsulate cisplatin (CDDP) embedded within a polymeric mucoadhesive CS matrix. CSM is designed to swell up when exposed to moisture, facilitating release of the NPs via diffusion across the matrix. CSM is intended to be administered topically and locally to mucosal tissues, with its initial indication being oral cancer (OC). Currently, intravenous (IV) administered CDDP is the gold standard chemotherapeutic agent used in the treatment of OC. However, its clinical use has been limited by its renal and hemotoxicity profile. We aim to locally administer CDDP via encapsulation in CS NPs and deliver them directly to the oral cavity with CSM. It is hypothesized that such a delivery device will greatly reduce any systemic toxicity and increase antitumor efficacy. This paper describes the methods for developing CSM and maintaining the integrity of CDDP NPs embedded in the CSM.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: J Nanotechnol Eng Med Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: J Nanotechnol Eng Med Ano de publicação: 2014 Tipo de documento: Article