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Restricted mobility of specific functional groups reduces anti-cancer drug activity in healthy cells.
Martins, Murillo L; Ignazzi, Rosanna; Eckert, Juergen; Watts, Benjamin; Kaneno, Ramon; Zambuzzi, Willian F; Daemen, Luke; Saeki, Margarida J; Bordallo, Heloisa N.
Afiliação
  • Martins ML; Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen, Denmark.
  • Ignazzi R; Instituto de Biociências - Universidade Estadual Paulista - CP 510, 18618-970 Botucatu-SP, Brazil.
  • Eckert J; Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen, Denmark.
  • Watts B; Department of Chemistry, University of South Florida, 4202 E. Fowler Ave., Tampa, Florida 33620, United States.
  • Kaneno R; Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Zambuzzi WF; Swiss Light Source, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
  • Daemen L; Instituto de Biociências - Universidade Estadual Paulista - CP 510, 18618-970 Botucatu-SP, Brazil.
  • Saeki MJ; Instituto de Biociências - Universidade Estadual Paulista - CP 510, 18618-970 Botucatu-SP, Brazil.
  • Bordallo HN; Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
Sci Rep ; 6: 22478, 2016 Mar 02.
Article em En | MEDLINE | ID: mdl-26932808
ABSTRACT
The most common cancer treatments currently available are radio- and chemo-therapy. These therapies have, however, drawbacks, such as, the reduction in quality of life and the low efficiency of radiotherapy in cases of multiple metastases. To lessen these effects, we have encapsulated an anti-cancer drug into a biocompatible matrix. In-vitro assays indicate that this bio-nanocomposite is able to interact and cause morphological changes in cancer cells. Meanwhile, no alterations were observed in monocytes and fibroblasts, indicating that this system might carry the drug in living organisms with reduced clearance rate and toxicity. X-rays and neutrons were used to investigate the carrier structure, as well as to assess the drug mobility within the bio-nanocomposite. From these unique data we show that partial mobility restriction of active groups of the drug molecule suggests why this carrier design is potentially safer to healthy cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article