000 nab a22 7a 4500
999 _c17074
_d17074
003 PC17074
005 20221117134412.0
008 221117b xxu||||| |||| 00| 0 eng d
040 _cH12O
041 _aeng
100 _93113
_aVillegas, María Rocío
_eInstituto de Investigación imas12
100 _92995
_aBaeza, Alejandro
_eInstituto de Investigación imas12
245 0 0 _aHybrid Collagenase Nanocapsules for Enhanced Nanocarrier Penetration in Tumoral Tissues. ACS Appl Mater Interfaces.
_h[artículo]
260 _bACS applied materials & interfaces,
_c2015
300 _a7(43):24075-81.
500 _aFormato Vancouver: Villegas MR, Baeza A, Vallet Regí M. Hybrid Collagenase Nanocapsules for Enhanced Nanocarrier Penetration in Tumoral Tissues. ACS Appl Mater Interfaces. 2015 Nov 4;7(43):24075-81.
501 _a PMID: 26461206
504 _aContiene 26 referencias
520 _aPoor penetration of drug delivery nanocarriers within dense extracellular matrices constitutes one of the main liabilities of current nanomedicines. The conjugation of proteolytic enzymes on the nanoparticle surface constitutes an attractive alternative. However, the scarce resistance of these enzymes against the action of proteases or other aggressive agents present in the bloodstream strongly limits their application. Herein, a novel nanodevice able to transport proteolytic enzymes coated with an engineered pH-responsive polymeric is presented. This degradable coat protects the housed enzymes against proteolytic attack at the same time that it triggers their release under mild acidic conditions, usually present in many tumoral tissues. These enzyme nanocapsules have been attached on the surface of mesoporous silica nanoparticles, as nanocarrier model, showing a significatively higher penetration of the nanoparticles within 3D collagen matrices which housed human osteosarcoma cells (HOS). This strategy can improve the therapeutic efficacy of the current nanomedicines, allowing a more homogeneous and deeper distribution of the therapeutic nanosystems in cancerous tissues.
710 _9625
_aInstituto de Investigación imas12
856 _uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc17074.pdf
_ySolicitar documento
942 _2ddc
_cART
_n0