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10.1021/acsnano.7b04979

http://scihub22266oqcxt.onion/10.1021/acsnano.7b04979
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suck abstract from ncbi


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pmid28806871      ACS+Nano 2017 ; 11 (9): 9413-9423
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  • Bioreducible Hydrophobin-Stabilized Supraparticles for Selective Intracellular Release #MMPMID28806871
  • Maiolo D; Pigliacelli C; Sanchez Moreno P; Violatto MB; Talamini L; Tirotta I; Piccirillo R; Zucchetti M; Morosi L; Frapolli R; Candiani G; Bigini P; Metrangolo P; Baldelli Bombelli F
  • ACS Nano 2017[Sep]; 11 (9): 9413-9423 PMID28806871show ga
  • One of the main hurdles in nanomedicine is the low stability of drug-nanocarrier complexes as well as the drug delivery efficiency in the region-of-interest. Here, we describe the use of the film-forming protein hydrophobin HFBII to organize dodecanethiol-protected gold nanoparticles (NPs) into well-defined supraparticles (SPs). The obtained SPs are exceptionally stable in vivo and efficiently encapsulate hydrophobic drug molecules. The HFBII film prevents massive release of the encapsulated drug, which, instead, is activated by selective SP disassembly triggered intracellularly by glutathione reduction of the protein film. As a consequence, the therapeutic efficiency of an encapsulated anticancer drug is highly enhanced (2 orders of magnitude decrease in IC(50)). Biodistribution and pharmacokinetics studies demonstrate the high stability of the loaded SPs in the bloodstream and the selective release of the payloads once taken up in the tissues. Overall, our results provide a rationale for the development of bioreducible and multifunctional nanomedicines.
  • |Animals[MESH]
  • |Antineoplastic Agents, Phytogenic/*administration & dosage/pharmacokinetics[MESH]
  • |Cell Line, Tumor[MESH]
  • |Drug Liberation[MESH]
  • |Female[MESH]
  • |Fungal Proteins/*chemistry[MESH]
  • |Gold/*chemistry[MESH]
  • |Humans[MESH]
  • |Hypocrea/*chemistry[MESH]
  • |Metal Nanoparticles/*chemistry[MESH]
  • |Mice, Inbred BALB C[MESH]


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