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1.
ACS Appl Mater Interfaces ; 10(41): 35495-35502, 2018 Oct 17.
Article in English | MEDLINE | ID: mdl-30251823

ABSTRACT

Black phosphorus (BP) nanosheets with unique biocompatibility and superior optical performance have attracted enormous attention in material science. However, their instability and poor solution-processability severely limit their clinical applications. In this work, we demonstrate the use of silk fibroin (SF) as an exfoliating agent to produce thin-layer BP nanosheets with long-term stability and facile solution-processability. Presence of SF prevents rapid oxidation and degradation of the resultant BP nanosheets, enhancing their performance in physiological environment. The SF-modified BP nanosheets exhibit subtle solution-processability and are fabricated into various BP-based material formats. As superior photothermal agents, BP-based wound dressings effectively prevent bacterial infection and promote wound repair. Therefore, this work opens new avenues for unlocking current challenges of BP nanosheet applications for practical biomedical purposes.


Subject(s)
Bacterial Infections/drug therapy , Fibroins , Nanocomposites , Phosphorus , Wound Healing/drug effects , Wound Infection/drug therapy , Animals , Cell Line , Fibroins/chemistry , Fibroins/pharmacology , Humans , Mice , Nanocomposites/chemistry , Nanocomposites/therapeutic use , Phosphorus/chemistry , Phosphorus/pharmacology
2.
Chem Commun (Camb) ; 54(25): 3142-3145, 2018 Mar 28.
Article in English | MEDLINE | ID: mdl-29527603

ABSTRACT

Gene therapy with small interfering RNA (siRNA) has been proved to be a promising technology to treat various diseases by hampering the production of target proteins. However, developing a delivery system that has high efficiency in transporting siRNA without obvious side effects remains a challenge. Herein, we designed a new survivin siRNA delivery system based on polyethyleneimine functionalized black phosphorus (BP) nanosheets which could suppress tumor growth by silencing survivin expression. Combined with the photothermal properties of the BP nanosheets, the presented delivery system shows excellent therapy efficiency for tumors. Therefore, the BP-based delivery system would be a promising tool for future clinical applications.


Subject(s)
Drug Delivery Systems , Gene Silencing/drug effects , Genetic Therapy , Nanostructures/chemistry , Phosphorus/chemistry , Phototherapy , Polyethyleneimine/chemistry , RNA, Small Interfering/pharmacology , Animals , Cell Proliferation/drug effects , Female , Humans , MCF-7 Cells , Mammary Neoplasms, Experimental/drug therapy , Mammary Neoplasms, Experimental/pathology , Mice , RNA, Small Interfering/administration & dosage
3.
Nanoscale ; 9(44): 17193-17198, 2017 Nov 16.
Article in English | MEDLINE | ID: mdl-29095468

ABSTRACT

Two-dimensional transition metal dichalcogenides (TMDs) have attracted rapidly increasing attention due to their fascinating properties and potential applications. However, scalable and cost-effective methods to produce thin-layer TMD nanosheets and their functional composites with environmental benignity are still limited. Herein, we develop a facile and environmentally friendly method for the scalable production of thin-layer TMD nanosheets in an aqueous medium by using silk fibroin, a natural and abundant biopolymer, as the exfoliating agent. Specifically, carboxyl-modified silk fibroin significantly improves the exfoliation efficiency, achieving the high-yield production of thin-layer MoSe2 nanosheets with good solution stabilization and excellent biocompatibility. Strong binding interactions endow the resultant MoSe2 nanosheets with unprecedentedly high concentrations. By virtue of the solution-processability of silk fibroin, MoSe2 hybrid nanosheets are readily fabricated into macroscopic freestanding films. Furthermore, due to the superior peroxidase-like activity of MoSe2 nanosheets, MoSe2-based films show rapid and effective wound disinfection and healing efficacy with the use of low-dose H2O2in vivo, avoiding the side effects of high-dose H2O2 in traditional medical therapy. This work may offer new opportunities to apply two-dimensional TMD nanosheets for clinical applications.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bandages , Fibroins/chemistry , Nanostructures , Selenium/chemistry , Animals , Bacillus subtilis/drug effects , Escherichia coli/drug effects , Hydrogen Peroxide , Mice , Molybdenum/chemistry , Skin Diseases, Bacterial/drug therapy , Wound Infection/drug therapy
4.
Nanoscale ; 9(8): 2695-2700, 2017 Feb 23.
Article in English | MEDLINE | ID: mdl-28186214

ABSTRACT

Uniform hydrophobic nanoparticles synthesized in nonpolar solvents possess excellent physio-chemical properties, showing great potential in biomedical applications. However, the presence of hydrophobic ligands on their surfaces limits their use under physiological conditions. Inspired by protein coronas present at the nano-bio interface, here we report a facile and universal method for phase transfer and surface bioengineering of hydrophobic nanoparticles using ß-sheet-rich silk fibroin, a FDA-approved natural protein. Due to its amphiphilicity and high mechanical stiffness, the ß-sheet-rich silk fibroin not only readily drags nanoparticles from an organic phase into aqueous media but also endows them with excellent monodispersity and long-term stability. The silk fibroin-coated nanoparticles can retain the magnetic and optical properties of the original nanoparticles, acting effectively as probes for biomedical imaging and biosensing. Furthermore, hydrophobic drugs can be easily adsorbed onto the protein coating via hydrophobic interaction, allowing the construction of promising theranostic nanoagents. Given these unique features, the strategy developed here possesses great promise in facilitating biomedical applications of hydrophobic nanomaterials.


Subject(s)
Fibroins/chemistry , Metal Nanoparticles , Protein Corona/chemistry , Animals , Bioengineering , Bombyx , Ferric Compounds , Hydrophobic and Hydrophilic Interactions , Protein Conformation, beta-Strand
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