Nanostructured Stealth Surfaces for Visible and Near-Infrared Light.

Nano Lett

Department of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, and Laboratory of Biophysical Chemistry, University of Heidelberg, Jahnstraße 29, 69120 Heidelberg, Germany.

Published: October 2016

So far, all previous attempts to apply nanostructures for perfect transmission have not achieved maximum transmittance beyond 99.5% due to the limited regularity of the nanoscale surface geometry: too low for many high-end applications. Here we demonstrate a nanostructured stealth surface, with minimal reflectance (<0.02%) and maximal transmittance (>99.8%) for a wavelength range, covering visible and near-infrared. Compared to multilayer thin film coatings for near-infrared applications our antireflective surfaces operate within a much broader wavelength range, are mechanical stable to resist human touch or contamination, show a 44% higher laser-induced damage threshold, and are suitable for bended interfaces such as microlenses as well.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.nanolett.6b03308DOI Listing

Publication Analysis

Top Keywords

nanostructured stealth
8
visible near-infrared
8
wavelength range
8
stealth surfaces
4
surfaces visible
4
near-infrared light
4
light previous
4
previous attempts
4
attempts apply
4
apply nanostructures
4

Similar Publications

Cyclic poly(2-methyl-2-oxazine) (-PMOZI) brush shells on Au nanoparticles (NPs) exhibit enhanced stealth properties toward serum and different cell lines compared to their linear PMOZI (-PMOZI) counterparts. While selectively recruiting immunoglobulins, -PMOZI shells reduce overall human serum (HS) protein binding and alter the processing of complement factor 3 (C3) compared to chemically identical linear shells. Polymer cyclization significantly decreases NP uptake by nonphagocytic cells and macrophages in both complement-deficient fetal bovine serum (FBS) and complement-expressing HS, indicating ineffective functional opsonization.

View Article and Find Full Text PDF

High-performance color-changing compounds, recognized as prominent smart materials, dynamically alter their color in response to external environmental stimuli. However, existing compounds exhibit limited responsiveness and color diversity, presenting challenges in the development of textiles responsive to multiple stimuli. This research introduces a novel design for dual-responsive color-changing microcapsules, employing a Pickering emulsion template method.

View Article and Find Full Text PDF

Purpose: In the bloodstream, nanoparticles (NPs) interact with serum proteins to form the protein corona, which includes both opsonins, promoting NP recognition and elimination, and dysopsonins, which can inhibit opsonin activity. Albumin, the most abundant serum protein, is part of this corona and can act as a dysopsonin, potentially hiding NPs from the immune system. This study aims to investigate how a covalently bound layer of human serum albumin (HSA) on polymeric NPs affects the protein corona and their behavior in the immune system.

View Article and Find Full Text PDF

Introduction: The treatment of glioblastoma is hindered by the blood-brain barrier (BBB) and rapid drug clearance by the immune system. To address these challenges, we propose a novel drug delivery system using liposomes modified with cell membrane fragments. These modified liposomes can evade the immune system, cross the BBB, and accumulate in tumor tissue through homotypic targeting, thereby delivering drugs like paclitaxel and carboplatin more effectively.

View Article and Find Full Text PDF

The regulation of immunosuppressive microenvironments in tumors through targeted drug delivery shows promise for immunochemotherapy in bladder cancer. Drawing inspiration from stealth tactics, a nano-vehicle camouflaged with platelets (PLTs) was developed to enable precise delivery and trigger pyroptosis for tumor immunotherapy. Erdafitinib (Erda) was nano-sized and encapsulated in PLTs to construct nano-Erda@PLT.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!