Employing antagonistic C-X-C motif chemokine receptor 4 antagonistic peptide functionalized NaGdF nanodots for magnetic resonance imaging-guided biotherapy of breast cancer.

C-X-C motif chemokine receptor 4 (CXCR4) is a promising therapeutic target of breast cancer because it is overexpressed on cell surface of all molecular subtypes of breast cancer including triplenegative breast cancer (TNBC). Herein, CXCR4 antagonistic peptide-NaGdF nanodot conjugates (termed as anti-CXCR4-NaGdF NDs) have been constructed for magnetic resonance imaging (MRI)-guided biotherapy of TNBC through conjugation of the C-X-C Motif Chemokine 12 (CXCL12)-derived cyclic peptide with tryptone coated NaGdF nanodots (5 ± 0.5 nm in diameter, termed as Try-NaGdF NDs).

Octahedral Distortion Co-Regulation via Dual Strategies toward Luminescence Enhancement for the MAInBr Perovskite Single Crystal.

A series of novel perovskite single crystals are innovatively grown. Aiming to enhance the luminescence performance, octahedral distortion co-regulation via dual strategies for the as-prepared perovskite single crystals is performed. The distortion of the octahedral structure strengthens the electron-phonon coupling and electron localization, resulting in a more stable self-trapped state, which thereby increases the potential for radiative recombination, accompanied by the self-trapped exciton emission.

Engineered Electronic Structure and Carrier Dynamics in Emerging CsAgNaFeCl Perovskite Single Crystals.

Lead-free double perovskites have attracted noteworthy attention due to their compositional flexibility and electronic diversity. In this study, we hydrothermally grow a new class of CsAgNaFeCl (0 ≤ ≤ 1) perovskite single crystals with high thermal stability. The substitution of B-site cation allows to regulate the crystallographic and band structure, which gives rise to enlarged band absorbance close to the near-infrared region (∼800 nm) via composition engineering.

Modification of electron structure on the semiconducting single-walled carbon nanotubes for effectively electrosensing guanine and adenine.

The as-prepared SWNTs are always a mixture of metallic (m-) and semiconducting (s-) tubes with quite different electrochemical properties which is a major barrier for their application in many fields. Based on the noncovalent interactions between planar aromatic molecules and SWNTs, the pyrene derivatives 1-docosyloxylmethylpyrene (DomP) was synthesized to separate the m-SWNTs and s-SWNTs via its significant selectivity toward s-SWNTs, i.e.

Novel Strategy for the Investigation on Chirality Selection of Single-Walled Carbon Nanotubes with DNA by Electrochemical Characterization.

There is a correlation between specific bases of DNA molecules and the chirality of single-walled carbon nanotubes (SWNTs), which contributes the recognition ability of DNA toward partner species of chiral SWNTs. A novel strategy of electrochemical characterization is reported here for the investigation on chirality selection of (7,6) and (6,5) SWNTs with various DNA sequences, and it is found that both DNA strand length and sequence composition significantly affected the interaction of chiral SWNTs with DNA. Then (7,6) and (6,5) SWNTs were distinguished from each other with DNA sequences chosen by electrochemical methods, which demonstrated an effective and excellent feasibility for the strategy and presented a new insight into DNA-SWNT applications.