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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 1 ·47367 · IF 2.188

Synthesis of a bio-based triazine derivative and its effects on flame retardancy of polypropylene composites

Dong Ma,Juan Li

A triazine derivative CC–Cy was synthesized using cytosine (Cy) and cyanuric chloride (CC). The CC–Cy was used as a charring agent and combined with ammonium polyphosphate (APP) to form an intumescent flame-retardant (IFR) system. The IFR system was applied to improve the flame retardancy of polypropylene (PP). Moreover, bisphenol-A bis(diphenyl phosphate) (BDP) was introduced in the IFR system to regulate the suitability between the IFR and PP. The results showed the PP containing 20 wt % APP and 5 wt % CC–Cy achieves the UL-94 V-2 rating. While the PP with 18 wt % APP/CC-Cy (4:1) and 3 wt % BDP obtains the UL-94 V-0 rating indicating the improved flame-retardant efficiency. Thermal degradation behaviors and char morphology both showed that the reactions between APP and CC–Cy promote the formation of char residues, and BDP works in gas phase to enhance the flame retardancy of PP composites. Thus, a synergistic IFR system based on APP, CC–Cy, and BDP is formed, which can protect PP from fire effectively. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 47367.

CAS / MDL: 2579-20-6 21868-80-4

研究领域: 材料科学 · 化学工程

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JOURNAL OF MEDICINAL CHEMISTRY · 2026 · IF 7.3

LvID-BDP: A Conotoxin-Based Fluorescent Probe for Visualizing α7 nAChR Expression in Intestinal Inflammation

Yao Tan,Tao Ma,Siyuan Li,Chenxing Xu,Yu Han,Dongting Zhangsun,Xiaopeng Zhu,Sulan Luo

The α7 nicotinic acetylcholine receptor (α7 nAChR) modulates neuroimmune signaling but remains poorly characterized in peripheral disease due to a lack of visualization tools. We developed the fluorescent probe LvID-BDP by conjugating a BODIPY fluorophore to the high-affinity α7 nAChR-targeting peptide LvID. LvID-BDP showed high quantum yield, robust photostability, and sufficient physiological stability for biological imaging. Electrophysiology characterized LvID-BDP as a potent α7 nAChR antagonist, exhibiting a half-maximal inhibitory concentration (IC50) of 119.2 nM while retaining high affinity and specificity for the receptor. In murine colon sections, LvID-BDP specifically labeled α7 nAChR, showing strong antibody colocalization (Pearson’s R = 0.87) while revealing macrophage-selective enrichment (Pearson’s R = 0.85). This probe detected α7 nAChR alterations in engineered and inflamed macrophages and quantified its expression in inflammatory bowel disease (IBD) tissues. LvID-BDP provides a valuable pharmacological tool for specific α7 nAChR visualization in peripheral disease contexts, advancing pathological mechanism research.

CAS / MDL: 1330-43-4 134-03-2 13746-66-2 7553-56-2

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