Green synthesis of water-compatible layer-by-layer assembled sandwich bread-like molecularly imprinted polymers for selective recognition of baicalin from Scutellariae Radix.

J Chromatogr A

Key Laboratory of Protection, Development and Utilization of Medicinal Resources in Liupanshan Area, Ministry of Education, College of Pharmacy, Ningxia Medical University, Yinchuan 750004, China; Key Laboratory of Ningxia Minority Medicine Modernization, Ministry of Education, Ningxia Medical Unive

Published: February 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Molecularly imprinted polymers (MIPs) are typically synthesized in organic solvents, leading to poor compatibility with water, weak affinity and selectivity for target molecules in aqueous media. To address these challenges, a green and sustainable synthesis of sandwich bread-like ATP@MIP was conducted using polyethylenimide (PEI) and deep eutectic solvent (DES) as hydrophilic bi-functional monomers via layer-by-layer self-assembly on the attapulgite (ATP) carrier. The new ATP@MIP can provide a higher density of imprinting sites with more orderly and uniform distribution due to inhibiting the competitive polymerization between PEI and DES, thereby significantly enhancing recognition ability. Moreover, the ATP@MIP was synthesized in water, aligning with green chemistry principles and establishing a sustainable preparation method for MIP materials. Equipped with the remarkable merits of good water compatibility, excellent selectivity (IF=3.6), high adsorption capacity (77.6 mg g) and desirable repeatability (8 times), the as-prepared materials were used as a solid phase extraction adsorbent for efficient separation and enrichment of baicalin from Scutellariae Radix. More importantly, the recognizing performance of ATP@MIP for baicalin increased 1.40-1.69 times than other MIP materials, and its excellent specificity was demonstrated in comparison with several common commercial adsorbents (C18, HLB, MCX and SAX). Therefore, this work introduces a feasible and green strategy to synthesize water-compatible MIP materials for highly selective enrichment and separation of active components from natural products.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.chroma.2025.465673DOI Listing

Publication Analysis

Top Keywords

mip materials
12
sandwich bread-like
8
molecularly imprinted
8
imprinted polymers
8
baicalin scutellariae
8
scutellariae radix
8
green
4
green synthesis
4
synthesis water-compatible
4
water-compatible layer-by-layer
4

Similar Publications

A novel molecularly imprinted polymer (MIP)-based electrochemical sensor has been developed for the selective detection of naringenin (NAR) in various real-world samples, including plant extracts, wine, and herbal supplements. To enhance the active surface area and porosity of the glassy carbon electrode (GCE), a 2D/0D nanocomposite composed of graphene oxide (GO) and cobalt ferrite (CFO) nanoparticles, CFO_GO, was incorporated into the sensor design. 4-aminobenzoic acid (4-ABA) was selected as the functional monomer to prepare the MIPs.

View Article and Find Full Text PDF

Amplified electrochemical detection of sulfadiazine based on Cu-BTC-encapsulated FeNi dual-atom catalysts with improved catalytic efficiency.

Anal Methods

September 2025

College of Environmental Science and Engineering, Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Niversity Engineering Research Center of Watershed Protection and Green Development, Guilin University of Technology, Guilin, 541006, China.

The amplification of detection signals is an important method for improving the sensitivity of electrochemical detection. This study presents an efficient strategy for preparing electrochemical catalytic materials using a simple self-assembly technique to encapsulate Fe single atoms (Fe-SAs) and Ni single atoms (Ni-SAs) in the Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC) metal-organic framework to form a Cu-BTC@FeNi-SAs catalytic system. Subsequently, Cu-BTC@FeNi-SAs was modified on the surface of a gold electrode, and sulfadiazine was used as a template to prepare a molecularly imprinted polymer (MIP) on the modified electrode.

View Article and Find Full Text PDF

The pervasive concern regarding veterinary drug residues in food necessitates advanced detection solutions, particularly addressing limitations of conventional methods reliant on large-scale instrumentation that incur prolonged analysis duration, complex sample preparation, and lack of real-time on-site capability. A portable "single response-on" molecularly imprinted ratiometric fluorescent paper-based sensor was developed for quantifying fleroxacin (FLX) residues in animal-derived foods, wherein B, N-co-doped MXene quantum dot (B, N-MQD) was synthesized and combined with BCP-Eu as dual-emission fluorophores, while FLX- molecularly imprinted polymer (FLX-MIP) was engineered using functionalized Nano-SiO as the carrier. Concentration-dependent fluorescence enhancement at 574 nm was exhibited with invariant reference signal at 411 nm, achieving a 36-fold lower detection limit (0.

View Article and Find Full Text PDF

Complementary biomolecular coassemblies direct energy transport for cardiac photostimulators.

Proc Natl Acad Sci U S A

September 2025

Department of Chemical and Biomolecular Engineering, Samueli School of Engineering, University of California, Irvine, CA 92697.

Charge and energy transport within living systems are fundamental processes that enable the autonomous function of excitable cells and tissues. To date, localized control of these transport processes has been enabled by genetic modification approaches to render light sensitivity to cells. Here, we present peptidic nanoassemblies as constituents of a cardiac biomaterial platform that leverages complementary sequence interactions to direct photoinduced energy transport at the cellular interface.

View Article and Find Full Text PDF

An ultrasensitive electrode modified with a molecularly imprinted PEDOT-TiO nanocomposite for voltammetric atrazine detection in environmental samples.

Talanta

August 2025

Department of Chemistry, Faculty of Natural and Exact Sciences, Universidad de Oriente, Av. Patricio Lumumba, Santiago de Cuba, 90100, Cuba.

Molecularly imprinted polymers (MIPs) have been studied to be used as a platform for electrochemical sensing devices, with special regard to the determination of pesticides. Due to MIP applicability, in the present research, we develop a glassy carbon electrode (GCE) modified with a molecularly imprinted nanocomposite based on the doping of poly(3,4-ethylenedioxythiophene) (PEDOT) with chitosan (Chit) and TiO nanoparticles for sensing atrazine in environmental samples. The construction of the MIP nanocomposite was divided into four parts, which include the chitosan-TiO layer formation by simple drop-casting on the GCE, the doping and electropolymerization of the Chit+TiO+PEDOT layer, cavity formation, and elution.

View Article and Find Full Text PDF