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Histamine is among the biogenic amines that are formed during the microbial decarboxylation of amino acids in various food products, posing a significant threat to both food safety and human health. Herein, we present a one-step synthesis of PEGylated gold nanoparticles (PEG-AuNPs) for rapid, simple, and cost-effective colorimetric histamine detection. PEG-AuNPs' surface plasmon resonance (SPR) range at 520-530 nm with a hydrodynamic size distribution of 20-40 nm. Fourier transform infrared (FT-IR) spectra confirmed the reduction of AuNPs at 1645 cm along with the other observed peaks at 2870, 1350, and 1100 cm as a strong evidence for the presence of PEG. Upon the addition of histamine to the PEG-AuNP solution, transmission electron microscopy (TEM) highlighted the aggregation of nanoparticles. In addition, red shifting and a decrease in the absorbance of the SPR peak along with the appearance of an additional peak at ∼690 nm was observed in the PEG-AuNP absorption spectra in the presence of histamine. Increasing the PEG concentration in the gold colloids leads to the formation of a protective barrier around the surface of nanoparticles, which influences the colloidal stability by impeding the aggregation of PEG-AuNPs upon histamine addition. The minimum colorimetric response of PEG-AuNPs to histamine concentration is 30 ppm, as assessed by the naked eye. The absorption ratio (/) showed a linear dynamic range from 20 to 100 ppm with a limit of detection of 9.357 μM. Additionally, the assay demonstrates a commendable selectivity toward histamine analyte.
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http://dx.doi.org/10.1021/acsomega.3c10050 | DOI Listing |
Drug Dev Res
September 2025
School of Pharmacy, The University of Jordan, Amman, Jordan.
Cancer treatment faces challenges like nonselective toxicity and drug resistance, prompting the need for innovative therapies. This study aimed to develop liposomal formulations for co-delivery of empagliflozin and rutin, evaluating their anticancer and antioxidant efficacy. PEGylated empagliflozin-loaded nanoliposomes (Empa-NLs) and empagliflozin-rutin co-loaded nanoliposomes (Empa-Rut NLs) were synthesized using the thin-film hydration technique.
View Article and Find Full Text PDFViruses
August 2025
Wits/SAMRC Antiviral Gene Therapy Research Unit, Infectious Diseases and Oncology Research Institute (IDORI), School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Parktown 2193, South Africa.
Chronic infection with the hepatitis B virus (HBV) results in over 1 million deaths annually. Although currently licensed treatments, including pegylated interferon-α and nucleoside/nucleotide analogs, can inhibit viral replication, they rarely eradicate covalently closed circular DNA (cccDNA) reservoirs. Moreover, vaccination does not offer therapeutic benefit to already infected individuals or non-responders.
View Article and Find Full Text PDFBiomacromolecules
August 2025
Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Quinine-based polymers have shown promise for effective delivery of nucleic acids; however, quinine's hydrophobicity has often resulted in uncontrolled aggregation (>1000 nm) of complexes. PEGylation is often used to improve the colloidal stability of nucleic acid delivery vehicles; however, this frequently results in reduced cellular internalization. Herein, we describe the synthesis of two diblock quinine polymers that utilize the carbohydrates glucose and galactose in place of PEG as the neutral hydrophilic block to deliver mRNA.
View Article and Find Full Text PDFBioorg Med Chem
August 2025
China State Institute of Pharmaceutical Industry, Shanghai, China. Electronic address:
Thrombopoietin (TPO) mimetic peptides activate c-Mpl receptor-mediated signaling to stimulate platelet production, possessing similar bioactivity to endogenous TPO. However, their clinical application is limited by rapid clearance in vivo (t₁₂ ≈ 1 h). To address this limitation, various long-acting modification strategies, such as PEGylation and Fc fusion, have been extensively developed.
View Article and Find Full Text PDFColloids Surf B Biointerfaces
December 2025
Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González 2, Sevilla 41012, Spain; Instituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Rocío, Avda. Manuel Siurot s/n, Sevilla 41013, Spain. Electronic a
Aim: While selective CB2 receptor agonists hold significant promise for mitigating inflammation and atherosclerosis, their poor physicochemical properties have hampered clinical translation. To overcome this, we engineered a sophisticated, nanoparticle-based delivery system designed for precise cannabinoid deposition at atheromatous plaque sites. Our approach utilized PEGylated PLGA nanoparticles (NPs), functionalized with a peptide ligand specifically targeting vascular cell adhesion molecule-1 (VCAM-1), a well-established biomarker of atherosclerotic lesions.
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