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Recent years have witnessed the gradual use of dendrimers to prepare and modify various separation materials, including adsorbents and chromatographic stationary phases. Polyamide-amine (PAMAM) has become one of the most widely used dendritic materials because it is simple to prepare, inexpensive, hypotoxic, and has excellent performance characteristics. PAMAM is advantageous as a modification material for adsorbents and chromatographic stationary phases compared to other traditional materials. Firstly, the large number of terminal groups on a PAMAM dendrimer provide abundant interaction sites on the surface of the functional matrix, which is beneficial for delivering superior adsorption capacity and separation selectivity. In addition, the hyperbranched structure of a PAMAM dendrimer facilitates higher grafting efficiency on the limited surface area of the matrix while simultaneously improving the uniformity of the functional groups grafted on the surface. Moreover, the controllable structure of PAMAM dendrimer effectively regulates the surface structure of separated materials. Moreover, the terminal amino functional groups of integer-generational PAMAM dendrimer are capable of carrying a high density of positive charges following protonation or quaternization, thereby facilitating good electrostatic interactions with negatively charged anionic substances that lead to excellent enrichment and separation effects. Based on the structural characteristics of integer generation PAMAM dendrimer and the mechanism of ionic interaction, the research progress of protonated or quaternized PAMAM dendrimer in the preparation of ionic adsorbents and ion chromatography stationary phases was summarized in this paper. Their future development potential and applications prospects are also discussed.
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http://dx.doi.org/10.3724/SP.J.1123.2024.06002 | DOI Listing |
Pharmaceutics
July 2025
Faculty of Pharmacy, Applied Science University, Amman 11937, Jordan.
: Alectinib, a second-generation tyrosine kinase inhibitor indicated for the treatment of non-small-cell lung cancer (NSCLC), exhibits suboptimal oral bioavailability, primarily attributable to its inherently low aqueous solubility and limited dissolution kinetics. This study aimed to enhance Alectinib's solubility and therapeutic efficacy by formulating a G4-NH2-PAMAM dendrimer complex. : The complex was prepared using the organic solvent evaporation method and characterized by DSC, FTIR, dynamic light scattering (DLS), and zeta potential measurements.
View Article and Find Full Text PDFInt J Pharm
October 2025
NICM Health Research Institute, Western Sydney University, Westmead, Australia. Electronic address:
Liver fibrosis is a progressive condition characterized by excessive accumulation of extracellular matrix components, which impairs liver function and can lead to cirrhosis or hepatocellular carcinoma. In this study, we designed a multifunctional poly(amidoamine) dendrimer-based gene delivery system (VA/CLU/COL-P@mp) to target activated hepatic stellate cells (aHSCs) and mitgate liver fibrosis. This platform leverages clusterin (CLU) for Kupffer cell evasion, collagenase I (COL) to enhance nanoparticle penetration through fibrotic ECM, and vitamin A for targeted binding to retinol-binding protein (RBP) receptors on aHSCs.
View Article and Find Full Text PDFJ Biomater Sci Polym Ed
August 2025
Department of Ophthalmology, Fifth Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, P.R. China.
Microcapsules are considered as one of the most promising drug carriers due to their exceptional characteristics. The cellular uptake of microcapsules is determined by physicochemical properties, yet comprehensive studies on thickness and shape effects are limited. In this study, we developed single-layered poly(amidoamine) (PAMAM) dendrimer microcapsules with tunable thicknesses and morphologies to systematically investigate their cellular internalization.
View Article and Find Full Text PDFBiomacromolecules
September 2025
Department of Chemistry, College of Arts and Sciences, Washington State University, 1470 NE College Avenue, Pullman, Washington 99164, United States.
Triple-negative breast cancer (TNBC) remains one of the most aggressive and treatment-resistant breast cancer subtypes due to poor drug bioavailability, systemic toxicity, and rapid resistance development. Camptothecin (Campto), a potent topoisomerase I inhibitor, has shown strong anticancer activity but suffers from poor solubility, instability, and off-target toxicity. Here, we report the synthesis and in vitro mechanistic evaluation of a novel dendrimer-drug conjugate, PD-Campto, composed of a generation 4 hydroxyl-terminated PAMAM dendrimer (PD) covalently linked to Campto via biodegradable ester linkers using copper(I)-catalyzed alkyne-azide click (CuAAC) chemistry.
View Article and Find Full Text PDFSci Rep
August 2025
Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, 51656-65931, Iran.
Breast cancer (BC) is one of the most common cancers in women, requiring comprehensive treatment strategies to reduce disease burden and costs. In this study, we developed an innovative dual nanoparticle system based on niosome containing PAMAM/Tirapazamine (N@P/T), and studied its efficacy combining in silico and experimental validation. Molecular docking and protein-protein interaction network analysis identified HIF1A as a central target for Tirapazamine (TPZ), revealing multiple high-confidence binding sites and interactions with key cancer-related pathways.
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