This study presents a novel approach to synthesize biocompatible single-chain polymeric nanoparticles (SCPN) under mild reaction conditions via organo-catalyzed ring-opening polymerization (ROP). Linear polymeric precursors containing pendent polymerizable caprolactone groups, made by reversible addition-fragmentation chain transfer (RAFT) polymerization, were intramolecularly cross-linked via ROP in the presence of benzyl alcohol (nucleophilic initiator) and methanesulfonic acid (organo catalyst) to form discrete, well-defined SCPN, as confirmed by GPC, DLS, H NMR, and AFM analysis. The formed SCPN are tunable in size (2-5 nm), depending on the molecular weight of the parent linear macromolecule. Furthermore, cytotoxicity studies revealed that the SCPN, which were covalently cross-linked by biodegradable polyester linkages, were nontoxic toward human embryonic kidney (HEK293T) cells. This study demonstrates the efficiency and versatility of this approach to generate uniformly sized soft nanoparticles with tunable dimensions that are potentially useful for a range of targeted applications, including drug delivery systems and membranes for gas separation technologies.
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http://dx.doi.org/10.1021/mz500225p | DOI Listing |
Biomacromolecules
October 2024
Centro de Física de Materiales (CFM) (CSIC-UPV/EHU), Materials Physics Center (MPC), Paseo Manuel de Lardizabal 5, E-20018 Donostia, Spain.
Protein single-chain nanoparticles can outperform synthetic nanoparticles in biomedical applications due to enhanced biocompatibility. Compared to synthetic (co)polymers, the chemical complexity of proteins challenges chain conformation control. Here, we investigate the impact of the precursor chain conformation of bovine serum albumin (BSA) on the nanoparticle structure after intramolecular cross-linking.
View Article and Find Full Text PDFACS Appl Bio Mater
September 2024
School of Chemistry, University of Hyderabad, Hyderabad-500046, Telangana, India.
Hydrated dispersions containing equimolar mixtures of cationic and anionic amphiphiles, referred to as catanionic systems, exhibit synergistic physicochemical properties, and mixing single-chain cationic and anionic lipids can lead to the spontaneous formation of vesicles as well as other phase structures. In the present work, we have characterized two catanionic systems prepared by mixing -acyltaurines (NATs) and sarcosine alkyl esters (SAEs) bearing 11 and 12 C atoms in the acyl/alkyl chains. Turbidimetric and isothermal titration calorimetric studies revealed that both NATs form equimolar complexes with SAEs having matching acyl/alkyl chains.
View Article and Find Full Text PDFACS Appl Bio Mater
July 2024
Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Av. dos Estados, 5001, Bloco A, Torre 3, Santo André, SP 09210-580, Brazil.
Human tissue kallikrein-related peptidase 7 (KLK7) is a serine protease implicated in the physiology of skin desquamation, and its uncontrolled activity can lead to chronic diseases such as psoriasis, atopic dermatitis, and Netherton syndrome. For this reason, kallikrein 7 has been identified as a potential therapeutic target. This work aimed to evaluate Pluronic (PL) hydrogels as topical carriers of four specific scFv-Fc antibodies to inhibit KLK7.
View Article and Find Full Text PDFMacromol Biosci
September 2024
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustraße 3, 14195, Berlin, Germany.
Mucus lines the epithelial cells at the biological interface and is the first line of defense against multiple viral infections. Mucins, the gel-forming components of mucus, are high molecular weight glycoproteins and crucial for preventing infections by binding pathogens. Consequently, mimicking mucins is a promising strategy for new synthetic virus inhibitors.
View Article and Find Full Text PDFInt J Mol Sci
February 2024
Research and Development Department, Miltenyi Biotec B.V. & Co. KG, 51429 Bergisch Gladbach, Germany.
Endotoxin, a synonym for lipopolysaccharide (LPS), is anchored in the outer membranes of Gram-negative bacteria. Even minute amounts of LPS entering the circulatory system can have a lethal immunoactivating effect. Since LPS is omnipresent in the environment, it poses a great risk of contaminating any surface or solution, including research products and pharmaceuticals.
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