Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
datasetposted on 01.04.2019, 00:00 by Rumana Parveen, Bandi Jayamma, Parthasarathi Dastidar
Following supramolecular synthon rationale in the context of crystal engineering, a nonsteroidal-anti-inflammatory-drug (NSAID), namely flufenamic acid (FA) and its β-alanine monopeptide derivative (FM), were converted to a series of primary ammonium monocarboxylate (PAM) salts. Majority of the PAM salts (∼90%) showed gelation with various solvents including water and methyl salicylate (important solvents in topical gel formulation). Structure–property correlation studies based on single-crystal X-ray diffraction (SXRD) and powder X-ray diffraction (PXRD) data provided intriguing insights into the structure of the gel network. Furthermore, one of the gelator salts (S7) displayed anticancer activity on a highly aggressive human breast cancer cell line (MDA-MB-231) ,as revealed by MTT, PEG2, and cell migration assays.
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powder X-ray diffractionPEG 2single-crystal X-ray diffractionPAMsupramolecular synthon rationalebreast cancer cell linegelator saltsanticancer activitySXRDPlausible Biomedical ApplicationSupramolecular Gels Derivedcell migration assayssolventmethyl salicylateFAMDA-MB -231FMNSAIDflufenamic acidPXRDammonium monocarboxylateβ- alanine monopeptideSimple Organic SaltsS 7gel formulationgel networkMTTcrystal engineering