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A well\u2010known nonsteroidal anti\u2010inflammatory drug, namely, indomethacin, was conjugated with six different <jats:sc>l<\/jats:sc>\u2010amino acids to generate the corresponding peptides having free carboxylic acid functionality, which reacted further with an antiviral drug, namely, amantadine, a primary amine, in 1:1 ratio to yield six primary ammonium monocarboxylate salts. Half of the synthesized salts showed gelation ability that included hydrogelation, organogelation and ambidextrous gelation. The gels were characterized by table\u2010top and dynamic rheology and different microscopic techniques. Further insights into the gelation mechanism were obtained by temperature\u2010dependent <jats:sup>1<\/jats:sup>H\u2005NMR spectroscopy, FTIR spectroscopy, photoluminescence and dynamic light scattering. Single\u2010crystal X\u2010ray diffraction studies on two gelator salts revealed the presence of 2D hydrogen\u2010bonded networks. One such ambidextrous gelator (capable of gelling both pure water and methyl salicylate, which are important solvents for biological applications) was promising in both mechanical (rheoreversible and injectable) and biological (self\u2010delivery) applications for future multidrug\u2010containing injectable delivery vehicles.<\/jats:p>","DOI":"10.1002\/chem.201602429","type":"journal-article","created":{"date-parts":[[2016,8,31]],"date-time":"2016-08-31T14:00:53Z","timestamp":1472652053000},"page":"14929-14939","source":"Crossref","is-referenced-by-count":23,"title":["Multidrug\u2010Containing, Salt\u2010Based, Injectable Supramolecular Gels for Self\u2010Delivery, Cell Imaging and Other Materials Applications"],"prefix":"10.1002","volume":"22","author":[{"given":"Rajdip","family":"Roy","sequence":"first","affiliation":[{"name":"Department of Organic Chemistry Indian Association for the Cultivation of Science (IACS)  2A and 2B Raja S. C. 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