2022
DOI: 10.1016/j.biopha.2022.112919
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Development of a new polymer network system carrier of essential oils

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Cited by 12 publications
(15 citation statements)
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“…In one of the mentioned references [ 9 ], the ethylene brassylate homopolymer was synthesised in bulk or solution with benzyl alcohol and various organic compounds as initiation systems, and the study highlighted the interdependence between the molecular mass of the polymer and the catalysts used. Our group investigated the polymerisation of EB with squaric acid (SA) at various rates, and the newly synthesised co-polymacrolactone systems presented increased functionality that opened new opportunities for the application of these compounds [ 20 , 21 ]. SA, a strong acid due to its polar units, is capable of chemical processes, can form intermolecular hydrogen bonds, and, furthermore, can develop polymeric networks with various applications, including medicinal chemistry [ 22 ].…”
Section: Introductionmentioning
confidence: 99%
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“…In one of the mentioned references [ 9 ], the ethylene brassylate homopolymer was synthesised in bulk or solution with benzyl alcohol and various organic compounds as initiation systems, and the study highlighted the interdependence between the molecular mass of the polymer and the catalysts used. Our group investigated the polymerisation of EB with squaric acid (SA) at various rates, and the newly synthesised co-polymacrolactone systems presented increased functionality that opened new opportunities for the application of these compounds [ 20 , 21 ]. SA, a strong acid due to its polar units, is capable of chemical processes, can form intermolecular hydrogen bonds, and, furthermore, can develop polymeric networks with various applications, including medicinal chemistry [ 22 ].…”
Section: Introductionmentioning
confidence: 99%
“…The use of PEBSA as a biopolymer-based functional structure in a new chemical system also contributes to the diversification of its range of uses. In addition, by using PEBSA, which has already demonstrated its biocompatibility in vivo [ 21 ], in creating a new structure by encapsulating a suitable specific compound, its versatility is highlighted again.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, the reducing in intensity of C=O stretching vibration (~1700 cm −1 ) and C–O stretching vibration bands (~1280 cm −1 ) corresponding to PEBSA, settle the above statement. Other bands identified in spectra are: 2925, 2856 and 1460 cm −1 assigned to C–H asymmetric, symmetric and bending vibration; peaks found between 1096 and 1105 cm −1 correspond to asymmetric C–O–C bridge stretching vibration; and C=C bending vibration from squaric acid units identified at 920 and 848 cm −1 [ 13 ].…”
Section: Resultsmentioning
confidence: 99%
“…Our group reported recently the synthesis of poly(ethylene brassylate-co-squaric acid) (PEBSA) performed by ethylene brassylate macrolactone ring-opening and copolycondensing with squaric acid [ 11 ]. In previous studies, our group paid particular attention to this copolymeracrolactone system with different ratios between comonomers [ 11 , 12 , 13 ]. PEBSA, which presents special properties, such as the possibility to create networks, biodegradability and good thermal stability, is also capable of incorporating essential oils—namely thymol (Thy) and carvacrol (CC).…”
Section: Introductionmentioning
confidence: 99%
“…One such compound is 3,4-dihydroxy-3-cyclobutene-1,2-dione, known as squaric acid (SA) [ 38 ]. It has a cyclic structure and was utilized as an effective crosslinker for MNPs coated with chitosan/collagen [ 19 ], and collagen/elastin hydrogels [ 39 ] or in preparing a copolymacrolactone for essential oil encapsulation [ 40 , 41 ]. The influence of SA on the cytotoxicity of collagen/elastin hydrogels was assessed, revealing that SA can be regarded as a safe option [ 39 ] to replace the readily available reagents as GA for enzyme immobilization on amino-functionalized MNPs.…”
Section: Introductionmentioning
confidence: 99%