2020
DOI: 10.1016/j.arabjc.2020.04.001
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Modified cotton fabrics with poly (3-(furan-2-carboamido) propionic acid) and poly (3-(furan-2-carboamido) propionic acid)/gelatin hydrogel for UV protection, antibacterial and electrical properties

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Cited by 15 publications
(7 citation statements)
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“…[ 7–14 ] The other heterocycles like pyrimidine, furan, pyrrole, indole, oxadiazole, benzoxazole, azetidine, thiophene, coumarin, benzofuran, pyrazole, quinoline oxazole, quinazoline, pyrimidine, thiazole, quinoline, pyrazole, and isoxazole also possess various pharmacological activities. [ 8,15–30 ]…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[ 7–14 ] The other heterocycles like pyrimidine, furan, pyrrole, indole, oxadiazole, benzoxazole, azetidine, thiophene, coumarin, benzofuran, pyrazole, quinoline oxazole, quinazoline, pyrimidine, thiazole, quinoline, pyrazole, and isoxazole also possess various pharmacological activities. [ 8,15–30 ]…”
Section: Introductionmentioning
confidence: 99%
“…[7][8][9][10][11][12][13][14] The other heterocycles like pyrimidine, furan, pyrrole, indole, oxadiazole, benzoxazole, azetidine, thiophene, coumarin, benzofuran, pyrazole, quinoline oxazole, quinazoline, pyrimidine, thiazole, quinoline, pyrazole, and isoxazole also possess various pharmacological activities. [8,[15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30] The Food and Drug Administration (FDA)-approved drugs in recent years contain biologically active heterocycles in their structures. The drugs like remdesivir (broad-spectrum antiviral drug), [31] avaprinitib (an antitumor drug), [32] pematinib (an anticancer drug used to treat cholangiocarcinoma), [33] remimazolam (sedative drug), [34] and oliceradine (pain medication) [35] approved in 2020 (Figure 1).…”
mentioning
confidence: 99%
“…In general, conjugated polymers have been described as an alternating single (σ-bond) and double (π-bond) bonds along the carbon atoms on the alternating units [2] such as polyaniline [3,4], polyacetylene [5,6], polyfuran [7], polystyrene [8,9], and Poly(vinyl carbazole) [10]. The hybridization of the carbon atom in the π-bond is sp 2 p z which overlap over the polymer skeleton, allowing the electron mobilization and charge transfer.…”
Section: Introductionmentioning
confidence: 99%
“…The conjugated polymer's diverse applications in various technologies have recently received a lot of attention due to their ability to combine the unique properties of conventional polymers such as low weight, good mechanical and flexibility with those of conventional semiconductors such as light emission and absorption, and tunable conductivity.Conjugated polymers, for example, have been used in a variety of critical applications, including electrods [13], solar cell [14,15], optoelectronic devices [16][17][18], supercapacitor [19,20], sensors [21,22], smart fabrics [7,23], transistors [24] and medical applications [25,26].…”
Section: Introductionmentioning
confidence: 99%
“…In addition, natural antimicrobial agents with environmental friendliness and nontoxicity were also frequently incorporated into polymeric materials [12,13] but have some disadvantages such as high extraction cost, low sterilization efficiency and weak thermal stability [14]. As synthetic antimicrobial agents, N-halamine compounds have been applied in medical dressings [15,16], filtration materials [17,18] and textiles [19,20] due to their excellent biocompatibility and high antibacterial activity [21][22][23]. Conveniently, after chlorination by household bleach solution, the N-H bond in N-halamine can be converted to the N-Cl bond, which has high antimicrobial efficiencies and rechargeable properties [24] and the level of chlorine loading represents the antibacterial activity to a certain extent [25,26].…”
Section: Introductionmentioning
confidence: 99%