2011
DOI: 10.1016/j.carbpol.2011.05.001
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One-step fabrication of biocompatible carboxymethyl cellulose polymeric particles for drug delivery systems

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Cited by 116 publications
(47 citation statements)
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“…Chemical-crosslinking provides CMC gels a more stable three-dimensional network. For example, divinyl sulfone [14], epichlorohydrin [15], aldehydes [16,17], fumaric acid [18] and citric acid [19] have been used as crosslinkers to form CMC and CMC composite gels. Monomers with double bond, such as N-isopropyl acrylamide [20] and partially neutralized acrylic acid/rectorite [21], have been initiated by ammonium persulfate and coupled onto CMC backbones via methylene bisacrylamide (crosslinker).…”
Section: Introductionmentioning
confidence: 99%
“…Chemical-crosslinking provides CMC gels a more stable three-dimensional network. For example, divinyl sulfone [14], epichlorohydrin [15], aldehydes [16,17], fumaric acid [18] and citric acid [19] have been used as crosslinkers to form CMC and CMC composite gels. Monomers with double bond, such as N-isopropyl acrylamide [20] and partially neutralized acrylic acid/rectorite [21], have been initiated by ammonium persulfate and coupled onto CMC backbones via methylene bisacrylamide (crosslinker).…”
Section: Introductionmentioning
confidence: 99%
“…Porém, cápsulas de alginato normalmente apresentam poros, o que permite a difusão da temperatura para o interior da cápsula (Mandal et al, 2006;Ding & Shah, 2009;Gouin, 2004). Outros materiais que podem ser utilizados na encapsulação de probióticos, como o carboximetilcelulose também apresentam o problema de gerar cápsulas porosas (Butun et al, 2011). Como alternativa, outros materiais de cápsulas podem ser incluídos como quitosana, trehalose, inulina, leite em pó, maltodextrina, farelo de arroz, entre outros para aumentar a proteção aos probióticos (Cavalheiro et al, 2015;Silva et al, 2015;Chitprasert et al, 2012).…”
Section: Emulsificaçãounclassified
“…In its chain structure, it presents a high number of hydroxyl groups suitable to be converted, by chemical modification, into cellulose esters [52]. These cellulose derivatives are more suitable to be applied in different areas, such as enteric coatings, hydrophobic matrices, and semi-permeable membranes for applications in pharmaceuticals, agriculture, and cosmetics [52][53][54]. Furthermore, the cellulose esters can be applied in the field of controlled release systems, due to their well established preparation processes, application safety and good handling properties [55].…”
Section: Cellulose Derivativesmentioning
confidence: 99%