Performance of alginate films for retention of l-[+]-ascorbic acid

In view of acting as controlled delivery systems for nutritional supplementation, therapy or antioxidant activity at interfaces, alginate films of different copolymer composition and glycerol plasticizer levels were developed in the presence of Ca2+ for achieving higher stability of l-[+]-ascorbic a...

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Detalles Bibliográficos
Otros Autores: De Nobili, María D., Curto, Lucrecia M., Delfino, José María, Soria, Marcelo Abel, Fissore, Eliana N., Rojas, Ana M.
Formato: Artículo
Lenguaje:Inglés
Materias:
Acceso en línea:http://ri.agro.uba.ar/files/intranet/articulo/2013denobili.pdf
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Aporte de:Registro referencial: Solicitar el recurso aquí
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245 1 0 |a Performance of alginate films for retention of l-[+]-ascorbic acid 
520 |a In view of acting as controlled delivery systems for nutritional supplementation, therapy or antioxidant activity at interfaces, alginate films of different copolymer composition and glycerol plasticizer levels were developed in the presence of Ca2+ for achieving higher stability of l-[+]-ascorbic acid [AA]. The ability of the alginate network to preserve AA from hydrolysis, tested by storage under vacuum at 25 C, only decreased with the relative humidity [RH] increase when alginates were mainly constituted by guluronic-guluronic acid blocks [GG], whereas also decreased with the glycerol level increase when mannuronic-mannuronic acid [MM] and/or alternating guluronic-mannuronic [GM + MG] flexible blocks were present in higher proportions. This result could be probably related to the lower capability of the latter alginate block compositions to immobilize water in the network as they are not able to constitute Ca2+ mediated junction zones where water molecules are highly retained. Films also studied under air storage showed that even at less favorable conditions of RH and glycerol levels, both GG and GM + MG enriched alginate networks in general preserved AA from oxidation. It also demonstrated that hydrolysis is the principal way by which AA is lost when supported in films. 
653 0 |a ALGINATE FILMS 
653 0 |a ANTIOXIDANT INTERFACE 
653 0 |a ASCORBIC ACID HYDROLYSIS 
653 0 |a BIOMOLECULE DELIVERY 
653 0 |a GLYCEROL 
653 0 |a ALGINIC ACID 
653 0 |a ASCORBIC ACID 
653 0 |a CALCIUM ALGINATE 
653 0 |a MANNURONIC ACID 
653 0 |a WATER 
653 0 |a DRUG HYDROLYSIS 
653 0 |a DRUG STABILITY 
653 0 |a HUMIDITY 
653 0 |a MOLECULE 
653 0 |a TEMPERATURE 
653 0 |a ALGINATES 
653 0 |a DRUG STORAGE 
653 0 |a HYDROLYSIS 
653 0 |a OXIDATION-REDUCTION 
653 0 |a PLASTICIZERS 
700 1 |a De Nobili, María D.  |9 70150 
700 1 |a Curto, Lucrecia M.  |9 72599 
700 1 |a Delfino, José María  |9 72600 
700 1 |9 49057  |a Soria, Marcelo Abel 
700 1 |a Fissore, Eliana N.  |9 68705 
700 1 |a Rojas, Ana M.  |9 70153 
773 |t International Journal of Pharmaceutics  |g vol.450, no.1-2 (2013), p.95-103 
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900 |a ^aDe'Nobili, M.D.^tDepartamento de Industrias, Facultad de Ciencias Exactas y Naturales, University of Buenos Aires, 1428 Buenos Aires, Argentina 
900 |a ^aCurto, L.M.^tDepartment of Biological Chemistry, Institute of Biochemistry and Biophysics - IQUIFIB (CONICET), University of Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina 
900 |a ^aDelfino, J.M.^tDepartment of Biological Chemistry, Institute of Biochemistry and Biophysics - IQUIFIB (CONICET), University of Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina 
900 |a ^aSoria, M.^tMicrobiologia Agricola, Instituto de Investigaciones en Biociencias Agricolas y Ambientales - INBA, Facultad de Agronomía, University of Buenos Aires, Av. San Martin 4453, 1417 Buenos Aires, Argentina 
900 |a ^aFissore, E.N.^tDepartamento de Industrias, Facultad de Ciencias Exactas y Naturales, University of Buenos Aires, 1428 Buenos Aires, Argentina 
900 |a ^aRojas, A.M.^tDepartamento de Industrias, Facultad de Ciencias Exactas y Naturales, University of Buenos Aires, 1428 Buenos Aires, Argentina 
900 |a ^tInternational Journal of Pharmaceutics^cInt. J. Pharm. 
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900 |a 95 
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900 |a Vol. 450, no. 1-2 
900 |a 103 
900 |a ALGINATE FILMS 
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900 |a ASCORBIC ACID HYDROLYSIS 
900 |a BIOMOLECULE DELIVERY 
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900 |a ALGINIC ACID 
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900 |a MOLECULE 
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900 |a HYDROLYSIS 
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900 |a In view of acting as controlled delivery systems for nutritional supplementation, therapy or antioxidant activity at interfaces, alginate films of different copolymer composition and glycerol plasticizer levels were developed in the presence of Ca2+ for achieving higher stability of l-[+]-ascorbic acid [AA]. The ability of the alginate network to preserve AA from hydrolysis, tested by storage under vacuum at 25 C, only decreased with the relative humidity [RH] increase when alginates were mainly constituted by guluronic-guluronic acid blocks [GG], whereas also decreased with the glycerol level increase when mannuronic-mannuronic acid [MM] and/or alternating guluronic-mannuronic [GM + MG] flexible blocks were present in higher proportions. This result could be probably related to the lower capability of the latter alginate block compositions to immobilize water in the network as they are not able to constitute Ca2+ mediated junction zones where water molecules are highly retained. Films also studied under air storage showed that even at less favorable conditions of RH and glycerol levels, both GG and GM + MG enriched alginate networks in general preserved AA from oxidation. It also demonstrated that hydrolysis is the principal way by which AA is lost when supported in films. 
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