Investigations on drug release systems using CMC crosslinked with ferric ions

Artificial Cells, Blood Substitutes, and Immobilization Biotechnology

Volumn 27, Issue 3, 1999, Pages 279-290

  Sungur, Sibel ^a  

^a ANKARA UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CELLULOSE DERIVATIVES; CROSSLINKING; DRUG PRODUCTS; DRYING; IONS; IRON;

CARBOXYMETHYLCELLULOSE; ERYTHROMYCIN;

CONTROLLED DRUG DELIVERY;

CARBOXYMETHYLCELLULOSE; ERYTHROMYCIN; FERRIC ION;

ARTICLE; CONTROLLED RELEASE FORMULATION; CROSS LINKING; DRUG DELIVERY SYSTEM; DRUG RELEASE; INTESTINE; PH; STOMACH;

EID: 0033006198     PISSN: 10731199     EISSN: None     Source Type: Journal    
DOI: 10.3109/10731199909117700     Document Type: Article

References (7)

1. Pozzi F, Furlani P Gazzaniga A, Davis SS, Wilding IR. The time clock system: A new oral dosage form for fast and complete release of drug after a predetermined lag time. J Cont Rel. 31: 99-108 (1994)
2. Göpferich A. Mechanisms of polymer degradation and erosion. Biomaterials. 17: 103-114 (1996)
3. Lowman AM, Peppas NA. Complexation graft copolymers as oral drug delivery systems. Polym Preprints. 38(2): 566-567 (1997)
4. Langer R. Polymer-controlled drug delivery systems. Acc Chem Res. 26(10): 537-542 (1993)
5. Encyclopedia of Chemical Technology, J. Wiley and Sons, Inc., New York (1986)
6. Fort J H, Presscott G C, Hinman J W, Caron E L. Colorimetric determination of erythromycin. Anal Chem. 25: 1195-1197 (1953)
7. Sungur S, Emregül E. Application of carboxymethylcellulose in controlled drug release. Macromol Rep. A33(Suppls. 5&6): 319-325 (1996)