Chitosomes as drug delivery systems for C-phycocyanin: Preparation and characterization

被引:61
作者
Manconi, M. [2 ]
Mura, S. [2 ]
Manca, M. L. [2 ]
Fadda, A. M. [2 ]
Dolz, M. [3 ]
Hernandez, M. J. [3 ]
Casanovas, A. [3 ]
Diez-Sales, O. [1 ]
机构
[1] Univ Valencia, Dept Pharmaceut & Pharmaceut Technol, E-46100 Valencia, Spain
[2] Univ Cagliari, Dpt Farmaco Chim Tecnol, I-09124 Cagliari, Italy
[3] Univ Valencia, Dpt Fis Terra & Termodinam, E-46100 Valencia, Spain
关键词
Liposomes coated; Drug delivery; Release study; Diffusion coefficient; Swelling; Mucoadhesive properties; MUCOADHESIVE PROPERTIES; ACID; ANTIOXIDANT; RELEASE; EXTRACT; BILIPROTEIN; ABSORPTION;
D O I
10.1016/j.ijpharm.2010.03.038
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this work was to investigate chitosomes, i.e. liposomes coated by a polyelectrolyte complex between chitosan (CH) and xantan gum (XG), as potential delivery system for oral administration of the protein C-phycocyanin. To this purpose several CH-XG-microcomplexes were prepared in aqueous lactic acid at different chitosan-xanthan gum percent ratios and rheological properties of the microcomplexes were studied to analyse the contribution of chitosan and xanthan gum in the reaction of microcomplexation. After establishing the best microcomplexes, chitosomes were prepared by coating C-phycocyanin loaded liposomes with the CH-XG hydrogels using spray-drying or freeze-drying. The chitosomes were characterized in terms of morphology, size distribution, zeta potential, swelling properties, drug release, and mucoadhesive properties. Rheological studies showed the influence of xanthan gum in the microcomplex properties. Moreover, obtained results demonstrated the effects of formulation and process variables on particle size, drug content, swelling, drug release, and especially on the mucoadhesiveness of C-PC chitosomes of CH-XG. In particular, chitosomes prepared by spray-drying technique using CH-XG in 0.5/8.0 (w/w) ratio showed a regular surface and a drug release characteristic for a Fickian diffusion of the active ingredient. The in vitro mucoadhesive study revealed that the spray-drying method is advantageous to prepare C-phycocyanin loaded chitosomes with excellent mucoadhesive properties for colonic drug delivery. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 100
页数:9
相关论文
共 37 条
[1]   Colloidal drug carriers: achievements and perspectives [J].
Barratt, G .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (01) :21-37
[2]   Antioxidant properties of a novel phycocyanin extract from the blue-green alga Aphanizomenon flos-aquae [J].
Benedetti, S ;
Benvenuti, F ;
Pagliarani, S ;
Francogli, S ;
Scoglio, S ;
Canestrari, F .
LIFE SCIENCES, 2004, 75 (19) :2353-2362
[3]   C-Phycocyanin:: A potent peroxyl radical scavenger in vivo and in vitro [J].
Bhat, VB ;
Madyastha, KM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (01) :20-25
[4]   Lipid vesicles and other colloids as drug carriers on the skin [J].
Cevc, G .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (05) :675-711
[5]   Rheological properties of progesterone microemulsions: Influence of xanthan and chitosan biopolymer concentration [J].
Corrias, F. ;
Dolz, M. ;
Herraez, M. ;
Diez-Sales, O. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 110 (02) :1225-1235
[6]   Rheological characterization of chitosan matrices:: Influence of biopolymer concentration [J].
Diez-Sales, O. ;
Dolz, M. ;
Hernandez, M. J. ;
Casanovas, A. ;
Herraez, M. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2007, 105 (04) :2121-2128
[7]   Transmission electron microscopy studies on pig gastric mucin and its interactions with chitosan [J].
Fiebrig, I ;
Harding, SE ;
Rowe, AJ ;
Hyman, SC ;
Davis, SS .
CARBOHYDRATE POLYMERS, 1995, 28 (03) :239-244
[8]   PHYCOBILIPROTEINS - A FAMILY OF VALUABLE, WIDELY USED FLUOROPHORES [J].
GLAZER, AN .
JOURNAL OF APPLIED PHYCOLOGY, 1994, 6 (02) :105-112
[9]   Anti-inflammatory activity of phycocyanin extract in acetic acid-induced colitis in rats [J].
González, R ;
Rodríguez, S ;
Romay, C ;
Ancheta, O ;
González, A ;
Armesto, J ;
Remirez, D ;
Merino, N .
PHARMACOLOGICAL RESEARCH, 1999, 39 (01) :55-59
[10]   Chitosan-based gastrointestinal delivery systems [J].
Hejazi, R ;
Amiji, M .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (02) :151-165