Characteristics of vitamin C encapsulated tripolyphosphate-chitosan microspheres as affected by chitosan molecular weight

被引:66
作者
Desai, K. G.
Liu, C.
Park, H. J.
机构
[1] Korea Univ, Sch Life Sci Biotechnol, Sungbuk Ku, Seoul 136701, South Korea
[2] Clemson Univ, Clemson, SC USA
关键词
vitamin C; chitosan; molecular weight; encapsulation; microspheres; tripolyphosphate; controlled release;
D O I
10.1080/02652040500435360
中图分类号
O69 [应用化学];
学科分类号
081704 [应用化学];
摘要
In this paper, the effect of chitosan molecular weight on the characteristics (size, encapsulation efficiency, zeta potential, surface morphology and release rate) of vitamin C encapsulated tripolyphosphate cross-linked chitosan (TPP-chitosan) microspheres. The molecular weight of chitosan had a noticeable influence on the size, encapsulation efficiency, zeta potential, surface morphology and controlled release behaviour of the vitamin C encapsulated TPP-chitosan microspheres. The mean particle size and encapsulation efficiencies of TPP-chitosan microspheres were 3.1, 4.9 and 6.7 mu m and 67.25, 60.43 and 52.74% for the microspheres prepared using low, medium and high molecular weight chitosan, respectively. All the TPP-chitosan microspheres (low, medium and high molecular weight) had positive charge on their surface. The zeta potential of the TPP-chitosan microspheres prepared using low, medium and high molecular weight chitosan was 41.25, 40.84 and 39.13 mV, respectively. The particle sizes of TPP-chitosan microspheres increased with increases in chitosan molecular weight. Molecular weight of chitosan did not affect significantly the % yield of TPP-chitosan microspheres prepared by spray-drying. The influence of chitosan molecular weight on the surface morphology of vitamin C encapsulated TPP-chitosan microspheres was examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). It was observed that, as the molecular weight of chitosan increases, TPP-chitosan microspheres with uniform spherical shape could be obtained. The physical state of vitamin C (amorphous or crystalline) in TPP-chitosan matrix was studied by X-ray diffraction (XRD) and it was found that vitamin C is dispersed at the molecular level (amorphous) in the TPP-chitosan matrix. Release rate of the vitamin C from TPP-chitosan microspheres was significantly affected by the chitosan molecular weight. The release rate decreased with increase in the chitosan molecular weight. The release of vitamin C from TPP-chitosan microspheres followed Fick's law of diffusion.
引用
收藏
页码:79 / 90
页数:12
相关论文
共 21 条
[1]
EVALUATION OF CHITOSAN CITRATE COMPLEXES AS MATRICES FOR CONTROLLED RELEASE FORMULATIONS USING A 3(2) FULL FACTORIAL DESIGN [J].
ADUSUMILLI, PS ;
BOLTON, SM .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1991, 17 (14) :1931-1945
[2]
Preparation and evaluation of sustained release cross-linked chitosan microspheres containing phenobarbitone [J].
Al-Helw, AA ;
Al-Angary, AA ;
Mahrous, GM ;
Al-Dardari, MM .
JOURNAL OF MICROENCAPSULATION, 1998, 15 (03) :373-382
[3]
Augustin MA, 2001, FOOD AUST, V53, P220
[4]
Swellable matrices for the controlled-release of diclofenac sodium: Formulation and in vitro studies [J].
Bravo, SA ;
Lamas, MC ;
Salomon, CJ .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2004, 9 (01) :75-83
[5]
Effect of temperature on the intrinsic viscosity and conformation of chitosans in dilute HCl solution [J].
Chen, RH ;
Tsaih, ML .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1998, 23 (02) :135-141
[6]
Encapsulation of vitamin C in tripolyphosphate cross-linked chitosan microspheres by spray drying [J].
Desai, KGH ;
Park, HJ .
JOURNAL OF MICROENCAPSULATION, 2005, 22 (02) :179-192
[7]
A simple and reliable spectrophotometric method for the determination of ascorbic acid in pharmaceutical preparations [J].
Farajzadeh, MA ;
Nagizadeh, S .
JOURNAL OF ANALYTICAL CHEMISTRY, 2003, 58 (10) :927-932
[8]
Spray-dried carbamazepine-loaded chitosan and HPMC microspheres: preparation and characterisation [J].
Filipovic-Grcic, J ;
Perissutti, B ;
Moneghini, M ;
Voinovich, D ;
Martinac, A ;
Jalsenjak, I .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (07) :921-931
[9]
Chitosan-based gastrointestinal delivery systems [J].
Hejazi, R ;
Amiji, M .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (02) :151-165
[10]
DETERMINATION OF DEGREE OF DEACETYLATION OF CHITOSAN BY H-1-NMR SPECTROSCOPY [J].
HIRAI, A ;
ODANI, H ;
NAKAJIMA, A .
POLYMER BULLETIN, 1991, 26 (01) :87-94