Application of PVP/HPMC miscible blends with enhanced mucoadhesive properties for adjusting drug release in predictable pulsatile chronotherapeutics

被引:121
作者
Karavas, Evangelos
Georgarakis, Emmanouel
Bikiaris, Dimitrios [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Chem, Lab Organ Chem Technol, Thessaloniki 54124, Greece
[2] Aristotle Univ Thessaloniki, Dept Chem, Dept Pharm, Thessaloniki 54124, Greece
[3] Pallini Attikis, Pharmaceut Ind, Athens, Greece
关键词
felodipine; poly(vinyl pyrrolidone); hydroxypropyl methyl-cellulose; miscible blends; pulsatile chronotherapeutics; mucoadhesive polymers;
D O I
10.1016/j.ejpb.2005.12.013
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The aim of the present study was to prepare pulsatile release formulations consisting of two-layered tablets appropriate for preventing ischemic heart diseases. For this reason the active core was constituted by a FELO/PVP 10/90 w/w solid dispersion while for the adjustment of the drug release time the coating layer was composed of PVP/HPMC blends at different compositions, acting as a stimulus responsible layer. These blends as was found by DSC studies are miscible in the entire composition range, ensured by the interactions taking place between hydroxyl groups of HPMC and carbonyl groups of PVP. The miscibility of the system enhances the mucoadhesive properties of the blends, compared with those of pure HPMC, which is desired for such applications. The enhancement was attributed to the higher rate of wetting and flexibility of the new matrices due to the faster dissolution of the PVP macromolecules. Upon exposure of the prepared tablets to the release medium it was found that the coating layer disintegrates first, followed by the immediate release of FELO from the active core. The delaying time is based on a complicated mechanism, which is a combination of swelling and erosion of the PVP/HPMC polymer blends. Varying the PVP/HPMC blend ratios, the exact time that FELO is released during a daytime can be effectively adjusted and this ability is expressed mathematically by the equation t = 0.028 C-1.5, where C is the concentration of HPMC in the blend. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 126
页数:12
相关论文
共 50 条
[1]
EVALUATION OF SOLUBILIZERS IN THE DRUG-RELEASE TESTING OF HYDROPHILIC MATRIX EXTENDED-RELEASE TABLETS OF FELODIPINE [J].
ABRAHAMSSON, B ;
JOHANSSON, D ;
TORSTENSSON, A ;
WINGSTRAND, K .
PHARMACEUTICAL RESEARCH, 1994, 11 (08) :1093-1097
[2]
A novel mucoadhesive polymer prepared by template polymerization of acrylic acid in the presence of chitosan [J].
Ahn, JS ;
Choi, HK ;
Cho, CS .
BIOMATERIALS, 2001, 22 (09) :923-928
[3]
CIRCADIAN-RHYTHM OF SERUM INTERLEUKIN-6 IN RHEUMATOID-ARTHRITIS [J].
ARVIDSON, NG ;
GUDBJORNSSON, B ;
ELFMAN, L ;
RYDEN, AC ;
TOTTERMAN, TH ;
HALLGREN, R .
ANNALS OF THE RHEUMATIC DISEASES, 1994, 53 (08) :521-524
[4]
CIRCADIAN VARIATION IN AIRWAY FUNCTION [J].
BARNES, PJ .
AMERICAN JOURNAL OF MEDICINE, 1985, 79 (6A) :5-9
[5]
Blends of polymers with similar glass transition temperatures: A DMTA and DSC study [J].
Bikiaris, D ;
Prinos, J ;
Botev, M ;
Betchev, C ;
Panayiotou, C .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 93 (02) :726-735
[6]
TREATMENT OF NOCTURNAL ASTHMA WITH PULSED-RELEASE ALBUTEROL [J].
BOGIN, RM ;
BALLARD, RD .
CHEST, 1992, 102 (02) :362-366
[7]
Choi HK, 1999, J APPL POLYM SCI, V73, P2749, DOI 10.1002/(SICI)1097-4628(19990923)73:13<2749::AID-APP23>3.0.CO
[8]
2-9
[9]
Modulation of the dissolution profiles from Geomatrix(R) multi-layer matrix tablets containing drugs of different solubility [J].
Conte, U ;
Maggi, L .
BIOMATERIALS, 1996, 17 (09) :889-896
[10]
A NEW IBUPROFEN PULSED RELEASE ORAL DOSAGE FORM [J].
CONTE, U ;
COLOMBO, P ;
LAMANNA, A ;
GAZZANIGA, A ;
SANGALLI, ME ;
GIUNCHEDI, P .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1989, 15 (14-16) :2583-2596