VISCOELASTICITY OF CELLULOSE POLYMERS AND MUCOCILIARY TRANSPORT ON FROG PALATES

被引:15
作者
LIN, SY
AMIDON, GL
WEINER, ND
GOLDBERG, AH
机构
[1] UNIV MICHIGAN,COLL PHARM,ANN ARBOR,MI 48109
[2] RUGBY DARBY GRP CO INC,ROCKVILLE CTR,NY 11570
关键词
CELLULOSE POLYMER; CONTOUR PLOT; MIXED SOLVENT SYSTEM; MOISTURE ABSORPTION; VISCOELASTICITY; MUCOCILIARY TRANSPORT;
D O I
10.1016/0378-5173(93)90390-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The viscoelastic properties of model polymer, hydroxypropylmethylcellulose (HPMC), in ternary solvent mixtures and the variation of viscoelastic properties under dilution with water were investigated. HPMC was dispersed in mixtures of glycerol formal (GF) or ethyl alcohol, propylene glycol (PG), and water. Each polymeric sample was oscillated at different frequencies with fixed stress amplitude and the changes in elastic modulus, viscous modulus, and apparent viscosity were measured at 30-degrees-C. The moisture absorption rate of HPMC in PG:GF solvent mixtures in a 94% relative humidified environment was also studied. A linear relationship between the elastic modulus or viscous modulus and polymer concentration was observed for the HPMC samples. The relative mucociliary transport rate tested on the non-depleted frog palate model revealed a curvilinear correlation with the loss tangent (a ratio of the viscous modulus to the elastic modulus) of the polymeric solution. Using GF as a solvent for HPMC resulted in a formation of a rigid gel with the highest elastic modulus and viscous modulus among solvents selected. A higher affinity for water was found for HPMC in the PG:GF 90:10 mixture compared with HPMC in the PG:GF 70:30 mixture. However, the elastic modulus and viscous modulus were much higher for HPMC in the PG:GF 70:30 mixture.
引用
收藏
页码:57 / 65
页数:9
相关论文
共 20 条
[1]  
BARNES H, 1989, AINTRO RHEOLOGY, P37
[2]  
BIRD RB, 1987, DYNAMICS POLYM LIQUI, V1, P55
[3]  
CHIEN Y W, 1984, Journal of Parenteral Science and Technology, V38, P32
[4]  
Doelker E., 1990, ABSORBENT POLYM TECH, V8, P125, DOI [10.1016/b978-0-444-88654-5.50011-x, DOI 10.1016/B978-0-444-88654-5.50011-X]
[5]  
Ferry J.D., 1980, VISCOELASTIC PROPERT, Vthird, P33
[6]  
GELMAN RA, 1979, AM REV RESPIR DIS, V120, P553
[7]   MODEL OF DISPOSITION OF DRUGS ADMINISTERED INTO THE HUMAN NASAL CAVITY [J].
GONDA, I ;
GIPPS, E .
PHARMACEUTICAL RESEARCH, 1990, 7 (01) :69-75
[8]   BIOADHESIVE INTRAORAL RELEASE SYSTEMS - DESIGN, TESTING AND ANALYSIS [J].
GURNY, R ;
MEYER, JM ;
PEPPAS, NA .
BIOMATERIALS, 1984, 5 (06) :336-340
[9]  
GURNY R, 1990, BIOADHESIVE DRUG DEL, P153
[10]   INTRANASAL DRUG DELIVERY BY SPRAY AND DROPS [J].
HARDY, JG ;
LEE, SW ;
WILSON, CG .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1985, 37 (05) :294-297