Mucoadhesive Polymers for Oral Transmucosal Drug Delivery: A Review

被引:47
作者
Bagan, Jose' [1 ]
Paderni, Carlo [2 ]
Termine, Nicoletta [2 ]
Campisi, Giuseppina [2 ]
Lo Russo, Lucio [3 ]
Compilato, Domenico [2 ]
Di Fede, Olga [2 ]
机构
[1] Univ Gen Hosp Valencia, Serv Stomatol, Valencia, Spain
[2] Univ Palermo, Dept Surg & Oncol Disciplines, Sect Odontostomatol Sci, Sect Oral Med V Margiotta, Palermo, Italy
[3] Univ Foggia, Dept Surg & Oncol Disciplines, Foggia, Italy
关键词
Mucoadhesion; oral transmucosal drug delivery; dosage form; drug controlled-release; mucoadhesive polymers; oral mucosa; mucosal permeability; MEMBRANE-COATING GRANULES; IN-VITRO EVALUATION; BIOADHESIVE POLYMERS; CLINICAL-TRIAL; APHTHOUS STOMATITIS; MUCUS GLYCOPROTEINS; SODIUM HYALURONATE; TABLET FORMULATION; POLY(ACRYLIC ACID); ABSORPTIVE MUCOSAE;
D O I
10.2174/138161212803307545
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The oral mucosa offers an interesting site for the application of dosage forms that release drugs within/throughout the oral mucosa, by assuring a high drug bioavailability for topic and systemic effects. However, the relative permeability of the oral mucosa and the washing effect related to the oral fluids and mechanical stresses must be considered in the formulation of oral dosage forms. Since a sustained drug release can be guaranteed only if dosage forms remain in contact with the oral site of absorption/application for a prolonged time, the development of mucoadhesive dosage forms is mandatory. The mucoadhesion is a complex phenomenon and the mucoadhesive bond consists of two different parts, the mucoadhesive polymers and the mucous substrate. In addition to factors related to the oral mucosa and oral environment features, the physical-chemical characteristics of mucoadhesive polymers must be also considered as factors influencing the mucoadhesive bonds. While it is not possible to modify the mucosal features or it is possible to modify or inhibit only in part certain mucosal processes, the knowledge of polymer properties influencing mucoadhesive bonds allows to modify or to control these properties in developing increasingly effective mucoadhesive systems. The aims of this review are to discuss the several mechanisms and factors behind the phenomenon of mucoadhesion with particular reference to the features of the oral environment, oral mucosa, and polymeric compounds influencing mucoadhesion process. Finally, a brief mention to the main mucoadhesive dosage forms designed for oral transmucosal drug delivery is made.
引用
收藏
页码:5497 / 5514
页数:18
相关论文
共 150 条
[1]  
Akbari Jafar, 2004, Farmaco, V59, P155
[2]   Comparative in vivo mucoadhesion studies of thiomer formulations using magnetic resonance imaging and fluorescence detection [J].
Albrecht, K. ;
Greindl, M. ;
Kremser, C. ;
Wolf, C. ;
Debbage, P. ;
Bernkop-Schnuerch, A. .
JOURNAL OF CONTROLLED RELEASE, 2006, 115 (01) :78-84
[3]   Buccoadhesive erodible disk for treatment of oro-dental infections: design and characterisation [J].
Ali, J ;
Khar, R ;
Ahuja, A ;
Kalra, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 238 (1-2) :93-103
[4]   BUCCAL ABSORPTION OF PROTIRELIN - AN EFFECTIVE WAY TO STIMULATE THYROTROPIN AND PROLACTIN [J].
ANDERS, R ;
MERKLE, HP ;
SCHURR, W ;
ZIEGLER, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (12) :1481-1483
[5]   Mucoadhesive polymeric platforms for controlled drug delivery [J].
Andrews, Gavin P. ;
Laverty, Thomas P. ;
Jones, David S. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 71 (03) :505-518
[6]   Development of Satranidazole Mucoadhesive Gel for the Treatment of Periodontitis [J].
Bansal, K. ;
Rawat, M. K. ;
Jain, A. ;
Rajput, A. ;
Chaturvedi, T. P. ;
Singh, S. .
AAPS PHARMSCITECH, 2009, 10 (03) :716-723
[7]   Transmucosal, oral controlled-release, and transdermal drug administration in human subjects: A crossover study with melatonin [J].
Benes, L ;
Claustrat, B ;
Horriere, F ;
Geoffriau, M ;
Konsil, J ;
Parrott, KA ;
DeGrande, G ;
McQuinn, RL ;
Ayres, JW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (10) :1115-1119
[8]   Mucoadhesive polymers:: strategies, achievements and future challenges [J].
Bernkop-Schnürch, A .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (11) :1553-1555
[9]   Thiolation of polycarbophil enhances its inhibition of intestinal brush border membrane bound aminopeptidase N [J].
Bernkop-Schnürch, A ;
Zarti, H ;
Walker, GF .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (11) :1907-1914
[10]   Thiolated polymers:: synthesis and in vitro evaluation of polymer-cysteamine conjugates [J].
Bernkop-Schnürch, A ;
Clausen, AE ;
Hnatyszyn, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 226 (1-2) :185-194