Preparation of thiomer microparticles and in vitro evaluation of parameters influencing their mucoadhesive properties

被引:31
作者
Albrecht, K. [1 ]
Zirm, E. J. [1 ]
Palmberger, T. F. [1 ]
Schlocker, W. [1 ]
Bernkop-Schnuerch, A. [1 ]
机构
[1] Univ Innsbruck, Inst Pharm, Dept Pharmaceut Technol, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
microparticulate delivery system; thiomers; polycarbophil-cysteine; water uptake; amount of thiol groups; mucoadhesion;
D O I
10.1080/03639040600712334
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
It was the aim of this study to develop mucoadhesive microparticulate delivery systems based on thiomers and to investigate parameters influencing their mucoadhesive properties. Microparticles were prepared via coazervation of thiolated or unmodified polycarbophil with fluorescein-diacetate as marker. The protective effect of the polymers toward enzymatic hydrolysis by intestinal enzymes was investigated. Mucoadhesion studies with microparticles, applied in dry and prehydrated form, were performed by ascertaining their residence time on intestinal mucosa. Furthermore, the influence of the amount of thiol groups on mucoadhesion was studied in vitro. Results showed that in comparison to unmodified polycarbophil, thiolated polycarbophil provided a more than 3-fold higher protective effect for the incorporated marker fluorescein-diacetate toward hydrolysis. When being applied in dry form 23.4 +/- 4.8% of the fluorescence marker being embedded in thiomer microparticles remained adhering to the intestinal mucosa within 3 h. In contrast, only 11.6 +/- 2.0% of the marker remained on the mucosa, when the thiomer microparticles were applied in prehydrated form. In addition, tests performed to assess the impact of the amount of thiol groups pointed out that a high amount of thiol groups is advantageous in order to further improve mucoadhesive properties. This knowledge should contribute to the design of highly efficient drug delivery systems being based on thiomer microparticles.
引用
收藏
页码:1149 / 1157
页数:9
相关论文
共 22 条
[1]   Polymers with thiol groups:: A new generation of mucoadhesive polymers? [J].
Bernkop-Schnürch, A ;
Schwarz, V ;
Steininger, S .
PHARMACEUTICAL RESEARCH, 1999, 16 (06) :876-881
[2]   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
[3]   Improvement in the mucoadhesive properties of alginate by the covalent attachment of cysteine [J].
Bernkop-Schnürch, A ;
Kast, CE ;
Richter, MF .
JOURNAL OF CONTROLLED RELEASE, 2001, 71 (03) :277-285
[4]  
Bernkop-Schnürch A, 2000, J PHARM SCI-US, V89, P901, DOI 10.1002/1520-6017(200007)89:7<901::AID-JPS7>3.0.CO
[5]  
2-0
[6]   The role of glutathione in the permeation enhancing effect of thiolated polymers [J].
Clausen, AE ;
Kast, CE ;
Bernkop-Schnürch, A .
PHARMACEUTICAL RESEARCH, 2002, 19 (05) :602-608
[7]   VARIATION IN GASTROINTESTINAL TRANSIT OF PHARMACEUTICAL DOSAGE FORMS IN HEALTHY-SUBJECTS [J].
COUPE, AJ ;
DAVIS, SS ;
WILDING, IR .
PHARMACEUTICAL RESEARCH, 1991, 8 (03) :360-364
[8]   SENSITIVE METHOD FOR LOCALIZATION OF DISULFIDE CONTAINING PEPTIDES IN COLUMN EFFLUENTS [J].
HABEEB, AFSA .
ANALYTICAL BIOCHEMISTRY, 1973, 56 (01) :60-65
[9]   GI TRANSIT OF POTENTIAL BIOADHESIVE FORMULATIONS IN MAN - A SCINTIGRAPHIC STUDY [J].
HARRIS, D ;
FELL, JT ;
SHARMA, HL ;
TAYLOR, DC .
JOURNAL OF CONTROLLED RELEASE, 1990, 12 (01) :45-53
[10]   Mucoadhesive ocular insert based on thiolated poly(acrylic acid):: development and in vivo evaluation in humans [J].
Hornof, M ;
Weyenberg, W ;
Ludwig, A ;
Bernkop-Schnürch, A .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (03) :419-428