Preparation and characterization of laminated thiolated chitosan-based freeze-dried wafers for potential buccal delivery of macromolecules

被引:37
作者
Boateng, Joshua S. [1 ]
Ayensu, Isaac [1 ]
机构
[1] Univ Greenwich Medway, Fac Sci & Engn, Dept Pharmaceut Chem & Environm Sci, Chatham ME4 4TB, Kent, England
关键词
BSA; buccal; enzyme inhibitor; protein; thiolated chitosan; wafer; IN-VITRO EVALUATION; PROTEIN DRUG-DELIVERY; B-PLA NANOPARTICLES; MUCOSAL DRUG; ABSORPTION; VIVO; PEPTIDE; FILMS; MUCOADHESIVE; POLYMERS;
D O I
10.3109/03639045.2014.884126
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study involves the development and functional characterization of a thiolated chitosan (CS) system for potential buccal delivery of proteins. Thiolated CS was synthesized by conjugating pure CS with thioglycolic acid and dialyzed to remove excess acid. Amount of thiol groups immobilized on CS was determined using L-cysteine calibration curve. The weight average molecular weights of CS and thiolated CS were monitored using gel permeation chromatography. Laminated wafers were obtained by pouring gels (containing bovine serum albumin; BSA, different amounts of glutathione as enzyme inhibitor and mucin to mimic salivary conditions) of the thiolated CS into moulds previously lined with impervious ethylcellulose (EC) films and freeze-dried. The resulting formulations were analyzed using attenuated total reflectance Fourier transform infrared (FTIR) spectroscopy, circular dichroism (CD) and scanning electron microscopy (SEM). The formulations were further characterized for functional buccal mucosa performance using hydration, swelling, mucoadhesion and in vitro drug dissolution studies. FTIR showed successful thiolation of CS's amine functionality, CD confirmed that BSA conformation remained unchanged throughout the gel formulation and freeze-drying process, whilst SEM showed a porous microstructure of the wafers and a uniform EC film laminate with no visible pores or cracks. The functional characterization studies showed that glutathione had significant effects on hydration, mucoadhesion and subsequently drug dissolution and release characteristics, whilst mucin affected the mucoadhesive properties of the wafers. It was concluded that BSA-loaded wafers containing 10% w/w glutathione as enzyme inhibitor was the formulation choice for potential buccal delivery and should be selected for further investigations.
引用
收藏
页码:611 / 618
页数:8
相关论文
共 45 条
[1]   Recent advances on chitosan-based micro- and nanoparticles in drug delivery [J].
Agnihotri, SA ;
Mallikarjuna, NN ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :5-28
[2]  
Ayensu I, 2012, J SCI TECH, V32, P11
[3]  
Ayensu I, 2011, AAPS J, V13, pM1144
[4]   In vitro characterisation of chitosan based xerogels for potential buccal delivery of proteins [J].
Ayensu, Isaac ;
Mitchell, John C. ;
Boateng, Joshua S. .
CARBOHYDRATE POLYMERS, 2012, 89 (03) :935-941
[5]   Effect of membrane dialysis on characteristics of lyophilised chitosan wafers for potential buccal delivery of proteins [J].
Ayensu, Isaac ;
Mitchell, John C. ;
Boateng, Joshua S. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2012, 50 (04) :905-909
[6]   Development and physico-mechanical characterisation of lyophilised chitosan wafers as potential protein drug delivery systems via the buccal mucosa [J].
Ayensu, Isaac ;
Mitchell, John C. ;
Boateng, Joshua S. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2012, 91 :258-265
[7]   Thiolated polymers-thiomers:: synthesis and in vitro evaluation of chitosan-2-iminothiolane conjugates [J].
Bernkop-Schnürch, A ;
Hornof, M ;
Zoidl, T .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 260 (02) :229-237
[8]   Comparison of the in vitro release characteristics of mucosal freeze-dried wafers and solvent-cast films containing an insoluble drug [J].
Boateng, Joshua S. ;
Matthews, Kerr H. ;
Auffret, Anthony D. ;
Humphrey, Mike J. ;
Eccleston, Gillian M. ;
Stevens, Howard N. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2012, 38 (01) :47-54
[9]   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
[10]   Chitosan nanoparticles as new ocular drug delivery systems:: in vitro stability, in vivo fate, and cellular toxicity [J].
de Campos, AM ;
Diebold, Y ;
Carvalho, ELS ;
Sánchez, A ;
Alonso, MJ .
PHARMACEUTICAL RESEARCH, 2004, 21 (05) :803-810