Open AccessPermeation‐enhancing effects of chitosan formulations on recombinant hirudin‐2 by nasal delivery in vitro and in vivo
Author(s) -
ZHANG Yujie,
MA Changhua,
LU Wanliang,
ZHANG Xuan,
WANG Xiaoliang,
SUN Jianning,
ZHANG Qiang
Publication year - 2005
Publication title -
acta pharmacologica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.514
H-Index - 90
eISSN - 1745-7254
pISSN - 1671-4083
DOI - 10.1111/j.1745-7254.2005.00174.x
Subject(s) - chemistry , chitosan , permeation , bioavailability , in vivo , pharmacology , nasal administration , ivivc , chromatography , absorption (acoustics) , in vitro , biochemistry , membrane , medicine , physics , microbiology and biotechnology , acoustics , biology , dissolution testing , biopharmaceutics classification system
Aim: To investigate the enhancing effects of chitosan with or without enhancers on nasal recombinant hirudin‐2 (rHV2) delivery in vitro and in vivo , and to evaluate the ciliotoxicity of these formulations. Methods: The permeation‐enhancing effect of various chitosan formulations was estimated by using the permeation coefficient of fluorescein isothiocyanate recombinant hirudin‐2 (FITC‐rHV2) across the excited rabbit nasal epithelium in vitro . The effect was further evaluated by measuring the blood concentration level after nasal absorption of FITC‐rHV2 in rats. The mucosal ciliotoxicity of different formulations was evaluated with an in situ toad palate model. Results: Chitosan at a concentration of 0.5% with or without various enhancers significantly increased the permeability coefficient (P) and relative bioavailability (Fr) of FITC‐rHV2 compared with the blank control. The addition of 1% sodium dodecylsulfate, 5%Brij35, 5%Tween80, 1.5% menthol, 1% glycyrrhizic acid monoammonium salt (GAM) or 4% Azone into the 0.5% chitosan solution resulted in a further increase in absorption (P<0.05) compared with 0.5% chitosan alone. But co‐administration of chitosan with 5% hydroxyl‐propyl‐beta‐cyclodextrin(HP‐β‐CD), 5%lecithin or 0.1% ethylenediamine tetraacetic acid (EDTA) was not more effective than using the 0.5% chitosan solution alone. Chitosan alone and with 5% HP‐β‐CD, 0.1% EDTA, 1% GAM or 5%Tween80 was relatively less ciliotoxic. Conclusion: Chitosan with or without some enhancers was able to effectively promote the nasal absorption of recombinant hirudin, while not resulting in severe mucosal ciliotoxicity. A chitosan formulation system would be a useful approach for the nasal delivery of recombinant hirudin.