Abstract
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.
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References
Walenga JM, Pifarre R, Fareed J . Recombinant hirudin as an antithrombotic agent. Drugs Future 1990; 15: 267–80.
Markwardt F, Fink G, Kaiser B, Klocking HP, Nowak G, Richter M, et al. Pharmacological survey of recombinant hirudin. Pharmazie 1988; 43: 202–7.
Doutremepuich C, Deharo E, Guyot M, Lalanne MC, Walenga JM, Fareed J . Antithrombotic activity of recombinant hirudin in rat: a comparative study with heparin. Thrombos Res 1989; 54: 435–45.
Markwardt F . The development of hirudin as an antithrombotic drug. Thromb Res 1994; 74: 1–23.
Markwardt F . Prospective clinical use of hirudin as an anticoagulant. Biomed Prog 1990; 3: 19–23.
Han YM, Lu YF, Wang ZH . Studies on the effects of anticoagulant and anti-thrombin after duodenal administration of recombinant hirudin in rats. Chin J Hematol 1999; 20: 483–4.
Yang XY, Wang XT, Zhang XN, Zhang Q . Gastrointestinal absorption of recombinant hirudin-2 in rats. J Pharmacol Exp Ther 2004; 308: 774–9.
Schipper NG, Olsson S, Hoogstraate JA, deBoer AG, Varum KM, Artursson P . Chitosan as absorption enhancers for poorly absorbable drugs. 2: Mechanism of absorption enhancement. Pharm Res 1997; 14: 923–9.
Aspden TJ, Mason JD, Jones NS, Lowe J, Skaugrud O, Illum L . Chitosan as a nasal delivery system: the effect of chitosan solutions on in vitro and in vivo mucociliary transport rates in human turbinates and volunteers. J Pharm Sci 1997; 86: 509–13.
Jiang XG, Cui JB, Fang XL, Wei Y, Xi NZ . Toxicity of drugs on nasal mucocilia and method of its evaluation. Acta Pharm Sin 1995; 30: 848–53.
Wang HD, Zhou SH . Marking techniques of biomedicine. Beijing: People's Medical Publishing House; 1995.
Griessbach U, Stürzebecher J, Markwardt F . Assay of hirudin in plasma using a chromogenic thrombin substrate. Thromb Res 1985; 37: 347–50.
Hosoya K, Kubo H, Natsume H, Sugibayashi K, Morimoto Y . Evaluation of enhancers to increase nasal absorption using chamber technique. Biol Pharm Bull 1994; 17: 316–22.
Chandler SG, Illum L, Tomas NM . Nasal absorption in rats. II Effect of enhancers on insulin absorption and nasal histology. Int J Pharm 1991; 76: 61–70.
Temesvari LA, Bush JM, Peterson MD, Novak KD, Titus MA, Cardelli JA . Examination of the endosomal and lysosomal pathways in Dictyostelium discoideum myosin I mutants. J Cell Sci 1996; 109: 663–73.
Illum L . Chitosan and its use as a pharmaceutical excipient. Pharm Res 1998; 15: 1326–31.
Illum L, Farraj NF, Davis SD . Chitosan as a novel basal delivery system for peptide drugs. Pharm Res 1994; 11: 1186–9.
Shojaei AH . Buccal mucosa as a route for systemic drug delivery: a review. J Pharm Pharm Sci 1998; 1: 15–30.
Rege BD, Kao JP, Polli JE . Effects of nonionic surfactants on membrane transporters in Caco-2 cell monolayers. Eur J Pharm Sci 2002; 16: 237–46.
Sugibayashi K, Nakayama S, Seki T, Hosoya K, Morimoto YJ . Mechanism of skin penetration-enhancing effect by laurocapram. Pharm Sci 1992; 81: 58–64.
Wang GS, Zabner J, Deering C, Launspach J, Shao JQ, Bodner M . Increasing epithelial junction permeability enhances gene transfer to airway epithelia in vivo. Am J Respir Cell Mol Biol 2000; 22: 129–38.
Marttin E, Verhoef JC, Cullander C, Romeijn SG, Nagelkerke JF, Merkus FW . Confocal laser scanning microscopic visualization of the transport of dextrans after nasal administration to rats: effects of absorption enhancer. Pharm Res 1997; 14: 631–7.
Yang T, Hussain A, Paulson J, Abbruscato TJ, Ahsan F . Cyclodextrins in nasal delivery of low-molecular-weight heparins: in vivo and in vitro studies. Pharm Res 2004; 21: 1127–36.
Merkus FW, Verhoef JC, Marttin E, Romeijn, SG, van der Kuy, PH, Hermens WA, et al. Cyclodextrins in nasal drug delivery. Adv Drug Deliv Rev 1999; 36: 41–57.
Yu SY, Zhao Y, Wu FL, Zang X, Lü WL, Zhang H . Nasal insulin delivery in the chitosan solution: in vitro and in vivo studies. Int J Pharm 2004; 281: 11–23.
Maitani Y, Nakamura K, Suenaga H, Kamata K, Takayama K, Nagai T . The effect of soybean-derived sterylglucoside and β-sitosterol β-D-glucoside on nasal absorption in rabbits. Int J Pharm 2000; 200: 17–26.
Kaplun-Frischoff Y, Touitou E . Testosterone skin permeation enhancement by menthol through formation of eutectic with drug and interaction with skin lipids. J Pharm Sci 1997; 86: 1394–9.
Sakai M, Imai T, Ohtake H, Azuma H, Otagiri M . Effects of absorption enhancers on cytoskeletal actin filaments in Caco-2cell monolayers. Life Sci 1998; 63: 45–54.
Sakai M, Imai T, Ohtake H, Azuma H, Otagiri M . Simultaneous use of sodium deoxycholate and dipotassium glycyrrhizinate enhances the cellular transport of poorly absorbed compounds across Caco-2 cell monolayers. J Pharm Biomed Anal 2004; 36: 915–9.
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Zhang, Yj., Ma, Ch., Lu, Wl. et al. Permeation-enhancing effects of chitosan formulations on recombinant hirudin-2 by nasal delivery in vitro and in vivo. Acta Pharmacol Sin 26, 1402–1408 (2005). https://doi.org/10.1111/j.1745-7254.2005.00174.x
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DOI: https://doi.org/10.1111/j.1745-7254.2005.00174.x