Abstract

PurposeThe effects of chitosan hydrochloride on the oral absorption of acyclovir in humans were studied to confirm the absorption enhancing effects reported for in vitro and rat studies, respectively.MethodsA controlled, open-label, randomized, 3-phase study was conducted in 12 healthy human volunteers. Zovirax 200 mg dispersible tablets co-administered with doses of 400 and 1000 mg chitosan HCl were compared with Zovirax only.ResultsThe expected increased absorption of acyclovir was not observed. On the contrary, mean area under the plasma concentration-time curve (AUC0-12 h) and maximal plasma concentration (Cmax) decreased following concomitant chitosan intake (1402 versus 1017 and 982.0 ng∙h/ml and 373 versus 208 and 235 ng/ml, respectively). In addition, Tmax increased significantly in presence of 1000 mg of chitosan from 1 to 2 h.ConclusionsThe results of this study in human volunteers did not confirm an absorption enhancing effect of chitosan. Reference values were comparable to literature data, whereas addition of chitosan resulted in significant opposite effects on Cmax, Tmax and AUC. Additional studies are needed to investigate the cause of the discrepancy. The observed variability and complex potential interactions may complicate the use of chitosan HCl in oral pharmaceutical formulations.Electronic supplementary materialThe online version of this article (doi:10.1007/s11095-014-1613-y) contains supplementary material, which is available to authorized users.

Highlights

  • Permeation enhancement has been a research topic in pharmaceutics for decades

  • Chitosan is a heteropolysaccharide derived from natural source; characterized by variable molecular weights, degrees of deacetylation (DD) and salt forms [10]

  • The aim of the study presented here was to test the effects of chitosan hydrochloride on the oral absorption of acyclovir in human volunteers

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Summary

Introduction

Increasing the absorption of drugs with low permeability may for instance aid the reduction of the variability in bioavailability as well as reduce the administered dose of an active substance. Examples of absorption modulators are acetylcystein, supposedly acting via reduction of the mucous layer by disrupting disulfide bridges; surfactants, polymers and chelating agents potentially interfering with the tight junctions, and substances interfering with absorption or efflux transporters [1,2,3]. Chitosan and its derivatives have been described as potential permeability enhancers acting via a disruptive effect on the tight junctions between the epithelial cells [4,5,6,7,8,9]. The aim of the study presented here was to test the effects of chitosan hydrochloride on the oral absorption of acyclovir in human volunteers

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