Chitosan has become a focus of major interest in recent years due to its excellent biocompatibility, biodegradability and non-toxicity. Although this material has already been extensively investigated in the design of different types of drug delivery systems, it is still little explored for stomach specific drug delivery systems. The objective of the present investigation was to explore the potential of low molecular mass chitosan (LMCH) as carrier for a hydrodynamically balanced system (HBS) for sustained delivery of water soluble drug ciprofloxacin hydrochloride (CP). Various formulations were prepared by physical blending of drug and polymer(s) in varying ratios followed by encapsulation into hard gelatin capsules. All the formulations remained buoyant in 0.1 mol L-1 HCl (pH 1.2) throughout the experiment. Effect of addition of xanthan gum (XG) or ethyl cellulose (EC) on drug release was also investigated. Zero order drug release was obtained from the formulations containing LMCH alone or in combination with XG, and in one instance also with EC. Our results suggest that LMCH alone or in combination with XG is an excellent material for stomach specific sustained delivery of CP from hydrodynamically balanced single unit capsules. Zbog svoje biokompatibilnosti, biorazgradljivosti i netoksičnosti kitozan je vrlo interesantan istraživačima u području farmaceutske tehnologije. Najviše se upotrebljavao u dizajniranju različitih sustava za isporuku lijekova ali vrlo malo za sustave za specifičnu isporuku u želucu. Cilj ovog rada bio je ispitati mogućnost upotrebe kitozana male molekulske mase (LMCH) kao nosača u hidrodinamički balansiranom sustavu (HBS) za usporenu isporuku vodotopljivog lijeka ciprofloksacin hidroklorida (CP). Pripravljene su različite formulacije stvaranjem fizičke smjese lijeka i polimera u različitim omjerima, koje su potom kapsulirane u želatinske kapsule. Svi su pripravci za vrijeme cijelog eksperimenta ostali plutati u 0,01mol L1 HCl (pH 1,2). Ispitivan je i učinak ksantan gume (XG) ili etilceluloze (EC) na oslobađanje lijeka. Oslobađanje lijeka nultog reda postignuto je iz formulacija koje sadrže samo LMCH ili LMCH u kombinaciji sa XG i u jednom slučaju s EC. Dobiveni rezultati pokazuju da je LMCH, sam ili u kombinaciji sa XG, izvrstan materijal za sustave za specifičnu isporuku CP iz hidrodinamički balansiranih kapsula.