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      Stability studies of lincomycin hydrochloride in aqueous solution and intravenous infusion fluids

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          Abstract

          Purpose

          The purpose of this study was to evaluate the chemical stability of Lincocin ® (lincomycin hydrochloride) in commonly used intravenous fluids at room temperature (25°C), at accelerated-degradation temperatures and in selected buffer solutions.

          Materials and methods

          The stability of Lincocin ® injection (containing lincomycin 600 mg/2 mL as the hydrochloride) stored at 25°C±0.1°C in sodium lactate (Hartmann’s), 0.9% sodium chloride, 5% glucose, and 10% glucose solutions was investigated over 31 days. Forced degradation of Lincocin ® in hydrochloric acid, sodium hydroxide, and hydrogen peroxide was performed at 60°C. The effect of pH on the degradation rate of lincomycin hydrochloride stored at 80°C was determined.

          Results

          Lincomycin hydrochloride w as found to maintain its shelf life at 25°C in sodium lactate (Hartmann’s) solution, 0.9% sodium chloride solution, 5% glucose solution, and 10% glucose solution, with less than 5% lincomycin degradation occurring in all intravenous solutions over a 31-day period. Lincomycin hydrochloride showed less rapid degradation at 60°C in acid than in basic solution, but degraded rapidly in hydrogen peroxide. At all pH values tested, lincomycin followed first-order kinetics. It had the greatest stability near pH 4 when stored at 80°C (calculated shelf life of 4.59 days), and was least stable at pH 2 (calculated shelf life of 0.38 days).

          Conclusion

          Lincocin ® injection was chemically found to have a shelf life of at least 31 days at 25°C when added to sodium lactate (Hartmann’s) solution, 0.9% sodium chloride solution, 5% glucose solution, and 10% glucose solution. Solutions prepared at approximately pH 4 are likely to have optimum stability.

          Most cited references11

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          British Pharmacopoeia

          (2005)
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            Stability of commonly used antibiotic solutions in an elastomeric infusion device.

            The Accufuser silicone-based elastomeric infusion device has recently been approved for the Canadian market.
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              Lincomycin. II. Characterization and gross structure

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                Author and article information

                Journal
                Drug Des Devel Ther
                Drug Des Devel Ther
                Drug Design, Development and Therapy
                Drug Design, Development and Therapy
                Dove Medical Press
                1177-8881
                2016
                07 March 2016
                : 10
                : 1029-1034
                Affiliations
                School of Pharmacy, Curtin University, Perth, WA, Australia
                Author notes
                Correspondence: Petra Czarniak, School of Pharmacy, Curtin University, Kent Street, Bentley, Perth, WA 6102, Australia, Tel +61 8 9266 7419, Fax +61 8 9266 2769, Email p.czarniak@ 123456curtin.edu.au
                Article
                dddt-10-1029
                10.2147/DDDT.S94710
                4789844
                27022242
                fcf89ea0-514e-44d0-ab6e-cd225450b27e
                © 2016 Czarniak et al. This work is published and licensed by Dove Medical Press Limited

                The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.

                History
                Categories
                Original Research

                Pharmacology & Pharmaceutical medicine
                lincomycin,stability,ph,intravenous fluids,iv additives
                Pharmacology & Pharmaceutical medicine
                lincomycin, stability, ph, intravenous fluids, iv additives

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