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Preparation and characterization of hyperbranched polyester conjugate of ciprofloxacin and its in vitro drug release studies

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Abstract

Hyperbranched polyester (HBP) based on the 3,5-dihydroxy benzoic acid was prepared by the self-poly condensation under standard trans-esterification conditions. The polyester possesses excellent solubility in common organic solvents. Molecular weight and intrinsic viscosity was determined by viscosity measurements. HBP has potential to act as efficient drug carrier systems. Using, ciprofloxacin hydrochloride drug as a model drug, studied the interaction between the drug and hyperbranched polyester with OH functionality. Analysis of the drug release was done by in vitro dissolution apparatus at pH 7.4 (phosphate buffer) media to understand the nature of transport of drug containing solution through the polymeric material. The results demonstrated that the HBP-drug was gradually release (10.4 %) the drug with phosphate buffer medium at 35 °C over a period of 24 h.

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Acknowledgments

This article dose not contain any studies with human and animal subjects performed by any of the authors. And all authors (S. Karpagam and M. Venkateswaran) declare that they have no conflict of interest. We thank VIT University for providing laboratory facilities, VIT-TBI and SAIF-IIT for recording spectral data.

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Correspondence to S. Karpagam.

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Karpagam, S., Venkateswaran, M. Preparation and characterization of hyperbranched polyester conjugate of ciprofloxacin and its in vitro drug release studies. Journal of Pharmaceutical Investigation 44, 1–7 (2014). https://doi.org/10.1007/s40005-013-0086-z

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  • DOI: https://doi.org/10.1007/s40005-013-0086-z

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