Affiliations 

  • 1 Department of Veterinary Pharmacology and Toxicology, Veterinary College, Hebbal, Bangalore, Karnataka, India
  • 2 Nano Research for Advanced Materials and Technologies,(1) Bangalore, Karnataka, India; Department of Biotechnology, Garden City College, Bangalore, Karnataka, India; Mazumdar Shaw Translational Research Center & Narayana Hrudayalaya Multi Specialty Hospital, Bangalore, Karnataka, India; Sri Vishnu College of Pharmacy, West Godavari District, Bhimavaram, Andhra Pradesh, India
  • 3 Faculty of Pharmaceutical sciences, Asian Metropolitan University, Batu-9, Kualalumpur, Selangor 43200, Malaysia. Electronic address: gunnaeswara79@gmail.com
  • 4 Department of Biotechnology, Garden City College, Bangalore, Karnataka, India
  • 5 Mazumdar Shaw Translational Research Center & Narayana Hrudayalaya Multi Specialty Hospital, Bangalore, Karnataka, India
  • 6 Sri Vishnu College of Pharmacy, West Godavari District, Bhimavaram, Andhra Pradesh, India
Int J Pharm, 2014 Aug 25;471(1-2):146-52.
PMID: 24858388 DOI: 10.1016/j.ijpharm.2014.05.033

Abstract

Enrofloxacin is a fluoroquinolone derivative used for treating urinary tract, respiratory and skin infections in animals. However, low solubility and low bioavailability prevented it from using on humans. Polyvinylpyrrolidone (PVP) is an inert, non toxic polymer with excellent hydrophilic properties, besides it can enhance bioavailability by forming drug polymer conjugates. With the aim of increasing solubility and bioavailability, enrofloxacin thin films were prepared using PVP as a polymer matrix. The obtained oral thin films exhibited excellent uniformity and mechanical properties. Swelling properties of the oral thin films revealed that the water uptake was enhanced by 21%. The surface pH has been found to be 6.8±0.1 indicating that these films will not cause any irritation to oral mucosa. FTIR data of the oral thin films indicated physical interaction between drug and polymer. SEM analysis revealed uniform distribution of drug in polymer matrix. In vitro drug release profiles showed enhanced release profiles (which are also pH dependant) for thin films compared to pure drug. Antibacterial activity was found to be dose dependent and maximum susceptibility was found on Klebsiella pneumonia making this preparation more suitable for respiratory infections.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.