JPTRM Vol. 2 No. 2 (November 2014)

Permanent URI for this collection

https://demodspace.chitkara.edu.in/handle/123456789/128

Browse

Browsing JPTRM Vol. 2 No. 2 (November 2014) by Subject "Chitosan"

Now showing 1 - 2 of 2
  • No Thumbnail Available
    Item
    Development And Characterization of Inhaled Chitosan Nanoparticles Loaded with Isoniazid
    (Chitkara University Publications, 2014-11-30) Junise V; R Saraswathi
    The objective of our study is to load first line anti-tubercular drug, Isoniazid in chitosan Nanoparticles in order to enhance bioavailability and to reduce dose frequency. The chitosan nanoparticles containing the drug Isoniazid were prepared by the method of spontaneous emulsification. Chitosan gel containing drug is cross linked with Glutaraldehyde and nanoparticle suspension obtained was centrifuged at 5000 rpm. It was then evaluated for Drug loading, swelling index, Mucoadhesive force, Zeta potential, DLS studies, DSC studies, SEM studies, In vitro Drug release, Pharmacokinetic Studies and Stability studies.Formulation 1(F1) shows maximum Drug Loading, Swelling index and mucoadhesive force. The positive zeta value was obtained for all formulations due to positive charge of polymer used in preparation of dispersion. The DLS plot of Formulations shows that Average particle diameter are in the range of 661.8-823.8nm. The SEM study revealed that the micrographs of cross linked chitosan nanoparticles have smooth surface. The thermogram of the formulations showed the shifting of endotherm. This indicates the possible change in the release kinetics and bioavailability of the drug. In vitro drug releases was found to be maximum for formulation F6. Pharmacokinetic evaluation shows all the formulation shows first order rate release profile and release mechanism from nanoparticles is diffusion controlled. Stability studies indicated that the developed chitosan nanoparticles are physically and chemically stable and retain their pharmaceutical properties at various environmental conditions over a period of 3 months.
  • No Thumbnail Available
    Item
    Preparation and Evaluation of Chitosan and PLGA Based Implants for the Delivery of Cefotaxime
    (Chitkara University Publications, 2014-11-30) Pankaj Gahiye; Sanjay Bajaj
    The poor bioavailability of cefotaxime and limitation of conventional system limits the delivery of antibacterial drug cefotaxime for bone infection treatment. In the current study in situ chitosan implant containing cefotaxime was developed. Injectable implantable drug delivery system containing Cefotaxime was prepared by physically mixing β-glycerophosphate with chitosan in different concentrations. The objective of this study was to standardize the concentrations of the ingredients so as to develop formulation that remains liquid when stored at 4ºC but forms a gel, in minimum time, when injected or when its temperature is raised to 37oC. Injectable in-situ implant before injection was clear and transparent. Gelation temperature significantly increase from 32.6°C ±0.1 to 48.43°C ±0.1 of all formulation. Percentage drug content of all formulation were found in the range of 82.42±1.93 to 99.43±0.55. The syringeability of the final solutions greatly decreased with the increase of chitosan concentration. The release pattern for all formulations was biphasic, comprising an initial burst effect followed by an almost sustained continuous phase. After an initial burst release, the drug entrapped into the chitosan/Gp gel was released slowly. Local delivery of chemotherapeutic agent by controlled- release polymers is a new strategy with the potential to maximize the antibacterial effect of a drug to treat bone infection. The system formulated with cefotaxime was found to be stable and the release profiles of a formulation with chitosan and beta-GP showed almost Higuchi equation release kinetics. The drug release of chitosan imlant containing cefotaxime was found to be more as compare to PLGA implant.