Abstract

Delivery of therapeutic moieties using water soluble Carbon dots (C-dots) have been pivotal to control the release of the drugs under physiological condition due to their high biocompatibility. Controlled Dopamine hydrochloride (DA), a potential neurotransmitter using C-dots as carriers is studied in the present work, in order to highlight its potential to deliver drugs related with neurological disorders such as Alzheimer's and Parkinson's disease. The tenure of the DA release under the considered environment at pH 7.4 was extended to 60 h after conjugation to C-dots, in comparison to bare DA under the same environment. The DA release was as per Hixson-Crowell model. In order to understand the impact of the C-dots-DA conjugate under physiological conditions, Nero 2A cells were taken under consideration. The conjugate was found to have least impact as far as the toxicity of the nanoparticles is concerned. Microtomy of tissue section of vital organs was also performed to see the internal effect of conjugate drug. No inimical effect of the conjugate was found on internal organs of experimental models during histological studies. Less toxicity was found on Neuro 2A cells by C-dots-DA conjugate as compared to alone DA. Body weight of mice was also taken into consideration after injecting 20 µg mL−1 of C-dots and C-dots-DA, we did not found any change in their body weight till 45 days of observation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.