Salah M Tawfik, Mirkomil Sharipov, Bui The Huy, Zayakhuu Gerelkhuu, Dana Biechele-Speziale and Yong-Ill Lee
Changwon National University, Republic of Korea
Egyptian Petroleum Research Institute, Egypt
Western Kentucky University, USA
Posters & Accepted Abstracts: J Nanomed Nanotechnol
A novel nano-carrier with great biocompatibility, imaging functionality and drug delivery ability has been developed. In this work, the carrier poly (ethylene glycol) bis (amine)-modified alginate (Al-NH-PEG-NH2) with folate (FA) as the targeting molecule (Al-NH-PEG-NH-FA) were synthesized to act as functionalizing agents for UCNPs. The synthesized polymer enhanced the stability, biocompatibility and up-conversion luminescent intensity (20-fold) of the UCNPs compared to bare UCNPs. The UCNP-Al-NH-PEG-NH-FA nano-carrier enabled the specific targeting of folate receptor-positive KB cells, as confirmed via in vitro near infrared (NIR) imaging. The anticancer drug doxorubicin (DOX) was loaded onto the nano-carrier with high drug loading efficacy (81.2%) then the pH-responsive drug releasing ability was measured. The release of DOX from the nano-carrier was pH dependent and the release rate was much faster at a lower pH (pH=5) than at a higher pH (pH=7.2). The in vitro evaluation of KB cells demonstrated that the DOX-loaded UCNP-Al-NH-PEG-NH-FA provided a sustained intracellular DOX release and a prolonged DOX accumulation in the nucleus, resulting in a prolonged therapeutic efficacy. Additionally, the DOX-loaded UCNP-Al-NH-PEG-NH-FA showed higher cytotoxicity towards the KB cells than free DOX. Thus, the biocompatible nonionic alginate-functionalized UCNPs hold substantial potential to be further developed as effective NIR imaging agents and drug-delivery carriers. salahtwfk85@yahoo.com