Targeted Nanoparticles Harboring Jasmine-Oil-Entrapped Paclitaxel for Elimination of Lung Cancer Cells

Shira Engelberg1, Yuexi Lin1, Yehuda G Assaraf2

  • 1The Laboratory of Biopolymers for Food and Health, Department of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

Insights

Jasmine oil enhances paclitaxel delivery in nanoparticles for non-small cell lung cancer treatment, improving drug loading and potency. This targeted approach offers a promising strategy for chemotherapy.

Area of Science:

  • Nanotechnology
  • Oncology
  • Drug Delivery

Background:

  • Targeted drug delivery systems aim to improve chemotherapy efficacy by concentrating drugs in tumor cells.
  • Current systems face challenges with low drug encapsulation efficiency, capacity, and premature release.
  • Non-small cell lung cancer (NSCLC) remains a significant therapeutic challenge requiring innovative treatment strategies.

Purpose of the Study:

  • To develop S15-aptamer (APT)-decorated PEG-PCL nanoparticles co-encapsulating paclitaxel (PTX) and Jasmine oil (JO) for targeted NSCLC therapy.
  • To evaluate the impact of JO on PTX encapsulation efficiency, capacity, and release kinetics.
  • To assess the synergistic cytotoxic effect of co-encapsulated PTX and JO on NSCLC cells.

Main Methods:

  • Co-encapsulation of PTX and JO within PEG-PCL nanoparticles.
  • Decoration of nanoparticles with S15-aptamer for targeted delivery to NSCLC cells.
  • Characterization of nanoparticle size, drug encapsulation efficiency (EE), encapsulation capacity (EC), and in vitro drug release.
  • Assessment of PTX cytotoxicity against A549 NSCLC cells and comparison with free drug and nanoparticles without JO.

Main Results:

  • Jasmine oil significantly enhanced PTX encapsulation efficiency from 23% to 87.8% and capacity from 35 ± 6 to 74 ± 8 µg/mg.
  • JO increased the residual PTX amount after 69 h from 18.3% to 65%, indicating reduced premature release.
  • Co-encapsulation with JO resulted in a 20-fold lower IC50 for PTX and a 6-fold more potent cell-killing effect against A549 cells compared to PTX without JO.

Conclusions:

  • Jasmine oil acts as an effective "adhesive" core, improving PTX loading and stability in targeted nanoparticles.
  • The synergistic effect of JO significantly enhances the anti-cancer activity of PTX-loaded nanoparticles against NSCLC.
  • This co-delivery strategy holds potential for improving hydrophobic chemotherapeutic efficacy in targeted cancer therapy.