Skip to main content
Log in

Oleanolicacid-Chitosan Nanocomplex Induced Apoptotic Cell Death Through Mitochondrial Dysfunction in Human Lung Carcinoma: An Improved Synergetic Drug System for Cancer Therapy

  • Original Paper
  • Published:
Journal of Cluster Science Aims and scope Submit manuscript

Abstract

Lung carcinoma is a forceful type of malignancy, having great elevated pace of morbidity and mortality with limited therapeutic options. The goal of current examination was to reveal the anticancer potential embedded in the oleanolic acid conjugated chitosan nanocomplex (OAC) in Human lung cancer cells (A-549). The OAC complex was characterized with DLS, Zeta potential, FTIR and SEM analysis. We found that the cytotoxic efficacy of OAC in Human lung cancer cells (A549) was dose dependent and also shows insignificant cytotoxicity towards to Human normal lung epithelial normal cells IMR-90. The influence of OAC nanocomplex on cell cycle phase distribution and also the mitochondrial membrane potential was assessed using flowcytometry. The results revealed that oleanolic acid nanocomplex system induced apoptotic cell death in a dose dependent manner. Subsequently the acridine orange and ethidium bromide staining (AO/EtBr) treatment was done with different concentrations of OAC nanocomplex had initiated a characteristic morphological alterations associated with apoptosis. The present findings concluded that OAC nanocomplex treatment brought about the loss in integrity of mitochondrial membrane potential, which occurred in treated human lung cancer cells. Thus the oleanolic acid nanocomplex could be utilized as a therapeutic mediator in the treatment of cancers in humans.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10

Similar content being viewed by others

References

  1. P. Boyle and B. Levin, Cancer Control, 2008, https://doi.org/10.1016/j.cma.2010.02.010.

    Article  Google Scholar 

  2. R. Allison, K. Moghissi, G. Downie and K. Dixon, Photodiagnosis and Photodynamic Therapy, 2011, 8, 231–239.

    Article  Google Scholar 

  3. W. C. Huang, K. T. Kuo, B. O. Adebayo, C. H. Wang, Y. J. Chen, K. Jin, T. H. Tsai and C. T. Yeh, Journal of Nutritional Biochemistry, 2018, 54, 140–150.

    Article  CAS  Google Scholar 

  4. S. Y. Qin, A. Q. Zhang, S. X. Cheng, L. Rong and X. Z. Zhang, Biomaterials, 2017, 112, 234–247.

    Article  CAS  Google Scholar 

  5. M. Sharma, R. Sharma, D. K. Jain and A. Saraf, International Journal of Biological Macromolecules, 2019, 135, 246–260.

    Article  CAS  Google Scholar 

  6. S. Natesan, C. Ponnusamy, A. Sugumaran, S. Chelladurai, S. Shanmugam Palaniappan and R. Palanichamy, International Journal of Biological Macromolecules, 2017, 104, 1853–1859.

    Article  CAS  Google Scholar 

  7. P. Pandey, K. Dua and H. Dureja, International Journal of Biological Macromolecules, 2019, 139, 1304–1316.

    Article  CAS  Google Scholar 

  8. J. Zhang, W. Xia, P. Liu, Q. Cheng, T. Tahirou, W. Gu and B. Li, Marine drugs, 2010, 8, 1962–87.

    Article  CAS  Google Scholar 

  9. B. Ates, A. Ulu, S. Köytepe, S. A. Ali Noma, V. S. Kolat and T. Izgi, RSC Advances, 2018, 8, 36063–36075.

    Article  CAS  Google Scholar 

  10. Z. B. Wang, P. Shan, S. Z. Li, Y. Zhou, X. Deng, J. L. Li, Y. Zhang, J. S. Gao and J. Xu, RSC Advances, 2016, 6, 96785–96797.

    Article  CAS  Google Scholar 

  11. M. Omidi, A. Yadegari and L. Tayebi, RSC Advances, 2017, 7, 10638–10649.

    Article  CAS  Google Scholar 

  12. J. Y. Yhee, S. Jeon, H. Y. Yoon, M. K. Shim, H. Ko, J. Min, J. H. Na, H. Chang, H. Han, J. H. Kim, M. Suh, H. Lee, J. H. Park, K. Kim and I. C. Kwon, Journal of Controlled Release, 2017, 267, 223–231.

    Article  CAS  Google Scholar 

  13. E. O. Fukushima, H. Seki, K. Ohyama, E. Ono, N. Umemoto, M. Mizutani, K. Saito and T. Muranaka, Plant and Cell Physiology, 2011, 52, 2050–2061.

    Article  CAS  Google Scholar 

  14. L. Jie, Journal of Ethnopharmacology, 1995, 49, 57–68.

    Article  Google Scholar 

  15. J. P. Fan, T. Kong, L. Zhang, S. Tong, Z. Y. Tian, Y. H. Duan and X. H. Zhang, Journal of Chemical and Engineering Data, 2011, 56, 2723–2725.

    Article  CAS  Google Scholar 

  16. L. Liu and X. Wang, Journal of Chemical and Engineering Data, 2007, 52, 2527–2528.

    Article  CAS  Google Scholar 

  17. J. A. Jesus, J. H. G. Lago, M. D. Laurenti, E. S. Yamamoto and L. F. D. Passero, Evidence-based Complementary and Alternative Medicine, 2015.

  18. X. Wang, X. long Ye, R. Liu, H. L. Chen, H. Bai, X. Liang, X. Di Zhang, Z. Wang, W. li Li and C. X. Hai, Chemico-Biological Interactions, 2010, https://doi.org/10.1016/j.cbi.2010.01.034.

  19. X. Wang, R. Liu, W. Zhang, X. Zhang, N. Liao, Z. Wang, W. Li, X. Qin and C. Hai, Molecular and Cellular Endocrinology, 2013, 376, 70–80.

    Article  CAS  Google Scholar 

  20. S. R. Yoo, S. J. Jeong, N. R. Lee, H. K. Shin and C. S. Seo, Pharmacognosy Magazine, 2017, 13, 339–344.

    Article  CAS  Google Scholar 

  21. H. Zhao, M. Zhou, L. Duan, W. Wang, J. Zhang, D. Wang and X. Liang, Molecules, 2013, 18, 3615–3629.

    Article  CAS  Google Scholar 

  22. Y. Y. Zhu, H. Y. Huang and Y. L. Wu, Molecular Medicine Reports, 2015, 12, 5012–5018.

    Article  CAS  Google Scholar 

  23. M. K. Shanmugam, A. H. Nguyen, A. P. Kumar, B. K. H. Tan and G. Sethi, Cancer Letters, 2012, 320, 158–170.

    Article  CAS  Google Scholar 

  24. J. Wei, M. Liu, H. Liu, H. Wang, F. Wang, Y. Zhang, L. Han and X. Lin, Journal of Applied Toxicology, 2013, 33, 756–765.

    Article  CAS  Google Scholar 

  25. X. Wang, H. Bai, X. Zhang, J. Liu, P. Cao, N. Liao, W. Zhang, Z. Wang and C. Hai, Carcinogenesis, 2013, 34, 1323–1330.

    Article  CAS  Google Scholar 

  26. Y. S. Wang, G. L. Li, S. Bin Zhu, F. C. Jing, R. D. Liu, S. S. Li, J. He and J. Du Lei, Chinese Journal of Polymer Science (English Edition), 2020, 38, 819–829.

  27. M. Hadidi, S. Pouramin, F. Adinepour, S. Haghani and S. M. Jafari, Carbohydrate Polymers, 2020, https://doi.org/10.1016/j.carbpol.2020.116075.

    Article  PubMed  Google Scholar 

  28. Y. Bao, S. Zhang, Z. Chen, A. T. Chen, J. Ma, G. Deng, W. Xu, J. Zhou, Z. Q. Yu, G. Yao and J. Chen, Molecular Pharmaceutics, 2020, 17, 1343–1351.

    Article  CAS  Google Scholar 

  29. C. Chang, L. Zhang, Y. Miao, B. Fang and Z. Yang, Journal of Cluster Science, 2020, https://doi.org/10.1007/s10876-020-01792-w.

    Article  Google Scholar 

  30. K. Saravanakumar, A. Sathiyaseelan, A. V. A. Mariadoss, E. Jeevithan, X. Hu, S. Shin and M. H. Wang, Carbohydrate Polymers, 2020, https://doi.org/10.1016/j.carbpol.2020.116407.

    Article  PubMed  Google Scholar 

  31. S. Vijayan, K. Divya and M. S. Jisha, Applied Nanoscience (Switzerland), 2019, 10, 715–728.

    Article  Google Scholar 

  32. J. Gao, Y. Zhao, C. Wang, H. Ji, J. Yu, C. Liu and A. Liu, International Journal of Biological Macromolecules, 2020, 158, 689–697.

    Article  CAS  Google Scholar 

  33. S. Ramya, S. Thiruvenkataswamy, K. Kavithaa, S. Preethi, H. Winster, V. Balachander, M. Paulpandi and A. Narayanasamy, Journal of Cluster Science, 2020, https://doi.org/10.1007/s10876-020-01789-5.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Adili Salai.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Abulaiti, A., Sun, W., Salai, A. et al. Oleanolicacid-Chitosan Nanocomplex Induced Apoptotic Cell Death Through Mitochondrial Dysfunction in Human Lung Carcinoma: An Improved Synergetic Drug System for Cancer Therapy. J Clust Sci 33, 89–99 (2022). https://doi.org/10.1007/s10876-020-01934-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10876-020-01934-0

Keywords

Navigation