146
Views
1
CrossRef citations to date
0
Altmetric
Articles

Development of asolectin-based liposomal formulation for controlled and targeted delivery of erlotinib as a model drug for EGFR monotherapy

, ORCID Icon, , ORCID Icon, &
Pages 386-395 | Received 30 Sep 2021, Accepted 07 Feb 2022, Published online: 28 Feb 2022

References

  • Bruno, R, et al., 2003. Preliminary population pharmacokinetics (P P K) and exposure-safety (E-S) relationships of erlotinib HCI in patients with metastatic breast cancer (MBC). In: Proceedings of the American Society of Clinical Oncology (ASCO '03), vol. 22, p. 205, Chicago, Ill, USA, June 2003.
  • Buck, E., et al., 2006. Inactivation of Akt by the epidermal growth factor receptor inhibitor erlotinib is mediated by HER-3 in pancreatic and colorectal tumor cell lines and contributes to erlotinib sensitivity. Molecular cancer therapeutics, 5 (8), 2051–2059.
  • Chin, T.M., et al., 2008. Reduced erlotinib sensitivity of epidermal growth factor receptor-mutant non-small cell lung cancer following cisplatin exposure: A cell culture model of second-line erlotinib treatment. Clinical cancer research, 14 (21), 6867–6876.
  • Daraee, H., et al., 2016. Application of liposomes in medicine and drug delivery. Artificial cells, nanomedicine, and biotechnology, 44 (1), 381–391.
  • Diep, C.H., et al., 2011. Synergistic effect between erlotinib and MEK inhibitors in KRAS wild-type human pancreatic cancer cells. Clinical cancer research, 17 (9), 2744–2756.
  • Dimov, N., et al., 2017. Formation and purification of tailored liposomes for drug delivery using a module-based micro continuous-flow system. Scientific reports, 7, 120–145.
  • Dwivedi, C., and Verma, S., 2013. Review on preparation and characterization of liposomes with application. Journal of scientific and innovative research and reviews, 2, 2320–4818.
  • Gerlowski, L.E., and Jain, R.K., 1986. Microvascular permeability of normal and neoplastic tissues. Microvascular Research, 31 (3), 288–305.
  • Hao, J., Yang, X., et al., 2016. Paeoniflorin potentiates the inhibitory effects of erlotinib in pancreatic cancer cell lines by reducing ErbB3 phosphorylation. Scientific reports, 6, 1–9.
  • Hua, S., and Wu, S.Y., 2013. The use of lipid-based nanocarriers for targeted pain therapies. Frontiers in pharmacology, 4, 143–147.
  • Khare, V., et al., 2014. Targeted drug delivery systems for pancreatic cancer. Journal of biomedical nanotechnology, 10 (12), 3462–3482.
  • Latha, S.T., Thangadurai, S.A., et al., 2017. Development and validation of RP-HPLC method for the estimation of erlotinib in pharmaceutical formulation. Arabian Journal of Chemistry, 10, S1138–S1144.
  • Le, U.M., Hartman, A., and Pillai, G., 2017. Enhanced selective cellular uptake and cytotoxicity of epidermal growth factor-conjugated liposomes containing curcumin on EGFRoverexpressed pancreatic cancer cells. Journal ofdrug target, 1, 1–8.
  • Long, J., et al., 2011. Overcoming drug resistance in pancreatic cancer. Expert opinion on therapeutic targets, 15 (7), 817–828.
  • Maitra, A., and Hruban, R.H., 2008. Pancreatic cancer. Annual review of pathology, 3, 157–188.
  • Meure, L.A., Foster, N.R., and Dehghani, F., 2008. Conventional and dense gas techniques for the production of liposomes: a review. AAPS Pharmscitech, 9 (3), 798–809.
  • Pathak, S.K., et al., 2012. Effect of cholesterol concentration on size of liposome. IOSR journal of pharmacy and biological sciences, 1 (1), 50–53.
  • Provenzano, P.P., and Hingorani, S.R., 2013. Hyaluronan, fluid pressure, and stromal resistance in pancreas cancer. British journal of cancer, 108 (1), 1–8.
  • Ranson, M., et al., 2010. A Phase I dose-escalation and bioavailability study of oral and intravenous formulations of erlotinib (Tarceva, OSI-774) in patients with advanced solid tumors of epithelial origin. Cancer chemotherapy and pharmacology, 66 (1), 53–58.
  • Saravanan, V.S., and Rao, B.M., 2013. Analytical method development and validation for the determination of erlotinib hydrochloride bulk and in pharmaceutical dosage form. Journal ofdrug delivery and therapy, 3, 50–54.
  • Segaert, S., and Cutsem, E.V., 2005. Clinical signs, pathophysiology and management of skin toxicity during therapy with epidermal growth factor receptor inhibitors. Annals of oncology, 16 (9), 1425–1433. vol.
  • Singh, P.K., et al., 2016. Macrophage-targeted chitosan anchored PLGA nanoparticles bearing doxorubicin and amphotericin B against visceral leishmaniasis. RSC Advances, 6 (75), 71705–71718.
  • Starling, N., Neoptolemos, J., and Cunningham, D., 2006. Role of erlotinib in the management of pancreatic cancer. Therapeutics and clinical risk management, 2 (4), 435–445.
  • Xu, H., et al., 2017. Novel therapeutic modalities and drug delivery – erlotinib liposomes modified with galactosylated lipid: in vitro and in vivo investigations. Artificial Cells, Nanomedicine, and Biotechnology, 1–6. 10.1080/21691401.2017.1396222

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.