Study2022Open access

Co-delivery of paclitaxel (PTX) and docosahexaenoic acid (DHA) by targeting lipid nanoemulsions for cancer therapy

Li B, Tan T, Chu W, Zhang Y, Ye Y, Wang S, Qin Y, Tang J, Cao X

Drug delivery · 39 citations

How it was studied

Design
In vitro/mechanistic study (classified by our AI screen)
Studied in
People, plus animal or lab work
Main outcome
Clinical events such as disease or death

Who paid for it

Funding
Independent funding
Government
Anhui Province Natural Science Foundation

Based on 1 listed funder(s) and full-text disclosure statement.

Publication

Published
2021-12-29 · Drug Deliv · vol. 29 · issue 1 · pp. 75–88
Publisher
Taylor & Francis
Cited
53 citations · more than 93% of similar papers · 2.8× the field average
Impact
Top 10% most cited in its field
References
54 works
Access
Open access (journal) · CC-BY
Research areas
Cancer, Lipids, and Metabolism · Nanoparticle-Based Drug Delivery · RNA Interference and Gene Delivery
Keywords
Paclitaxel, Docosahexaenoic acid, Nanocarriers, Cytotoxicity, Pharmacology, Drug delivery, Cancer cell, Toxicity, In vivo, Breast cancer, Apoptosis, Cancer, Cancer research, Chemistry, In vitro, Drug, Medicine, Fatty acid, Biology, Polyunsaturated fatty acid, Biochemistry, Internal medicine
MeSH
cell line, tumor, animals, mice, inbred balb c, humans, mice, mice, nude, paclitaxel, folic acid, antineoplastic agents, phytogenic, emulsions, drug carriers, xenograft model antitumor assays, apoptosis, cell survival, dose-response relationship, drug, female, nanoparticles, mcf-7 cells, drug liberation, raw 264.7 cells, tumor-associated macrophages

9 authors

From CN

  • Bo LiAnhui Medical University; State Administration of Traditional Chinese Medicine of the People's Republic of China; First Affiliated Hospital of Anhui Medical University
  • Tingfei TanAnhui Medical University; State Administration of Traditional Chinese Medicine of the People's Republic of China; First Affiliated Hospital of Anhui Medical University
  • Weiwei ChuAnhui Medical University; State Administration of Traditional Chinese Medicine of the People's Republic of China; First Affiliated Hospital of Anhui Medical University
  • Ying ZhangAnhui Medical University; First Affiliated Hospital of Anhui Medical University
  • Yuanzi YeAnhui Medical University; First Affiliated Hospital of Anhui Medical University
  • Shanshan WangAnhui Medical University; State Administration of Traditional Chinese Medicine of the People's Republic of China; First Affiliated Hospital of Anhui Medical University

Abstract

Breast cancer is one of the most common types of cancer in female patients with high morbidity and mortality. Multi-drug chemotherapy has significant advantages in the treatment of malignant tumors, especially in reducing drug toxicity, increasing drug sensitivity and reducing drug resistance. The objective of this research is to fabricate lipid nanoemulsions (LNs) for the co-delivery of PTX and docosahexaenoic acid (DHA) with folic acid (FA) decorating (PTX/DHA-FA-LNs), and investigate the anti-tumor activity of the PTX/DHA-FA-LNs against breast cancer both in vitro and in vivo. PTX/DHA-FA-LNs showed a steady release of PTX and DHA from the drug delivery system (DDS) without any burst effect. Furthermore, the PTX/DHA-FA-LNs exhibited a dose-dependent cytotoxicity and a higher rate of apoptosis as compared with the other groups in MCF-7 cells. The cellular uptake study revealed that this LNs were more readily uptaken by MCF-7 cells and M2 macrophages in vitro. Additionally, the targeted effect of PTX/DHA-FA-LNs was aided by FA receptor-mediated endocytosis, and its cytotoxicity was proportional to the cellular uptake efficiency. The anti-tumor efficiency results showed that PTX/DHA-FA-LNs significant inhibited tumor volume growth, prolonged survival time, and reduced toxicity when compared with the other groups. These results indicated that DHA increases the sensitivity of tumor cells and tumor-associated macrophages (ATM2) to PTX, and synergistic effects of folate modification in breast cancer treatment, thus PTX/DHA-FA-LNs may be a promising nanocarrier for breast cancer treatment.

Abstract via Europe PMC. Copyright remains with the authors or publisher (CC BY).

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