1. Academic Validation
  2. Chitosan oligosaccharide decorated liposomes combined with TH302 for photodynamic therapy in triple negative breast cancer

Chitosan oligosaccharide decorated liposomes combined with TH302 for photodynamic therapy in triple negative breast cancer

  • J Nanobiotechnology. 2021 May 19;19(1):147. doi: 10.1186/s12951-021-00891-8.
Yinan Ding 1 Rui Yang 2 Weiping Yu 1 Chunmei Hu 3 Zhiyuan Zhang 4 Dongfang Liu 1 Yanli An 5 Xihui Wang 1 Chen He 1 Peidang Liu 1 Qiusha Tang 6 Daozhen Chen 7
Affiliations

Affiliations

  • 1 Medical School of Southeast University, Nanjing, 210009, China.
  • 2 Research Institute for Reproductive Health and Genetic Diseases, The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, Wuxi, 214002, China.
  • 3 Department of Tuberculosis, The Second Affiliated Hospital of Southeast University (The Second Hospital of Nanjing), Nanjing, 210009, China.
  • 4 Department of Neurosurgery, Nanjing Jinling Hospital, Nanjing University, Nanjing, 210002, China.
  • 5 Affiliated Zhongda Hospital of Southeast University, Nanjing, 210009, China.
  • 6 Medical School of Southeast University, Nanjing, 210009, China. [email protected].
  • 7 Research Institute for Reproductive Health and Genetic Diseases, The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, Wuxi, 214002, China. [email protected].
Abstract

Background: Triple negative breast Cancer (TNBC) is an aggressive tumor with extremely high mortality that results from its lack of effective therapeutic targets. As an adhesion molecule related to tumorigenesis and tumor metastasis, cluster of differentiation-44 (also known as CD44) is overexpressed in TNBC. Moreover, CD44 can be effectively targeted by a specific hyaluronic acid analog, namely, chitosan oligosaccharide (CO). In this study, a CO-coated Liposome was designed, with Photochlor (HPPH) as the 660 nm LIGHT mediated photosensitizer and evofosfamide (also known as TH302) as the hypoxia-activated prodrug. The obtained liposomes can help diagnose TNBC by fluorescence imaging and produce antitumor therapy by synergetic photodynamic therapy (PDT) and chemotherapy.

Results: Compared with the nontargeted liposomes, the targeted liposomes exhibited good biocompatibility and targeting capability in vitro; in vivo, the targeted liposomes exhibited much better fluorescence imaging capability. Additionally, liposomes loaded with HPPH and TH302 showed significantly better antitumor effects than the other monotherapy groups both in vitro and in vivo.

Conclusion: The impressive synergistic antitumor effects, together with the superior fluorescence imaging capability, good biocompatibility and minor side effects confers the liposomes with potential for future translational research in the diagnosis and CD44-overexpressing Cancer therapy, especially TNBC.

Keywords

CD44; Chitosan oligosaccharide; Liposomes; Photodynamic therapy; Triple negative breast cancer.

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