# Acriflavine-empowered IR780-PTX albumin nanoparticles for reinforced synergistic photochemotherapy

**Authors:** Dazhao Li, Tong Wang, Hongchao Liu, Yao Yao, Taiyuan Lu, Rong Wang, Xinyi Jiang, Xiaoyang Zhang, Minjie Sun, Ya Peng, Yilin Yang, Naiyuan Shao, Dawei Ding, Feng Zhi

PMC · DOI: 10.1007/s44307-026-00097-9 · Advanced Biotechnology · 2026-03-11

## TL;DR

Researchers developed a new treatment combining chemotherapy and phototherapy to overcome challenges in treating glioma tumors.

## Contribution

A novel combination of IR780-PTX nanoparticles and acriflavine hydrogels is introduced to enhance photochemotherapy in hypoxic tumors.

## Key findings

- The IR780-PTX nanoparticles and ACF hydrogels work together to provide an extraordinary antitumor effect.
- ACF suppresses HIF-1 activity and HSP70 upregulation, improving phototherapy efficacy in hypoxic conditions.
- This approach shows promise for treating tumors with severe hypoxia or therapy-induced resistance.

## Abstract

Traditional chemotherapy and radiotherapy for glioma are challenging due to the hypoxia in tumor microenvironment and the inability of chemotherapeutic agents to enter into tumor cells. Phototherapy is a novel therapeutic approach against various tumors in recent years. When combined with chemotherapy, the antitumor efficacy of phototherapy is superior than each alone. However, the combination of chemotherapy and phototherapy is still hampered by the hypoxic tumor microenvironment which upregulates the expression of hypoxia-inducible factor 1 (HIF-1) and its downstream pathways, as well as the thermoresistance caused by the overexpression of heat shock proteins (HSPs). To solve this, the biocompatible albumin-based nanoparticles (NPs) are developed to co-deliver IR780 iodine (IR780) and paclitaxel (PTX) simultaneously at an optimized ratio (IR780-PTX NPs) for synergistic photochemotherapy. Moreover, acriflavine (ACF), a chemical inhibitor of HIF-1, is formulated into intratumorally formed hydrogels to reinforce synergistic photochemotherapy. The continuously released ACF from hydrogel not only relieves the impact of photodynamic therapy-exacerbated tumor hypoxia by suppressing HIF-1 activity, but also efficiently attenuates HSP70 upregulation. The collaboration between IR780-PTX NPs and ACF hydrogels leads to an extraordinary antitumor effect in vitro and in vivo. The reinforced synergistic photochemotherapy via a single molecule by overcoming HIF-1 activity and HSP overexpression provides an effective therapeutic example to treat tumors, especially in those undergone severe hypoxia and/or therapy-induced thermoresistance.

The online version contains supplementary material available at 10.1007/s44307-026-00097-9.

## Linked entities

- **Proteins:** HIF1A (hypoxia inducible factor 1 subunit alpha), HSPA1A (heat shock protein family A (Hsp70) member 1A)
- **Chemicals:** acriflavine (PubChem CID 443101), paclitaxel (PubChem CID 36314)
- **Diseases:** glioma (MONDO:0021042)

## Full-text entities

- **Genes:** HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}, HSP90B2P (heat shock protein 90 beta family member 2, pseudogene) [NCBI Gene 7190] {aka GRP94P1, GRP94b, HSP, HSPCP2, TRA1P1, TRAP1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}
- **Diseases:** tumor (MESH:D009369), glioma (MESH:D005910), hypoxia (MESH:D000860), hypoxic (MESH:D002534)
- **Chemicals:** PTX (MESH:D017239), ACF (MESH:D000167), IR780 (MESH:C548458), IR780 iodine (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979732/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979732/full.md

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Source: https://tomesphere.com/paper/PMC12979732