# Polysorbate-Based Carriers Encapsulating Oxygen-Deficient Nanoparticles for Targeted and Effective Chemo-Sonodynamic Therapy of Glioblastoma

**Authors:** Hyeon Ju Kang, Quan Truong Hoang, Nguyen Cao Nguyen, Binh Thi Thanh Pham, Thuy Giang Nguyen Cao, Vasanthan Ravichandran, Min Suk Shim

PMC · DOI: 10.3390/ijms262010235 · International Journal of Molecular Sciences · 2025-10-21

## TL;DR

Researchers developed a targeted therapy for glioblastoma using nanocarriers that cross the blood-brain barrier and combine chemotherapy with sonodynamic treatment.

## Contribution

FA-conjugated polysorbate nanocarriers encapsulating DOX and MnWOx for BBB-crossing chemo-sonodynamic therapy of GBM.

## Key findings

- FA-T-DOX@MnWOx nanocarriers enhanced DOX uptake in U87MG glioblastoma cells.
- MnWOx nanoparticles in the carriers triggered ROS generation and apoptosis under ultrasound.
- The nanocarriers effectively crossed an in vitro blood-brain barrier model.

## Abstract

Glioblastoma multiforme (GBM) is the most aggressive brain tumor with a high recurrence rate and mortality. A major obstacle to the effective treatment of GBM is the blood–brain barrier (BBB), which hinders the transfer of therapeutic cargo to the tumor lesion. Polysorbate-coated drug carriers are known to efficiently cross the BBB via apolipoprotein E (ApoE)-mediated transcytosis. In this study, we developed cancer-targeted nanocarriers using folic acid (FA)-conjugated polysorbate (Tween 80, T80) for safe and efficient chemo-sonodynamic combination therapy against GBM. T80-based nanocarriers effectively co-encapsulated doxorubicin (DOX, chemotherapeutic agent) and oxygen-deficient MnWOx nanoparticles (sonosensitizer). FA-conjugated T80 nanocarriers encapsulating DOX and MnWOx (FA-T-DOX@MnWOx) boosted the cellular uptake of DOX in human glioblastoma U87MG cells. The efficient ability of the T80-based drug carriers to cross the BBB was demonstrated using an in vitro transwell BBB model. In addition, sonosensitizer MnWOx nanoparticles in the T80-based carriers triggered GSH depletion, synergistically enhancing intracellular reactive oxygen species (ROS) generation in U87MG cells upon US irradiation. As a result, FA-T-DOX@MnWOx combined with US triggered significant apoptosis in U87MG cells. This study demonstrated that FA-conjugated, MnWOx-loaded, T80-based nanocarriers capable of crossing the BBB hold significant potential for treating GBM through a combined chemo-sonodynamic therapy.

## Linked entities

- **Proteins:** APOE (apolipoprotein E)
- **Chemicals:** doxorubicin (PubChem CID 31703), folic acid (PubChem CID 135398658), Tween 80 (PubChem CID 443315)
- **Diseases:** Glioblastoma multiforme (MONDO:0018177)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}
- **Diseases:** cancer (MESH:D009369), GBM (MESH:D005909), brain tumor (MESH:D001932)
- **Chemicals:** Polysorbate (MESH:D011136), GSH (MESH:D005978), Oxygen (MESH:D010100), DOX (MESH:D004317), ROS (MESH:D017382), FA (MESH:D005492), DOX@MnWOx (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** U87MG — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_0022)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12564566/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12564566/full.md

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Source: https://tomesphere.com/paper/PMC12564566