# A high-efficiency automatic pressure-relief drug transfer device for anticancer medications with superior closed performance

**Authors:** Liming Xie, Guanfeng Chen, Qianqian Ouyang, Weiyan Quan, Xiaoming Xie, Xiaoling Chen, Lefan Li, Sidong Li, Rizhi Chen, Rongqiong Luo, Zhiqing Qiu

PMC · DOI: 10.3389/fphar.2025.1579771 · Frontiers in Pharmacology · 2025-04-25

## TL;DR

A new drug transfer device reduces exposure risks for healthcare workers by preventing leakage during handling of hazardous medications.

## Contribution

A novel closed-system drug-transfer device with automatic pressure relief that significantly reduces drug leakage during transfers.

## Key findings

- CSTD(JLY) significantly reduces drug leakage compared to traditional syringes.
- The device's automatic pressure-relief structure decreases resistance during drug transfer.
- The device improves safety for healthcare workers and patients by minimizing exposure risks.

## Abstract

Preventing exposure to hazardous drugs is crucial for healthcare workers to avoid health risks. To mitigate healthcare workers’ risks when handling hazardous drugs, we developed a novel closed-system drug-transfer device (CSTD) called CSTD(JLY). This CSTD has an automatic pressure-relief structure. Hence, it can significantly decrease the resistance in the push/pull of a piston rod if an operator transfers drugs, thereby reducing the burden on the hands of the operator during drug transfer.

We investigated the closed performance of the novel CSTD (JLY) by comparing it with the performance of a syringe. We selected a simulation drug (fluorescein sodium), commonly used drugs (lansoprazole, nimodipine, and tropisetron), and a commonly used anti-cancer agent (cyclophosphamide) to conduct exposure evaluation.

Compared with a syringe, CSTD(JLY) could reduce drug leakage significantly. Our novel CSTD with an automatic pressure-relief structure had superior closed performance. CSTD(JLY) could solve the problem of liquid-drug leakage during drug transfer.

This feature could reduce the exposure risk healthcare workers and patients.

## Linked entities

- **Chemicals:** fluorescein sodium (PubChem CID 10608), lansoprazole (PubChem CID 3883), nimodipine (PubChem CID 4497), tropisetron (PubChem CID 656665), cyclophosphamide (PubChem CID 2907)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), anti (MESH:D006679)
- **Chemicals:** fluorescein sodium (MESH:D019793), tropisetron (MESH:D000077526), nimodipine (MESH:D009553), cyclophosphamide (MESH:D003520), lansoprazole (MESH:D064747)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12061688/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12061688/full.md

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Source: https://tomesphere.com/paper/PMC12061688