# Microneedle-Based Technologies for Long-Acting Transdermal Drug Delivery in Wearable Devices

**Authors:** Jiaxin Luo, Yinqi Dai, Xin Cheng, Zifeng Wang, Zhigang Zhu

PMC · DOI: 10.3390/s26010239 · Sensors (Basel, Switzerland) · 2025-12-30

## TL;DR

This review explores how microneedle-based systems can deliver drugs through the skin over long periods using wearable devices.

## Contribution

The paper introduces design strategies and materials for sustained drug release using biodegradable polymers and advanced drug carriers in microneedles.

## Key findings

- Biodegradable polymers like PLA, PLGA, and PCL enable prolonged drug release through tunable degradation rates.
- Incorporating liposomes and nanoparticles into microneedles enhances drug-loading capacity and extends release duration.
- Challenges for clinical translation include manufacturing consistency, sterility, and long-term safety validation.

## Abstract

This review systematically outlines recent advances in long-acting microneedle-based transdermal drug delivery systems. It begins by introducing the fundamental principles of microneedles (MNs) as a minimally invasive technology and categorizes them by delivery mechanism into solid, coated, dissolving, hollow, hydrogel-forming, and biodegradable types. The review then discusses the design strategies and material platforms engineered for sustained drug release. A key focus is on biodegradable synthetic polymers, such as polylactic acid (PLA), poly (lactic-co-glycolic acid) (PLGA), and polycaprolactone (PCL), and natural polymers like silk fibroin (SF) and chitosan (CS), which enable prolonged drug release through their tunable degradation rates. Furthermore, it describes the incorporation of advanced drug carriers, including liposomes and polymeric nanoparticles/microparticles, into MNs to further extend release duration and enhance drug-loading capacity. Finally, the major challenges for clinical translation are addressed, including ensuring batch-to-batch consistency in manufacturing, maintaining sterility, and the necessity for more comprehensive validation of long-term in vivo efficacy and safety.

## Linked entities

- **Chemicals:** polylactic acid (PubChem CID 61503), chitosan (PubChem CID 129662530)

## Full-text entities

- **Chemicals:** CS (MESH:D048271), PLGA (MESH:D000077182), PCL (MESH:C016240), PLA (MESH:C033616)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12788315/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12788315/full.md

## References

133 references — full list in the complete paper: https://tomesphere.com/paper/PMC12788315/full.md

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Source: https://tomesphere.com/paper/PMC12788315