Microneedles: Classification, Fabrication, And Applications

Aug 22, 2026

 

Microneedles (MNs) are microscale needle structures designed for transdermal drug delivery, interstitial fluid sampling, signal detection, biosensing, and other biomedical applications. Benefiting from their painless, minimally invasive, and user-friendly​ nature, MNs have attracted extensive research attention. A typical MN ranges from 25 to 2000 μm in length, with a tip size of 10–20 μm-significantly sharper than conventional hypodermic needles. This geometry enables MNs to easily penetrate the stratum corneum​ (the skin's outermost barrier) and create microchannels, while deliberately avoiding contact with nerve fibers and blood vessels located in the epidermis and dermis.

The concept of MN fabrication was first proposed in 1976​ to overcome the limitations of traditional transdermal drug delivery. Since the 1990s, driven by advances in modern microfabrication technologies, a wide variety of MNs have been successfully developed and widely applied in the biomedical field.

Following our previous discussion on microneedle patches and the latest advances in transdermal delivery, Engineering for Life (EFL) presents this comprehensive classification of MNs based on their structural and functional characteristics, along with representative fabrication methods and case studies.


Five Major Types of Microneedles

(Reference: Advanced Drug Delivery Reviews, 2019 - https://doi.org/10.1016/j.addr.2019.10.004)


1. Solid Microneedles (SMNs)

Solid microneedles are fabricated on a planar substrate, typically arranged in arrays ranging from 5×5 to 20×20, resembling a spiked plate.

Category

Details

Fabrication

Direct cutting from solid materials via laser ablation or mechanical/chemical etching; also produced by master molding and electroplating.

Drug Delivery

SMNs are first inserted into the skin to create micro-pores. After removal, a drug-loaded patch is applied, and the drug diffuses slowly through the residual channels into deeper tissues. Alternatively, SMNs can scratch the skin surface to form linear micro-injuries, facilitating drug diffusion.

Advantages

High mechanical stiffness allows easy and reliable skin penetration.

Disadvantages

Brittleness leads to a risk of needle fracture during transportation, handling, or insertion.

📌 Case Study: Fabrication and characterization of gold-coated solid silicon microneedles with improved biocompatibility- https://doi.org/10.1007/s00170-018-2596-3


2. Hollow Microneedles (HMNs)

Hollow microneedles are essentially conventional hypodermic needles scaled down to micrometer dimensions. They can be configured as a single needle or an array mounted on a base, which may be connected to an external device providing a driving force to inject liquid or drugs through the internal lumen.

Category

Details

Fabrication

Thermoplastic extrusion-stretching processes, among others.

Drug Delivery

Similar to subcutaneous injection-liquid drugs are driven by pressure through the HMN lumen into the skin.

Advantages

Enables precise, on-demand dose control tailored to individual patients.

Disadvantages

Skin tightness may limit the delivery rate and total fluid volume.

📌 Case Study: https://doi.org/10.1063/5.0008983


3. Coated Microneedles (CMNs)

Coated microneedles are fabricated using biodegradable and biocompatible materials, capable of rapidly delivering high-molecular-weight drugs into the skin. Drugs are stored in a solid phase as a coating on the needle surface, which enhances long-term stability.

Category

Details

Fabrication

Dip-coating, roll-coating, layer-by-layer coating, and spray-coating.

Drug Delivery

After insertion, the water-soluble drug coating dissolves from the MN surface into the skin, followed by needle retraction.

Advantages

Cost-effective, simple to operate, and capable of delivering large drug doses.

Disadvantages

Coating may detach during insertion; dissolution kinetics in skin affect drug release but are difficult to control precisely.

📌 Case Study: A novel method for fabrication of coated microneedles with homogeneous and controllable drug dosage for transdermal drug delivery- https://doi.org/10.1007/s13346-022-01123-8


4. Dissolving Microneedles (DMNs)

Dissolving microneedles are fabricated from biocompatible, water-soluble matrix materials, eliminating concerns about needle fracture residue and biocompatibility. Upon insertion, the needle tips dissolve in the interstitial fluid, naturally releasing the encapsulated drug.

Category

Details

Fabrication

Two-step casting, droplet-blowing, centrifugal lithography, photopolymerization, and drawing lithography.

Drug Delivery

Biodegradable polymers and water-soluble sugar-based drugs are encapsulated within the matrix. DMNs fully degrade or dissolve in the skin, achieving complete drug release.

Advantages

Excellent biocompatibility; simplified single-step administration (no patch removal needed); no biohazardous sharp waste.

Disadvantages

Limited drug loading capacity; moderate mechanical strength affecting skin penetration; potential loss of drug bioactivity during fabrication or storage.

📌 Case Study: https://doi.org/10.1016/j.ijpharm.2021.120749


5. Hydrogel-Forming Microneedles (HFMNs)

Hydrogel-forming microneedles are prepared from hydrogel-forming polymeric matrices. Upon insertion, these arrays rapidly absorb interstitial fluid, causing the hydrogel to swell and form continuous, unobstructed conduits​ for sustained drug permeation.

Category

Details

Fabrication

Mold-based methods and Digital Light Processing (DLP) projection lithography.

Drug Delivery

HFMNs swell in situ to create hydrogel conduits that enable controlled drug diffusion into the skin.

Advantages

(a) High drug loading with controllable release profiles; (b) Crosslinked polymer materials avoid needle fracture and associated skin injury; (c) Swellable-but-non-dissolving design enables sustained, predictable drug release.

Disadvantages

Mechanical stiffness remains a challenge due to the inherent flexibility of hydrogel polymers.


Summary Comparison Table

Type

Key Feature

Delivery Mechanism

Main Limitation

Solid (SMN)

High stiffness

Poke & patch

Brittleness / fracture risk

Hollow (HMN)

Internal lumen

Pressure-driven injection

Limited by skin tightness

Coated (CMN)

Drug on surface

Dissolving coating

Uncontrolled dissolution kinetics

Dissolving (DMN)

Fully degradable matrix

In-situ dissolution

Low drug loading, stability concerns

Hydrogel (HFMN)

Swellable polymer

Swelling-created conduits

Insufficient stiffness


Note: This classification and technical summary is compiled by Engineering for Life (EFL). For further resources or collaboration opportunities, please contact EFL directly.