Optical Trapping: A Non-Contact Technique for Fragile Microparticle Micromanipulation
29 December 2025
Optical Trapping: A Non-Contact Technique for Fragile Microparticle Micromanipulation
29 December 2025
Written by:
Dr. Muhamad Safuan Mat Yeng
Senior Lecturer
Physics Department,
Faculty of Science and Mathematics,
Universiti Pendidikan Sultan Idris
Dr. Shahrul Kadri Ayop
Associate Professor
Physics Department,
Faculty of Science and Mathematics,
Universiti Pendidikan Sultan Idris
A fragile microparticle, such as a red blood cell, bacteria, ovum, sperm, DNA, or others, can be easily broken down when physically held by tweezers during a specific procedure or application. This fragile microparticle must be carefully handled to be applied for specific uses, such as physical measurement analysis, including elasticity, stiffness, micro rheology, and others [1–3]. To prevent this fragile microparticle from being easily broken down or flawed, a novel micromanipulation method without physical contact was explored using optical tweezers [4 - 5]. Optical tweezers use an intensely focused beam of light to hold and manipulate a fragile microparticle contactlessly, a process called optical trapping [6]. Optical trapping was discovered by Arthur Ashkin in 1990, and he was awarded the Nobel Prize in Physics in 2018 [7]. Optical tweezers work by tightly focusing a laser beam through an objective lens to form a laser spot in the sample [8]. When the objective lens focuses the laser beam, an optical force is generated, trapping the fragile microparticle in the laser spot. Figure 1 shows the optical trapping of a fragile microparticle of Lactobacillus exposed to the optical trap from (a) to (f) viewed from the monitor camera. The single rod-shaped cell is trapped, with its central axis aligned along the beam propagation direction.
Figure 1: (a) (b) and (c); The Lactobacillus is free to move in the water. (d) and (e); The Lactobacillus approaches the optical trap. (f); The Lactobacillus gets trapped in the optical trap .
[The black arrow indicates the Lactobacillus and the red dashed circle indicates the optical trap]
Optical Trapping Process
How do the fragile microparticles get trapped at the laser focus? Figure 2 shows the principle of optical trapping. The optical force due to the laser beam is mainly composed of two components [9]. The first optical force component is the pulling gradient force [10]. The gradient force depends on the intensity gradient of the laser beam used. For instance, if the laser beam has a Gaussian profile, the most intense region will be at the beam centre, which corresponds to the strength of the pulling gradient force. As a result, the gradient force will pull the fragile microparticle toward the centre of the laser spot. The second component of the optical force is the pushing scattering force [10]. The pushing scattering force will push the particle away from the laser spot along the laser beam propagation. In short, the pulling gradient force and the pushing scattering force interact to balance each other so that the particle can be trapped or held at the centre of the laser focus.
Figure 2: The principle of optical trapping.
Optical Trapping Parameter Condition for Stable Trapping
Laser Power
The optical trapping procedure, particularly when handling the fragile microparticle, must consider several parameters to achieve successful, stable optical trapping. Stable and successful optical trapping means that the fragile microparticle being studied can be held and not escape from the laser spot during the monitoring period. The first parameter to consider is the laser power used for optical trapping [11 - 12]. The laser power is directly proportional to the optical force generated to hold the fragile microparticle. This means that using high laser power will produce a strong optical force. Since the optical trapping procedure focuses on holding and controlling the fragile microparticle, higher laser power is not recommended, as it might damage or destroy it. However, if the laser power is too low, the resulting optical force will be weaker, and the fragile microparticle cannot be held or controlled. Hence, it is required to use a laser power within a suitable range for optical trapping of the fragile microparticle. In addition, the wavelength selection for the trapping laser is also crucial in a specific application. For example, an infrared laser is preferable for trapping a biological sample in water, as the heating effect can be suppressed.
Particle Size
The second parameter to consider for the optical trapping of the fragile microparticle is its size [12]. The researcher must consider the size of the fragile microparticle that needs to be held or controlled by the optical tweezers. Since the optical trapping produced a pico-newton force, choosing the correct size for the trap becomes crucial. If the selected size of the fragile microparticle is larger, there is a probability that the process of holding and confining becomes harder as the optical force is weaker. From another perspective, if the selected fragile microparticle size is too small, it is also challenging to hold, as the small fragile microparticle would experience a larger optical force and be pushed away from the laser spot. The specific optical tweezers model, such as OTKB/M from Thorlabs, has a limited resolution of ~500nm, meaning that fragile microparticles smaller than 500nm cannot be observed during optical trapping. Despite this limitation, the use of dye and spectroscopy techniques combined with optical tweezers might help to observe the fragile particle during optical trapping.
As a conclusion, optical trapping of the fragile microparticle is possible when the technical aspects of the optical trapping conditions, such as laser power and size, are considered. Even though the trapping conditions for each fragile microparticle would differ, it is the researcher's skills to determine the appropriate optical trapping conditions. For future work, the researcher might explore the possibility of assisting gamete fertilisation, a comprehensive study of red blood cell deformation, and the manipulation of microorganisms, such as bacterial motion, using optical trapping.
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