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Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
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Rate-programmed drug delivery systems (DDS) are designed to release drugs at specific, controlled rates to maintain consistent therapeutic levels. These systems are categorized based on their release mechanisms, including dissolution-controlled DDS, diffusion-controlled DDS, and combined dissolution-diffusion-controlled DDS.In dissolution-controlled DDS, the release rate depends on the slow dissolution of the drug itself or the surrounding matrix. Drugs with inherently slow dissolution rates,...
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Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also...
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Updated: May 5, 2026

Cell Squeezing as a Robust, Microfluidic Intracellular Delivery Platform
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Acoustic Controllable Spatiotemporal Cell Micro-oscillation for Noninvasive Intracellular Drug Delivery.

Xiaoqi Gao1,2,3, Dayang Li1, Shukun Zhao2,3

  • 1Department of Electronic Engineering, School of Electronic Science and Engineering, Xiamen University, Xiamen 361012, P. R. China.

Analytical Chemistry
|September 6, 2024
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Summary
This summary is machine-generated.

Acoustic waves precisely control cell oscillations, enhancing drug delivery efficiency and cell membrane permeability. This gentle method significantly increases intracellular drug concentration without compromising cell viability.

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Area of Science:

  • Biotechnology
  • Cellular Mechanics
  • Nanomedicine

Background:

  • Efficient intracellular cargo delivery is vital for drug evaluation, nanomedicine, and gene therapy.
  • Current methods often face challenges in balancing high delivery efficiency with cell viability.

Purpose of the Study:

  • To develop an acoustic-mediated mechanism for precise intracellular drug delivery.
  • To enhance cell membrane permeability using controlled cell oscillations.

Main Methods:

  • Utilized phase shifting keying-based spatiotemporal acoustic tweezers to create controllable oscillating cell arrays.
  • Applied oscillating radiation force and fluid shear stress to disturb cell membrane mobility and enhance permeability.
  • Tunable parameters included oscillation frequency, direction, amplitude, and speed.

Main Results:

  • Achieved active delivery of doxorubicin into cells, resulting in an intracellular concentration over 8 times higher than controls.
  • Demonstrated excellent biocompatibility with no significant compromise in cell activity.
  • Showcased tunable cell oscillation from 10⁻² to 10² Hz.

Conclusions:

  • The proposed
  • dancing acoustic waves
  • scheme offers a flexible, gentle, and high-throughput strategy for intracellular cargo delivery.
  • This method advances cell manipulation in spatial and temporal domains, benefiting nanobiological research and medical treatments.