| 英文摘要 |
Microfluidic chip technology has been widely employed in biomedical diagnostics, single-cell analysis, and on-site testing; however, conventional systems typically rely on bulky and expensive external pumps and tubing, which limit portability and deployment in resource-limited settings. Recently, low-vacuum-driven microfluidics has emerged as a promising approach that exploits pre-evacuated chambers or vacuum pouches, as well as the gas solubility and permeability of polydimethylsiloxane (PDMS), to generate a stable and predictable negative pressure as the driving force, thereby enabling power-free or low-power fluidic control. In this study, we first review the fundamental principles of low-vacuum-driven microfluidic systems, including pressure-driven laminar flow, degassing mechanisms in PDMS, and the dynamics of vacuum release, and we compare them with conventional syringe-pump-based and capillary-driven systems. We then analyze representative application examples, such as the vacuum pouch microfluidic system for thin-film micromixers and on-site detection, syringe-assisted vacuum-driven micropumps providing constant flow rates, and transient on-chip vacuum for shear-free mammalian cell loading and patterning. These case studies demonstrate that low-vacuum-driven architectures offer advantages in system simplification, cost reduction, portability, and ease of integration with disposable cartridges, while challenges remain in terms of vacuum retention time, long-term flow stability, and precise quantitative control. Finally, we discuss design guidelines and future perspectives for implementing low-vacuum-driven microfluidic chips in biomedical assays and point-of-care diagnostics, aiming to support subsequent device development and system integration efforts. |