Methods, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Methods, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Sensors and Actuators A Physical, Год журнала: 2024, Номер 376, С. 115625 - 115625
Опубликована: Июнь 24, 2024
The integration of CRISPR technology with microfluidic-based biosensors has greatly expanded its applications in medicine and molecular biology. This combination offers enhanced sensitivity selectivity medical diagnostics. CRISPR-powered microfluidics enables the accurate quantification DNA RNA associated diseases such as cancer, viral infections, bacterial diseases. precise targeting capabilities allow for detection specific genetic sequences, aiding early diagnosis, disease monitoring, treatment assessment. improves specificity by leveraging programmable nature coupling it signal readouts. However, challenges assay optimization, standardization, device fabrication need to be addressed. Additionally, complexity presents potential limitations terms off-target effects unintended modifications. Overall, holds tremendous diagnostics, but further research development are required fully exploit benefits clinical settings.
Язык: Английский
Процитировано
21Theranostics, Год журнала: 2025, Номер 15(8), С. 3275 - 3288
Опубликована: Фев. 18, 2025
Rationale: The ultrasensitive and accurate detection of driver mutations is critical for early cancer screening precision medicine. Current methods face challenges in balancing sensitivity, specificity, speed, which limits their clinical utility. Therefore, a rapid, sensitive, specific method essential detecting cancer-related SNPs. Methods: This study introduces SPEAR (Specific Point mutation Evaluation via CRISPR-Cas Assisted Recognition), novel methodology combining NEAR (Nicking Enzyme Amplification Reaction) isothermal amplification with SNP-specific recognition by Cas12b RNP one-pot configuration to detect single nucleotide polymorphisms (SNPs). leverages the power efficiently amplify target DNA, followed recognition. integrated approach ensures rapid precise system reaction. Results: was applied blood samples mutations, results obtained approximately 30 min. enables gene at single-molecule level it can targets 0.1% ratio despite strong background interference. exhibits single-base resolution allowing multiple SNPs It outperforms first-generation sequencing (FGS) both convenience while remaining compatible next-generation (NGS). Conclusion: offers convenient SNPs, significant potential applications, including real-time molecular diagnostics
Язык: Английский
Процитировано
3ACS Sensors, Год журнала: 2023, Номер 8(12), С. 4420 - 4441
Опубликована: Ноя. 18, 2023
CRISPR/Cas system is becoming an increasingly influential technology that has been repositioned in nucleic acid detection. A preamplification step usually required to improve the sensitivity of CRISPR/Cas-based The striking biological features CRISPR/Cas, including programmability, high and sequence specificity, single-base resolution. More strikingly, target-activated trans-cleavage could act as a biocatalytic signal transductor amplifier, thereby empowering it potentially perform detection without step. reports such work are on rise, which not only scientifically significant but also promising for futuristic end-user applications. This review started with introduction methods acids diagnostics (CRISPR-Dx). Next, we objectively discussed pros cons steps CRISPR-Dx. We then illustrated highlighted recently developed strategies CRISPR/Cas-powered amplification-free can be realized through uses ultralocalized reactors, cascade reactions, ultrasensitive systems, or others. Lastly, challenges perspectives were proposed. It expected this makes researchers better understand current emerging field, provides insight designing novel CRISPR-Dx win practicable use near future.
Язык: Английский
Процитировано
41Lab on a Chip, Год журнала: 2023, Номер 23(5), С. 938 - 963
Опубликована: Янв. 1, 2023
We review recent advances in CRISPR-based nucleic acid detection using microfluidic devices and discuss the capabilities, limitations, potential of this emerging technology.
Язык: Английский
Процитировано
35ACS Sensors, Год журнала: 2023, Номер 8(10), С. 3623 - 3642
Опубликована: Окт. 11, 2023
Over the past few decades, pathogens have posed a threat to human security, and rapid identification of should be one ideal methods prevent major public health security outbreaks. Therefore, there is an urgent need for highly sensitive specific approaches identify quantify pathogens. Clustered Regularly Interspaced Short Palindromic Repeats CRISPR/Cas systems Argonaute (Ago) belong Microbial Defense Systems (MDS). The guided, programmable, targeted activation nucleases by both them leading way new generation detection. We compare these two in terms similarities differences. In addition, we discuss future challenges prospects development biosensors, especially electrochemical biosensors. This review expected afford researchers entering this multidisciplinary field useful guidance provide inspiration more innovative biosensors
Язык: Английский
Процитировано
27Critical Reviews in Food Science and Nutrition, Год журнала: 2023, Номер 64(32), С. 12061 - 12082
Опубликована: Сен. 10, 2023
Food safety problems have become one of the most important public health issues worldwide. Therefore, development rapid, effective and robust detection is great importance. Amongst a range methods, nucleic acid isothermal amplification (NAIA) plays role in food detection. However, widespread application remains limited due to few shortcomings. CRISPR/Cas system has emerged as powerful tool detection, which could be readily integrated with NAIA improve sensitivity, specificity, adaptability versatility dependability. currently there was lack comprehensive summary regarding integration field In this review, recent advances based on CRISPR/Cas-integrated were comprehensively reviewed. To begin with, summarized. Then, types working principles introduced. The applications for mainly introduced objectively discussed. Lastly, current challenges future opportunities proposed. summary, technology expected an approach leading safer more reliable industry.
Язык: Английский
Процитировано
24TrAC Trends in Analytical Chemistry, Год журнала: 2024, Номер 172, С. 117594 - 117594
Опубликована: Фев. 8, 2024
The precision and versatility of CRISPR-based techniques, combined with the advantages nucleic acid-based nanotechnology, hold great promise in transforming landscape molecular diagnostics. While significant progress has been made, current platforms primarly focus on acid detection. To expand applicability fully leverage offered by diagnostics, ongoing efforts explore strategies to develop CRISPR sensors capable detecting a diverse range analytes beyond acids. In addition, challenges still persist adaptation for point-of-care (POC) applications, involving concerns such as portability automation, well complexities associated multiplexing. Here, we provide detailed classification comprehensive discussion facilitating conversion non-nucleic target binding into CRISPR-powered outputs an emphasis their corresponding design principles. Furthermore, second part review outlines potential solutions seamlessly integrating these user-friendly rapid tests specifically tailored (POC).
Язык: Английский
Процитировано
18Talanta, Год журнала: 2024, Номер 278, С. 126467 - 126467
Опубликована: Июнь 28, 2024
Язык: Английский
Процитировано
12Lab on a Chip, Год журнала: 2023, Номер 23(6), С. 1467 - 1492
Опубликована: Янв. 1, 2023
Critical development of CRISPR-based diagnostics coupled with nucleic acid amplification and amplification-free techniques; various purposes CRISPR including determination, quantification, multiplexed point-of-care diagnostics.
Язык: Английский
Процитировано
23ACS Synthetic Biology, Год журнала: 2024, Номер 13(6), С. 1633 - 1646
Опубликована: Июнь 11, 2024
A growing number of applications require simultaneous detection multiplexed nucleic acid targets in a single reaction, which enables higher information density combination with reduced assay time and cost. Clustered regularly interspaced short palindromic repeats (CRISPR) the CRISPR-Cas system have broad for acids due to their strong specificity, high sensitivity, excellent programmability. However, realizing is still challenging nonspecific collateral cleavage activity, limited signal reporting strategies, possible cross-reactions. In this review, we summarize principles, features based on further discuss challenges perspective.
Язык: Английский
Процитировано
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