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1.
ACS Sens ; 9(5): 2294-2309, 2024 05 24.
Article in English | MEDLINE | ID: mdl-38654679

ABSTRACT

Bioanalyte collection by blood draw is a painful process, prone to needle phobia and injuries. Microneedles can be engineered to penetrate the epidermal skin barrier and collect analytes from the interstitial fluid, arising as a safe, painless, and effective alternative to hypodermic needles. Although there are plenty of reviews on the various types of microneedles and their use as drug delivery systems, there is a lack of systematization on the application of polymeric microneedles for diagnosis. In this review, we focus on the current state of the art of this field, while providing information on safety, preclinical and clinical trials, and market distribution, to outline what we believe will be the future of health monitoring.


Subject(s)
Needles , Polymers , Humans , Polymers/chemistry , Drug Delivery Systems/instrumentation , Animals , Microinjections/instrumentation , Microinjections/methods , Monitoring, Physiologic/instrumentation , Monitoring, Physiologic/methods
2.
Bioelectrochemistry ; 154: 108553, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37672968

ABSTRACT

Alzheimer's disease (AD) is the most common dementia type and a leading cause of death and disability in the elderly. Diagnosis is expensive and invasive, urging the development of new, affordable, and less invasive diagnostic tools. The identification of changes in the expression of non-coding RNAs prompts the development of diagnostic tools to detect disease-specific blood biomarkers. Building on this idea, this work reports a novel electrochemical microRNA (miRNA) biosensor for the diagnosis of AD, based on carbon screen-printed electrodes (C-SPEs) modified with two gold nanostructures and a complementary anti-miR-34a oligonucleotide probe. This biosensor showed good target affinity, reflected on a 100 pM to 1 µM linearity range and a limit of detection (LOD) of 39 pM in buffer and 94 aM in serum. Moreover, the biosensor's response was not affected by serum compounds, indicating selectivity for miR-34a. The biosensor also detected miR-34a in the cell culture medium of a common AD model, stimulated with a neurotoxin to increase miR-34a secretion. Overall, the proposed biosensor makes a solid case for the introduction of a novel, inexpensive, and minimally invasive tool for the early diagnosis of AD, based on the detection of a circulating miRNA overexpressed in this pathology.


Subject(s)
Alzheimer Disease , MicroRNAs , Aged , Humans , Alzheimer Disease/diagnosis , Alzheimer Disease/genetics , MicroRNAs/genetics , Carbon , Cell Culture Techniques , Electrodes
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