Chemotherapy
has seen great progress in the development of performant
treatment strategies. Nanovesicles such as liposomes and polymersomes
demonstrated great potential in cancer therapy. However, these nanocarriers
deliver their content passively, which faces a lot of constraints
during blood circulation. The main challenge resides in degradation
and random delivery to normal tissues. Hence, targeting drug delivery
using specific molecules (such as antibodies) grafted over the surface
of these nanocarriers came as the answer to overcome many problems
faced before. The advantage of using antibodies is their antigen/antibody
recognition, which provides a high level of specificity to reach treatment
targets. This review discusses the many techniques of nanocarrier
functionalization with antibodies. The aim is to recognize the various
approaches by describing their advantages and deficiencies to create
the most suitable drug delivery platform. Some methods are more suitable
for other applications rather than drug delivery, which can explain
the low success of some proposed targeted nanocarriers. In here, a
critical analysis of how every method could impact the recognition
and targeting capacity of some nanocarriers (liposomes and polymersomes)
is discussed to make future research more impactful and advance the
field of biomedicine further.
Real-time detection of substance use is an approach of
high interest
leading to the optimization of behavioral interventions and drug abuse
intervention. The current methods in use suffer many limitations and
need high logistical and laboratory requirements. Biosensors have
shown a great potential in overcoming these limitations. In the present
study, the electrochemical biosensor composed of a screen-printed
electrode (SPE) was designed for the detection of synthetic cannabinoid
(SC). Antibody-immobilized magnetic nanoparticles were also used to
create a surface on the transducer with magnetic interactions in order
to detect JWH-073 as a SC model. The use of immobilized magnetic nanoparticles
to create working surfaces makes the electrode a reusable SPE which
can be reutilized after the cleansing. To examine and observe any
possible changes on the surface due to its interaction with the analyte,
different electrochemical techniques such as differential pulse voltammetry,
cyclic voltammetry, and electrochemical impedance spectrometry were
applied. Based on the obtained results, the linearity of the biosensor
was found between 5 and 400 ng/mL, and the detection limit was calculated
as 22 ng/mL (n = 6) using the 3 Sb/m formula. The
biosensor functionality was studied in the presence of some related
interferents that showed lower responses than JWH-073, thus demonstrating
the good selectivity of the prepared biosensor. Finally, the sensory
platform was used to test synthetic urine sample, and the results
were compared with obtained results from liquid chromatography quadrupole
time-of-flight mass spectrometry (LC-QTOF/MS), which showed that the
proposed method could be utilized to identify abuse drugs.
As COVID-19 has reached pandemic status and the number of cases continues to grow, widespread availability of diagnostic testing is critical in helping identify and control the emergence of this rapidly spreading and serious illness. However, a lacking in making a quick reaction to the threat and starting early development of diagnostic sensing tools has had an important impact globally. In this regard, here we will review critically the current developed diagnostic tools in response to the COVID-19 pandemic and compare the different types through the discussion of their pros and cons such as nucleic acid detection tests (including PCR and CRISPR), antibody and protein-based diagnosis tests. In addition, potential technologies that are under development such as on-site diagnosis platforms, lateral flow, and portable PCR units are discussed. Data collection and epidemiological analysis could also be an interesting factor to incorporate with the emerging technologies especially with the wide access to smartphones. Lastly, a SWOT analysis and perspectives on how the development of novel sensory platforms should be treated by the different decision-makers are analyzed.
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