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Wearable sweat sensors are reshaping healthcare monitoring, providing real-time data on hydration and electrolyte levels with user-friendly, noninvasive devices. This paper introduces a highly portable two-channel microfluidic device for simultaneous sweat sampling and the real-time detection of volatile organic compound (VOC) biomarkers. This innovative wearable microfluidic system is tailored for monitoring diabetes through the continuous and noninvasive tracking of acetone and ammonia VOCs, and it seamlessly integrates with smartphones for easy data management. The core of this system lies in the utilization of carbon polymer dots (CPDs) and carbon dots (CDs) derived from monomers such as catechol, resorcinol, o-phenylenediamine, urea, and citric acid. These dots are seamlessly integrated into hydrogels made from gelatin and poly(vinyl alcohol), resulting in an advanced solid-state fluorometric sensor coating on a cellulose paper substrate. These sensors exhibit exceptional performance, offering linear detection ranges of 0.05-0.15 ppm for acetone and 0.25-0.37 ppm for ammonia, with notably low detection limits of 0.01 and 0.08 ppm, respectively. Rigorous optimization of operational parameters, encompassing the temperature, sample volume, and assay time, has been undertaken to maximize device performance. Furthermore, these sensors demonstrate impressive selectivity, effectively discerning between biologically similar substances and other potential compounds commonly present in sweat. As this field matures, the prospect of cost-effective, continuous, personalized health monitoring through wearable VOC sensors holds significant potential for overcoming barriers to comprehensive medical care in underserved regions. This highlights the transformative capacity of wearable VOC sweat sensing in ensuring equitable access to advanced healthcare diagnostics, particularly in remote or geographically isolated areas.

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Ultraviolet (UV) radiation exposure is one of the most important risk factor among workers. it may stimulate health outcomes such as multiple skin injuries and blinding eye diseases. So, UV protection is mainly important for people who expose to it. Modification of cotton textiles by nanomaterials is a new approach to overcome this problem. So, the aim of this study is to review studies conducted on using ZnO nanoparticles for improving ultraviolet protection of cotton textiles. The search strategy was provided by cochrane guideline. 45 studies were regarded as appropriate. The results show that UPF for textiles has improved by coated ZnO. However, UPF was depended on the physicochemical characteristics of ZnO and textiles such as yarn structure, effect of woven fabric construction, fabric porosity, and impurity of textiles and laundering conditions. Also, plasma technology has improved UPF, it is recommended that more studies be done to achieve better results.

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Analysis of volatile organic compounds (VOCs) secreted in urine, blood, breath, etc. is a new method for monitoring the metabolism and biochemistry of the human body. However, due to the complexity of samples, a pre-concentration step is necessary before the final analysis with gas chromatography-mass spectroscopy (GC-MS). Therefore, miniaturized extraction methods such as solid-phase microextraction (SPME) can be a promising and simple pre-concentration technique. Different strategies have been adopted for the fabrication or modification of SPME fibers. This study presents the preparation and characterization of glass optical fibers coated with ZnO nanorods functionalized with gallic acid (ZnO@GA nanorod) as SPME adsorbent in GC-MS. ZnO@GA nanorods were synthesized separately and then coated onto the fibers. The coated fibers were characterized by using field emission scanning electron microscopy coupled with energy dispersive analysis of X-rays (FESEM/EDAX) and Fourier transform infrared spectroscopy (FTIR) techniques. Possessing a high surface to volume ratio of ZnO nanorods and functional groups of GA, the ZnO@GA nanorod-based SPME fibers exhibited good extraction performance for VOCs comparing with the commercial polydimethylsiloxane (PDMS) coated fibers. Under optimal conditions (NaCl concentration, 30% w/v; extraction time of 25 min; pH, 5-7 and stirring rate of 400 rpm) ZnO@GA nanorods coated fibers achieved low detection limits (0.32-4.8 µg/L), low quantification limits (1.8-16.3 µg/L) and good linearity (5-1000 µg/L) for selected VOCs. The repeatability (n = 3) for a single fiber was within the range of 4.1-7.9% (intra-day) and 5.7-9.6% (inter-day) while the reproducibility (n = 3) of fiber-to-fiber were in the range of 4.7% and 9.9%. This method was successfully used for the determination of six VOCs in water and urine with satisfactory recoveries of 90-112%. ZnO@GA nanorod coated fibers, despite possessing a much thinner coating compared to the commercial fibers, revealed a better overall extraction efficiency towards VOCs. These results indicated that the ZnO@GA provided a promising alternative in sample pretreatment and analysis in GC-MS.

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The aim of this study was to evaluate the efficiency of using a natural substance, curcumin, encapsulated in CD44-targeting hyaluronate-polylactide (HA-PLA) nanoparticles (NPs) for the modulation of macrophage polarity from the pro-inflammatory M1 to anti-inflammatory M2 phenotype. For this purpose, the characterization of the NPs was monitored using 1HNMR, FTIR, DLS and FE-SEM. The effects of curcumin-encapsulated HA-PLA NPs on the viability of LPS/IFN-γ stimulated peritoneal macrophages were determined using MTT assay. The cellular uptake of free curcumin and nano-formulated curcumin was assessed using confocal microscopy. Also, the expression levels of iNOS-2 (M1 marker), Arg-1 (M2 marker) and also pro-inflammatory cytokines were measured by real-time PCR. Data showed that the nano-formulated curcumin with spherical shape, an average diameter of 102.5 nm and high cellular uptake was significantly less toxic to peritoneal macrophages. Furthermore, the nano-formulated curcumin effectively indicated a reduction in iNOS-2 and an increase in Arg-1 levels than free curcumin. The change in macrophage phenotype by curcumin-encapsulated HA-PLA NPs could suppress the inflammation in LPS/IFN-γ stimulated macrophages as evidenced by a major reduction in pro-inflammatory cytokines. Conclusively, the results suggested that the curcumin formulation with CD44-targeting HA-PLA NPs might be a promising platform for the treatment of inflammatory diseases.

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Despite the great value of current exogenous contrast agents for providing main diagnostic information, they still have certain drawbacks such as short blood half life, nonspecific biodistribution, fast clearance, slight renal toxicity and poor contrast in fat patients. Nanoparticles (NPs) are used as novel contrast agents that represent a promising strategy for the non invasive diagnosis. As a platform, nanoparticulates are compatible for developing targeted contrast agents. Advances in nanotechnology will provide enhanced sensitivity and specificity for tumor imaging enabling earlier detection of metastases. This article focuses on fundamental issue such as biological interactions, clearance routes, coating of NPs and presents a wide discussion about most recent category of NPs that are used as contrast agents and thebenefits/concerns issues associated with their use in clinical procedures.

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Poor water solubility and low oral bioavailability limit the clinical application of Erlotinib as an anticancer. For this purpose, we encapsulated erlotinib in the solid lipid nanoparticles (SLN) and designed a spray-dried dry powder inhalable (DPI) formulation. Erlotinib-loaded SLNs were prepared using self-nanoemulsifying and characterized for physicochemical properties. Pulmonary deposition of spray-dried DPI formulation was performed using Next Generation Impactor. The particle size and zeta potential of Erlotinib-loaded SLNs were 300 to 800 nm and -18 to -32 mV, respectively. High drug entrapment efficiency in the narrow range of 80-85% was achieved. Cytotoxicity results indicated that cell growth inhibition of free drug and drug loaded nanoparticles is dose- and time-dependent. Inhalable dry powders prepared from drug-loaded SLNs were found to have a fine particle fraction in the range of 6.92±0.99 -11.24±2.4%, mean mass aerodynamic diameter in the range of 4.52±0.1 to 6.67±0.5 µm. The findings revealed that the proposed inhalable dry powder formulation loaded with erlotinib SLN has potential in lung cancer therapy through pulmonary route.

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Lipid nanoparticles (LNPs) have attracted special interest during last few decades. Solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) are two major types of Lipid-based nanoparticles. SLNs were developed to overcome the limitations of other colloidal carriers, such as emulsions, liposomes and polymeric nanoparticles because they have advantages like good release profile and targeted drug delivery with excellent physical stability. In the next generation of the lipid nanoparticle, NLCs are modified SLNs which improve the stability and capacity loading. Three structural models of NLCs have been proposed. These LNPs have potential applications in drug delivery field, research, cosmetics, clinical medicine, etc. This article focuses on features, structure and innovation of LNPs and presents a wide discussion about preparation methods, advantages, disadvantages and applications of LNPs by focusing on SLNs and NLCs.