Specific Reaction Research Articles

A melanin-like polymer bearing phenylboronic units as a suitable bioplatform for living cell display technology

Surface display of functional groups with specific reactivity around living cells is an emerging, low cost and highly eco-compatible technology that serves multiple applications, ranging from basic biochemical studies to biomedicine, therapeutics and environmental sciences. Conversely to classical methods exploiting hazardous organic synthesis of precursors or monovalent functionalization via genetics, here we perform functional decoration of individual living microalgae using suitable biocoatings based on polydopamine, a melanin-like synthetic polymer. Here we demonstrate the one-pot synthesis of a functional polydopamine bearing phenylboronic units which can decorate the living cell surfaces via a direct ester formation between boronic units and surface glycoproteins. Furthermore, biosorption of fluorescent sugars on functionalized cell membranes is triggered, demonstrating that these organic coatings act as biocompatible soft shells, still functional and reactive after cell engineering.

Development of Methods to Generate Radical Species and Synthetic Applications

Radicals are chemical species bearing an isolated single electron. They have developed in a complementary manner to the two-electron species such as anions and cations. Radical species are classified into different groups according to their electronic states, such as cation radicals, neutral radicals, anion radicals, and biradicals, each of which has high reactivity and induces specific reactions. The authors have been developing studies on radical species to establish the generation methods and to control their reactivity. The author has found that heavy atom-containing compounds can undergo photochemical reactions that generate radical species through direct S0→Tn transitions. The S0→Tn absorption band exists in a longer wavelength region than the corresponding S0→Sn band, and thus light in the near-visible light region can be used for the reactions. Although the absorption efficiency of the S0→Tn transition is not high, it is possible to selectively excite heavy atom-containing molecules by irradiation of near-visible light, thus making it possible to control the generation and reactivity of radical species. The author also succeeded in developing a ligand that is activated by visible light irradiation to generate the monovalent palladium radical species. By using this ligand, it was possible to efficiently generate radical species of transition metals. Furthermore, depending on the valence of the palladium used, radical species with opposite properties could be generated.

Harnessing the Power of PM6:Y6 Semitransparent Photoanodes by Computational Balancement of Photon Absorption in Photoanode/Photovoltaic Organic Tandems: >7 mA cm−2 Solar Synthetic Fuels Production at Bias‐Free Potentials

This study first demonstrates the potential of organic photoabsorbing blends in overcoming a critical limitation of metal oxide photoanodes in tandem modules: insufficient photogenerated current. Various organic blends, including PTB7‐Th:FOIC, PTB7‐Th:O6T‐4F, PM6:Y6, and PM6:FM, were systematically tested. When coupled with electron transport layer (ETL) contacts, these blends exhibit exceptional charge separation and extraction, with PM6:Y6 achieving saturation photocurrents up to 16.8 mA cm−2 at 1.23 VRHE (oxygen evolution thermodynamic potential). For the first time, a tandem structure utilizing organic photoanodes has been computationally designed and fabricated and the implementation of a double PM6:Y6 photoanode/photovoltaic structure resulted in photogenerated currents exceeding 7 mA cm−2 at 0 VRHE (hydrogen evolution thermodynamic potential) and anodic current onset potentials as low as −0.5 VRHE. The herein‐presented organic‐based approach paves the way for further exploration of different blend combinations to target specific oxidative reactions by selecting precise donor/acceptor candidates among the multiple existing ones.

Iraqi patients with a single-nucleotide polymorphism of interleukin-10 -1082G/A and interleukin-6 -174G/C susceptibility to asthma

The effects of genetic variations in the IL-10 -1082G/A gene and IL-6 -174G/C gene, as well as the genotypes and alleles linked to the prevalence of asthma disease, were investigated using a molecular and immunological study. Between October 2018 and the end of July 2020, 40 healthy individuals (20 females and 20 males) served as a control group for the study, which involved 50 asthmatic patients (31 females and 19 males) at the Allergy Centre, Al-Anbar Teaching Hospital, in Al-Anbar City. The study used the Single Specific Primer-Polymerase Chain Reaction (SSP-PCR) technique to show that the single nucleotide polymorphisms IL-10 -1082G/A and IL-6 -174G/C had a considerably high prevalence rate (P<0.05) among asthma case and that there was an association between the polymorphism and the asthma risk. The findings indicate that asthma patients had considerably higher (P<0.05) IL-10 A alleles and heterozygous GA genotypes (1082G/A) compared to the control group. Genetic variations affecting IL-10 production and the genotypes affecting IL-10 serum levels are associated with the occurrence of asthma and are attributed to the IL-10 -1082G/A promoter gene polymorphism. There was a strong correlation between cytokine levels, of disease development, and the genotypes of the AA and AG genes, indicating that IL-10 -1082A/G predisposition to asthma may be influenced by the gene promoter polymorphism. Asthma development and immunological markers (IL-10) are substantially correlated. One theory links allergic rhinitis to both the development of asthma and its risk. Inducing long-term immunological and clinical tolerance in patients was a good use of HDM immunotherapy. The current study's findings indicate a substantial difference between the asthma patients and the control group in terms of gene type and allele frequency of the IL-6 -174G/C polymorphism. The patients exhibited a higher prevalence of the G allele and the GG homozygous genotype than the control group. Therefore, it was shown that those with GG genotypes had a 2-fold increased probability of having asthma, indicating that patients were more prone to the condition.

Human leukocyte antigen HLA-B*57:01 status in HIV-1 patients developing hypersensitivity reactions in Benin: a pilot study

BackgroundAntiretroviral drugs in people living with HIV-1 (PLHIV-1) often trigger side effects which may lead to discontinuation or failure of treatment. Human Leukocyte Antigen B*57:01 (HLA-B*57:01) allele is known to predict hypersensitivity reactions to Abacavir. Very few data are available on the prevalence of HLA-B*57:01 allele in PLHIV-1 in African countries. This study aimed to screen for HLA-B*57:01 allele in PLHIV-1 in Benin.MethodsThis pilot study was carried out on one hundred ten PLHIV-1 enrolled in two health facilities in Benin. Socio-demographic and clinical data were collected. Biological data were determined and HLA-B*57:01 allele was genotyped, using Single Specific Primer-Polymerase Chain Reaction in blood samples.Results70% of participants were female. PLHIV-1 were under TDF + 3TC + DTG (47.2%) or TDF + 3TC + EFV (57.3%). Their median age was 41 [36-48.75] years and the average CD4 + T cell count was 249 [130-381.25] cells/µl. The average viral load in treatment failure PLHIV-1 was 4.7 [3.9–5.2] Log10. At the inclusion date, twenty-nine (26.4%) PLHIV-1 under TDF + 3TC + EFV have developed hypersensitivity reactions. None of 110 patients had shown HLA-B*5701 allele.ConclusionOur study revealed that HLA-B*57:01 allele was very rare in PLHIV-1 in Benin, suggesting that its screening before starting the Abacavir regimen did not seem necessary.

Recent Developments in Selenylation of Alkynes

Alkynes are simple yet important organic feedstocks. The selenylation of alkynes is able to produce complex selenium‐containing compounds in a facile way. Although there are some reviews about the selenylation of alkynes, most of them focus on one specific reaction or what types of products that can be obtained. There is a lack of attention given to the various uses of different selenium reagents and their mechanisms. This review mainly focuses on recent advances (2013‐2023) based on diverse selenium reagents. Mechanisms and how the added reagents work will be discussed. Different reaction types, including difunctionalization, Se‐annulation, spiro‐cyclization, C‐Se coupling, click reaction will be recorded in this review. The regioselectivity can be achieved through various mechanisms, including radicals, seleniraniums or electrophilic cyclization. We hope it will do help for future research in this area.

Recent updates on diet‐derived gut microbial metabolites

AbstractEmerging evidence indicates that the health‐beneficial effects of ingested food components depend on in part, their upper and lower gastrointestinal uptake and metabolism and the gut microbial composition of the host. Several dietary components, such as polyphenols, are poorly absorbed in the upper intestinal compartments and extensively metabolized by the colonic microbiota resulting in the production of an array of metabolites. These microbiota‐mediated products possess specific solubility, reactivity, bioavailability, and biological activities. However, identifying and characterizing a wide range of metabolites is challenging due to the high chemical diversity of dietary components and interindividual variability of the gut microbiota. It is, therefore, critical to design an animal model that effectively mimics human microbial metabolism and use multidisciplinary omics approaches such as metabolomics to detect and identify a wide range of metabolites. Here, we provide the current state of knowledge of major diet‐derived gut microbial metabolites and their potential biological activities.

Optical Label-Free Aptasensor Based on Weak Value Amplification for Real-Time and Ultrasensitive Detection of IgE.

Allergy is a prevalent disease, and the potential allergic population is expanding with industrialization and changes in people's living standards. Serum immunoglobulin E (IgE) level is one of the critical indicators for determining allergy. Here, we proposed a simple, real-time monitoring, low chip cost, label-free aptamer biosensing strategy based on weak value amplification (WVA) for the quantitative detection of IgE in serum samples, enabling early and accurate diagnosis of allergic or hypersensitive patients. The aptasensor combined an imaging weak measurement system with the high specificity of the aptamer for the marker IgE. By modifying the amino group at the 3-terminal end, the anti-IgE aptamers can attach to a dopamine-modified prism's surface and selectively recognize IgE in human serum. In the presence of IgE, a specific binding reaction occurred, resulting in a change in the refractive index of the reactive region's surface, manifested as a change in the light intensity of the camera acquired experimental images. As the concentration of IgE increased, the relative light intensity advanced sequentially. The WVA-aptasensing strategy achieved a wide detection range of 0.01 ng/mL to 2 μg/mL in phosphate buffered saline buffer, with the resolution as low as 4.3 pg/mL. IgE testing experiments in human serum have proved the feasibility of our methods in detecting complex samples. In addition, the method specifically recognized IgE without interference from other proteins. We believe that our proposed sensing strategy opens up new possibilities for ultrahigh sensitivity screening of IgE and can be expanded to detecting other biomolecules.

Bioinspired Cellular Membrane Vesicles Derived from Bacterial and Erythrocyte Ghosts: Development and Applications as a Smart Drug Delivery System

This study emphasizes the importance and application of bioinspired cellular membrane vesicles as smart drug delivery carriers. The lessons can be learned from nature for the smart drug delivery system. Biological membranes are essential to provide stable and functional compartments, preserve cellular architecture, and promote selective signaling and transportation, which are mediated by embedded integral or peripheral proteins. Bioinspired mimicking of natural components in organisms has demonstrated their potential to serve as an innovative system for theranostic applications. However, mimicking the cell membrane in an artificial system is complex because of the multifarious biological structures. The primary advantage of these bioinspired delivery systems is the systematic biodistribution that nonnative delivery systems could not possess. This review will present biomimics resulting from self-assembling amphiphilic polymers. The promising artificial self-assemblies tagged with biomolecules by encapsulation, hybridization, or insertion can serve as means for the development of a smart drug delivery system. Moreover, in case the developed system is stimuli-responsive, the system allows for the triggered or on demand release of payload with in situ specific reaction. In conclusion, cellular membrane vesicles offer an important approach to efficient drug-targeted treatments at the molecular and cellular levels. Here, bioinspired cellular membrane vesicles are discussed along with their applications. Relevant examples of bioinspired membrane mimics are included for an overview of drug delivery candidates. The advantages of using biomimetic membranes and current limitations for future improvements are also included.

Phosphorus-Water Interaction Drives Active Center Evolution into the Water-Adaptive Structure in the High-Humidity NH3-SCR Reaction.

The impact of water on catalyst activity remains inconclusive due to its dependence on the specific reaction environment. To maximize the exploitation of water's promoting effect, we employed ammonia selective catalytic reduction (NH3-SCR) as a probe reaction and proposed a phosphorus modification strategy for Cu-ZSM-5 catalysts. The objective of this approach was to construct water-adaptive microstructures through directional arrangement. To investigate the effect of phosphorus on the transformation of framework copper sites in humid environments, we conducted comprehensive characterizations and density functional theory calculation. Results reveal that water molecules cleave the oxygen bridges between phosphorus oxide and copper, leading to the formation of active isolated [Cu(OH)]+ groups and phosphate. The phosphate species weaken the interaction between exchanged Cu2+ groups and the zeolite framework, leading to the generation of highly migratory hydrated Cu2+ species. This work will potentially guide the rational design of water-adaptive catalysts for gas pollution abatement in a humid environment.

The characteristics and mechanism NO formation during hydroxylated fuels/NH3 oxidation in oxy-fuel atmospheres

Oxy-fuel combustion, as an important technology to realize CCUS in the field of combustion, needs to control the generation of pollutants such as NOx while realizing CO2 capture, and the conversion of fuel-N to N2 is crucial. Previous experiments have provided insights into the influence of different atmospheres on NO during oxy-fuel combustion of alcohols. However, the specific reaction mechanism underlying how the atmosphere and hydroxyl fuels impact NO generation through the free radical pool remains unclear. In this study, the formation and reduction of NO during the oxidation of CH3OH/NH3 and C2H5OH/NH3 in O2/CO2, O2/H2O and O2/CO2/H2O atmospheres with oxy-fuel condition were investigated by simulation. In the NO generation stage, different H2O, CO2, O2 and fuel types have little effect on the peak of NO although they change the NH3→NO reaction path. In the process of NO reduction, stage 1 is the main reaction phase of NO→N2, and both CO2 and H2O are beneficial for the reduction of NO. But the reduction of NO by H2O was more pronounced. In the case of simultaneous addition of H2O and CO2, the reducing effect of H2O and CO2 alone on NO was attenuated. On the other hand, the reduction effect exerted by H2O and CO2 was stronger in high than in low oxygen-fuel ratio, stronger in C2H5OH than in CH3OH. The reduction of NO by H2O and CO2 is based on the general equation NO→N2+O2. H2O is used to promote the reaction in the positive direction by consuming O2 to convert it to H and OH, so that more of the element O is converted to OH than O2 to inhibit the production of NO. The CO2 contributes to the formation of less O2 during the reduction of N2 from NO by promoting reaction NO + N→O + N2, while the additional OH increases the "capacity" of O2 in the NO→N2+O2 reaction.

Development of polyimide nanofiber aerogels with a 3D multi-level pore structure: A new sensor for colorimetric detection of breath acetone

Polyimide nanofiber aerogels loaded with thymol blue and hydroxylamine sulfate (TB-HAS@PI NFAs) were synthesized and employed as a novel sensor for colorimetric detection of breath acetone (BrAce). The enhancement of 3D multi-level pore structure of TB-HAS@PI NFAs for sensing performance was elucidated through systematical characterization results. Because the designed sensing system relied on the specific reaction of HAS with acetone, TB-HAS@PI NFAs exhibited a more sensitive response ability to acetone, ensuring that the colorimetric sensing detection will not be interfered by other coexisting gas in exhaled breath. Moreover, the sensor demonstrated a rapid response, with color changes quantitatively measured within 30 s of exposure to acetone gas. Importantly, the feasibility and accuracy of established method were confirmed through comparison with GC–MS. This research provided a promising strategy for daily health management of healthy people and diabetics.

Solvatochromism mechanism of perylene diimide radicals stabilized by low barrier hydrogen bond and detection of formaldehyde in real food samples

Formaldehyde (FA) is widely used for food preservation and whitening because of its preservative and bleaching effects. Excessive FA seriously endangers human health, so monitoring FA-treated food is of great significance for food safety. In this paper, perylene diimide radicals with the chirality (BTFPDI) and water-solubility (TFPDI-bPEI) were designed respectively based on our previous studies. Property of solvatochromism induced by these perylene diimide radicals aggregation was demonstrated by the concentration and temperature dependent absorption spectrum and the circular dichroism spectrum. Further the colorimetric monitoring of trace FA in gaseous and liquid was realized by the condensation reaction of FA with amine to induce TFPDI-bPEI aggregation. After the addition of FA, TFPDI-bPEI molecule aggregated in aqueous solution due to the specific reaction of a large number of –NH2 groups with FA, resulting in a blue-shift of the maximum absorption peak from 780 nm to 561 nm, and the detection limit as low as 0.86 μM to FA and the response time of only 20 s. This method could further detect FA in food with good recoveries and detect FA in contaminated food samples.

Optimization of synthesis parameters for polyamide 610: Strategic tailoring for superior latent heat performance

The study systematically optimizes the synthesis of polyamide 610 with the aim of improving latent heat and melting temperature to meet the demanding requirements of high-temperature heat storage applications using Response Surface Methodology (RSM). The results clarify the critical impact of reaction times, washing solvents, and molar ratios on these vital thermal characteristics. Samples exhibiting exceptional latent heat capacities at various mole ratios were further analyzed using Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Fourier Transform Infrared Spectroscopy (FTIR), and X-ray Diffraction (XRD). The TGA assessments were instrumental in determining the thermal degradation behaviors of the materials. At the same time, The DSC analysis was used for the determination of thermal properties of the materials, FTIR provided detailed insights into their molecular structures, and XRD elucidated the crystalline structure of the materials. The findings reveal that a specific mole ratio is essential for achieving superior thermal properties, indicative of the polymer's resilience and structural stability. It was evident that samples with a balanced molar ratio (1:1) and specific reaction time (60 min) showed the best latent heat, surpassing 80 J g-1, and melting temperatures up to 210 °C. A notable aspect of this research is the use of Sebacic Acid instead of the conventional Sebacoyl Chloride for synthesizing polyamide 610. The choice of Sebacic Acid was made due to its lower toxicity and the fact that its byproducts are easier to remove than those from sebacoyl chloride, which produces hydrochloric acid as a byproduct. The presence of HCL can lead to side reactions and negatively impact the reaction process. By using Sebacic Acid, we reduce the risk of such contaminants, thereby enhancing the thermal stability and performance of polyamide 610. This greener approach not only aligns with sustainable practices but also has significant implications for the performance of the polymer. In addition, the integration of RSM with comprehensive characterization techniques has been pivotal in elucidating the critical influence of synthesis parameters on material properties. This enhanced understanding holds the potential for significant contributions to the development of advanced materials for latent heat storage applications, combining sustainability with high performance.

Acute Ongoing Nociception Delays Recovery of Consciousness from Sevoflurane Anesthesia via a Midbrain Circuit.

Although anesthesia provides favorable conditions for surgical procedures, recent studies have revealed that the brain remains active in processing noxious signals even during anesthesia. However, whether and how these responses affect the anesthesia effect remains unclear. The ventrolateral periaqueductal gray (vlPAG), a crucial hub for pain regulation, also plays an essential role in controlling general anesthesia. Hence, it was hypothesized that the vlPAG may be involved in the regulation of general anesthesia by noxious stimuli. Here, we found that acute noxious stimuli, including capsaicin-induced inflammatory pain, acetic acid-induced visceral pain, and incision-induced surgical pain, significantly delayed recovery from sevoflurane anesthesia in male mice, whereas this effect was absent in the spared nerve injury-induced chronic pain. Pretreatment with peripheral analgesics could prevent the delayed recovery induced by acute nociception. Furthermore, we found that acute noxious stimuli, induced by the injection of capsaicin under sevoflurane anesthesia, increased c-Fos expression and activity in the GABAergic neurons of the ventrolateral periaqueductal gray. Specific reactivation of capsaicin-activated vlPAGGABA neurons mimicked the effect of capsaicin and its chemogenetic inhibition prevented the delayed recovery from anesthesia induced by capsaicin. Finally, we revealed that the vlPAGGABA neurons regulated the recovery from anesthesia through the inhibition of ventral tegmental area dopaminergic neuronal activity, thus decreasing dopamine (DA) release and activation of DA D1-like receptors in the brain. These findings reveal a novel, cell- and circuit-based mechanism for regulating anesthesia recovery by nociception, and it is important to provide new insights for guiding the management of the anesthesia recovery period.

A Novel Fluorescent Probe for Nitroreductase Detection and Imaging of cancer Cells under Hypoxia Conditions.

Nitroreductase (NTR) is to be pivotal in the biodegradation of nitroaromatics. NTR is produced in tumor tissues under hypoxic conditions, which is one of the markers for early tumor diagnosis. In this study, a novel probe FD-NTR was developed for NTR detection. Probe FD-NTR can exhibit a specific reaction with NTR in the presence of NADH. The probe displayed satisfactory selectivity and sensitivity towards NTR with a calculated detection limit of 12 ng/mL. Under the conditions of low cytotoxic hypoxia, the FD-NTR probe has shown successful application in imaging both MCF-7 cells and tumor tissues, which indicated that the FD-NTR probe holds promising application prospects for detecting NTR in tumors.

Progress of natural sesquiterpenoids in the treatment of hepatocellular carcinoma.

Hepatocellular carcinoma is one of the common malignant tumors of digestive tract, which seriously threatens the life of patients due to its high incidence rate, strong invasion, metastasis, and prognosis. At present, the main methods for preventing and treating HCC include medication, surgery, and intervention, but patients frequently encounter with specific adverse reactions or side effects. Many Traditional Chinese medicine can improve liver function, reduce liver cancer recurrence and have unique advantages in the treatment of HCC because of their acting mode of multi-target, multi-pathway, multi-component, and multi-level. Sesquiterpenoids, a class of natural products which are widely present in nature and exhibit good anti-tumor activity, and many of them possess good potential for the treatment of HCC. This article reviewed the anti-tumor activities, natural resources, pharmacological mechanism of natural sesquiterpenoids against HCC, providing the theoretical basis for the prevention and treatment of HCC and a comprehensive understanding of their potential for development of new clinical drugs.

Synergistic nitrate removal: Coupling electrocatalysis and chemical reduction for exceptional nitrogen selectivity

Nitrate pollution in natural water bodies poses a severe threat to human health and the environment. Developing efficient and environmentally friendly nitrate removal methods has become a global need. Electrochemical techniques offer a cost-effective strategy for nitrate remediation; however, the complexity of the reaction and the formation of multiple by-products make the selective production of harmless nitrogen a challenging task. This study proposes a novel two-step strategy to achieve high efficiency and selectivity in converting nitrate into nitrogen. First, a membrane electrode consisting of silver nanowires (Ag NWs) is used to electrochemically reduce nitrate to nitrite through a direct electron transfer pathway. Whether in a static electrolytic cell or a flow cell, the process has very high nitrite selectivity and Faraday efficiencies, with Faraday efficiency up to 98.40 % and selectivity up to 99.90 % at −1.0 V vs Ag/AgCl. Subsequently, the nitrite is converted into nitrogen through a specific reaction with sulfamic acid with near 100 % conversion and selectivity. By coupling these two reactions, the selectivity for converting nitrate to nitrogen can reach more than 99 %. In addition, the membrane electrode can be readily used in a flow-through electrolytic cell to treat nitrates at a maximum rate of 150 L h−1 m−2. When operated at 50 L h−1 m−2, the membrane electrode demonstrates relatively stable performance for 100 h, reducing nitrates at 1.61 mM to below 0.81 mM (50 ppm), as recommended by the World Health Organization for drinking water. This novel synergistic approach not only enhances nitrogen selectivity but also simplifies the process of electrocatalytic nitrate reduction, making it a promising method for nitrate removal.

Reactivity Manipulation of Ionic Liquid Based on Alkyl Primary Ammonium: Protonation Control Using 4‐tert‐Butylpyridine Additive for Effective Spontaneous Passivation of Perovskite via Hole Transport Material Deposition

Alkyl‐primary‐ammonium‐based room‐temperature ionic liquids (RTILs) designed to exhibit specific reactivities allowing functions that cannot be achieved by other RTILs have recently emerged. The archetype of the reactive RTILs is n‐octylammonium bis(trifluoromethanesulfonyl)imide (OA‐TFSI), which has promising functions as an additive for hole transport materials (HTMs) in perovskite solar cells (PSCs); the high reactivity of the OA cations on the perovskite surface allows spontaneous perovskite passivation via HTM deposition, effectively improving the photovoltaic (PV) performance. However, although the reactivity manipulation of the reactive RTILs is instrumental for exploiting their potential functions and exploring their application scope, methods for reactivity control have not been developed. Herein, it is proposed that the coaddition of a pyridine derivative (4‐tert‐butylpridine: TBP) can effectively manipulate the reactivity of OA‐TFSI by controlling the protonation between OA and the 2,2′,7,7′‐tetrakis‐(N,N‐di‐4‐methoxyphenylamino)‐9,9′‐spirobifluorene (Spiro‐OMeTAD) HTM. The TBP prevents OA deprotonation presumably via stabilization of the OA cation, thus retaining its ammonium form, which allows efficient spontaneous perovskite passivation, effectively enhancing the PV performance. This reveals the protonation preference in the OA‐TFSI system, which is opposite to that in conventional RTILs. This first proposal of a method in manipulating reactivity of the reactive RTILs will contribute to the development of materials science.

Solar energy powered biodiesel synthesis from linseed oil – A novel experimental study

In developing countries such as India, there is a significant dependency on fossil fuels, which make up a substantial 70 % of their overall energy requirements. Nevertheless, this reliance becomes increasingly precarious as global reserves of fossil fuels continue to deplete due to their extensive consumption. Biodiesel offers a sustainable alternative to conventional fossil fuels, contributing to reduced greenhouse gas emissions and enhanced energy security. This research centres on developing a solar energy powered transesterification system for biodiesel production using a KOH catalyst. The main goal is to address technological, economic, and sustainability challenges in biodiesel manufacturing. Extensive experiments were conducted over five days to thoroughly assess the efficiency of this innovative solar reactor. The innovative solar biodiesel synthesis system consistently achieves an impressive average biodiesel conversion rate of 90.8 % when operated under specific reaction conditions. Furthermore, the system's energy efficiency, calculated at 9.08×10−5g/J, outperforms the energy efficiency of traditional methods. Additionally, the properties of the biodiesel produced fall well within the specified limits defined by the ASTM D6751 standards. These collective findings underscore the considerable potential of proposed novel reactor as an eco-friendly and sustainable approach to biodiesel production.