Curcumin Solution Research Articles

Novel method to improve oxidative stability of safflower oil: An artificial oil body loaded with curcumin coupled rosmarinic acid

Safflower oil is easily oxidized; therefore, its oxidative stability can be improved using artificial oil bodies (AOBs). AOBs were assembled using safflower oil, phospholipids, and a conjugate comprising safflower caleosin (Ctcaleosin) and rosmarinic acid. AOBs coupled with rosmarinic acid exhibited better physical and thermal stability. The conjugate comprising safflower caleosin and rosmarinic acid was obtained by forming stable C-N covalent bonds. Circular dichroism spectroscopy analysis revealed that α-helix levels increased in safflower caleosin in the conjugate, which could be ascribed to the improvement in the stability and flexibility of safflower caleosin anchored by rosmarinic acid. Rosmarinic acid covering the surface of the AOBs and curcumin (Cur) located in the core of the artificial oil bodies significantly improved the physical and lipid oxidation stabilities of the artificial oil bodies. In vitro, release assay confirmed that curcumin in safflower caleosin-rosmarinic acid conjugate-modified AOBs loaded with curcumin (RAOBC) had a slower release efficiency than the free curcumin solution. The hemolysis assay confirmed the biological safety of RAOBC. The assembly of RAOBC can prevent the oxidation and deterioration of safflower oil, broadening its application in industry.

Development of transferosomes for topical ocular drug delivery of curcumin

BackgroundTransferosomes (TFS) are ultra-deformable elastic bilayer vesicles that have previously been used to enhance gradient driven penetration through the skin. This study aimed to evaluate the potential of TFS for topical ocular drug delivery and to compare their penetration enhancing properties in different ocular tissues. MethodsCurcumin-loaded TFS were prepared using Tween 80 as the edge activator. Drug release and precorneal retention of the TFS were evaluated in vitro, while their ocular biocompatibility and bioavailability were evaluated ex vivo using a curcumin solution in medium chain triglycerides as the oily control. ResultsThe TFS had a narrow size distribution with a particle size less than 150 nm and an entrapment efficiency greater than 99.96 %. Burst release from the TFS was minimal and the formulation showed good corneal biocompatibility. Moreover, enhanced corneal and conjunctival drug penetration with significantly greater and deeper drug delivery was observed with TFS. ConclusionTFS offer a promising platform for ocular delivery of hydrophobic drugs. This study, for the first time, elucidates the effect of tissue morphology and osmotic gradients on drug penetration in different ocular tissues.

Development of a Healing, Antimicrobial, and Anti‐Inflammatory Gel Containing Cellulose and Curcumin for Wound Treatment

AbstractThis work presents the production of a gel containing bacterial cellulose and curcumin and the anti‐inflammatory and healing activity assayed according to an animal model (BC‐curcumin). The methodology consisted of the production of bacterial cellulose (BC) using a glycerol‐based culture medium, subsequentially purified and transformed into a powder and added to an ethanolic curcumin solution, acting as a carrier matrix of a bioactive compound, as well as this component present in the gel proposal, promotes the prolonged liberation of curcumin. The BC and BC‐curcumin were characterized by infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. The antimicrobial activity of the developed gel was confirmed through halo inhibition zone assay and minimum inhibitory concentration against strains of Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli, whose presenting halos with diameters of 21, 26, and 14 mm, and concentrations of 63.78, 6.16 and 136.65 μg mL−1 for the three microorganisms, respectively. The healing and anti‐inflammatory activities were observed according to in vivo assays using Wistar rats, which demonstrated a high healing potential, also confirmed by histopathological study of the tissue samples extracted from the healing area.

Precise-color-mutation designing and programmable drop-on-demand printing for intelligent package of shrimp

Biosafe colorimetric labels that can accurately evaluate food freshness have been widely investigated in recent years. The colorimetric macro-array sensor, with the composite solution of curcumin, alizarin and acetic-acid as the indicator, was prepared by means of a self-developed 2D printing device to detect shrimp freshness. The results evidenced the sensor which had high stability, uniform color distribution and great sensitivity could be drop-on-demand printed in batches under the premise of micro-printing. When the TVB-N content of shrimp exceeded 20 mg/100g at all observed temperatures, the sensor abruptly turned from yellow to reddish-brown meanwhile the ΔE value raised sharply, indicating that there was a color mutation at the critical value of shrimp freshness. The macro-array sensor could be recognized by the smartphone to obtain the correlation between the color information (RGB) and TVB-N content, by which the shrimp freshness was determined. Furthermore, the correlation was verified through the WeChat mini-program. When the R value was less than 200 or the G value was below 140, the sensor was brown, suggesting the sample was inedible. Consequently, the system can be applied in food quality control throughout the supply chain.

Enhancing curcumin nanoparticle synthesis through wet-milling: Comparative analysis of physico-chemical and antimicrobial properties of nano-curcumin with micro-curcumin

Curcumin efficacy is limited due to its low water-solubility and absorption, making curcumin nanoparticles (CN) useful alternatives. This study aimed to optimize CN synthesis through wet-milling using Response Surface Methodology (RSM) – Box-Behnken Design (BBD), considering mean particle size, followed by a comparison between CN synthesized under optimum conditions with curcumin. CN presented the least particle size (35.9 ± 0.1 nm) with a polydispersity index (PDI) of 0.0621 ± 0.0093, radical scavenging ability (RSA) of 89.97% ± 0.57, solubility of 10.46 ± 0.03 μg/mL and dissolution rate of 97.9% ± 1.4 under optimum conditions (curcumin solution concentration of 3.73 mg/mL, flow rate of 0.16 mL/min and ultrasonication time of 38.24 min). However, curcumin showed an average particle size of 671.1 ± 0.9 nm, PDI of 0.2060 ± 0.0104, RSA of 78.11% ± 1.05, solubility of 0.96 ± 0.07 μg/mL and dissolution rate of 11.9% ± 1.7, while being more thermodynamically stable. Fourier Transform Infrared (FTIR) spectroscopy demonstrated that both curcumin and CN had an identical chemical structure. X-Ray Diffraction (XRD) and Differential Scanning Calorimetry (DSC) showed lower crystallinity of CN, and microbiological analysis confirmed their stronger antimicrobial activity as compared with curcumin. Our findings revealed that optimizing the synthesis parameters of CN can improve the resulting nanoparticles’ characteristics, supporting their bioavailability and application as antimicrobial and antioxidant agents in food storage.

Curcumin effects on age-related changes in oral immunity: an in vivo study.

The current study aimed to investigate the effects of ageing on oral immunity using β-defensin (DEFB) 1/2 as a marker and evaluate the effects of curcumin (CUR) on these processes. The study sample included thirty male C57BL/6J mice divided into three groups based on the treatment method used. The young control (YC) and old control (OC) groups received 0·5 % methylcellulose-400 (CUR vehicle) orally for 5 days, whereas the CUR group of older mice received a CUR solution suspended in 0·5 % methylcellulose-400 (dose: 3·0 mg/kg body). DEFB1/2 and immune indicator levels were measured in the saliva and salivary glands post-treatment. The saliva volume and protein content were significantly reduced in the OC group compared with the YC group. CUR administration restored these parameters, decreased DEFB1 expression in the salivary gland and increased DEFB1/2 secretion and DEFB2 expression. These findings were supported by epigenetic gene regulation and partial cytokine activation from changes in WD40 repeat protein 5, TNF alpha and IL-1beta. CUR can partially restore age-related changes in oral immune responses and promote oral health, thereby preventing frailty in the older population through a nutritional therapeutic pathway.

Curcumin-Assisted Synthesis of MoS2 Nanoparticles as an Electron Transport Material in Perovskite Solar Cells.

Recently, two-dimensional (2D) transition metal dichalcogenides (2D TMDs), such as molybdenum sulfide (MoS2) and molybdenum selenide (MoSe2), have been presented as effective materials for extracting the generated holes from perovskite layers. Thus, the work function of MoS2 can be tuned in a wide range from 3.5 to 4.8 eV by adjusting the number of layers, chemical composition, elemental doping, surface functionalization, and surface states, depending on the synthetic approach. In this proposed work, we attempt to synthesize MoS2 nanoparticles (NPs) from bulk MoS2 using two steps: (1) initial exfoliation of bulk MoS2 into few-layer MoS2 by using curcumin-cholesteryl-derived organogels (BCC-ED) and curcumin solution in ethylene diamine (C-ED) under sonication; (2) ultrasonication of the subsequently obtained few-layer MoS2 at 60-80 °C, followed by washing of the above chemicals. The initial treatment with the BCC-ED/C-ED undergoes exfoliation of bulk MoS2 resulted in few-layer MoS2, as evidenced by the morphological analysis using SEM. Further thinning or reduction of the size of the few-layer MoS2 by prolonged ultrasonication at 60-80 °C, followed by repeated washing with DMF, resulted in uniform nanoparticles (MoS2 NPs) with a size of ~10 nm, as evidenced by morphological analysis. Since BCC-ED and C-ED produced similar results, C-ED was utilized for further production of NPs over BCC-ED owing to the ease of removal of curcumin from the MoS2 NPs. Utilization of the above synthesized MoS2 NPs as an ETL layer in the cell structure FTO/ETL/perovskite absorber/spiro-OMeTAD/Ag enhanced the efficiency significantly. The results showed that MoS2 NPs as an ETL exhibited a power conversion efficiency (PEC) of 11.46%, a short-circuit current density of 18.65 mA/cm2, an open-circuit voltage of 1.05 V, and a fill factor of 58.66%, at the relative humidity of 70 ± 10% (open-air conditions) than that of the ED-treated MoS2 devices without curcumin. These results suggest that the synergistic effect of both curcumin and ED plays a critical role in obtaining high-quality MoS2 NPs, beneficial for efficient charge transport, lowering the crystal defect density/trap sites and reducing the charge recombination rate, thus, significantly enhancing the efficiency.

Mechanism of Ocular Penetration of Lipophilic Drugs from Lipophilic Vehicles

Since eyedrops have conventionally been formulated in aqueous vehicles, ocular pharmacokinetic studies are generally performed using aqueous buffers to identify physicochemical properties of the drug and the vehicles that influence drug absorption. In recent years, biocompatible lipophilic vehicles are increasingly finding application in ocular drug delivery; however, the mechanism of drug penetration from these non-aqueous vehicles is poorly understood. This study aims to compare ocular penetration of the model lipophilic drug curcumin when incorporated into lipophilic vehicles. To elucidate whether intrinsic solubility in the lipophilic vehicle influences ocular penetration, a curcumin solution and suspension were prepared in medium chain triglycerides (MCT) and squalane, respectively. Ocular penetration and distribution of curcumin from both vehicles was compared and evaluated qualitatively and quantitatively ex vivo. Significantly greater and faster penetration was observed from the squalane suspension than from the MCT solution in all ocular tissues. Our results suggest that the ability of lipophilic drugs to partition out of lipophilic vehicles and into cell membranes, rather than their intrinsic solubility in the lipophilic vehicle, determines the rate and extent of their ocular penetration.

Novel pH-responsive hybrid hydrogels for controlled delivery of curcumin: Overcoming conventional constraints and enhancing cytotoxicity in MCF-7 cells

Traditional drug delivery techniques often have drawbacks such inadequate bioavailability, quick clearance, and non-specific targeting, which may result in unfavorable side effects. Hybrid nanocarriers composed of nanoclay have the potential to be a viable solution to these problems. The goal of this work was to design a biocompatible hybrid nanocarrier that would release curcumin under regulated conditions to specific locations, especially cancer cells. FTIR, XRD, and FESEM were used to effectively construct and evaluate our polyvinyl pyrrolidone/polyethylene glycol/montmorillonite (PVP/PEG/MMT) hybrid hydrogels, verifying their synthesis and intended features. Zeta potential and DLS studies showed a suitable size distribution (∼300 nm) and high stability. The curcumin encapsulation efficiency and release profile were assessed using the use of UV spectrophotometry and the dialysis bag technique. The findings showed a gradual and continuous release that was highly impacted by the acidic environment (which mimicked the characteristics of cancer cells), suggesting pH-responsive activity. The MTT test was used in vitro cytotoxicity experiments to show that curcumin-loaded nanocarriers were more effective against MCF-7 cancer cells than curcumin in solution. Increased rates of necrosis and apoptosis in cancer cells treated with the nanocarrier formulation were further validated by flowcytometry. According to these results, PVP/PEG/MMT hybrid hydrogels have a lot of potential as a cutting-edge drug delivery strategy for curcumin. They may be able to overcome some of the drawbacks of traditional techniques and improve the effectiveness of treatment against cancer cells.

Antibacterial effect ofcurcumin onSalmonella Typhimurium: Invitro and food model studies.

Salmonellosis isamajor foodborne disease transmitted from contaminated poultry products worldwide. Although awide variety ofchemical agents are used inthe prevention offoodborne Salmonellaspp. infections, consumers prefer natural additives, that donot harm human health and donot impair the characteristics offood. Curcumin isayellow-coloured, hydrophobic polyphenol obtained from the rhizome ofthe Curcuma longaL. plant known asturmeric. The purpose ofthis study was toevaluate curcumin's antibacterial activity against S.Typhimurium inchicken meat and invitro. Inthe first step, chicken samples were experimentally contaminated with S.Typhimurium atalevel of2.8×10-7CFU/ml. Then, they were kept ina1, 2, and 3% curcumin solution for 15minutes. Atthe end ofthe treatment, chicken samples were stored at+4°C. The number ofS.Typhimurium inchicken samples was determined according toENISO6579-1. Inthe result ofthe study, thenumber ofS.Typhimurium decreased by2.37, 2.71, and 2.84log levels atthe end ofthe 6thday asaresult ofthe 1, 2 and 3% curcumin treatment, respectively. The MIC value ofcurcumin was determined tobe 362μg/ml for S.Typhimurium.

Integration of Ethanol and the Immune Modulator Curcumin for Immunoablation of Hepatocellular Carcinoma

PurposeTo investigate immuno-ethanol ablation using an ethanol and immune adjuvant formulation as a potent immunoablation approach that can achieve an enhanced anticancer effect in the treatment of hepatocellular carcinoma (HCC). Materials and MethodsEthanol concentration– and exposure time–dependent cellular responses were investigated. Curcumin was combined with ethanol as an immunoablation agent. Cellular uptake of curcumin, cancer cell killing, and inflammatory markers of ethanol-curcumin treatment were characterized. To evaluate the potential in vivo anticancer immunity of ethanol-curcumin treatment, each right and left lobe of rat liver was concurrently inoculated with N1S1 HCC cells and a mixture of treated N1S1 cells (ethanol only or ethanol-curcumin) in Sprague Dawley rats (each group: 5 rats; control: nontreated N1S1 cells). Tumor growth and immune response were characterized with 7T magnetic resonance (MR) imaging, flow cytometry analysis, and immunohistology. ResultsAn optimized ethanol-curcumin (10% ethanol and 0.5% weight/volume (w/v) curcumin solution) treatment contributed to an enhanced cellular uptake of curcumin, increased cancer cell killing, and decreased inflammatory reaction. Ethanol-curcumin–treated N1S1 cell implantation in the rat liver demonstrated N1S1 HCC tumor rejection. The secondary tumor growth by nontreated N1S1 cell inoculation was significantly suppressed at the same time. Activated anticancer immunity was evidenced by significantly increased CD8+ T cell infiltration (3.5-fold) and CD8+–to–regulatory T cell ratio (4.5-fold) in the experimental group compared with those in the control group. ConclusionsEnhanced anticancer effect of immuno-ethanol ablation could be achieved with ethanol-curcumin agent. The results underscore the importance of optimized immunoablation therapeutic procedures for enhanced therapeutic outcomes.

In-flight electro-neutralisation electrospray for pulmonary drug delivery

Pulmonary drug delivery does not only provide non-invasive therapy for local lung diseases but also remarkably enhances systemic absorption of therapeutics owing to the tremendous surface area of the lung and fast transport of active molecules across the respiratory epithelia. In comparison to traditional delivery systems, electrohydrodynamic atomisation (EHDA) is superior in terms of size and production rate control but the high surface charges of resulting particles prohibit its use in drug delivery. To overcome this challenge, we developed an in-flight electro-neutralisation electrospray (IFENE) method which enables the generation of mists of particles in respirable size range with little to no charge. Our approach uses low-frequency alternating current (AC) to produce charge-neutralised sprays with initial velocity due to oppositely charged droplets combination. Experiments and simulations with pure liquid as the working solution were conducted to reveal the underlying mechanism. The applied frequency is found to be the main factor that influences spray stability and formation. Poly (vinylidene fluoride) (PVDF) and PVDF with curcumin solution were electrosprayed via IFENE, producing sprays of organic particles with controlled sizes and neutralised charges. The capability of coupling particle generation in the respirable size range (below 5 μm) and charge reduction (under 400 femtoamperes), along with its simple setup makes IFENE a promising platform technology in inhalation drug delivery.

UV-A-Induced Photoisomerization and Photodimerization of Curcumin: An Ion Mobility Mass Spectrometry Study.

Curcumin, the bioactive compound present in spice plant turmeric, has been shown to exhibit selective phototoxic activities toward mammalian cancer cells, and it is being used extensively as a photosensitizer (PS) in photodynamic therapies (PDT). However, so far, the fate of curcumin toward photochemical transformations is not well understood. Here we report our findings of a number of novel photochemical reaction channels of curcumin in water-methanol mixture, like photoisomerization, photodimerization, and photooxidation (H2-loss). The reaction was performed by irradiating the curcumin solution with ultraviolet (UV) light of wavelength 350 nm, which is abundant in the earth's troposphere. Product identification and structure elucidation are done by employing an integrated method of drift tube ion mobility mass spectrometry (DTIMS) in combination with high-performance liquid chromatography (HPLC) and collision-induced dissociation (CID) of the mass-selected molecular ions. Two photoisomers of curcumin produced as a result of trans-cis configurational changes about C═C double bonds in the excited state have been identified, and it has been shown that they could serve as the precursors for formation of isomeric dimers via [2 + 2] cycloaddition and H2-loss products. Comparisons of the experimentally measured collision cross-section (CCS) values of the reactant and product ions obtained by the DTIMS method with those predicted by the electronic structure theory are found to be very effective for the discrimination of the produced photoisomers. The observed photochemical reaction channels are potentially significant toward uses of curcumin as a photosensitizer in photodynamic therapy.

Evaluation of The Genoprotective Effect of Curcumin Against Methotrexate in Bone Marrow and Spleen Cells in Mice

Curcumin is a yellow pigment produced from the rhizomes of the Curcuma longa plant and a primary chemo preventive component of turmeric is used as a spice and food coloring ingredient. Curcumin has a large number of pharmacological activities, such as anticancer, anti-diabetic, antioxidant, anti-infectious, and anti-inflammatory properties.Investigation of the geno-protective effect of curcumin on methotrexate induces chromosomal aberrations of spleen and bone marrow cells. In this study, 32 mice were used and divided into four groups (eight mice at each group) as follows: Group1 (negative control): Dimethyl sulfoxide was given intraperitoneally to mice every day for ten days.Group2 (positive control): Mice were received a single dose (20mg/kg) of methotrexate intraperitoneally Group3: Mice were received (200mg/kg) of curcumin solution intraperitoneally for ten successive days.Group4: Mice were received (200mg/kg) of curcumin solution intraperitoneally for ten successive days and on the day 11, a single dose of methotrexate ( 20 mg/kg ) was injected intraperitoneally . In animals treated with methotrexate, significant elevations of the chromosomal aberrations were observed along with a decline in the mitotic index. Meanwhile, there was a considerable elevation of the mitotic index and no detectable chromosomal changes in the curcumin-supplemented mice. The number of abnormal cells was reduced significantly in the curcumin-treated group in comparison with the methotrexate-treated group. The ability of curcumin to inhibit methotrexate's cytotoxic effects was shown by the compound's ability to raise the mitotic index. According to this finding, curcumin approved to be a protective agent against genotoxic effects of methotrexate. Keywords: Curcumin, Chromosomal aberrations, Methotrexate, Mitotic index, Mice

Influence of photodynamic action on pure and mixed cultures of gram-negative bacteria: related to growth mechanisms

Gram-negative bacteria present a significant challenge to conventional treatments due to their structurally complex cell walls, setting them apart from their gram-positive counterparts. These structural distinctions, coupled with various antimicrobial resistance mechanisms, make them highly resilient. Photodynamic inactivation (PDI) has emerged as a promising technique to address this challenge, capitalizing on oxidative stress induced by the synergy of light and a photosensitizer (PS). In this study, we delved into the application of PDI and its repercussions on both Klebsiella pneumoniae and Escherichia coli bacteria, in both pure cultures and mixed populations. Our investigation encompassed an analysis of changes in growth curves when influenced by photodynamic and the response to the susceptibility to gentamicin. Methods: Various concentrations (50 μM, 100 μM, and 150 μM) of synthetic curcumin solutions served as PS in treatment groups. Additionally, solvents such as dimethyl sulfoxide and 0.1% sodium dodecyl sulfate (SDS) were evaluated to enhance PS mobility and absorption. Growth curves for pure and mixed cultures were established, both pre- and post-PDI, and in the presence of 0.1% SDS. Blue light irradiation at 30 J cm−2 and 450 nm was employed. The minimum inhibitory concentration (MIC) of the antibiotic was determined with and without PDI + SDS. Results: While PDI did not achieve optimal bacterial reduction for these strains, it did introduce oxidative damage that has the potential to affect other critical aspects of the temporal progression of cultures and their responses to antibiotics. Conclusion: This study shows that even with the minimal impact of PDI in the presence of 0.1% SDS, observable alterations in bacterial growth profiles and MIC values occur and can be used in favor of treatment involving such infections.

A Systematic Evaluation of Curcumin Concentrations and Blue Light Parameters towards Antimicrobial Photodynamic Therapy against Cariogenic Microorganisms.

Dental caries is a highly preventable and costly disease. Unfortunately, the current management strategies are inadequate at reducing the incidence and new minimally invasive strategies are needed. In this study, a systematic evaluation of specific light parameters and aqueous curcumin concentrations for antimicrobial photodynamic therapy (aPDT) was conducted. Aqueous solutions of curcumin were first prepared and evaluated for their light absorbance after applying different ~56 mW/cm2 blue light treatments in a continuous application mode. Next, these same light treatments as well as different application modes were applied to the curcumin solutions and the molar absorptivity coefficient, reactive oxygen species (ROS) release, minimum inhibitory concentration (MIC), and minimum bactericidal concentration (MBC) for Streptococcus mutans and the MIC and minimum fungicidal concentration (MFC) for Candida albicans were measured. After up to 1 min of light treatment, the molar absorptivity of curcumin when added to culture media was lower than that for water only; however, at higher energy levels, this difference was not apparent. There was a noted dependence on both ROS type and cariogenic microorganism species on the sensitivity to both blue light treatment and application mode. In conclusion, this study provides new information towards improving the agonistic potential of aPDT associated with curcumin against cariogenic microorganisms.

A chitosan/alginate coated nano-liposome to improve intestinal absorption of curcumin for oral administration.

Attempts to improve low absorption and rapid metabolic conversion of curcumin were made by developing curcumin-loaded bilayer nanoliposomes coated with chitosan and alginate for intestinal-specific drug delivery. A curcumin-loaded nano-liposome was prepared with optimized formulations with phosphatidylcholine, curcumin, chitosan, and alginate. The particle size of the optimized formulation was approximately 400nm, and the encapsulation efficiency was more than 99%. In the in vitro release study, curcumin release from the curcumin-loaded nanoliposome with double layers of chitosan/alginate (CNL-CH/AL) was suppressed in the simulated gastric fluid (SGF, pH 1.2) and enhanced in the simulated intestinal fluid (SIF, pH 6.8). In the in vivo pharmacokinetic study in rats, the CNL-CH/AL-treated group showed a prolonged absorption pattern of curcumin and the area under the plasma concentration-time curve from 0 to 24h (AUC0-24) was improved 109-fold compared to the control group treated with a curcumin solution without a nanocarrier.

Aerosol assisted synthesis of a pH responsive curcumin anticancer drug nanocarrier using chitosan and alginate natural polymers

In recent years, several nanocarrier synthesis methods have been developed. In cancer therapy, the use of smart nanocarriers is of interest. Smart nanocarriers respond to their environment and can release their cargo in a controlled manner under the action of internal or external stimuli. In this work, we report on the development of an aerosol-assisted method for the synthesis of curcumin-loaded chitosan/alginate-based polymeric nanocarrier (CurNCs). A custom-fabricated multi-nebulizer system was utilized for the synthesis of CurNCs. The developed system comprises three main parts a sprayer, an electric heater tunnel, and a collector. Curcumin and chitosan solutions were sprayed using a pneumatic multinebulizer into the electric heater tunnel to form chitosan-curcumin assemblies. Then, the aerosol was guided into the collector solution containing sodium alginate and tri-poly phosphate aqueous solution for further cross-linkage. The synthesized CurNCs were characterized using TEM, DLS, and FTIR techniques. The TEM size of the nanoparticles was 8.62 ± 2.25 nm. The release experiments revealed that the nanocarrier is sensitive to the environment pH as more curcumin is released at acidic pH values (as is the case for cancerous tissues) compared to physiological pH. The curcumin content of the nanocarrier was 77.27 mg g−1 with a drug loading efficiency of 62%. The in-vitro cytotoxicity of the synthesized nanocarrier was evaluated against the MCF7 breast cancer cell line. The IC50 concentrations for CurNCs and curcumin were obtained as 14.86 and 16.45 mg mL−1, respectively. The results showed that while the empty nanocarrier shows non-significant cytotoxicity, the CurNCs impact the cell culture and cause prolonged cell deaths. Overall, pH-responsive curcumin polymeric nanocarrier was synthesized using a custom fabricated aerosol-based method. The method enabled fast and feasible synthesis of the nanocarrier with high efficiency.

Effect of Birch Sap as Solvent and Source of Bioactive Compounds in Casein and Gelatine Films.

Birch sap consists of a natural water-based solution with valuable compounds such as minerals, sugars, organic acids and phenolic compounds that can be used advantageously in the preparation of edible films. In this study, gelatine- and casein-based films were prepared using birch sap as biopolymer solvent and source of bioactive compounds with the aim of developing new bioactive materials for food packaging. The physical, mechanical, barrier, antioxidant and iron-chelating properties of the obtained films were investigated. Birch sap enhanced the mechanical properties of the films by increasing puncture strength and flexibility, as well as their ultraviolet-visible light barrier properties. In addition, the presence of bioactive compounds endowed the birch sap films with an antioxidant capacity of almost 90% and an iron-chelating capacity of 40-50% with respect to the control films. Finally, to test these films as food packaging material, a photosensitive curcumin solution was packed and exposed to ultraviolet light. Tested films were able to protect curcumin against photodegradation, and the presence of bioactive compounds inside the birch-sap-enriched materials offered an additional 10% photoprotective effect compared to control films. Results showed the potential of birch sap as an environmentally friendly biopolymer solvent and plasticizer that can improve the mechanical and photoprotective properties of the prepared materials.

Antifungal activity of green-synthesized curcumin-coated silver nanoparticles alone and in combination with fluconazole and itraconazole against Candida and Aspergillus species.

Regarding the wide-spectrum antimicrobial effects of curcumin and silver, this study aimed to evaluate the antifungal activity of green-synthesized curcumin-coated silver nanoparticles (Cur-Ag NPs) against a set of Candida and Aspergillus species. Cur-Ag NPs were synthesized by mixing 200 µL of curcumin solution (40 mM) and 15 mL of deionized water. The mixture was stirred for 3-5 min, followed by the addition of 2.5 mL of silver nitrate solution (2.5 mM). The resulting solution was incubated for 3 days. Antifungal susceptibility of 30 fungal isolates of Aspergillus and Candida to fluconazole and itraconazole, as well as the activity of Cur-Ag NPs against the isolates, were determined, both alone and in combination, using broth microdilution according to the Clinical and Laboratory Standards Institute guidelines. Cur-Ag NPs demonstrated promising antifungal activity, particularly against Candida species. The geometric mean value of the minimum inhibitory concentration of Cur-Ag NPs was significantly lower than that of fluconazole for all the studied fungi. Similarly, it was lower than those of itraconazole in C. albicans and A. fumigatus. The minimum fungicidal concentrations of Cur-Ag NPs were markedly better than those of fluconazole but still inferior to those of itraconazole. Cur-Ag NPs demonstrated indisputable antifungal activity and great potential that can be harnessed to combat fungal infections, particularly those caused by azole-resistant strains of Aspergillus and Candida.