Droplet Polydispersity Research Articles

Emulsifying property of Schinopsis brasiliensis gum in oil-in-water emulsions

Gums are polysaccharide compounds widely used by food, pharmaceutical and biomedical industries for different purposes, in particular due to their ability to stabilize emulsions. In this work, the raw gum of Schinopsis brasiliensis Engl., popularly known as Barauna (GB) was employed in different oil/water formulations in order to evaluate its emulsifying activity in comparison with the commercial Arabic gum (GA) as a positive control. Rheological properties of GB and GA were also evaluated and similar behavior was observed. To study the emulsifying activity of each sample, a three-stage experimental design combined with a 24 full factorial design was developed. At each stage, parameters such as sample concentration, oil concentration, agitation speed and agitation time were recorded. The evaluation of the physical-chemical properties of the emulsions indicated that the stirring speed and oil concentration were the variables that most influenced the stability of emulsions. Regardless of the type of the gum, the emulsions prepared with the highest agitation speed (25000 rpm) and lowest oil concentration (1.0%v/v), in general, showed smaller droplet size and polydispersity index (PDI), and, therefore, greater stability. Emulsions prepared with GB (4.0 mg/mL) were stable for a longer period of time (28 days) than those obtained with GA. These results suggest that the optimization of the speed and time of agitation for the samples preparation containing GB could result in emulsions with the highest potential to achieve the ultrafine (nano) dimensions required for pharmaceutical, medical and food industry applications.

Droplet pair breakup in microfluidic expansion channel

Previous studies on droplet splitting mainly focus on monodisperse droplets, and the understanding of the breakup of polydisperse droplet systems is still lacking. In this work, we experimentally study the breakup of droplet pairs in the expansion region of microfluidic channel. The results show that with the increase in the size ratio of the droplets in the droplet pair, the breakup mode of droplet pairs changes from rear droplet breakup to front droplet breakup, and then to front droplet alternate breakup. The expansion angle can affect the critical size ratio of the splitting mode transition, but it cannot change the transition trend. The expansion angle plays a major role in the splitting time and distance of the droplet pair. When the expansion angle is increased, the splitting time of the droplet pair is reduced and the splitting distance is shorter. Our study extends the understanding of the breakup of non-monodisperse droplet systems and provides a feasible approach for the selective and controllable splitting of droplets, which is important for laboratory-on-a-chip droplet volume manipulation and has potential applications.

Effect of Surfactant Concentration on Physicochemical and Antibacterial Properties of Eugenol Nanoemulsions

Introduction:: Nanoencapsulation has gained popularity in recent decades due to its numerous benefits, such as improved stability, oxidation resistance, retention of volatile ingredients, controlled release, delivery of multiple active ingredients in a row, improvement in organoleptic properties, reduction of toxic side effects, and water solubility. Methods:: The present study was aimed to prepare eugenol nanoemulsions (EuNEs) using non-ionic surfactant (Tween 80) by ultrasound-assisted techniques and to evaluate the effects of surfactant concentration on their droplets size, polydispersity index (PDI), zeta potential, storage stability, antioxidant, and antibacterial activities. Antimicrobial activity of the prepared nanoemulsions was tested against Gram-positive; Staphylococcus aureus, Bacillus subtilis and Gram-negative; Escherichia coli, and Alcaligenes faecalis bacteria using well diffusion method. Results:: The results showed that the droplet size decreased after a threshold Tween 80 concentration (10%), while PDI value increased with the increase in surfactant concentration (Tween 80). method: The droplets size, poly dispersity index (PDI), zeta potential, storage stability, antioxidant, and antibacterial activities of the prepared nanoemusions were characterized. Conclusion:: The prepared EuNEs exhibited good antibacterial activity against all the four bacterial strains: E. coli, A. faecalis, S. aureus, and B. subtilis. conclusion: No phase separation, creaming, layering or deposition of large oil droplet were observed in the prepared nanoemulsions (EuNE-5, EuNE-7.5, and EuNE-10) except in case of 15%, v/v Tween 80 (EuNE-15) during 30 days of storage

Development of Polymeric Micelles for Combined Delivery of Luteolin and Doxorubicin for Cancer Therapy.

Background: Luteolin (LUT) is a bioactive compound with several pharmacological activities including anticancer effect. Doxorubicin (DOX) is an anthracycline chemotherapeutic drug that have proven to be effective in treating various types of cancers. Polymeric micelles (PMs) containing biologically active materials have emerged as prospective dosage forms with high drug-loading, which can add therapeutic benefit to the poorly water-soluble compounds and novel chemical entities. PMs are effective in delivering several drugs, such as anticancer drugs, antifungal drugs, flavonoids and drugs targeting the brain. The aim of the current study is to develop PMs for LUT and DOX as a combined delivery system for cancer therapy. Methods: PMs were prepared using 2.5% of each of LUT and DOX with varying compositions of Poloxamer 188, Poloxamer 407, Vitamin E (TPGS), Poloxamer 123 and Gellucire 44/14 at room temperature. Particle size, polydispersity index, zeta potential, were achieved using Zetasizer Nano particle size analyzer and the sizes were further confirmed with transmission electron microscopy (TEM). Prepared PMs were further characterized using powder X-ray diffraction (PXRD) and fourier transform infrared spectroscopy (FTIR). An MTT assay was performed on breast cancer (MCF-7) cells and liver cancer (HepG2) cells to determine the cytotoxic effect of the different PMs formulations. Results: PMs were successfully developed and optimized using 74.3% Poloxamer 407 with 20.7% Vitamin E (TPGS), and 70% Poloxamer 407 with 25% Gellucire 44/14, respectively. The droplet size and polydispersity index were found to be 62.03 ± 3.99 nm, 91.96 ± 5.80 nm and 0.33 ± 0.05, 0.59± 0.03, respectively for PMs containing TPGS and Gellucire 44/14. Zeta potentials of the PMs containing TPGS and Gellucire 44/14 were recorded as -2.27 ±0.11mV and -7.78 ± 0.10 mV, respectively. The PMs showed a spherical structure with approximately 50-90 nm range evident by TEM analysis. The PXRD spectra of PMs powder presented the amorphization of LUT and DOX. The FTIR spectra of LUT-loaded and DOX-loaded PMs were identical, suggesting consistent PMs composition. The MTT assay showed that the representative combined drug loaded PMs treatment led to a reduction in the viability of MCF-7 and HepG2 cells compared to drug free PMs and pure LUT, DOX alone. Conclusions: PMs with LUT and DOX exhibited significant cytotoxic effects against breast and liver cancer cells and could thus be an important new pharmaceutical formulation to treat cancer.

Ultrasound reforms droplets.

Size-controlled monodisperse droplets are indispensable in food, cosmetics, and healthcare industries. Although emulsion formation from bulk phases is well-explored, a robust in situ method to continuously reform existing emulsions is unavailable. Remarkably, we introduce a continuous flow acousto-microfluidics technique which enables simultaneous trapping-coalescence-splitting of droplets to reform an existing polydisperse emulsion into size-controlled droplets with improved monodispersity. In contrast to conventional approaches, our platform enables controlling droplet characteristics in situ by regulating acoustic power without altering hydrodynamical parameters thereby improving response time and facilitates continuous nozzle-less clogging-free droplet generation from a liquid plug in a chamber instead of from a liquid stream at a narrow junction. The technique can process polydisperse droplets produced not only due to fluid-source fluctuations or unstable jetting regime but also externally by non-microfluidic or inexpensive setups. Our theoretical scaling suggests that the sum of capillary (Ca) and acousto-capillary (Caa) numbers ∼ (1), and predicts the generated droplet size, both agreeing well with the experimental findings. We identify acousto-visco-capillary number, Caav = (Ca Caa)1/2, which governs the generated droplet size. We also explore and characterize acoustic streaming- and coalescence-based mixing of samples inside the trapped plug. Distinctively, our platform is amenable to continuous mixing of inhomogeneous droplets, offering monodisperse mixed-sample droplets, and holds the potential to match current throughput standards through suitable design modifications.

Impact of Lallemantia royleana seed mucilage on the physicochemical, textural, rheological, and in-mouth breakdown behavior properties of cold-set whey protein isolate emulsion-filled gel

This work focused on the Lallemantia royleana seed mucilage (LRSM) effect on the rheological, physicochemical, and microstructural attributes, and the in vivo oral breakdown of cold-set emulsion-filled gel (EFG) based on the whey protein isolate (WPI). Emulsions containing 0.1 and 0.5% LRSM displayed the largest and smallest droplet sizes (3.38 vs. 1.26 μm) and polydispersity index (0.60 vs. 0.23), respectively. Also, the 0.1–0.5% LRSM-WPI EFGs compared to the control had greater elastic modulus in the linear viscoelastic (LVE) region (7006.1–7167.8 vs. 4438.3 Pa), flow-point stress (484.6–540.1 vs. 327.8 Pa), network strength (7227.8–7451.2 vs. 5380.1 Pa.s1z), network extension (10.91–11.44 vs. 10.05), lower LVE limit (1.74–2.26 vs. 2.53 %), same loss tangent (0.17), similar frequency dependence of elastic modulus (0.087–0.091 vs. 0.095), and inhomogeneous microstructures. Hardness, springiness, and chewiness at 0.1% and adhesiveness and cohesiveness at 0.5% LRSM-WPI EFGs were the highest. Raising the LRSM from 0% to 0.5% improved the water-holding capacity (75.49%–87.68%), swelling ratio (0.20%–2.59%), and decreased syneresis (11.08%–9.13%). The 0.5% LRSM-WPI EFG compared to the control needed a higher chew duration (16.22 vs. 11.80 s) and chew cycle (24.76 vs. 18.31), and its bolus had a smaller particle size (0.94 vs. 1.65 mm).

Effect of Different Hydrophilic-lipophilic Balance (HLB) on Droplet Size, Polydispersity Index and Stability of Lemon Myrtle Nanoemulsion

Using mixed non-ionic surfactants Tween/Span, we determined the required hydrophilic-lipophilic balance (HLB) value on the oil in water nanoemulsion of lemon myrtle essential oil. In this study, Span 80 mixed with Tween 80, and Span 20 mixed with Tween 20 were used as mixed non-ionic surfactant. The droplet size, polydispersity index and stability of the lemon myrtle nanoemulsion at different HLB values were obtained over a period of 28 days. Both mixed surfactants have similar required HLB value at HLB 14 due to their smallest droplet size and lowest polydispersity index during the early nanoemulsion preparation. However, after a period of 28 days, nanoemulsion with Span 80-Tween 80 surfactant mixture was more stable compared to Span 20-Tween 20 surfactant mixture. Therefore, HLB 14 using Span 80-Tween 80 surfactant mixture has been selected as the required HLB for lemon myrtle nanoemulsion due to its stability and consistency of droplet size in 28 days.

The Effect of High-Pressure Homogenization Conditions on the Physicochemical Properties and Stability of Designed Fluconazole-Loaded Ocular Nanoemulsions.

The growing interest in high-energy emulsification is a result of its scalability, which is important from an industrial perspective and allows for a more reproducible and efficient production of pharmaceutical formulations. The aim of this study was to evaluate the effect of composition, mainly a fixed surfactant/cosurfactant (Smix) ratio, their concentration, and the parameters of high-pressure homogenization (HPH) processing on the quality and stability of ophthalmic fluconazole-loaded nanoemulsions. After a physicochemical analysis of nanoemulsions containing 20% w/w of oil, as optimal conditions for the HPH process, three cycles at a pressure of 1000 bar were established, obtaining formulations with an average droplet diameter size in the range of 80.63-129.68 nm and PDI values below 0.25. While it was expected that an increasing cosurfactant concentration decreased the droplet size, in the case of formulations containing Tween 20 and 10% w/w of cosurfactants, "over-processing" was observed, identified by the droplet size and polydispersity index increase. Consecutively, the selected formulations were evaluated for in vitro drug release in Franz's cell, antifungal activity, and 30-day stability using NMR spectroscopy. An antifungal activity test showed no significant difference in the antifungal activity between optimal fluconazole-loaded nanoemulsions and a 0.3% aqueous drug solution, but previously, research showed that prepared formulations were characterized by a higher viscosity and satisfactory prolonged release compared to a control. In a 30-day stability study, it was observed that higher HLB values of the used surfactants decreased the stability of the formulations in the following order: Kolliphor EL, Tween 80, Tween 20. The NMR spectra confirmed that Kolliphor EL-based formulations ensured the higher stability of the nanoemulsion composition in comparison to Tween 80 and a better stabilizing effect of propylene glycol as a cosurfactant in comparison to PEG 200. Therefore, the optimization of HPH technology should be focused on the selection of Smix and the Smix:oil ratio in order to prepare stable formulations of high quality.

In vivo and in vitro transdermal availability of Ibuprofen using novel solubility enhancing fluid nanosized carrier systems

The objective of this study was to explore the benefits of transdermal drug delivery systems as an alternative option for patients who are unable to tolerate oral administration of drugs, such as ibuprofen (IB). To achieve this, nonionic surfactants and three cosolvents were employed to develop new microemulsions (MEs) that contained IB as nanocarriers. The aim was to enhance the solubility and bioavailability of the drug after transdermal administration. The MEs were characterised by droplet size, polydispersity index (PDI), and rheological properties. Furthermore, the flux of IB was evaluated by Franz diffusion cells using excised rat skin and in vivo bioavailability using rats. The results showed that the MEs had ideal viscosity and droplet size below 100 nm. Moreover, using the developed MEs, an improvement in the solubility (170 mg/mL) and flux through the rat skin (94.6 ± 8.0 µg/cm2.h) was achieved. In addition, IB demonstrated a maximum plasma level of 0.064 mg/mL after 8 h of transdermal administration in rats using the ME with an increase in the bioavailability of about 1.5 times in comparison to the commercial IB gel. In conclusion, the developed nonionic MEs containing IB can be ideal nanocarriers and promising formulations for the transdermal administration of IB.

Characterization and Determination of the Antibacterial Activity of Baccharis dracunculifolia Essential-Oil Nanoemulsions.

The aim of this study was to evaluate the antibacterial activity of nanoemulsions of Baccharis dracunculifolia essential oil. The volatile compounds of the essential oil were identified using gas chromatography-mass spectrometry. The properties of the nanoemulsions (droplet size, polydispersity index, pH, and electrical conductivity) were determined. The antibacterial activities of the essential oil and its nanoemulsions were evaluated using MIC, MBC, and disk diffusion. The microorganisms used were: Gram-positive bacteria (Staphylococcus aureus ATCC 25923, Bacillus cereus ATCC 14579, Streptococcus mutans ATCC 25175, and Enterococcus faecalis ATCC 29212) and Gram-negative bacteria (Pseudomonas aeruginosa ATCC 27853, Klebsiella pneumoniae ATCC BAA-1706, Salmonella enterica ATCC 14028, and Escherichia coli ATCC 25922). The major volatile compounds of the B. dracunculifolia essential oil were limonene (19.36%), (E)-nerolidol (12.75%), bicyclogermacrene (10.76%), and β-pinene (9.60%). The nanoemulsions had a mean droplet size between 13.14 and 56.84 nm. The nanoemulsions presented lower and statistically significant MIC values compared to the essential oil, indicating enhancement of the bacteriostatic action. The disk diffusion method showed that both the nanoemulsions and the essential oil presented inhibition zones only for Gram-positive bacteria, while there were no results against Gram-negative bacteria, indicating that B. dracunculifolia essential oil has a better antimicrobial effect on Gram-positive microorganisms.

Citronella essential oil-based nanoemulsion as a post-emergence natural herbicide

A natural herbicide nanoemulsion was fabricated from citronella (Cymbopogon nardus L.) essential oil (CEO) and a nonionic surfactant Tween 60 mixed with Span 60 at hydrophilic-lipophilic balance 14 using a microfluidization method. The main constituents of CEO were citronellol (35.244%), geraniol (21.906%), and citronellal (13.632%). CEO nanoemulsion droplet size and polydispersity index (PI) were evaluated by dynamic light scattering (DLS). The smallest droplet size (33.2 nm, PI 0.135) was obtained from a microfluidizer at 20,000 psi, 7 cycles. Nanoemulsion droplet in transmission electron microscopy correlated with DLS confirmed CEO to successfully produce nanoemulsion. The herbicidal activity of the nanoemulsion as a foliar spray was evaluated against Echinochloa cruss-galli and Amaranthus tricolor as representative narrow- and broadleaf weed plants, both of which presented visual toxicity symptoms. The modes of action of the nanoemulsion were then determined in terms of membrane integrity (relative electrolyte leakage; REL), malondialdehyde (MDA), and photosynthetic pigment contents. The results showed increase in REL and MDA which indicated the destruction of the treated plants; additionally, chlorophylls and carotenoid contents were decreased. Consequently, CEO nanoemulsion may have the possibility to act as a natural herbicide resource, and natural herbicides from citronella nanoemulsions could be good alternatives for use in sustainable agriculture.

Computational Investigation of the Water Droplet Effects on Shapes of Ice on Airfoils

The paper presents the results of studying the effects of droplet diameters on the NACA0012 airfoil ice accretion, which have been obtained in the 3D numerical simulation of icing. To simulate the motion of water droplets as a multiphase medium, the Eulerian approach is used, which assumes that water droplets have spherical shapes, do not undergo deformation and breakup, do not interact with each other, and that coalescence/fragmentation of droplets does not take place. Both monodisperse (of the same size) and polydisperse (of various sizes) droplets are considered; they are represented by the spectral Langmuir distributions. These spectral distributions take into account the polydisperse nature of droplets and provide a higher efficiency in predicting ice shapes. The obtained ice shapes on an airfoil are compared with the available experimental and calculated data. It should be noted according to the simulation results that the use of the standard size of droplet diameter equal to 20 μm does not allow for obtaining correct shapes of ice on the leading edge of the wing profile not at all temperature regimes. For temperatures from −20 °C to −10 °C, there is a noticeable difference compared to the experimental data. At the same time, for this temperature range, the use of the Langmuir spectral distribution of droplet diameters relative to 15 μm provides a better agreement of the formed ice forms with the experiment.

Nanoemulsions as a Promising Carrier for Topical Delivery of Etodolac: Formulation Development and Characterization.

This research primarily focuses on the development of innovative topical nanoemulsions for etodolac, aimed at surmounting its inherent limitations. The preparation of etodolac nanoemulsions is accomplished through a combination of high shear homogenization and ultrasonication methods. The optimization of the formulation components is systematically conducted using the design of experiments methodology. The droplet size (DS), polydispersity index (PDI), and zeta potential (ZP) of the optimized formulation were assessed using the differential light scattering (DLS) technique. Surface morphology examinations were conducted using electron microscopy, while interactions between excipients and the drug were analyzed through FTIR analysis. Additionally, in vitro release and ex vivo permeability studies were carried out. Furthermore, anti-inflammatory activity was evaluated in the context of a carrageenan-induced paw edema model in rats. The DS, PDI, and ZP of the optimal formulation were 163.5 nm, 0.141, and -33.1 mV, respectively. The in vitro release profile was assessed as a sustained release by following a non-Fickian drug transport. The flux of etodolac nanoemulsions and coarse dispersions were 165.7 ± 11.7 µg/cm2 h and 59.7 ± 15.2 µg/cm2 h, respectively. Enhanced edema inhibition was observed at 13.4%, 36.5%, and 50.65% for the 6th, 8th, and 24th hours, respectively. Taken together, these results confirmed that nanoemulsions are promising carriers for the topical delivery of etodolac.

Innovative Microemulsion Loaded with Unusual Dimeric Flavonoids from Fridericia platyphylla (Cham.) L.G. Lohmann Roots.

Fridericia platyphylla (Cham.) L.G. Lohmann is a species native to the Brazilian cerrado, with promising bioactivity. The organic fraction of the roots is rich in unusual dimeric flavonoids, reported as potential candidates for cancer treatment. The exploration of these flavonoids is very important, considering their diverse biological activities and the need for innovative therapeutic options. This work aimed to develop and characterize a microemulsion loaded with a non-polar fraction (DCM). The constituents were chosen, and the pseudo-ternary diagram was constructed to determine the region of microemulsion formation. The microemulsions blank (ME), with 3% (ME3) and 5% (ME5) of fraction DCM, were characterized in terms of droplet size, zeta potential, and polydispersity index. Both MEs showed particle sizes <100 nm; only ME3 exhibited better values for polydispersity index and zeta potential and was therefore selected for further study. The organoleptic and physicochemical characteristics were evaluated, revealing limpidity and transparency typical of these microstructures, physiologically acceptable pH, refractive index of 1.42±0.01, and density of 1.017 g/cm3±0.01. The stability tests showed good stability profiles even after exposure to extreme thermal conditions, with minimal changes in pH and the content of the incorporated fraction. The in vitro release study demonstrated that ME3 enabled the controlled release of the fraction, with a cumulative amount released over 60% within 6 h. Furthermore, fraction DCM and ME3 exhibited no toxicity in Tenebrio molitor larvae. The developed microemulsion exhibited excellent properties, so this study represents the first successful attempt to develop a formulation that incorporates the dimeric flavonoid fraction.

Development of Bedaquiline-Loaded SNEDDS Using Quality by Design (QbD) Approach to Improve Biopharmaceutical Attributes for the Management of Multidrug-Resistant Tuberculosis (MDR-TB).

Background: The ever-growing emergence of antibiotic resistance associated with tuberculosis (TB) has become a global challenge. In 2012, the USFDA gave expedited approval to bedaquiline (BDQ) as a new treatment for drug-resistant TB in adults when no other viable options are available. BDQ is a diarylquinoline derivative and exhibits targeted action on mycobacterium tuberculosis, but due to poor solubility, the desired therapeutic action is not achieved. Objective: To develop a QbD-based self-nanoemulsifying drug delivery system of bedaquiline using various oils, surfactants, and co-surfactants. Methods: The quality target product profile (QTPP) and critical quality attributes (CQAs) were identified with a patient-centric approach, which facilitated the selection of critical material attributes (CMAs) during pre-formulation studies and initial risk assessment. Caprylic acid as a lipid, propylene glycol as a surfactant, and Transcutol-P as a co-surfactant were selected as CMAs for the formulation of bedaquiline fumarate SNEDDS. Pseudo-ternary phase diagrams were constructed to determine the optimal ratio of oil and Smix. To optimize the formulation, a Box-Benkhen design (BBD) was used. The optimized formulation (BDQ-F-SNEDSS) was further evaluated for parameters such as droplet size, polydispersity index (PDI), percentage transmittance, dilution studies, stability studies, and cell toxicity through the A549 cell. Results: Optimized BDQ-F-SNEDDS showed well-formed droplets of 98.88 ± 2.1 nm with a zeta potential of 21.16 mV. In vitro studies showed enhanced drug release with a high degree of stability at 25 ± 2 °C, 60 ± 5% and 40 ± 2 °C, 75 ± 5%. Furthermore, BDQ-F-SNEDDS showed promising cell viability in A549 cells, indicating BDQ-F-SNEDDS as a safer formulation for oral delivery. Conclusion: Finally, it was concluded that the utilization of a QbD approach in the development of BDQ-F-loaded SNEDDS offers a promising strategy to improve the biopharmaceutical properties of the drug, resulting in potential cost and time savings.

Size distribution of migrating particles and droplets under gravity in concentrated dispersions measured with static multiple light scattering

HypothesisLight scattering techniques can provide a non-intrusive measurement of particle and droplet size distribution but are limited to relatively diluted liquid dispersions. Measurement of particle velocity distributions (PVD) and particle/droplet size distributions (PSD) in diluted to highly concentrated solid suspensions and emulsions can be performed by coupling the static multiple light scattering technique (SMLS) to mathematical models describing the vertical motion under gravity of polydisperse particles and droplets. ExperimentsMeasurement of the PSD using SMLS was performed on silica particles dispersed in water with monomodal, bimodal and trimodal PSDs ranging from 570 nm and 7.90 µm. Quasi-monodisperse certified latex particles with 815 nm mean diameter dispersed in water and non-controlled emulsions of hexadecane-water emulsions at volume fractions ranging from 0.005 % to 20 % were also characterized with SMLS. These measurements were compared to certified size distributions, and to laser diffraction and dynamic light scattering measurements. FindingsRobust, highly resolutive and concentration-dependent measurement of the PVD and PSD of solid particles and droplets was achieved for diluted to highly concentrated liquid dispersions. As interactions between particles or droplets are dependent on the dispersed phase concentration, accurate characterization of as-formulated industrial liquid dispersions can be performed with SMLS.

Are Most Micrometer Droplets (>10 μm) Wasted in Electrospray Ionization? An Insight from Real-Time High-Speed Imaging.

Electrospray ionization (ESI) is one of the main techniques used in mass spectrometry (MS) of nonvolatile compounds. ESI is a disordered process, in which a large number of polydisperse droplets are projected from a fluctuating Taylor cone and jet protruding ESI emitter. Here, we disclose a system for sectioning electrospray plumes to discrete packets with millisecond and submillisecond lifetime, which are introduced to the MS orifice, one at a time. A high-speed camera was triggered at 10,000 frames per second to capture consecutive images of the electrospray packets transmitted to the mass spectrometer. We further correlated the high-speed images of electrospray packets with MS signals of a test analyte (acetaminophen). Following computational treatment of the images, we determined the number of droplet observations (<300), average diameter of droplets (∼10-20 μm), and average volume of droplets (few tens of picoliters) in the individual electrospray packets. The result shows that most micrometer droplets (>10 μm) do not have any significant contribution to the MS signals. This finding is in agreement with the prior conjecture that most of the MS signals are mainly attributed to nanodroplets. Based on this finding, one can deduce that only a small number of the initial microdroplets effectively carry analyte molecules that undergo ionization. We discuss that, in future, one may propose a way to "recharge" the emitted initial micrometer droplets to increase the efficiency of conventional ESI setups.

Population balance modelling of an electrocoalescer

The mechanism of dehydration of a water-in-oil emulsion is complex and involves the growth of an emulsion of polydispersed water droplets in oil, under an electric field, and their gravitational settling and phase separation. In this work, a simple configuration is chosen to understand the mechanism of this complex process. A population balance-based model is developed to predict the performance of an electrocoalescer. The model explicitly accounts for the coalescence of water drops by the action of dipolar forces and gravity settling. A distributed parameter plug flow and a tank-in-series model are developed to account for the gravity settling. The dynamics of electrocoalescence are captured by analyzing the drop size distribution and mean diameter along with the height of the coalescer and time. A simplified model - considering that monodispersity prevails throughout the process is also developed, and the separation curves are compared with the polydispersed system. The effect of operational parameters, such as the strength of the electric field, water cut, viscosity of oil, the height of the coalescer, and polydispersity in the initial drop size distribution, is investigated. The main insight from this work is that there are essentially three stages of electrocoalescence, a slow initial incubation stage where droplets grow to around 1 mm in size without much settling, followed by a rapid settling of these droplets to set in the fast coalescence stage where most water is removed to result in a lean emulsion, followed by a slow simultaneous electrocoalescence and separation stage of this lean emulsion to result in a final separation. A scaled masterplot for the performance of an electrocoalescer, encompassing the effect of the process parameters is obtained. The model also suggests that electrocoalescence essentially leads to a polydisperse system and a population balance approach is critical to its analysis.

Development, stabilization, and characterization of nanoemulsion of vitamin D3-enriched canola oil.

In this study, the oil-in-water nanoemulsion (NE) was prepared and loaded with vitamin D3 in food-grade (edible) canola oil and stabilized by Tween 80 and Span 80 by using a water titration technique with droplet sizes of 20 to 200 nm. A phase diagram was established for the influence of water, oil, and S-Mix concentration. The outcomes revealed that the particle size of blank canola oil nanoemulsion (NE) ranged from 60.12 to 62.27 (d.nm) and vitamin D3 NE ranged from 93.92 to 185.5 (d.nm). Droplet size and polydispersity index (PDI) of both blank and vitamin D3-loaded NE results were less than 1, and zeta potential results for blank and vitamin D3 loaded NE ranged from -9.71 to -15.32 mV and -7.29 to -13.56 mV, respectively. Furthermore, the pH and electrical conductivity of blank NE were 6.0 to 6.2 and 20 to 100 (μs/cm), respectively, whereas vitamin D3-loaded NE results were 6.0 to 6.2 and 30 to 100 (μs/cm), respectively. The viscosity results of blank NE ranged from 0.544 to 0.789 (mPa.s), while that of vitamin D3-loaded NE ranged from 0.613 to 0.793 (mPa.s). In this study, the long-term stability (3 months) of canola oil NE containing vitamin D3 at room temperature (25 C) and high temperature (40 C) was observed.

Enhancement of Bottle Gourd Oil Activity via Optimized Self-Dispersing Lipid Formulations (SDLFs) to Mitigate Isoproterenol-Evoked Cardiac Toxicity in Rats via Modulating BMP, MMP2, and miRNA-21 and miRNA-23a Genes' Expression.

Bottle gourd (BG) oil (family Cucurbitaceae) has several pharmacological activities including a reduction of the hazard of cardiovascular and atherosclerosis conditions. This work aimed to develop and optimize self-dispersing lipid formulations (SDLFs) of BG oil by applying a full 32 factorial design. The formulation variables (oil concentration and surfactant mixture ratio) showed an obvious impact on the characters of the prepared BG-SDLFs including droplet size (DS), polydispersity index (PDI), emulsification time (ET), and transmission percentage (Tr%). The optimum BG-SDLF composed of 30% oil and Tween 80/Cremophor® RH40 (1:1) showed good emulsification characteristics and a better drug release profile compared with BG oil. In vivo study in isoproterenol-injected rats showed that BG oil and the optimized BG-SDLF improved cardiac function, by elevating the miRNA-23a gene expression level and decreasing miRNA-21 gene expression. They also caused the inhibition of the plasma B-type natriuretic peptide (BNP), N-terminal proatrial natriuretic peptide (NT-pro-BNP), cystatin c, galectin-3, lipoprotein-associated phospholipase A2 (Lp-PLA2), matrix metallopeptidase 2 (MMP2), cardiac troponin I (cTnI), and cardiac troponin T (cTnT). Our study demonstrated that BG oil and the optimized BG-SDLF provided a cardioprotection against isoproterenol-induced cardiac toxicity with better results in groups treated with the optimized BG-SDLF.