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Turbisoft software

Manufactured by Microtrac
Sourced in France

TurbiSoft is a software application developed by Microtrac for the analysis and characterization of particle size and distribution. The software's core function is to provide users with the ability to capture, analyze, and report on data collected from Microtrac's particle sizing instruments.

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5 protocols using turbisoft software

1

Characterization and Stability Evaluation of Vesicular Carriers

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The mean size, size distribution, and z-potential were evaluated by a Zetasizer Nano ZS (Malvern Instruments Ltd., Worchestershire, United Kingdom), following a 1:50 dilution of the samples. Zetasizer Nano is a dynamic light-scattering spectrophotometer (DLS) and a third-order cumulant fitting correlation function was used for sample analysis. This instrument was equipped with a 4.5 mW laser diode operating at 670 nm, which was the light source; the back-scattered photons were detected at 173°. Before starting the analyses, the medium refractive index (1.330), medium viscosity (1.0 mPa × s), and dielectric constant (80.4) were set. The samples were placed in quartz cuvettes to be analyzed [26 (link)].
To evaluate the stability of the prepared vesicular carriers, Turbiscan Lab® Expert, equipped with a Turbiscan Lab Cooler, was used. The photon transmitted (T) and backscattered (BS) through the samples, placed in a cylindrical glass tube, was detected [27 (link)]. The kinetic stability of the samples was evaluated from the data, obtained by TurbiSoft software (Formulaction, L’Union, France). Measurements were taken for 1 h at room temperature (24 ± 1 °C).
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2

Nanoparticle Characterization and Stability Evaluation

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Mean size, size distribution and z-potential were evaluated using a Zetasizer Nano ZS (Malvern Instruments Ltd., Worchestershire, UK), which is a dynamic light-scattering spectrophotometer [46 (link)]. A third-order cumulant fitting was applied as a correlation function. The instrument used a 4.5 mW laser diode operating at 670 nm for size analysis and back-scattered photons were detected at 173°. The medium refractive index (1.330), medium viscosity (1.0 mPa × s), and dielectric constant (80.4) were set before the experiments. Polycarbonate cuvettes were used for the analysis.
The stability of the carriers was determined by using a Turbiscan Lab® Expert [25 (link)], equipped with a Turbiscan Lab Cooler. Briefly, the samples were placed into a cylindrical glass tube and measurements were carried out for 1 h. The photon which was transmitted (T) and backscattered (BS) was recorded. Analysis was carried out at the temperature of 24 ± 1 °C. The analyses were performed using the TurbiSoft software (Formulaction, L’Union, France) and the obtained data were used to evaluate the kinetic stability of the formulations.
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3

Evaluating Formulation Stability via Turbiscan

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A long-term stability study over time of both empty and drug-loaded precursor solutions was performed using a Turbiscan® Lab Expert apparatus equipped with a Turbiscan Lab Cooler. Each precursor solution was gently placed in a cylindrical glass tube and sealed with a suitable plug. Before starting the analysis, the sample was placed into the instrument vial slot, where it was left to equilibrate at 37 ± 0.5 °C (operative temperature) for five minutes. The measurements were conducted for 3 h, during which time the integrated TurbiSoft software (Formulaction, L’Union, France) recorded alterations in delta-backscattering (ΔBS) and delta-transmission (ΔT) profiles as a function of time and vial height [48 (link)], ultimately determining the destabilization kinetic profile by measuring the Turbiscan stability index (TSI). TSI values were directly derived from a sophisticated formula by the software according to Equation (3), as previously reported [49 (link)]: TSI=ih|scani(h)scani1(h)|H
where scani(h) is the average of backscattering recorded at each time (i) of measurement, scani−1(h) is the average of backscattering for the i−1 time of measurement and H represents the sample height. The stability of samples was compared in terms of TSI, considering that TSI values can change from 0 for highly stable systems to 100 for highly unstable compounds [50 ,51 (link)].
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4

Characterization and Stability of Ethosomes

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Mean size, polydispersity index (PdI) and zeta potential were evaluated by photon correlation spectroscopy (ZetaSizer Nano ZS, Malven Instruments Ltd., Worcestorshire, UK) [36 (link)]. The experiments were carried out using a 4.5 mW laser diode operating at 670 nm as a light source. Ethosome® samples were suitably diluted with filtered water–ethanol mixtures at the same ratio used for ethosome® preparation (Sartorius membrane filters 0.22 μm), thus avoiding the multiscattering phenomena, and then placed in quartz cuvettes. Mean size and size distribution data of various ethosome® formulations are the mean of five different batches ± standard deviation.
The stability of ethosomes® was evaluated using a Turbiscan Lab® Expert instrument [37 (link),38 (link)], equipped with a Turbiscan Lab Cooler. Briefly, samples were placed into a cylindrical glass tube and measurements were carried out for 3 h. The photon which was transmitted (T) and backscattered (BS) through the whole height (6 mm) of the sample was recorded. Analysis was carried out at 24 ± 1 °C and TurbiSoft software (Formulaction, L’Union, France) was used for data collection and evaluation of the kinetic stability of ethosome® formulations.
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5

Monitoring Curcumin Dispersion Aggregation

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The aggregation of the MC-curcumin dispersions after GDL addition was followed by multiple light scattering measurements using a Turbiscan Classic MA2000 apparatus (Formulaction, France)
operating with a pulsed near infrared light source at 850 nm. Backscattered intensities all along the sample, more precisely between 15 and 45 mm above the bottom of the test tube, were then recorded every 5 min after GDL addition (corresponding to time zero). With Turbisoft software (Formulaction), the first scan recorded at time zero was substracted from following scans in order to highlight temporal evolution of backscattered intensity (ΔBS). The entire Turbiscan device was thermostated at 20 °C. Turbiscan measurements were acquired 3 min after GDL addition and sample stirring. Assays were performed in triplicate.
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