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Pt3100d

Manufactured by Kinematica
Sourced in Switzerland

The PT3100D is a high-performance homogenizer designed for laboratory applications. It features a powerful motor and a range of interchangeable homogenizing tools to accommodate various sample volumes and viscosities. The device is capable of efficiently dispersing, emulsifying, and homogenizing a wide variety of materials.

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10 protocols using pt3100d

1

Hydrophilic Matrix Film Preparation

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The hydrophilic matrix, CNP–TPP–CNC, was heated up at 75 ± 5 °C in a water bath to melt the BW lipid phase. The BW was weighed precisely (25% and 50% w/w on a dry basis of the film matter) and then introduced slowly in the matrix suspensions and homogenized at 14,000 rpm for 10 min using high-speed rotor-stator (POLYTRON PT-3100D-Kinematica, Swiss). The hot film-forming emulsion was quickly poured into hydrophobic Petri dishes to cast into films; then, cooled to room temperature in an ice bath. After that, the films were held in an air circulating chamber with constant relative humidity (50% RH) and temperature (20 °C) for 24 hours before peeling off the films. The transparent film samples were stored in desiccators at 60% RH for further characterizations.
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2

Soluble Solids and Tannins Analysis

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These analyses were also carried out with whole fruits and by also separating the secondary epidermis (generated during drying) and internal fruit flesh. To determine total soluble solids (TSS), the samples of each fruit were crushed by a Polytron homogenizer (model PT 3100D, Kinematica, Switzerland). To avoid tannins interfering with total soluble solid measurements, the insolubilization of tannins was previously done following the method of Sugiura et al. [14 ]. Measurements were recorded with a refractometer (Atagomod. PR1) and the results were expressed as °Brix.
Soluble tannins (ST) were determined by the Folin-Denis method [15 ], as described by Arnal and Del Río [16 (link)], and the results were expressed as a percentage of dry weight (DW).
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3

Resveratrol-Loaded PLGA Particle Fabrication

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Poly(lactide-co-glycolide) (PLG) particles were prepared using a single oil-in-water emulsification/solvent evaporation
method as described previously with modifications (Murphy et al., 2018 (link)). Briefly, PLG was
dissolved in dichloromethane (DCM) at 6% (weight/weight, hereafter labeled as 6%) and resveratrol (Sigma) was dissolved in 100%
ethanol at 40 mg/mL. The organic phase, which consisted of varying volume ratios of ethanol and DCM, was added to an aqueous
solution of polyvinyl alcohol (PVA) at 1 or 2% (weight/volume, hereafter labeled as 1 or 2%) in a 1:7 volume ratio and homogenized
using a Kinematica PT3100D homogenizer. The emulsion was then added to an aqueous solution of PVA and stirred for 5 hours,
allowing the DCM and ethanol to evaporate and the particles to harden. The volume of PVA solution in the solvent evaporation
beaker was 5 times greater than the emulsion mixture. The particles were then passed through a 40 μm filter, collected via
centrifugation, and washed 4 times in ultrapure water. Particles were frozen at −20°C and lyophilized overnight.
Particles were then stored protected from light, under vacuum, at room temperature.
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4

Scalable Synthesis of Biodegradable Polymer Particles

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PLG particles were formed using a single oil-in-water emulsification followed by solvent extraction method, reported previously by our group23 (link)–25 (link). Briefly, 50:50 PLG was dissolved in dichloromethane at 4% (wt/wt). 0.6 mL of the 4% PLG solution was added dropwise to 4 mL of an aqueous solution of 0.2% (wt/v) poly(vinyl alcohol) (PVA) or modified PVA and emulsified at 11,000 rpm for 5 minutes using a Kinematica PT3100D homogenizer. Particle formation occurred by adding the emulsion to 16 mL of ultrapure water and then stirring the mixture for 1 hour. The particles were then passed through a 40 μm filter and collected via centrifugation at 250×g. The particles were then washed 4 times by suspending them in ultrapure water and then collecting them via centrifugation (250×g). Washed particles were frozen at −20°C and lyophilized overnight. Recovered particles were stored under vacuum in a dry environment at room temperature. For coumarin 6 loaded particles, all conditions were the same except coumarin 6 was added to the organic phase at 0.3 mg/mL.
Particle mass yield was calculated by dividing the mass of recovered particles by the mass of PLG emulsified. Particle mass yield was calculated according to equation 2.
Mass Yield (%)=(MPTMPLG)*100
Where MPT is the mass of particles recovered from the emulsion, MPLG is the mass of PLG added to the emulsion.
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5

PLGA Microspheres for Pyrene Encapsulation

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Microspheres were formulated according to a modified solvent evaporation technique previously used by us. 26 The core oil was replaced by an equal amount of PLGA to produce microspheres rather than core-shell particles. PLGA (0.133 g) and pyrene (4 mg) were dissolved in DCM (3.2 mL) and acetone (200 mL), which was added slowly over 2 minutes to an aqueous phase containing 1 wt% PVA dispersant (2.5 mL). This was done while homogenizing at 4000 rpm with a Kinematica PT3100D homogenizer equipped with dispersing aggregate PT-DA07/2EC-F101. After 60 minutes of homogenization, the formed emulsion was diluted with an additional volume of aqueous phase (2.5 mL) and left under gentle stirring at 300 rpm overnight for the volatile solvents to evaporate.
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6

Muscle Protein and DNA Quantification

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Muscle samples of 100 mg were weighed and added to pre-cooled saline at a 1:10 (w/v) ratio and then homogenized with a homogenizer (PT-3100D, Kinematica, Malters, Switzerland) to prepare 10% tissue homogenate for further analysis. The concentration of muscle protein was determined using Coomassie brilliant blue kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Muscle DNA content was measured by UV spectrophotometry method [55 (link)].
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7

Nanochitosan Particle Synthesis

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Nanochitosan (NCH) particles were synthesized by the ionotropic gelation method. Four milliliters of TPP solution was introduced drop-wise in a beaker glass containing 40 mL of CH solution under constant high-speed stirring at 10,000 rpm rate, room temperature, for 5 min using rotor-stator homogenizer (POLYTRON PT-3100D-Kinematica, Luzern, Swiss). The cross-linking reaction of TPP and Chitosan was then completed under ultrasonic irradiation for 20 min using an ultrasonic processor (Vibra Cell, Type 72434, 100 Watts, horn diameter: 1.0 mm, Fisher Scientific, Illkirch-Graffenstaden, France).
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8

Muscle Protein and DNA Analysis

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The muscle samples were homogenised with a tissue homogeniser (PT-3100D; Kinematica) in ice-cold PBS EDTA (0•05 M-Na 3 PO 4 , 2•0 M-NaCl, 2 × 10 -3 M-EDTA, pH 7•4) using a 1:10 (w/v) ratio. Protein concentration of muscle homogenates was determined by a published method (31) using a detergent-compatible protein assay (Bio-Rad Laboratories) and bovine serum albumin as standards. Muscle DNA content was evaluated by a fluorometric assay (32) .
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9

Aging Oil Sample Preparation and Homogenization

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The experimental procedure is illustrated in Fig. 1. Firstly, 1.5 L aging oil samples were placed in 2 L beakers, which were then sealed and kept in a large static-sinking water bath (Changzhou Putian Instrument Manufacturing Co., Ltd., SY-1) at 80 °C for more than 3 h (to mitigate the history effect). The aging oil samples in the beaker were then homogenized using a high-speed homogenizer (Kinematica AG, Switzerland, PT 3100 D; 11,000 r/min for 2 mins). Finally, 50 ml of the homogenized sample was dispensed into 50 ml beakers and placed in a small thermostatic water bath (Gongyi Yuhua Instrument Co., Ltd., HH-S2) at 40 °C (to ensure a consistent initial temperature of the samples during ultrasonic irradiation) for spare use.

The experimental flow chart.

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10

Adipose Back-fat Tissue Homogenisation

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Homogenisation of the adipose back-fat tissue was performed using a Kinematica Polytron PT3100D with a PT 12/2 dispersing aggregate (Kinematica, CH).
The mass spectrometer method was developed on a Sciex 6500 QTRAP MS/MS (AB Sciex, USA) connected to a laser diode thermal desorption (LDTD) model 960S with built-in atmospheric pressure chemical ionisation (APCI) (Phytronix, Quebec, Canada).
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