Analysis of Freeze-Drying and Rehydration of Açai (Euterpe oleracea Martius)

2015 ◽  
Vol 365 ◽  
pp. 11-16
Author(s):  
R.J. Brandão ◽  
M.M. Prado ◽  
L.G. Marques
Keyword(s):  
Mass Transfer ◽  
Energy Demand ◽  
Freeze Drying ◽  
Moisture Diffusion ◽  
Euterpe Oleracea ◽  
Power Ultrasound ◽  
Ultrasound Waves ◽  
Freeze Dried ◽  
Peleg’S Equation ◽  
Kinetics Of

The freeze-drying rate is essentially low, since it is controlled by internal moisture diffusion. In addition, the application of vacuum and low temperature during the process presents a higher energy demand. Therefore, the search for new strategies to improve water mobility during freeze-drying constitutes a topic of relevant research. The aim of this work was to evaluate the use of power ultrasound to improve freeze-drying characteristics of açai, quantifying the influence of the applied power on both the drying and rehydration kinetics of the material. Açai (Euterpe oleracea Martius) samples were sonicated with two different frequency levels, 20 kHz and 40 kHz, and two sonication times, 3 min and 10 min. Page’s equation considering internal and external resistances to mass transfer provided a good fit of freeze-drying kinetics, while the Peleg’s equation was found to be suitable for describing the rehydration kinetics of freeze-dried açai. Pretreatment of açai with ultrasound waves was not effective. Ultrasound-induced structural disruption in the açai skin hindered the mass transfer during both freeze-drying and rehydration processes.

scholarly journals Morphology and Release Kinetics of Protein-Loaded Porous Poly(L-Lactic Acid) Spheres Prepared by Freeze-Drying Technique

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Takashi Sasaki ◽  
Kazuki Tanaka ◽  
Daisuke Morino ◽  
Kensuke Sakurai
Keyword(s):  
Lactic Acid ◽  
Freeze Drying ◽  
Release Kinetics ◽  
Particle Surface ◽  
Spherical Particles ◽  
Freeze Dried ◽  
Model Drug ◽  
Drug Compound ◽  
Kinetics Of ◽  
Step Mechanism

Freeze-drying a biodegradable polymer, poly(L-lactic acid) (PLLA), from 1,4-dioxane solutions provided very porous spherical particles of ca. 3 mm in radius with specific surface area of 8–13 m2 g−1. The surface of the particle was found to be less porous compared with its interior. To apply the freeze-dried PLLA (FDPLLA) to drug delivery system, its morphology and drug releasing kinetics were investigated, bovine serum albumin (BSA) being used as a model drug compound. Immersion of FDPLLA into a BSA aqueous solution gave BSA-loaded FDPLLA, where mass fraction of the adsorbed BSA reached up to 79%. Time-dependent release profile of BSA in water suggested a two-step mechanism: (1) very rapid release of BSA deposited on and near the particle surface, which results in an initial burst, and (2) leaching of BSA from the interior of the particle by the diffusion process. It was suggested that the latter process is largely governed by the surface porosity. The porosity of both the interior and surface was found to decrease remarkably as the concentration of the original PLLA/1,4-dioxane solution increases, C0. Thus, C0 is a key parameter that controls the loading and releasing of BSA.

scholarly journals Freeze-Drying of Blueberries: Effects of Carbon Dioxide (CO2) Laser Perforation as Skin Pretreatment to Improve Mass Transfer, Primary Drying Time, and Quality

Foods ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 211 ◽  
Author(s):  
Pablo Munzenmayer ◽  
Jaime Ulloa ◽  
Marlene Pinto ◽  
Cristian Ramirez ◽  
Pedro Valencia ◽  
...  
Keyword(s):  
Mass Transfer ◽  
Co2 Laser ◽  
Freeze Drying ◽  
Sharp Decrease ◽  
Linear Increase ◽  
Vapor Flow ◽  
Drying Time ◽  
Transfer Resistance ◽  
Freeze Dried ◽  
Phenomenological Perspective

Freeze-dried berry fruits are generally consumed as they are, whole and without peeling or cutting, as the conservation of their original shape and appearance is often desired for the final product. However, usually, berries are naturally wrapped by an outer skin that imparts a barrier to vapor flow during freeze-drying, causing berry busting. Photo-sequence, experimental, and theoretical methodologies were applied to evaluate the application of CO2 laser microperforations to blueberry skin. Under the same set of freeze-drying conditions, blueberries with and without perforations were processed. The results showed that the primary drying time was significantly reduced from 17 ± 0.9 h for nontreated berries to 13 ± 2.0 h when nine microperforations per berry fruit were made. Concomitantly, the quality was also significantly improved, as the percentage of nonbusted blueberries at the end of the process increased from an average of 47% to 86%. From a phenomenological perspective, the analysis of the mass transfer resistance of nontreated fruits, in agreement with reported studies, showed a Type II curvature, with a sharp decrease at low time, followed by a linear increase. In contrast, blueberries with nine perforations depicted a Type III regime, with a saturation curvature toward the time axis. It was demonstrated that CO2-laser microperforation has high potential as a skin pretreatment for the freeze-drying of blueberries.

Aerosol survival of Serratia marcescens as a function of oxygen concentration, relative humidity, and time

1974 ◽  
Vol 20 (11) ◽  
pp. 1529-1534 ◽  
Author(s):  
C. S. Cox ◽  
S. J. Gagen ◽  
Jean Baxter
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Relative Humidity ◽  
Serratia Marcescens ◽  
Oxygen Concentration ◽  
Freeze Drying ◽  
Cytoplasmic Membrane ◽  
Cell Wall Synthesis ◽  
Freeze Dried ◽  
Kinetics Of

Previously the kinetics of loss of viability of freeze-dried Serratia marcescens 8UK were determined by Cox and Heckly as a function of oxygen concentration and time. Results are presented here when dehydration is brought about by aerosolization into atmospheres of low relative humidity (RH) rather than by freeze-drying. As for freeze-dried S. marcescens, oxygen was toxic and viable decay followed the same kinetics with respect to oxygen concentration and time. The influence of RH upon viable decay (which was not studied in the previous report) was that above 65% RH oxygen was not toxic but was progressively more toxic as the humidity was further reduced. Kinetic analyses of the results indicate that the site for the toxic action of oxygen lies in the interspace between the cytoplasmic membrane and the cell wall. Such a finding is consistent with other data which suggest that cell division and (or) cell wall synthesis in bacteria are inhibited by oxygen.

Drying of a Low Porosity Product (Carrot) as Affected by Power Ultrasound

2008 ◽  
Vol 273-276 ◽  
pp. 764-769 ◽  
Author(s):  
J.V. García-Pérez ◽  
J.A. Cárcel ◽  
J. Benedito ◽  
E. Riera ◽  
A. Mulet
Keyword(s):  
Mass Transfer ◽  
Electric Power ◽  
Ultrasonic Transducer ◽  
Energy Levels ◽  
Drying Kinetics ◽  
Acoustic Energy ◽  
Convective Drying ◽  
Power Ultrasound ◽  
Kinetics Of ◽  
Low Porosity

The main aim of this work was to assess the influence of power ultrasound on mass transfer process during convective drying of a low porosity product submitted to different acoustic energy levels. Drying kinetics of carrot cubes (side 8.5 mm) were carried out at 40 °C and 1 m/s applying different electric power levels to the ultrasonic transducer: 0, 10, 20, 30, 40, 50, 60, 70, 80 and 90 W. Drying kinetics were modelled considering the diffusion theory. From the results, a significant (p<0.05) influence of power ultrasound application on drying kinetics of carrot cubes was found. Drying rate increased as the electric power applied got higher. The influence was only observed above an acoustic energy threshold, which corresponded to an electric power applied to the transducer of 20-30 W. From this threshold, a linear relationship was found between the average effective moisture diffusivity or the mass transfer coefficient and the electric power applied to the transducer.

scholarly journals Simulation of the process kinetics and analysis of physicochemical properties in the freeze drying of kale

2018 ◽  
Vol 32 (1) ◽  
pp. 49-56 ◽  
Author(s):  
Dariusz Dziki ◽  
Renata Polak ◽  
Stanisław Rudy ◽  
Andrzej Krzykowski ◽  
Urszula Gawlik-Dziki ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Freeze Drying ◽  
Total Phenolics ◽  
Drying Time ◽  
Browning Index ◽  
Drying Temperature ◽  
Freeze Dried ◽  
Hue Angle ◽  
Phenolics Content ◽  
Kinetics Of

AbstractInvestigations were performed to study the freeze-drying process of kale (Brassica oleraceaL. varacephala). The process of freeze-drying was performed at temperatures of 20, 40, and 60°C for whole pieces of leaves and for pulped leaves. The kinetics of the freeze-drying of both kale leaves and kale pulp were best described by the Page model. The increasing freeze-drying temperature from 20 to 60°C induced an approximately two-fold decrease in the drying time. Freeze-drying significantly increased the value of the lightness, delta Chroma, and browning index of kale, and had little influence on the hue angle. The highest increase in the lightness and delta Chroma was observed for whole leaves freeze-dried at 20°C. An increase in the drying temperature brought about a slight decrease in the lightness, delta Chroma and the total colour difference. Pulping decreased the lightness and hue angle, and increased browning index. Freeze-drying engendered a slight decrease in the total phenolics content and antioxidant activity, in comparison to fresh leaves. The temperature of the process and pulping had little influence on the total phenolics content and antioxidant activity of dried kale, but significantly decreased the contents of chlorophyllaand chlorophyllb.

Scanning Electron Microscopy-cuticular Lesions on the Roundworm Ascaris Suum

1970 ◽  
Vol 28 ◽  
pp. 114-115
Author(s):  
P. A. Madden ◽  
W. R. Anderson
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Freeze Drying ◽  
Room Temperature ◽  
Secondary Electron ◽  
Distilled Water ◽  
Freeze Dried ◽  
Silver Paint ◽  
To Come ◽  
Scanning Electron

The intestinal roundworm of swine is pinkish in color and about the diameter of a lead pencil. Adult worms, taken from parasitized swine, frequently were observed with macroscopic lesions on their cuticule. Those possessing such lesions were rinsed in distilled water, and cylindrical segments of the affected areas were removed. Some of the segments were fixed in buffered formalin before freeze-drying; others were freeze-dried immediately. Initially, specimens were quenched in liquid freon followed by immersion in liquid nitrogen. They were then placed in ampuoles in a freezer at −45C and sublimated by vacuum until dry. After the specimens appeared dry, the freezer was allowed to come to room temperature slowly while the vacuum was maintained. The dried specimens were attached to metal pegs with conductive silver paint and placed in a vacuum evaporator on a rotating tilting stage. They were then coated by evaporating an alloy of 20% palladium and 80% gold to a thickness of approximately 300 A°. The specimens were examined by secondary electron emmission in a scanning electron microscope.

Revealing gross three-dimensional structure in the SEM

1987 ◽  
Vol 45 ◽  
pp. 656-657
Author(s):  
Sterling P. Newberry
Keyword(s):  
Freeze Drying ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Small Object ◽  
Final Solution ◽  
Dimensional Representation ◽  
X Ray ◽  
Three Dimensional Representation ◽  
Freeze Dried ◽  
Critical Point Drying

The beautiful three dimensional representation of small object surfaces by the SEM leads one to search for ways to open up the sample and look inside. Could this be the answer to a better microscopy for gross biological 3-D structure? We know from X-Ray microscope images that Freeze Drying and Critical Point Drying give promise of adequately preserving gross structure. Can we slice such preparations open for SEM inspection? In general these preparations crush more readily than they slice. Russell and Dagihlian got around the problem by “deembedding” a section before imaging. This some what defeats the advantages of direct dry preparation, thus we are reluctant to accept it as the final solution to our problem. Alternatively, consider fig 1 wherein a freeze dried onion root has a window cut in its surface by a micromanipulator during observation in the SEM.

scholarly journals Effect of Freeze Drying and Simulated Gastrointestinal Digestion on Phenolic Metabolites and Antioxidant Property of the Natal Plum (Carissa macrocarpa)

Foods ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1420
Author(s):  
Faith Seke ◽  
Vimbainashe E. Manhivi ◽  
Tinotenda Shoko ◽  
Retha M. Slabbert ◽  
Yasmina Sultanbawa ◽  
...  
Keyword(s):  
Freeze Drying ◽  
Array Detector ◽  
Gastrointestinal Digestion ◽  
Liquid Chromatograph ◽  
Antioxidant Power ◽  
Intestinal Phase ◽  
Glucosidase Activity ◽  
Freeze Dried ◽  
Small Intestinal ◽  
The Impact

Natal plums (Carissa macrocarpa) are a natural source of bioactive compounds, particularly anthocyanins, and can be consumed as a snack. This study characterized the impact of freeze drying and in vitro gastrointestinal digestion on the phenolic profile, antioxidant capacity, and α-glucosidase activity of the Natal plum (Carissa macrocarpa). The phenolic compounds were quantified using high performance liquid chromatography coupled to a diode-array detector HPLC-DAD and an ultra-performance liquid chromatograph (UPLC) with a Waters Acquity photodiode array detector (PDA) coupled to a Synapt G2 quadrupole time-of-flight (QTOF) mass spectrometer. Cyanidin-3-O-β-sambubioside (Cy-3-Sa) and cyanidin-3-O-glucoside (Cy-3-G) were the dominant anthocyanins in the fresh and freeze-dried Natal plum powder. Freeze drying did not affect the concentrations of both cyanidin compounds compared to the fresh fruit. Both cyanidin compounds, ellagic acid, catechin, epicatechin syringic acid, caffeic acid, luteolin, and quercetin O-glycoside from the ingested freeze-dried Natal plum powder was quite stable in the gastric phase compared to the small intestinal phase. Cyanidin-3-O-β-sambubioside from the ingested Natal plum powder showed bioaccessibility of 32.2% compared to cyanidin-3-O-glucoside (16.3%). The degradation of anthocyanins increased the bioaccessibility of gallic acid, protocatechuic acid, coumaric acid, and ferulic acid significantly, in the small intestinal digesta. The ferric reducing antioxidant power (FRAP), 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) activities, and inhibitory effect of α-glucosidase activity decreased in the small intestinal phase. Indigenous fruits or freeze-dried powders with Cy-3-Sa can be a better source of anthocyanin than Cy-3-G due to higher bioaccessibility in the small intestinal phase.

Process for production of microencapsulated anthocyanin pigments from Rosa pimpinellifolia L. fruits: optimization of aqueous two-phase extraction, microencapsulation by spray and freeze-drying, and storage stability evaluation

2020 ◽  
Vol 16 (9) ◽  
Author(s):  
Halil İbrahim Odabaş ◽  
Ilkay Koca
Keyword(s):  
Freeze Drying ◽  
Fold Increase ◽  
Drying Methods ◽  
Phase Extraction ◽  
Extraction Temperature ◽  
Two Phase ◽  
Freeze Dried ◽  
Anthocyanin Pigments ◽  
Promising Source ◽  
Aqueous Two Phase Extraction

AbstractRosa pimpinellifolia L. fruits (RPF) are promising source of anthocyanin pigments. The objectives of this study were to optimization of the aqueous two-phase extraction (ATPE) process of anthocyanin from RPF and microencapsulation of anthocyanin-rich RPF extract. The optimal ATPE conditions were as follows: 0% HCl, 30% ethanol, 19% ammonium sulfate, and liquid to solid ratio 51.71, 97.71 min, and 30°C extraction temperature. Predicted anthocyanin yield at the optimum conditions was 1578.90 mg cyanidin 3-glucoside equivalent/100 g dry fruit. ATPE resulting in 1.80-fold increase in the purity of anthocyanins when compared to conventional solvent extraction (CSE). The composition of the anthocyanins were determined with HPLC-QTOF-MS. Freeze-drying and spray-drying methods were employed for the production of microencapsulated anthocyanin pigments. The half times of microencapsulated anthocyanins at 4, 25 and 37°C were determined as 12.16, 6.60 and 3.12 months for freeze-dried microcapsules, and 16.50, 9.24 and 4.29 months for spray-dried microcapsules, respectively.

Preparation and Characterization of Chitosan-Based Scaffolds for Biomedical Applications

2006 ◽  
Vol 514-516 ◽  
pp. 1005-1009 ◽  
Author(s):  
José V. Araújo ◽  
J.A. Lopes da Silva ◽  
Margarida M. Almeida ◽  
Maria Elisabete V. Costa
Keyword(s):  
Biomedical Applications ◽  
Freeze Drying ◽  
Average Pore Size ◽  
Composite Scaffolds ◽  
Average Pore ◽  
Chitosan Matrix ◽  
Freeze Dried ◽  
Porous Chitosan ◽  
Interconnected Structure

Porous chitosan/brushite composite scaffolds were prepared by a freeze-drying technique, starting from brushite suspensions in chitosan solutions. The obtained scaffolds showed a regular macroporous and interconnected structure with brushite particles uniformly distributed in the chitosan matrix. The variation of the brushite concentration affected the microstructure of the final freeze-dried scaffold, in particular, its porosity and its average pore size. The yield strengths of the composite scaffolds could also be improved by the increase of the brushite content.

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