Porosity and Water Activity Effects on Stability of Crystalline β‐Carotene in Freeze‐Dried Solids

Abstract: Stability of entrapped crystalline β‐carotene as affected by water activity, solids microstructure, and composition of freeze‐dried systems was investigated. Aliquots (1000 mm³, 20% w/w solids) of solutions of maltodextrins of various dextrose equivalents (M040: DE6, M100: DE11, and M250: DE25.5), M100‐sugars (1:1 glucose, fructose and sucrose), and agar for gelation with dispersed β‐carotene were frozen at ?20, ?40, or ?80 °C and freeze‐dried. Glass transition and α‐relaxation temperatures were determined with differential scanning calorimetry and dynamic mechanical analysis, respectively. β‐Carotene contents were monitored spectrophotometrically. In the glassy solids, pore microstructure had a major effect on β‐carotene stability. Small pores with thin walls and large surface area allowed β‐carotene exposure to oxygen which led to a higher loss, whereas structural collapse enhanced stability of β‐carotene by decreasing exposure to oxygen. As water plasticized matrices, an increase in molecular mobility in the matrix enhanced β‐carotene degradation. Stability of dispersed β‐carotene was highest at around 0.2 a_w, but decreasing structural relaxation times above the glass transition correlated well with the rate of β‐carotene degradation at higher a_w. Microstructure, a_w, and component mobility are important factors in the control of stability of β‐carotene in freeze‐dried solids Practical Application: β‐Carotene expresses various nutritional benefits; however, it is sensitive to oxygen and the degradation contributes to loss of nutritional values as well as product color. To increase stability of β‐carotene in freeze‐dried foods, the amount of oxygen penetration need to be limited. The modification of freeze‐dried food structures, for example, porosity and structural collapse, components, and humidity effectively enhance the stability of dispersed β‐carotene in freeze‐dried solids.     

Enzyme stability of microencapsulated Bifidobacterium animalis ssp. lactis Bb12 after freeze drying and during storage in low water activity at room temperature

Abstract: Stability of enzymes such as β‐galactosidase (β‐gal), β‐glucosidase (β‐glu), lactate dehydrogenase (LDH), pyruvate kinase (PK), hexokinase (HK), and ATPase of microencapsulated Bifidobacterium animalis ssp. lactis Bb12 after freeze‐drying and after 10 wk of storage at low water activity (a_w) at room temperature was studied. Bacteria were microencapsulated using alginate formulation with or without mannitol fortification (sodium alginate and mannitol [SAM] and sodium alginate [SA], respectively) by creating gel beads followed by freeze drying. Two types of dried gel beads were then stored at low a_w, such as 0.07, 0.1, and 0.2; storage in an aluminum foil was used as control. All storage was carried out at room temperature of 25 °C for 10 wk. Measurement of β‐gal, β‐glu, LDH, PK, HK, and ATPase (with or without exposure to pH 2.0 for 2 h) activities was carried out before freeze drying, after freeze drying, and after 10 wk of storage. There was a significant decrease in almost all enzyme activities, except that of PK. SAM and SA showed no different effect on maintaining enzyme activities during freeze drying. Storage for 10 wk at room temperature at various low a_w using SAM and SA system had a significant effect on retention of most enzymes studied, except that of PK and LDH. Storage at a_w of 0.07 and 0.1 was more effective in maintaining enzyme activities than storage at a_w of 0.2 and in an aluminum foil. However, mannitol fortification into alginate system did not significantly improve retention of enzymes during 10 wk of storage.     

Degradation kinetics of beetroot pigment encapsulated in polymeric matrices

Kinetic studies on the degradation of water‐soluble beetroot pigment, mainly consisting of the betalain betanin, encapsulated in three different matrices (pullulan and two maltodextrin samples differing in their molecular weight) were carried out under various water activity (a_w = 0.23, 0.43, 0.64, 0.75 and 0.84) and temperature (30, 40 and 50 °C) conditions. The water sorption behaviour of these materials was also examined. Degradation of the pigment was monitored by absorbance measurements at 537 nm (λ_max of betanin). The highest values of the rate constants for degradation were observed at an intermediate water activity level (a_w = 0.64) for all matrices and all three storage temperatures examined. An attempt to relate the degradation kinetics to the molecular mobility of the wall material was not successful. Pigment losses were observed even at temperatures below the glass transition temperature (T_g) of the polymeric matrices, although degradation was largely slowed down in the glassy state. In the vicinity of the T_g zone, where all polymers go through a glass → rubber transition, there was not a distinct change in the reaction rate, which could reflect the pronounced changes in molecular mobility of the wall material. In fact, some of the lower degradation rates were observed mostly under conditions where the matrices were fully plasticised (ie rubbery) and ‘collapsed’, implying that the degradation kinetics is not governed by factors related only to the physical state of the polymeric wall material. © 2001 Society of Chemical Industry     

Fruit snacks from raspberries: influence of drying parameters on colour degradation and bioactive potential

Raspberries were dehydrated using air and freeze‐drying with wet and dry sugar infusion pretreatments. Product quality factors such as colour, bioactive compounds, antioxidant capacity and sensorial characteristics were analysed. Special emphasis was placed on the analysis of anthocyanin degradation and its relationship with colour deterioration and with polymeric compounds development and browning. Freeze‐dried raspberries presented a higher retention of bioactive compounds and a lower content of polymeric compounds than air‐dried ones. Dried samples without pretreatment (control) showed the highest retention of total phenolic content (freeze‐dried ≈82% and air‐dried ≈37% retention), but the lowest sensory acceptability. Although sugar infusion pretreatments caused an important loss of bioactive compounds (9–18% of TPC retention), a higher sensorial acceptability was obtained. Pretreatments with bisulphite and acid allowed obtaining the best quality attributes in terms of anthocyanin and polyphenol content, antiradical activity and colour retention. Polyphenol intake through pretreated dried raspberries (115–299 mg gallic ac./100 g intake) would be higher in some cases than that of usually consumed foods as vegetables, cereals and several fresh fruits.     

Browning reactions during storage of low-moisture Australian sultanas: Further evidence for arginine-mediated Maillard reactions during storage, and some effects of vine-shading and harvest date

Sultana grapevines (Vitis Vinifera L. cv. Sultana syn. Thompson Seedless) were subjected to four shading regimes: 50% shading (1), 25% shading (2), fully exposed‐top of canopy (3) and beneath canopy (4) and harvested early (21 February) and late (13 March) in the 1996/1997 sultana season. Grapes from each of the eight field‐treatment combinations represented a range of maturities (14.4 to 23.50^oBrix). Grape samples from each of the treatments were dipped and dried to 18% moisture, with half of each of the sultana samples further reduced in moisture by sunfinishing on plastic sheets in direct sun. These field treatments resulted in sixteen unique dried sultana bulk samples with a range of initial chemico‐physical properties; a_w (0.481–0.691), skin‐polyphenoloxidase (PPO) activity (4.40–9.05 μmol O₂/g.minute) free arginine in skin tissues (1.0–5.10 mg/g) and protein (16.40–27.18 mg/g). Sultanas were stored at 10^oC and 30^oC in either the presence or absence of oxygen for 10 months, and changes in CIE L*a*b* tristimulus values, hue‐angle (h_ab*) and chroma (C_ab*) were monitored. Significant changes in sultana colour occurred in samples stored at 30^oC, especially in higher a_w non‐sunfinished sultanas. Although browning was more intense in the presence of oxygen, significant browning also occurred in the absence of oxygen. Lower concentrations of 5‐hydroxy methylfurfural, a key marker of Maillard browning in samples stored at 30^oC in the presence of oxygen, indicated that the non‐enzymatic reactions were sensitive to oxygen. Changes in the concentration of trans‐caftaric acid, the main substrate of grape PPO, were also measured during sultana drying. Storage browning (changes in L*, b*, h_ab*, C_ab*)in dried sultanas could be predicted by regression models using pre‐storage a_w, free‐skin arginine or Kjeldahl protein after 10 months' storage between 10^oC and 30^oC. Non‐enzymatic and Maillard‐type reactions (sensitive to both oxygen and a_w), made an important contribution to sultana storage browning. We provide only weak evidence that either shaded (immature) or green fruit was more susceptible to storage browning.     

Browning reactions during storage of low-moisture Australian sultanas: Evidence for arginine-mediated Maillard reactions

Browning during storage of low‐moisture dried Vitis Vinifera L. cv. Sultana (Thompson Seedless) grapes was examined in a multifactorial treatment and storage trial. Grapevines were subjected to two different levels of sun exposure, harvested fruit was dipped and subjected to different drying treatments to obtain a range of initial moisture contents (a_w= 0.419–0.558). The storage effects of temperature (10^oC and 30^oC), and the presence of oxygen on colour change (CIE L*a*b* tristimulus values, hue‐angle (h_ab*)) and chroma (C_ab*) over a fourteen‐month period were observed. The most significant changes in colour were measured for samples stored at 30^oC, both aerobically and anaerobically, although the largest changes occurred in the presence of oxygen. Initial a_w had a strong effect on colour changes; higher a_w non‐sunfinished samples underwent more significant browning compared to lower a_w sunfinished controls regardless of their oxygen status. Changes in the concentration of the free‐arginine and free‐proline, the most abundant free amino acids in sultanas, were monitored throughout the storage period. Free arginine decreased significantly at 30^oC in both the absence and presence of oxygen, whereas free proline increased (at both 10^oC and 30^oC), implying that free proline did not play a role in browning reactions at those temperatures. In addition to the decreases in free arginine, the concentration of 5‐hydroxymethyl furfural (5‐HMF), a marker of Maillard browning reactions, increased significantly in samples stored at 30^oC. Significant differences in the concentrations of 5‐HMF under the two oxygen conditions indicated sultana Maillard reactions, and possibly other non‐enzymatic browning processes, were oxygen sensitive.     

Death rates of Salmonellae in fishmeals with different water activities. I. During storage

Fishmeals with different moisture contents, having water activities (a_w) ranging from 0.34 to 0.71, were infected with strains of Salmonella oranienburg or S. senftenberg and were stored at 15, 20 and 30°c, packed in nitrogen or air. The initial death rates (calculated over storage periods of 70 days) were not appreciably influenced by reduction of a_w from 0.71 to 0.54. Further reduction of a_w to 0.34 caused a decrease of the initial death rate, in particular in meals stored at 15 or 20°c. As compared with fishmeals packed in air, meals packed in nitrogen showed a decrease of initial death rates, especially in meals with the lowest a_w and stored at 15 and 20°c. Death rates calculated over longer storage periods were smaller than initial death rates, in particular in meals with a_w 0.54 stored at 15 and 20°c and meals with a_w 0.34 stored at 15, 20 and 30°c. Pelletisation of meals with a_w 0.72-0.74 caused a 10²-10³-fold reduction of initial Salmonella counts. The death rates of salmonellae which survived the pelletisation treatments were of about the same order as found for the initial death rates of salmonellae in non-pelletised meals with about the same a_w.     

Water Adsorption of Peanut Kernels in a Closed System with Respect to Moisture Transfer

Adsorption isotherms of peanut kernels, Tainan # 9 and #11, were determined at 30°C and used as reference to determine the a_w at equilibrium. The changes of the apparent a_w and moisture of three weighed dried kernels in closed systems stored with distilled water were determined in an electric hygrometer and a series of vessels at 30°C. A nonequilibrium state of moisture and apparent a_w gradients of the kernels was observed in the early stages of 144 hr storage. In a 90 min experiment with the hygrometer at 30°C, the vapor adsorption rate and final apparent a_w decreased in order with the increase of the number of kernels, from 1 to 7, stored with saturated K₂Cr₂O₇ salt (a_w= 0.98 at 30°C). Vapor adsorption rate and final apparent a_w of Tainan # 9 were slightly higher than those of # 11.     

Effect of hydrocolloid addition and microwave-assisted freeze drying on the characteristics of foamed raspberry puree

Foamed fruit purees can be dried and consumed as snacks. This study compares the characteristics of foamed raspberry puree dried via microwave-assisted freeze drying and conventional freeze drying. The effect of potato protein (PP) (as a foaming agent), maltodextrin (MD) (as a foam stabilizer), and microwave power on the product characteristics was investigated. The puree contained 18%–20% higher content of anthocyanins and ascorbic acid than unprocessed raspberries. The retention of ascorbic acid and anthocyanins increased with increasing concentrations of MD and PP. Both drying methods resulted in 66%–81% retention of ascorbic acid and 53%–84% retention of total anthocyanins. The higher drying rates obtained at higher maltodextrin concentrations resulted in higher ascorbic acid and anthocyanin retention. The total color difference was significantly higher for the foam with 30% MD (w/w) at 2.0 W g⁻¹, accounting for the formation of hot spots. Protein concentration did not have a considerable effect on product color. Increasing the maltodextrin concentration yielded a harder foam structure, while increasing the protein concentration had the opposite effect. Overall, microwave-assisted freeze drying was found to be a promising alternative to conventional freeze drying, as it offers a more efficient drying process with comparable product quality.     

Effect of caking and stickiness on the retention of spray‐dried encapsulated orange peel oil

Flavour microcapsules containing amorphous carbohydrate as wall material can undergo changes such as crystallisation, clumping, sticking and caking during handling and storage. Such physical changes may lead to the release of entrapped flavours. The objective of this study was to investigate the effect of storage temperature and water activity on caking, stickiness and glass transition temperatures and to evaluate the relative degree of protection provided to orange peel oil entrapped in mesquite (Prosopis juliflora) gum by spray drying. The powders were stored at water activities (a_w) ranging from 0.108 to 0.972 at 25 and 35 °C. The surface caking temperature (T_sc) and advance caking temperature (T_ac) were determined by the modified ampoule and sealed glass tube methods respectively. The glass transition temperature was determined by differential scanning calorimetry. Changes in the amount of encapsulated oil were determined by Clevenger hydrodistillation. As expected, both T_sc and T_ac decreased with increasing storage a_w. Above a_w 0.628 the powders caked and collapsed during storage at 35 °C. Below a_w 0.628 the capsules were not damaged and high retention levels (above 90%) were obtained. Increasing a_w in the range 0.743–0.972 caused progressive dissolution of the wall polymer, and the retention level dropped sharply. The volatiles are protected and retained by mesquite gum as long as the capsule structure remains intact. Copyright © 2003 Society of Chemical Industry     

Phytochemical stability in dried apple and green tea functional products as related to moisture properties

In this study, apple products made with and without added green tea extract were freeze-dried and stored for up to 45 days at 30 °C in low and intermediate moisture environments (water activity, a_w, 0.11, 0.22, 0.32, 0.57, and 0.75). Kinetic models were developed for the changes in color and decreases in contents of selected green tea and apple monomeric and polymeric flavanols and ascorbic acid. Moisture isotherms were developed for each product. At various moisture levels, the glass transition temperature (T_g) was measured by DSC and water mobility by ¹H NMR. Chemical changes were related to T_g, a_w, and water mobility in the products.Phytochemical degradation occurred more rapidly at higher moisture contents, except for caffeine which was stable. In the product containing apple with green tea, the content of monomeric flavan-3-ols decreased by 34% and 39% after 45 days of storage at a_w of 0.56 and 0.75, respectively. Phytochemical degradation correlated with increasing a_w, T_g, and water mobility. This study showed that, in general, storage at a_w 0.75 most affected phytochemical stability and color.     

Drying characteristics and thermal degradation kinetics of hardness,anthocyanin content and colour in purple‐ and red‐fleshed potato (Solanum tuberosum L.) during hot air drying

Purple‐fleshed potatoes (PFP) and red‐fleshed potatoes (RFP) were dried using hot air. The hardness, anthocyanin content and colour in PFP and RFP during drying were evaluated at 60, 70 and 80 °C. The hardness was characterised by a softening stage in the early drying period, followed by a hardening stage. The times to reach at the transition were 420, 300 and 240 min at 60, 70 and 80 °C, respectively, for PFP, and 480, 360 and 240 min for RFP. However, the moisture content of both PFP and RFP at the transition time was identical at 0.3 (d.b.). The two stages of hardness changes were well described by combining two modified first‐order kinetics models. The activation energy (E_a) for the degradation of anthocyanin in PFP and RFP was 25.12 and 28.43 kJ mol^?1, respectively. The E_a values demonstrated that the thermal sensitivity of PFP was higher than that of RFP.     

Effect of water activity on the inactivation kinetics of Escherichia coli O157:H7 by electron beam in ground beef, chicken breast meat, and trout fillets

Water activity (a_w) of ground beef, chicken breast meat, and trout fillets was modified to intermediate (a_w 0.98–0.99) and lowest (a_w 0.94–0.96) levels. The meat samples with modified and unaltered (native, a_w 1.00) a_w were inoculated with Escherichia coli O157:H7 and subjected to electron beam (e‐beam). Survivor curves were plotted and the D₁₀‐values were calculated. The D₁₀‐values ranged from 0.22 kGy for trout at native a_w to 0.33 kGy for beef at intermediate, and chicken and trout at lowest a_w. Regardless of the species, a_w reduction increased E. coli resistance to e‐beam, suggesting that even small depletion of unbound water from food increases survival. The difference of the D₁₀‐values between the samples at intermediate and lowest a_w was insignificant. E‐beam could be used before a_w‐reducing techniques are applied to food products. However, this would require stringent microbial control following e‐beam processing. The ‘tailing’ of survivors was observed for some samples with reduced a_w.     

Changes during storage of dried Moringa oleifera leaves prepared by heat pump‐assisted dehumidified air drying

Moringa oleifera leaves contain phytochemicals that are retained during heat pump‐assisted dehumidified air drying. Changes in phytochemicals, antioxidant capacity and colour were evaluated at 15–35 °C, during storage of dried leaves in polypropylene (PP) or high barrier (PET/Al/PE) packaging for up to 6 months. The a_w of samples in PP increased from 0.373 to 0.669. Decreases in total phenolics were greatest at 35 °C in PP (48%) and least at 15 °C in PET/Al/PE (19%). There were few significant changes in DPPH inhibition after 2 months storage. There was little change in kaempferol and some increase in quercetin. During storage, samples became less green, suggesting breakdown in chlorophyll had occurred. The degradation of flavonoids followed first‐order kinetics. The half‐life for total flavonoids ranged from 2.13 to 1.47 months for samples stored in PP and from 2.59 to 1.83 months for samples stored in PET/Al/PE.     

Using Dielectric Relaxation Spectroscopy to Characterize the Glass Transition Time of Polydextrose

Dielectric relaxation spectroscopy was used to characterize the glass transition time, t_g, of polydextrose, where the glass transition temperature, T_g, and water activity, a_w (relative humidity), were held constant during polydextrose relaxation. The t_g was determined from a shift in the peak frequency of the imaginary capacitance spectrum with time. It was found that when the peak frequency reaches 30 mHz, polydextrose undergoes glass transition. Glass transition time, t_g, is the time for polydextrose to undergo glass transition at a specific T_g and a_w. Results lead to a modified state diagram, where T_g is depressed with increasing a_w. This curve forms a boundary: (a) below the boundary, polydextrose does not undergo glass transition and (b) above the boundary, polydextrose rapidly undergoes glass transition. As the boundary curve is specified by a t_g value, it can assist in the selection of storage conditions. An important point on the boundary curve is at a_w = 0, where T_g0 = 115 °C. The methodology can also be used to calculate the stress‐relaxation viscosity of polydextrose as a function of T_g and a_w, which is important when characterizing the flow properties of polydextrose initially in powder form.     

Growth and Enterotoxin A Production by Staphylococcus aureus in Precooked Bacon in the Intermediate Moisture Range

Different water activities were obtained in precooked bacon by varying the frying time. Water activity (a_w) correlated best to the moisture, salt and protein content. When stored aerobically at 37°C, S. aureus A100 was capable of rapid growth in precooked bacon at a a_w of 0.84 or above, whereas at 20°C a a_w of 0.88 or higher was required. Under anaerobic storage at 37°C, growth was observed at a a_w of 0.90, and at 20°C slight growth was noted at a a_w of 0.91. The increase in the minimal a_w required for aerobic growth at the lower temperature was reflected in the differences between the isotherms obtained at 37°C and 20°C. The maximum populations achieved were higher for samples stored aerobically. Enterotoxin A (19–821 ng/g) was found in all aerobically stored samples where growth occurred. Enterotoxin A (38–109 ng/g) was also found in all anaerobically incubated samples where the population of S. aureus increased more than one logarithmic cycle.     

Effect of Dehydration on Raspberries: Polyphenol and Anthocyanin Retention, Antioxidant Capacity, and Antiadipogenic Activity

ABSTRACT:  Fresh and dried raspberries prepared by freeze drying (FD), microwave-vacuum (MIVAC), hot-air drying (HAD), and a combination of hot-air drying and microwave-vacuum (HAD/MIVAC) drying methods were evaluated for polyphenol retention, total polyphenol and anthocyanin contents, total antioxidant capacity, and antiadipogenic activity (the inhibition of fat cell development). Ellagic acid and quercetin were present in the largest concentrations in fresh and dehydrated raspberries. Dehydration led to a loss of polyphenols and anthocyanins and antioxidant capacity. Polyphenols (aglycone form) were retained in the greatest amount: 20% (freeze dried) to 30% (HAD/MIVAC) (fresh = 100%). A total of 30% of polyphenols (glycoside form) were retained in raspberries dried by the HAD/MIVAC methods with 5% of retention observed for raspberries dried by FD, HAD, or MIVAC. FD and MIVAC resulted in higher retention of anthocyanins (aglycone form) than other drying methods. It was also observed that antioxidant activity was reduced by dehydration. Adipogenesis was inhibited by polyphenolic glycosides (30%) and aglycones (30% to 40%) in fresh and HAD/MIVAC raspberries. Extracts from dried raspberries by HAD/MIVAC methods were relatively more effective at inhibiting adipogenesis compared to HAD and FD dried raspberries.     

Effects of Water Activity on the Lipid Oxidation and Antioxidants of Dried Laver (Porphyra) During Storage in the Dark

Lipid oxidation and antioxidant degradation in dried laver (Porphyra) were determined during storage at water activities (A_w) of 0.11, 0.30, 0.51, 0.75, or 0.89 in the dark at 40 °C for 15 d. Lipid oxidation was evaluated by measuring peroxide value (POV) and conjugated dienoic acid (CDA) contents, and fatty acid composition was analyzed by gas chromatography. Contents of polyphenols, tocopherols, and porphyran were determined by spectrophotometry, HPLC, and gravimetry, respectively. The POV and CDA contents of the dried laver lipids increased during storage as A_w increased from 0.11 to 0.30, 0.51, 0.75, and 0.89, whereas the relative content of eicosapentaenoic acid was decreased; however, the contents of polyphenols, α‐tocopherol, and porphyran in dried laver showed the reverse phenomena. Lipid oxidation and antioxidant degradation in dried laver sharply increased at an A_w of 0.51. Polyphenols, α‐tocopherol, and porphyran contributed to reduction of lipid oxidation in dried laver. The degree of lipid oxidation of dried laver was more dependent on the concentration of α‐tocopherol than that of either polyphenols or porphyran during storage in the dark. The results strongly suggest that the quality of dried laver can be improved by preserving tocopherols as much as possible while decreasing A_w during storage.     

Storage stability of the natural colourant from Justicia spicigera microencapsulated in protective colloids blends by spray‐drying

Muitle (Justicia spicigera), a Mexican native plant, produces a purple aqueous extract (MAE) because of its anthocyanin content. The aim of this work was to microencapsulate MAE by spray‐drying in two different protective colloids blends in a 1:1 weight ratio: gum Arabic‐mesquite gum (GA50‐MD50) and mesquite gum‐maltodextrin DE10 (MG50‐MD50), yielding the microcapsules M_GA50‐MD50 and M_MG50‐MD50. The minimum integral entropy of the microcapsules was determined at 20, 35 and 40 °C, and the resulting water activities (a_W) were 0.555, 0.592, 0.627 for M_GA50‐MD50 and 0.581, 0.587, 0.648 for M_MG50‐MD50, respectively. These a_W temperature sets were considered as the most adequate conditions for achieving maximum storage stability of the microcapsules. Total anthocyanin content (TAC) and total colour change (ΔE) suffered considerable degradation at all storage conditions, but that degradation was significantly inhibited by encapsulating MAE in the biopolymers blends especially that made up by MG50‐MD50.     

Effects of conventional and nonconventional drying on the stability of Bifidobacterium animalis subsp. lactis INL1

Freeze, spray, vacuum, microwave vacuum‐ and microwave freeze‐drying were applied to Bifidobacterium animalis subsp. lactis INL1. Freeze and microwave freeze‐drying showed the highest survival after drying. When a storage test (25 °C; oxygen) was performed, these cultures were the most sensitive ones at a_w = 0.23, but the addition of lactose improved their stability after 8 weeks. Flow cytometry was useful to assess viability after drying but not during storage. Our results show that dehydration technologies other than freeze‐drying might be suitable alternatives that deserve further investigation for the preservation of sensitive probiotic bacteria. Microwave drying rendered cultures of comparable characteristics to their conventional counterparts, requiring significantly shorter drying times.