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1 d within a dry matrix of roe proteins during spray drying.
2 rium infantis and Lactobacillus plantarum by spray drying.
3 w/w) and then encapsulated in powder form by spray drying.
4 varian cancer cell line, ID8 was prepared by spray drying.
5 d with maltodextrin (MD) (20, w/v%) prior to spray drying.
6 (HOSO+SFE)) were encapsulated with Capsul by spray drying.
7 y the binding of allicin in combination with spray drying.
8 h/without lecithin and/or sodium alginate by spray drying.
9 Lactobacillus plantarum, A17 and B21, during spray drying.
10 ated onto porous starch as an alternative to spray drying.
11 (DCH and MCD, respectively) were obtained by spray drying.
12 roencapsulated with whey protein isolate via spray drying.
13 ations were unstable and crystallized during spray drying.
14 x and its effect on probiotic endurance upon spray drying.
15 oom-temperature stability for months through spray drying.
16 concentrate (SPC) by using calcium salts and spray-drying.
17 as well as its antimicrobial activity during spray-drying.
18 composite design (CP-C and UF-C systems) by spray-drying.
19 o-glycolide) microparticles were prepared by spray-drying.
20 wines that had previously been subjected to spray-drying.
21 tribution around 9 mum), microcapsules after spray drying and double emulsions after redispersion sho
26 ordo grape skin aqueous extract, produced by spray-drying and freeze-drying using polydextrose (5%) a
27 grape skin extract was microencapsulated by spray-drying and freeze-drying, using gum arabic (GA), p
29 based encapsulation such as electrospinning, spray drying, antisolvent, amylose inclusion complexatio
30 iven sample pH and temperature regime during spray drying benefits the survivability of S. boulardii
32 lubilized drug form--coated crystals made by spray drying (CCSD), was formulated and progressed into
35 as subjected to different drying techniques: spray drying, freeze drying and vacuum drying with the t
36 aqueous wild blueberry pomace extracts, then spray drying, freeze drying, or vacuum oven drying to pr
46 The objective of this work was to study the spray drying of jussara pulp using ternary mixtures of g
50 icles carrying HDM allergen were produced by spray-drying of an aqueous solution containing HDM aller
54 microencapsulation with gum Arabic by using spray drying on the odour profile and volatile compounds
56 -derived pigments showed no influence of the spray-drying process on these functional constituents.
57 rge porous NP (LPNP) aggregates occurs via a spray-drying process that ensures the drying time of the
59 ticle size measurements indicated that while spray-drying promoted the aggregation of nisin-pectin co
61 ypes of drying methods: hot air-drying (HD), spray drying (SD), lyophilisation (LD), and ultrasonic c
63 aring nanoporous carrier through non-organic spray drying showed to be a facile approach to enhance t
64 al of large porous particle (LPP) systems by spray drying solutions of polymeric and nonpolymeric NPs
69 encapsulate nisin (5g/L concentration) using spray-drying technique and to evaluate how complexation
72 olyunsaturated fatty acid (PUFA) enrichment, spray-drying temperature (160 degrees C vs. 180 degrees
76 pheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precurs
77 ects (Sl:Ca, 1:1), were microencapsulated by spray-drying using maltodextrin as the encapsulating mat
78 prove their stability and hydrophilicity) by spray-drying, using maltodextrin crosslinked with citric
80 apsulation of betalains from cactus fruit by spray drying was evaluated as a stabilization strategy f
81 interface of the emulsion droplets prior to spray drying was stabilized with several hydrophilic emu
86 by complexation with pectin or alginate and spray-drying were studied by using UV-Vis absorption and
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