Degree Of Crosslinking Research Articles

Thermo-oxidative crosslinking of carbon fiber reinforced PEEK (Polyetheretherketone) for additive manufactured ceramic matrix composites

Carbon fiber reinforced polyetheretherketone (CF-PEEK) samples were fabricated using material extrusion. These additive manufactured green bodies are later processed to their final application as ceramic matrix composites (CMC) by the liquid silicon infiltration (LSI) route. Past studies showed that the application of material extrusion for the fabrication of CMC requires an additional stabilization-step after 3D-printing in order to prevent the remelting of CF-PEEK during the high temperature process of pyrolysis. The thermally induced crosslinking of the CF-PEEK parts ensured shape accuracy and avoided remelting during the pyrolysis afterwards but is limited by the melting temperature of PEEK (T m ∼ 343 °C). The study revealed a correlation between the annealing conditions time and temperature and the degree of crosslinking. Based on the analytical results from differential scanning calorimetry (DSC), a kinetic model was calculated, allowing predictions in dependence of the annealing temperature and time. Rheological and shape stability investigations of thermally annealed specimens verified the analytic results. The main findings of the study highlight an increasing degree of crosslinking with increasing annealing temperature and time.

Heterogeneous organo/metal cooperative catalysis: One-pot immobilization of Pd(PPh3)4 and chiral phosphoric acid to hollow mesoporous polystyrene nanospheres for efficient asymmetric α-allylation of aldehydes

The widely used combinations of palladium catalysts and chiral phosphoric acids face with the problems of cooperative catalysis and low-cost immobilization of binary catalysts in heterogeneous catalysis, due to the significant decline in the freedom of anchored catalysts. In this paper, the one-pot immobilization of both chiral phosphoric acid (TRIP) and Pd(PPh3)4 to hollow mesoporous polystyrene nanospheres (HMPNs) via Friedel-Crafts alkylation is developed to fabricate HMPNs-supported dual organo/metal catalysts (Pd(PPh3)4#TRIP@HMPNs) at a low cost. The efficient cooperative catalysis of anchored TRIP and Pd(PPh3)4 with good to excellent yields (8993 %) and enantioselectivities (8087 % ee) is achieved in the direct asymmetric α-allylation of aldehydes with allylic alcohols. The higher molar ratio of TRIP to Pd(PPh3)4 and a lower crosslinking degree of HMPNs are beneficial to the cooperative catalysis of the anchored catalysts. Overall, this paper showcases a success in solving the key problems in heterogeneous asymmetric metal/oragano catalysis.

Ozone induced structural variation in OSA waxy rice starch: Effects on the thermal behavior of starch and its stabilized pickering emulsion

Waxy rice starch (St) was modified by pre-OSA esterification reaction followed by ozone treatment. The molecular structure of this modified product (OSA-OSt) was characterized, and the thermal behaviors and its stabilized Pickering emulsion were evaluated. 1HNMR and XPS results discovered that ozone initially oxidized the hydroxyl groups in the amorphous region of starch (preferentially C2/C3) along with a degree of crosslinking, enhancing the molecular orderliness. This led to an increase in water-holding capability (29.15%) and swelling power (52.8 g/g), and a decrease in solubility (0.35%). TGA, RVA, and DSC indicated that oxidation-induced crosslinking within a brief treatment period enhanced the starch's thermal stability. The structural change enabled the formation of a weak gel structure during the heating process, which displayed high thermal and freeze-thaw stability. The work proves ozone is an effective way of improving the thermal behavior of OSA-starch and its emulsion for subsequent applications in numerous food products.

β-Cyclodextrin-enabled, densely cross-linked anion-exchange membranes for fuel cell applications

Polyarylpiperidinium anion exchange membranes (AEMs) have been widely studied in anion exchange membrane fuel cells and alkaline electrolyzed water due to their excellent alkali resistance stability. In this work, we report the design and fabrication of poly(p-triphenylene-piperidinyl) (PTP) AEMs quaternized and cross-linked by bromo-β-cyclodextrin (β-CD-Br7). In this type of membranes, the densely cross-linked and quaternized sites derived from β-CD-Br7 can help to construct continuous ion transport channels to facilitate ion conduction. Although the ion exchange capacity (IEC) tended to decrease with increasing cross-linking degree, the qPTP-CD5 membrane with 5 % cross-linking (IEC = 2.3 mmol g−1) produced the most significant microphase separation and the highest conductivity (125.6 mS cm−1 at 80 °C). The membrane also exhibited impressive alkaline stability, with 94.6 % conductivity retention in 1 M NaOH at 80 °C after 1000 h and 90.7 % conductivity retention after 1500 h. Finally, the peak power density of the fuel cell assembled with qPTP-CD5 membranes was 1.216 W cm−2 at 80 °C and there was no significant voltage degradation when operated at 200 mA cm−2 current density for 40 h. This work demonstrates that β-CD can function as a good “platform” for simultaneous cross-linking and quaternization to fabricate high performance AEM.

Enzymatically cross-linked arabinoxylan hydrogel: Effect of glucose oxidase on the gel characteristics and oral colon-targeted delivery for Naja atra neurotoxin

Water-extracted arabinoxylan (WEAX) can form covalent hydrogels and has potential applications in colon-targeted drug delivery. However, it is not clear which structural characteristics of WEAX gels can better facilitate drug release in the colon as a microbial triggered system. In this study, different rheological properties of WEAX gels were prepared through oxidative cross-linking using glucose oxidase (GOX) with varying amounts for oral colon-targeted released Naja atra neurotoxin (NANT). It was found that the WEAX hydrogel with an adequate strong cross-linking degree minimized NANT loss in the gastrointestinal tract and improved its release in the colon in vitro. Moreover, NANT was fixed to the wall of the gel network by noncovalent binding and could maintain its secondary structure in the WEAX–NANT hydrogel. The WEAX–NANT hydrogel had an obvious analgesic effect in the in vivo mice test. The results revealed that the WEAX–NANT hydrogel with a strong cross-linking degree was better at releasing NANT.

Evaluation of Porcine-Derived Collagen Membranes for Soft Tissue Augmentation in the Oral Cavity: An In Vivo Study.

The use of porcine-derived collagen membranes (PDCM) to improve intraoral soft tissue rehabilitation remains under investigation. Different degrees of crosslinking have yielded differences in resorption time and inflammation surrounding collagen membranes. The aim of this study was to evaluate the in vivo performance of bilayered PDCMs with varying degrees of crosslinking for the regeneration of oral soft tissue defects. Bilateral split-thickness oral mucosa defects were created in mandibles of beagles (n=17) and assigned to one of the following: bilayer PDCM (high crosslinking porcine dermis in sheet form-H-xlink) and (low crosslinking porcine dermis in sheet form-L-xlink), bilayer PDCM (non-crosslinked predicate collagen membrane in spongy form-Ctrl), or negative control (Sham) and compared with positive control (unoperated). Animals were euthanized after 4-, 8-, or 12-weeks of healing to evaluate soft tissue regeneration and remodeling through histomorphometric analyses. H-xlink membranes presented delayed healing with a poorly developed epithelial layer (analogous to the sham group) across time points. Relative to Ctrl at 8 and 12 weeks, defects treated with H-xlink presented no difference in semiquantitative scores (P > 0.05), while L-xlink exhibited greater healing (P = 0.042, P = 0.043, at 8 and 12 weeks, respectively). Relative to positive control, L-xlink exhibited similar healing at 8 weeks and greater healing at 12 weeks (P = 0.037) with a well-developed epithelial layer. Overall, groups treated with L-xlink presented with greater healing relative to the positive control after 12 weeks of healing and may serve as an alternative to autologous grafts for intraoral soft tissue regeneration.

1H pulsed NMR measurement of reactivity of silane coupling agents for conservation of cultural heritage sites

AbstractThe network structure and reactivity of suitable restoration agent consisting of silane coupling agents (SCAs) of the brittle walls of a cultural heritage site located underground in a desert area in Egypt were investigated using 1H pulsed nuclear magnetic resonance (pulse NMR). It should possess both high coagulation strength and ductility to ensure that it can withstand an earthquake; it should also contain ethoxy rather than methoxy groups, which generate toxic methanol. The solidification rate for the SCA or oligomer with ethoxy groups was lower than those with methoxy groups; however, the final polycondensates showed the same relaxation time (hardness). The difference spectrum was developed newly to analyze the network structure combined higher strength and ductility. The distribution of crosslinking degree of such polycondensates was narrow, and the amount of lower crosslinking degree was small. On the other hand, the distribution was wide in the polycondensates with ductility but lower strength. From the compression tests of model sand solidified with the restoration agent for both methoxy and ethoxy types showed the superior properties combined higher strength and ductility. The pulse NMR experiment was useful for estimating the solidification rate and the network structure.

Impact of Co-60 γ-ray irradiation on the cross-linking and stability of fish collagen: Structural changes and digestibility

Irradiation can promote the cross-linking of collagen to enhance its biological properties, but the molecular changes in irradiated collagen have few been investigated. This study aimed to explore the impact of irradiation treatment on the molecular structure stabilization and cross-linking degree of skin collagen. The results showed that collagen in solution was more susceptible to Co-60 gamma irradiation than that in fish skin and in sponge forms. The solubility of collagen in solution decreased by more than 80% and the carbonyl content increased by more than 4 times compared with the control group after 12 kGy irradiation. Spectroscopic analysis and sodium dodecyl sulfate - polyacrylamide gel electrophoresis (SDS-PAGE) showed that collagen in solution was cross-linked, especially at high irradiation doses. However, the triple helical structure of skin collagen and collagen sponge remained intact. Furthermore, irradiation also reduced the sensitivity of collagen to collagenase. Gastrointestinal digestion results showed that the antioxidant activity of collagen increased at 1–3 kGy doses and decreased at 9–12 kGy doses. Collagen irradiated at high doses (9–12 kGy) was more difficult to digest and had a larger average particle size. This study provides a potential new approach for the preparation of stable fishery-derived collagen with excellent antioxidant activity and resistance to digestion by irradiation treatment.

Dehydration-modulated pomelo peel cellulose nanofiber interlayer customized polyamide membrane with highly uniform pores for efficient nanofiltration

The development of high-performance polyamide nanofiltration (PA NF) membranes by introducing interlayers holds promise for efficient desalination. In this study, a novel PA NF membrane was prepared by incorporating the special biomass interlayer, which consisted of dehydration-modulated pomelo peel cellulose nanofiber (PCNF). Due to the removal of water, the proportion of exposed oxygen-containing functional groups within the PCNF interlayer increased significantly, and thus the diffusion of piperazine (PIP) could be slowed down effectively. Consequently, the diffusion-restricted PIP was enriched and anchored by PCNF and formed a PA layer with a unique layered structure in the interfacial polymerization (IP) reaction. The surface PA layer with lower a cross-linking degree could optimize water transport pathways and improve membrane permeability (28.67 LMH/bar). Meanwhile, the bottom PA layer, which was closely interspersed with PCNF, reduced pore size of the membrane and enhanced the rejection of Na2SO4 (98.63%). This study reveals a low-cost and eco-friendly strategy for preparing effective biomass interlayers, which provides a feasible approach for designing high-performance NF membranes.

Development of hyaluronic acid hydrogel containing prednisolone-encapsulated nonphospholipid liposomes for the treatment of rheumatoid arthritis.

Rheumatoid arthritis (RA) requires therapeutic approaches that alleviate symptoms and inhibit the progression of joint damage. Glucocorticoids (GCs) have been a cornerstone of RA treatment, yet their use is often limited by side effects. Recent advancements suggest that liposome-based delivery systems can improve GC biodistribution, minimizing toxicity. This study introduces an innovative tool for RA treatment using prednisone-encapsulated nonphospholipid liposomes (NPLs) in combination with a hyaluronic acid (HA) hydrogel. Our methodology involved incorporating prednisone (PR) with palmitic acid and cholesterol to formulate stable NPLs using a thin-film hydration technique. The synthesized PR-NPLs, characterized by a mean size of 150 nm, demonstrated uniform distribution and higher drug encapsulation in comparison with conventional phospholipid liposomes. In vitro assays revealed that PR-NPL markedly reduced inflammatory responses in macrophages. Additionally, we successfully incorporated PR-NPL into an HA hydrogel, employing a photoinitiated cross-linking process. This novel composite offered modulable PR release, governed by the degree of hydrogel cross-linking. The developed system presents a promising advancement in RA management, especially suited for intraarticular injections. It potentially enables targeted, controlled drug release with a reduced risk of side effects, signifying a significant improvement over existing RA therapies.

Reducing the degree of crosslinking of peptidoglycan in Listeria monocytogenes promoted the secretion of membrane vesicles.

Listeria monocytogenes (LM) is a Gram-positive (G+) bacterium that secretes nanoscale membrane vesicles (MVs). LM MVs comprise various bacterial components and may have potential as an antigen or drug-delivery vehicle; however, the low yield of the LM MVs limits related research. G+-bacterial MVs germinate from the bacterial plasma membrane and must pass through a thick crosslinked peptidoglycan layer for release. Herein, we aimed to increase the release of MVs by reducing the degree of crosslinking of peptidoglycan. We knocked out two genes related to the longitudinal crosslinking of peptidoglycan, dal and dat, and supplemented the knocked-out dal gene through plasmid expression to obtain a stably inherited recombinant strain LMΔdd::pCW633. The structure, particle size, and main protein components of MVs secreted by this recombinant strain were consistent with those secreted from the wild strain, but the yield of MVs was considerably increased (p < 0.05). Furthermore, Listeria ivanovii (LI) was found to secrete MVs that differed in the composition of the main proteins compared with those of LM MVs. The abovementioned method was also feasible for promoting the secretion of MVs from the attenuated LM strain and LI wild-type and attenuated strains. Our study provides a new method to increase the secretion of MVs derived from Listeria that could be extended to other G+ bacteria.

Moderate-temperature curing of epoxidized soybean oil for highly efficient coated fertilizer

The use of bio-oil-based polymers in fertilizer coatings has drawn significant academic interest. However, the challenge remains to eliminate toxic chemicals while enhancing comprehensive properties. This study focused on synthesizing a degradable polymer from epoxidized soybean oil (ESO) without organic solvent at low temperature (120°C), accomplished through a modified curing agent (MCA). This MCA was made of an acidic eutectic mixture of phthalic anhydride (PA) and its glycerides, produced from inexpensive, low-toxic phthalic anhydride and glycerol. The process utilized a small quantity of zinc acetate (0.5 wt%) to facilitate the formation of phthalic triglyceride in the MCA and mitigate PA sublimation, resulting in the enhanced cross-link degree, superior mechanical properties and hydrophobicity of the ESO-based resin (ESOR). Under optimal preparation conditions, the solvent-free ESOR-coated fertilizer exhibited an extended longevity of 53 days, with an 80 % phosphorus release. This coating material can undergo hydrolytic degradation in soil and in-situ conversion into carboxylates. These findings hold significant potential for advancing the applications of ESOR in green and sustainable agriculture.

Synthesis of hydrogels from biomaterials and their potential application in tissue engineering

In this study, a series of hydrogels were synthesized from chitosan(s) that was crosslinking with glutaraldehyde at different concentrations. Ascorbic acid in an acidic medium was used to facilitate non-covalent interactions. The chitosan(s) was obtained from shrimp cytoskeleton; while ascorbic acid was extracted from xoconostle juice. The hydrogel reaction was monitored by UV–vis spectroscopy (550 nm) to determine the reaction kinetics and reaction order at 60 °C. The hydrogels structures were characterized by NMR, FT-IR, HR-MS and SEM, while the degree of cross-linking was examined with TGA-DA. The extracellular matrices were obtained as stable hydrogels where reached maximum crosslinking was of 7 %, independent of glutaraldehyde quantity added. The rheological properties showed a behavior of weak gels and a dependence of crosslinking agent concentration on strength at different temperatures. The cytotoxicity assay showed that the gels had no adverse effects on cellular growth for all concentrations of glutaraldehyde.

Green bifunctional unsaturated fatty acid modulated interfacial polymerization for augmented nanofiltration performance

Facile and precise regulation of the selective layer structure is challenging but highly crucial for the development of nanofiltration (NF) technology. In this work, we present an innovative strategy to modulate the polyamide physicochemical structure by introducing oleic acid (OA) into the organic boundary during interfacial polymerization (IP) process. As a naturally extracted product, OA is a kind of unsaturated fatty acid with a carboxylic head and a C17 alkyl chain tail. The presence of OA in organic phase allows to diminish the interfacial tension and accelerate the diffusion of piperazine (PIP) towards the organic boundary. Meanwhile, in situ reaction of OA with PIP during IP process yields organic particles that are embedded in the selective layer and alter its morphology. These two effects can result in opposite influence on membrane performance. Under the optimized OA dosage of 1 %, the MgSO4 rejection boosted from 70.8 % to 97.4 % while maintaining a high pure water permeability up to 16.4 ± 0.1 L m−2 h−1 bar−1. This improvement is closely attributed to the augmented crosslinking degree and lessened MWCO/average pore size. In comparison to the control sample, the membrane surface changed from a smooth to a clustered morphology while the film thickness increased. This is mainly caused by the embedding of organic particles into the selection layer. This advancement provides a convenient and effective method for the design of high-performance NF membranes.

Scalable Production of 2D Non‐Layered Metal Oxides through Metal–Organic Gel Rapid Redox Transformation

Two‐dimensional (2D) nonlayered metal compounds with porous structure show broad application prospects in electrochemistry‐related fields due to their abundant active sites, open ions/electrons diffusion channels, and faradaic reactions. However, scalable and universal synthesis of 2D porous compounds still remains challenging. Here, inspired by blowing gum, a metal‐organic gel (MOG) rapid redox transformation (MRRT) strategy is proposed for the mass production of a wide variety of 2D porous metal oxides. Adequate crosslinking degree of MOG precursor and its rapid redox with NO3‐ are critical for generating gas pressure from interior to exterior, thus blowing the MOG into 2D carbon nanosheets, which further act as self‐sacrifice template for formation of oxides with porous and ultrathin structure. The versatility of this strategy is demonstrated by the fabrication of 39 metal oxides, including 10 transition metal oxides, one II‐main group oxide, two III‐main group oxides, 22 perovskite oxides, four high‐entropy oxides. As an illustrative verification, the 2D transition metal oxides exhibit excellent capacitive deionization (CDI) performance. Moreover, the assembled CDI cell could act as desalting battery to supply electrical energy during electrode regeneration. This MRRT strategy offers opportunities for achieving universal synthesis of 2D porous oxides with nonlayered structures and studying their electrochemistry‐related applications.

Scalable Production of 2D Non-Layered Metal Oxides through Metal-Organic Gel Rapid Redox Transformation.

Two-dimensional (2D) nonlayered metal compounds with porous structure show broad application prospects in electrochemistry-related fields due to their abundant active sites, open ions/electrons diffusion channels, and faradaic reactions. However, scalable and universal synthesis of 2D porous compounds still remains challenging. Here, inspired by blowing gum, a metal-organic gel (MOG) rapid redox transformation (MRRT) strategy is proposed for the mass production of a wide variety of 2D porous metal oxides. Adequate crosslinking degree of MOG precursor and its rapid redox with NO3 - are critical for generating gas pressure from interior to exterior, thus blowing the MOG into 2D carbon nanosheets, which further act as self-sacrifice template for formation of oxides with porous and ultrathin structure. The versatility of this strategy is demonstrated by the fabrication of 39 metal oxides, including 10 transition metal oxides, one II-main group oxide, two III-main group oxides, 22 perovskite oxides, four high-entropy oxides. As an illustrative verification, the 2D transition metal oxides exhibit excellent capacitive deionization (CDI) performance. Moreover, the assembled CDI cell could act as desalting battery to supply electrical energy during electrode regeneration. This MRRT strategy offers opportunities for achieving universal synthesis of 2D porous oxides with nonlayered structures and studying their electrochemistry-related applications.

Holographic surface relief diffraction gratings made of hydrogels for direct label-free biosensing of IgGs

This work describes the development of a label-free (LF) biosensing platform for the direct detection of targets based on diffractive structures fabricated with acrylamide-based hydrogels biofunctionalized with proteins and antibodies. Hydrogels containing Bovine Serum Albumin protein (BSA) with different crosslinking degrees were synthesized and characterized to find the optimal conditions for the suitable fabrication of surface relief gratings (SRGs). The bioavailability of BSA-functionalized hydrogels for the specific recognition of anti-BSA antibodies was verified by fluorescence detection. After the hydrogel-based SRG fabrication, diffraction efficiency measures at two different laser wavelengths were used for the direct LF detection of anti-BSA antibodies. The limit of detection in the sub mg L−1 range was read. Additionally, SRGs were prepared with hydrogels biofunctionalized with anti-rabbit antibodies for the direct detection of IgGs from rabbit serum, obtaining similar analytical performance without the necessity of labeling or applying amplification strategies.

Synthesis, characterization and evaluation of in vitro potential antimicrobial efficiency of new chitosan hydrogels and their CuO nanocomposites

The phenomenon of microbial resistance and its resulting biofilms to traditional antibiotics is worsening over time. Therefore, the discovery of alternative substances that inhibit microbial activities through mechanisms different from those of known antibiotics requires attention. So, chitosan was crosslinked using different amounts of oxalyl dihydrazide yielding four novel hydrogels; ODHCs-I, ODHCs-II, ODHCs-III, and ODHCs-IV of crosslinking degree 12.17, 20.67, 31.67, and 43.17, respectively. Different amounts of CuO nanoparticles were impregnated into ODHCs-IV, obtaining ODHCs-IV/CuONPs-1 %, ODHCs-IV/CuONPs-3 % and ODHCs-IV/CuONPs-5 % composites. Their structure was emphasized using FTIR, SEM, XRD, TEM, EDX and elemental analysis. Their in vitro antimicrobial and anti-biofilm activities improved with increasing ODH and CuONPs content. ODHCs-IV exhibited minimal inhibition concentration (2 μg/mL) against S. pyogenes that was much lower than Vancomycin (3.9 μg/mL). ODHCs-IV/CuONPs-5 % displayed better inhibition performance than Vancomycin and Amphotericin B against Gram-positive-bacteria and fungi, respectively, and comparable one to that of Vancomycin against Gram-negative-bacteria. ODHCs-IV/CuONPs-5 % displayed much lower minimal biofilm inhibition concentrations (1.95 to 3.9 μg/mL) as compared with those of ODHCs-IV (7.81 and 15.63 μg/mL), against C. albicans, S. pyogenes, and K. pneumonia. ODHCs-IV/CuONPs-5 % composite is safe on normal human cells. Oxalyl dihydrazide and CuONPs amalgamated into chitosan in one formulation promoted its antimicrobial efficiency.

Recyclable Covalent Adaptable Polystyrene Networks Using Boronates and TetraAzaADamantanes.

With an ever-increasing annual production of polymers and the accumulation of polymer waste leading to progressively adverse environmental consequences, it has become important that all polymers can be efficiently recycled at the end of their life cycle. Especially thermosets are intrinsically difficult to recycle because of their permanent covalent cross-links. A possible solution is to switch from using thermosets to covalent adaptable networks, sparking the rapid development of novel dynamic covalent chemistries and derived polymer materials. Next to development of these innovative polymer materials, there is also an evident advantage of merging the virtues of covalent adaptable networks with the proven material properties of widely used commodity plastics, by introducing dynamic covalent bonds in these original thermoplastic materials to obtain recyclable thermosets. Here we report the synthesis and characterization of a polystyrene polymer, functionalized with TetraAzaADamantanes and cross-linked with dynamic covalent boronic esters. The material properties were characterized for different degrees of cross-linking. The materials showed good solvent resistance with a high remaining insoluble fraction. In line with the typical behavior of traditional covalent adaptable networks, the prepared polystyrene-based boronate-TetraAzaADamantane materials were able to undergo stress relaxation. The material relaxation was also shown to be tunable by mixing with an acid catalyst. Lastly, the materials could be recycled at least 2 times.

Lactiplantibacillus plantarum ACCC 11095 microencapsulated by lotus seeds cross-linked resistant starch: Survival under simulated gastrointestinal conditions and its structural changes

Under simulated gastrointestinal digestion, we investigated the protective and releasing effects of lotus seed cross-linked resistant starch (LSCS) with low, medium, and high cross-linking degree toward Lactiplantibacillus plantarum ACCC 11095 and associated structural changes. Probiotic microcapsules (PM) made of high crosslinking starch showed better encapsulation rates (48.81%) and released 6.26 log CFU/g of viable bacteria after digestion, which helped colonize and exert probiotic effects in the intestinal tract. Scanning electron microscopy and Fourier Transform Infrared spectroscopy confirmed better high crosslinking starch protection for probiotic bacteria. This was closely related to PM embedded materials. Correlation analysis showed that agglomeration between high crosslinking starch starch granules in PM was significantly enhanced, and amorphous zones were hydrolyzed to a lesser extent, providing better Lactiplantibacillus plantarum ACCC 11095 protection. Thus, high crosslinking starch demonstrated potential as an oral probiotic carrier in terms of cost, suitability for functional foods, and commercialization potential.