Novel Developments on Stimuli-Responsive Probiotic Encapsulates: From Smart Hydrogels to Nanostructured Platforms

: Biomaterials engineering and biotechnology have advanced signiﬁcantly towards probiotic encapsulation with encouraging results in assuring sufﬁcient bioactivity. However, some major challenges remain to be addressed, and these include maintaining stability in different compartments of the gastrointestinal tract (GIT), favoring adhesion only at the site of action, and increasing residence times. An alternative to addressing such challenges is to manufacture encapsulates with stimuli-responsive polymers, such that controlled release is achievable by incorporating moieties that respond to chemical and physical stimuli present along the GIT. This review highlights, therefore, such emerging delivery matrices going from a comprehensive description of addressable stimuli in each GIT compartment to novel synthesis and functionalization techniques to currently employed materials used for probiotic’s encapsulation and achieving multi-modal delivery and multi-stimuli responses. Next, we explored the routes for encapsulates design to enhance their performance in terms of degradation kinetics, adsorption, and mucus and gut microbiome interactions. Finally, we present the clinical perspectives of implementing novel probiotics and the challenges to assure scalability and cost-effectiveness, prerequisites for an eventual niche market penetration.


Introduction
The term "probiotic" has been complimented since its first appearance in the 1960s. It was initially defined as a substance secreted by microorganisms that has beneficial effects on the human body [1,2]. Then, in 1980, some specific characteristics were added to this definition. Additional claims stated that probiotics are "strains that have a beneficial impact, non-toxic, non-allergic, and nonpathogenic, available in large quantities as viable cells, suitable for the environment of the gut, and storable as well as stable" [1]. The Food and Agriculture Organization (FAO) and the World Health Organization (WHO) defined probiotics as "live microorganisms that, when administered in adequate amounts, confer a health benefit on the host" [1][2][3][4]. Additionally, both organizations have classified products containing live organisms into four categories: (a) live or active cultures; (b) probiotics in food or supplements without a health claim; (c) probiotics in food or supplements with a specific health claim; and (d) probiotic drugs [2].
Probiotic strains generally belong to the following genera: Lactobacillus, Bifidobacterium, Saccharomyces, Pediococcus, Streptococcus, and Leuconostoc [1]. Lactobacillus and Bifidobacterium are the most common strains. Different aspects need to be considered when selecting probiotic strains, and these include stomach pH and bile tolerance, adherence to epithelial Hence, the scope of this review is focused only on the engineering of probiotics delivery to improve the GIT's health.

Gastrointestinal Tract (GIT) Stimuli as Tool for Design
Besides biomaterials formulation based on polymer science serving as a helpful tool for novel probiotic encapsulation, the need for a complete understanding of the environment for oral administration is a field of intensive research as it is key to assuring optimal performance of encapsulates in the GIT. Additionally, GIT conditions set a baseline to guide the required physicochemical properties for designing novel encapsulates. While in some cases, the harsh conditions of the GIT and its innate reactive stimuli appeared as a major obstacle to reaching the site of action of several encapsulates (Figure 1), novel engineering approaches have considered responses to such stimuli for the development of polymeric networks programmed to undergo volume changes, structural transitions, partial degradation, and structural network rearrangements [24]. Thus, the proper understating of the ionic strength, redox potential, pH, and enzymatic stimuli [25,26] present in the GIT is essential to rationally design multi-structured matrices capable of active response to the conditions of each GIT component while protecting the probiotic cargoes [27]. The addressable stimuli for developing biomaterials showing such dynamic responses are discussed below. and targeted delivery of pharmacological compounds. We exemplify how frequently used techniques for encapsulation can be extrapolated to rationally fabricate novel 3D matrices capable of responding actively to their surroundings and overcoming current issues, and taking advantage of the harsh conditions of the GIT to improve their functionalities. In addition, through this review, we point out pivotal points to set a straightforward approach to rational design potential stimuli-responsive encapsulates to reach clinical applicability. Hence, the scope of this review is focused only on the engineering of probiotics delivery to improve the GIT's health.

Gastrointestinal Tract (GIT) Stimuli as Tool for Design
Besides biomaterials formulation based on polymer science serving as a helpful tool for novel probiotic encapsulation, the need for a complete understanding of the environment for oral administration is a field of intensive research as it is key to assuring optimal performance of encapsulates in the GIT. Additionally, GIT conditions set a baseline to guide the required physicochemical properties for designing novel encapsulates. While in some cases, the harsh conditions of the GIT and its innate reactive stimuli appeared as a major obstacle to reaching the site of action of several encapsulates (Figure 1), novel engineering approaches have considered responses to such stimuli for the development of polymeric networks programmed to undergo volume changes, structural transitions, partial degradation, and structural network rearrangements [24]. Thus, the proper understating of the ionic strength, redox potential, pH, and enzymatic stimuli [25,26] present in the GIT is essential to rationally design multi-structured matrices capable of active response to the conditions of each GIT component while protecting the probiotic cargoes [27]. The addressable stimuli for developing biomaterials showing such dynamic responses are discussed below.   Table 1 synthesized the function and characteristics of essential enzymes present throughout the GIT, but details will be explained below. The chemical digestion starts in the oral cavity and consists of ptyalin (or alpha-amylase) and lingual lipase. The bolus is then swallowed into the esophagus and transits along it to reach the stomach [28]. Pepsin is the principal enzyme involved in protein digestion (i.e., hydrolysis of proteins). These enzymes are active in the acidic medium of the stomach by the secreted hydrochloric acid (HCl) and bile coming from the liver. Oxyntic and pyloric glands are two types of glands in the gastric mucosa that help during the chemical digestion process taking place in the stomach. The oxyntic glands contain parietal cells that secrete HCl at a pH of 0.8 to eliminate pathogenic microorganisms and denature proteins for further enzymatic degradation by pepsin. The G-cells in the pyloric glands secrete the hormone gastrin, which stimulates the secretion of HCl by parietal cells [28].

Salivary amylase
It digests starch into maltose and maltotriose by working at an optimum pH of 6.7 to 7. This cleavage decreases the glucose-polymer chain length and the viscosity of starch. [28,29] Lingual lipase It catalyzes the hydrolysis of fatty acids. It hydrolyzes the ester bonds in the triglycerides to form diacylglycerols and monoacylglycerols. [28,30] Stomach Pepsin It breaks down the internal peptide bonds of proteins at an optimal pH from 2 to 3. [28]

Small intestine
Pancreatic amylase It digests starch in the duodenal portion into maltose and maltotriose. [29] Trypsin It is an endopeptidase that hydrolyzes the internal peptide bonds of proteins. It converts chymotrypsinogen, procarboxypeptidase, and proelastase to their active forms. [28,31] Pectinase It causes the degradation of pectin chains, a polysaccharide found in the cell wall of plants. [32,33] Peptidase It plays a role in protein digestion before absorption. [34] Lipase It is produced in the pancreas and oversees fat digestion. It breaks down triglycerides into free fatty acids and glycerol. [35] The pancreas produces several digestive enzymes (i.e., pancreatic amylase, pancreatic lipase, trypsinogen, chymotrypsinogen, procarboxypeptidase, and proelastase) that reach the stomach to sections away from the acidic environment and the small intestine where they work optimally at more basic pH values (pH 6 to 7) due to the presence of bicarbonate secreted by the pancreas [28].
The small intestine comprises the duodenum, the jejunum, and the ileum. Pancreatic amylase is released into the duodenum to further digest incoming starch molecules. The acinar cells (exocrine cells of the pancreas) produce and transport the digestive enzymes. These cells have insulin receptors, where insulin binds to assure a normal acinar cell function, regulating the pancreatic amylase secretion and starch digestion [29].
The surface area available for absorption of peptides and proteins in the large intestine is reduced due to a lack of villi, microvilli, and crypts. Here, the considerable amount of bacteria present facilitates the digestion of residual food into caloric substances for subsequent absorption [30].

Ionic Strength and Redox Potential
Among the commonly found chemical stimuli present in the GIT, ionic strength and reduction-oxidation (redox) potency provide crucial cues for in situ extracellular matrix changes as a function of the systemic response of mammalian body functions [24]. Thus, the existence of monovalent and bivalent ions as well as reactive oxygen species (ROS) and nitrogen-oxygen species (NOS) are produced under different ionic strength and redox conditions, and therefore represent an addressable route to ionize polymeric structures [36].
The ionic strength of a solution or media is comprehended as the measure of the concentration of electrically charged species in a solution [37], which changes with the different fluids present throughout the GIT and can be advantageous for the release of on-cargo matrices commonly employed in oral drug release. Moreover, they can be exploited for controlling the response of polymeric biomaterials (e.g., swelling, dissolution, and degradation) [38][39][40][41][42], which, in turn, is critical for the survival of the probiotics [43][44][45]. Moreover, marked changes in the ionic potential of GIT fluids allow the control disaggregation of foods and ingestible encapsulates by destabilization of polypeptide bonds and polymeric structural rearrangements.
Typical ionic strength values vary from 0.051 to 0.151 mol/L in the gastric fluid of the stomach and between 0.070-0.166 mol/L in the intestinal fluid [46]. However, as ionic strength is defined by the reactive species at equilibrium present in each GIT compartment, the state of ionic power is also regulated by the food intake and location within the GIT [41].
The redox potency is used to describe a system's overall reducing or oxidizing capacity through the presence of chemically reactive species [41]. Its relevance in biological science stems from its role in shaping the structure and function of microbial communities, as demonstrated by the precise communication in the gut microbiome and epithelial cells in the mucosa layers [47,48]. In particular, the redox balance in the GIT is mainly mediated by the presence of ROS, NOS, thiol/disulfide redox systems (i.e., glutathione/glutathione disulfide (GSH/GSSG), cysteine/cystine (Cys/CySS), and reduced and oxidized thioredoxin (Trx/TrxSS) redox couples), which are predominant molecules that interfere in preserving tissue redox homeostasis, metabolic functions, and cellular integrity. For instance, maintaining mucus fluidity and absorption of nutrients and protecting against chemical-induced oxidant injury at the luminal surface is largely achieved by dynamically adjusting the thiol-disulfide status [36].

Polymeric Platforms and Delivery Systems of Probiotics
The selection of optimal material for probiotic encapsulation and the appropriate processing route are key parameters to ensure an efficient delivery strategy, where early degradation by GIT stimuli and harsh conditions are largely avoided. Nevertheless, selecting the materials for superior performance in complex physiological environments such as the GIT is a task made challenging not only by the obstacles to be overcome to reach the target site but also by the need to maintain high biological activities and positive responses to the changing surroundings [49,50]. The fast-growing notion that encapsulates can be composed of active biomaterials should be driven by matching the material's properties with expected responses through the GIT. Particularly, polymers exhibit versatile molecular moieties that have been widely exploited to fabricate chemical and physical delivery platforms with properties that can be finely tuned by adjusting interchain interactions [51]. Chemical polymeric scaffolds are formed by covalent bonds between adjacent chains, while the physical ones are maintained together by charged polyvalent surfactants or ion interactions [24].
Moreover, their versatile processability schemes facilitate obtaining different morphologies, functionalities, and the possibility to form composites with nanostructured materials in search of an enhanced response when subjected to a stimulus [52][53][54]. Typical polymeric encapsulates comprise microparticles, microspheres, microcapsules, hydrogels, and, more recently, nanocomposite 3D matrices. However, despite the success in preparing encapsulation systems capable of maintaining biological activity, more concerted stimuli responsiveness and higher resistance to harsh environments remain a significant constraint for moving to clinical setups [52]. Accordingly, the following section will discuss the most used materials and processing schemes for probiotic encapsulation in conjunction with alternatives to take advantage of their resultant properties to overcome the different challenges of each GIT compartment.

Polymeric Materials in Probiotic Encapsulation
In protected-delivery technologies, a suitable polymeric material should be able to preserve its core from adverse environmental conditions (e.g., reduce the acid-induced degradation of probiotics by gastric fluids in the stomach), exhibit inertness with the encapsulated materials, promote a controlled release of the encapsulate, achieve higher encapsulation efficiencies of bioactive compounds on a per mass basis and, ultimately, favor high levels of absorption into the targeted organs (i.e., the overall efficacy of the compounds) [27,55,56]. All the selected materials must also be biodegradable and biocompatible since they will be in direct contact with various types of cells [27,57].
Chitosan is a very abundant polysaccharide obtained from chitin and is composed of (1,4)-linked 2-amino-deoxy-b-d-glucan [68]. It also shows high biocompatibility and biodegradability under physiological conditions. For these reasons, it has enabled several encapsulation applications in the food and pharmaceutical industries, including liposome coating, chitosan-alginate coating, controlled delivery of small molecules and biologicals, and the release of bioactive metabolites (e.g., essential oils, probiotics, vitamins, antioxidants, and flavors). The unique cationic character of chitosan allows forming multi-layer systems with anionic alginate for probiotic encapsulation, which can bring efficient protection to cargoes, reduced porosity, stability at various pH ranges, and reduced leakage of the encapsulated probiotic. In experiments where the gastric environment was simulated, chitosan coating was more efficient than poly-l-lysine and alginate coatings in protecting probiotics, which represents a possible route to overcome the challenges of oral delivery [68]. Furthermore, chitosan coating with drying processes can prolong the long-term storage of some probiotics at different temperatures [69].
Another frequently studied material for encapsulation is gelatin, a commercially available denatured protein obtained by the hydrolysis of collagen from the skin and bones of bovines or fish. This protein might be positively or negatively charged, depending on whether an acidic or alkaline method was used for its extraction, which can be exploited to design multifunctional controlled release systems [70]. For example, gelatin-coated alginate capsules and microspheres can protect labile drugs from the stomach's acidic environment, enabling their release in the target intestinal area, whose environment has a basic pH [71]. Other studies have reported that the addition of fish gelatin significantly raised polymer matrix density and improved the physical integrity of alginate capsules because of a more stable and ordered 3D structure. Some other aspects, such as the survival rate of microorganisms during the GIT's passage, are enhanced compared to non-encapsulated cells [72].
Poly-l-lysine is a cationic, non-ribosomal, non-toxic, biocompatible, biodegradable, and antimicrobial homopolymer produced by modified strains of Streptomyces albulus. Lysine is frequently used as a preservative and food additive [73], and studied as an alginate bead coating. The marked antimicrobial activity of most cationic polymers poses a major challenge because they tend to inhibit the growth of some microorganism strains, depending on pH and incubation times. That is the case not only of lysine but also of chitosan and polyethyleneimines [74]. However, different in vitro studies that have implemented mixed manufacturing techniques, such as freeze-frying, have shown that poly-l-lysine coatings for alginate capsules are well-suited to maintain cells' growth and proliferation at low pH values and viability for a storage period of up to 16 weeks at 4 • C [22].
The materials mentioned above correspond to the most popular and studied polymers for survival enhancement and protection of probiotics in hostile environments, such as those found in the compartments of the GIT. Many other materials might be suitable for producing capsules and coatings for this application, including polyethyleneimines, poly(2-dimethyl(aminoethyl)methacrylate), dextran, pectin, Arabic gum, starch, sodium caseinate, polyvinyl alcohol, polyethylene glycol, polyacrylic acid, and succinylated or acylated carrageenan [22,73,75,76].

Hydrogels
Hydrogels have drawn particular attention among encapsulation alternatives for probiotics, given their ease of processing, the wide range of materials available for their fabrication, and their capability to form three-dimensional networks that protect the probiotic's integrity [77]. Remarkably, the inertness of hydrogels in environments with high water activity makes them suitable to entrap molecules and microorganisms, and ensure their integrity and viability in physiological environments [78]. However, one of the main concerns about implementing hydrogels is the proper tuning of mechanical performance, along with optimal porosity to enable microorganism survival while maintaining sufficient cell entrapment and a considerable degree of swelling [79]. This has been addressed by chemically modified polymers through different routes, including the addition of ionizable functional groups, functionalized backbones, and combined polymeric blending [50,80,81].
One of the most intensive research areas is the development of strategies for tuning degradation rates and matrix porosities to improve their performance in protecting encapsulated living organisms [87]. This has been achieved by the supramolecular design of monomeric structures and by controlling polymerization reactions with carefully applied light and thermal stimuli [88,89]. Depending on the polymerization scheme selected (i.e., bulk polymerization, solution polymerization, suspension polymerization, emulsion polymerization, and graft polymerization), macroscopic and microscopic properties such as porosity and polymeric mesh size might change significantly [90]. Notably, the capacity of engineering the tortuosity and interconnectivity of hydrogels' mesh has been reported as critical for the smart release of the encapsulated cargoes [91]. Further control over such a process can be achieved by chemical modifications with hygroscopic polymers such as polyethyleneglycol, which leads to the enhanced mucoadhesiveness of the encapsulates by both physical entanglement and hydrogen bonding with the base encapsulating polymer [92,93]. Therefore, the following section will discuss the fast-growing area of stimuli-responsive hydrogels, emphasizing how they can be activated, de-activated, or re-activated for a particular delivery purpose [94].

Microencapsulates
Microparticles, microcapsules, and microspheres usually made of food-grade polymers, such as alginate, chitosan, carboxymethyl cellulose, cellulose acetate phthalate, xanthan gum, starch, carrageenan, gelatin, and pectin [59,110], have demonstrated to be protective barriers of high performance against the GIT's environmental conditions [111][112][113][114][115]. These microencapsulates' dimensions usually range between 1 and 1000 µm [25]. According to recent studies, an effective microencapsulation system should maintain the stability of the probiotics during storage, protect them from the harsh conditions of the upper GIT, release them in the colon, and finally, promote their ability to colonize the mucosal surfaces [25,[116][117][118].
Microparticles typically consist of a core composed of one to several ingredients surrounded by a wall or barrier of uniform or non-uniform thickness, either single-layered or multi-layered. The design of microencapsulated ingredients requires knowledge of (1) the core, (2) the materials for encapsulation, (3) the interactions between the core, matrix, and the environment, (4) the stability of the microencapsulated ingredients under storage conditions and when incorporated into food matrices, and (5) the mechanisms that control the release of the core [56,59,110]. Matrix degradation, and consequently, the release of its contents, can be controlled to occur at different times. Larger particles generally release encapsulated compounds more slowly and over more extended periods, while particle size reduction favors adhesiveness and therefore prolonged GI transit time, leading to a higher drug bioavailability [56,59,110,119].

Nanostructured Platforms
One of the leading strategies to improve microencapsulates' tolerance to different GIT environments and ensure their efficient delivery is physical and chemical blending with stimuli-responsive and high mechanical performance nanomaterials [144][145][146]. This approach allows superior control over probiotic delivery due to the unique properties attainable by forming nanocomposites and the possibility of providing multimodal delivery platforms (i.e., including more than one encapsulated component) where survival of probiotics is increased substantially [147,148]. Accordingly, several nanostructured materials have been explored in the fabrication of next-generation delivery platforms, including polymeric and iron oxide-based nanoparticles, nanosheets (e.g., graphene oxide-GO and phyllosilicate clays), nanoliposomes, micelles, and nanoparticles derived from naturally occurring polymers such as nanocellulose and starch nanocrystals [149][150][151].
The dispersion of nanoparticles (NPs) into polymeric arrangements (to form nanocomposites) is attractive mainly due to their intrinsic capacity to fill out pores, therefore avoiding the diffusion of molecules such as hydrogen ions, bile salts, or digestive enzymes that may lead to the undesirable degradation of the encapsulated probiotics [152]. For instance, magnesium oxide (MgO) NPs have been incorporated into alginate-gelatin microgels, which resulted in a more stable encapsulation of probiotics when compared to unmodified microgels. The MgO NPs help neutralize the hydrogen ions present in the gastric fluids, which diminishes the acid-induced degradation of probiotics and maintains a neutral pH inside the microgels [27]. Alternatively, the use of NPs can help improve some physicochemical properties of the encapsulates, such as hardness, compressibility, cohesiveness, and adhesiveness. This is the case of chitosan NPs, which have been reported to enhance the mucoadhesive properties of hydrogels [153]. Through this approach, the interaction with the intestinal mucus is improved by the electrostatic interaction and physical entanglements of the chitosan-containing matrices facilitated by the positive charge of chitosan.
Another approach suggests that combining polymeric platforms with nanocrystals derived from polysaccharides (e.g., cellulose and starch) enhances mechanical stability and shelling properties [154], and increases the surface area for target delivery [155]. For instance, when cellulose nanocrystals (NCs) are combined with alginate during the microencapsulation process, the dissolution time increases while porosity is reduced significantly [156]. Moreover, ionic interaction between the material and the nanocellulose filler reduces the infiltration of gastric fluids, preventing the degradation of probiotics [157]. When starch NCs are implemented as fill-in alginate-based delivery platforms, thicker barrier protection against gastric and intestinal juices provides a stable mechanism to decrease probiotics mortality [149].
Remarkably, novel developments in the fabrication of nanocarbon-based materials (e.g., reduced graphene oxide, graphene quantum dots, graphene nanoribbons), silicabased nanocarriers, and inorganic nanoparticles have enabled the fabrication of emerging nanocomposites with improved mechanical strengths, high drug loading, and reduced toxicity [144,158,159]. These features have been reported to not only favor the controlled release of on-cargo molecules but also increase the survival of encapsulated living organisms (e.g., probiotics and mammalian cells) [160,161]. Similarly, clay mineral silicates have gained popularity given their unique cationic exchange properties that can be exploited to fabricate water barriers due to hydrogen bonding [162,163]. Kim and colleagues reported superior shape integrity for bentonite/alginate-based encapsulates during gastric fluid exposure and appropriate disintegration in the intestinal area upon oral administration in mice [158]. Relevant nanocomposites for probiotic encapsulation are listed in Table 4. Other recent reports suggest that incorporating nanostructured materials into delivery platforms makes it possible to accompany the encapsulation of probiotics with other therapeutic and bioactive molecules, thereby providing a route for multimodal controlled release [80,164].

Improving Functionalities of Polymeric Matrices for Probiotic Encapsulation
Although processing schemes and properties of the materials are vital parameters for controlling their response, the rational design of polymeric multi-responsive platforms capable of taking advantage of innate GIT stimuli is a groundbreaking alternative to overcome current issues. Accordingly, given the predominant role of singular stimuli along GIT sections, multi-layer platforms of micro and nanostructured matrices or supramolecular encapsulates appear well-suited to actively respond to environments with particular physicochemical conditions. In this regard, one of the significant challenges is the precise control of interactions between polymeric components such that the obtained 3D constructs only respond to a set of stimuli of interest. This section is dedicated to correlating the engineering of polymer responses with the innate stimuli of the GIT (discussed in Section 2) through processing schemes explored in Section 3 ( Figure 2).

pH-Responsive Matrices
As pH changes through the GIT are evident (Section 2.1), the use of ionizable polymers that undergo physical and chemical changes is a current alternative to take advantage of the presence of amines, carboxylic acids, hydroxyls, sulfonic acids, and imines [165]. This approach relies on the chemical reactivity of the pendant functional groups in the backbone of polymeric structures to provide responsiveness and cargo release through careful control of swelling-deswelling processes resulting from electrostatic repulsion (i.e., ionic strength). Thus, pH-responsive moieties in polymers offer an alternative to control the probiotic's release based on desired pH conditions at the delivery region of the GIT.

pH-Responsive Matrices
As pH changes through the GIT are evident (Section 2.1), the use of ionizable polymers that undergo physical and chemical changes is a current alternative to take advantage of the presence of amines, carboxylic acids, hydroxyls, sulfonic acids, and imines [165]. This approach relies on the chemical reactivity of the pendant functional groups in the backbone of polymeric structures to provide responsiveness and cargo release through careful control of swelling-deswelling processes resulting from electrostatic repulsion (i.e., ionic strength). Thus, pH-responsive moieties in polymers offer an alternative to control the probiotic's release based on desired pH conditions at the delivery region of the GIT.
pH-responsive polymers can be classified as (a) cationic or (b) anionic, based on their capability to donate or accept electrons from the medium [166]. While cationic polymers (e.g., chitosan, poly(ethylenimine), poly(2-dimethyl(aminoethyl) methacrylate), and poly(l-lysine)) are characterized by the presence of ionizable basic groups at low pH (pH < pKa), anionic polymers (e.g., alginate, hyaluronic acid, polymethyl methacrylate) are characterized by acidic functional groups ionizable at higher pH (pH > pKa) [82,167]. The differential ionizable capabilities of cationic and anionic polymers are key features that can be exploited to improve the response of novel multi-layer encapsulates. The high-water solubility of anionic polymers at acidic pH and low-water solubility at neutral makes them suitable to overcome the oral cavity pH and gradually dissolve in the stomach. In contrast, cationic polymers are suitable for overcoming oral and stomach pH environments providing stability when they reach the upper small intestine and colon, as they swell in basic and neutral environments. These features lead to two possible alternatives to fabricate probiotics encapsulates: (a) the single use of anionic polymers and (b) the combined use of cationic and anionic polymers in multi-structured approaches that encompass the cleavage of sensitive polymers, as shown in Table 5. In this regard, multi-structured platforms based on microencapsulates fabricated with cationic colloidal micelles and chemically crosslinked polyremes combined with nanofunctional fillers dispersed in anionic hydrogels seem to be a promising alternative to entrap probiotics successfully [168].
Moreover, anionic (or polyacidic) matrices for small intestine and colon delivery of probiotics have been reported to respond actively to changes in osmotic pressure differences for cargo release [168]. The involved osmotic force induces swelling and promotes pore opening, and as a result, the facilitated release of probiotics through the formed meshed network. Concerning this, several studies have reported that by tuning the core resistance for small intestine delivery and rationally incorporating surface functional groups, the survival of the probiotic could be improved by more than 70% [104,169].
With the appropriate selection of encapsulation schemes and materials (i.e., ensuring survival in the stomach environment and rapid release in the small intestine), it is possible to synthesize encapsulates with superior resistance to acidic environments and rapid depolymerization in neutral environments [170]. Moreover, by combining polycationic co-polymers and polypeptides, the resulting matrices exhibit reduced permeability, and improved stability in physiological media has been demonstrated to be an efficient alternative for the fabrication of pH-responsive materials [104]. As shown by Gately et al., polymers such as shellac can be employed as sources of ionizable groups to tune degradation rates as a function of the pH while simultaneously taking advantage of the high chemical stability and natural bioadhesiveness of this polymer [171].
Alternatively, recent reports indicate that pH-responsive drug encapsulates exploit environmental pH as stimuli for releasing molecules upon cleavage of acid-sensitive bonds [104]. Such an approach has also been implemented successfully in encapsulating metabolizable sugars and salts, which have been demonstrated to improve probiotics' organoleptic properties and prolong their shelf life [172,173]. Moreover, this approach largely addresses the limited availability of the encapsulated nutrients at the site of action due to unspecific release and fluid infiltration along the transit through the GIT [174].  pH-dependent electrostatic interactions between raw materials enable an almost impermeable protective matrix at low pH and the appearance of pores at neutral pH. [180] Ca-alginate/protamine Co-extrusion Microcapsule L. casei Blockage of diffusion channels at acidic pH and easy degradation at a neutral pH environment. [169]

Enzyme-Responsive Matrices
The materials that respond to enzymes must contain substrate mimics or recognition elements that can be identified by enzymes (i.e., specific amino acid sequences), and the substrates must be accessible by enzymes [181]. Conversely, the action of the enzymes can induce either chemical or physical modifications in the matrices that lead to their degradation and, in turn, the release of encapsulated molecules [24].
The presence of different enzymes along the GIT can help release the probiotics at the site of action by the cleavage of specific moieties on the matrices [24]. Pathophysiological conditions such as inflammatory diseases of the GIT (e.g., ulcerative colitis and inflammatory bowel disease) can be potentially targeted by probiotics as they have been reported to upregulate matrix metalloproteinases (MMP) and esterases, which can degrade certain polymeric materials [31].
From a design point of view, the enzyme-responsive material must contain substrate mimics recognition motifs for effective active site binding or substrates capable of interacting with the enzyme molecules without imparting detrimental conformational changes (i.e., significant secondary and tertiary structural changes) [181]. Although to our knowledge, this approach has not been implemented for probiotic encapsulation and delivery purposes, it might be suitable for this task, given the possibility of incorporating wellknown ester molecules (e.g., triglycerol monostearate and ascorbyl palmitate) into the polymeric matrices, which are recognizable by several promiscuous enzymes [154,182]. Additionally, exogenous enzymes can be potentially crosslinked with polymeric matrices such that their release upon degradation at the site of action accelerates probiotics and other cargo delivery even further.
Some natural polymers like pectin can be degraded enzymatically without any chemical modification. Zhu and colleagues developed a pectin-based system for colon-specific delivery assisted by the pectinase enzymes resident therein [33]. The enzyme degradation kinetics of pectin has been enhanced by blending it with other polymers such as ethylcellulose, hydroxypropylmethylcellulose, chitosan, poly(lysine), and polyacrylate derivatives containing quaternary ammonium groups to take advantage of the enzymatic repertoire of the bacterial flora in the presence of co-encapsulated enzyme co-factors to potentiate their action [183]. Lai and colleagues exposed guar gum to a simulated colonic fluid containing β-mannanase and demonstrated in situ pore generation by ionic interactions and the subsequent cargo release [184]. Other materials used for colon targeting include amylose combined with ethylcellulose, galactomannan, inulin, and dextran [185]. In particular, dextran has been reported to excel in targeted colon delivery applications due to its relatively high chemical stability throughout the GIT, and its breakdown by dextranases thought to be exclusively present in the colon microflora [186].

Ionic Strength and Redox-Responsive Matrices
Ion-responsive matrices react to the ionic composition of the surrounding medium, where such composition determines the magnitude and range of electrostatic interactions resulting from ion binding and electrostatic screening effects [187]. By altering electrostatic interactions between the polymer chains, it is possible to change their 3D network organization radically.
Ionic strength has proven to have a marked effect on charged poly(N-isopropyl acrylamide) (PolyNIPAM) hydrogels, altering their swelling/shrinking behavior [37,184]. In this regard, it has been observed that a strongly charged hydrogel is likely to swell at low ionic strengths due to the strong interchain electrostatic repulsion but shrinks at high ionic strengths due to electrostatic screening effects [187]. Therefore, once a critical ionic strength level is reached, the hydrogel undergoes a conformational change from a swollen to a compact state, resulting in a regime of impeded diffusion [41,188].
The swelling and shrinking characteristics imparted by ionic strength or pH changes may also alter the electrostatic interactions between a substance and the encapsulating 3D polymeric matrix. Additionally, several ion-responsive matrices are also pH-responsive. An example of a pH/ionic strength and temperature-sensitive hydrogel has been reported for insulin delivery [189]. In this case, the release profile was evaluated in vitro, showing a negligible release in simulated gastric fluid and sustained release in simulated intestinal fluid, making it suitable for the intended site of action. The charge-inducing effect of the medium can explain the observed release mechanism of this type of matrices. For instance, under conditions where the encapsulated substance and the polymers have opposite charges, there will be an electrostatic attraction between them, leading to retention within the hydrogel matrix. In contrast, under conditions where the encapsulated substance and the polymers have identical charges (or one of them is uncharged), there will be an electrostatic repulsion (or no electrostatic attraction), leading to release from the hydrogel matrix [187].
Redox-responsive polymeric matrices can respond to biological stimuli generated by the presence of oxidants or reducing agents in the medium or to changes in the redox conditions [53]. In this case, matrices are equipped with chemical groups such as disulfide bonds, organometallic compounds, viologens, or tetrathiafulvalene, widely used to induce redox responsiveness.
Recent studies highlight that enzymatically generated ROS have been shown to function as second messengers in many signal transduction pathways via the transient oxidative activity on sensor proteins bearing thiol groups sensitive to oxidant molecules. Examples of redox-sensitive proteins include tyrosine phosphatases that regulate MAPK pathways, the focal adhesion kinase, and several components responsible for NF-kB activation [190].
A pH/redox-dual responsive nanoemulsion-embedded composite hydrogel could be a promising candidate for efficient oral delivery and controlled intestinal release of magnesium and other ions. The hydrogel is synthesized by crosslinking a biocompatible, pH-responsive pseudo-peptide, poly(L-lysine isophthalamide), and the redox-sensitive molecule L-cystine dimethyl ester dihydrochloride. As reported by Huang et al. [191], these hydrogels exhibit a compact structure at acidic gastric pH but become highly swollen or degraded under neutral pH and reduce conditions of the intestinal environment. The authors highlight that the ion release profiles indicated that the nanoemulsion-embedded composite hydrogel could retain and protect magnesium ions in the simulated gastric fluid buffer at pH 1.2 but efficiently release them in the simulated intestinal fluid buffer at pH 6.8 in the presence of 1,4-dithiothreitol as a reducing agent.
Likewise, Liu et al. introduced a redox/pH dual stimulus-responsive cellulose hydrogel that was prepared by incorporating enamine and disulfide bonds in the same system at physiological pH. The cellulose hydrogel was obtained by mixing aqueous solutions of cellulose acetoacetate and cystamine dihydrochloride at room temperature. The cellulose hydrogel showed reversible sol-gel transitions in response to pH and redox potential changes [192].
Xiao et al. [77] developed a redox-responsiveness hydrogel to encapsulate the probiotic microorganism L. rhamnosus with the final goal of treating bacterial enteritis. This hydrogel was prepared by the auto-crosslinking of thiolated hyaluronic acid. Upon exposure to H 2 S, which is excreted by intestinal pathogens, the hydrogel degrades locally and rapidly releases the cargoes, thereby competing with source pathogens for binding to the host. Further endurance experiments indicated that encapsulation of L. rhamnosus led to a significant increase in viability that was maintained even after transit throughout the GIT. Compared with free cells, encapsulated L. rhamnosus showed a superior therapeutic effect for Salmonella-induced enteritis and negligible toxicity in vivo. Taken together, their results demonstrated the feasibility of implementing redox-responsive hydrogels for the encapsulation and targeted delivery of orally administered therapeutic probiotics by taking advantage of altered intestinal conditions observed during the invasion of pathogens.
However, despite the recent advances in the field, ionic strength and redox-responsive polymeric matrices are still in their infancy, and therefore much work will be needed to move to an eventual clinical translation.

Physiological Barriers to Overcome
Although the stimuli-responsiveness of probiotic encapsulates is a vital attribute to accomplish therapeutic action in the intestine, successful colonization of the GIT is a pivotal aspect for conferring sufficient host-interaction [26]. Therefore, the design of delivery vehicles must take into consideration the interaction details of the encapsulated microorganisms ( Figure 3) with the barrier receptors to promote their adsorption. Probiotics are commonly rejected during this process, as they are sensed as invaders by the gut microbiome. This colonization resistance is one of the most critical issues to overcome for the long-term success of probiotic therapies. This has been addressed by tuning the degradation kinetics of the delivery matrix for maintaining adhesion to the intestinal mucosa for more extended periods. In this section, we discuss key aspects of probiotics colonization to the GIT and provide a set of recommendations for the rational design of polymeric matrices for probiotics encapsulation. to H2S, which is excreted by intestinal pathogens, the hydrogel degrades locally and rapidly releases the cargoes, thereby competing with source pathogens for binding to the host. Further endurance experiments indicated that encapsulation of L. rhamnosus led to a significant increase in viability that was maintained even after transit throughout the GIT. Compared with free cells, encapsulated L. rhamnosus showed a superior therapeutic effect for Salmonella-induced enteritis and negligible toxicity in vivo. Taken together, their results demonstrated the feasibility of implementing redox-responsive hydrogels for the encapsulation and targeted delivery of orally administered therapeutic probiotics by taking advantage of altered intestinal conditions observed during the invasion of pathogens. However, despite the recent advances in the field, ionic strength and redox-responsive polymeric matrices are still in their infancy, and therefore much work will be needed to move to an eventual clinical translation.

Physiological Barriers to Overcome
Although the stimuli-responsiveness of probiotic encapsulates is a vital attribute to accomplish therapeutic action in the intestine, successful colonization of the GIT is a pivotal aspect for conferring sufficient host-interaction [26]. Therefore, the design of delivery vehicles must take into consideration the interaction details of the encapsulated microorganisms ( Figure 3) with the barrier receptors to promote their adsorption. Probiotics are commonly rejected during this process, as they are sensed as invaders by the gut microbiome. This colonization resistance is one of the most critical issues to overcome for the long-term success of probiotic therapies. This has been addressed by tuning the degradation kinetics of the delivery matrix for maintaining adhesion to the intestinal mucosa for more extended periods. In this section, we discuss key aspects of probiotics colonization to the GIT and provide a set of recommendations for the rational design of polymeric matrices for probiotics encapsulation.

Composition of the Gut Microbiome
The gut microbiome involves a complex ecosystem of microorganisms (i.e., bacteria, viruses, protozoa, and fungi) and their collective genetic material [193]. When this ecosystem exists in a state of mutually beneficial symbiosis, the microbiome is considered healthy and beneficial for the host [194]. Some of the primary functions of gut microbiota include nutrient metabolism, xenobiotic and drug metabolism, maintenance of structural integrity of the gut mucosal barrier, immunomodulation, and protection against pathogens [195].
The concentration of microbiota gradually increases throughout the GIT, starting with a small number of microorganisms in the stomach and finalizing with a high one in the colon [17]. This can be explained by the low pH and the presence of bile or pancreatic enzymes in the stomach and proximal duodenum, where bacteria fail to survive or proliferate [17].
Most gut microorganisms are strictly anaerobic and belong to the phyla Firmicutes, Bacteriodetes, and Proteobacteria [17,193]. Other gut bacteria with a minor presence in the healthy gut (usually below 1%) belong to the phyla Actinobacteria, Verrumicrobia, Acidobacteria, or Fusobacteria [17].
Human microbiome composition varies according to the location in the GIT. Predominant bacterial genera in the oral cavity include Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Spirochaetes, and Fusobacteria [196,197]. However, the predominant ones in saliva are Gemella, Veillonella, Neisseria, Fusobacterium, Streptococcus, Prevotella, Pseudomonas, and Actinomyces [196,198]. The most abundant bacteria in the human esophagus belong to the phylum Firmicutes and the genus Streptococcus [17,196]. In this, bacterial communities are dominated either by Streptococcus, Prevotella, and Veillonella, or Haemophilus and Rothia [17,196,199]. The low pH of the stomach is not an obstacle to finding a diverse microbiota. The genera commonly found in the corpus and antrum include Bacillales incertae seidis, Streptococcaceae, Enterobacteriaceae, Leptotrichiaceae, Veillonellaceae, and Pseudomonadaceae [17,196,200,201]. The small intestine exhibits unique microbial compositional profiles as opposed to the previous compartments. Duodenum, jejunum, and ileum are dominated by Proteobacteria and Lactobacillales [196,202]. Duodenum harbors similar genera as the stomach (i.e., Bacillales incertae sedis, Streptococcaceae, Enterobacteriaceae, Leptorichiaeceae, Veillonellaceae, and Pseudomonadaceae) [200], jejunum and ileum most common communities consist of streptococci, lactobacilli, Gammaproteobacteria, the Enterococcus group, and the Bacteroides group [17,77,199]. The terminal ileum exhibits a composition closer to that of the colon, which typically includes Clostridiaceae, Lachnospiraceae, Peptostreptococcaceae, Ruminococcaceae, Enterobacteriaceae, and Bacteroidaceae [17,196,200]. Lastly, the colon is mostly colonized by bacterial phyla such as Bacteroidetes, Firmicutes, Verrucomicrobia, Proteobacteria, and Actinobacteria [196,201]. However, the intestine is also colonized by archaea, bacteriophages, viruses, unicellular eukaryotes, and fungi. The human gut harbors several fungi, including the genera Aspergillus, Candida, Cryptococcus, and Penicillium, which account for about 0.2-0.3% of the total gut microbiota [17].

Colonization Resistance
The gut microbiome provides resistance against colonization by exogenous microorganisms [203]. Although the involved mechanisms have not been fully elucidated, some of the identified underlying processes include secretion of antimicrobial products, nutrient competition, support of gut barrier integrity, and bacteriophage deployment [203,204].
The mechanisms of colonization have been classified into direct and indirect. In the first case, the resistance refers strictly to exogenous microbial colonization [26], mainly through killing and competition for resources. This set of mechanisms tends to act between more closely related species [204]. Killing or growth suppression can be mediated by bacteriocins-short, toxic peptides produced in the ribosomes of specific bacterial specieswhich can disturb processes involving RNA and DNA and also mediate pore formation in the cell membrane of microorganisms [26,[204][205][206][207][208]. Other antibacterial factors, like bacteriophages, can play an important role in excluding specific gut bacteria, thereby contributing to colonization resistance by lysing and transferring genetic information [204].
Also, metabolic byproducts such as short-chain fatty acids (SCFAs) (e.g., acetic, propionic, and butyric acid) can have an inhibitory effect on the growth of bacteria [204]. SCFAs are mainly produced by bacteria through fermentation of nondigestible carbohydrates [204] and can impair bacterial growth by changing intracellular pH and altering metabolic routes [203]. Bile acids, which are amphipathic and cholesterol-derived molecules secreted into the small intestine [204], also exhibit antimicrobial properties [203]. Deoxycholic acid, a secondary bile acid, is bactericidal to many bacteria by membrane disruption and subsequent leakage of the cellular content [203,[209][210][211][212]. Finally, nutrient and space competition occur more easily in bacterial strains that belong to the same species. Microbiota nutrients absorption and physical competition for adhesion sites (often glycan structures) could prevent the proliferation of pathogens [203,204].
Alternatively, indirect colonization resistance usually stimulates the innate or adaptive immune system. However, non-immune defenses might also be involved [204]. In this regard, the first non-immune barriers are the mucus layers in the small intestine, cecum, and colon. The gut barrier consists of the inner and outer mucus layers, the epithelial barrier, and its immune barrier. The inner mucus layer is very robust and firmly attached to the epithelium, forming a physical barrier for bacteria. This prevents direct interaction of microbial pathogens with the epithelial layer and a potential inflammatory response [203]. As described by Pickard et al., the mucus is decorated by various glycans that serve as nutrient sources or adhesion receptors for microbes. These can be cleaved by bacterial enzymes, and the resulting free sugars (e.g., fucose) can suppress pathogen or pathobiont virulence. The host can also oxidize sugars via reactive nitrogen species produced by inducible nitric oxide synthase [204].
In concern to the immune response, the innate immunity is briefly stimulated by microbe-associated molecular patterns produced by bacteria and viruses, via toll-like receptors (TLRs) and the protein MyD88, on either epithelial cells or dendritic cells. ILC3 and Th17 cells can be activated to produce the interleukin IL-22, which has been reported to promote the secretion of antimicrobial peptides such as Reg3g from epithelial cells. Also, by the acquired immunity, B cells produce IgA and IgG antibodies, targeting symbionts or pathogens in the intestinal lumen and preventing possible systemic infections [204].

Mucosal Adhesion in Probiotics Colonization
After overcoming the harsh conditions of the GIT, the benefits of probiotics largely depend on successful mucosa colonization [26]. Thus, enhanced interaction between encapsulated probiotics at the small intestine and colon level needs to be considered with careful attention to engineer systems with the capability of increasing the bioaccessibility of the delivered microorganisms and extending their residence times [213,214]. In this regard, a rational design of the encapsulates surface biochemistry is critical for an appropriate material-intestinal surface interaction to enhance the adhesion of mucosal and intestinal epithelial cells (IECs). Such design must be based on the structural features of the mucosal layer that is mainly composed of polymerized glycoproteins, also known as mucins, and specific cell surfaces ligands [215]. However, the microorganism binding to the mucosa and the IECs is a complex process that comprises several irreversible and reversible stages. Initially, probiotics bind to the mucosa by the interplay of non-specific physical interactions and forces, e.g., Van der Waals attraction and electrostatic and hydrophobic interactions [213]. The irreversible stages involve molecular specific reactions mediated by mucus-binding proteins (MBPs) [216,217], fibronectin-binding proteins (FBPs) [218], surface-layer proteins (SLPs) [219], and non-protein molecules present on the probiotics' surface, such as teichoic acids (TA) [220] and exopolysaccharides (EPS) [221]. However, intestinal probiotic adhesion and further colonization can be compromised by competitive exclusion where intestinal bacteria compete for adhesion sites [222].
Over the years, several attempts have been made to increase the adhesion of probiotics to negatively charged intestinal mucus by coating the encapsulates with positively charged polymers such as chitosan and different types of nanomaterials [93,223,224]. In fact, strengthening mucus/polymer interactions makes it possible to form transient gels due to intermolecular entanglements between ionizable monomers and mucins. Such gels represent a clear opportunity as platforms to increase the residence time of the encapsulate carriers [93]. Similarly, hydrogen bonding, hydrophobic interaction potential, electrostatic interactions, and lectin/sugar recognition are reported to be key parameters in the design of more robust mucoadhesives [93,225,226]. Furthermore, as polymer/mucus binding at the GIT mainly proceeds by hydrogen bonding, water molecules can interact with mucus strongly, limiting polymer interactions. Thus, incorporating hygroscopic materials such as polyethylene glycol (PEG) in encapsulates has increased mucoadhesion [92]. Also, this approach has been reported to open tight epithelial junctions to improve the mucus/polymer contact area [153].

Prebiotics Co-Immobilization as an Alternative to Improve Probiotics Colonization
Prebiotics are non-viable substrates that serve as nutrients for beneficial microorganisms, including probiotic and indigenous strains [227]. An exogenous probiotic strain must compete for nutrients and space with microorganisms in the indigenous microbiome. Therefore, prebiotics have been considered alternative nutritional substrates that could potentially lower strain competition and favor colonization of probiotics [228,229]. Prebiotics such as fructooligosaccharides (FOS) [230], xylooligosaccharides (XOS) [231], galactooligosaccharides (GOS) [229], and inulin [232] have demonstrated their potential for helping overcome colonization resistance of probiotics [26]. However, detailed studies on the impact of prebiotics are rather scarce and therefore represent an opportunity to engineer next-generation probiotics.

Future Directions for Probiotic Encapsulation and Clinical Practice
From a clinical perspective, the delivery of probiotics has shown promising results in clinical trials to prevent, mitigate and treat specific diseases such as traveler's diarrhea, antibiotic-associated diarrhea, acute diarrhea in children, intestine bowel syndrome, inflammatory bowel disease, and atopic dermatitis [233]. One of the most attractive features of probiotics implementation is their possible extrapolation from the food industry to specific disease treatment without incurring further scrutiny by governmental agencies (e.g., Food and Drug Administration-FDA) since probiotics are considered functional foods and not pharmacological compounds [234,235]. However, relevant clinical data have revealed ambiguous results and a lack of data on possible side effects, recommendations on proper probiotic selection for single disease treatment, and their exact mechanism of action [236]. For this purpose, 1831 clinical trials have been conducted to better understand probiotics' interaction with the human body, as reported in the ClinicalTrials.gov database (accessed 18 January 2022).
Moreover, besides the fast-growing research on probiotics encapsulation using polymers, the translation of such technologies remains limited, as evidenced by just one clinical trial found in the ClinicalTrials.gov database (accessed 18 January 2022). Despite this limited number of studies at the clinical level, several studies conducted in vitro report on promising probiotics encapsulates capable of overcoming the GIT's harsh conditions, as demonstrated by more than 13,000 patents awarded in this field (lens.org, accessed 19 January 2022). Nevertheless, as for the clinical trials, preclinical models are also scarce, and only 32 research articles have been published to date, including the term "in vivo" (PubMed.gov, accessed 19 January 2022). This trend is exacerbated even further when the term "stimuli-responsive" is included in the patent search algorithm, as only 802 patents were available (lens.org, accessed 19 January 2022).
The limited translation of current and emerging probiotics encapsulation technologies strongly indicates that there is still a long way to go before stimuli-responsive matrices reach clinical implementation. In this regard, one of the most important obstacles to overcome is to design and manufacture cost-effective encapsulation processes, as they largely define scalability and the requirements of approved food additives [104]. Conversely, scaling up routes should be considered from the beginning of the developments such that the economic output and long-term sustainability is assured. Moreover, to facilitate complying with numerous regulatory requirements for clinical research and, ultimately, the claim substantiation and market access [237], the developments should consider stimuliresponsive materials already approved for human use.

Conclusions
Recent technological advancements in encapsulation facilitate the formulation of probiotics' site-selective delivery with high cell viability and prolonged stabilities and residence times. Among such advancements are stimuli-responsive polymeric matrices, which offer an avenue for the precise delivery of probiotics by taking advantage of changes in physicochemical conditions throughout the GIT. These include changes in pH, ionic strength, redox potential, and even mechanical stress. Among the developed matrices, hydrogels and the nanostructured platforms stand out for their ease of modification and processing, versatility to facilitate multimodal delivery, and the possibility to finely tune multi-stimuli responsiveness to address multiple components of the GIT. The most popular and studied matrices involve alginate and its derivatives coated with chitosan or gelatin, as they have proven to tolerate the harsh conditions of the GIT and maintain superior probiotics viability.
Thus far, most smart platforms for probiotics delivery take advantage of pH-responsiveness for engineering site-selective delivery vehicles. Emerging materials have considered other stimuli and, most recently, the action of enzymes either native to the GIT or added exogenously to the matrix to favor selective degradation and release at the site of the action. Besides protection of the probiotic as it transits through the GIT, sufficient host interaction is only achievable upon successful colonization of the delivered strains, determined by possible competition with indigenous microorganisms. One way to overcome this limitation is by administering prebiotics, which are nutritional substrates that favor the proliferation of beneficial microorganisms. Additionally, polymers with specific moieties can interact selectively with mucus to form transient gels that might extend the residence time. Despite the progress over the past few years, the rational design of encapsulates for targeted probiotic delivery is still in its infancy. Therefore, much work needs to be invested in elucidating the routes for developing materials that involve simple manufacturing schemes that can be scaled up to address the increasingly higher demand for these products. Also, this might help accelerate the defining of conditions for relevant pre-clinical and clinical tests.

Conflicts of Interest:
The authors declare no conflict of interest.