In this Special Issue, we focus on biomineralization/pathological biomineralization systems and the synthesis of bioinspired materials. This Special Issue promotes the current trend of “green chemistry”, and, as such, in all published papers, only aqueous solutions and eco-friendly additives were used for the production of well-characterized bioinspired materials.
This Special Issue contains four papers: three original research papers and one review. Here, a brief introduction of these papers is provided.
Kontrec et al. [1] in their paper indicate a significant contribution of initial pH to the overall effect of all parameters relevant to precipitation processes and biomineralization. This paper reports on the influence of initial pH and type of stirring on the kinetics, phase composition, size, and morphology of spontaneously precipitated calcium carbonate (CaCO3). CaCO3 is one of the most widespread biominerals formed via biomineralization in calcifying organisms. Precipitation processes are the physicochemical basis of biomineralization. The main parameter controlling the precipitation of CaCO3 is supersaturation, but other parameters, such as the concentration of constituent ions and dissolved carbon dioxide (CO2) [2], the presence of additives [3,4], temperature [5], pH [6], ionic strength [7] and hydrodynamics [8], are also known to influence and control CaCO3 precipitation and, consequently, together with the variety of biological constituents and processes, influence biomineralization. Bearing in mind that the supersaturation, ionic strength, and activity ratio of constituent ions a(Ca2+)/a(CO32−) influence the phase composition and morphology of the precipitated CaCO3, in the work presented in this paper, the initial values of these parameters in all experiments were identical.
Amongst the sixty different types of biominerals, one of the most interesting to humans is calcium phosphate (CaP), the main inorganic component of vertebrate skeletons, and it is also prominent in pathological biomineralization [9,10]. The inclusion of additives in the precipitation system affects the rate and mechanism of CaP formation as well as the properties of the formed solid phase(s). Erceg et al. [11] investigated the influence of different classes of amino acids (AAs), namely, charged (aspartic acid and lysine), polar (asparagine and serine), and non-polar (phenylalanine) amino acids, under conditions similar to physiological conditions. The observed differences in the effects that AAs exert on CaP precipitation, as well as the differences in the behavior of AAs of the same class, indicated that classification based on charge and polarity cannot satisfactorily explain the different effects. Rather, these relatively simple molecules should be studied as specific entities. The obtained results point to the likely complex role of AAs in biological mineralization but also to a rather simple method of controlling CaPs properties, which are of importance in the preparation of multifunctional bone regeneration materials.
Urolithiasis is a multifactorial disease with a high incidence and high recurrence rate, characterized by formation of solid deposits in the urinary tract. Petrović et al. [12] have presented in detail an overview of the relevant papers showing that the incidence and prevalence of urolithiasis are constantly increasing, thus presenting an important public health issue, but there is still much to be learned about the stone formation, initial crystallization, and interaction of crystals and epithelial cells. They pointed out that there is a lack of understanding about the bioactive component of plant extracts as well as their safety. Moreover, some plant extracts have been shown to be damaging to the kidneys [13]. Future research should address these issues in order to understand if these therapeutics even reach the kidneys in an in vivo model.
Šafranko et.al. [14] proposed the optimal conditions to obtain the maximum content of the two most dominant calcium oxalate hydrate phases (monohydrate, CaC2O4•H2O, COM, and dihydrate, CaC2O4•2H2O, COD) using response surface methodology (RSM). In their study, the influence of temperature, system pH, and the presence of gallic acid on the individual hydrate phase of calcium oxalate formation was investigated. Gallic acid is one of the most abundant phenolic acids, and it is widely distributed throughout the plant kingdom where it is present either in free form or, more commonly, as a constituent of tannins [15]. Regarding its biological activity, gallic acid exerts antibacterial, antiviral, anti-inflammatory, and antioxidant effects [16,17].
By performing statistical analysis, it was observed that a higher temperature, lower system pH, and lower amounts of added gallic acid promoted the formation of the COM hydrate phase of calcium oxalate. However, a lower temperature, higher system pH, and higher amounts of added gallic acid favored the formation of COD. According to the desirability function approach, the optimal conditions for obtaining the maximum content of COM and COD were determined and experimentally verified, showing good agreement with the predicted data with suitable deviations of ±5%. These findings could contribute to efficient process optimization, thereby allowing for specific hydrate phases of calcium oxalate to be obtained while elucidating the possible effects of the operating conditions on crystal formation in the pathological biomineralization of kidney stones.
The editors thank all of the authors who participated in this Special Issue, as well as the reviewers who provided constructive comments on all submissions. We would like to thank the editorial staff at Crystals for their fast and professional handling of all submissions.
Biomineralization/pathological biomineralization is an important and interesting topic, and green synthesis is a novel and exciting direction for bio-inspired material production. We hope that this Special Issue will serve as a useful reference.
Funding
This research received no external funding.
Conflicts of Interest
The authors declare no conflict of interest.
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