Extended and oriented nanostructures are desirable for many applications, but direct fabrication of complex nanostructures with controlled crystalline morphology, orientation and surface architectures remains a significant challenge. Here we report a low-temperature, environmentally benign, solution-based approach for the preparation of complex and oriented ZnO nanostructures, and the systematic modification of their crystal morphology. Using controlled seeded growth and citrate anions that selectively adsorb on ZnO basal planes as the structure-directing agent, we prepared large arrays of oriented ZnO nanorods with controlled aspect ratios, complex film morphologies made of oriented nanocolumns and nanoplates (remarkably similar to biomineral structures in red abalone shells) and complex bilayers showing in situ column-to-rod morphological transitions. The advantages of some of these ZnO structures for photocatalytic decompositions of volatile organic compounds were demonstrated. The novel ZnO nanostructures are expected to have great potential for sensing, catalysis, optical emission, piezoelectric transduction, and actuations.

Complex and oriented ZnO nanostructures

Nanoscale hydroxyapatite particles for bone tissue engineering

Synthesis methods for nanosized hydroxyapatite with diverse structures.

A targeted drug delivery system is the need of the hour. Guiding magnetic iron oxide nanoparticles with the help of an external magnetic field to its target is the principle behind the development of superparamagnetic iron oxide nanoparticles (SPIONs) as novel drug delivery vehicles. SPIONs are small synthetic γ-Fe2O3 (maghemite) or Fe3O4 (magnetite) particles with a core ranging between 10 nm and 100 nm in diameter. These magnetic particles are coated with certain biocompatible polymers, such as dextran or polyethylene glycol, which provide chemical handles for the conjugation of therapeutic agents and also improve their blood distribution profile. The current research on SPIONs is opening up wide horizons for their use as diagnostic agents in magnetic resonance imaging as well as for drug delivery vehicles. Delivery of anticancer drugs by coupling with functionalized SPIONs to their targeted site is one of the most pursued areas of research in the development of cancer treatment strategies. SPIONs have also demonstrated their efficiency as nonviral gene vectors that facilitate the introduction of plasmids into the nucleus at rates multifold those of routinely available standard technologies. SPION-induced hyperthermia has also been utilized for localized killing of cancerous cells. Despite their potential biomedical application, alteration in gene expression profiles, disturbance in iron homeostasis, oxidative stress, and altered cellular responses are some SPION-related toxicological aspects which require due consideration. This review provides a comprehensive understanding of SPIONs with regard to their method of preparation, their utility as drug delivery vehicles, and some concerns which need to be resolved before they can be moved from bench top to bedside.

/pdf/superparamagnetic-iron-oxide-nanoparticles-magnetic-r8ry68tylh.pdf

Superparamagnetic iron oxide nanoparticles: magnetic nanoplatforms as drug carriers

Calcium orthophosphates are the main mineral constituents of bones and teeth, and there is great interest in understanding the physical mechanisms that underlie their growth, dissolution, and phase stability. By definition, all calcium orthophosphates consist of three major chemical elements: calcium (oxidation state +2), phosphorus (oxidation state +5), and oxygen (oxidation state −2).1 The orthophosphate group (PO43−) is structurally different from meta (PO3−), pyro (P2O74−), and poly (PO3)nn−. In this review, only calcium orthophosphates will be discussed. The chemical composition of many calcium orthophosphates includes hydrogen, either as an acidic orthophosphate anion such as HPO42− or H2PO4−, and/or incorporated water as in dicalcium phosphate dihydrate (CaHPO4 · 2H2O).1 Most calcium orthophosphates are sparingly soluble in water, but all dissolve in acids; the calcium to phosphate molar ratios (Ca/P) and the solubilities are important parameters to distinguish between the phases (Table 1) with crystallographic data summarized in Table 2. In general, the lower the Ca/P ratio, the more acidic and soluble the calcium phosphate phase.2 It is now generally recognized that the crystallization of many calcium phosphates involves the formation of metastable precursor phases that subsequently dissolve as the precipitation reactions proceed. Thus, complex intermediate phases can participate in the crystallization process. Moreover, the in vivo presence of small peptides, proteins, and inorganic additives other than calcium and phosphate has a considerable influence on crystallization, making it difficult to predict the possible phases that may form.3 Studies of apatite mineral formation are complicated by the possibility of forming several calcium phosphate phases. The least soluble, hydroxyapatite (HAP), is preferentially formed under neutral or basic conditions. In more acidic solutions, phases such as brushite (DCPD) and octacalcium phosphate (OCP) are often encountered. Even under ideal HAP precipitation conditions, the precipitates are generally nonstoichiometric, suggesting the formation of calcium-deficient apatites. Both DCPD and OCP have been implicated as possible precursors to the formation of apatite. This may occur by the initial precipitation of DCPD and/or OCP followed by transformation to a more apatitic phase. Although DCPD and OCP are often detected during in vitro crystallization, in vivo studies of bone formation rarely show the presence of these acidic calcium phosphate phases. In the latter case, the situation is more complicated, since a large number of ions and molecules are present that can be incorporated into the crystal lattice or adsorbed at the crystallite surfaces. In biological apatite, DCPD and OCP are usually detected only during pathological calcification, where the pH is often relatively low. In normal in vivo calcifications, these phases have not been found, suggesting the involvement of other precursors or the formation of an initial amorphous calcium phosphate phase (ACP) followed by transformation to apatite.



Table 1

Ca/P Molar Ratios, Chemical Formulas, and Solubilitiesa of Some Calcium Orthophosphate Minerals1,3,4





Table 2

Crystallographic Data of Calcium Orthophosphates1,4,5



In this review, we will discuss some important parameters related to crystal nucleation and growth/dissolution including the supersaturation/undersaturation, pH, ionic strength and the ratio of calcium to phosphate activities (Table 3). We then focus on the dynamics of crystallization/dissolution in the presence of additive molecules pertinent to biogenic calcium phosphate minerals.



Table 3

Crystal Growth Controls and Their Effect on the Bulk Solution and the Crystal Surfaces6




2. Biologically Related Calcium Phosphate Phases
2.1. Structure, Composition, and Phase Stability


2.1.1. Amorphous Calcium Phosphate (ACP) 
During the synthesis of HAP crystals through the interaction of calcium and phosphate ions in neutral to basic solution, a precursor amorphous phase is formed that is structurally and chemically distinct from HAP.7 However, calculations have shown that the phase consisted of individual or groups of HAP unit cells.8 Chemical analysis of the precursor phase indicated this noncrystalline phase to be a hydrated calcium phosphate (Ca3(PO4)2 · xH2O) with a Ca/P ratio 1.50,8 consisting of roughly spherical Ca9(PO4)6 “Posner’s clusters” (PC) close-packed to form larger spherical particles with water in the interstices.9 PCs appeared to be energetically favored in comparison to alternative candidates including Ca3(PO4)2 and Ca6(PO4)4 clusters.10 The structure of PCs in isolated form is notably different from that in a HAP environment.11 In particular, the chirality feature of PCs found in the HAP environment is suggested to disappear in an isolated form and in aqueous solution. The reconsideration of PCs as possible components in the actual structural model of ACP resulted from the cluster growth model of the HAP crystal.12 Ab initio calculations confirmed that stable isomers exist on the [Ca3(PO4)2]3 potential energy surface (PES).12,13 These isomers correspond to compact arrangements, i.e., arrangements in which the Ca and PO4 are disposed closely together. Their geometries are compatible with the terms “roughly spherical” used in Posner’s hypothesis. The calculations performed on the monomer and dimer PES revealed that the relative energies of the different isomers are governed by a specific bonding pattern in which a calcium atom interacts with two PO43− groups, forming four CaO bonds.12,13 The compact isomers on the trimer PES are energetically favored in comparison to monomer or dimer isomers. This is rationalized by the appearance of a specific bonding pattern for the trimer case in which a calcium forms six CaO bonds with six different PO4 groups. This type of bonding in encountered in HAP.13

It is now generally agreed that, both in vitro and in vivo, precipitation reactions at sufficiently high supersaturation and pH result in the initial formation of an amorphous calcium phosphate with a molar calcium/phosphate ratio of about 1.18–2.50. The chemical composition of ACP is strongly dependent on the solution pH: ACP phases with Ca/P ratios in the range of 1.18:1 precipitated at pH 6.6 to 1.53:1 at pH 11.7 and even as high as 2.5:1.4 Two amorphous calcium phosphates, ACP1 and ACP2, have been reported with the same composition, but differing in morphology and solubility.14,15 The formation of ACP precipitate with little long-range order tends to consist of aggregates of primary nuclei (roughly spherical clusters) with composition Ca9(PO4)65 dependent on the conditions of formation. It hydrolyzes almost instantaneously to more stable phases. These amorphous clusters served as seeds during HAP crystallization via a stepwise assembly process12 and were presumed to pack randomly with respect to each other,16 forming large 300–800 A spheres. Recent experimental studies found that ACP has definite local atomic microcrystalline order rather than a random network structure. NMR of thoroughly dried ACP suggests that the tightly held water resides in the interstices between clusters,17 but these are probably not of intrinsic importance in the structure of ACP. It is well-known that ACP contains 10–20% by weight of tightly bound water, which is removed by vacuum drying at elevated temperature.9 However, drying does not alter the calcium and phosphorus atomic arrangement. The side band intensities of dried ACP suggest that its chemical shift anisotropy is similar to or identical with that of normal ACP.17 ACP has an apatitic short-range structure, but with a crystal size so small that it appears to be amorphous by X-ray analysis. This is supported by extended X-ray absorption fine structure (EXAFS) on biogenic and synthetic ACP samples.18–20

The CaP amorphous phase transforms to HAP microcrystalline in the presence of water. The lifetime of the metastable amorphous precursor in aqueous solution was reported to be a function of the presence of additive molecules and ions, pH, ionic strength, and temperature.21 The transformation kinetics from ACP to HAP, which can be described by a ”first-order” rate law, is a function only of the pH of the mediating solution at constant temperature. The solution-mediated transformation depends upon the conditions which regulate both the dissolution of ACP and the formation of the early HAP nuclei.22 Tropp et al. used 31P NMR to demonstrate that the strength of ACP side bands is due to a characteristic structural distortion of unprotonated phosphate and not to a mixture of protonated and unprotonated phosphates,17 suggesting that ACP could contain substantial amounts of protonated phosphate not in the form of any known phase of calcium phosphate crystals. Yin and Stott suggested that, in the transformation from ACP to HAP, ACP need only dissociate into clusters rather than undergo complete ionic solvation. The cluster with C1 symmetry is the most stable isomer in vacuum. The interaction of Posner’s cluster with sodium ions and especially with protons leads to a considerable stability increase, and surprisingly, the cluster with six protons and six OH− recovers the C3 symmetry and similar atomic arrangement that it has as a structural unit in the HAP crystal. This may be a key factor in the transformation from ACP to HAP crystal.23

In general, ACP is a highly unstable phase that hydrolyzes almost instantaneously to more stable phases. In the presence of other ions and macromolecules or under in vivo conditions, ACP may persist for appreciable periods3 and retain the amporphous state under some specific experimental conditions.24

/pdf/calcium-orthophosphates-crystallization-and-dissolution-1c1riyx5dd.pdf

Calcium orthophosphates: crystallization and dissolution.

Nanosized Hydroxyapatite Precipitation from Homogeneous Calcium/Citrate/Phosphate Solutions Using Microwave and Conventional Heating

Mechanical properties of visible light-cured resins reinforced with hydroxyapatite for dental restoration.

The adsorption of citrate on hydroxyapatite (HA) has been studied at 25°C, pH 6 and 8, and at 37°C, pH 8 The experimental results agree with the Langmuir adsorption model at low citrate concentrations, with similar values of the affinity coefficient K  The amount adsorbed Q decreases with the increase of pH and the rise in temperature However, the fraction of sites occupied on the HA surface is the same at both values of pH On the other hand, the desorption is higher at pH 8 and zeta potential values of suspensions prepared from HA preadsorbed with citrate are negative and decrease with the rise of pH The adsorption takes place by ionic exchange of phosphate by citrate ions at the solid-solution interface, caused by a higher affinity of citrate than phosphate species for the Ca-sites on the HA surface To explain experimental data we propose a model where citrate species interact in different ways: cit 3− interacts weakly in a bidentate manner (1 citrate per 2 Ca sites), whereas the Hcit 2− interaction is stronger (1 citrate per 1 Ca site) than the previous one, possibly due to certain resonance between a monodentate (using 1 -COO − group) and a surface–chelate interaction (using 2 -COO − groups)

The Role of pH in the Adsorption of Citrate Ions on Hydroxyapatite

The interpretation of the precipitation data of hydroxyapatite in MSMPR systems presents several problems due to the lack of consistency of the classical nucleation-growth-agglomeration mechanism in the analysis of the Crystal Size Distribution In the proposed model, the mechanism of formation of particles starts with a nucleation episode, followed by the aggregation of supercritical nuclei ruled by surface energy excess, which counterbalance the repulsive forces between particles The aggregates agglomerate, forming solid bridges, and the agglomerates continue to grow as distinct particles due to repulsive forces

A. López-Macipe

Papers

Nanosized Hydroxyapatite Precipitation from Homogeneous Calcium/Citrate/Phosphate Solutions Using Microwave and Conventional Heating

Mechanical properties of visible light-cured resins reinforced with hydroxyapatite for dental restoration.

The Role of pH in the Adsorption of Citrate Ions on Hydroxyapatite

Hydroxyapatite precipitation: A case of nucleation-aggregation-agglomeration-growth mechanism

Calcium carbonate precipitation from aqueous solutions containing Aerosol OT